System Message

OK

Cancel

LOADING

Gene Symbol:: KRAS
Entrez Gene ID: 3845
Gene Name:: KRAS proto-oncogene, GTPase
Gene Aliases: C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A, K-RAS4B, KI-RAS, KRAS1, KRAS2, NS, NS3, RALD, RASK2
Gene Chromosome Location: Chr.12: on Build GRCh38
UniGene: Hs.505033
Species:: Human
Primer Chromosome Location: Chr.12: 25245217-25245462 on Build GRCh38 View in UCSC browser
Amplicon Length: 246
Primer Sequences: Log in to view
Ampliseq ID's

Genomic Map
Assay Details
More Information

Assay Details

Gene Information

Phenotype

Literature Links:

KRAS PubMed Links

SNP ID

rs753482944

rs193929331

rs755397559

rs104894365

rs121913530

rs112445441

rs121913529

rs771188508

rs766045811

rs749956607

rs397517040

rs755305645

rs104894361

rs377354475

rs780220170

rs747140926

rs794727277

rs534412138

rs104894366

rs113623140

rs397517039

rs147406419

rs750997877

rs727503109

rs730880472

rs754767487

rs121913538

rs779370636

rs776785730

rs727503110

rs370230526

rs121913535

rs606231202

rs779282636

rs121913236

rs748695743

Back To Top

More Information

Set Membership:

Between 200-400 bp

Panther Classification:

Molecular Function -

small GTPase

Gene Ontology Categories:

Function(s) Process(es)

Format:

Each primer will be delivered in a single tube, dried-down

Quick Reference Guide

Primer Designer^™ Tool Quick Reference

Back To Top

Primer ID	Hs00679698_CE
Primer 5'-tail Option
Purification
Primer Pair /FWD/REV
Synthesis Scale	25 nmol
Availability	Made To Order
Catalog #'s	A15629,A15630
Price

1000Genome	Applied Biosystems^®	HapMap
Global - Not Available	Caucasian - Not Available	CEPH (CEU) - Not Available
EAS - Not Available	African American - Not Available	YRI (Yoruba) - Not Available
SAS - Not Available	Chinese - Not Available	CHB (Han Chinese) - Not Available
AFR - Not Available	Japanese - Not Available	JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available

1000Genome	Applied Biosystems^®	HapMap
Global - Not Available	Caucasian - Not Available	CEPH (CEU) - Not Available
EAS - Not Available	African American - Not Available	YRI (Yoruba) - Not Available
SAS - Not Available	Chinese - Not Available	CHB (Han Chinese) - Not Available
AFR - Not Available	Japanese - Not Available	JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available

1000Genome	Applied Biosystems^®	HapMap
Global - Not Available	Caucasian - Not Available	CEPH (CEU) - Not Available
EAS - Not Available	African American - Not Available	YRI (Yoruba) - Not Available
SAS - Not Available	Chinese - Not Available	CHB (Han Chinese) - Not Available
AFR - Not Available	Japanese - Not Available	JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available

1000Genome	Applied Biosystems^®	HapMap
Global - Not Available	Caucasian - Not Available	CEPH (CEU) - Not Available
EAS - Not Available	African American - Not Available	YRI (Yoruba) - Not Available
SAS - Not Available	Chinese - Not Available	CHB (Han Chinese) - Not Available
AFR - Not Available	Japanese - Not Available	JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available

KRAS
	Accession	Protein	COSMIC ID	Mutation	AA
RefSeq	NM_004985.4	NP_004976.2	1318028	c.108A>G	p.I36M
			20818	c.57G>T	p.L19F
			27637	c.100C>T	p.P34S
			5751853	c.75G>GT	p.N26fs*1
			1169214	c.101C>T	p.P34L
			523	c.36T>C	p.G12G
			5415923	c.37_39GGC>AAG	p.G13K
			87280	c.38_39GC>AA	p.G13E
			1360888	c.28G>A	p.G10R
			24602	c.15A>T	p.K5N
			30566	c.35_36GT>AG	p.G12E
			5945259	c.79C>T	p.H27Y
			531	c.38_39GC>AT	p.G13D
			4387522	c.35_36GT>TG	p.G12V
			1605974	c.30A>C	p.G10G
			6009012	c.2T>C	p.M1T
			535	c.39C>G	p.G13G
			506	c.15A>C	p.K5N
			3727814	c.91G>A	p.E31K
			6474353	c.8A>G	p.E3G
			12654	c.30_31insGGA	p.G10_A11insG
			5369708	c.32_34CTG>TTT	p.A11_G12>VC
			5751775	c.34_35insA	p.G12fs*22
			514	c.34_35GG>CT	p.G12L
			132886	c.13A>G	p.K5E
			6930965	c.101C>G	p.P34R
			5752016	c.33_34insA	p.G12fs*22
			4855091	c.62T>G	p.I21R
			524	c.36T>A	p.G12G
			219781	c.39_40insGGC	p.G13_V14insG
			4169161	c.59C>T	p.T20M
			87281	c.36_37TG>AT	p.G13C
			6867641	c.101C>A	p.P34Q
			13643	c.34_35GG>AA	p.G12N
			541	c.52G>A	p.A18T
			5945943	c.29_29delG	p.G10fs*5
			53283	c.37_38GG>AA	p.G13N
			249887	c.41T>G	p.V14G
			30567	c.38_39GC>AG	p.G13E
			6904437	c.34_35GG>GT	p.G12V
			6978960	c.84T>G	p.F28L
			1666928	c.48_49insTGG	p.K16_S17insW
			6022433	c.37_38insCTGGTG	p.G12_G13insAG
			507	c.24A>G	p.V8V
			33721	c.64C>T	p.Q22*
			7335344	c.109G>A	p.E37K
			6921315	c.76A>T	p.N26Y
			12655	c.36_37insGGT	p.G12_G13insG
			1685355	c.37_38GG>TT	p.G13F
			5546585	c.40G>T	p.V14L
			1163765	c.47A>G	p.K16R
			515	c.35_36GT>TC	p.G12V
			536	c.39C>T	p.G13G
			3735049	c.45C>T	p.G15G
			7409996	c.77A>T	p.N26I
			4696724	c.45C>G	p.G15G
			12721	c.38_39GC>TT	p.G13V
			19907	c.67C>A	p.L23I
			6853642	c.34_35insTGG	p.A11_G12insV
			521	c.35G>A	p.G12D
			5413585	c.35_36GT>CA	p.G12A
			87301	c.33_34insGGAGCT	p.A11_G12insGA
			1360858	c.103A>G	p.T35A
			6948221	c.31_35GCTGG>ACTGA	p.A11_G12>TD
303833	c.36_37insGCG	p.G12_G13insA
529	c.37G>C	p.G13R
1562184	c.25G>A	p.V9I
7335322	c.45C>A	p.G15G
6438042	c.17T>A	p.L6H
110699	c.29G>A	p.G10E
51382	c.50G>A	p.S17N
36281	c.34_36GGT>TGG	p.G12W
12705	c.27_28insGTA	p.V9_G10insV
1168054	c.90C>A	p.D30E
12722	c.40G>A	p.V14I
4745557	c.36_37TG>AC	p.G13R
522	c.35G>C	p.G12A
303853	c.68T>G	p.L23R
87313	c.71T>A	p.I24N
4384683	c.99T>G	p.D33E
6950487	c.33_34TG>CT	p.G12C
1360871	c.60G>A	p.T20T
5479419	c.111+6T>C	p.?
530	c.38_39GC>TG	p.G13V
7335340	c.73C>T	p.Q25*
328030	c.33T>C	p.A11A
1562186	c.35_36insAGCTGG	p.G12_G13insAG
6438043	c.1-11G>A	p.?
1159170	c.36T>G	p.G12G
534	c.38G>T	p.G13V
1256064	c.106A>T	p.I36L
513	c.34_36GGT>TGC	p.G12C
519	c.35_36GT>AA	p.G12E
539	c.44G>A	p.G15D
7409178	c.34_35GG>GA	p.G12D
6937870	c.111+1G>A	p.?
527	c.37G>T	p.G13C
544	c.65A>G	p.Q22R
14209	c.35_36GT>AC	p.G12D
7335309	c.14A>G	p.K5R
6269668	c.26T>A	p.V9D
5985091	c.37_38GG>CC	p.G13P
6903502	c.77A>G	p.N26S
5347015	c.20T>G	p.V7G
6438040	c.3G>A	p.M1I
511	c.32C>T	p.A11V
12703	c.57G>C	p.L19F
520	c.35G>T	p.G12V
26146	c.91G>C	p.E31Q
6945837	c.75G>C	p.Q25H
1360856	c.105A>C	p.T35T
540	c.49A>G	p.S17G
5879376	c.38_39insTGG	p.G13_V14insG
528	c.37G>A	p.G13S
1511785	c.99T>A	p.D33E
545	c.66G>A	p.Q22Q
99692	c.83T>C	p.F28S
512	c.34_35GG>TT	p.G12F
12704	c.80A>T	p.H27L
517	c.34G>A	p.G12S
537	c.39C>A	p.G13G
49167	c.57_58GA>TG	p.L19_T20>FA
6238199	c.3G>T	p.M1I
5945990	c.65A>T	p.Q22L
525	c.37_38GG>AT	p.G13I
542	c.53C>A	p.A18D
938160	c.69A>G	p.L23L
6955152	c.66G>T	p.Q22H
249888	c.34_36GGT>AGA	p.G12R
7335302	c.41T>C	p.V14A
30568	c.38_40GCG>ACA	p.G13_V14>DI
6022434	c.40_41insGCG	p.G13_V14insG
532	c.38G>A	p.G13D
5490624	c.53C>G	p.A18G
509	c.27T>C	p.V9V
1666974	c.37_38GG>TA	p.G13Y
3384260	c.31G>A	p.A11T
1166617	c.31_32insGAG	p.G10_A11insG
516	c.34G>T	p.G12C
1716372	c.34_36GGT>CTG	p.G12L
3735050	c.53C>T	p.A18V
538	c.43G>A	p.G15S
518	c.34G>C	p.G12R
87289	c.58A>T	p.T20S
6934711	c.7G>T	p.E3*
543	c.64C>A	p.Q22K
6254986	c.100C>A	p.P34T
49168	c.35G>M	p.G12X
526	c.37_39GGC>CGT	p.G13R
25081	c.34_35GG>TA	p.G12Y
30620	c.19G>A	p.V7M
7335307	c.34_35GG>CA	p.G12H
938161	c.59C>G	p.T20R
4589939	c.7_8insT	p.E3fs*3
6903500	c.5C>T	p.T2I
6959653	c.34_35GG>TC	p.G12S
14208	c.104C>T	p.T35I
6438039	c.22G>A	p.V8I
6024195	c.29G>T	p.G10V
533	c.38G>C	p.G13A
34144	c.34_35GG>AT	p.G12I
7335388	c.43G>T	p.G15C
510	c.31G>C	p.A11P
12657	c.35delG	p.G12fs*3
NM_033360.3	NP_203524.1	6867640	c.101C>A	p.P34Q
		4169156	c.50G>A	p.S17N
		4384684	c.43G>A	p.G15S
		6474354	c.3G>A	p.M1I
		2202573	c.53C>A	p.A18D
		4696723	c.45C>G	p.G15G
		1135366	c.35G>A	p.G12D
		6238198	c.3G>T	p.M1I
		1360868	c.65A>G	p.Q22R
		6937869	c.111+1G>A	p.?
		1159169	c.36T>G	p.G12G
		6955151	c.66G>T	p.Q22H
		4169160	c.59C>T	p.T20M
		5490623	c.53C>G	p.A18G
		3384257	c.38G>C	p.G13A
		4745556	c.36_37TG>AC	p.G13R
		6537633	c.33T>C	p.A11A
		6254985	c.100C>A	p.P34T
		1360869	c.64C>A	p.Q22K
		1152506	c.34G>A	p.G12S
		5374884	c.34_35GG>AT	p.G12I
		1562183	c.25G>A	p.V9I
		4169150	c.91G>A	p.E31K
		1166616	c.31_32insGAG	p.G10_A11insG
		5751852	c.75G>GT	p.N26fs*1
		1605973	c.30A>C	p.G10G
		6072204	c.34_35GG>TA	p.G12Y
		1140135	c.34_35GG>TT	p.G12F
		1360859	c.101C>T	p.P34L
		6978959	c.84T>G	p.F28L
		6853641	c.34_35insTGG	p.A11_G12insV
		6934710	c.7G>T	p.E3*
		5479418	c.111+6T>C	p.?
		1157797	c.34G>C	p.G12R
		1562185	c.35_36insAGCTGG	p.G12_G13insAG
		6951529	c.40_41insGCG	p.G13_V14insG
		4384682	c.99T>G	p.D33E
		6474352	c.8A>G	p.E3G
		5752015	c.33_34insA	p.G12fs*22
		1212766	c.57G>T	p.L19F
		1605975	c.13A>G	p.K5E
		6914042	c.38_39GC>AA	p.G13E
		2202572	c.68T>G	p.L23R
		1140136	c.34G>T	p.G12C
		1360866	c.69A>G	p.L23L
		3772370	c.36T>C	p.G12G
		1360887	c.28G>A	p.G10R
		1152504	c.38G>T	p.G13V
		6948220	c.31_35GCTGG>ACTGA	p.A11_G12>TD
		4389083	c.53C>T	p.A18V
		1256063	c.106A>T	p.I36L
		6921314	c.76A>T	p.N26Y
		1140133	c.35G>T	p.G12V
		1360855	c.105A>C	p.T35T
		6697729	c.36T>A	p.G12G
		1152505	c.37G>T	p.G13C
		1511784	c.99T>A	p.D33E
		6950486	c.33_34TG>CT	p.G12C
		6961527	c.38_39GC>TG	p.G13V
		6474350	c.29G>T	p.G10V
		5751774	c.34_35insA	p.G12fs*22
		1318027	c.108A>G	p.I36M
		1360857	c.103A>G	p.T35A
		1140134	c.35G>C	p.G12A
6930964	c.101C>G	p.P34R
6903499	c.5C>T	p.T2I
1360882	c.41T>G	p.V14G
4169138	c.29G>A	p.G10E
6945836	c.75G>C	p.Q25H
4387521	c.35_36GT>TG	p.G12V
6269667	c.26T>A	p.V9D
3384258	c.37G>C	p.G13R
1152501	c.71T>A	p.I24N
1360876	c.57G>C	p.L19F
4169139	c.44G>A	p.G15D
1152503	c.39C>T	p.G13G
1360883	c.40G>A	p.V14I
6903501	c.77A>G	p.N26S
6959652	c.34_35GG>TC	p.G12S
4387523	c.34_35GG>CT	p.G12L
5879375	c.38_39insTGG	p.G13_V14insG
1140132	c.38G>A	p.G13D
6919675	c.38_39GC>TT	p.G13V
4855090	c.62T>G	p.I21R
3384259	c.31G>A	p.A11T
1152502	c.59C>G	p.T20R
XM_006719069.3	XP_006719132.1	-	-	-
XM_011520653.2	XP_011518955.1	-	-	-
XM_017019292.1	XP_016874781.1	-	-	-
XM_017019293.1	XP_016874782.1	-	-	-
GenBank	AF493917.1	AAM12631.1	-	-	-
	AK292510.1		-	-	-
	BC013572.2	AAH13572.1	-	-	-
	BC029545.1		-	-	-
	BT007153.1	AAP35817.1	-	-	-
	ENST00000311936.0		-	-	-
	M17087.1	AAA36555.1	-	-	-
	M35504.1	AAA35689.1	-	-	-
	M35505.1	AAA35690.1	-	-	-
	M54968.1	AAB41942.1	-	-	-

System Message

Genomic Map

Assay Details

Gene Information

Phenotype

Literature Links:

SNP ID

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count

Allele Nomenclature

Chromosome Location

Allele Frequency

Submission count