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- SNP ID:
- rs75932628
- Gene
-
LOC105375056TREM2TREML1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.6: 41161514 - 41161514 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
TCCCAGCTGGCGGCACCAGGCCTTG[C/T]GCCTCCCCCAGTGCTTCATGGAGTC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605086
MIM: 609714
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Literature Links: |
LOC105375056 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| LOC105375056 - uncharacterized LOC105375056 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| TREM2 - triggering receptor expressed on myeloid cells 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001271821.1 | 244 | Missense Mutation | NP_001258750.1 | |||
| NM_018965.3 | 244 | Missense Mutation | NP_061838.1 | |||
| XM_006715116.3 | 244 | Intron | XP_006715179.1 | |||
| TREML1 - triggering receptor expressed on myeloid cells like 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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