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SNP ID:
rs75932628
Gene
LOC105375056 TREM2 TREML1
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

Assay ID C_100657057_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 605086 MIM: 609714

Literature Links:

 LOC105375056 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.00)
(1.00)
Caucasian - Not Available CEPH (CEU) - Not Available
EAS
T (0.00)
(1.00)
African American - Not Available YRI (Yoruba) - Not Available
SAS
T (0.00)
(1.00)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
T (0.00)
(1.00)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
T (0.01)
(0.99)
AMR
T (0.00)
(1.00)
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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