Product Details

SNP ID: rs199795809
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:41158767 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTTTTCCTCCCATCATCTTCCTTCA[C/T]GTGTCTCTCAGCCCTGCAATAGTCC
Phenotype: MIM: 605086 MIM: 609714
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: LOC105375056 PubMed Links

Gene Details

Gene: LOC105375056
Gene Name: uncharacterized LOC105375056

There are no transcripts associated with this gene.

Gene: TREM2
Gene Name: triggering receptor expressed on myeloid cells 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271821.1	794	Missense Mutation	ATG,GTG	M166V	NP_001258750.1
NM_018965.3	794	Silent Mutation	ACA,ACG	T230T	NP_061838.1
XM_006715116.3	794	Silent Mutation	ACA,ACG	T143T	XP_006715179.1

Gene: TREML1
Gene Name: triggering receptor expressed on myeloid cells like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271807.1	794	Intron			NP_001258736.1
NM_001271808.1	794	Intron			NP_001258737.1
NM_178174.3	794	Intron			NP_835468.1
XM_017010822.1	794	Intron			XP_016866311.1
XM_017010823.1	794	Intron			XP_016866312.1
XM_017010824.1	794	Intron			XP_016866313.1
XM_017010825.1	794	Intron			XP_016866314.1

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