Product Details

SNP ID
rs143618766
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:150803455 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TACGAGAAACGGGGTGGTACATACT[C/G]GGTAAGTTCAGGGAAGGGCATGGGA
Phenotype
MIM: 610334 MIM: 610385
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
TMEM176A PubMed Links

Gene Details

Gene
TMEM176A
Gene Name
transmembrane protein 176A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018487.2 554 Missense Mutation TCG,TGG S114W NP_060957.2
XM_011516376.2 554 Missense Mutation TCG,TGG S131W XP_011514678.1
XM_011516377.2 554 Missense Mutation TCG,TGG S131W XP_011514679.1
XM_011516378.2 554 Missense Mutation TCG,TGG S131W XP_011514680.1
XM_017012393.1 554 Missense Mutation TCG,TGG S114W XP_016867882.1
Gene
TMEM176B
Gene Name
transmembrane protein 176B
There are no transcripts associated with this gene.

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