Product Details

SNP ID
rs189771808
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:97757363 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAATGGAGTGGTGGACCACAGGCC[A/G]CTGGTGTTACCGAGGACCGACTGCG
Phenotype
MIM: 615659
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TMEM131 PubMed Links

Gene Details

Gene
TMEM131
Gene Name
transmembrane protein 131
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015348.1 5791 Silent Mutation AGC,AGT S1796S NP_056163.1
XM_005263909.1 5791 Silent Mutation AGC,AGT S1813S XP_005263966.1
XM_005263910.1 5791 Silent Mutation AGC,AGT S1812S XP_005263967.1
XM_005263911.1 5791 Silent Mutation AGC,AGT S1774S XP_005263968.1
XM_005263912.3 5791 Silent Mutation AGC,AGT S1757S XP_005263969.1
XM_011510869.1 5791 Silent Mutation AGC,AGT S1751S XP_011509171.1

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