Product Details

SNP ID
rs147030072
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:97757200 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACGGGTTGTAGGTCTGTCCCAAGT[A/C]GTCAGCTGGACTGGAGGTGGAGGGA
Phenotype
MIM: 615659
Polymorphism
A/C, Transversion 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 5954 Missense Mutation NP_056163.1
XM_005263909.1 5954 Missense Mutation XP_005263966.1
XM_005263910.1 5954 Missense Mutation XP_005263967.1
XM_005263911.1 5954 Missense Mutation XP_005263968.1
XM_005263912.3 5954 Missense Mutation XP_005263969.1
XM_011510869.1 5954 Missense Mutation XP_011509171.1

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