Product Details

SNP ID
rs201625536
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:97758979 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCGACTCCCAAAGGTATGAAGGGC[C/T]ACTATTAAACTCGTTCCAGCTCCTC
Phenotype
MIM: 615659
Polymorphism
C/T, 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 5684 Missense Mutation AGC,GGC S1761G NP_056163.1
XM_005263909.1 5684 Missense Mutation AGC,GGC S1778G XP_005263966.1
XM_005263910.1 5684 Missense Mutation AGC,GGC S1777G XP_005263967.1
XM_005263911.1 5684 Missense Mutation AGC,GGC S1739G XP_005263968.1
XM_005263912.3 5684 Missense Mutation AGC,GGC S1722G XP_005263969.1
XM_011510869.1 5684 Missense Mutation AGC,GGC S1716G XP_011509171.1

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