Product Details

SNP ID
rs202229445
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:97758951 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCCAGGAAGGACTGGGATCTGTC[A/G]CTGGCGACTCCCAAAGGTATGAAGG
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 5712 Missense Mutation GCG,GTG A1770V NP_056163.1
XM_005263909.1 5712 Missense Mutation GCG,GTG A1787V XP_005263966.1
XM_005263910.1 5712 Missense Mutation GCG,GTG A1786V XP_005263967.1
XM_005263911.1 5712 Missense Mutation GCG,GTG A1748V XP_005263968.1
XM_005263912.3 5712 Missense Mutation GCG,GTG A1731V XP_005263969.1
XM_011510869.1 5712 Missense Mutation GCG,GTG A1725V XP_011509171.1

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