Product Details

SNP ID
rs200561143
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:97757157 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGGTCCGAGCTTCTTCTTCCAATC[A/G]TGGGGCTCCATATCCGCCACGGGTT
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 5997 Missense Mutation NP_056163.1
XM_005263909.1 5997 Missense Mutation XP_005263966.1
XM_005263910.1 5997 Missense Mutation XP_005263967.1
XM_005263911.1 5997 Missense Mutation XP_005263968.1
XM_005263912.3 5997 Missense Mutation XP_005263969.1
XM_011510869.1 5997 Missense Mutation XP_011509171.1

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