Product Details

SNP ID
rs201320556
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:97757121 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATTTAATTCTCGTGAGGAAAGTGC[A/G]AATTAGACCAAGGGTCCGAGCTTCT
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 6033 Missense Mutation TCG,TTG S1877L NP_056163.1
XM_005263909.1 6033 Missense Mutation TCG,TTG S1894L XP_005263966.1
XM_005263910.1 6033 Missense Mutation TCG,TTG S1893L XP_005263967.1
XM_005263911.1 6033 Missense Mutation TCG,TTG S1855L XP_005263968.1
XM_005263912.3 6033 Missense Mutation TCG,TTG S1838L XP_005263969.1
XM_011510869.1 6033 Missense Mutation TCG,TTG S1832L XP_011509171.1

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