Product Details

SNP ID
rs199651021
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:97757172 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTCCAATCGTGGGGCTCCATATC[C/T]GCCACGGGTTGTAGGTCTGTCCCAA
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 5982 Missense Mutation CAG,CGG Q1860R NP_056163.1
XM_005263909.1 5982 Missense Mutation CAG,CGG Q1877R XP_005263966.1
XM_005263910.1 5982 Missense Mutation CAG,CGG Q1876R XP_005263967.1
XM_005263911.1 5982 Missense Mutation CAG,CGG Q1838R XP_005263968.1
XM_005263912.3 5982 Missense Mutation CAG,CGG Q1821R XP_005263969.1
XM_011510869.1 5982 Missense Mutation CAG,CGG Q1815R XP_011509171.1

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