Product Details

SNP ID
rs199691225
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:97757299 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCGTGTTTGCTGGAGTGGTGAAGG[A/G]AAGGGCGCTGCTAAGGTTGCTGGAC
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 5855 Missense Mutation CCC,TCC P1818S NP_056163.1
XM_005263909.1 5855 Missense Mutation CCC,TCC P1835S XP_005263966.1
XM_005263910.1 5855 Missense Mutation CCC,TCC P1834S XP_005263967.1
XM_005263911.1 5855 Missense Mutation CCC,TCC P1796S XP_005263968.1
XM_005263912.3 5855 Missense Mutation CCC,TCC P1779S XP_005263969.1
XM_011510869.1 5855 Missense Mutation CCC,TCC P1773S XP_011509171.1

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