Product Details

SNP ID
rs189291071
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:128675656 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTCTGCTCCTTTCTGACCCATGT[A/G]CCTGAGGCTGATTTCCAGGTCACTA
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FAM71F2 PubMed Links

Gene Details

Gene
FAM71F2
Gene Name
family with sequence similarity 71 member F2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001012454.5 276 Silent Mutation GTA,GTG V54V NP_001012457.3
NM_001128926.3 276 Intron NP_001122398.1
NM_001290254.1 276 UTR 5 NP_001277183.1
NM_001290255.1 276 Intron NP_001277184.1
XM_011516128.2 276 Silent Mutation GTA,GTG V54V XP_011514430.1
XM_011516129.2 276 Silent Mutation GTA,GTG V54V XP_011514431.1
XM_011516130.2 276 Silent Mutation GTA,GTG V54V XP_011514432.1
XM_011516131.2 276 Silent Mutation GTA,GTG V54V XP_011514433.1
XM_011516132.2 276 Intron XP_011514434.1
XM_011516134.2 276 Intron XP_011514436.1
XM_011516135.2 276 Intron XP_011514437.1
XM_011516136.2 276 Intron XP_011514438.1
XM_017012147.1 276 Intron XP_016867636.1
XM_017012149.1 276 Silent Mutation GTA,GTG V54V XP_016867638.1

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