Product Details

SNP ID
rs149355931
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:80501871 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGAAGACGGTGCTGAGATCACCTG[A/G]TATCATGCAGCTAACCACAAGGCAC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FAM151B PubMed Links

Gene Details

Gene
FAM151B
Gene Name
family with sequence similarity 151 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_205548.2 160 Nonsense Mutation TGA,TGG *35W NP_991111.2
XM_006714564.3 160 Nonsense Mutation TGA,TGG *34W XP_006714627.2
XM_011543234.2 160 Nonsense Mutation TGA,TGG *51W XP_011541536.1
XM_011543235.2 160 Intron XP_011541537.1
XM_011543236.2 160 Intron XP_011541538.1
XM_011543237.2 160 Intron XP_011541539.1
XM_017009166.1 160 UTR 5 XP_016864655.1
XM_017009167.1 160 Intron XP_016864656.1
XM_017009168.1 160 UTR 5 XP_016864657.1
XM_017009169.1 160 Intron XP_016864658.1
XM_017009170.1 160 Intron XP_016864659.1

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