Product Details

SNP ID
rs145389845
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:138622411 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGGATGGTGAGAACTTTAGAATTG[G/T]TTTGGGTAAGTTAGTGCTGTTTCCG
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
FAIM PubMed Links

Gene Details

Gene
FAIM
Gene Name
Fas apoptotic inhibitory molecule
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001033030.1 1029 Missense Mutation GGT,GTT G146V NP_001028202.1
NM_001033031.1 1029 Missense Mutation GGT,GTT G134V NP_001028203.1
NM_001033032.1 1029 Missense Mutation GGT,GTT G112V NP_001028204.1
NM_018147.3 1029 Missense Mutation GGT,GTT G112V NP_060617.1
XM_011512950.2 1029 Missense Mutation GGT,GTT G166V XP_011511252.1

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