Product Details

SNP ID
rs201507534
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:27732611 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTTCTTCCTTAACAGTAAAACCA[A/G]TACAATATGCAAGAAATGTGCTCAG
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FAM76A PubMed Links

Gene Details

Gene
FAM76A
Gene Name
family with sequence similarity 76 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001143912.1 257 Missense Mutation AAT,AGT N86S NP_001137384.1
NM_001143913.1 257 Missense Mutation AAT,AGT N86S NP_001137385.1
NM_001143914.1 257 Missense Mutation AAT,AGT N52S NP_001137386.1
NM_001143915.1 257 Missense Mutation AAT,AGT N52S NP_001137387.1
NM_152660.2 257 Missense Mutation AAT,AGT N52S NP_689873.1
XM_017000543.1 257 Missense Mutation AAT,AGT N52S XP_016856032.1

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