Product Details

SNP ID

rs6670793

Assay Type

Functionally tested

NCBI dbSNP Submissions

56

Location

Chr.1:27734063 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTGTCAGTATTGCAACATAATTGC[A/G]GCATTTATTGGGAATAAATGCCAGC

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	438	Silent Mutation	GCA,GCG	A112A	NP_001137384.1
NM_001143913.1	438	Silent Mutation	GCA,GCG	A112A	NP_001137385.1
NM_001143914.1	438	Silent Mutation	GCA,GCG	A78A	NP_001137386.1
NM_001143915.1	438	Intron			NP_001137387.1
NM_152660.2	438	Silent Mutation	GCA,GCG	A78A	NP_689873.1
XM_017000543.1	438	Silent Mutation	GCA,GCG	A78A	XP_016856032.1

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