Product Details

SNP ID

rs147172208

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:33585384 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCTTCTGCCACGGTGGCATCTCTG[C/G]GGGTGGAGGTTCGATTTCATTGGGT

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM98A PubMed Links

Gene Details

Gene

FAM98A

Gene Name

family with sequence similarity 98 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001304538.1	1090	Missense Mutation	CCA,GCA	P122A	NP_001291467.1
NM_015475.4	1090	Missense Mutation	CCA,GCA	P317A	NP_056290.3

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