Product Details

SNP ID

rs186026933

Assay Type

Functionally tested

NCBI dbSNP Submissions

16

Location

Chr.1:52642871 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGTCTTCTCTTCCCAGCATTGGCG[C/G]TCTCATAGGCCTGTCCGTAGCAGCA

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM159A PubMed Links

Gene Details

Gene

FAM159A

Gene Name

family with sequence similarity 159 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042693.2	1611	Missense Mutation	GCT,GGT	A64G	NP_001036158.1
XM_011541377.2	1611	Missense Mutation	GCT,GGT	A68G	XP_011539679.1
XM_011541378.2	1611	Missense Mutation	GCT,GGT	A68G	XP_011539680.1

View Full Product Details