Product Details

SNP ID

rs2305962

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.5:64695646 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TGGCCTTAAGCTTCAACACTTAGAG[C/G]CTTCTTCCACTCAAGAAGGTAATCA

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM159B PubMed Links

Gene Details

Gene

FAM159B

Gene Name

family with sequence similarity 159 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001164442.1	647	Missense Mutation	CCT,GCT	P111A	NP_001157914.1

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