Product Details

SNP ID

rs145825874

Assay Type

Functionally tested

NCBI dbSNP Submissions

14

Location

Chr.1:52642873 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCTTCTCTTCCCAGCATTGGCGCT[C/T]TCATAGGCCTGTCCGTAGCAGCAGT

Phenotype

Polymorphism

C/T, Transition 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	1613	Missense Mutation	CTC,TTC	L65F	NP_001036158.1
XM_011541377.2	1613	Missense Mutation	CTC,TTC	L69F	XP_011539679.1
XM_011541378.2	1613	Missense Mutation	CTC,TTC	L69F	XP_011539680.1

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