Product Details

SNP ID

rs11880862

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:16185238 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGGGCGCCAAATTCGGAAGTGTGG[C/T]AGCAGATAGGAATCGAAGGGCACTC

Phenotype

MIM: 614554

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM32A PubMed Links

Gene Details

Gene

FAM32A

Gene Name

family with sequence similarity 32 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014077.3	55	Intron			NP_054796.1
XM_011527898.1	55	Nonsense Mutation	CAG,TAG	Q14*	XP_011526200.1

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