Product Details

SNP ID

rs199653947

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:16185687 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGAAGCAATGGGAACGAGCAAAAA[C/G]AACGAGGAGGAGAAGCGGCGCGGCC

Phenotype

MIM: 614554

Polymorphism

C/G, Transversion 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	397	Intron			NP_054796.1
XM_011527898.1	397	Missense Mutation	CAA,GAA	Q128E	XP_011526200.1

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