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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