Product Details

SNP ID
rs200348508
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:113316810 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGTGGTCCATTCTGAGTAAGTGA[A/C]TTCCTCTGTTAAAACTTGCACACAA
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
WDR31 PubMed Links

Gene Details

Gene
WDR31
Gene Name
WD repeat domain 31
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001006615.2 1259 Missense Mutation AGT,ATT S223I NP_001006616.1
NM_001012361.3 1259 Missense Mutation AGT,ATT S348I NP_001012361.1
NM_145241.4 1259 Missense Mutation AGT,ATT S347I NP_660284.1
XM_011518194.2 1259 Missense Mutation AGT,ATT S323I XP_011516496.1

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