Product Details

SNP ID
rs200885820
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:48600458 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TACGGGGCCACACCCGTGGTGTCTC[C/T]GACTTCGCCTGGTCCCTCTCCAATG
Phenotype
MIM: 300512
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
WDR13 PubMed Links

Gene Details

Gene
WDR13
Gene Name
WD repeat domain 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001166426.1 821 Silent Mutation TCC,TCT S129S NP_001159898.1
NM_017883.4 821 Silent Mutation TCC,TCT S221S NP_060353.2
XM_006724539.1 821 Silent Mutation TCC,TCT S221S XP_006724602.1
XM_006724541.3 821 Silent Mutation TCC,TCT S129S XP_006724604.1
XM_011543947.2 821 Silent Mutation TCC,TCT S221S XP_011542249.1

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