Product Details

SNP ID
rs201297563
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:63598870 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCTATTTTCATACTCTCTTTCTTT[C/G]TAAAGGTCTTCTCTATAGCTCCAGG
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
WDR89 PubMed Links

Gene Details

Gene
WDR89
Gene Name
WD repeat domain 89
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001008726.2 1835 Missense Mutation ACA,AGA T358R NP_001008726.1
NM_001258272.1 1835 Missense Mutation ACA,AGA T358R NP_001245201.1
NM_080666.3 1835 Missense Mutation ACA,AGA T358R NP_542397.1
XM_011536383.2 1835 Missense Mutation ACA,AGA T396R XP_011534685.1
XM_011536385.2 1835 Missense Mutation ACA,AGA T358R XP_011534687.1

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