Product Details

SNP ID
rs139071345
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:48967957 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGTACACACATACCTGGCGCCCCA[C/T]CCTGTTGTTGTGGATTCGCATTCGT
Phenotype
MIM: 601906
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
WNT10B PubMed Links

Gene Details

Gene
WNT10B
Gene Name
Wnt family member 10B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003394.3 542 Missense Mutation ATG,GTG M234V NP_003385.2
XM_011538722.1 542 Missense Mutation ATG,GTG M112V XP_011537024.1
XM_011538724.1 542 Missense Mutation GAT,GGT D158G XP_011537026.1
XM_017019919.1 542 Missense Mutation ATG,GTG M112V XP_016875408.1

View Full Product Details