Product Details

SNP ID
rs2040862
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:138084300 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGTCCCAAGGTAGGATGATCTCCAG[C/T]TTCTGTTTTTACCCACTGAGGGCCC
Phenotype
MIM: 606360
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
WNT8A PubMed Links

Gene Details

Gene
WNT8A
Gene Name
Wnt family member 8A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001300938.1 Intron NP_001287867.1
NM_001300939.1 Intron NP_001287868.1
NM_058244.3 Intron NP_490645.1
XM_011543625.2 Intron XP_011541927.2
XM_017009824.1 Intron XP_016865313.1
XM_017009825.1 Intron XP_016865314.1
XM_017009826.1 Intron XP_016865315.1

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