Product Details

SNP ID
rs11113753
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:108130957 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCACCTGGTCTCTGAGGATCATTTT[A/G]GAGCCGCCCCTGTGGTCACAGCCCC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
WSCD2 PubMed Links

Gene Details

Gene
WSCD2
Gene Name
WSC domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001304447.1 Intron NP_001291376.1
NM_014653.3 Intron NP_055468.2
XM_017020243.1 Intron XP_016875732.1
XM_017020244.1 Intron XP_016875733.1
XM_017020245.1 Intron XP_016875734.1
XM_017020246.1 Intron XP_016875735.1
XM_017020247.1 Intron XP_016875736.1
XM_017020248.1 Intron XP_016875737.1
XM_017020249.1 Intron XP_016875738.1
XM_017020250.1 Intron XP_016875739.1
XM_017020251.1 Intron XP_016875740.1
XM_017020252.1 Intron XP_016875741.1

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