Product Details

SNP ID
rs200146764
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:168292242 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTACTACATAGACCACACGAACCG[C/T]ACCACCAGCTGGATCGACCCGCGGG
Phenotype
MIM: 610533
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
WWC1 PubMed Links

Gene Details

Gene
WWC1
Gene Name
WW and C2 domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001161661.1 140 Silent Mutation CGC,CGT R30R NP_001155133.1
NM_001161662.1 140 Silent Mutation CGC,CGT R30R NP_001155134.1
NM_015238.2 140 Silent Mutation CGC,CGT R30R NP_056053.1
XM_005265850.1 140 Silent Mutation CGC,CGT R30R XP_005265907.1
XM_005265853.2 140 Silent Mutation CGC,CGT R30R XP_005265910.1
XM_011534485.1 140 Silent Mutation CGC,CGT R30R XP_011532787.1
XM_011534486.1 140 Silent Mutation CGC,CGT R30R XP_011532788.1
XM_011534487.1 140 Silent Mutation CGC,CGT R30R XP_011532789.1
XM_011534488.1 140 Silent Mutation CGC,CGT R30R XP_011532790.1
XM_011534489.1 140 Silent Mutation CGC,CGT R30R XP_011532791.1
XM_011534490.1 140 Silent Mutation CGC,CGT R30R XP_011532792.1
XM_011534491.1 140 Silent Mutation CGC,CGT R30R XP_011532793.1
XM_017009276.1 140 Silent Mutation CGC,CGT R30R XP_016864765.1
XM_017009277.1 140 Intron XP_016864766.1
XM_017009278.1 140 Intron XP_016864767.1

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