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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