Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCTACTACATAGACCACACGAACCG[C/T]ACCACCAGCTGGATCGACCCGCGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 610533 | ||||||||||||||||||||
Literature Links: |
WWC1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
WWC1 - WW and C2 domain containing 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001161661.1 | 140 | Silent Mutation | CGC,CGT | R,R 30 | NP_001155133.1 | |
NM_001161662.1 | 140 | Silent Mutation | CGC,CGT | R,R 30 | NP_001155134.1 | |
NM_015238.2 | 140 | Silent Mutation | CGC,CGT | R,R 30 | NP_056053.1 | |
XM_005265850.1 | 140 | Silent Mutation | CGC,CGT | R,R 30 | XP_005265907.1 | |
XM_005265853.2 | 140 | Silent Mutation | CGC,CGT | R,R 30 | XP_005265910.1 | |
XM_011534485.1 | 140 | Silent Mutation | CGC,CGT | R,R 30 | XP_011532787.1 | |
XM_011534486.1 | 140 | Silent Mutation | CGC,CGT | R,R 30 | XP_011532788.1 | |
XM_011534487.1 | 140 | Silent Mutation | CGC,CGT | R,R 30 | XP_011532789.1 | |
XM_011534488.1 | 140 | Silent Mutation | CGC,CGT | R,R 30 | XP_011532790.1 | |
XM_011534489.1 | 140 | Silent Mutation | CGC,CGT | R,R 30 | XP_011532791.1 | |
XM_011534490.1 | 140 | Silent Mutation | CGC,CGT | R,R 30 | XP_011532792.1 | |
XM_011534491.1 | 140 | Silent Mutation | CGC,CGT | R,R 30 | XP_011532793.1 | |
XM_017009276.1 | 140 | Silent Mutation | CGC,CGT | R,R 30 | XP_016864765.1 | |
XM_017009277.1 | 140 | Intron | XP_016864766.1 | |||
XM_017009278.1 | 140 | Intron | XP_016864767.1 |