Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 601282 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PLEC PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
PLEC - plectin | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000445.4 | 13014 | Silent Mutation | TTC,TTT | F,F 4383 | NP_000436.2 | |
NM_201378.3 | 13014 | Silent Mutation | TTC,TTT | F,F 4342 | NP_958780.1 | |
NM_201379.2 | 13014 | Silent Mutation | TTC,TTT | F,F 4334 | NP_958781.1 | |
NM_201380.3 | 13014 | Silent Mutation | TTC,TTT | F,F 4493 | NP_958782.1 | |
NM_201381.2 | 13014 | Silent Mutation | TTC,TTT | F,F 4324 | NP_958783.1 | |
NM_201382.3 | 13014 | Silent Mutation | TTC,TTT | F,F 4356 | NP_958784.1 | |
NM_201383.2 | 13014 | Silent Mutation | TTC,TTT | F,F 4360 | NP_958785.1 | |
NM_201384.2 | 13014 | Silent Mutation | TTC,TTT | F,F 4356 | NP_958786.1 | |
XM_005250976.3 | 13014 | Silent Mutation | TTC,TTT | F,F 4498 | XP_005251033.1 | |
XM_005250978.3 | 13014 | Silent Mutation | TTC,TTT | F,F 4365 | XP_005251035.1 | |
XM_005250979.4 | 13014 | Silent Mutation | TTC,TTT | F,F 4361 | XP_005251036.1 | |
XM_005250980.4 | 13014 | Silent Mutation | TTC,TTT | F,F 4361 | XP_005251037.1 | |
XM_005250981.3 | 13014 | Silent Mutation | TTC,TTT | F,F 4347 | XP_005251038.1 | |
XM_005250982.3 | 13014 | Silent Mutation | TTC,TTT | F,F 4339 | XP_005251039.1 | |
XM_005250983.2 | 13014 | Silent Mutation | TTC,TTT | F,F 4333 | XP_005251040.1 | |
XM_005250984.4 | 13014 | Silent Mutation | TTC,TTT | F,F 4329 | XP_005251041.1 | |
XM_006716588.3 | 13014 | Silent Mutation | TTC,TTT | F,F 4388 | XP_006716651.1 | |
XM_006716589.2 | 13014 | Silent Mutation | TTC,TTT | F,F 4338 | XP_006716652.1 | |
XM_006716590.3 | 13014 | Silent Mutation | TTC,TTT | F,F 4338 | XP_006716653.1 | |
XM_011517130.2 | 13014 | Silent Mutation | TTC,TTT | F,F 4361 | XP_011515432.1 | |
XM_011517131.2 | 13014 | Silent Mutation | TTC,TTT | F,F 4333 | XP_011515433.1 | |
XM_011517132.2 | 13014 | Silent Mutation | TTC,TTT | F,F 3238 | XP_011515434.1 |