Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AATGTAAGCTATGGGTCGAACTTGA[G/T]CCGGTGTTATGGTAGCAATGTCAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 615383 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FIGNL1 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
|
FIGNL1 - fidgetin like 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042762.2 | 2280 | Missense Mutation | GAT,GCT | D,A 634 | NP_001036227.1 | |
NM_001287492.1 | 2280 | Missense Mutation | GAT,GCT | D,A 634 | NP_001274421.1 | |
NM_001287493.1 | 2280 | Missense Mutation | GAT,GCT | D,A 634 | NP_001274422.1 | |
NM_001287494.1 | 2280 | Missense Mutation | GAT,GCT | D,A 634 | NP_001274423.1 | |
NM_001287495.1 | 2280 | Missense Mutation | GAT,GCT | D,A 634 | NP_001274424.1 | |
NM_001287496.1 | 2280 | Missense Mutation | GAT,GCT | D,A 523 | NP_001274425.1 | |
NM_022116.4 | 2280 | Missense Mutation | GAT,GCT | D,A 634 | NP_071399.2 | |
XM_011515470.2 | 2280 | Missense Mutation | GAT,GCT | D,A 634 | XP_011513772.1 | |
XM_017012501.1 | 2280 | Missense Mutation | GAT,GCT | D,A 634 | XP_016867990.1 | |
XM_017012502.1 | 2280 | Missense Mutation | GAT,GCT | D,A 634 | XP_016867991.1 |