Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 615123 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANKRD13A PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU)
|
||||||
EAS
|
African American - Not Available | YRI (Yoruba)
|
||||||
SAS
|
Chinese - Not Available | JPT (Japanese)
|
||||||
AFR
|
Japanese - Not Available | CHB (Han Chinese)
|
||||||
EUR
|
||||||||
AMR
|
ANKRD13A - ankyrin repeat domain 13A | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033121.1 | 1773 | Missense Mutation | CCT,CTT | P,L 505 | NP_149112.1 | |
XM_005253980.2 | 1773 | Missense Mutation | CCT,CTT | P,L 506 | XP_005254037.1 | |
XM_005253981.3 | 1773 | Missense Mutation | CCT,CTT | P,L 505 | XP_005254038.1 | |
XM_005253982.3 | 1773 | Missense Mutation | CCT,CTT | P,L 504 | XP_005254039.1 | |
XM_005253984.1 | 1773 | Missense Mutation | CCT,CTT | P,L 418 | XP_005254041.1 | |
XM_011538937.1 | 1773 | Missense Mutation | CCT,CTT | P,L 458 | XP_011537239.1 | |
XM_011538938.2 | 1773 | Silent Mutation | ACC,ACT | T,T 452 | XP_011537240.1 | |
XM_017020157.1 | 1773 | Missense Mutation | CCT,CTT | P,L 468 | XP_016875646.1 | |
XM_017020158.1 | 1773 | Missense Mutation | CCT,CTT | P,L 466 | XP_016875647.1 | |
XM_017020159.1 | 1773 | Missense Mutation | CCT,CTT | P,L 417 | XP_016875648.1 | |
XM_017020160.1 | 1773 | Missense Mutation | CCT,CTT | P,L 417 | XP_016875649.1 | |
XM_017020161.1 | 1773 | Missense Mutation | CCT,CTT | P,L 416 | XP_016875650.1 | |
XM_017020162.1 | 1773 | Silent Mutation | ACC,ACT | T,T 450 | XP_016875651.1 | |
XM_017020163.1 | 1773 | Missense Mutation | CCT,CTT | P,L 340 | XP_016875652.1 |
C12orf76 - chromosome 12 open reading frame 76 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |