Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTTCATCACAATAACCAGGTCTGC[C/T]GTCAGAATAGTGTGTACTCGATGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 601439 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ABCC9 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
|
ABCC9 - ATP binding cassette subfamily C member 9 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005691.3 | 5342 | Intron | NP_005682.2 | |||
NM_020297.3 | 5342 | Silent Mutation | ACA,ACG | T,T 1512 | NP_064693.2 | |
XM_005253284.3 | 5342 | Silent Mutation | ACA,ACG | T,T 1512 | XP_005253341.1 | |
XM_005253286.3 | 5342 | Silent Mutation | ACA,ACG | T,T 1512 | XP_005253343.1 | |
XM_005253287.4 | 5342 | UTR 3 | XP_005253344.1 | |||
XM_005253288.3 | 5342 | Silent Mutation | ACA,ACG | T,T 1512 | XP_005253345.1 | |
XM_005253289.3 | 5342 | Silent Mutation | ACA,ACG | T,T 1499 | XP_005253346.1 | |
XM_005253290.3 | 5342 | Silent Mutation | ACA,ACG | T,T 1465 | XP_005253347.1 | |
XM_006719025.3 | 5342 | UTR 3 | XP_006719088.1 | |||
XM_011520545.2 | 5342 | Silent Mutation | ACA,ACG | T,T 1512 | XP_011518847.1 |