Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAAAAGTACCTTTGACAAACCCAAG[A/T]CAGATGGGGAACAAAAAACAAAAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602468 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PPP1R9A PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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
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AMR
|
PPP1R9A - protein phosphatase 1 regulatory subunit 9A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166160.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | NP_001159632.1 | |
NM_001166161.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | NP_001159633.1 | |
NM_001166162.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | NP_001159634.1 | |
NM_001166163.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | NP_001159635.1 | |
NM_017650.2 | 397 | Missense Mutation | ACA,TCA | T,S 39 | NP_060120.2 | |
XM_011516380.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_011514682.1 | |
XM_011516381.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_011514683.1 | |
XM_011516382.2 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_011514684.1 | |
XM_011516383.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_011514685.1 | |
XM_011516389.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_011514691.1 | |
XM_017012394.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867883.1 | |
XM_017012395.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867884.1 | |
XM_017012396.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867885.1 | |
XM_017012397.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867886.1 | |
XM_017012398.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867887.1 | |
XM_017012399.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867888.1 | |
XM_017012400.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867889.1 | |
XM_017012401.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867890.1 | |
XM_017012402.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867891.1 | |
XM_017012403.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867892.1 | |
XM_017012404.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867893.1 | |
XM_017012405.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867894.1 | |
XM_017012406.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867895.1 | |
XM_017012407.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867896.1 | |
XM_017012408.1 | 397 | Intron | XP_016867897.1 | |||
XM_017012409.1 | 397 | Missense Mutation | ACA,TCA | T,S 39 | XP_016867898.1 | |
XM_017012410.1 | 397 | UTR 5 | XP_016867899.1 | |||
XM_017012411.1 | 397 | Intron | XP_016867900.1 |