Product Details
- SNP ID
-
rs113253337
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:94910228 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GAAAAGTACCTTTGACAAACCCAAG[A/T]CAGATGGGGAACAAAAAACAAAAGA
- Phenotype
-
MIM: 602468
- Polymorphism
- A/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
PPP1R9A
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs12536183] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- PPP1R9A
- Gene Name
- protein phosphatase 1 regulatory subunit 9A
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001166160.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
NP_001159632.1 |
NM_001166161.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
NP_001159633.1 |
NM_001166162.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
NP_001159634.1 |
NM_001166163.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
NP_001159635.1 |
NM_017650.2 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
NP_060120.2 |
XM_011516380.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_011514682.1 |
XM_011516381.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_011514683.1 |
XM_011516382.2 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_011514684.1 |
XM_011516383.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_011514685.1 |
XM_011516389.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_011514691.1 |
XM_017012394.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867883.1 |
XM_017012395.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867884.1 |
XM_017012396.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867885.1 |
XM_017012397.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867886.1 |
XM_017012398.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867887.1 |
XM_017012399.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867888.1 |
XM_017012400.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867889.1 |
XM_017012401.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867890.1 |
XM_017012402.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867891.1 |
XM_017012403.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867892.1 |
XM_017012404.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867893.1 |
XM_017012405.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867894.1 |
XM_017012406.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867895.1 |
XM_017012407.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867896.1 |
XM_017012408.1 |
397 |
Intron |
|
|
XP_016867897.1 |
XM_017012409.1 |
397 |
Missense Mutation |
ACA,TCA |
T39S |
XP_016867898.1 |
XM_017012410.1 |
397 |
UTR 5 |
|
|
XP_016867899.1 |
XM_017012411.1 |
397 |
Intron |
|
|
XP_016867900.1 |
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