Product Details

SNP ID
rs145318043
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:94910585 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTGCATGAATCAGGACAGAACAAC[C/T]GCTATTCCCCAAAGAAAGAGAAAGC
Phenotype
MIM: 602468
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PPP1R9A PubMed Links

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_001166160.1 754 Missense Mutation CGC,TGC R158C NP_001159632.1
NM_001166161.1 754 Missense Mutation CGC,TGC R158C NP_001159633.1
NM_001166162.1 754 Missense Mutation CGC,TGC R158C NP_001159634.1
NM_001166163.1 754 Missense Mutation CGC,TGC R158C NP_001159635.1
NM_017650.2 754 Missense Mutation CGC,TGC R158C NP_060120.2
XM_011516380.1 754 Missense Mutation CGC,TGC R158C XP_011514682.1
XM_011516381.1 754 Missense Mutation CGC,TGC R158C XP_011514683.1
XM_011516382.2 754 Missense Mutation CGC,TGC R158C XP_011514684.1
XM_011516383.1 754 Missense Mutation CGC,TGC R158C XP_011514685.1
XM_011516389.1 754 Missense Mutation CGC,TGC R158C XP_011514691.1
XM_017012394.1 754 Missense Mutation CGC,TGC R158C XP_016867883.1
XM_017012395.1 754 Missense Mutation CGC,TGC R158C XP_016867884.1
XM_017012396.1 754 Missense Mutation CGC,TGC R158C XP_016867885.1
XM_017012397.1 754 Missense Mutation CGC,TGC R158C XP_016867886.1
XM_017012398.1 754 Missense Mutation CGC,TGC R158C XP_016867887.1
XM_017012399.1 754 Missense Mutation CGC,TGC R158C XP_016867888.1
XM_017012400.1 754 Missense Mutation CGC,TGC R158C XP_016867889.1
XM_017012401.1 754 Missense Mutation CGC,TGC R158C XP_016867890.1
XM_017012402.1 754 Missense Mutation CGC,TGC R158C XP_016867891.1
XM_017012403.1 754 Missense Mutation CGC,TGC R158C XP_016867892.1
XM_017012404.1 754 Missense Mutation CGC,TGC R158C XP_016867893.1
XM_017012405.1 754 Missense Mutation CGC,TGC R158C XP_016867894.1
XM_017012406.1 754 Missense Mutation CGC,TGC R158C XP_016867895.1
XM_017012407.1 754 Missense Mutation CGC,TGC R158C XP_016867896.1
XM_017012408.1 754 Intron XP_016867897.1
XM_017012409.1 754 Missense Mutation CGC,TGC R158C XP_016867898.1
XM_017012410.1 754 UTR 5 XP_016867899.1
XM_017012411.1 754 Intron XP_016867900.1

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