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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