Mutation

Primary Site >> Stomach Cancer

Gene >> PPP1R36

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298705
Start	64587255:64587255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773A>G
AA Mutation	p.Glu258Gly(p.E258G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298705
Start	64565664:64565664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767950225
CDS Mutation	c.406C>T
AA Mutation	p.Arg136Trp(p.R136W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298705
Start	64587360:64587360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878T>C
AA Mutation	p.Phe293Ser(p.F293S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298705
Start	64589159:64589159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090A>G
AA Mutation	p.Ile364Val(p.I364V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298705
Start	64588233:64588233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147167561
CDS Mutation	c.1020C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298705
Start	64586873:64586873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298705
Start	64588203:64588203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142941569
CDS Mutation	c.990C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298705
Start	64568408:64568408(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.500delA
AA Mutation	p.Asn167ThrfsTer12(p.N167Tfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000298705
Start	64552812:64552812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript