Mutation

Primary Site >> Stomach Cancer

Gene >> PIAS1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68153654:68153654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893G>A
AA Mutation	p.Arg298Gln(p.R298Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68086508:68086508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.227C>T
AA Mutation	p.Ser76Phe(p.S76F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249636
Start	68146630:68146630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779657844
CDS Mutation	c.758C>T
AA Mutation	p.Thr253Ile(p.T253I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249636
Start	68153625:68153625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249636
Start	68173797:68173797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376194188
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249636
Start	68187610:68187610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184857997
CDS Mutation	c.1731G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249636
Start	68086599:68086599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145053928
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000249636
Start	68175721:68175721(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1259delA
AA Mutation	p.Lys420ArgfsTer17(p.K420Rfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000249636
Start	68187617:68187617(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1742delT
AA Mutation	p.Phe581SerfsTer13(p.F581Sfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000249636
Start	68146583:68146583(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.716delA
AA Mutation	p.Asn239MetfsTer47(p.N239Mfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000249636
Start	68146614:68146614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742C>T
AA Mutation	p.Arg248Ter(p.R248*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript