Mutation

Primary Site >> Stomach Cancer

Gene >> PIBF1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326291
Start	72795489:72795489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484A>G
AA Mutation	p.Thr162Ala(p.T162A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326291
Start	72973610:72973610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1984T>C
AA Mutation	p.Ser662Pro(p.S662P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326291
Start	72797945:72797945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591A>C
AA Mutation	p.Glu197Asp(p.E197D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326291
Start	72821940:72821940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.764A>G
AA Mutation	p.Gln255Arg(p.Q255R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326291
Start	72931196:72931196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1762G>A
AA Mutation	p.Glu588Lys(p.E588K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000326291
Start	72973636:72973636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2010A>C
AA Mutation	p.Gln670His(p.Q670H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000326291
Start	72795475:72795475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376737770
CDS Mutation	c.470G>A
AA Mutation	p.Arg157His(p.R157H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000326291
Start	72783507:72783507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781616914
CDS Mutation	c.38A>G
AA Mutation	p.Asn13Ser(p.N13S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326291
Start	72783496:72783496(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.33delA
AA Mutation	p.Val12Ter(p.V12*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326291
Start	72854116:72854116(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1286delA
AA Mutation	p.Lys429ArgfsTer4(p.K429Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript