Mutation

Primary Site >> Stomach Cancer

Gene >> COL8A2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303143
Start	36097670:36097670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2011G>A
AA Mutation	p.Asp671Asn(p.D671N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303143
Start	36097922:36097922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759403098
CDS Mutation	c.1759G>A
AA Mutation	p.Ala587Thr(p.A587T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303143
Start	36098401:36098401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1280G>A
AA Mutation	p.Gly427Asp(p.G427D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303143
Start	36097929:36097929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1752C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303143
Start	36098520:36098520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1161A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303143
Start	36097752:36097752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765161350
CDS Mutation	c.1929G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303143
Start	36097830:36097830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776159463
CDS Mutation	c.1851C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303143
Start	36099013:36099013(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.668delG
AA Mutation	p.Gly223ValfsTer14(p.G223Vfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303143
Start	36098997:36098997(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769991029
CDS Mutation	c.684delC
AA Mutation	p.Gly229AlafsTer8(p.G229Afs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303143
Start	36098888:36098888(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.793delG
AA Mutation	p.Glu265SerfsTer13(p.E265Sfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303143
Start	36099097:36099098(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.583dupG
AA Mutation	p.Glu195GlyfsTer7(p.E195Gfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303143
Start	36098601:36098602(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1079dupC
AA Mutation	p.Gly361TrpfsTer18(p.G361Wfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303143
Start	36098887:36098888(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.793dupG
AA Mutation	p.Glu265GlyfsTer77(p.E265Gfs*77)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript