Mutation

Primary Site >> Stomach Cancer

Gene >> COL9A2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372748
Start	40310134:40310134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369221204
CDS Mutation	c.769G>A
AA Mutation	p.Ala257Thr(p.A257T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372748
Start	40304516:40304516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1175A>G
AA Mutation	p.Glu392Gly(p.E392G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372748
Start	40307716:40307716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754230024
CDS Mutation	c.941C>T
AA Mutation	p.Thr314Met(p.T314M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372748
Start	40314264:40314264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.190C>T
AA Mutation	p.Pro64Ser(p.P64S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372748
Start	40301241:40301241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2011G>A
AA Mutation	p.Gly671Arg(p.G671R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372748
Start	40304517:40304517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174G>A
AA Mutation	p.Glu392Lys(p.E392K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372748
Start	40310135:40310135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150444024
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372748
Start	40303946:40303946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1350C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372748
Start	40307749:40307749(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.908delC
AA Mutation	p.Pro303GlnfsTer15(p.P303Qfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000372748
Start	40303186:40303186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1549-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript