Mutation

Primary Site >> Stomach Cancer

Gene >> CHRNA3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326828
Start	78601858:78601858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784G>A
AA Mutation	p.Val262Ile(p.V262I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326828
Start	78617076:78617076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325A>G
AA Mutation	p.Met109Val(p.M109V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326828
Start	78601660:78601660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781008848
CDS Mutation	c.982G>A
AA Mutation	p.Val328Met(p.V328M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326828
Start	78601927:78601927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61737495
CDS Mutation	c.715C>T
AA Mutation	p.Arg239Cys(p.R239C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326828
Start	78601669:78601669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569381256
CDS Mutation	c.973G>A
AA Mutation	p.Val325Met(p.V325M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000326828
Start	78601926:78601926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766076436
CDS Mutation	c.716G>A
AA Mutation	p.Arg239His(p.R239H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326828
Start	78602183:78602183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202207061
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326828
Start	78601644:78601644(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.998delC
AA Mutation	p.Pro333ArgfsTer10(p.P333Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000326828
Start	78596645:78596645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1477G>T
AA Mutation	p.Gly493Ter(p.G493*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript