Mutation

Primary Site >> Stomach Cancer

Gene >> DAPK3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3961033:3961033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745312042
CDS Mutation	c.758G>A
AA Mutation	p.Arg253His(p.R253H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3959166:3959166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1300G>A
AA Mutation	p.Val434Met(p.V434M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3959150:3959150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1316G>A
AA Mutation	p.Arg439His(p.R439H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3964785:3964785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.269T>A
AA Mutation	p.Val90Asp(p.V90D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3964980:3964980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.74C>T
AA Mutation	p.Ala25Val(p.A25V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3959616:3959616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850C>T
AA Mutation	p.Arg284Cys(p.R284C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3969702:3969702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775366216
CDS Mutation	c.34C>T
AA Mutation	p.His12Tyr(p.H12Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301264
Start	3969679:3969679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.57G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301264
Start	3964937:3964937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301264
Start	3959302:3959302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1164C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301264
Start	3964963:3964963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91C>A
Mutation Classification	Silent
Feature Type	Transcript