Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DAPK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3964270:3964270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.527A>T
AA Mutation	p.Asn176Ile(p.N176I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3964759:3964759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.295G>A
AA Mutation	p.Gly99Arg(p.G99R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3964304:3964304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493G>A
AA Mutation	p.Ala165Thr(p.A165T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3964908:3964908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146T>C
AA Mutation	p.Leu49Pro(p.L49P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000301264
Start	3960102:3960102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547931912
CDS Mutation	c.785G>A
AA Mutation	p.Arg262Gln(p.R262Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301264
Start	3964760:3964760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775587396
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301264
Start	3964302:3964302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777773890
CDS Mutation	c.495G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DAPK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3961016:3961016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775G>T
AA Mutation	p.Asp259Tyr(p.D259Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3964334:3964334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463C>A
AA Mutation	p.Pro155Thr(p.P155T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000301264
Start	3964633:3964633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.421A>C
AA Mutation	p.Lys141Gln(p.K141Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301264
Start	3961144:3961144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.647C>T
AA Mutation	p.Pro216Leu(p.P216L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript