Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CASP14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000427043
Start	15056066:15056066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751321912
CDS Mutation	c.706C>T
AA Mutation	p.Arg236Trp(p.R236W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427043
Start	15055437:15055437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765384541
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427043
Start	15053882:15053882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549293146
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000427043
Start	15055507:15055507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598G>T
AA Mutation	p.Gly200Ter(p.G200*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CASP14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000427043
Start	15052264:15052264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77227419
CDS Mutation	c.13C>T
AA Mutation	p.Arg5Trp(p.R5W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000427043
Start	15055994:15055994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200139686
CDS Mutation	c.634C>T
AA Mutation	p.Arg212Trp(p.R212W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000427043
Start	15053584:15053584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61731993
CDS Mutation	c.130C>T
AA Mutation	p.Arg44Trp(p.R44W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000427043
Start	15053900:15053900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.345G>T
AA Mutation	p.Lys115Asn(p.K115N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript