Colon Cancer: Gene >> ZDHHC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348579
Start	67398581:67398581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.806T>C
AA Mutation	p.Ile269Thr(p.I269T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348579
Start	67395045:67395045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1187C>T
AA Mutation	p.Ala396Val(p.A396V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000348579
Start	67398223:67398223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769302084
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Trp(p.R306W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000348579
Start	67398261:67398261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.878G>A
AA Mutation	p.Gly293Glu(p.G293E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000348579
Start	67398220:67398220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141973581
CDS Mutation	c.919C>T
AA Mutation	p.Pro307Ser(p.P307S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZDHHC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348579
Start	67406339:67406339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759312519
CDS Mutation	c.113G>A
AA Mutation	p.Arg38Gln(p.R38Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348579
Start	67399410:67399410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.475G>A
AA Mutation	p.Gly159Ser(p.G159S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript