Colon Cancer: Gene >> CHAF1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314103
Start	36416316:36416316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768250753
CDS Mutation	c.1630C>T
AA Mutation	p.Arg544Trp(p.R544W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314103
Start	36387662:36387662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.191G>A
AA Mutation	p.Arg64His(p.R64H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314103
Start	36416293:36416293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1607A>G
AA Mutation	p.Gln536Arg(p.Q536R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314103
Start	36413166:36413166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1344C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314103
Start	36412923:36412923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200643242
CDS Mutation	c.1101C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CHAF1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314103
Start	36397432:36397432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.499T>G
AA Mutation	p.Phe167Val(p.F167V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript