Colon Cancer: Gene >> DNAJC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000602402
Start	95760074:95760074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.581G>A
AA Mutation	p.Arg194Gln(p.R194Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000602402
Start	95677337:95677337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82G>A
AA Mutation	p.Gly28Ser(p.G28S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000602402
Start	95757752:95757752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502G>A
AA Mutation	p.Gly168Arg(p.G168R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000602402
Start	95790998:95790998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144153992
CDS Mutation	c.1483G>A
AA Mutation	p.Gly495Arg(p.G495R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000602402
Start	95763711:95763711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.917T>C
AA Mutation	p.Val306Ala(p.V306A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000602402
Start	95723343:95723343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.295C>T
AA Mutation	p.Gln99Ter(p.Q99*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DNAJC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000602402
Start	95760179:95760179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686G>A
AA Mutation	p.Ser229Asn(p.S229N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript