Colon Cancer: Gene >> CDC37

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222005
Start	10391685:10391685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1003C>T
AA Mutation	p.Arg335Cys(p.R335C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222005
Start	10403385:10403385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95G>T
AA Mutation	p.Arg32Leu(p.R32L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222005
Start	10396067:10396067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239A>G
AA Mutation	p.Glu80Gly(p.E80G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222005
Start	10396058:10396058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248G>A
AA Mutation	p.Arg83His(p.R83H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222005
Start	10395948:10395948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.358A>G
AA Mutation	p.Ser120Gly(p.S120G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222005
Start	10393436:10393436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000222005
Start	10393085:10393085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.981+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CDC37

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222005
Start	10393301:10393301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript