Colon Cancer: Gene >> CCHCR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376266
Start	31145458:31145458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1462C>T
AA Mutation	p.Arg488Cys(p.R488C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376266
Start	31151110:31151110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547A>G
AA Mutation	p.Thr183Ala(p.T183A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376266
Start	31145254:31145254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1521G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376266
Start	31143093:31143093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754888343
CDS Mutation	c.2094G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCHCR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376266
Start	31150200:31150200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961T>C
AA Mutation	p.Ser321Pro(p.S321P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376266
Start	31143402:31143402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748422751
CDS Mutation	c.1912C>T
AA Mutation	p.Arg638Cys(p.R638C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376266
Start	31150972:31150972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774674896
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Trp(p.R229W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript