Colon Cancer: Gene >> UQCRC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000203407
Start	48599136:48599136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435C>T
AA Mutation	p.Arg479Cys(p.R479C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000203407
Start	48601393:48601393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781G>A
AA Mutation	p.Ala261Thr(p.A261T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000203407
Start	48604772:48604772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306G>T
AA Mutation	p.Lys102Asn(p.K102N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000203407
Start	48605823:48605823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244G>A
AA Mutation	p.Glu82Lys(p.E82K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000203407
Start	48609239:48609239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133G>A
AA Mutation	p.Val45Met(p.V45M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000203407
Start	48604322:48604322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537G>A
AA Mutation	p.Met179Ile(p.M179I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UQCRC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000203407
Start	48600547:48600547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1148C>T
AA Mutation	p.Ala383Val(p.A383V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000203407
Start	48605841:48605841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.226G>A
AA Mutation	p.Asp76Asn(p.D76N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript