Colon Cancer: Gene >> XRCC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262887
Start	43554738:43554738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322G>A
AA Mutation	p.Val108Ile(p.V108I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262887
Start	43544225:43544225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1631A>G
AA Mutation	p.Gln544Arg(p.Q544R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262887
Start	43575425:43575425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34T>C
AA Mutation	p.Cys12Arg(p.C12R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262887
Start	43552113:43552113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.986G>A
AA Mutation	p.Gly329Asp(p.G329D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262887
Start	43544201:43544201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1655G>A
AA Mutation	p.Gly552Glu(p.G552E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262887
Start	43551580:43551580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1190C>T
AA Mutation	p.Pro397Leu(p.P397L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262887
Start	43543475:43543475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754226766
CDS Mutation	c.1819G>A
AA Mutation	p.Val607Ile(p.V607I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262887
Start	43552025:43552025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> XRCC1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262887
Start	43543633:43543633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1767A>G
Mutation Classification	Silent
Feature Type	Transcript