Colon Cancer: Gene >> XRCC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352127
Start	103708543:103708543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143410843
CDS Mutation	c.172C>T
AA Mutation	p.Arg58Trp(p.R58W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352127
Start	103708602:103708602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758434542
CDS Mutation	c.113T>C
AA Mutation	p.Leu38Pro(p.L38P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352127
Start	103707114:103707114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777400049
CDS Mutation	c.295C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352127
Start	103698864:103698864(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.975delC
AA Mutation	p.Ser326ProfsTer43(p.S326Pfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352127
Start	103707180:103707181(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.228dupC
AA Mutation	p.Thr77HisfsTer28(p.T77Hfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000352127
Start	103699362:103699362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000352127
Start	103699181:103699181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.775-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> XRCC3

No Mutation Annotation!