Colon Cancer: Gene >> XRCC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359321
Start	152649272:152649272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.213A>C
AA Mutation	p.Glu71Asp(p.E71D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359321
Start	152648826:152648826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.659A>G
AA Mutation	p.Asp220Gly(p.D220G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359321
Start	152648914:152648914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571C>A
AA Mutation	p.Leu191Ile(p.L191I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359321
Start	152649004:152649004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481A>G
AA Mutation	p.Asn161Asp(p.N161D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359321
Start	152649064:152649064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421C>T
AA Mutation	p.Pro141Ser(p.P141S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359321
Start	152648684:152648684(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.801delA
AA Mutation	p.Lys267AsnfsTer30(p.K267Nfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000359321
Start	152660773:152660773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750903875
CDS Mutation	c.49C>T
AA Mutation	p.Arg17Ter(p.R17*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> XRCC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359321
Start	152660712:152660712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.110C>T
AA Mutation	p.Ser37Leu(p.S37L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript