Colon Cancer: Gene >> XRCC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359308
Start	41646968:41646968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846G>T
AA Mutation	p.Lys282Asn(p.K282N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359308
Start	41646960:41646960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838G>T
AA Mutation	p.Ala280Ser(p.A280S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359308
Start	41656923:41656923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1312C>T
AA Mutation	p.Pro438Ser(p.P438S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359308
Start	41657020:41657020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749612494
CDS Mutation	c.1409G>A
AA Mutation	p.Arg470His(p.R470H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359308
Start	41650838:41650838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1076A>G
AA Mutation	p.His359Arg(p.H359R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359308
Start	41661346:41661346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1538C>T
AA Mutation	p.Ala513Val(p.A513V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359308
Start	41647069:41647069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947C>T
AA Mutation	p.Thr316Ile(p.T316I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359308
Start	41646971:41646971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359308
Start	41663782:41663782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369068201
CDS Mutation	c.1797G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359308
Start	41637651:41637651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359308
Start	41653603:41653603(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1207delC
AA Mutation	p.Arg403AlafsTer25(p.R403Afs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359308
Start	41658287:41658287(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1457delA
AA Mutation	p.His486ProfsTer12(p.H486Pfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359308
Start	41628150:41628151(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.122dupT
AA Mutation	p.Leu41PhefsTer3(p.L41Ffs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> XRCC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359308
Start	41636678:41636678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497T>C
AA Mutation	p.Ile166Thr(p.I166T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359308
Start	41656938:41656938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1327A>G
AA Mutation	p.Lys443Glu(p.K443E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359308
Start	41636764:41636764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.583G>T
AA Mutation	p.Asp195Tyr(p.D195Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript