Colon Cancer: Gene >> XRCC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338635
Start	83204903:83204903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727C>T
AA Mutation	p.Leu243Phe(p.L243F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338635
Start	83353130:83353130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.899G>T
AA Mutation	p.Arg300Met(p.R300M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338635
Start	83195885:83195885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431T>C
AA Mutation	p.Leu144Pro(p.L144P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338635
Start	83353163:83353163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932A>G
AA Mutation	p.Lys311Arg(p.K311R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338635
Start	83353139:83353139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.908C>A
AA Mutation	p.Ser303Tyr(p.S303Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000338635
Start	83111070:83111070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760546308
CDS Mutation	c.182T>C
AA Mutation	p.Met61Thr(p.M61T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338635
Start	83353227:83353227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.996C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338635
Start	83195834:83195834(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.382delT
AA Mutation	p.Cys128ValfsTer25(p.C128Vfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338635
Start	83195872:83195872(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.422delA
AA Mutation	p.Asn141MetfsTer12(p.N141Mfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000338635
Start	83203551:83203551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> XRCC4

No Mutation Annotation!