Colon Cancer: Gene >> XRN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377191
Start	21348410:21348410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753036714
CDS Mutation	c.1843C>T
AA Mutation	p.Arg615Trp(p.R615W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377191
Start	21326316:21326316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.113C>T
AA Mutation	p.Ala38Val(p.A38V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377191
Start	21331782:21331782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664G>T
AA Mutation	p.Asp222Tyr(p.D222Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377191
Start	21330668:21330668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539A>T
AA Mutation	p.Asp180Val(p.D180V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377191
Start	21365625:21365625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377677641
CDS Mutation	c.2377C>T
AA Mutation	p.Arg793Trp(p.R793W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377191
Start	21328565:21328565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322C>T
AA Mutation	p.Arg108Cys(p.R108C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377191
Start	21328587:21328587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344G>A
AA Mutation	p.Arg115His(p.R115H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377191
Start	21333952:21333952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1083C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377191
Start	21356109:21356109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2050T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377191
Start	21332320:21332320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774996547
CDS Mutation	c.738G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377191
Start	21346460:21346460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1575T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377191
Start	21340813:21340813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372167550
CDS Mutation	c.1371G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000377191
Start	21356646:21356646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2179G>T
AA Mutation	p.Glu727Ter(p.E727*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000377191
Start	21333550:21333550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.865G>T
AA Mutation	p.Glu289Ter(p.E289*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000377191
Start	21339068:21339068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1258G>T
AA Mutation	p.Glu420Ter(p.E420*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> XRN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377191
Start	21339060:21339060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1250G>A
AA Mutation	p.Arg417Gln(p.R417Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377191
Start	21386989:21386989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2770G>T
AA Mutation	p.Asp924Tyr(p.D924Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377191
Start	21330515:21330515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462A>C
AA Mutation	p.Arg154Ser(p.R154S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377191
Start	21348413:21348413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1846A>G
AA Mutation	p.Lys616Glu(p.K616E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377191
Start	21332320:21332320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774996547
CDS Mutation	c.738G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000377191
Start	21333580:21333580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895G>T
AA Mutation	p.Gly299Ter(p.G299*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript