Colon Cancer: Gene >> CXXC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285106
Start	50282912:50282912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1766G>A
AA Mutation	p.Arg589His(p.R589H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285106
Start	50283731:50283731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1498C>T
AA Mutation	p.Arg500Cys(p.R500C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285106
Start	50282732:50282732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1832A>G
AA Mutation	p.Lys611Arg(p.K611R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285106
Start	50283527:50283527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1562C>T
AA Mutation	p.Thr521Ile(p.T521I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285106
Start	50285129:50285129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.785C>T
AA Mutation	p.Ala262Val(p.A262V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285106
Start	50286067:50286067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568303411
CDS Mutation	c.414G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285106
Start	50282677:50282677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1887C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285106
Start	50284473:50284473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745491958
CDS Mutation	c.1110G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285106
Start	50285074:50285074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.840A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285106
Start	50285233:50285233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141965165
CDS Mutation	c.681G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CXXC1

No Mutation Annotation!