Colon Cancer: Gene >> DTX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257600
Start	113058362:113058362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.170G>A
AA Mutation	p.Arg57His(p.R57H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257600
Start	113095172:113095172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1517G>A
AA Mutation	p.Arg506His(p.R506H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257600
Start	113077539:113077539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257600
Start	113077464:113077464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257600
Start	113095372:113095372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1596C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257600
Start	113096765:113096765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754668631
CDS Mutation	c.1689C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257600
Start	113077473:113077473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.309G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257600
Start	113077527:113077527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257600
Start	113095393:113095393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1617C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DTX1

No Mutation Annotation!