Colon Cancer: Gene >> RDH5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257895
Start	55724448:55724448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.860C>T
AA Mutation	p.Ala287Val(p.A287V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257895
Start	55723940:55723940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624C>A
AA Mutation	p.Phe208Leu(p.F208L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257895
Start	55721240:55721240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370781214
CDS Mutation	c.56G>A
AA Mutation	p.Arg19Lys(p.R19K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257895
Start	55721741:55721741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000257895
Start	55723911:55723911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759835915
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Ter(p.R199*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	start_lost
Transcription ID	ENST00000257895
Start	55721185:55721185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750520220
CDS Mutation	c.1A>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RDH5

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257895
Start	55724368:55724368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.780C>T
Mutation Classification	Silent
Feature Type	Transcript