Colon Cancer: Gene >> DRAXIN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294485
Start	11711917:11711917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709G>T
AA Mutation	p.Asp237Tyr(p.D237Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294485
Start	11709323:11709323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500T>C
AA Mutation	p.Leu167Pro(p.L167P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294485
Start	11712390:11712390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758315246
CDS Mutation	c.808G>A
AA Mutation	p.Glu270Lys(p.E270K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294485
Start	11715155:11715155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775629878
CDS Mutation	c.884C>T
AA Mutation	p.Pro295Leu(p.P295L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294485
Start	11712375:11712375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200827019
CDS Mutation	c.793G>A
AA Mutation	p.Glu265Lys(p.E265K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294485
Start	11709417:11709417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.594T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DRAXIN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294485
Start	11706430:11706430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533314493
CDS Mutation	c.172C>T
AA Mutation	p.Arg58Cys(p.R58C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294485
Start	11719660:11719660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1014G>A
Mutation Classification	Silent
Feature Type	Transcript