Colon Cancer: Gene >> DUSP26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256261
Start	33592129:33592129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520A>G
AA Mutation	p.Thr174Ala(p.T174A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256261
Start	33592123:33592123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545078102
CDS Mutation	c.526G>A
AA Mutation	p.Val176Met(p.V176M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256261
Start	33592148:33592148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256261
Start	33593606:33593606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138833176
CDS Mutation	c.363G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DUSP26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256261
Start	33593550:33593550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147770891
CDS Mutation	c.419C>T
AA Mutation	p.Ala140Val(p.A140V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256261
Start	33593554:33593554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376826832
CDS Mutation	c.415C>T
AA Mutation	p.Arg139Trp(p.R139W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript