Colon Cancer: Gene >> DUSP7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000495880
Start	52054083:52054083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.809G>A
AA Mutation	p.Gly270Asp(p.G270D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000495880
Start	52050981:52050981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094A>C
AA Mutation	p.Lys365Thr(p.K365T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000495880
Start	52053954:52053954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.938C>T
AA Mutation	p.Ala313Val(p.A313V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000495880
Start	52050917:52050917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1158G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000495880
Start	52051094:52051094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.981C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000495880
Start	52054266:52054266(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.626delG
AA Mutation	p.Gly209AlafsTer131(p.G209Afs*131)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DUSP7

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000495880
Start	52053998:52053998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.894C>A
Mutation Classification	Silent
Feature Type	Transcript