Colon Cancer: Gene >> DUSP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366899
Start	221738979:221738979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.766C>A
AA Mutation	p.Leu256Ile(p.L256I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366899
Start	221706374:221706374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751183346
CDS Mutation	c.904G>A
AA Mutation	p.Ala302Thr(p.A302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366899
Start	221738946:221738946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799C>A
AA Mutation	p.Leu267Met(p.L267M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366899
Start	221739712:221739712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366899
Start	221739034:221739034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.711T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366899
Start	221706162:221706162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366899
Start	221739724:221739724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546322180
CDS Mutation	c.21C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366899
Start	221706447:221706447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767093804
CDS Mutation	c.831G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000366899
Start	221739051:221739051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694G>T
AA Mutation	p.Glu232Ter(p.E232*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DUSP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366899
Start	221702507:221702507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1354A>T
AA Mutation	p.Met452Leu(p.M452L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript