Colon Cancer: Gene >> DUSP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000240100
Start	29340227:29340227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.450T>G
AA Mutation	p.Phe150Leu(p.F150L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000240100
Start	29337388:29337388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375453930
CDS Mutation	c.823C>T
AA Mutation	p.Arg275Cys(p.R275C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000240100
Start	29350217:29350217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62G>A
AA Mutation	p.Arg21Gln(p.R21Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000240100
Start	29338419:29338419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662G>T
AA Mutation	p.Gly221Val(p.G221V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000240100
Start	29338426:29338426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754443801
CDS Mutation	c.655G>A
AA Mutation	p.Ala219Thr(p.A219T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000240100
Start	29340206:29340206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774219516
CDS Mutation	c.471C>A
AA Mutation	p.Phe157Leu(p.F157L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240100
Start	29337059:29337059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1152G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000240100
Start	29338496:29338497(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.584dupG
AA Mutation	p.Pro196SerfsTer42(p.P196Sfs*42)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DUSP4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240100
Start	29337221:29337221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990C>T
Mutation Classification	Silent
Feature Type	Transcript