Colon Cancer: Gene >> DUSP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279488
Start	89351763:89351763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.277G>A
AA Mutation	p.Asp93Asn(p.D93N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000279488
Start	89350997:89350997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429C>A
AA Mutation	p.Phe143Leu(p.F143L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000279488
Start	89351005:89351005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.421G>A
AA Mutation	p.Ala141Thr(p.A141T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000279488
Start	89349492:89349492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.908T>C
AA Mutation	p.Val303Ala(p.V303A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000279488
Start	89350815:89350815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611C>T
AA Mutation	p.Pro204Leu(p.P204L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000279488
Start	89349489:89349489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.911C>T
AA Mutation	p.Thr304Ile(p.T304I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000279488
Start	89351947:89351947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.93C>A
AA Mutation	p.Asn31Lys(p.N31K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000279488
Start	89351692:89351692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.348G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000279488
Start	89350920:89350921(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.505_506delGG
AA Mutation	p.Gly169ProfsTer6(p.G169Pfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000279488
Start	89350611:89350611(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.815delT
AA Mutation	p.Phe272SerfsTer8(p.F272Sfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DUSP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279488
Start	89350596:89350596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830C>A
AA Mutation	p.Ser277Tyr(p.S277Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript