Colon Cancer: Gene >> DUSP8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331588
Start	1558192:1558192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.617G>A
AA Mutation	p.Ser206Asn(p.S206N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331588
Start	1565729:1565729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757458616
CDS Mutation	c.98G>A
AA Mutation	p.Arg33His(p.R33H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331588
Start	1557483:1557483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.913G>A
AA Mutation	p.Ala305Thr(p.A305T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331588
Start	1563965:1563965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256G>A
AA Mutation	p.Val86Met(p.V86M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331588
Start	1563913:1563913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308G>A
AA Mutation	p.Ser103Asn(p.S103N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331588
Start	1563966:1563966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145547062
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331588
Start	1563939:1563939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282G>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DUSP8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331588
Start	1563941:1563941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280C>T
AA Mutation	p.Arg94Trp(p.R94W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript