Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DMTF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331242
Start	87182311:87182311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.794G>A
AA Mutation	p.Arg265Gln(p.R265Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331242
Start	87191014:87191014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1481T>A
AA Mutation	p.Phe494Tyr(p.F494Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331242
Start	87188226:87188226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199931097
CDS Mutation	c.1336C>T
AA Mutation	p.Arg446Cys(p.R446C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331242
Start	87174658:87174658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559006713
CDS Mutation	c.508C>T
AA Mutation	p.Arg170Cys(p.R170C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331242
Start	87182273:87182273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748180758
CDS Mutation	c.756G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331242
Start	87188128:87188128(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1244delA
AA Mutation	p.Asn415ThrfsTer28(p.N415Tfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DMTF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331242
Start	87179671:87179671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762676722
CDS Mutation	c.646C>T
AA Mutation	p.Arg216Cys(p.R216C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331242
Start	87182290:87182290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773C>A
AA Mutation	p.Ser258Tyr(p.S258Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331242
Start	87184523:87184523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947G>A
AA Mutation	p.Arg316His(p.R316H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript