Colon Cancer: Gene >> DMKN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339686
Start	35499970:35499970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1347G>T
AA Mutation	p.Lys449Asn(p.K449N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339686
Start	35500007:35500007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1310C>T
AA Mutation	p.Ala437Val(p.A437V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339686
Start	35505752:35505752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1100A>C
AA Mutation	p.Lys367Thr(p.K367T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339686
Start	35512737:35512737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.480G>T
AA Mutation	p.Gln160His(p.Q160H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339686
Start	35512674:35512674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339686
Start	35500006:35500006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757140536
CDS Mutation	c.1311G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339686
Start	35513167:35513167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.309C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339686
Start	35513398:35513398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339686
Start	35513073:35513073(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.403delG
AA Mutation	p.Val135CysfsTer52(p.V135Cfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339686
Start	35498893:35498893(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs764025438
CDS Mutation	c.1364delG
AA Mutation	p.Gly455GlufsTer19(p.G455Efs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000339686
Start	35512631:35512631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586G>T
AA Mutation	p.Gly196Ter(p.G196*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339686
Start	35511490:35511491(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.838_839insCA
AA Mutation	p.Gly280AlafsTer98(p.G280Afs*98)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DMKN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339686
Start	35511428:35511428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371442207
CDS Mutation	c.901G>A
AA Mutation	p.Gly301Ser(p.G301S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339686
Start	35500538:35500538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547354931
CDS Mutation	c.1282G>A
AA Mutation	p.Asp428Asn(p.D428N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339686
Start	35512474:35512474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631G>A
AA Mutation	p.Ala211Thr(p.A211T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339686
Start	35513121:35513121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>T
AA Mutation	p.Asp119Tyr(p.D119Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339686
Start	35513146:35513146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339686
Start	35505954:35505954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1071T>C
Mutation Classification	Silent
Feature Type	Transcript