Colon Cancer: Gene >> DLG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000419354
Start	197136625:197136625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1036A>G
AA Mutation	p.Asn346Asp(p.N346D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000419354
Start	197051655:197051655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751084251
CDS Mutation	c.2530C>T
AA Mutation	p.Arg844Cys(p.R844C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000419354
Start	197119470:197119470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1325C>T
AA Mutation	p.Ala442Val(p.A442V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000419354
Start	197065746:197065746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2195T>G
AA Mutation	p.Ile732Ser(p.I732S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000419354
Start	197104929:197104929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1619C>A
AA Mutation	p.Thr540Lys(p.T540K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000419354
Start	197140174:197140174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778A>G
AA Mutation	p.Thr260Ala(p.T260A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000419354
Start	197136556:197136556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105G>T
AA Mutation	p.Asp369Tyr(p.D369Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000419354
Start	197138296:197138296(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	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000419354
Start	197044726:197044726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2612T>A
AA Mutation	p.Ile871Asn(p.I871N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000419354
Start	197090948:197090948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1724C>A
AA Mutation	p.Ser575Tyr(p.S575Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000419354
Start	197194468:197194468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440A>C
AA Mutation	p.Asn147Thr(p.N147T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000419354
Start	197081101:197081101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1954C>T
AA Mutation	p.Arg652Ter(p.R652*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000419354
Start	197194569:197194570(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.338_339insTTCATAACAATAATAAAT
AA Mutation	p.Glu113delinsAspSerTerGlnTerTerIle(p.E113delinsDS*Q**I)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000419354
Start	197130665:197130666(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1125_1126insTTAAGCA
AA Mutation	p.Asn376LeufsTer12(p.N376Lfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000419354
Start	197149742:197149742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DLG1

No Mutation Annotation!