Colon Cancer: Gene >> DLL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170288440:170288440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761280644
CDS Mutation	c.469G>A
AA Mutation	p.Glu157Lys(p.E157K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170286261:170286261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.708T>G
AA Mutation	p.Phe236Leu(p.F236L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170285662:170285662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769T>C
AA Mutation	p.Cys257Arg(p.C257R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170283633:170283633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1646G>A
AA Mutation	p.Cys549Tyr(p.C549Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170283477:170283477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1802A>T
AA Mutation	p.Asp601Val(p.D601V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170285366:170285366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920C>T
AA Mutation	p.Thr307Met(p.T307M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170285318:170285318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968C>A
AA Mutation	p.Ala323Asp(p.A323D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170285399:170285399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.887A>C
AA Mutation	p.Lys296Thr(p.K296T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170285105:170285105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1063C>A
AA Mutation	p.Pro355Thr(p.P355T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366756
Start	170283245:170283245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776288082
CDS Mutation	c.2034G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366756
Start	170283821:170283821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1458G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366756
Start	170283030:170283030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150208957
CDS Mutation	c.2124C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366756
Start	170283938:170283938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369504757
CDS Mutation	c.1341C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366756
Start	170285269:170285269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146213588
CDS Mutation	c.1017C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366756
Start	170285586:170285586(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.845delG
AA Mutation	p.Gly282AlafsTer8(p.G282Afs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366756
Start	170283523:170283523(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1756delG
AA Mutation	p.Glu586ArgfsTer5(p.E586Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366756
Start	170285585:170285586(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs760008381
CDS Mutation	c.845dupG
AA Mutation	p.Leu283ProfsTer14(p.L283Pfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DLL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170283328:170283328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767441798
CDS Mutation	c.1951G>A
AA Mutation	p.Asp651Asn(p.D651N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170288368:170288368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541G>A
AA Mutation	p.Glu181Lys(p.E181K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170283582:170283582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1697T>C
AA Mutation	p.Val566Ala(p.V566A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366756
Start	170285621:170285621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810G>T
AA Mutation	p.Gln270His(p.Q270H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366756
Start	170288378:170288378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366756
Start	170283741:170283741(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1538delG
AA Mutation	p.Gly513ValfsTer24(p.G513Vfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript