Colon Cancer: Gene >> JAG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331782
Start	105157719:105157719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462T>A
AA Mutation	p.Asp154Glu(p.D154E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331782
Start	105168065:105168065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.109C>A
AA Mutation	p.Leu37Met(p.L37M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331782
Start	105155819:105155819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778791847
CDS Mutation	c.646G>A
AA Mutation	p.Asp216Asn(p.D216N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331782
Start	105142789:105142789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3623C>T
AA Mutation	p.Ser1208Leu(p.S1208L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331782
Start	105150762:105150762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444T>C
AA Mutation	p.Tyr482His(p.Y482H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331782
Start	105142892:105142892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148815369
CDS Mutation	c.3520G>A
AA Mutation	p.Val1174Ile(p.V1174I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331782
Start	105148155:105148155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746789751
CDS Mutation	c.2209G>A
AA Mutation	p.Ala737Thr(p.A737T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331782
Start	105145747:105145747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368191747
CDS Mutation	c.2936G>A
AA Mutation	p.Arg979His(p.R979H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331782
Start	105149271:105149271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1652G>A
AA Mutation	p.Cys551Tyr(p.C551Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000331782
Start	105145046:105145046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766346968
CDS Mutation	c.2968G>A
AA Mutation	p.Ala990Thr(p.A990T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000331782
Start	105148194:105148194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2170G>A
AA Mutation	p.Gly724Ser(p.G724S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331782
Start	105148797:105148797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1968C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331782
Start	105147869:105147869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2268G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331782
Start	105142785:105142785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753118216
CDS Mutation	c.3627G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331782
Start	105151645:105151645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777609396
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331782
Start	105152020:105152020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331782
Start	105155871:105155871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765995003
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331782
Start	105142872:105142872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331782
Start	105148144:105148144(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2220delC
AA Mutation	p.Gly741AlafsTer21(p.G741Afs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331782
Start	105150749:105150750(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1456_1457delTG
AA Mutation	p.Cys486ProfsTer48(p.C486Pfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331782
Start	105150875:105150875(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1418delG
AA Mutation	p.Gly473AlafsTer7(p.G473Afs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000331782
Start	105146450:105146450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2644G>T
AA Mutation	p.Gly882Ter(p.G882*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> JAG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331782
Start	105145768:105145768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372934981
CDS Mutation	c.2915G>A
AA Mutation	p.Arg972His(p.R972H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript