Colon Cancer: Gene >> DPP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000541961
Start	66509231:66509231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2194G>A
AA Mutation	p.Ala732Thr(p.A732T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000541961
Start	66486619:66486619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440G>A
AA Mutation	p.Cys147Tyr(p.C147Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000541961
Start	66482298:66482298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756979162
CDS Mutation	c.98A>G
AA Mutation	p.Tyr33Cys(p.Y33C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000541961
Start	66493124:66493124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1241C>T
AA Mutation	p.Ala414Val(p.A414V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000541961
Start	66495440:66495440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766673185
CDS Mutation	c.1528C>T
AA Mutation	p.Arg510Trp(p.R510W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000541961
Start	66491546:66491546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851G>A
AA Mutation	p.Ser284Asn(p.S284N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000541961
Start	66485237:66485237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.335C>T
AA Mutation	p.Thr112Ile(p.T112I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000541961
Start	66486655:66486655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755183144
CDS Mutation	c.476G>A
AA Mutation	p.Arg159Gln(p.R159Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000541961
Start	66482390:66482390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190A>G
AA Mutation	p.Ser64Gly(p.S64G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000541961
Start	66504683:66504684(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs772006461
CDS Mutation	c.1956dupC
AA Mutation	p.Glu653ArgfsTer14(p.E653Rfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DPP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000541961
Start	66482238:66482238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38G>A
AA Mutation	p.Gly13Asp(p.G13D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000541961
Start	66492828:66492828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1101G>T
AA Mutation	p.Lys367Asn(p.K367N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541961
Start	66491308:66491308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541961
Start	66504656:66504656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756177410
CDS Mutation	c.1923C>T
Mutation Classification	Silent
Feature Type	Transcript