Colon Cancer: Gene >> DPP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360534
Start	162018798:162018798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351C>T
AA Mutation	p.Pro451Ser(p.P451S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360534
Start	162009269:162009269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1859A>G
AA Mutation	p.Asp620Gly(p.D620G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360534
Start	162017114:162017114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1462G>T
AA Mutation	p.Asp488Tyr(p.D488Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360534
Start	162008588:162008588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149643982
CDS Mutation	c.1961C>T
AA Mutation	p.Ala654Val(p.A654V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360534
Start	162024931:162024931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896A>T
AA Mutation	p.Tyr299Phe(p.Y299F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360534
Start	162073416:162073416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.77T>C
AA Mutation	p.Val26Ala(p.V26A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360534
Start	162035183:162035183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755T>C
AA Mutation	p.Val252Ala(p.V252A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360534
Start	162024892:162024892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935C>A
AA Mutation	p.Ser312Tyr(p.S312Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360534
Start	162018754:162018754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1395G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360534
Start	161995313:161995313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2112T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360534
Start	161995331:161995331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750468748
CDS Mutation	c.2094T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000360534
Start	162046983:162046983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.217G>T
AA Mutation	p.Glu73Ter(p.E73*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000360534
Start	162033653:162033654(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.775-1_775insAA
AA Mutation	p.Ala259LysfsTer5(p.A259Kfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000360534
Start	162033540:162033540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761173556
CDS Mutation	c.887+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DPP4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360534
Start	162016795:162016795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1540C>T
Mutation Classification	Silent
Feature Type	Transcript