Colon Cancer: Gene >> DPEP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393847
Start	67992515:67992515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761580112
CDS Mutation	c.385G>A
AA Mutation	p.Ala129Thr(p.A129T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393847
Start	67991865:67991865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150079633
CDS Mutation	c.635C>T
AA Mutation	p.Thr212Met(p.T212M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000393847
Start	67989396:67989396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997C>T
AA Mutation	p.His333Tyr(p.H333Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393847
Start	67992072:67992072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753813676
CDS Mutation	c.512C>T
AA Mutation	p.Ser171Leu(p.S171L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393847
Start	67989390:67989390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540505554
CDS Mutation	c.1003G>A
AA Mutation	p.Asp335Asn(p.D335N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393847
Start	67989351:67989351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1042A>T
AA Mutation	p.Ile348Phe(p.I348F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393847
Start	67990114:67990114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767211201
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393847
Start	67991172:67991172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393847
Start	67993092:67993093(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs547189498
CDS Mutation	c.120dupC
AA Mutation	p.Arg41GlnfsTer26(p.R41Qfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DPEP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393847
Start	67990097:67990097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944C>T
AA Mutation	p.Ser315Phe(p.S315F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393847
Start	67987875:67987875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1183C>A
Mutation Classification	Silent
Feature Type	Transcript