Colon Cancer: Gene >> DPPA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335658
Start	109329038:109329038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>T
AA Mutation	p.Gly244Cys(p.G244C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335658
Start	109337477:109337477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41C>T
AA Mutation	p.Ala14Val(p.A14V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335658
Start	109330593:109330593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610G>T
AA Mutation	p.Ala204Ser(p.A204S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335658
Start	109330712:109330712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491A>G
AA Mutation	p.His164Arg(p.H164R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000335658
Start	109332029:109332030(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.180dupG
AA Mutation	p.Leu61AlafsTer4(p.L61Afs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000335658
Start	109332033:109332033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.179-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000335658
Start	109328888:109328888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DPPA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335658
Start	109330583:109330583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201448153
CDS Mutation	c.620C>T
AA Mutation	p.Ala207Val(p.A207V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335658
Start	109333890:109333891(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.157dupA
AA Mutation	p.Met53AsnfsTer7(p.M53Nfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript