Colon Cancer: Gene >> ATG4D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309469
Start	10551957:10551957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1027T>C
AA Mutation	p.Tyr343His(p.Y343H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309469
Start	10552278:10552278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1196C>T
AA Mutation	p.Ala399Val(p.A399V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309469
Start	10549014:10549014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748483612
CDS Mutation	c.946G>A
AA Mutation	p.Val316Met(p.V316M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309469
Start	10553009:10553009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1367G>A
AA Mutation	p.Arg456His(p.R456H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309469
Start	10552226:10552226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150808873
CDS Mutation	c.1144C>T
AA Mutation	p.Arg382Cys(p.R382C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000309469
Start	10546922:10546922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781286935
CDS Mutation	c.577C>T
AA Mutation	p.Arg193Cys(p.R193C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000309469
Start	10552121:10552121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1122G>T
AA Mutation	p.Glu374Asp(p.E374D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000309469
Start	10544996:10544996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359T>G
AA Mutation	p.Leu120Arg(p.L120R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000309469
Start	10552904:10552904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1262C>A
AA Mutation	p.Ala421Asp(p.A421D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000309469
Start	10552227:10552227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371466606
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382His(p.R382H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000309469
Start	10552265:10552265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201291151
CDS Mutation	c.1183G>A
AA Mutation	p.Val395Met(p.V395M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309469
Start	10547092:10547092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309469
Start	10545111:10545111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309469
Start	10546870:10546870(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776471163
CDS Mutation	c.530delC
AA Mutation	p.Pro177LeufsTer75(p.P177Lfs*75)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ATG4D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309469
Start	10548954:10548954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752546576
CDS Mutation	c.886G>A
AA Mutation	p.Glu296Lys(p.E296K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309469
Start	10544981:10544981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344A>G
AA Mutation	p.Asp115Gly(p.D115G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript