Colon Cancer: Gene >> GCDH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222214
Start	12897827:12897827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1207C>T
AA Mutation	p.His403Tyr(p.H403Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222214
Start	12896308:12896308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.739G>T
AA Mutation	p.Ala247Ser(p.A247S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222214
Start	12897830:12897830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201509112
CDS Mutation	c.1210G>A
AA Mutation	p.Ala404Thr(p.A404T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222214
Start	12897848:12897848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760155287
CDS Mutation	c.1228G>A
AA Mutation	p.Val410Met(p.V410M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222214
Start	12897410:12897410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748275416
CDS Mutation	c.1064G>A
AA Mutation	p.Arg355His(p.R355H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222214
Start	12897406:12897406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1060G>T
AA Mutation	p.Gly354Cys(p.G354C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000222214
Start	12896351:12896351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.782C>G
AA Mutation	p.Thr261Arg(p.T261R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000222214
Start	12897317:12897317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.971T>C
AA Mutation	p.Val324Ala(p.V324A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000222214
Start	12897794:12897794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1174A>G
AA Mutation	p.Asn392Asp(p.N392D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000222214
Start	12896296:12896296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549254182
CDS Mutation	c.727C>T
AA Mutation	p.Arg243Trp(p.R243W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000222214
Start	12897302:12897302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.957-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GCDH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222214
Start	12891839:12891839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136C>T
AA Mutation	p.Pro46Ser(p.P46S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222214
Start	12893504:12893504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356C>T
AA Mutation	p.Ser119Leu(p.S119L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222214
Start	12896933:12896933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222214
Start	12897787:12897787(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs755038561
CDS Mutation	c.1173delG
AA Mutation	p.Asn392MetfsTer9(p.N392Mfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript