Colon Cancer: Gene >> GSTM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256594
Start	109737136:109737136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613G>C
AA Mutation	p.Asp205His(p.D205H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256594
Start	109739904:109739904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.53C>T
AA Mutation	p.Ala18Val(p.A18V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256594
Start	109737154:109737154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199933862
CDS Mutation	c.595G>A
AA Mutation	p.Ala199Thr(p.A199T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256594
Start	109738129:109738129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202208381
CDS Mutation	c.334C>T
AA Mutation	p.Arg112Cys(p.R112C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256594
Start	109737492:109737492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544T>C
AA Mutation	p.Phe182Leu(p.F182L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256594
Start	109739876:109739876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.81C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256594
Start	109739870:109739870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.87T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000256594
Start	109737657:109737657(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.467delA
AA Mutation	p.Lys156SerfsTer30(p.K156Sfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000256594
Start	109739479:109739479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Ter(p.R47*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000256594
Start	109738165:109738165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298C>T
AA Mutation	p.Arg100Ter(p.R100*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GSTM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256594
Start	109738105:109738105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.358T>C
AA Mutation	p.Tyr120His(p.Y120H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256594
Start	109737155:109737155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561954445
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript