Colon Cancer: Gene >> MTF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370298
Start	93110293:93110293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.69G>T
AA Mutation	p.Lys23Asn(p.K23N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370298
Start	93120556:93120556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805A>C
AA Mutation	p.Ile269Leu(p.I269L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370298
Start	93133978:93133978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576246655
CDS Mutation	c.1317A>G
AA Mutation	p.Ile439Met(p.I439M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370298
Start	93129391:93129391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103C>G
AA Mutation	p.Thr368Arg(p.T368R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370298
Start	93110231:93110231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7G>T
AA Mutation	p.Asp3Tyr(p.D3Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370298
Start	93110283:93110283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189234488
CDS Mutation	c.59G>A
AA Mutation	p.Arg20Gln(p.R20Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370298
Start	93129328:93129328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347Gln(p.R347Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370298
Start	93133757:93133757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1215A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370298
Start	93136865:93136865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1620T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370298
Start	93133723:93133723(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759847587
CDS Mutation	c.1188delA
AA Mutation	p.Gly397GlufsTer6(p.G397Efs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000370298
Start	93120548:93120548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.798-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MTF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370298
Start	93110283:93110283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189234488
CDS Mutation	c.59G>A
AA Mutation	p.Arg20Gln(p.R20Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370298
Start	93133752:93133752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1210C>T
AA Mutation	p.Arg404Cys(p.R404C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370298
Start	93133776:93133776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1234A>C
AA Mutation	p.Lys412Gln(p.K412Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370298
Start	93110357:93110357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133A>C
AA Mutation	p.Lys45Gln(p.K45Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000370298
Start	93129294:93129294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1006G>T
AA Mutation	p.Glu336Ter(p.E336*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript