Colon Cancer: Gene >> MTF1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373036
Start	37838625:37838625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.779G>A
AA Mutation	p.Arg260Gln(p.R260Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373036
Start	37838652:37838652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779682329
CDS Mutation	c.752G>A
AA Mutation	p.Arg251Gln(p.R251Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373036
Start	37815174:37815174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2224G>A
AA Mutation	p.Glu742Lys(p.E742K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373036
Start	37857633:37857633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26A>G
AA Mutation	p.Asn9Ser(p.N9S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373036
Start	37857458:37857458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373036
Start	37822412:37822412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1476G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373036
Start	37815142:37815142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2256C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373036
Start	37815388:37815388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2010C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373036
Start	37840000:37840000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.567C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373036
Start	37838722:37838722(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.682delA
AA Mutation	p.Thr228ArgfsTer19(p.T228Rfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373036
Start	37822503:37822503(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1385delC
AA Mutation	p.Pro462LeufsTer83(p.P462Lfs*83)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000373036
Start	37857348:37857349(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.310_311insCCAGCTAAA
AA Mutation	p.His104delinsProSerTerAsn(p.H104delinsPS*N)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373036
Start	37835200:37835201(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.868_869insACACACC
AA Mutation	p.Phe290TyrfsTer7(p.F290Yfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MTF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373036
Start	37823739:37823739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763643120
CDS Mutation	c.1142C>T
AA Mutation	p.Thr381Met(p.T381M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000373036
Start	37815513:37815513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1885G>T
AA Mutation	p.Glu629Ter(p.E629*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript