Colon Cancer: Gene >> NMT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258960
Start	45103811:45103811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1267T>C
AA Mutation	p.Tyr423His(p.Y423H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258960
Start	45103050:45103050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148483868
CDS Mutation	c.1093G>A
AA Mutation	p.Val365Ile(p.V365I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258960
Start	45104914:45104914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1388A>T
AA Mutation	p.Glu463Val(p.E463V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258960
Start	45096206:45096206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517T>C
AA Mutation	p.Tyr173His(p.Y173H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258960
Start	45098501:45098501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.833A>G
AA Mutation	p.Gln278Arg(p.Q278R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258960
Start	45103868:45103868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1324G>A
AA Mutation	p.Ala442Thr(p.A442T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258960
Start	45103753:45103753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1209G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258960
Start	45098526:45098526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258960
Start	45081694:45081694(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.188delA
AA Mutation	p.Lys63ArgfsTer17(p.K63Rfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000258960
Start	45102972:45102972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1015C>T
AA Mutation	p.Arg339Ter(p.R339*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000258960
Start	45103878:45103878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1332+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NMT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258960
Start	45104862:45104862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336G>A
AA Mutation	p.Gly446Arg(p.G446R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000258960
Start	45097174:45097174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643C>T
AA Mutation	p.Arg215Ter(p.R215*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript