Colon Cancer: Gene >> NMT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378165
Start	15112954:15112954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201047504
CDS Mutation	c.1180G>A
AA Mutation	p.Gly394Ser(p.G394S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378165
Start	15128396:15128396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.953G>T
AA Mutation	p.Arg318Ile(p.R318I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378165
Start	15141426:15141426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772878315
CDS Mutation	c.242C>T
AA Mutation	p.Ser81Leu(p.S81L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378165
Start	15135301:15135301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364T>A
AA Mutation	p.Trp122Arg(p.W122R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378165
Start	15135302:15135302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363T>A
AA Mutation	p.Phe121Leu(p.F121L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378165
Start	15135287:15135287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777341889
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378165
Start	15141500:15141501(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.167dupA
AA Mutation	p.Glu57GlyfsTer15(p.E57Gfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NMT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378165
Start	15133313:15133313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540952796
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Cys(p.R148C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378165
Start	15109829:15109829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1349A>G
AA Mutation	p.Asp450Gly(p.D450G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378165
Start	15112814:15112814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530895662
CDS Mutation	c.1320G>A
Mutation Classification	Silent
Feature Type	Transcript