Colon Cancer: Gene >> NOXA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341349
Start	137433226:137433226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.872C>A
AA Mutation	p.Pro291His(p.P291H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341349
Start	137431313:137431313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.776G>C
AA Mutation	p.Arg259Pro(p.R259P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341349
Start	137428124:137428124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352A>G
AA Mutation	p.Lys118Glu(p.K118E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341349
Start	137434019:137434019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1234G>A
AA Mutation	p.Ala412Thr(p.A412T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341349
Start	137426286:137426286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753935714
CDS Mutation	c.216G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341349
Start	137428061:137428061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745570386
CDS Mutation	c.289C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341349
Start	137433970:137433970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753151253
CDS Mutation	c.1185C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341349
Start	137431278:137431278(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.745delC
AA Mutation	p.Leu249SerfsTer66(p.L249Sfs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000341349
Start	137431235:137431235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NOXA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341349
Start	137428104:137428104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145080773
CDS Mutation	c.332C>T
AA Mutation	p.Thr111Met(p.T111M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341349
Start	137428064:137428064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769178904
CDS Mutation	c.292G>C
AA Mutation	p.Ala98Pro(p.A98P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript