Colon Cancer: Gene >> ENOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338144
Start	130667673:130667673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.851G>A
AA Mutation	p.Arg284His(p.R284H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338144
Start	130670036:130670036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779235219
CDS Mutation	c.710G>A
AA Mutation	p.Arg237His(p.R237H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338144
Start	130667691:130667691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759616146
CDS Mutation	c.833G>A
AA Mutation	p.Arg278Gln(p.R278Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338144
Start	130679644:130679644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747944133
CDS Mutation	c.445G>A
AA Mutation	p.Glu149Lys(p.E149K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338144
Start	130637351:130637351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1276G>A
AA Mutation	p.Asp426Asn(p.D426N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000338144
Start	130679666:130679666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423G>T
AA Mutation	p.Glu141Asp(p.E141D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000338144
Start	130667623:130667623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901C>T
AA Mutation	p.Arg301Cys(p.R301C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000338144
Start	130656689:130656689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199818795
CDS Mutation	c.1108C>T
AA Mutation	p.Arg370Cys(p.R370C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000338144
Start	130665678:130665678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066C>T
AA Mutation	p.Arg356Trp(p.R356W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000338144
Start	130670192:130670192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770968891
CDS Mutation	c.554G>A
AA Mutation	p.Arg185His(p.R185H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338144
Start	130679645:130679645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771959613
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338144
Start	130679729:130679729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.360C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338144
Start	130665664:130665664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779849967
CDS Mutation	c.1080C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338144
Start	130634996:130634997(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1493dupA
AA Mutation	p.Asn498LysfsTer3(p.N498Kfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ENOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338144
Start	130709282:130709282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10G>T
AA Mutation	p.Asp4Tyr(p.D4Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript