Colon Cancer: Gene >> ENAH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366844
Start	225511831:225511831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1451C>T
AA Mutation	p.Ala484Val(p.A484V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366844
Start	225514624:225514624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781433637
CDS Mutation	c.1190C>T
AA Mutation	p.Ala397Val(p.A397V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366844
Start	225519356:225519356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149587286
CDS Mutation	c.644G>A
AA Mutation	p.Arg215His(p.R215H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366844
Start	225514683:225514683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1131C>A
AA Mutation	p.Phe377Leu(p.F377L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366844
Start	225505033:225505033(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1559delA
AA Mutation	p.Asn520IlefsTer39(p.N520Ifs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000366844
Start	225519261:225519261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739C>T
AA Mutation	p.Arg247Ter(p.R247*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366844
Start	225519414:225519415(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.584_585dupGA
AA Mutation	p.Gln196AspfsTer57(p.Q196Dfs*57)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ENAH

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000366844
Start	225498380:225498380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1705G>T
AA Mutation	p.Glu569Ter(p.E569*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript