Colon Cancer: Gene >> HOXB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311626
Start	48552297:48552297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178G>A
AA Mutation	p.Ala60Thr(p.A60T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311626
Start	48552218:48552218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257C>T
AA Mutation	p.Pro86Leu(p.P86L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311626
Start	48550798:48550798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832G>A
AA Mutation	p.Ala278Thr(p.A278T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311626
Start	48550880:48550880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.750G>T
AA Mutation	p.Lys250Asn(p.K250N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311626
Start	48550536:48550536(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1094delC
AA Mutation	p.Pro365LeufsTer64(p.P365Lfs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311626
Start	48550857:48550857(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.773delG
AA Mutation	p.Gly258AlafsTer19(p.G258Afs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000311626
Start	48550794:48550794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836T>A
AA Mutation	p.Leu279Ter(p.L279*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311626
Start	48552374:48552375(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs771928715
CDS Mutation	c.100dupC
AA Mutation	p.Gln34ProfsTer68(p.Q34Pfs*68)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HOXB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311626
Start	48551055:48551055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575G>A
AA Mutation	p.Arg192Gln(p.R192Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311626
Start	48552232:48552232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243G>T
AA Mutation	p.Glu81Asp(p.E81D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript