Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HMOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219700
Start	4505575:4505575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.51G>T
AA Mutation	p.Lys17Asn(p.K17N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219700
Start	4507822:4507822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151216051
CDS Mutation	c.314G>A
AA Mutation	p.Arg105Gln(p.R105Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219700
Start	4507945:4507945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17880805
CDS Mutation	c.437C>T
AA Mutation	p.Pro146Leu(p.P146L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219700
Start	4509708:4509708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369456522
CDS Mutation	c.903C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219700
Start	4509456:4509456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.741G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000219700
Start	4505567:4505568(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.50dupA
AA Mutation	p.Asn18GlufsTer15(p.N18Efs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000219700
Start	4507993:4507994(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.491dupG
AA Mutation	p.Gln165ProfsTer26(p.Q165Pfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HMOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219700
Start	4509718:4509718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.913G>A
AA Mutation	p.Ala305Thr(p.A305T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219700
Start	4505580:4505580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.56C>T
AA Mutation	p.Ser19Phe(p.S19F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219700
Start	4507856:4507856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.348C>A
AA Mutation	p.Phe116Leu(p.F116L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript