Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HOXD9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249499
Start	176122848:176122848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80G>A
AA Mutation	p.Gly27Asp(p.G27D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249499
Start	176123084:176123084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316G>A
AA Mutation	p.Ala106Thr(p.A106T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249499
Start	176123982:176123982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.866G>A
AA Mutation	p.Arg289His(p.R289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000249499
Start	176122872:176122872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104C>T
AA Mutation	p.Ala35Val(p.A35V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000249499
Start	176123430:176123431(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs758440041
CDS Mutation	c.668dupG
AA Mutation	p.Thr224AsnfsTer48(p.T224Nfs*48)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HOXD9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249499
Start	176123417:176123417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649G>A
AA Mutation	p.Ala217Thr(p.A217T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249499
Start	176123946:176123946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830C>T
AA Mutation	p.Ala277Val(p.A277V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249499
Start	176124019:176124019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.903G>T
AA Mutation	p.Glu301Asp(p.E301D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000249499
Start	176124154:176124154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038G>T
AA Mutation	p.Glu346Asp(p.E346D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249499
Start	176123947:176123947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000249499
Start	176123567:176123567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799C>T
AA Mutation	p.Gln267Ter(p.Q267*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript