Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HOXA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222728
Start	27145812:27145812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548G>A
AA Mutation	p.Arg183His(p.R183H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222728
Start	27147346:27147346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774234211
CDS Mutation	c.404C>T
AA Mutation	p.Pro135Leu(p.P135L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222728
Start	27147428:27147428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322G>A
AA Mutation	p.Glu108Lys(p.E108K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222728
Start	27145876:27145876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484T>C
AA Mutation	p.Tyr162His(p.Y162H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222728
Start	27147489:27147489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222728
Start	27147524:27147524(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.226delG
AA Mutation	p.Ala76ProfsTer68(p.A76Pfs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HOXA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222728
Start	27145894:27145894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761372561
CDS Mutation	c.466C>T
AA Mutation	p.Arg156Cys(p.R156C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222728
Start	27145806:27145806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.554G>A
AA Mutation	p.Arg185His(p.R185H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222728
Start	27145664:27145664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript