Colon Cancer: Gene >> HOXA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343060
Start	27095579:27095579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334G>A
AA Mutation	p.Ala112Thr(p.A112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343060
Start	27095792:27095792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121G>A
AA Mutation	p.Ala41Thr(p.A41T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343060
Start	27095501:27095501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412C>T
AA Mutation	p.Pro138Ser(p.P138S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343060
Start	27095580:27095580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343060
Start	27095376:27095376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.537C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343060
Start	27094710:27094710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762883582
CDS Mutation	c.738G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343060
Start	27095687:27095687(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.226delC
AA Mutation	p.Gln76SerfsTer38(p.Q76Sfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343060
Start	27095738:27095738(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.175delG
AA Mutation	p.Val59CysfsTer55(p.V59Cfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HOXA1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343060
Start	27094626:27094626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343060
Start	27095686:27095687(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.226dupC
AA Mutation	p.Gln76ProfsTer102(p.Q76Pfs*102)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript