Colon Cancer: Gene >> HOXA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317201
Start	27108708:27108708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539C>A
AA Mutation	p.Ala180Asp(p.A180D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317201
Start	27110288:27110288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353C>T
AA Mutation	p.Ala118Val(p.A118V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317201
Start	27108664:27108664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Cys(p.R195C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317201
Start	27108660:27108660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587C>T
AA Mutation	p.Thr196Met(p.T196M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317201
Start	27110520:27110520(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	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317201
Start	27108254:27108254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317201
Start	27108692:27108692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317201
Start	27108149:27108149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1098C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317201
Start	27110512:27110512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317201
Start	27108343:27108343(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.904delC
AA Mutation	p.Gln302ArgfsTer74(p.Q302Rfs*74)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317201
Start	27108269:27108293(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.954_978delCTGCGCACCCCCGCCACCCCCACAG
AA Mutation	p.Ser318ArgfsTer50(p.S318Rfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HOXA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317201
Start	27110513:27110513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128G>A
AA Mutation	p.Gly43Asp(p.G43D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317201
Start	27107980:27107980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371241609
CDS Mutation	c.1267G>A
AA Mutation	p.Asp423Asn(p.D423N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317201
Start	27108539:27108539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.708G>T
AA Mutation	p.Lys236Asn(p.K236N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript