Colon Cancer: Gene >> POU3F3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361360
Start	104856712:104856712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202C>T
AA Mutation	p.Ala401Val(p.A401V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361360
Start	104856670:104856670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1160C>T
AA Mutation	p.Ala387Val(p.A387V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361360
Start	104856928:104856928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1418C>T
AA Mutation	p.Thr473Met(p.T473M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361360
Start	104856759:104856759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249G>A
AA Mutation	p.Val417Ile(p.V417I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361360
Start	104856976:104856976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1466C>T
AA Mutation	p.Pro489Leu(p.P489L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361360
Start	104856527:104856527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361360
Start	104856485:104856485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758983648
CDS Mutation	c.975C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361360
Start	104856551:104856551(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1043delG
AA Mutation	p.Gly348AlafsTer21(p.G348Afs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361360
Start	104856408:104856408(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.899delG
AA Mutation	p.Gly300AlafsTer69(p.G300Afs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> POU3F3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361360
Start	104856710:104856710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143105467
CDS Mutation	c.1200C>T
Mutation Classification	Silent
Feature Type	Transcript