Colon Cancer: Gene >> IFNA13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000610660
Start	21367934:21367934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.77A>T
AA Mutation	p.Asp26Val(p.D26V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000610660
Start	21368000:21368000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747627050
CDS Mutation	c.11C>T
AA Mutation	p.Ser4Leu(p.S4L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000610660
Start	21367537:21367537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.474G>T
AA Mutation	p.Lys158Asn(p.K158N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000610660
Start	21367656:21367656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355G>A
AA Mutation	p.Asp119Asn(p.D119N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000610660
Start	21367871:21367871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.140G>T
AA Mutation	p.Arg47Ile(p.R47I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000610660
Start	21367677:21367677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334G>A
AA Mutation	p.Glu112Lys(p.E112K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000610660
Start	21367956:21367956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.55T>C
AA Mutation	p.Ser19Pro(p.S19P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IFNA13

No Mutation Annotation!