Colon Cancer: Gene >> IRF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367021
Start	209790783:209790783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772C>T
AA Mutation	p.Pro258Ser(p.P258S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367021
Start	209796426:209796426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301A>G
AA Mutation	p.Lys101Glu(p.K101E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367021
Start	209796412:209796412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.315G>T
AA Mutation	p.Met105Ile(p.M105I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367021
Start	209796453:209796453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274G>A
AA Mutation	p.Glu92Lys(p.E92K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367021
Start	209790639:209790639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916G>T
AA Mutation	p.Val306Phe(p.V306F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367021
Start	209790760:209790760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367021
Start	209790538:209790538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1017A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_deletion;splice_region_variant
Transcription ID	ENST00000367021
Start	209801242:209801250(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.164_172delCCATTTTTA
AA Mutation	p.Thr55_Phe57del(p.T55_F57del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IRF6

No Mutation Annotation!