Colon Cancer: Gene >> IRF7

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000397574
Start	614797:614797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394G>A
AA Mutation	p.Glu132Lys(p.E132K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397574
Start	613215:613215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs786205223
CDS Mutation	c.1228T>G
AA Mutation	p.Phe410Val(p.F410V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397574
Start	613458:613458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745316844
CDS Mutation	c.985G>A
AA Mutation	p.Val329Ile(p.V329I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397574
Start	613963:613963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754G>A
AA Mutation	p.Ala252Thr(p.A252T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397574
Start	612655:612655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1502A>C
AA Mutation	p.Gln501Pro(p.Q501P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397574
Start	614522:614522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.407C>T
AA Mutation	p.Thr136Met(p.T136M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397574
Start	614299:614299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554A>G
AA Mutation	p.Gln185Arg(p.Q185R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397574
Start	613429:613429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760052779
CDS Mutation	c.1014G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397574
Start	613300:613300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755335495
CDS Mutation	c.1143C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397574
Start	613297:613297(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1146delA
AA Mutation	p.Pro384GlnfsTer68(p.P384Qfs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397574
Start	614364:614365(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.487_488dupCA
AA Mutation	p.Ala164MetfsTer35(p.A164Mfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IRF7

No Mutation Annotation!