Colon Cancer: Gene >> WIF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286574
Start	65121184:65121184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8G>A
AA Mutation	p.Arg3Gln(p.R3Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286574
Start	65120490:65120490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215A>T
AA Mutation	p.Lys72Ile(p.K72I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286574
Start	65051465:65051465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024G>A
AA Mutation	p.Glu342Lys(p.E342K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286574
Start	65066729:65066729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.642T>G
AA Mutation	p.Cys214Trp(p.C214W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286574
Start	65077823:65077823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781329359
CDS Mutation	c.320G>A
AA Mutation	p.Arg107His(p.R107H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000286574
Start	65120455:65120455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250A>G
AA Mutation	p.Ile84Val(p.I84V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286574
Start	65051391:65051391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757666764
CDS Mutation	c.1098C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286574
Start	65051373:65051373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> WIF1

No Mutation Annotation!