Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MDFIC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393486
Start	114979611:114979611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323G>A
AA Mutation	p.Gly108Glu(p.G108E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393486
Start	115015850:115015850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656A>T
AA Mutation	p.Asp219Val(p.D219V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393486
Start	114942374:114942374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.194C>A
AA Mutation	p.Pro65His(p.P65H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393486
Start	114979750:114979750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393486
Start	115015812:115015812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552071640
CDS Mutation	c.618C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393486
Start	115015731:115015731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393486
Start	114942297:114942297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779960274
CDS Mutation	c.117T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393486
Start	114979674:114979674(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.391delA
AA Mutation	p.Met131CysfsTer11(p.M131Cfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MDFIC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393486
Start	114979718:114979718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430G>A
AA Mutation	p.Asp144Asn(p.D144N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393486
Start	114979659:114979659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764638487
CDS Mutation	c.371C>T
AA Mutation	p.Ser124Leu(p.S124L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393486
Start	114979625:114979625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>A
AA Mutation	p.Ala113Thr(p.A113T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript