Colon Cancer: Gene >> MSI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257552
Start	120364725:120364725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298G>A
AA Mutation	p.Ala100Thr(p.A100T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257552
Start	120368039:120368039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.236C>T
AA Mutation	p.Ala79Val(p.A79V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257552
Start	120346251:120346251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931A>G
AA Mutation	p.Thr311Ala(p.T311A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257552
Start	120353367:120353367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.665T>A
AA Mutation	p.Phe222Tyr(p.F222Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257552
Start	120356993:120356993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561G>T
AA Mutation	p.Lys187Asn(p.K187N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257552
Start	120364739:120364739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284C>T
AA Mutation	p.Ala95Val(p.A95V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257552
Start	120346306:120346306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756975620
CDS Mutation	c.876G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257552
Start	120357882:120357882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555470172
CDS Mutation	c.468G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257552
Start	120346295:120346295(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.887delC
AA Mutation	p.Pro296LeufsTer57(p.P296Lfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MSI1

No Mutation Annotation!