Colon Cancer: Gene >> DSN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373750
Start	36771078:36771078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150G>T
AA Mutation	p.Glu50Asp(p.E50D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373750
Start	36771086:36771086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552571192
CDS Mutation	c.142G>A
AA Mutation	p.Val48Ile(p.V48I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373750
Start	36758147:36758147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761761654
CDS Mutation	c.665G>A
AA Mutation	p.Arg222His(p.R222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373750
Start	36770893:36770893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335C>A
AA Mutation	p.Pro112His(p.P112H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373750
Start	36768020:36768020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745734102
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373750
Start	36771045:36771045(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.183delA
AA Mutation	p.Gly63GlufsTer39(p.G63Efs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000373750
Start	36762531:36762531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520G>T
AA Mutation	p.Glu174Ter(p.E174*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DSN1

No Mutation Annotation!