Colon Cancer: Gene >> MLF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000203630
Start	6749895:6749895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.512G>A
AA Mutation	p.Arg171His(p.R171H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000203630
Start	6750734:6750734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.249G>A
AA Mutation	p.Met83Ile(p.M83I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000203630
Start	6749887:6749887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520G>C
AA Mutation	p.Asp174His(p.D174H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000203630
Start	6749995:6749995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745833590
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Trp(p.R138W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000203630
Start	6751971:6751971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134A>G
AA Mutation	p.Asp45Gly(p.D45G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000203630
Start	6749931:6749932(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.475dupG
AA Mutation	p.Asp159GlyfsTer28(p.D159Gfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MLF2

No Mutation Annotation!