Colon Cancer: Gene >> FLOT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376389
Start	30741299:30741299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245C>A
AA Mutation	p.Ala82Glu(p.A82E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376389
Start	30741828:30741828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.83G>T
AA Mutation	p.Arg28Leu(p.R28L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376389
Start	30730135:30730135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774019896
CDS Mutation	c.1141G>T
AA Mutation	p.Val381Leu(p.V381L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376389
Start	30740563:30740563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503G>A
AA Mutation	p.Arg168Gln(p.R168Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376389
Start	30742179:30742179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11C>T
AA Mutation	p.Thr4Ile(p.T4I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376389
Start	30741660:30741660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.164T>C
AA Mutation	p.Val55Ala(p.V55A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376389
Start	30730036:30730036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201200201
CDS Mutation	c.1240G>A
AA Mutation	p.Val414Met(p.V414M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376389
Start	30740232:30740232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747715326
CDS Mutation	c.649G>A
AA Mutation	p.Glu217Lys(p.E217K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376389
Start	30741298:30741298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541162560
CDS Mutation	c.246G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000376389
Start	30730523:30730523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.994C>T
AA Mutation	p.Arg332Ter(p.R332*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FLOT1

No Mutation Annotation!