Colon Cancer: Gene >> PLEKHO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369124
Start	150158967:150158967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674C>A
AA Mutation	p.Ala225Glu(p.A225E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369124
Start	150159304:150159304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1011G>T
AA Mutation	p.Lys337Asn(p.K337N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369124
Start	150159507:150159507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782430585
CDS Mutation	c.1214G>A
AA Mutation	p.Arg405Gln(p.R405Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369124
Start	150159504:150159504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1211A>G
AA Mutation	p.Tyr404Cys(p.Y404C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369124
Start	150151040:150151040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.159C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369124
Start	150159352:150159352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1059G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369124
Start	150159054:150159054(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.766delC
AA Mutation	p.Gln256ArgfsTer6(p.Q256Rfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000369124
Start	150159293:150159293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000C>T
AA Mutation	p.Arg334Ter(p.R334*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PLEKHO1

No Mutation Annotation!