Colon Cancer: Gene >> PLEKHF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000436066
Start	29674422:29674422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Cys(p.R195C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000436066
Start	29673895:29673895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.56A>C
AA Mutation	p.Glu19Ala(p.E19A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000436066
Start	29674209:29674209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370A>T
AA Mutation	p.Ser124Cys(p.S124C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000436066
Start	29674542:29674542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.703G>A
AA Mutation	p.Ala235Thr(p.A235T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000436066
Start	29673995:29673995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371222738
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000436066
Start	29674079:29674079(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.244delC
AA Mutation	p.Leu82TrpfsTer20(p.L82Wfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PLEKHF1

No Mutation Annotation!