Colon Cancer: Gene >> CENPH

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000283006
Start	69195791:69195791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314G>T
AA Mutation	p.Arg105Met(p.R105M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283006
Start	69194691:69194691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200925138
CDS Mutation	c.235G>A
AA Mutation	p.Glu79Lys(p.E79K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283006
Start	69197075:69197075(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.344delA
AA Mutation	p.Asn115ThrfsTer16(p.N115Tfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000283006
Start	69202571:69202571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CENPH

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283006
Start	69194690:69194690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234C>T
Mutation Classification	Silent
Feature Type	Transcript