Colon Cancer: Gene >> VASP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245932
Start	45522772:45522772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775G>A
AA Mutation	p.Gly259Arg(p.G259R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245932
Start	45525990:45525990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1092G>T
AA Mutation	p.Glu364Asp(p.E364D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000245932
Start	45521330:45521330(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.356delC
AA Mutation	p.Pro119LeufsTer34(p.P119Lfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000245932
Start	45522354:45522354(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.498delC
AA Mutation	p.Ala167LeufsTer101(p.A167Lfs*101)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000245932
Start	45523878:45523878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.910+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000245932
Start	45522219:45522219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> VASP

No Mutation Annotation!