Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> VASH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000517399
Start	212972635:212972635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553T>C
AA Mutation	p.Tyr185His(p.Y185H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000517399
Start	212972758:212972758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676A>T
AA Mutation	p.Ser226Cys(p.S226C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000517399
Start	212972830:212972830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748C>A
AA Mutation	p.Leu250Met(p.L250M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000517399
Start	212951788:212951788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000517399
Start	212951800:212951800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VASH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000517399
Start	212972640:212972640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558C>A
AA Mutation	p.Phe186Leu(p.F186L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000517399
Start	212972954:212972954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.872G>T
AA Mutation	p.Arg291Ile(p.R291I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000517399
Start	212951695:212951695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.153C>A
Mutation Classification	Silent
Feature Type	Transcript