Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HYAL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357750
Start	50319616:50319616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874G>A
AA Mutation	p.Val292Ile(p.V292I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357750
Start	50318157:50318157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1394C>T
AA Mutation	p.Ala465Val(p.A465V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357750
Start	50320410:50320410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80C>T
AA Mutation	p.Ala27Val(p.A27V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357750
Start	50319752:50319752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149978009
CDS Mutation	c.738G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357750
Start	50319947:50319947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782813686
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000357750
Start	50318306:50318306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1245G>A
AA Mutation	p.Trp415Ter(p.W415*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HYAL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357750
Start	50319916:50319916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782059591
CDS Mutation	c.574C>T
AA Mutation	p.Arg192Cys(p.R192C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357750
Start	50320223:50320223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201798244
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357750
Start	50320442:50320442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48G>T
Mutation Classification	Silent
Feature Type	Transcript