Colon Cancer: Gene >> HYAL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336307
Start	50295305:50295305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298C>T
AA Mutation	p.Pro100Ser(p.P100S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336307
Start	50294906:50294906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.697T>C
AA Mutation	p.Trp233Arg(p.W233R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336307
Start	50294903:50294903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.700C>A
AA Mutation	p.Leu234Ile(p.L234I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336307
Start	50293677:50293677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.939A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336307
Start	50294895:50294895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781876186
CDS Mutation	c.708C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000336307
Start	50293517:50293517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> HYAL3

No Mutation Annotation!