Colon Cancer: Gene >> RASSF7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397583
Start	562444:562444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490A>T
AA Mutation	p.Arg164Trp(p.R164W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397583
Start	562174:562174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220G>A
AA Mutation	p.Gly74Arg(p.G74R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397583
Start	562540:562540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.586C>G
AA Mutation	p.Leu196Val(p.L196V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397583
Start	562380:562380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.426G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000397583
Start	563395:563395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.952-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RASSF7

No Mutation Annotation!