Colon Cancer: Gene >> RASSF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357043
Start	50331676:50331676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655C>G
AA Mutation	p.His219Asp(p.H219D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357043
Start	50331664:50331664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376674291
CDS Mutation	c.667C>T
AA Mutation	p.Arg223Cys(p.R223C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357043
Start	50337996:50337996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.278G>A
AA Mutation	p.Cys93Tyr(p.C93Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357043
Start	50331578:50331578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201678786
CDS Mutation	c.753C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357043
Start	50330721:50330724(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.892_895delGACG
AA Mutation	p.Asp298ProfsTer77(p.D298Pfs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357043
Start	50330589:50330589(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1027delC
AA Mutation	p.Ter345AspfsTer31(p.*345Dfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RASSF1

Mutation ID	1
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000357043
Start	50331557:50331557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.772+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript