Colon Cancer: Gene >> RASSF6

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000342081
Start	73576308:73576308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037T>C
AA Mutation	p.Phe346Ser(p.F346S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342081
Start	73576660:73576660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149223773
CDS Mutation	c.889G>A
AA Mutation	p.Ala297Thr(p.A297T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342081
Start	73593548:73593548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286T>C
AA Mutation	p.Trp96Arg(p.W96R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342081
Start	73598667:73598667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342081
Start	73585198:73585198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342081
Start	73582195:73582195(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.759delA
AA Mutation	p.Lys253AsnfsTer25(p.K253Nfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000342081
Start	73576444:73576444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1000G>T
AA Mutation	p.Glu334Ter(p.E334*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342081
Start	73611819:73611820(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.72_73insTTGATCTTGTT
AA Mutation	p.Asp25LeufsTer13(p.D25Lfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RASSF6

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000342081
Start	73576627:73576627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922G>T
AA Mutation	p.Glu308Ter(p.E308*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript