Colon Cancer: Gene >> LY96

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284818
Start	74010066:74010066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268C>T
AA Mutation	p.Arg90Cys(p.R90C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284818
Start	73991546:73991546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104C>G
AA Mutation	p.Thr35Ser(p.T35S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284818
Start	74026830:74026830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.373A>C
AA Mutation	p.Lys125Gln(p.K125Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284818
Start	74026829:74026829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284818
Start	73991458:73991458(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.22delT
AA Mutation	p.Ser8ProfsTer45(p.S8Pfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000284818
Start	74004858:74004858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.175G>T
AA Mutation	p.Gly59Ter(p.G59*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LY96

Mutation ID	1
Mutation Consequence	stop_lost
Transcription ID	ENST00000284818
Start	74029054:74029054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.483G>T
AA Mutation	p.Ter161TyrextTer6(p.*161Yext*6)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript