Colon Cancer: Gene >> MEN1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000337652
Start	64807893:64807893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs794728620
CDS Mutation	c.667C>T
AA Mutation	p.Arg223Trp(p.R223W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337652
Start	64804713:64804713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1469G>A
AA Mutation	p.Arg490Gln(p.R490Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337652
Start	64809930:64809930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180G>C
AA Mutation	p.Glu60Asp(p.E60D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337652
Start	64804621:64804621(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs794728642
CDS Mutation	c.1561delC
AA Mutation	p.Arg521GlyfsTer43(p.R521Gfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MEN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337652
Start	64809790:64809790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320C>G
AA Mutation	p.Pro107Arg(p.P107R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337652
Start	64807569:64807569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781C>A
AA Mutation	p.Leu261Ile(p.L261I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript