Colon Cancer: Gene >> MAD2L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000235310
Start	11676902:11676902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151024263
CDS Mutation	c.278G>A
AA Mutation	p.Arg93His(p.R93H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000235310
Start	11675163:11675163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513G>T
AA Mutation	p.Trp171Cys(p.W171C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000235310
Start	11674795:11674795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142776270
CDS Mutation	c.616C>T
AA Mutation	p.Arg206Cys(p.R206C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235310
Start	11675097:11675097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28924114
CDS Mutation	c.579G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000235310
Start	11676048:11676048(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.425delC
AA Mutation	p.Pro142GlnfsTer45(p.P142Qfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAD2L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000235310
Start	11675095:11675095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581C>T
AA Mutation	p.Ser194Leu(p.S194L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000235310
Start	11676892:11676892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288G>T
AA Mutation	p.Glu96Asp(p.E96D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript