Colon Cancer: Gene >> MDM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258149
Start	68828877:68828877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630G>T
AA Mutation	p.Glu210Asp(p.E210D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258149
Start	68839725:68839725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1370T>C
AA Mutation	p.Val457Ala(p.V457A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258149
Start	68835925:68835925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549965230
CDS Mutation	c.781G>A
AA Mutation	p.Asp261Asn(p.D261N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258149
Start	68839393:68839393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038A>C
AA Mutation	p.Glu346Asp(p.E346D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258149
Start	68839838:68839838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483T>C
AA Mutation	p.Tyr495His(p.Y495H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258149
Start	68839382:68839382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027G>A
AA Mutation	p.Asp343Asn(p.D343N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258149
Start	68836745:68836746(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.914_915insCAATCAGA
AA Mutation	p.Leu305PhefsTer16(p.L305Ffs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MDM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258149
Start	68835844:68835844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700G>T
AA Mutation	p.Val234Leu(p.V234L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript