Colon Cancer: Gene >> NPM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296930
Start	171390073:171390073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.81A>T
AA Mutation	p.Lys27Asn(p.K27N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296930
Start	171400842:171400842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376742289
CDS Mutation	c.586A>G
AA Mutation	p.Ile196Val(p.I196V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296930
Start	171387955:171387955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7G>T
AA Mutation	p.Asp3Tyr(p.D3Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296930
Start	171392957:171392957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503A>G
AA Mutation	p.Asp168Gly(p.D168G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296930
Start	171392932:171392932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478G>C
AA Mutation	p.Ala160Pro(p.A160P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296930
Start	171392931:171392932(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.477_478insACCA
AA Mutation	p.Ala160ThrfsTer3(p.A160Tfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000296930
Start	171392966:171392984(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.517_524+11delGATGAAGAGTAAGTATGAT
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NPM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296930
Start	171400863:171400863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607A>C
AA Mutation	p.Asn203His(p.N203H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript