Colon Cancer: Gene >> SPI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378538
Start	47378334:47378334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.20T>A
AA Mutation	p.Met7Lys(p.M7K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378538
Start	47358964:47358964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373T>A
AA Mutation	p.Ser125Thr(p.S125T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378538
Start	47359883:47359883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300G>A
AA Mutation	p.Met100Ile(p.M100I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378538
Start	47375701:47375701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.74C>T
AA Mutation	p.Thr25Met(p.T25M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378538
Start	47359987:47359987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113825984
CDS Mutation	c.196G>A
AA Mutation	p.Ala66Thr(p.A66T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378538
Start	47359984:47359984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199G>A
AA Mutation	p.Glu67Lys(p.E67K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378538
Start	47355383:47355383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378538
Start	47360017:47360017(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.166delC
AA Mutation	p.His56ThrfsTer130(p.H56Tfs*130)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SPI1

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378538
Start	47359886:47359886(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.297delC
AA Mutation	p.Met100TrpfsTer86(p.M100Wfs*86)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript