Colon Cancer: Gene >> SPIB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000595883
Start	50428203:50428203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656G>T
AA Mutation	p.Arg219Leu(p.R219L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000595883
Start	50422957:50422957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259G>T
AA Mutation	p.Gly87Trp(p.G87W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000595883
Start	50428209:50428209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563144649
CDS Mutation	c.662G>A
AA Mutation	p.Arg221His(p.R221H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000595883
Start	50422933:50422933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758882487
CDS Mutation	c.235G>A
AA Mutation	p.Glu79Lys(p.E79K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595883
Start	50428084:50428084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.537G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595883
Start	50428090:50428090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000595883
Start	50422908:50422908(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.214delC
AA Mutation	p.Gln72ArgfsTer108(p.Q72Rfs*108)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000595883
Start	50423007:50423007(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.309delT
AA Mutation	p.Ala104HisfsTer76(p.A104Hfs*76)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SPIB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000595883
Start	50422882:50422882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769582985
CDS Mutation	c.184G>A
AA Mutation	p.Asp62Asn(p.D62N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595883
Start	50428231:50428231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595883
Start	50423619:50423619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.354G>A
Mutation Classification	Silent
Feature Type	Transcript