Colon Cancer: Gene >> DGCR8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351989
Start	20089795:20089795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007G>A
AA Mutation	p.Gly336Glu(p.G336E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000351989
Start	20086048:20086048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85G>T
AA Mutation	p.Ala29Ser(p.A29S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000351989
Start	20092844:20092844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1642A>G
AA Mutation	p.Ile548Val(p.I548V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000351989
Start	20091470:20091470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1342T>C
AA Mutation	p.Phe448Leu(p.F448L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000351989
Start	20087253:20087253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.812G>A
AA Mutation	p.Ser271Asn(p.S271N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000351989
Start	20091877:20091877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1513A>G
AA Mutation	p.Ile505Val(p.I505V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351989
Start	20106661:20106661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763037264
CDS Mutation	c.1959C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351989
Start	20106215:20106215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145970507
CDS Mutation	c.1827C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351989
Start	20086431:20086431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351989
Start	20087266:20087266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753194485
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351989
Start	20086614:20086614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758334658
CDS Mutation	c.651C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000351989
Start	20090182:20090192(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1231_1241delCTAGGGGCTGA
AA Mutation	p.Leu411GlyfsTer19(p.L411Gfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000351989
Start	20086289:20086289(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.329delC
AA Mutation	p.Pro110LeufsTer9(p.P110Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000351989
Start	20091449:20091449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321C>T
AA Mutation	p.Arg441Ter(p.R441*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000351989
Start	20092909:20092909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1705+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DGCR8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351989
Start	20089715:20089715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927G>T
AA Mutation	p.Met309Ile(p.M309I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript