Colon Cancer: Gene >> DDX21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354185
Start	68967023:68967023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144769035
CDS Mutation	c.910C>T
AA Mutation	p.Arg304Cys(p.R304C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354185
Start	68970219:68970219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255C>A
AA Mutation	p.His419Asn(p.H419N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354185
Start	68982784:68982784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200756197
CDS Mutation	c.2324G>A
AA Mutation	p.Arg775Gln(p.R775Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354185
Start	68967056:68967056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943A>T
AA Mutation	p.Thr315Ser(p.T315S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354185
Start	68982671:68982671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2211G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354185
Start	68982677:68982677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746814470
CDS Mutation	c.2217C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354185
Start	68969088:68969088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1203T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354185
Start	68969019:68969019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354185
Start	68960063:68960063(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.350delA
AA Mutation	p.Asn117MetfsTer9(p.N117Mfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354185
Start	68962140:68962141(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.590_591insACATCACT
AA Mutation	p.Ile198HisfsTer12(p.I198Hfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DDX21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354185
Start	68960011:68960011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.293A>C
AA Mutation	p.Lys98Thr(p.K98T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354185
Start	68978956:68978956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2017G>T
AA Mutation	p.Val673Phe(p.V673F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript