Colon Cancer: Gene >> DDX53

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327968
Start	23000287:23000287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230C>T
AA Mutation	p.Ser77Leu(p.S77L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327968
Start	23000589:23000589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.532T>G
AA Mutation	p.Phe178Val(p.F178V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327968
Start	23001250:23001250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368434907
CDS Mutation	c.1193G>A
AA Mutation	p.Arg398His(p.R398H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327968
Start	23000304:23000304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247C>G
AA Mutation	p.Gln83Glu(p.Q83E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327968
Start	23000089:23000089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.32C>T
AA Mutation	p.Ala11Val(p.A11V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327968
Start	23000271:23000271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214A>G
AA Mutation	p.Lys72Glu(p.K72E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327968
Start	23001351:23001351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1294A>G
AA Mutation	p.Asn432Asp(p.N432D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327968
Start	23001512:23001512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373240695
CDS Mutation	c.1455C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327968
Start	23000315:23000315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778444531
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327968
Start	23001830:23001830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1773G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327968
Start	23001579:23001579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1522C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DDX53

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327968
Start	23001078:23001078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1021G>T
AA Mutation	p.Asp341Tyr(p.D341Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327968
Start	23001785:23001785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768469586
CDS Mutation	c.1728G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327968
Start	23000586:23000587(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.529_530insT
AA Mutation	p.Asn177IlefsTer14(p.N177Ifs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript