Colon Cancer: Gene >> DDX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000505374
Start	55781086:55781086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534079199
CDS Mutation	c.517G>A
AA Mutation	p.Glu173Lys(p.E173K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000505374
Start	55815343:55815343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2017G>A
AA Mutation	p.Glu673Lys(p.E673K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000505374
Start	55786632:55786632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979G>T
AA Mutation	p.Asp327Tyr(p.D327Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000505374
Start	55815083:55815083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1898G>A
AA Mutation	p.Arg633His(p.R633H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000505374
Start	55790608:55790608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1205G>T
AA Mutation	p.Gly402Val(p.G402V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000505374
Start	55815157:55815157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1972A>C
AA Mutation	p.Lys658Gln(p.K658Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000505374
Start	55815007:55815007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1822A>C
AA Mutation	p.Asn608His(p.N608H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000505374
Start	55760259:55760259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000505374
Start	55760216:55760216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000505374
Start	55813745:55813745(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1693delA
AA Mutation	p.Ile565TyrfsTer35(p.I565Yfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000505374
Start	55780044:55780044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475G>T
AA Mutation	p.Gly159Ter(p.G159*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000505374
Start	55792640:55792640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1303-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DDX4

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000505374
Start	55760201:55760201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129A>C
AA Mutation	p.Glu43Asp(p.E43D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000505374
Start	55760224:55760224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.152G>T
AA Mutation	p.Arg51Ile(p.R51I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000505374
Start	55763250:55763250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281G>T
AA Mutation	p.Arg94Ile(p.R94I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000505374
Start	55785328:55785328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000505374
Start	55815424:55815424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2097+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000505374
Start	55792640:55792640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1303-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript