Colon Cancer: Gene >> DDX27

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371764
Start	49236499:49236499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1769T>C
AA Mutation	p.Ile590Thr(p.I590T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371764
Start	49236179:49236179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1550T>C
AA Mutation	p.Leu517Pro(p.L517P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371764
Start	49236415:49236415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779990675
CDS Mutation	c.1685G>A
AA Mutation	p.Arg562His(p.R562H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371764
Start	49228789:49228789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761573110
CDS Mutation	c.874G>A
AA Mutation	p.Val292Met(p.V292M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371764
Start	49223281:49223281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.407A>C
AA Mutation	p.Lys136Thr(p.K136T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371764
Start	49234989:49234989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1421A>G
AA Mutation	p.Lys474Arg(p.K474R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371764
Start	49235000:49235000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759121430
CDS Mutation	c.1432C>T
AA Mutation	p.Arg478Cys(p.R478C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000371764
Start	49236152:49236152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760415513
CDS Mutation	c.1523G>A
AA Mutation	p.Arg508His(p.R508H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371764
Start	49221502:49221502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371764
Start	49226465:49226465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.729G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000622530
Start	49238971:49238971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1803C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371764
Start	49228725:49228725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs238166
CDS Mutation	c.810C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371764
Start	49221532:49221532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371764
Start	49233330:49233330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000371764
Start	49242635:49242635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2251G>T
AA Mutation	p.Glu751Ter(p.E751*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000371764
Start	49224986:49224986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.601G>T
AA Mutation	p.Gly201Ter(p.G201*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DDX27

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371764
Start	49235072:49235072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1504C>T
AA Mutation	p.Arg502Trp(p.R502W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371764
Start	49222979:49222979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356A>C
AA Mutation	p.Glu119Ala(p.E119A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000371764
Start	49243628:49243628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2298-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript