Colon Cancer: Gene >> DDX41

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000507955
Start	177512179:177512179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1649C>T
AA Mutation	p.Ala550Val(p.A550V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000507955
Start	177511859:177511859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1801A>G
AA Mutation	p.Met601Val(p.M601V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000507955
Start	177516126:177516126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366G>T
AA Mutation	p.Glu122Asp(p.E122D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000507955
Start	177512370:177512370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1573C>T
AA Mutation	p.Arg525Cys(p.R525C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000507955
Start	177512338:177512338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1605C>A
AA Mutation	p.Phe535Leu(p.F535L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000507955
Start	177512789:177512789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1390G>A
AA Mutation	p.Gly464Arg(p.G464R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000507955
Start	177513720:177513720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778864620
CDS Mutation	c.1063G>A
AA Mutation	p.Glu355Lys(p.E355K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000507955
Start	177511920:177511920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148650463
CDS Mutation	c.1740C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000507955
Start	177511917:177511917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1743C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000507955
Start	177516123:177516123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.369C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000507955
Start	177513032:177513032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DDX41

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000507955
Start	177514704:177514704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932G>A
AA Mutation	p.Arg311Gln(p.R311Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript