Colon Cancer: Gene >> DDX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225792
Start	64500632:64500632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358T>C
AA Mutation	p.Val453Ala(p.V453A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225792
Start	64499991:64499991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1777T>C
AA Mutation	p.Tyr593His(p.Y593H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000225792
Start	64503431:64503431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.648A>C
AA Mutation	p.Arg216Ser(p.R216S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225792
Start	64500036:64500036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782608247
CDS Mutation	c.1732G>A
AA Mutation	p.Gly578Arg(p.G578R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225792
Start	64504259:64504259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.270G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225792
Start	64503815:64503815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs79187435
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225792
Start	64500264:64500264(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1504delA
AA Mutation	p.Arg502GlyfsTer87(p.R502Gfs*87)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225792
Start	64500054:64500055(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1713_1714insAACTATCTTGTCA
AA Mutation	p.Asp572AsnfsTer6(p.D572Nfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225792
Start	64500720:64500721(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1269_1270insATTAATTGCTT
AA Mutation	p.Asp424IlefsTer31(p.D424Ifs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DDX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225792
Start	64500137:64500137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1631G>A
AA Mutation	p.Ser544Asn(p.S544N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript