Colon Cancer: Gene >> DDX6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000526070
Start	118763237:118763237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.716A>G
AA Mutation	p.His239Arg(p.H239R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000526070
Start	118755475:118755475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1203A>C
AA Mutation	p.Gln401His(p.Q401H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000526070
Start	118756275:118756275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159A>G
AA Mutation	p.Asn387Asp(p.N387D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000526070
Start	118756316:118756316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118G>A
AA Mutation	p.Arg373Gln(p.R373Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000526070
Start	118781154:118781154(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.231delA
AA Mutation	p.Lys77AsnfsTer7(p.K77Nfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000526070
Start	118786155:118786155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97G>T
AA Mutation	p.Gly33Ter(p.G33*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DDX6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000526070
Start	118756316:118756316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118G>A
AA Mutation	p.Arg373Gln(p.R373Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript