Colon Cancer: Gene >> DKK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220812
Start	42375772:42375772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374249506
CDS Mutation	c.170G>A
AA Mutation	p.Arg57His(p.R57H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220812
Start	42374134:42374134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202061584
CDS Mutation	c.641G>A
AA Mutation	p.Arg214Gln(p.R214Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220812
Start	42377038:42377038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8C>T
AA Mutation	p.Ala3Val(p.A3V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220812
Start	42374191:42374191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584A>G
AA Mutation	p.Asp195Gly(p.D195G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000220812
Start	42374155:42374155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620C>T
AA Mutation	p.Thr207Ile(p.T207I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000220812
Start	42374167:42374167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772507402
CDS Mutation	c.608G>A
AA Mutation	p.Arg203Gln(p.R203Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000220812
Start	42374858:42374858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318G>T
AA Mutation	p.Glu106Asp(p.E106D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000220812
Start	42375734:42375734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770888126
CDS Mutation	c.208C>T
AA Mutation	p.Arg70Trp(p.R70W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220812
Start	42374114:42374114(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.661delA
AA Mutation	p.Ile221Ter(p.I221*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DKK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220812
Start	42374859:42374859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317A>C
AA Mutation	p.Glu106Ala(p.E106A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220812
Start	42374167:42374167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772507402
CDS Mutation	c.608G>A
AA Mutation	p.Arg203Gln(p.R203Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript