Colon Cancer: Gene >> ZIC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287538
Start	137567311:137567311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620C>T
AA Mutation	p.Thr207Met(p.T207M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287538
Start	137567182:137567182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748579579
CDS Mutation	c.491G>A
AA Mutation	p.Gly164Glu(p.G164E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287538
Start	137567713:137567713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022G>A
AA Mutation	p.Arg341His(p.R341H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287538
Start	137566759:137566759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.68G>A
AA Mutation	p.Arg23His(p.R23H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287538
Start	137567601:137567601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.910C>T
AA Mutation	p.Arg304Trp(p.R304W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287538
Start	137567331:137567331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640G>A
AA Mutation	p.Ala214Thr(p.A214T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287538
Start	137566750:137566750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.59G>C
AA Mutation	p.Gly20Ala(p.G20A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287538
Start	137569984:137569984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318G>T
AA Mutation	p.Asp440Tyr(p.D440Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000287538
Start	137567688:137567688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997C>A
AA Mutation	p.Pro333Thr(p.P333T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000287538
Start	137568992:137568992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1151C>T
AA Mutation	p.Ser384Leu(p.S384L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000287538
Start	137567329:137567329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.638G>A
AA Mutation	p.Gly213Asp(p.G213D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287538
Start	137567393:137567393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287538
Start	137569017:137569017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780449661
CDS Mutation	c.1176G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287538
Start	137567090:137567090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.399T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287538
Start	137567597:137567597(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.910delC
AA Mutation	p.Arg304GlyfsTer104(p.R304Gfs*104)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZIC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287538
Start	137567430:137567430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739A>T
AA Mutation	p.Ile247Phe(p.I247F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287538
Start	137567624:137567624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000287538
Start	137569897:137569897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1231G>T
AA Mutation	p.Glu411Ter(p.E411*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript