Colon Cancer: Gene >> ZIC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147411083:147411083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971G>T
AA Mutation	p.Arg324Met(p.R324M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147412577:147412577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1042G>A
AA Mutation	p.Asp348Asn(p.D348N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147410681:147410681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569C>A
AA Mutation	p.Ala190Asp(p.A190D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147410729:147410729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617C>T
AA Mutation	p.Ala206Val(p.A206V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147412631:147412631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756221956
CDS Mutation	c.1096A>G
AA Mutation	p.Met366Val(p.M366V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147410405:147410405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.293G>A
AA Mutation	p.Arg98Gln(p.R98Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147410647:147410647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535G>A
AA Mutation	p.Gly179Ser(p.G179S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147412678:147412678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1143G>T
AA Mutation	p.Met381Ile(p.M381I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147411055:147411055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943C>T
AA Mutation	p.Arg315Cys(p.R315C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147410818:147410818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706G>A
AA Mutation	p.Ala236Thr(p.A236T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147413480:147413480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs75992939
CDS Mutation	c.1273T>C
AA Mutation	p.Ser425Pro(p.S425P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147412605:147412605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1070C>T
AA Mutation	p.Thr357Met(p.T357M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282928
Start	147410439:147410439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282928
Start	147410403:147410403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282928
Start	147410742:147410742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZIC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147410850:147410850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738C>G
AA Mutation	p.Phe246Leu(p.F246L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147410948:147410948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836A>G
AA Mutation	p.Glu279Gly(p.E279G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282928
Start	147412647:147412647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112A>G
AA Mutation	p.Tyr371Cys(p.Y371C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282928
Start	147410946:147410946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282928
Start	147410688:147410688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759778746
CDS Mutation	c.576G>A
Mutation Classification	Silent
Feature Type	Transcript