Colon Cancer: Gene >> OTX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282549
Start	63056030:63056030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779A>G
AA Mutation	p.His260Arg(p.H260R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282549
Start	63055757:63055757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.506G>C
AA Mutation	p.Ser169Thr(p.S169T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282549
Start	63053034:63053034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44T>A
AA Mutation	p.Leu15Gln(p.L15Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282549
Start	63055685:63055685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434C>T
AA Mutation	p.Ser145Phe(p.S145F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282549
Start	63055529:63055529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278G>A
AA Mutation	p.Cys93Tyr(p.C93Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282549
Start	63056269:63056269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1018T>G
AA Mutation	p.Cys340Gly(p.C340G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282549
Start	63056299:63056299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048C>T
AA Mutation	p.Arg350Trp(p.R350W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282549
Start	63055554:63055554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282549
Start	63056220:63056220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282549
Start	63056106:63056106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.855G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282549
Start	63056139:63056139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OTX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282549
Start	63055894:63055894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643G>A
AA Mutation	p.Ala215Thr(p.A215T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript