Colon Cancer: Gene >> FOXL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320241
Start	86578821:86578821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781452561
CDS Mutation	c.98C>T
AA Mutation	p.Ala33Val(p.A33V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320241
Start	86579046:86579046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323T>C
AA Mutation	p.Val108Ala(p.V108A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320241
Start	86578781:86578781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765582433
CDS Mutation	c.58C>G
AA Mutation	p.Leu20Val(p.L20V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320241
Start	86579073:86579073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350C>T
AA Mutation	p.Pro117Leu(p.P117L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000320241
Start	86578739:86578739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16G>A
AA Mutation	p.Asp6Asn(p.D6N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000320241
Start	86579054:86579054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331C>T
AA Mutation	p.Pro111Ser(p.P111S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000320241
Start	86578916:86578916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193G>A
AA Mutation	p.Ala65Thr(p.A65T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320241
Start	86579611:86579611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320241
Start	86578768:86578768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.45G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FOXL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320241
Start	86579082:86579082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359G>A
AA Mutation	p.Gly120Asp(p.G120D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320241
Start	86578790:86578790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.67C>A
AA Mutation	p.Pro23Thr(p.P23T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320241
Start	86578906:86578906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320241
Start	86579625:86579625(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.903delC
AA Mutation	p.Ser302ProfsTer11(p.S302Pfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript