Colon Cancer: Gene >> FOXN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261302
Start	89162868:89162868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019C>A
AA Mutation	p.Ala340Asp(p.A340D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261302
Start	89412161:89412161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316G>A
AA Mutation	p.Asp106Asn(p.D106N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261302
Start	89162490:89162490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1397T>C
AA Mutation	p.Ile466Thr(p.I466T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261302
Start	89162709:89162709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369372657
CDS Mutation	c.1178C>T
AA Mutation	p.Thr393Met(p.T393M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261302
Start	89162581:89162581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199923188
CDS Mutation	c.1306C>T
AA Mutation	p.Pro436Ser(p.P436S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261302
Start	89412133:89412133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344C>A
AA Mutation	p.Pro115His(p.P115H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261302
Start	89162713:89162713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754903884
CDS Mutation	c.1174G>A
AA Mutation	p.Asp392Asn(p.D392N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261302
Start	89162602:89162602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1285A>G
AA Mutation	p.Lys429Glu(p.K429E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261302
Start	89412181:89412181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296C>A
AA Mutation	p.Ala99Asp(p.A99D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261302
Start	89162699:89162699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143673672
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261302
Start	89412190:89412190(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763678909
CDS Mutation	c.287delC
AA Mutation	p.Pro96HisfsTer42(p.P96Hfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261302
Start	89412129:89412129(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.348delC
AA Mutation	p.Tyr117ThrfsTer21(p.Y117Tfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FOXN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261302
Start	89412316:89412316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147377124
CDS Mutation	c.161C>T
AA Mutation	p.Ala54Val(p.A54V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261302
Start	89412331:89412331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754294736
CDS Mutation	c.146G>A
AA Mutation	p.Arg49Gln(p.R49Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript