Colon Cancer: Gene >> FOXN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226247
Start	28524082:28524082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113C>T
AA Mutation	p.Ala38Val(p.A38V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226247
Start	28529164:28529164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770C>A
AA Mutation	p.Ala257Glu(p.A257E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226247
Start	28524701:28524701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774400145
CDS Mutation	c.322G>A
AA Mutation	p.Ala108Thr(p.A108T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226247
Start	28524585:28524585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769969790
CDS Mutation	c.206G>A
AA Mutation	p.Arg69His(p.R69H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000226247
Start	28535198:28535198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1627G>A
AA Mutation	p.Gly543Arg(p.G543R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000226247
Start	28529207:28529207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.813A>C
AA Mutation	p.Lys271Asn(p.K271N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226247
Start	28524032:28524032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758840390
CDS Mutation	c.63C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226247
Start	28524877:28524877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.498G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000226247
Start	28537232:28537232(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1748delC
AA Mutation	p.Pro583LeufsTer5(p.P583Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000226247
Start	28534814:28534814(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1247delC
AA Mutation	p.Pro416GlnfsTer134(p.P416Qfs*134)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FOXN1

No Mutation Annotation!