Colon Cancer: Gene >> ADHFE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396623
Start	66452074:66452074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770694758
CDS Mutation	c.856G>A
AA Mutation	p.Ala286Thr(p.A286T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396623
Start	66448951:66448951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553493479
CDS Mutation	c.715A>C
AA Mutation	p.Ser239Arg(p.S239R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396623
Start	66445402:66445402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538C>A
AA Mutation	p.Pro180Thr(p.P180T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396623
Start	66442812:66442812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112C>G
AA Mutation	p.Pro38Ala(p.P38A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396623
Start	66447282:66447282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569C>A
AA Mutation	p.Thr190Asn(p.T190N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396623
Start	66442804:66442804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104G>A
AA Mutation	p.Gly35Glu(p.G35E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000396623
Start	66457140:66457140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778193632
CDS Mutation	c.1136G>A
AA Mutation	p.Arg379Gln(p.R379Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000396623
Start	66456843:66456843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013G>T
AA Mutation	p.Gly338Val(p.G338V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396623
Start	66460381:66460381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369719961
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396623
Start	66460456:66460456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200821866
CDS Mutation	c.1311G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396623
Start	66444615:66444615(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.224delA
AA Mutation	p.Asn75MetfsTer4(p.N75Mfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ADHFE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396623
Start	66444741:66444741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346G>C
AA Mutation	p.Asp116His(p.D116H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396623
Start	66444611:66444611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396623
Start	66460381:66460381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369719961
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396623
Start	66444599:66444599(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.209delA
AA Mutation	p.Asn70ThrfsTer9(p.N70Tfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript