Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> APOH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000205948
Start	66223718:66223718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763687723
CDS Mutation	c.395C>T
AA Mutation	p.Pro132Leu(p.P132L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000205948
Start	66214474:66214474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35449692
CDS Mutation	c.961G>A
AA Mutation	p.Glu321Lys(p.E321K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000205948
Start	66214579:66214579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856T>A
AA Mutation	p.Phe286Ile(p.F286I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000205948
Start	66216886:66216886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686A>C
AA Mutation	p.Lys229Thr(p.K229T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000205948
Start	66214550:66214550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885A>T
AA Mutation	p.Lys295Asn(p.K295N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000205948
Start	66228130:66228131(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.130_131insAATGTGA
AA Mutation	p.Gly44GlufsTer60(p.G44Efs*60)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> APOH

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205948
Start	66220621:66220621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367862167
CDS Mutation	c.537G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205948
Start	66223759:66223759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150179394
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000205948
Start	66228089:66228089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172C>T
AA Mutation	p.Arg58Ter(p.R58*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000205948
Start	66212166:66212166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1005G>A
AA Mutation	p.Trp335Ter(p.W335*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript