Colon Cancer: Gene >> INPP5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368594
Start	132710452:132710452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643G>A
AA Mutation	p.Asp215Asn(p.D215N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368594
Start	132710405:132710405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596C>A
AA Mutation	p.Pro199His(p.P199H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368594
Start	132777690:132777690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576088004
CDS Mutation	c.997G>A
AA Mutation	p.Ala333Thr(p.A333T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368594
Start	132726840:132726840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667G>A
AA Mutation	p.Glu223Lys(p.E223K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368594
Start	132781880:132781880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374027590
CDS Mutation	c.1178G>A
AA Mutation	p.Arg393Gln(p.R393Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368594
Start	132780872:132780872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1113C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368594
Start	132710445:132710445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778625312
CDS Mutation	c.636C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368594
Start	132690427:132690427(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.347delA
AA Mutation	p.Asn116ThrfsTer25(p.N116Tfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000368594
Start	132650419:132650419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220G>T
AA Mutation	p.Glu74Ter(p.E74*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> INPP5A

No Mutation Annotation!