Colon Cancer: Gene >> INPP5E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371712
Start	136439109:136439109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748786705
CDS Mutation	c.311A>T
AA Mutation	p.Glu104Val(p.E104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371712
Start	136432520:136432520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346C>A
AA Mutation	p.Pro449His(p.P449H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371712
Start	136434805:136434805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871G>A
AA Mutation	p.Ala291Thr(p.A291T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371712
Start	136438864:136438864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556C>T
AA Mutation	p.Pro186Ser(p.P186S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371712
Start	136430407:136430407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1672G>A
AA Mutation	p.Val558Ile(p.V558I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371712
Start	136434043:136434043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1028C>T
AA Mutation	p.Ser343Phe(p.S343F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371712
Start	136432482:136432482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200837258
CDS Mutation	c.1384G>A
AA Mutation	p.Ala462Thr(p.A462T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371712
Start	136433048:136433048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779363781
CDS Mutation	c.1187G>A
AA Mutation	p.Arg396His(p.R396H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371712
Start	136431014:136431014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1653G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371712
Start	136431864:136431864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770801327
CDS Mutation	c.1509G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371712
Start	136430408:136430408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1671C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> INPP5E

No Mutation Annotation!