Colon Cancer: Gene >> INPP5J

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331075
Start	31133416:31133416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759418802
CDS Mutation	c.2342G>A
AA Mutation	p.Arg781His(p.R781H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331075
Start	31127970:31127970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1807G>A
AA Mutation	p.Asp603Asn(p.D603N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331075
Start	31127982:31127982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369582455
CDS Mutation	c.1819C>T
AA Mutation	p.Arg607Cys(p.R607C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331075
Start	31133442:31133442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2368G>A
AA Mutation	p.Val790Ile(p.V790I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331075
Start	31126973:31126973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547A>G
AA Mutation	p.Tyr516Cys(p.Y516C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331075
Start	31128503:31128503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374379847
CDS Mutation	c.2042G>A
AA Mutation	p.Arg681His(p.R681H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331075
Start	31127015:31127015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760092310
CDS Mutation	c.1589G>A
AA Mutation	p.Arg530His(p.R530H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331075
Start	31123109:31123109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95C>T
AA Mutation	p.Ala32Val(p.A32V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331075
Start	31133107:31133107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2203A>G
AA Mutation	p.Arg735Gly(p.R735G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000331075
Start	31134150:31134150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2752C>T
AA Mutation	p.Arg918Cys(p.R918C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000331075
Start	31127387:31127387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1642G>A
AA Mutation	p.Ala548Thr(p.A548T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331075
Start	31133205:31133205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2301C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331075
Start	31133223:31133223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767376371
CDS Mutation	c.2319C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> INPP5J

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331075
Start	31133169:31133169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544342010
CDS Mutation	c.2265G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331075
Start	31124928:31124928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.189G>A
Mutation Classification	Silent
Feature Type	Transcript