Colon Cancer: Gene >> INPP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322522
Start	190371049:190371049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577408029
CDS Mutation	c.847C>T
AA Mutation	p.Arg283Cys(p.R283C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322522
Start	190371340:190371340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777831500
CDS Mutation	c.1138C>T
AA Mutation	p.Arg380Trp(p.R380W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322522
Start	190371362:190371362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1160T>C
AA Mutation	p.Leu387Pro(p.L387P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322522
Start	190369223:190369223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587C>T
AA Mutation	p.Pro196Leu(p.P196L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322522
Start	190370852:190370852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650G>A
AA Mutation	p.Gly217Glu(p.G217E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322522
Start	190371315:190371315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1113A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322522
Start	190371034:190371035(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.840_841dupTG
AA Mutation	p.Gly281ValfsTer45(p.G281Vfs*45)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322522
Start	190360253:190360254(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.152_153insTC
AA Mutation	p.Leu52ArgfsTer11(p.L52Rfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> INPP1

No Mutation Annotation!