Colon Cancer: Gene >> INPP4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262992
Start	142145941:142145941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1619A>G
AA Mutation	p.Asp540Gly(p.D540G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262992
Start	142193127:142193127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1141C>T
AA Mutation	p.Leu381Phe(p.L381F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262992
Start	142405217:142405217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244G>A
AA Mutation	p.Glu82Lys(p.E82K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262992
Start	142108104:142108104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2363T>A
AA Mutation	p.Met788Lys(p.M788K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262992
Start	142431184:142431184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.76G>A
AA Mutation	p.Asp26Asn(p.D26N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262992
Start	142028903:142028903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568595082
CDS Mutation	c.2654G>A
AA Mutation	p.Arg885His(p.R885H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262992
Start	142431237:142431237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.23C>T
AA Mutation	p.Ala8Val(p.A8V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262992
Start	142173695:142173695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1296T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262992
Start	142402944:142402944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262992
Start	142270696:142270696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757828894
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000262992
Start	142305537:142305537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Ter(p.R142*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262992
Start	142145972:142145973(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1587dupG
AA Mutation	p.Lys530GlufsTer15(p.K530Efs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> INPP4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262992
Start	142270672:142270672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.606G>T
AA Mutation	p.Gln202His(p.Q202H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262992
Start	142237951:142237951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.749G>A
AA Mutation	p.Arg250Gln(p.R250Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262992
Start	142260530:142260530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650G>T
AA Mutation	p.Ser217Ile(p.S217I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript