Colon Cancer: Gene >> PIP4K2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000619039
Start	38770449:38770449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1157C>T
AA Mutation	p.Thr386Met(p.T386M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000619039
Start	38780522:38780522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.437G>A
AA Mutation	p.Arg146His(p.R146H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000619039
Start	38779522:38779522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.515T>C
AA Mutation	p.Val172Ala(p.V172A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000619039
Start	38780472:38780472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.487A>G
AA Mutation	p.Ile163Val(p.I163V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000619039
Start	38779427:38779427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610G>A
AA Mutation	p.Val204Met(p.V204M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000619039
Start	38779510:38779510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.527G>A
AA Mutation	p.Gly176Asp(p.G176D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619039
Start	38771252:38771252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.828C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619039
Start	38780572:38780572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.387T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619039
Start	38777789:38777789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.705G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619039
Start	38771222:38771222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767674989
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PIP4K2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000619039
Start	38784322:38784322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779273477
CDS Mutation	c.275G>A
AA Mutation	p.Arg92His(p.R92H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000619039
Start	38799277:38799277(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.148delG
AA Mutation	p.Val50Ter(p.V50*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript