Colon Cancer: Gene >> PATZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266269
Start	31335826:31335826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1373G>A
AA Mutation	p.Arg458His(p.R458H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266269
Start	31345001:31345001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.602G>A
AA Mutation	p.Gly201Asp(p.G201D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266269
Start	31344720:31344720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883G>T
AA Mutation	p.Gly295Cys(p.G295C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266269
Start	31344539:31344539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1064T>G
AA Mutation	p.Val355Gly(p.V355G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266269
Start	31345276:31345276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140597902
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266269
Start	31345070:31345070(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.533delC
AA Mutation	p.Pro178LeufsTer12(p.P178Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266269
Start	31344749:31344750(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.853_854delGG
AA Mutation	p.Gly285ProfsTer14(p.G285Pfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PATZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266269
Start	31345168:31345168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435G>A
AA Mutation	p.Met145Ile(p.M145I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266269
Start	31327180:31327180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1775T>C
AA Mutation	p.Val592Ala(p.V592A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript