Colon Cancer: Gene >> IRX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329734
Start	54285549:54285549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376056612
CDS Mutation	c.332C>T
AA Mutation	p.Pro111Leu(p.P111L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329734
Start	54285220:54285220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.661G>A
AA Mutation	p.Asp221Asn(p.D221N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329734
Start	54285490:54285490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391C>T
AA Mutation	p.Pro131Ser(p.P131S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329734
Start	54285063:54285063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.818C>T
AA Mutation	p.Ala273Val(p.A273V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329734
Start	54285890:54285890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758083649
CDS Mutation	c.161C>T
AA Mutation	p.Ser54Leu(p.S54L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329734
Start	54284275:54284275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1422C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329734
Start	54285437:54285437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.444G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329734
Start	54285175:54285175(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.706delG
AA Mutation	p.Glu236ArgfsTer24(p.E236Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329734
Start	54285156:54285156(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.725delG
AA Mutation	p.Gly242AlafsTer18(p.G242Afs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IRX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329734
Start	54285057:54285057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824G>A
AA Mutation	p.Arg275His(p.R275H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329734
Start	54285106:54285106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775T>G
AA Mutation	p.Leu259Val(p.L259V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329734
Start	54285175:54285175(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.706delG
AA Mutation	p.Glu236ArgfsTer24(p.E236Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript