Colon Cancer: Gene >> IRX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231357
Start	1879620:1879620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376873295
CDS Mutation	c.620C>T
AA Mutation	p.Thr207Met(p.T207M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231357
Start	1881833:1881833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272C>T
AA Mutation	p.Ser91Leu(p.S91L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231357
Start	1878400:1878400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129G>A
AA Mutation	p.Ala377Thr(p.A377T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000231357
Start	1881927:1881927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.178G>A
AA Mutation	p.Ala60Thr(p.A60T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000231357
Start	1879650:1879650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590G>A
AA Mutation	p.Arg197His(p.R197H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231357
Start	1878740:1878740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.789C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231357
Start	1879610:1879610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763072295
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231357
Start	1879571:1879571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231357
Start	1878041:1878041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1488C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231357
Start	1881823:1881823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231357
Start	1879772:1879772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.468G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231357
Start	1879646:1879646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.594G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IRX4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231357
Start	1878740:1878740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.789C>T
Mutation Classification	Silent
Feature Type	Transcript