Colon Cancer: Gene >> EGR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000545030
Start	73292125:73292125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102G>A
AA Mutation	p.Ala368Thr(p.A368T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000545030
Start	73293213:73293213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414G>T
AA Mutation	p.Arg138Ser(p.R138S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000545030
Start	73292005:73292005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1222G>A
AA Mutation	p.Ala408Thr(p.A408T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000545030
Start	73292237:73292237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000545030
Start	73292777:73292777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762746716
CDS Mutation	c.450C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000545030
Start	73291703:73291703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1524G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000545030
Start	73291727:73291727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1500C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000545030
Start	73291616:73291616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1611C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000545030
Start	73292300:73292300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144909297
CDS Mutation	c.927G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EGR4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000545030
Start	73292264:73292264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.963C>T
Mutation Classification	Silent
Feature Type	Transcript