Colon Cancer: Gene >> EGR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317216
Start	22692823:22692823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.122A>G
AA Mutation	p.Asp41Gly(p.D41G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317216
Start	22690583:22690583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054G>A
AA Mutation	p.Ala352Thr(p.A352T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317216
Start	22690618:22690618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1019G>A
AA Mutation	p.Arg340His(p.R340H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317216
Start	22690589:22690589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1048C>T
AA Mutation	p.Arg350Cys(p.R350C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317216
Start	22690714:22690714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923G>A
AA Mutation	p.Arg308Gln(p.R308Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317216
Start	22691180:22691180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457C>A
AA Mutation	p.Leu153Ile(p.L153I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000317216
Start	22691123:22691123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.514T>C
AA Mutation	p.Ser172Pro(p.S172P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000317216
Start	22690510:22690510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1127C>A
AA Mutation	p.Pro376His(p.P376H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000317216
Start	22691104:22691104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.533C>T
AA Mutation	p.Ser178Leu(p.S178L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000317216
Start	22690948:22690948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.689C>T
AA Mutation	p.Thr230Ile(p.T230I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000317216
Start	22691440:22691440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777341372
CDS Mutation	c.197C>A
AA Mutation	p.Pro66Gln(p.P66Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317216
Start	22691259:22691259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754227276
CDS Mutation	c.378G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317216
Start	22691370:22691370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317216
Start	22691259:22691259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317216
Start	22691034:22691034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317216
Start	22691117:22691117(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.520delC
AA Mutation	p.Gln174ArgfsTer17(p.Q174Rfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EGR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317216
Start	22690786:22690786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851G>A
AA Mutation	p.Arg284His(p.R284H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317216
Start	22690650:22690650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317216
Start	22691331:22691331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript