Colon Cancer: Gene >> ELK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247161
Start	47638038:47638038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799C>T
AA Mutation	p.Pro267Ser(p.P267S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247161
Start	47637053:47637053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1148G>C
AA Mutation	p.Ser383Thr(p.S383T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000247161
Start	47638167:47638167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774244991
CDS Mutation	c.670C>T
AA Mutation	p.Pro224Ser(p.P224S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000247161
Start	47641239:47641239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203A>G
AA Mutation	p.Tyr68Cys(p.Y68C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000247161
Start	47639082:47639082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.467C>T
AA Mutation	p.Ser156Leu(p.S156L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000247161
Start	47639101:47639101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.448C>T
AA Mutation	p.Arg150Trp(p.R150W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247161
Start	47637022:47637022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247161
Start	47637043:47637043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147990079
CDS Mutation	c.1158G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ELK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247161
Start	47641311:47641311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131G>A
AA Mutation	p.Arg44Gln(p.R44Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript