Colon Cancer: Gene >> ELP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350638
Start	31603793:31603793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539T>G
AA Mutation	p.Phe180Cys(p.F180C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350638
Start	31783399:31783399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750204793
CDS Mutation	c.1150C>T
AA Mutation	p.His384Tyr(p.H384Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350638
Start	31783463:31783463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1214C>T
AA Mutation	p.Ala405Val(p.A405V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000350638
Start	31783394:31783394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776578960
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382Gln(p.R382Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350638
Start	31520082:31520082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250C>A
AA Mutation	p.Leu84Ile(p.L84I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350638
Start	31603835:31603835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581T>G
AA Mutation	p.Leu194Arg(p.L194R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000350638
Start	31627129:31627129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748618717
CDS Mutation	c.673A>G
AA Mutation	p.Thr225Ala(p.T225A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350638
Start	31632288:31632288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350638
Start	31539732:31539732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ELP4

No Mutation Annotation!