Colon Cancer: Gene >> ELAVL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371823
Start	50195575:50195575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523G>A
AA Mutation	p.Val175Met(p.V175M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371823
Start	50200934:50200934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899T>C
AA Mutation	p.Phe300Ser(p.F300S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371823
Start	50201023:50201023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.988C>T
AA Mutation	p.Arg330Cys(p.R330C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371823
Start	50201113:50201113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078G>A
AA Mutation	p.Gly360Arg(p.G360R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371823
Start	50201089:50201089(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	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371823
Start	50144975:50144975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.28C>A
AA Mutation	p.Pro10Thr(p.P10T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371823
Start	50195583:50195583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531C>A
AA Mutation	p.Phe177Leu(p.F177L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371823
Start	50195744:50195744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692G>A
AA Mutation	p.Arg231Gln(p.R231Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371823
Start	50197434:50197434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740A>G
AA Mutation	p.Asp247Gly(p.D247G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371823
Start	50197459:50197459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761380670
CDS Mutation	c.765C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371823
Start	50200959:50200959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138724011
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371823
Start	50193782:50193782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528644967
CDS Mutation	c.372G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000371823
Start	50145053:50145053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106C>T
AA Mutation	p.Gln36Ter(p.Q36*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000371823
Start	50200808:50200808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ELAVL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371823
Start	50201087:50201087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1052C>T
AA Mutation	p.Ala351Val(p.A351V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371823
Start	50201175:50201175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1140C>A
Mutation Classification	Silent
Feature Type	Transcript