Colon Cancer: Gene >> ELAVL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359227
Start	11458167:11458167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607G>A
AA Mutation	p.Ala203Thr(p.A203T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359227
Start	11458469:11458469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476A>G
AA Mutation	p.Asp159Gly(p.D159G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359227
Start	11466647:11466647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749068597
CDS Mutation	c.190G>A
AA Mutation	p.Asp64Asn(p.D64N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359227
Start	11454642:11454642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.988G>A
AA Mutation	p.Val330Met(p.V330M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359227
Start	11454559:11454559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1071C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359227
Start	11454685:11454685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.945C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359227
Start	11458237:11458237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114284954
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359227
Start	11466711:11466711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148509524
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359227
Start	11458135:11458135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369079979
CDS Mutation	c.639G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ELAVL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359227
Start	11458194:11458194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580G>A
AA Mutation	p.Ala194Thr(p.A194T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359227
Start	11466710:11466710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144705960
CDS Mutation	c.127G>A
AA Mutation	p.Val43Ile(p.V43I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript