Colon Cancer: Gene >> EEF1A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217182
Start	63495880:63495880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300G>T
AA Mutation	p.Lys100Asn(p.K100N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217182
Start	63495092:63495092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.334G>A
AA Mutation	p.Ala112Thr(p.A112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217182
Start	63495070:63495070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356G>A
AA Mutation	p.Gly119Asp(p.G119D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217182
Start	63495891:63495891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.289G>A
AA Mutation	p.Asp97Asn(p.D97N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217182
Start	63488308:63488308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757556226
CDS Mutation	c.1382C>T
AA Mutation	p.Ala461Val(p.A461V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000217182
Start	63495035:63495035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391G>A
AA Mutation	p.Gly131Arg(p.G131R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000217182
Start	63488395:63488395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1295C>T
AA Mutation	p.Thr432Met(p.T432M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000217182
Start	63489077:63489077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105G>A
AA Mutation	p.Ala369Thr(p.A369T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000217182
Start	63494972:63494972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454G>A
AA Mutation	p.Val152Met(p.V152M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000217182
Start	63490613:63490613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895C>G
AA Mutation	p.Leu299Val(p.L299V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000217182
Start	63494857:63494857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569T>C
AA Mutation	p.Phe190Ser(p.F190S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000217182
Start	63493242:63493242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778585590
CDS Mutation	c.667G>A
AA Mutation	p.Ala223Thr(p.A223T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217182
Start	63489135:63489135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1047C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217182
Start	63490560:63490560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750037526
CDS Mutation	c.948G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217182
Start	63497740:63497740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.24C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217182
Start	63488382:63488382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000217182
Start	63493195:63493195(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.714delC
AA Mutation	p.Thr239ArgfsTer40(p.T239Rfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000217182
Start	63493194:63493195(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.714dupC
AA Mutation	p.Thr239HisfsTer50(p.T239Hfs*50)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EEF1A2

No Mutation Annotation!