Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EIF5B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99376608:99376608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1814C>T
AA Mutation	p.Ala605Val(p.A605V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99368585:99368585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1381A>G
AA Mutation	p.Lys461Glu(p.K461E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99376383:99376383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1589A>C
AA Mutation	p.Asn530Thr(p.N530T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99379082:99379082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1906G>A
AA Mutation	p.Val636Ile(p.V636I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99390643:99390643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2686C>T
AA Mutation	p.Pro896Ser(p.P896S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99390366:99390366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2551G>A
AA Mutation	p.Ala851Thr(p.A851T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99360255:99360255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374733590
CDS Mutation	c.55C>T
AA Mutation	p.Leu19Phe(p.L19F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99363770:99363770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1045G>A
AA Mutation	p.Ala349Thr(p.A349T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99390693:99390693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2736A>C
AA Mutation	p.Glu912Asp(p.E912D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99394748:99394748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3119G>A
AA Mutation	p.Arg1040Lys(p.R1040K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99364323:99364323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1135361
CDS Mutation	c.1190G>A
AA Mutation	p.Arg397Lys(p.R397K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289371
Start	99394532:99394532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3036A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289371
Start	99376405:99376405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1611G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289371
Start	99361645:99361645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758137614
CDS Mutation	c.744G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289371
Start	99361744:99361744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.843A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289371
Start	99390248:99390248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2433T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000289371
Start	99396867:99396868(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3362_3363delAG
AA Mutation	p.Gln1121ArgfsTer13(p.Q1121Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000289371
Start	99382889:99382889(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2244delA
AA Mutation	p.Lys748AsnfsTer29(p.K748Nfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000289371
Start	99361244:99361244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343G>T
AA Mutation	p.Glu115Ter(p.E115*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EIF5B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99382170:99382170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2073G>T
AA Mutation	p.Glu691Asp(p.E691D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289371
Start	99361446:99361446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545C>A
AA Mutation	p.Ser182Tyr(p.S182Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289371
Start	99389831:99389831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2385T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000289371
Start	99360484:99360484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181G>T
AA Mutation	p.Glu61Ter(p.E61*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript