Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PCBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70088042:70088042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299T>A
AA Mutation	p.Leu100Gln(p.L100Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70088419:70088419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676G>A
AA Mutation	p.Gly226Arg(p.G226R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70088042:70088042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299T>C
AA Mutation	p.Leu100Pro(p.L100P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70088614:70088614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.871A>G
AA Mutation	p.Ile291Val(p.I291V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70088048:70088048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305T>C
AA Mutation	p.Leu102Pro(p.L102P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70088048:70088048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.305T>G
AA Mutation	p.Leu102Arg(p.L102R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70088048:70088048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305T>A
AA Mutation	p.Leu102Gln(p.L102Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303577
Start	70087929:70087929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201447568
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PCBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70088557:70088557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.814G>T
AA Mutation	p.Ala272Ser(p.A272S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70088242:70088242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499C>A
AA Mutation	p.Leu167Met(p.L167M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70088042:70088042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299T>A
AA Mutation	p.Leu100Gln(p.L100Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70088761:70088761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1018C>A
AA Mutation	p.Gln340Lys(p.Q340K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70088048:70088048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305T>A
AA Mutation	p.Leu102Gln(p.L102Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303577
Start	70087790:70087790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47T>A
AA Mutation	p.Ile16Asn(p.I16N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript