Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLC5A12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396005
Start	26703628:26703628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724A>C
AA Mutation	p.Thr242Pro(p.T242P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396005
Start	26673434:26673434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1675T>C
AA Mutation	p.Cys559Arg(p.C559R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396005
Start	26681058:26681058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1472G>A
AA Mutation	p.Ser491Asn(p.S491N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396005
Start	26711346:26711346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>A
AA Mutation	p.Gly140Arg(p.G140R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396005
Start	26721703:26721703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396005
Start	26721664:26721664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.51C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396005
Start	26703846:26703846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396005
Start	26721611:26721611(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.104delA
AA Mutation	p.Lys35ArgfsTer14(p.K35Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC5A12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396005
Start	26721702:26721702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13A>T
AA Mutation	p.Asn5Tyr(p.N5Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396005
Start	26673407:26673407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702G>A
AA Mutation	p.Glu568Lys(p.E568K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396005
Start	26721634:26721634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.81C>A
AA Mutation	p.Phe27Leu(p.F27L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396005
Start	26703937:26703937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536A>C
AA Mutation	p.Lys179Thr(p.K179T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396005
Start	26692576:26692576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066T>C
Mutation Classification	Silent
Feature Type	Transcript