Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLC16A12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371790
Start	89436255:89436255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093C>A
AA Mutation	p.Leu365Ile(p.L365I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371790
Start	89441248:89441248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308C>A
AA Mutation	p.Pro103Gln(p.P103Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371790
Start	89443849:89443849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.211A>T
AA Mutation	p.Ile71Phe(p.I71F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371790
Start	89443807:89443807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551632763
CDS Mutation	c.253G>A
AA Mutation	p.Ala85Thr(p.A85T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371790
Start	89436155:89436155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1193C>T
AA Mutation	p.Thr398Ile(p.T398I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371790
Start	89436139:89436139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1209G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371790
Start	89443841:89443841(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs770429879
CDS Mutation	c.219delT
AA Mutation	p.Phe73LeufsTer22(p.F73Lfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC16A12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371790
Start	89438881:89438881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755537113
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Trp(p.R251W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371790
Start	89433137:89433137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1478C>A
AA Mutation	p.Ser493Tyr(p.S493Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371790
Start	89433270:89433270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1345T>C
AA Mutation	p.Ser449Pro(p.S449P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript