Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLC16A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000587091
Start	74525769:74525769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1046A>G
AA Mutation	p.Glu349Gly(p.E349G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000587091
Start	74531368:74531368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1435G>A
AA Mutation	p.Ala479Thr(p.A479T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000587091
Start	74521093:74521093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.534T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000587091
Start	74531428:74531428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1495C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC16A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000587091
Start	74525835:74525835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112G>A
AA Mutation	p.Arg371His(p.R371H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000587091
Start	74531412:74531412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1479C>G
AA Mutation	p.Ile493Met(p.I493M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000587091
Start	74531353:74531353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1420G>A
AA Mutation	p.Gly474Arg(p.G474R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000587091
Start	74524732:74524732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949C>A
AA Mutation	p.Arg317Ser(p.R317S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript