Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LDHB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350669
Start	21646964:21646964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.182G>A
AA Mutation	p.Gly61Glu(p.G61E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350669
Start	21642074:21642074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200163319
CDS Mutation	c.473G>A
AA Mutation	p.Arg158His(p.R158H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350669
Start	21644058:21644058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759971220
CDS Mutation	c.298C>T
AA Mutation	p.Arg100Cys(p.R100C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350669
Start	21638456:21638456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610G>T
AA Mutation	p.Gly204Cys(p.G204C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_lost
Transcription ID	ENST00000350669
Start	21635542:21635542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005A>C
AA Mutation	p.Ter335CysextTer7(p.335Cext7)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LDHB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350669
Start	21637076:21637076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832G>T
AA Mutation	p.Val278Leu(p.V278L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350669
Start	21638367:21638367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699G>T
AA Mutation	p.Lys233Asn(p.K233N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350669
Start	21642044:21642044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503C>A
AA Mutation	p.Ser168Tyr(p.S168Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350669
Start	21637074:21637075(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.833dupT
AA Mutation	p.Met281AspfsTer5(p.M281Dfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript