Mutation

Primary Site >> Stomach Cancer

Gene >> OGDH

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44673874:44673874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.721C>T
AA Mutation	p.Pro241Ser(p.P241S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44624428:44624428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85G>A
AA Mutation	p.Ala29Thr(p.A29T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44676061:44676061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118A>G
AA Mutation	p.Asn373Ser(p.N373S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44645346:44645346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200566080
CDS Mutation	c.242G>A
AA Mutation	p.Arg81His(p.R81H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44673908:44673908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755G>A
AA Mutation	p.Arg252Gln(p.R252Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44681801:44681801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1288C>T
AA Mutation	p.Pro430Ser(p.P430S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44681836:44681836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140074828
CDS Mutation	c.1323C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44694528:44694528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574777186
CDS Mutation	c.1620C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44693885:44693885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1396C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44696993:44696993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs57529168
CDS Mutation	c.1980G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44698242:44698242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2409C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44696936:44696936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1923T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222673
Start	44676144:44676144(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1205delA
AA Mutation	p.Lys402ArgfsTer67(p.K402Rfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222673
Start	44666801:44666801(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.587delG
AA Mutation	p.Gly196AspfsTer85(p.G196Dfs*85)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222673
Start	44707628:44707629(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2847dupC
AA Mutation	p.Asn950GlnfsTer3(p.N950Qfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript