Mutation

Primary Site >> Stomach Cancer

Gene >> OPCML

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132657173:132657173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314T>C
AA Mutation	p.Val105Ala(p.V105A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132942937:132942937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156C>A
AA Mutation	p.Ser52Arg(p.S52R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132437257:132437257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629C>T
AA Mutation	p.Ala210Val(p.A210V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132420203:132420203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1028T>G
AA Mutation	p.Ile343Ser(p.I343S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000524381
Start	133532285:133532285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40A>T
AA Mutation	p.Thr14Ser(p.T14S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132436693:132436693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751A>G
AA Mutation	p.Met251Val(p.M251V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132657194:132657194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.293A>G
AA Mutation	p.Tyr98Cys(p.Y98C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000524381
Start	133532316:133532316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9T>A
AA Mutation	p.His3Gln(p.H3Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132437275:132437275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611C>T
AA Mutation	p.Ala204Val(p.A204V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132657276:132657276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770223558
CDS Mutation	c.211C>T
AA Mutation	p.Arg71Cys(p.R71C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000331898
Start	132657237:132657237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746134342
CDS Mutation	c.250A>G
AA Mutation	p.Ile84Val(p.I84V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132420244:132420244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132437253:132437253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780275496
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132657238:132657238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132942979:132942979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331898
Start	132529134:132529134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000331898
Start	132437358:132437358(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.528delA
AA Mutation	p.Gly177AlafsTer5(p.G177Afs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	stop_lost
Transcription ID	ENST00000331898
Start	132420195:132420195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1036T>C
AA Mutation	p.Ter346ArgextTer1(p.346Rext1)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript