Mutation

Primary Site >> Stomach Cancer

Gene >> TOP3A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321105
Start	18277681:18277681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756711722
CDS Mutation	c.2821G>A
AA Mutation	p.Ala941Thr(p.A941T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321105
Start	18278238:18278238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759758444
CDS Mutation	c.2264G>C
AA Mutation	p.Gly755Ala(p.G755A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321105
Start	18278164:18278164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2338C>T
AA Mutation	p.His780Tyr(p.H780Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321105
Start	18285496:18285496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1622A>G
AA Mutation	p.His541Arg(p.H541R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321105
Start	18308418:18308418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550633885
CDS Mutation	c.247A>G
AA Mutation	p.Thr83Ala(p.T83A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000321105
Start	18305151:18305151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772020353
CDS Mutation	c.460G>A
AA Mutation	p.Glu154Lys(p.E154K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321105
Start	18302620:18302620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765303480
CDS Mutation	c.603C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321105
Start	18285516:18285516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321105
Start	18301981:18301981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.819T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321105
Start	18278054:18278054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781217267
CDS Mutation	c.2448C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321105
Start	18278231:18278231(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2271delC
AA Mutation	p.Arg758GlyfsTer15(p.R758Gfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321105
Start	18314651:18314651(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.128delA
AA Mutation	p.Asn43ThrfsTer16(p.N43Tfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000321105
Start	18308358:18308358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307C>T
AA Mutation	p.Arg103Ter(p.R103*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript