Mutation

Primary Site >> Stomach Cancer

Gene >> SEMA3A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84194535:84194535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52G>A
AA Mutation	p.Ala18Thr(p.A18T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84134822:84134822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242A>T
AA Mutation	p.Asp81Val(p.D81V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83961660:83961660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2027T>G
AA Mutation	p.Leu676Arg(p.L676R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265362
Start	83977194:83977194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1655G>A
AA Mutation	p.Arg552His(p.R552H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84134823:84134823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376684446
CDS Mutation	c.241G>A
AA Mutation	p.Asp81Asn(p.D81N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83961730:83961730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1957G>A
AA Mutation	p.Glu653Lys(p.E653K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83981405:83981405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377259138
CDS Mutation	c.1568C>T
AA Mutation	p.Ala523Val(p.A523V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83985439:83985439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1491G>C
AA Mutation	p.Lys497Asn(p.K497N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83963254:83963254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566466269
CDS Mutation	c.1811C>T
AA Mutation	p.Ala604Val(p.A604V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84060519:84060519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493G>A
AA Mutation	p.Gly165Ser(p.G165S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84129155:84129155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301G>A
AA Mutation	p.Asp101Asn(p.D101N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	84005425:84005425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778384312
CDS Mutation	c.1274C>T
AA Mutation	p.Thr425Met(p.T425M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83961443:83961443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2244G>T
AA Mutation	p.Lys748Asn(p.K748N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265362
Start	83961741:83961741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1946G>T
AA Mutation	p.Cys649Phe(p.C649F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265362
Start	83961443:83961443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755748248
CDS Mutation	c.2244G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265362
Start	84060496:84060496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265362
Start	83961695:83961695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1992C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000265362
Start	83961499:83961499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2188C>T
AA Mutation	p.Arg730Ter(p.R730*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000265362
Start	83961746:83961747(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1936_1940dupAATTA
AA Mutation	p.Tyr647Ter(p.Y647*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000265362
Start	84110526:84110526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397G>T
AA Mutation	p.Gly133Ter(p.G133*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000265362
Start	83961424:83961425(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2262_2263insTGGAGCATGTTGGTTGCCAGGGGACCCTGAGC
AA Mutation	p.Lys755TrpfsTer10(p.K755Wfs*10)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript