Mutation

Primary Site >> Stomach Cancer

Gene >> EBF3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355311
Start	129962208:129962208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374A>T
AA Mutation	p.Asp125Val(p.D125V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355311
Start	129843183:129843183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546805685
CDS Mutation	c.1148C>T
AA Mutation	p.Ala383Val(p.A383V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355311
Start	129873560:129873560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673G>A
AA Mutation	p.Val225Met(p.V225M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355311
Start	129963731:129963731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.38C>T
AA Mutation	p.Thr13Met(p.T13M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355311
Start	129963522:129963522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136G>A
AA Mutation	p.Gly46Ser(p.G46S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355311
Start	129837940:129837940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1780C>T
AA Mutation	p.Pro594Ser(p.P594S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355311
Start	129840960:129840960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1445A>G
AA Mutation	p.Asn482Ser(p.N482S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355311
Start	129962197:129962197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385C>T
AA Mutation	p.Arg129Cys(p.R129C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000355311
Start	129840988:129840988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150680609
CDS Mutation	c.1417G>A
AA Mutation	p.Val473Ile(p.V473I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000355311
Start	129840916:129840916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138447716
CDS Mutation	c.1489G>A
AA Mutation	p.Ala497Thr(p.A497T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000355311
Start	129867234:129867234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946C>G
AA Mutation	p.Pro316Ala(p.P316A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000355311
Start	129873530:129873530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703C>T
AA Mutation	p.His235Tyr(p.H235Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355311
Start	129840848:129840848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147171591
CDS Mutation	c.1557C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355311
Start	129840321:129840321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1683C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355311
Start	129963643:129963643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355311
Start	129867214:129867214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151206880
CDS Mutation	c.966C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355311
Start	129958959:129958959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.460C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355311
Start	129867821:129867821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.873G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355311
Start	129842246:129842246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771823461
CDS Mutation	c.1242C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355311
Start	129848455:129848455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200561162
CDS Mutation	c.1065C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355311
Start	129840887:129840887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372476626
CDS Mutation	c.1518G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355311
Start	129873519:129873519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355311
Start	129867839:129867839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149960200
CDS Mutation	c.855C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355311
Start	129963487:129963487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765038813
CDS Mutation	c.171G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355311
Start	129867861:129867861(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.833delG
AA Mutation	p.Gly278ValfsTer6(p.G278Vfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355311
Start	129963733:129963733(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.36delG
AA Mutation	p.Thr13ArgfsTer3(p.T13Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript