Mutation

Primary Site >> Stomach Cancer

Gene >> EBF1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313708
Start	158840078:158840078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587A>C
AA Mutation	p.Gln196Pro(p.Q196P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313708
Start	158777422:158777422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027A>G
AA Mutation	p.Ile343Val(p.I343V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313708
Start	158731130:158731130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064G>A
AA Mutation	p.Gly355Asp(p.G355D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313708
Start	158840039:158840039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626G>A
AA Mutation	p.Arg209Gln(p.R209Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313708
Start	158823229:158823229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768597902
CDS Mutation	c.725G>A
AA Mutation	p.Arg242Gln(p.R242Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313708
Start	158777442:158777442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007A>G
AA Mutation	p.Lys336Arg(p.K336R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313708
Start	159097114:159097114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151C>T
AA Mutation	p.Arg51Trp(p.R51W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000313708
Start	158714180:158714180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1128A>C
AA Mutation	p.Glu376Asp(p.E376D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000313708
Start	158712292:158712292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1411G>A
AA Mutation	p.Val471Met(p.V471M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000313708
Start	158712172:158712172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1531G>A
AA Mutation	p.Ala511Thr(p.A511T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000313708
Start	158823230:158823230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776402214
CDS Mutation	c.724C>T
AA Mutation	p.Arg242Trp(p.R242W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000313708
Start	158708135:158708135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1588C>A
AA Mutation	p.Leu530Ile(p.L530I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313708
Start	158712995:158712995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751083175
CDS Mutation	c.1344C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313708
Start	158823204:158823204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778456440
CDS Mutation	c.750G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313708
Start	159097013:159097013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371377954
CDS Mutation	c.252C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313708
Start	158796432:158796432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751933144
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313708
Start	158823294:158823294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.660T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313708
Start	158777500:158777500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313708
Start	158796384:158796384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313708
Start	158708124:158708125(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1598dupA
AA Mutation	p.Asn533LysfsTer65(p.N533Kfs*65)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	21
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000313708
Start	158714115:158714115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1191+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript