Mutation

Primary Site >> Stomach Cancer

Gene >> ESPL1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53286448:53286448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3712C>A
AA Mutation	p.Pro1238Thr(p.P1238T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53288048:53288048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531311020
CDS Mutation	c.4253G>A
AA Mutation	p.Arg1418Gln(p.R1418Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53277102:53277102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1960C>T
AA Mutation	p.Arg654Trp(p.R654W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53292320:53292320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5839A>C
AA Mutation	p.Ser1947Arg(p.S1947R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53283496:53283496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3035T>C
AA Mutation	p.Leu1012Ser(p.L1012S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000257934
Start	53292808:53292808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5999A>G
AA Mutation	p.Tyr2000Cys(p.Y2000C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53288565:53288565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4574A>T
AA Mutation	p.Glu1525Val(p.E1525V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53292291:53292291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5810C>T
AA Mutation	p.Pro1937Leu(p.P1937L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53290850:53290850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5374G>A
AA Mutation	p.Ala1792Thr(p.A1792T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53285996:53285996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3260A>G
AA Mutation	p.Gln1087Arg(p.Q1087R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53292858:53292858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6049C>T
AA Mutation	p.Arg2017Trp(p.R2017W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53276652:53276652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149272357
CDS Mutation	c.1733C>T
AA Mutation	p.Pro578Leu(p.P578L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53279841:53279841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2474C>T
AA Mutation	p.Thr825Ile(p.T825I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53277895:53277895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2299C>T
AA Mutation	p.Arg767Trp(p.R767W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53286586:53286586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3850A>G
AA Mutation	p.Thr1284Ala(p.T1284A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53269046:53269046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104C>T
AA Mutation	p.Ala35Val(p.A35V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53286610:53286610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3874T>C
AA Mutation	p.Trp1292Arg(p.W1292R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000257934
Start	53277826:53277826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2230T>C
AA Mutation	p.Ser744Pro(p.S744P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257934
Start	53286432:53286432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3696G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257934
Start	53274945:53274945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1635A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257934
Start	53269641:53269641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257934
Start	53286165:53286165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3429A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257934
Start	53286294:53286294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765718188
CDS Mutation	c.3558C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257934
Start	53290150:53290150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5179C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257934
Start	53284085:53284085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200962229
CDS Mutation	c.3105C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257934
Start	53283449:53283449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2988C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257934
Start	53291803:53291803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5634A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257934
Start	53289120:53289120(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4741delC
AA Mutation	p.Leu1581Ter(p.L1581*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000257934
Start	53269962:53269962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1020C>A
AA Mutation	p.Cys340Ter(p.C340*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000257934
Start	53272739:53272739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1388T>A
AA Mutation	p.Leu463Ter(p.L463*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257934
Start	53292598:53292599(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5941dupG
AA Mutation	p.Glu1981GlyfsTer6(p.E1981Gfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript