Mutation

Primary Site >> Stomach Cancer

Gene >> ASAP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130126018:130126018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1453G>C
AA Mutation	p.Gly485Arg(p.G485R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130112240:130112240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2255C>T
AA Mutation	p.Ala752Val(p.A752V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130060668:130060668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3103G>A
AA Mutation	p.Ala1035Thr(p.A1035T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130358073:130358073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130T>C
AA Mutation	p.Ser44Pro(p.S44P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130076356:130076356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2693C>A
AA Mutation	p.Pro898His(p.P898H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130061061:130061061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2710A>G
AA Mutation	p.Arg904Gly(p.R904G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130112204:130112204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774096816
CDS Mutation	c.2291G>A
AA Mutation	p.Arg764Gln(p.R764Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130159906:130159906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968A>G
AA Mutation	p.Tyr323Cys(p.Y323C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130214615:130214615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761895160
CDS Mutation	c.346A>G
AA Mutation	p.Thr116Ala(p.T116A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130134321:130134321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1192G>T
AA Mutation	p.Ala398Ser(p.A398S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130060931:130060931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2840C>T
AA Mutation	p.Ala947Val(p.A947V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130112169:130112169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778257995
CDS Mutation	c.2326G>A
AA Mutation	p.Val776Ile(p.V776I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130058010:130058010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3259A>G
AA Mutation	p.Thr1087Ala(p.T1087A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130061021:130061021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745406996
CDS Mutation	c.2750C>T
AA Mutation	p.Pro917Leu(p.P917L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130118631:130118631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1652G>T
AA Mutation	p.Arg551Met(p.R551M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130057983:130057983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764209195
CDS Mutation	c.3286G>A
AA Mutation	p.Val1096Ile(p.V1096I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130060821:130060821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2950C>G
AA Mutation	p.Pro984Ala(p.P984A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130057982:130057982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3287T>C
AA Mutation	p.Val1096Ala(p.V1096A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130079905:130079905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2639C>T
AA Mutation	p.Ser880Leu(p.S880L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000518721
Start	130118532:130118532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1751C>T
AA Mutation	p.Ala584Val(p.A584V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518721
Start	130060636:130060636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3135C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518721
Start	130137018:130137018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1101G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518721
Start	130060804:130060804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2967G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518721
Start	130214610:130214610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766538059
CDS Mutation	c.351G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518721
Start	130116974:130116974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753375926
CDS Mutation	c.1902G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518721
Start	130127943:130127943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376825464
CDS Mutation	c.1365C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518721
Start	130401929:130401929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518721
Start	130159908:130159908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.966A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518721
Start	130061020:130061020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377622334
CDS Mutation	c.2751G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518721
Start	130159880:130159880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.994C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518721
Start	130092112:130092112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2433A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518721
Start	130092133:130092133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2412C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000518721
Start	130214641:130214641(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.320delT
AA Mutation	p.Leu107Ter(p.L107*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000518721
Start	130214636:130214636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.325C>T
AA Mutation	p.Arg109Ter(p.R109*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000518721
Start	130060797:130060798(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2973dupC
AA Mutation	p.Lys992GlnfsTer25(p.K992Qfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000518721
Start	130136969:130136970(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1149dupA
AA Mutation	p.Ser384IlefsTer3(p.S384Ifs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript