Mutation

Primary Site >> Stomach Cancer

Gene >> SIPA1L2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232490977:232490977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1703A>G
AA Mutation	p.Glu568Gly(p.E568G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232483849:232483849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1924G>A
AA Mutation	p.Gly642Ser(p.G642S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232445688:232445688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187055622
CDS Mutation	c.3194C>T
AA Mutation	p.Thr1065Met(p.T1065M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232493537:232493537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1607G>T
AA Mutation	p.Arg536Met(p.R536M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232445538:232445538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3344A>G
AA Mutation	p.Asp1115Gly(p.D1115G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232514211:232514211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129T>C
AA Mutation	p.Cys377Arg(p.C377R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232515149:232515149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749117335
CDS Mutation	c.191C>T
AA Mutation	p.Pro64Leu(p.P64L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232425732:232425732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4487G>T
AA Mutation	p.Arg1496Met(p.R1496M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232445581:232445581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3301G>A
AA Mutation	p.Ala1101Thr(p.A1101T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232441775:232441775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3531G>T
AA Mutation	p.Arg1177Ser(p.R1177S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232439156:232439156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3983C>T
AA Mutation	p.Ala1328Val(p.A1328V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232402397:232402397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5017C>T
AA Mutation	p.Arg1673Trp(p.R1673W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232461025:232461025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2957G>A
AA Mutation	p.Arg986His(p.R986H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232479634:232479634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2078G>A
AA Mutation	p.Arg693Lys(p.R693K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232514156:232514156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184C>T
AA Mutation	p.Ala395Val(p.A395V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262861
Start	232404127:232404127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4814T>C
AA Mutation	p.Leu1605Pro(p.L1605P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232404139:232404139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4802A>G
AA Mutation	p.His1601Arg(p.H1601R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232439181:232439181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143814948
CDS Mutation	c.3958G>A
AA Mutation	p.Ala1320Thr(p.A1320T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232441778:232441778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3528C>G
AA Mutation	p.Ser1176Arg(p.S1176R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232514378:232514378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369266455
CDS Mutation	c.962G>A
AA Mutation	p.Arg321His(p.R321H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232428467:232428467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4354G>A
AA Mutation	p.Asp1452Asn(p.D1452N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232428520:232428520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4301A>T
AA Mutation	p.Gln1434Leu(p.Q1434L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232514736:232514736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.604G>T
AA Mutation	p.Gly202Cys(p.G202C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232514085:232514085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255G>A
AA Mutation	p.Glu419Lys(p.E419K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232514671:232514671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.669A>T
AA Mutation	p.Lys223Asn(p.K223N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232443641:232443641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3398G>A
AA Mutation	p.Gly1133Asp(p.G1133D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232445740:232445740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192387110
CDS Mutation	c.3142G>A
AA Mutation	p.Asp1048Asn(p.D1048N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232514601:232514601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739G>A
AA Mutation	p.Ala247Thr(p.A247T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232514335:232514335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005G>C
AA Mutation	p.Gln335His(p.Q335H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232415529:232415529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4727G>T
AA Mutation	p.Trp1576Leu(p.W1576L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232513877:232513877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569418675
CDS Mutation	c.1463G>A
AA Mutation	p.Arg488His(p.R488H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232425718:232425718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752185568
CDS Mutation	c.4501T>C
AA Mutation	p.Phe1501Leu(p.F1501L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232515113:232515113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.227T>C
AA Mutation	p.Val76Ala(p.V76A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232514903:232514903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773246161
CDS Mutation	c.437T>C
AA Mutation	p.Val146Ala(p.V146A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232432392:232432392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367638550
CDS Mutation	c.4111G>A
AA Mutation	p.Val1371Met(p.V1371M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000262861
Start	232425765:232425765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748564960
CDS Mutation	c.4454G>A
AA Mutation	p.Arg1485His(p.R1485H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262861
Start	232443634:232443634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201047593
CDS Mutation	c.3405C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262861
Start	232445609:232445609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765501159
CDS Mutation	c.3273G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262861
Start	232441363:232441363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3570C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262861
Start	232479714:232479714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754022709
CDS Mutation	c.1998G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262861
Start	232460973:232460973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3009C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262861
Start	232445669:232445669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3213T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262861
Start	232514761:232514761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.579A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262861
Start	232479684:232479684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373874564
CDS Mutation	c.2028C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262861
Start	232439326:232439326(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3813delC
AA Mutation	p.Cys1272AlafsTer18(p.C1272Afs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	46
Mutation Consequence	stop_gained
Transcription ID	ENST00000262861
Start	232445659:232445659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3223C>T
AA Mutation	p.Gln1075Ter(p.Q1075*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	47
Mutation Consequence	stop_gained
Transcription ID	ENST00000262861
Start	232490933:232490933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1747C>T
AA Mutation	p.Arg583Ter(p.R583*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	48
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000262861
Start	232402390:232402390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5022+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript