Mutation

Primary Site >> Stomach Cancer

Gene >> CELSR1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46365249:46365249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141057075
CDS Mutation	c.8536G>A
AA Mutation	p.Val2846Ile(p.V2846I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46411671:46411671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4700C>T
AA Mutation	p.Ala1567Val(p.A1567V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46464160:46464160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199506726
CDS Mutation	c.3730G>A
AA Mutation	p.Val1244Ile(p.V1244I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46463758:46463758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4132T>A
AA Mutation	p.Cys1378Ser(p.C1378S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46409773:46409773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5041G>A
AA Mutation	p.Gly1681Arg(p.G1681R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46398559:46398559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5491G>C
AA Mutation	p.Val1831Leu(p.V1831L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46396624:46396624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5824G>A
AA Mutation	p.Gly1942Arg(p.G1942R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46534518:46534518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2653G>A
AA Mutation	p.Ala885Thr(p.A885T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46533794:46533794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774178984
CDS Mutation	c.3377G>A
AA Mutation	p.Cys1126Tyr(p.C1126Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46364733:46364733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8558A>G
AA Mutation	p.Asp2853Gly(p.D2853G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46533938:46533938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3233C>T
AA Mutation	p.Ser1078Leu(p.S1078L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46369792:46369792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7772G>A
AA Mutation	p.Gly2591Asp(p.G2591D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46534323:46534323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2848A>G
AA Mutation	p.Ile950Val(p.I950V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46377183:46377183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199555924
CDS Mutation	c.7462G>A
AA Mutation	p.Val2488Ile(p.V2488I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46409031:46409031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5191G>A
AA Mutation	p.Ala1731Thr(p.A1731T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46391749:46391749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6032A>C
AA Mutation	p.His2011Pro(p.H2011P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46396662:46396662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374468252
CDS Mutation	c.5786C>T
AA Mutation	p.Pro1929Leu(p.P1929L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46536266:46536266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905C>T
AA Mutation	p.Thr302Met(p.T302M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46464132:46464132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3758T>G
AA Mutation	p.Val1253Gly(p.V1253G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46369763:46369763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777578706
CDS Mutation	c.7801G>A
AA Mutation	p.Asp2601Asn(p.D2601N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46536045:46536045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1126C>T
AA Mutation	p.Arg376Cys(p.R376C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46464331:46464331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748498695
CDS Mutation	c.3559G>A
AA Mutation	p.Val1187Ile(p.V1187I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46533788:46533788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370921649
CDS Mutation	c.3383C>A
AA Mutation	p.Pro1128Gln(p.P1128Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262738
Start	46390394:46390394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770797108
CDS Mutation	c.6343A>G
AA Mutation	p.Met2115Val(p.M2115V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46463953:46463953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763382137
CDS Mutation	c.3937G>A
AA Mutation	p.Glu1313Lys(p.E1313K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46409156:46409156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5066C>T
AA Mutation	p.Pro1689Leu(p.P1689L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46373047:46373047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542670900
CDS Mutation	c.7595C>T
AA Mutation	p.Thr2532Ile(p.T2532I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46534290:46534290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2881G>A
AA Mutation	p.Val961Met(p.V961M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000262738
Start	46536234:46536234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.937C>T
AA Mutation	p.Arg313Cys(p.R313C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46463909:46463909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745703075
CDS Mutation	c.3981C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46397819:46397819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374010740
CDS Mutation	c.5556C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46364555:46364555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141928741
CDS Mutation	c.8736C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46439353:46439353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374497127
CDS Mutation	c.4242C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46377249:46377249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7396C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46535998:46535998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1173C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46464113:46464113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147056983
CDS Mutation	c.3777C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46535863:46535863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1308G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46533658:46533658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371346729
CDS Mutation	c.3513G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46390479:46390479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6258G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46398557:46398557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5493C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46536391:46536391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372012495
CDS Mutation	c.780G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46533790:46533790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3381C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46535764:46535764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267606282
CDS Mutation	c.1407C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46464152:46464152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35364113
CDS Mutation	c.3738C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46534861:46534861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2310G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46463747:46463747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150510873
CDS Mutation	c.4143C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46410498:46410498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4833A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262738
Start	46364133:46364133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767367866
CDS Mutation	c.8898G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262738
Start	46380894:46380894(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7150delG
AA Mutation	p.Ala2384LeufsTer85(p.A2384Lfs*85)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	50
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262738
Start	46535330:46535330(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1841delG
AA Mutation	p.Gly614AlafsTer54(p.G614Afs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	51
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262738
Start	46364574:46364574(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.8717delC
AA Mutation	p.Pro2906ArgfsTer24(p.P2906Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	52
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262738
Start	46365271:46365271(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.8514delA
AA Mutation	p.Lys2838AsnfsTer45(p.K2838Nfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	53
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262738
Start	46369187:46369187(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7944delA
AA Mutation	p.Ile2650SerfsTer5(p.I2650Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	54
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262738
Start	46367055:46367055(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.8143delG
AA Mutation	p.Val2715CysfsTer20(p.V2715Cfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	55
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262738
Start	46410526:46410526(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4805delG
AA Mutation	p.Gly1602ValfsTer104(p.G1602Vfs*104)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	56
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262738
Start	46535986:46535987(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1184dupG
AA Mutation	p.Ala396ArgfsTer140(p.A396Rfs*140)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript