Primary Site >> Stomach Cancer
Gene >> HUWE1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53586808:53586808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4716G>T |
| AA Mutation | p.Lys1572Asn(p.K1572N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53647390:53647390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.329G>A |
| AA Mutation | p.Arg110Gln(p.R110Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53600253:53600253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3028G>C |
| AA Mutation | p.Glu1010Gln(p.E1010Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53631003:53631003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.794A>G |
| AA Mutation | p.His265Arg(p.H265R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53559455:53559455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142176360 |
| CDS Mutation | c.7814G>A |
| AA Mutation | p.Arg2605His(p.R2605H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53559461:53559461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146149373 |
| CDS Mutation | c.7808G>A |
| AA Mutation | p.Arg2603Gln(p.R2603Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53563770:53563770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7081G>A |
| AA Mutation | p.Gly2361Arg(p.G2361R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53628824:53628824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1042G>A |
| AA Mutation | p.Asp348Asn(p.D348N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53647543:53647543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.176A>G |
| AA Mutation | p.Asp59Gly(p.D59G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53595332:53595332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3235G>T |
| AA Mutation | p.Val1079Phe(p.V1079F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53628835:53628835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1031G>T |
| AA Mutation | p.Ser344Ile(p.S344I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53537559:53537559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12134G>A |
| AA Mutation | p.Arg4045Gln(p.R4045Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53547729:53547729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10580T>C |
| AA Mutation | p.Val3527Ala(p.V3527A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53586528:53586528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4786A>G |
| AA Mutation | p.Thr1596Ala(p.T1596A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53534689:53534689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782063282 |
| CDS Mutation | c.12658C>T |
| AA Mutation | p.Arg4220Cys(p.R4220C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53580944:53580944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5603A>G |
| AA Mutation | p.Asn1868Ser(p.N1868S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53539044:53539044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11669A>G |
| AA Mutation | p.His3890Arg(p.H3890R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53573875:53573875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6187A>G |
| AA Mutation | p.Lys2063Glu(p.K2063E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53546523:53546523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10828C>T |
| AA Mutation | p.Arg3610Trp(p.R3610W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53543863:53543863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11357G>A |
| AA Mutation | p.Arg3786Gln(p.R3786Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53549300:53549300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9694C>T |
| AA Mutation | p.Arg3232Cys(p.R3232C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53602618:53602618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2917A>G |
| AA Mutation | p.Lys973Glu(p.K973E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53544598:53544598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782484577 |
| CDS Mutation | c.11213G>A |
| AA Mutation | p.Arg3738His(p.R3738H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53559377:53559377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7892A>G |
| AA Mutation | p.Gln2631Arg(p.Q2631R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53547807:53547807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782741075 |
| CDS Mutation | c.10502C>T |
| AA Mutation | p.Thr3501Met(p.T3501M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53561890:53561890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7373A>G |
| AA Mutation | p.Asp2458Gly(p.D2458G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53548216:53548216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10093C>T |
| AA Mutation | p.Arg3365Trp(p.R3365W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53539026:53539026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11687G>A |
| AA Mutation | p.Ser3896Asn(p.S3896N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53604814:53604814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2517A>C |
| AA Mutation | p.Lys839Asn(p.K839N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53548119:53548119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10190A>G |
| AA Mutation | p.Asn3397Ser(p.N3397S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53549069:53549069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9925C>T |
| AA Mutation | p.Arg3309Cys(p.R3309C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53536560:53536560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs797045618 |
| CDS Mutation | c.12245G>A |
| AA Mutation | p.Arg4082His(p.R4082H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53563818:53563818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7033G>A |
| AA Mutation | p.Glu2345Lys(p.E2345K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53535473:53535473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12560G>A |
| AA Mutation | p.Arg4187His(p.R4187H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53548035:53548035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10274G>A |
| AA Mutation | p.Ser3425Asn(p.S3425N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53542517:53542517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11402C>T |
| AA Mutation | p.Ala3801Val(p.A3801V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262854 |
| Start | 53614585:53614585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2210C>T |
| AA Mutation | p.Ala737Val(p.A737V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262854 |
| Start | 53604706:53604706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2625T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262854 |
| Start | 53548067:53548067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782459089 |
| CDS Mutation | c.10242C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262854 |
| Start | 53560352:53560352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7572C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262854 |
| Start | 53562141:53562141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7308G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262854 |
| Start | 53534171:53534171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12858T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262854 |
| Start | 53552808:53552808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8580C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262854 |
| Start | 53583623:53583623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5455C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262854 |
| Start | 53554690:53554690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8437A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262854 |
| Start | 53625194:53625194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1554C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262854 |
| Start | 53603453:53603453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144396302 |
| CDS Mutation | c.2791C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262854 |
| Start | 53588385:53588385(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs35102400 |
| CDS Mutation | c.4611delT |
| AA Mutation | p.Phe1537LeufsTer4(p.F1537Lfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262854 |
| Start | 53549069:53549070(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.9924dupG |
| AA Mutation | p.Arg3309AlafsTer2(p.R3309Afs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262854 |
| Start | 53551364:53551365(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.8997dupC |
| AA Mutation | p.Ser3000LeufsTer4(p.S3000Lfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | splice_donor_variant;intron_variant |
| Transcription ID | ENST00000262854 |
| Start | 53634219:53634234(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.567+2_567+17delTAAGTAACTCTTTGGG |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |