Primary Site >> Stomach Cancer
Gene >> PCDH10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151243:133151243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1103G>T |
| AA Mutation | p.Ser368Ile(p.S368I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150382:133150382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.242G>A |
| AA Mutation | p.Arg81His(p.R81H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152487:133152487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2347A>G |
| AA Mutation | p.Ser783Gly(p.S783G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133163094:133163094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2915A>T |
| AA Mutation | p.Asn972Ile(p.N972I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133163032:133163032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2853T>A |
| AA Mutation | p.Asp951Glu(p.D951E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151726:133151726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1586G>A |
| AA Mutation | p.Arg529His(p.R529H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150304:133150304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199719551 |
| CDS Mutation | c.164C>T |
| AA Mutation | p.Thr55Met(p.T55M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151927:133151927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1787C>T |
| AA Mutation | p.Pro596Leu(p.P596L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152094:133152094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs535858980 |
| CDS Mutation | c.1954C>T |
| AA Mutation | p.Arg652Trp(p.R652W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151953:133151953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1813G>A |
| AA Mutation | p.Ala605Thr(p.A605T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151504:133151504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1364A>G |
| AA Mutation | p.Asp455Gly(p.D455G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151518:133151518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1378G>A |
| AA Mutation | p.Ala460Thr(p.A460T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150440:133150440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.300G>T |
| AA Mutation | p.Glu100Asp(p.E100D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150856:133150856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.716G>A |
| AA Mutation | p.Arg239Gln(p.R239Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151419:133151419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1279G>A |
| AA Mutation | p.Asp427Asn(p.D427N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151086:133151086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.946T>G |
| AA Mutation | p.Leu316Val(p.L316V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152355:133152355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2215C>T |
| AA Mutation | p.Arg739Cys(p.R739C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151974:133151974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750931587 |
| CDS Mutation | c.1834G>A |
| AA Mutation | p.Glu612Lys(p.E612K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151548:133151548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1408G>A |
| AA Mutation | p.Val470Met(p.V470M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152223:133152223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2083G>C |
| AA Mutation | p.Gly695Arg(p.G695R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133155012:133155012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2786C>A |
| AA Mutation | p.Ala929Asp(p.A929D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150610:133150610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754653138 |
| CDS Mutation | c.470G>A |
| AA Mutation | p.Arg157His(p.R157H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133154996:133154996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2770G>A |
| AA Mutation | p.Asp924Asn(p.D924N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150310:133150310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.170C>A |
| AA Mutation | p.Pro57His(p.P57H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151384:133151384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1244T>C |
| AA Mutation | p.Ile415Thr(p.I415T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152082:133152082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1942C>T |
| AA Mutation | p.Arg648Cys(p.R648C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151525:133151525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1385G>A |
| AA Mutation | p.Arg462His(p.R462H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151134:133151134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.994G>T |
| AA Mutation | p.Asp332Tyr(p.D332Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151147:133151147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1007A>T |
| AA Mutation | p.Asn336Ile(p.N336I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151947:133151947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1807G>A |
| AA Mutation | p.Val603Met(p.V603M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151380:133151380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1240A>C |
| AA Mutation | p.Thr414Pro(p.T414P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151381:133151381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1241C>A |
| AA Mutation | p.Thr414Asn(p.T414N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151210:133151210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1070A>C |
| AA Mutation | p.Glu357Ala(p.E357A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133163087:133163087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772263978 |
| CDS Mutation | c.2908C>T |
| AA Mutation | p.Arg970Cys(p.R970C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151800:133151800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1660C>A |
| AA Mutation | p.Leu554Met(p.L554M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151549:133151549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1409T>C |
| AA Mutation | p.Val470Ala(p.V470A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133163063:133163063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2884G>A |
| AA Mutation | p.Asp962Asn(p.D962N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150609:133150609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.469C>T |
| AA Mutation | p.Arg157Cys(p.R157C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152055:133152055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1915C>T |
| AA Mutation | p.Arg639Cys(p.R639C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150772:133150772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.632G>T |
| AA Mutation | p.Gly211Val(p.G211V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151240:133151240(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1100T>C |
| AA Mutation | p.Val367Ala(p.V367A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152202:133152202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2062G>A |
| AA Mutation | p.Gly688Arg(p.G688R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150292:133150292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.152G>A |
| AA Mutation | p.Arg51His(p.R51H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150945:133150945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.805G>A |
| AA Mutation | p.Val269Met(p.V269M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152619:133152619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2479C>A |
| AA Mutation | p.Pro827Thr(p.P827T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151798:133151798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1658C>T |
| AA Mutation | p.Ala553Val(p.A553V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151351:133151351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1211G>A |
| AA Mutation | p.Arg404His(p.R404H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152088:133152088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1948C>A |
| AA Mutation | p.Pro650Thr(p.P650T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151204:133151204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1064C>T |
| AA Mutation | p.Ala355Val(p.A355V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151915:133151915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1775G>A |
| AA Mutation | p.Arg592His(p.R592H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152016:133152016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1876A>G |
| AA Mutation | p.Met626Val(p.M626V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152046:133152046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1906G>A |
| AA Mutation | p.Gly636Arg(p.G636R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150576:133150576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.436G>A |
| AA Mutation | p.Ala146Thr(p.A146T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151159:133151159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1019C>T |
| AA Mutation | p.Ala340Val(p.A340V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152065:133152065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1925G>A |
| AA Mutation | p.Arg642His(p.R642H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152709:133152709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2569G>A |
| AA Mutation | p.Val857Ile(p.V857I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151520:133151520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1380G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152012:133152012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540013540 |
| CDS Mutation | c.1872C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151901:133151901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1761T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151742:133151742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1602G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151608:133151608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1468C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151115:133151115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.975A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150239:133150239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.99C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151052:133151052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.912G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151922:133151922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1782G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152687:133152687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777683475 |
| CDS Mutation | c.2547G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151124:133151124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.984G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152660:133152660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2520C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152471:133152471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2331G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150617:133150617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.477C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150233:133150233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.93C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151778:133151778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1638G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133163062:133163062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2883T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 74 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150383:133150383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538631045 |
| CDS Mutation | c.243C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 75 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133152207:133152207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773534266 |
| CDS Mutation | c.2067C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 76 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133163002:133163002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766245596 |
| CDS Mutation | c.2823T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 77 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151388:133151388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1248T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 78 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151889:133151889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533621614 |
| CDS Mutation | c.1749G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 79 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150494:133150494(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.360delC |
| AA Mutation | p.Ser121LeufsTer7(p.S121Lfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 80 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000264360 |
| Start | 133163072:133163072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2893C>T |
| AA Mutation | p.Gln965Ter(p.Q965*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 81 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151163:133151164(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1024_1025insTT |
| AA Mutation | p.Cys342PhefsTer5(p.C342Ffs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 82 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150812:133150813(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.678_679dupCC |
| AA Mutation | p.Gln227ProfsTer44(p.Q227Pfs*44) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 83 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264360 |
| Start | 133151125:133151126(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.987dupA |
| AA Mutation | p.Ala330SerfsTer23(p.A330Sfs*23) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 84 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264360 |
| Start | 133150812:133150813(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs762465989 |
| CDS Mutation | c.679dupC |
| AA Mutation | p.Gln227ProfsTer19(p.Q227Pfs*19) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |