Primary Site >> Stomach Cancer
Gene >> MUC17
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101039406:101039406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7990G>A |
| AA Mutation | p.Val2664Met(p.V2664M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101032674:101032674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1258T>A |
| AA Mutation | p.Ser420Thr(p.S420T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101037838:101037838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6422C>T |
| AA Mutation | p.Ser2141Leu(p.S2141L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101035398:101035398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3982C>T |
| AA Mutation | p.Pro1328Ser(p.P1328S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101037541:101037541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373744994 |
| CDS Mutation | c.6125G>A |
| AA Mutation | p.Arg2042Gln(p.R2042Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101031174:101031174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.137A>G |
| AA Mutation | p.Asp46Gly(p.D46G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101040226:101040226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8810C>A |
| AA Mutation | p.Thr2937Asn(p.T2937N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101041684:101041684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10268C>A |
| AA Mutation | p.Pro3423His(p.P3423H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101032369:101032369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527980140 |
| CDS Mutation | c.953C>T |
| AA Mutation | p.Thr318Met(p.T318M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101034207:101034207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2791G>A |
| AA Mutation | p.Asp931Asn(p.D931N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101043225:101043225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11809A>G |
| AA Mutation | p.Thr3937Ala(p.T3937A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101041291:101041291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370607705 |
| CDS Mutation | c.9875C>T |
| AA Mutation | p.Thr3292Met(p.T3292M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101035383:101035383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3967G>A |
| AA Mutation | p.Glu1323Lys(p.E1323K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101041003:101041003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9587C>A |
| AA Mutation | p.Thr3196Asn(p.T3196N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101038018:101038018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6602C>G |
| AA Mutation | p.Ser2201Cys(p.S2201C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101039713:101039713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8297C>A |
| AA Mutation | p.Ser2766Tyr(p.S2766Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101043333:101043333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11917A>G |
| AA Mutation | p.Thr3973Ala(p.T3973A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101058016:101058016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13454G>T |
| AA Mutation | p.Arg4485Met(p.R4485M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101034402:101034402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2986G>A |
| AA Mutation | p.Ala996Thr(p.A996T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101036334:101036334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4918A>G |
| AA Mutation | p.Thr1640Ala(p.T1640A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101040409:101040409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142796970 |
| CDS Mutation | c.8993C>T |
| AA Mutation | p.Pro2998Leu(p.P2998L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101031913:101031913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.497C>A |
| AA Mutation | p.Thr166Asn(p.T166N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101037577:101037577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140147544 |
| CDS Mutation | c.6161C>T |
| AA Mutation | p.Thr2054Met(p.T2054M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101037807:101037807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762599323 |
| CDS Mutation | c.6391A>G |
| AA Mutation | p.Ser2131Gly(p.S2131G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101033627:101033627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2211G>T |
| AA Mutation | p.Met737Ile(p.M737I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101041354:101041354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9938C>A |
| AA Mutation | p.Thr3313Asn(p.T3313N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101042080:101042080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753070467 |
| CDS Mutation | c.10664G>A |
| AA Mutation | p.Ser3555Asn(p.S3555N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101042695:101042695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11279T>A |
| AA Mutation | p.Val3760Asp(p.V3760D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101036029:101036029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4613C>T |
| AA Mutation | p.Pro1538Leu(p.P1538L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101034379:101034379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760274671 |
| CDS Mutation | c.2963C>T |
| AA Mutation | p.Thr988Ile(p.T988I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101032057:101032057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.641G>T |
| AA Mutation | p.Gly214Val(p.G214V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101032588:101032588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769590935 |
| CDS Mutation | c.1172G>A |
| AA Mutation | p.Gly391Glu(p.G391E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101037601:101037601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6185A>C |
| AA Mutation | p.Asn2062Thr(p.N2062T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101039050:101039050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7634C>T |
| AA Mutation | p.Pro2545Leu(p.P2545L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101058031:101058031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs534194993 |
| CDS Mutation | c.13469C>T |
| AA Mutation | p.Thr4490Met(p.T4490M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101032177:101032177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.761G>A |
| AA Mutation | p.Ser254Asn(p.S254N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101037732:101037732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6316A>C |
| AA Mutation | p.Ser2106Arg(p.S2106R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101040314:101040314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8898T>G |
| AA Mutation | p.Ser2966Arg(p.S2966R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101042395:101042395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10979T>G |
| AA Mutation | p.Val3660Gly(p.V3660G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101031999:101031999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.583A>C |
| AA Mutation | p.Ser195Arg(p.S195R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101042728:101042728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11312G>A |
| AA Mutation | p.Ser3771Asn(p.S3771N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101032986:101032986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1570G>A |
| AA Mutation | p.Ala524Thr(p.A524T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101041819:101041819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763016905 |
| CDS Mutation | c.10403C>T |
| AA Mutation | p.Thr3468Met(p.T3468M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101039971:101039971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8555C>A |
| AA Mutation | p.Thr2852Lys(p.T2852K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101031789:101031789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.373A>G |
| AA Mutation | p.Ser125Gly(p.S125G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101036310:101036310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4894C>G |
| AA Mutation | p.Leu1632Val(p.L1632V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101043136:101043136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11720C>T |
| AA Mutation | p.Thr3907Ile(p.T3907I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101032172:101032172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.756A>C |
| AA Mutation | p.Gln252His(p.Q252H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101033571:101033571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768351156 |
| CDS Mutation | c.2155G>A |
| AA Mutation | p.Val719Met(p.V719M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101041335:101041335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9919G>A |
| AA Mutation | p.Asp3307Asn(p.D3307N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101043451:101043451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12035G>A |
| AA Mutation | p.Ser4012Asn(p.S4012N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101037315:101037315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568723888 |
| CDS Mutation | c.5899C>T |
| AA Mutation | p.Pro1967Ser(p.P1967S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101033952:101033952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2536T>C |
| AA Mutation | p.Ser846Pro(p.S846P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101037172:101037172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5756C>T |
| AA Mutation | p.Ser1919Leu(p.S1919L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101041410:101041410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746129310 |
| CDS Mutation | c.9994A>G |
| AA Mutation | p.Thr3332Ala(p.T3332A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101035389:101035389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3973A>G |
| AA Mutation | p.Thr1325Ala(p.T1325A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101040397:101040397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8981T>A |
| AA Mutation | p.Val2994Asp(p.V2994D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101043678:101043678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12262G>A |
| AA Mutation | p.Ala4088Thr(p.A4088T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101034469:101034469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3053C>G |
| AA Mutation | p.Thr1018Ser(p.T1018S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101039179:101039179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7763G>A |
| AA Mutation | p.Ser2588Asn(p.S2588N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101035606:101035606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141608296 |
| CDS Mutation | c.4190C>T |
| AA Mutation | p.Pro1397Leu(p.P1397L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101043736:101043736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150141937 |
| CDS Mutation | c.12320C>T |
| AA Mutation | p.Thr4107Met(p.T4107M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101032114:101032114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.698C>T |
| AA Mutation | p.Ala233Val(p.A233V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101033560:101033560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2144C>T |
| AA Mutation | p.Thr715Ile(p.T715I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101051820:101051820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12961G>A |
| AA Mutation | p.Ala4321Thr(p.A4321T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306151 |
| Start | 101043155:101043155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11739C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 67 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306151 |
| Start | 101051659:101051659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149949866 |
| CDS Mutation | c.12921G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 68 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306151 |
| Start | 101048966:101048966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200175178 |
| CDS Mutation | c.12657G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 69 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306151 |
| Start | 101042756:101042756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138649661 |
| CDS Mutation | c.11340C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 70 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306151 |
| Start | 101043578:101043578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754413687 |
| CDS Mutation | c.12162G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 71 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306151 |
| Start | 101043194:101043194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751369976 |
| CDS Mutation | c.11778A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 72 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306151 |
| Start | 101034377:101034377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2961C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 73 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306151 |
| Start | 101038565:101038565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138267850 |
| CDS Mutation | c.7149C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |