Primary Site >> Stomach Cancer
Gene >> JPH3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284262 |
| Start | 87644432:87644432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.557C>T |
| AA Mutation | p.Ala186Val(p.A186V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284262 |
| Start | 87696587:87696587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772668984 |
| CDS Mutation | c.2174C>T |
| AA Mutation | p.Ala725Val(p.A725V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284262 |
| Start | 87644423:87644423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.548C>G |
| AA Mutation | p.Pro183Arg(p.P183R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284262 |
| Start | 87603258:87603258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.112G>A |
| AA Mutation | p.Glu38Lys(p.E38K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284262 |
| Start | 87603297:87603297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.151G>A |
| AA Mutation | p.Gly51Ser(p.G51S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284262 |
| Start | 87696634:87696634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2221A>G |
| AA Mutation | p.Ile741Val(p.I741V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284262 |
| Start | 87644953:87644953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200494558 |
| CDS Mutation | c.1078C>T |
| AA Mutation | p.Arg360Cys(p.R360C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284262 |
| Start | 87644743:87644743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.868G>T |
| AA Mutation | p.Gly290Cys(p.G290C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284262 |
| Start | 87644608:87644608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142136496 |
| CDS Mutation | c.733C>T |
| AA Mutation | p.Arg245Cys(p.R245C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284262 |
| Start | 87644401:87644401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546917046 |
| CDS Mutation | c.526G>A |
| AA Mutation | p.Ala176Thr(p.A176T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284262 |
| Start | 87644334:87644334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199746547 |
| CDS Mutation | c.459C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284262 |
| Start | 87690310:87690310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1950C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284262 |
| Start | 87644814:87644814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144601410 |
| CDS Mutation | c.939C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284262 |
| Start | 87644676:87644676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200310769 |
| CDS Mutation | c.801C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |