SUGP1
SURP and G-patch domain containing 1
Summary
SF4 is a member of the SURP family of splicing factors.[supplied by OMIM, Sep 2003]
Known Variants65 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1360283108 | 19:19,387,476 | G/C | — | uncertain significance |
| rs747671249 | 19:19,387,776 | G/A | — | uncertain significance |
| rs2512945866 | 19:19,387,830 | A/C | — | uncertain significance |
| rs199748454 | 19:19,387,849 | A/C | — | uncertain significance |
| rs4808191 | 19:19,388,060 | C/T | upstream gene variant | — |
| rs12981974 | 19:19,388,071 | G/A | — | — |
| rs2512947075 | 19:19,388,657 | T/C | — | uncertain significance |
| rs1322992365 | 19:19,389,509 | T/C | — | uncertain significance |
| rs149904112 | 19:19,390,126 | G/T | — | uncertain significance |
| rs1223071035 | 19:19,390,135 | C/A | — | uncertain significance |
| rs2061079358 | 19:19,390,180 | A/G | — | uncertain significance |
| rs11555053 | 19:19,390,185 | G/A | — | benign |
| rs1057524594 | 19:19,391,062 | G/T | — | uncertain significance |
| rs8100204 | 19:19,393,714 | G/A | intron variant | — |
| rs188247550 | 19:19,396,616 | C/T | intron variant | — |
| rs188431569 | 19:19,403,998 | C/T | intron variant | — |
| rs11666553 | 19:19,407,171 | C/A | intron variant | — |
| rs10401969 | 19:19,407,718 | T/C | intron variant | — |
| rs1372375128 | 19:19,407,810 | A/G | — | uncertain significance |
| rs761900209 | 19:19,407,852 | G/C | — | uncertain significance |
| rs750287204 | 19:19,407,864 | T/C | — | uncertain significance |
| rs373152885 | 19:19,407,933 | G/A | — | uncertain significance |
| rs2061233036 | 19:19,407,959 | G/C | — | uncertain significance |
| rs749403249 | 19:19,407,978 | C/A | — | uncertain significance |
| rs138311992 | 19:19,408,026 | G/A | — | uncertain significance |
| rs749011248 | 19:19,408,035 | G/A | — | uncertain significance |
| rs147240341 | 19:19,408,044 | C/G | — | uncertain significance |
| rs141056245 | 19:19,408,067 | C/A | — | uncertain significance |
| rs1254145923 | 19:19,408,095 | A/T | — | uncertain significance |
| rs552434494 | 19:19,408,112 | C/T | — | uncertain significance |
| rs758349812 | 19:19,408,133 | C/T | — | uncertain significance |
| rs117961479 | 19:19,410,750 | G/A | intron variant | — |
| rs57915152 | 19:19,412,045 | G/C | — | — |
| rs17751061 | 19:19,413,092 | C/G | missense variant | — |
| rs2512974059 | 19:19,413,101 | T/C | — | uncertain significance |
| rs747940911 | 19:19,413,180 | C/T | — | uncertain significance |
| rs199857058 | 19:19,413,183 | C/T | — | uncertain significance |
| rs1248975414 | 19:19,414,186 | G/A | — | uncertain significance |
| rs745392386 | 19:19,414,192 | T/C | — | uncertain significance |
| rs2512975703 | 19:19,414,193 | T/C | — | uncertain significance |
| rs1461507420 | 19:19,414,201 | T/C | — | uncertain significance |
| rs1187232115 | 19:19,414,564 | T/G | — | uncertain significance |
| rs905905668 | 19:19,414,594 | C/T | — | uncertain significance |
| rs2512976692 | 19:19,414,602 | A/G | — | uncertain significance |
| rs149077181 | 19:19,416,660 | T/C | — | uncertain significance |
| rs201270493 | 19:19,416,701 | G/A | — | likely benign |
| rs1599865570 | 19:19,416,711 | T/C | — | uncertain significance |
| rs553015469 | 19:19,416,736 | C/A | — | uncertain significance |
| rs2061314641 | 19:19,416,801 | G/A | — | uncertain significance |
| rs2061314772 | 19:19,416,814 | T/G | — | likely benign |
| rs369935862 | 19:19,416,835 | C/T | — | likely benign |
| rs558513662 | 19:19,416,870 | G/A | — | uncertain significance |
| rs739846 | 19:19,419,071 | G/A | intron variant | — |
| rs779302963 | 19:19,420,927 | G/C | — | uncertain significance |
| rs199887237 | 19:19,420,981 | T/A | — | uncertain significance |
| rs200879181 | 19:19,420,986 | G/A | — | uncertain significance |
| rs2315024 | 19:19,423,817 | T/A | intron variant | — |
| rs112253053 | 19:19,425,145 | T/A | intron variant | — |
| rs141578579 | 19:19,427,232 | C/T | — | uncertain significance |
| rs958958803 | 19:19,427,263 | C/A | — | uncertain significance |
| rs199730578 | 19:19,427,319 | C/T | — | uncertain significance |
| rs149607008 | 19:19,427,323 | G/A | — | likely benign |
| rs541344524 | 19:19,427,886 | G/C | — | — |
| rs543667961 | 19:19,428,527 | T/C | — | — |
| rs139043355 | 19:19,431,293 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.