GPATCH1
G-patch domain containing 1
Summary
Predicted to enable RNA binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Part of catalytic step 2 spliceosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs766935903 | 19:33,572,151 | G/C | — | uncertain significance |
| rs7252505 | 19:33,575,064 | G/A | intron variant | — |
| rs150368616 | 19:33,579,109 | G/T | — | uncertain significance |
| rs768936104 | 19:33,579,117 | G/A | — | uncertain significance |
| rs760152552 | 19:33,579,129 | G/A | — | uncertain significance |
| rs200492580 | 19:33,579,157 | C/G | — | uncertain significance |
| rs1021350790 | 19:33,581,707 | T/C | — | uncertain significance |
| rs745420155 | 19:33,581,727 | G/A | — | uncertain significance |
| rs1972586266 | 19:33,581,737 | C/A | — | uncertain significance |
| rs374456620 | 19:33,584,344 | G/A | — | uncertain significance |
| rs752843732 | 19:33,584,367 | G/A | — | uncertain significance |
| rs1972620006 | 19:33,584,371 | C/A | — | uncertain significance |
| rs1972620093 | 19:33,584,379 | C/T | — | uncertain significance |
| rs144397243 | 19:33,584,385 | C/T | — | uncertain significance |
| rs767665955 | 19:33,585,094 | G/A | — | uncertain significance |
| rs369545403 | 19:33,585,125 | G/T | — | uncertain significance |
| rs770609275 | 19:33,585,160 | C/T | — | uncertain significance |
| rs2513883268 | 19:33,587,275 | A/G | — | likely benign |
| rs1455961163 | 19:33,587,282 | G/A | — | uncertain significance |
| rs1376103024 | 19:33,588,704 | A/G | — | uncertain significance |
| rs1972681051 | 19:33,588,791 | A/T | — | uncertain significance |
| rs757583926 | 19:33,592,418 | C/T | — | uncertain significance |
| rs200016315 | 19:33,592,419 | G/A | — | uncertain significance |
| rs1157416063 | 19:33,597,614 | C/T | — | uncertain significance |
| rs768707692 | 19:33,597,686 | A/G | — | uncertain significance |
| rs373062301 | 19:33,597,703 | T/C | — | uncertain significance |
| rs192904363 | 19:33,597,773 | G/T | — | uncertain significance |
| rs10416218 | 19:33,599,127 | T/C | intron variant | — |
| rs2287679 | 19:33,600,764 | T/C | missense variant | — |
| rs772837945 | 19:33,600,798 | G/C | — | uncertain significance |
| rs147651445 | 19:33,600,804 | G/A | — | uncertain significance |
| rs754967838 | 19:33,600,821 | C/T | — | uncertain significance |
| rs749564199 | 19:33,600,866 | C/T | — | uncertain significance |
| rs201456156 | 19:33,600,898 | G/A | — | uncertain significance |
| rs1393166835 | 19:33,602,673 | G/C | — | uncertain significance |
| rs376267518 | 19:33,602,701 | C/T | — | uncertain significance |
| rs377165973 | 19:33,602,702 | G/A | — | uncertain significance |
| rs141437478 | 19:33,602,758 | G/A | — | uncertain significance |
| rs372282579 | 19:33,602,798 | G/A | — | uncertain significance |
| rs145630625 | 19:33,603,392 | A/G | — | uncertain significance |
| rs1355214485 | 19:33,603,426 | T/C | — | uncertain significance |
| rs369277459 | 19:33,603,432 | T/C | — | uncertain significance |
| rs941379016 | 19:33,603,510 | C/G | — | uncertain significance |
| rs756704990 | 19:33,604,693 | C/T | — | uncertain significance |
| rs1192098426 | 19:33,604,714 | A/T | — | uncertain significance |
| rs375992337 | 19:33,604,761 | A/G | — | uncertain significance |
| rs149390547 | 19:33,604,773 | T/C | — | likely benign |
| rs771674088 | 19:33,605,191 | A/C | — | uncertain significance |
| rs1194047919 | 19:33,605,295 | A/T | — | uncertain significance |
| rs10416265 | 19:33,605,300 | A/G | missense variant | — |
| rs201482751 | 19:33,608,785 | A/T | — | uncertain significance |
| rs140347639 | 19:33,608,818 | T/C | — | uncertain significance |
| rs2513907333 | 19:33,608,843 | A/C | — | uncertain significance |
| rs760787927 | 19:33,608,926 | G/A | — | uncertain significance |
| rs901560392 | 19:33,608,929 | A/T | — | uncertain significance |
| rs200972181 | 19:33,610,003 | T/A | — | uncertain significance |
| rs760249876 | 19:33,610,009 | C/T | — | uncertain significance |
| rs73039449 | 19:33,616,077 | T/C | — | benign |
| rs745453494 | 19:33,617,575 | G/A | — | uncertain significance |
| rs774171885 | 19:33,617,590 | C/G | — | uncertain significance |
| rs16967824 | 19:33,617,599 | G/A | — | benign |
| rs199830028 | 19:33,617,614 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.