HHIPL1
HHIP like 1
Summary
This gene encodes a protein that belongs to the glucose/sorbosone dehydrogenase family. The encoded protein also contains a domain that binds folate and reduced folic acid derivatives. [provided by RefSeq, Jul 2016]
Known Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11160533 | 14:100,075,773 | C/T | regulatory region variant | — |
| rs4905865 | 14:100,076,059 | T/G | regulatory region variant | — |
| rs12893887 | 14:100,111,565 | G/A | synonymous variant | — |
| rs2504276942 | 14:100,111,579 | T/G | — | uncertain significance |
| rs767779810 | 14:100,111,707 | G/A | — | uncertain significance |
| rs1228079576 | 14:100,111,784 | G/T | — | uncertain significance |
| rs35911833 | 14:100,115,799 | C/T | regulatory region variant | — |
| rs769281410 | 14:100,118,574 | A/C | — | uncertain significance |
| rs2504298849 | 14:100,118,576 | G/A | — | uncertain significance |
| rs199936947 | 14:100,118,594 | G/A | — | uncertain significance |
| rs766506953 | 14:100,118,597 | G/A | — | uncertain significance |
| rs146699172 | 14:100,118,610 | C/T | — | uncertain significance |
| rs986728022 | 14:100,118,612 | C/A | — | uncertain significance |
| rs200203805 | 14:100,118,618 | C/A | — | uncertain significance |
| rs766596893 | 14:100,118,672 | C/T | — | uncertain significance |
| rs759635561 | 14:100,118,675 | G/A | — | uncertain significance |
| rs765262191 | 14:100,118,684 | C/T | — | uncertain significance |
| rs549263452 | 14:100,118,766 | C/T | — | uncertain significance |
| rs769901251 | 14:100,118,879 | G/A | — | uncertain significance |
| rs145984890 | 14:100,118,894 | G/A | — | uncertain significance |
| rs140080680 | 14:100,118,927 | C/T | — | uncertain significance |
| rs376667018 | 14:100,118,928 | G/A | — | uncertain significance |
| rs772231324 | 14:100,119,050 | C/T | — | uncertain significance |
| rs2055960354 | 14:100,119,122 | G/T | — | uncertain significance |
| rs2056057420 | 14:100,123,349 | G/T | — | uncertain significance |
| rs1198627686 | 14:100,123,381 | G/C | — | uncertain significance |
| rs375024067 | 14:100,123,395 | G/A | — | uncertain significance |
| rs2473244642 | 14:100,123,407 | T/C | — | uncertain significance |
| rs144827737 | 14:100,123,434 | G/A | — | uncertain significance |
| rs12897285 | 14:100,124,055 | T/C | intron variant | — |
| rs755723325 | 14:100,125,767 | C/T | — | uncertain significance |
| rs1278649634 | 14:100,125,796 | G/A | — | uncertain significance |
| rs776689209 | 14:100,125,838 | C/T | — | uncertain significance |
| rs767386626 | 14:100,125,887 | C/A | — | uncertain significance |
| rs774230122 | 14:100,125,930 | C/T | — | likely benign |
| rs572979321 | 14:100,125,935 | C/A | — | uncertain significance |
| rs374815884 | 14:100,125,943 | G/A | — | uncertain significance |
| rs778098930 | 14:100,125,955 | G/T | — | uncertain significance |
| rs754475370 | 14:100,126,078 | G/A | — | uncertain significance |
| rs2504330632 | 14:100,126,085 | C/T | — | uncertain significance |
| rs2504335517 | 14:100,126,626 | T/G | — | uncertain significance |
| rs769018561 | 14:100,126,637 | G/A | — | uncertain significance |
| rs1337189026 | 14:100,126,649 | A/G | — | uncertain significance |
| rs2056130999 | 14:100,126,685 | C/G | — | uncertain significance |
| rs193920989 | 14:100,126,712 | G/C | — | uncertain significance |
| rs766908100 | 14:100,129,274 | A/G | — | uncertain significance |
| rs777230313 | 14:100,129,352 | G/A | — | uncertain significance |
| rs2895811 | 14:100,133,942 | T/A | — | — |
| rs2056279470 | 14:100,134,612 | G/A | — | uncertain significance |
| rs2504374405 | 14:100,138,676 | C/G | — | uncertain significance |
| rs1246703043 | 14:100,141,457 | C/T | — | uncertain significance |
| rs1377483778 | 14:100,141,499 | C/T | — | uncertain significance |
| rs926048708 | 14:100,141,520 | G/T | — | uncertain significance |
| rs2504383318 | 14:100,141,547 | A/C | — | uncertain significance |
| rs927547754 | 14:100,141,613 | G/A | — | uncertain significance |
| rs1378988828 | 14:100,141,617 | T/C | — | uncertain significance |
| rs568054581 | 14:100,141,644 | G/A | — | uncertain significance |
| rs554216426 | 14:100,141,668 | G/A | — | uncertain significance |
| rs2504384168 | 14:100,141,674 | G/A | — | uncertain significance |
| rs1218168306 | 14:100,141,688 | G/A | — | uncertain significance |
| rs1196514949 | 14:100,141,694 | G/A | — | uncertain significance |
| rs761132705 | 14:100,141,782 | G/A | — | uncertain significance |
| rs764316680 | 14:100,141,787 | G/T | — | uncertain significance |
| rs2056378999 | 14:100,141,788 | T/C | — | likely benign |
| rs1383626402 | 14:100,141,850 | G/C | — | uncertain significance |
| rs754614733 | 14:100,141,871 | C/G | — | uncertain significance |
| rs1054086375 | 14:100,141,887 | A/G | — | uncertain significance |
| rs775070784 | 14:100,141,910 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.