NHLRC3
NHL repeat containing 3
Summary
This gene encodes a protein containing NCL-1, HT2A and Lin-41 (NHL) family repeats. Mammalian NHL-repeat containing proteins may be involved in a variety of enzymatic processes, including protein modification through ubiquitination. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Aug 2012]
Known Variants23 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1251188134 | 13:39,612,781 | C/G | — | uncertain significance |
| rs756879023 | 13:39,612,789 | T/G | — | uncertain significance |
| rs139618208 | 13:39,612,819 | C/T | — | uncertain significance |
| rs778069617 | 13:39,613,294 | G/A | — | uncertain significance |
| rs997927216 | 13:39,613,339 | G/T | — | uncertain significance |
| rs1007107832 | 13:39,613,369 | G/A | — | uncertain significance |
| rs202055145 | 13:39,613,400 | T/C | — | uncertain significance |
| rs769173699 | 13:39,613,409 | T/C | — | uncertain significance |
| rs186016810 | 13:39,613,783 | C/T | — | uncertain significance |
| rs139647635 | 13:39,613,822 | C/A | — | uncertain significance |
| rs374721683 | 13:39,613,839 | G/A | — | uncertain significance |
| rs373055809 | 13:39,616,302 | G/C | — | uncertain significance |
| rs1159914140 | 13:39,616,359 | A/G | — | uncertain significance |
| rs772023282 | 13:39,616,365 | A/G | — | uncertain significance |
| rs376811167 | 13:39,616,431 | A/G | — | uncertain significance |
| rs142754977 | 13:39,621,838 | T/G | — | uncertain significance |
| rs145374636 | 13:39,621,888 | T/A | — | uncertain significance |
| rs143599770 | 13:39,621,920 | A/G | — | uncertain significance |
| rs145181998 | 13:39,621,923 | A/C | — | uncertain significance |
| rs139652592 | 13:39,621,928 | A/C | — | uncertain significance |
| rs41286951 | 13:39,621,933 | C/T | missense variant | — |
| rs144310707 | 13:39,621,967 | C/G | — | uncertain significance |
| rs776584716 | 13:39,622,034 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.