PHF10
PHD finger protein 10
Summary
This gene contains a predicted ORF that encodes a protein with two zinc finger domains. The function of the encoded protein is not known. Sequence analysis suggests that multiple alternatively spliced transcript variants are derived from this gene but the full-length nature of only two of them is known. These two splice variants encode different isoforms. A pseudogene for this gene is located on Xq28. [provided by RefSeq, Jul 2008]
Known Variants23 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1372177914 | 6:170,104,113 | T/G | — | uncertain significance |
| rs780408412 | 6:170,104,155 | C/G | — | uncertain significance |
| rs148902304 | 6:170,104,181 | C/T | — | uncertain significance |
| rs138138680 | 6:170,105,313 | G/A | — | uncertain significance |
| rs373802598 | 6:170,105,378 | G/A | — | uncertain significance |
| rs771642444 | 6:170,105,716 | A/G | — | likely benign |
| rs4286788 | 6:170,105,725 | T/C | — | benign |
| rs759984393 | 6:170,105,738 | A/G | — | uncertain significance |
| rs373121095 | 6:170,105,799 | T/G | — | likely benign |
| rs12663375 | 6:170,110,243 | G/A | downstream gene variant | — |
| rs34227712 | 6:170,110,361 | C/T | — | uncertain significance |
| rs2537317787 | 6:170,110,385 | T/C | — | uncertain significance |
| rs7762018 | 6:170,113,244 | C/A | intron variant | — |
| rs141042911 | 6:170,114,894 | C/A | — | uncertain significance |
| rs2537330480 | 6:170,121,153 | T/C | — | uncertain significance |
| rs1352816821 | 6:170,121,167 | G/A | — | uncertain significance |
| rs1276288844 | 6:170,121,205 | A/C | — | uncertain significance |
| rs530092231 | 6:170,123,957 | C/T | — | uncertain significance |
| rs1018219018 | 6:170,123,984 | G/A | — | uncertain significance |
| rs899656396 | 6:170,123,985 | G/C | — | uncertain significance |
| rs1441979774 | 6:170,123,991 | G/A | — | uncertain significance |
| rs954755915 | 6:170,124,002 | G/A | — | uncertain significance |
| rs1789252501 | 6:170,124,006 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.