TAF1L
TATA-box binding protein associated factor 1 like
Summary
This locus is intronless, and apparently arose in the primate lineage from retrotransposition of the transcript from the multi-exon TAF1 locus on the X chromosome. The gene is expressed in male germ cells, and the product has been shown to function interchangeably with the TAF1 product. [provided by RefSeq, Aug 2015]
Known Variants102 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1423191848 | 9:32,630,123 | C/T | — | uncertain significance |
| rs753724498 | 9:32,630,241 | G/A | — | likely benign |
| rs753541946 | 9:32,630,344 | G/C | — | uncertain significance |
| rs575169099 | 9:32,630,349 | A/C | — | uncertain significance |
| rs1300239639 | 9:32,630,410 | T/A | — | uncertain significance |
| rs758042199 | 9:32,630,422 | T/A | — | uncertain significance |
| rs772388404 | 9:32,630,469 | C/G | — | uncertain significance |
| rs139164755 | 9:32,630,548 | G/A | — | likely benign |
| rs149951568 | 9:32,630,562 | G/C | — | uncertain significance |
| rs771118521 | 9:32,630,603 | C/G | — | uncertain significance |
| rs145062474 | 9:32,630,615 | G/A | missense variant | — |
| rs547706504 | 9:32,630,671 | T/A | — | uncertain significance |
| rs781319177 | 9:32,630,726 | T/C | — | likely benign |
| rs767781428 | 9:32,630,807 | C/T | — | uncertain significance |
| rs2489665930 | 9:32,630,836 | T/C | — | uncertain significance |
| rs1044009811 | 9:32,630,848 | G/C | — | uncertain significance |
| rs903800906 | 9:32,630,899 | T/C | — | uncertain significance |
| rs750860273 | 9:32,630,957 | C/T | — | uncertain significance |
| rs148347388 | 9:32,630,993 | T/G | — | uncertain significance |
| rs2489666418 | 9:32,631,032 | G/C | — | uncertain significance |
| rs545988745 | 9:32,631,218 | G/A | — | uncertain significance |
| rs773657347 | 9:32,631,254 | G/A | — | uncertain significance |
| rs759663955 | 9:32,631,284 | C/A | — | uncertain significance |
| rs528038779 | 9:32,631,389 | G/A | — | uncertain significance |
| rs535208015 | 9:32,631,392 | G/A | — | uncertain significance |
| rs746394860 | 9:32,631,454 | C/T | — | uncertain significance |
| rs2489667916 | 9:32,631,490 | T/C | — | uncertain significance |
| rs959223349 | 9:32,631,559 | G/A | — | uncertain significance |
| rs2489668202 | 9:32,631,577 | A/G | — | uncertain significance |
| rs2489668523 | 9:32,631,728 | C/T | — | uncertain significance |
| rs140558556 | 9:32,631,781 | G/C | — | conflicting classifications of pathogenicity |
| rs768522210 | 9:32,631,905 | T/A | — | uncertain significance |
| rs761527217 | 9:32,631,907 | A/G | — | uncertain significance |
| rs201130609 | 9:32,631,915 | A/T | — | uncertain significance |
| rs147664591 | 9:32,631,928 | C/T | — | uncertain significance |
| rs757557186 | 9:32,631,934 | C/A | — | uncertain significance |
| rs140751314 | 9:32,631,935 | G/A | — | uncertain significance |
| rs1031292234 | 9:32,631,944 | C/T | — | uncertain significance |
| rs1822524588 | 9:32,632,022 | T/C | — | uncertain significance |
| rs2489669559 | 9:32,632,123 | A/G | — | uncertain significance |
| rs533375922 | 9:32,632,129 | C/T | — | uncertain significance |
| rs550382128 | 9:32,632,132 | C/T | — | likely benign |
| rs772629563 | 9:32,632,376 | G/A | — | uncertain significance |
| rs773530597 | 9:32,632,391 | T/C | — | uncertain significance |
| rs764176652 | 9:32,632,432 | C/T | — | uncertain significance |
| rs746088854 | 9:32,632,516 | T/C | — | uncertain significance |
| rs572372548 | 9:32,632,535 | G/C | — | uncertain significance |
| rs147191242 | 9:32,632,604 | T/C | — | uncertain significance |
| rs1054005211 | 9:32,632,708 | A/G | — | uncertain significance |
| rs2489672179 | 9:32,632,789 | G/C | — | uncertain significance |
| rs142256340 | 9:32,632,860 | A/G | — | likely benign |
| rs774112603 | 9:32,632,895 | T/C | — | uncertain significance |
| rs760948209 | 9:32,632,915 | C/T | — | uncertain significance |
| rs139281774 | 9:32,632,940 | A/G | — | uncertain significance |
| rs368539318 | 9:32,632,952 | T/A | — | uncertain significance |
| rs61734890 | 9:32,632,963 | T/C | — | uncertain significance |
| rs1351770270 | 9:32,633,040 | C/T | — | uncertain significance |
| rs34787787 | 9:32,633,044 | C/T | — | uncertain significance |
| rs1225126506 | 9:32,633,057 | G/A | — | uncertain significance |
| rs753174528 | 9:32,633,060 | G/A | — | uncertain significance |
| rs764426328 | 9:32,633,070 | C/A | — | uncertain significance |
| rs191743642 | 9:32,633,195 | A/T | — | uncertain significance |
| rs1254969000 | 9:32,633,206 | T/C | — | uncertain significance |
| rs1389480172 | 9:32,633,263 | T/C | — | uncertain significance |
| rs2489674246 | 9:32,633,282 | G/T | — | uncertain significance |
| rs55827525 | 9:32,633,307 | T/C | — | likely benign |
| rs1328769489 | 9:32,633,414 | A/G | — | uncertain significance |
| rs138806882 | 9:32,633,479 | G/A | — | uncertain significance |
| rs1353987821 | 9:32,633,566 | T/C | — | uncertain significance |
| rs376973127 | 9:32,633,594 | T/C | — | uncertain significance |
| rs532747728 | 9:32,633,683 | C/T | — | uncertain significance |
| rs140084525 | 9:32,633,767 | C/T | — | uncertain significance |
| rs1485360008 | 9:32,633,770 | A/T | — | uncertain significance |
| rs143756087 | 9:32,633,780 | G/A | — | uncertain significance |
| rs778095037 | 9:32,633,831 | G/C | — | uncertain significance |
| rs1479181668 | 9:32,633,881 | A/T | — | uncertain significance |
| rs1447055934 | 9:32,633,888 | T/C | — | uncertain significance |
| rs918249317 | 9:32,634,050 | T/C | — | uncertain significance |
| rs574024094 | 9:32,634,113 | T/G | — | uncertain significance |
| rs1312353532 | 9:32,634,193 | C/T | — | uncertain significance |
| rs765455049 | 9:32,634,217 | C/T | — | uncertain significance |
| rs373008575 | 9:32,634,226 | C/A | — | uncertain significance |
| rs779690335 | 9:32,634,244 | G/T | — | uncertain significance |
| rs1387637404 | 9:32,634,285 | A/C | — | uncertain significance |
| rs756069082 | 9:32,634,481 | C/T | — | likely benign |
| rs747811095 | 9:32,634,518 | T/G | — | uncertain significance |
| rs138133234 | 9:32,634,586 | G/A | — | uncertain significance |
| rs751081950 | 9:32,634,595 | T/A | — | uncertain significance |
| rs143742964 | 9:32,634,752 | G/A | — | uncertain significance |
| rs781399503 | 9:32,634,785 | A/C | — | uncertain significance |
| rs2489678832 | 9:32,634,796 | A/G | — | uncertain significance |
| rs55991718 | 9:32,634,811 | C/G | — | benign |
| rs764701675 | 9:32,634,908 | C/T | — | uncertain significance |
| rs138027604 | 9:32,635,111 | G/C | — | uncertain significance |
| rs2489679871 | 9:32,635,112 | G/A | — | uncertain significance |
| rs2489679897 | 9:32,635,119 | C/G | — | uncertain significance |
| rs983895495 | 9:32,635,333 | G/T | — | uncertain significance |
| rs764175922 | 9:32,635,336 | G/A | — | uncertain significance |
| rs1321541962 | 9:32,635,451 | C/T | — | uncertain significance |
| rs750929210 | 9:32,635,510 | G/C | — | uncertain significance |
Showing 100 of 102 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.