CHAF1A
chromatin assembly factor 1 subunit A
Summary
Chromatin assembly factor I (CAF1) is a nuclear complex consisting of p50, p60 (CHAF1B; MIM 601245), and p150 (CHAF1A) subunits that assembles histone octamers onto replicating DNA in vitro (Kaufman et al., 1995 [PubMed 7600578]).[supplied by OMIM, Mar 2008]
Known Variants74 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2512252126 | 19:4,402,790 | G/A | — | uncertain significance |
| rs1177305767 | 19:4,402,797 | G/A | — | uncertain significance |
| rs243340 | 19:4,403,800 | T/A | — | — |
| rs370633320 | 19:4,408,947 | G/A | — | uncertain significance |
| rs997164464 | 19:4,409,004 | G/A | — | likely benign |
| rs1358937015 | 19:4,409,005 | C/T | — | uncertain significance |
| rs2230633 | 19:4,409,006 | C/G | — | benign |
| rs1568429634 | 19:4,409,080 | A/T | — | uncertain significance |
| rs775109223 | 19:4,409,115 | G/A | — | likely benign |
| rs2512263282 | 19:4,409,125 | T/C | — | uncertain significance |
| rs140374238 | 19:4,409,164 | C/T | — | uncertain significance |
| rs141725942 | 19:4,409,184 | C/T | — | uncertain significance |
| rs1022490964 | 19:4,409,248 | G/A | — | uncertain significance |
| rs778512366 | 19:4,409,319 | A/G | — | uncertain significance |
| rs779932686 | 19:4,409,409 | C/T | — | uncertain significance |
| rs2512264424 | 19:4,409,425 | T/C | — | uncertain significance |
| rs781225000 | 19:4,409,496 | A/G | — | uncertain significance |
| rs148594897 | 19:4,409,518 | T/G | — | uncertain significance |
| rs779078357 | 19:4,409,535 | G/C | — | uncertain significance |
| rs151103031 | 19:4,409,548 | C/G | — | uncertain significance |
| rs905637000 | 19:4,409,589 | A/G | — | likely benign |
| rs527960356 | 19:4,409,601 | A/G | — | uncertain significance |
| rs776588955 | 19:4,409,652 | T/G | — | uncertain significance |
| rs769961874 | 19:4,409,692 | C/T | — | uncertain significance |
| rs1270309250 | 19:4,409,740 | C/A | — | uncertain significance |
| rs112018734 | 19:4,409,752 | G/A | — | uncertain significance |
| rs56411083 | 19:4,410,646 | G/A | intron variant | — |
| rs149123603 | 19:4,418,029 | T/A | — | uncertain significance |
| rs56227586 | 19:4,418,515 | C/G | — | — |
| rs769517946 | 19:4,422,597 | G/A | — | uncertain significance |
| rs2512286571 | 19:4,422,617 | G/A | — | uncertain significance |
| rs1432165653 | 19:4,422,650 | G/C | — | uncertain significance |
| rs2512286680 | 19:4,422,665 | A/C | — | uncertain significance |
| rs201112361 | 19:4,422,705 | G/A | — | uncertain significance |
| rs2512288388 | 19:4,423,362 | A/C | — | uncertain significance |
| rs759526977 | 19:4,423,855 | C/T | — | uncertain significance |
| rs753582271 | 19:4,428,731 | G/A | — | uncertain significance |
| rs150835577 | 19:4,428,739 | G/A | — | uncertain significance |
| rs758852937 | 19:4,428,744 | C/A | — | uncertain significance |
| rs528742438 | 19:4,428,792 | C/G | — | uncertain significance |
| rs752206987 | 19:4,428,865 | C/T | — | uncertain significance |
| rs746820349 | 19:4,429,455 | G/A | — | uncertain significance |
| rs752262036 | 19:4,429,478 | G/A | — | uncertain significance |
| rs1568438575 | 19:4,429,592 | G/T | — | uncertain significance |
| rs2512303758 | 19:4,430,564 | G/A | — | uncertain significance |
| rs2512303775 | 19:4,430,571 | A/T | — | uncertain significance |
| rs2512306918 | 19:4,432,085 | A/G | — | uncertain significance |
| rs372020675 | 19:4,432,148 | C/T | — | uncertain significance |
| rs756362611 | 19:4,432,184 | G/A | — | uncertain significance |
| rs568115192 | 19:4,432,197 | C/G | — | uncertain significance |
| rs371300311 | 19:4,432,198 | G/A | — | uncertain significance |
| rs199658685 | 19:4,433,145 | G/A | — | uncertain significance |
| rs1353703224 | 19:4,433,205 | T/G | — | uncertain significance |
| rs1974221746 | 19:4,433,237 | A/G | — | likely benign |
| rs2512310296 | 19:4,433,288 | G/A | — | uncertain significance |
| rs139033845 | 19:4,433,394 | C/T | — | uncertain significance |
| rs146377841 | 19:4,433,439 | C/T | — | uncertain significance |
| rs1460349295 | 19:4,433,487 | G/T | — | uncertain significance |
| rs2512310950 | 19:4,433,514 | A/C | — | uncertain significance |
| rs1158862966 | 19:4,433,522 | A/T | — | uncertain significance |
| rs12459919 | 19:4,434,503 | C/G | — | — |
| rs11666856 | 19:4,437,450 | A/G | intron variant | — |
| rs369272426 | 19:4,442,279 | C/T | — | uncertain significance |
| rs201873003 | 19:4,442,327 | C/T | — | uncertain significance |
| rs201581960 | 19:4,442,913 | G/A | — | likely benign |
| rs758282754 | 19:4,442,942 | G/T | — | uncertain significance |
| rs1330779150 | 19:4,442,960 | G/C | — | uncertain significance |
| rs147615871 | 19:4,442,978 | A/G | — | likely benign |
| rs140478541 | 19:4,442,981 | G/A | — | likely benign |
| rs897730451 | 19:4,443,006 | C/T | — | uncertain significance |
| rs78869060 | 19:4,444,742 | A/G | downstream gene variant | — |
| rs34822893 | 19:4,445,775 | C/T | downstream gene variant | — |
| rs113231772 | 19:4,447,187 | C/T | downstream gene variant | — |
| rs969036491 | 19:4,450,000 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.