LIN54
lin-54 DREAM MuvB core complex component
Summary
LIN54 is a component of the LIN, or DREAM, complex, an essential regulator of cell cycle genes (Schmit et al., 2009 [PubMed 19725879]).[supplied by OMIM, Dec 2010]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1482275802 | 4:83,849,322 | C/T | — | uncertain significance |
| rs1415377276 | 4:83,849,353 | C/A | — | uncertain significance |
| rs2547254927 | 4:83,849,386 | G/T | — | uncertain significance |
| rs1483765738 | 4:83,849,440 | C/A | — | uncertain significance |
| rs373076659 | 4:83,852,236 | C/T | — | likely benign |
| rs375103636 | 4:83,852,287 | C/T | — | uncertain significance |
| rs28539166 | 4:83,853,986 | T/C | — | — |
| rs6848366 | 4:83,856,661 | G/A | intron variant | — |
| rs1232902027 | 4:83,858,426 | G/A | — | uncertain significance |
| rs1305496598 | 4:83,859,639 | C/T | — | uncertain significance |
| rs2547268658 | 4:83,859,641 | T/A | — | uncertain significance |
| rs2547270043 | 4:83,860,736 | C/G | — | uncertain significance |
| rs1334637543 | 4:83,860,786 | T/C | — | uncertain significance |
| rs2547270849 | 4:83,861,112 | T/C | — | uncertain significance |
| rs13119433 | 4:83,863,303 | C/G | — | — |
| rs55957664 | 4:83,864,043 | A/C | downstream gene variant | — |
| rs13147892 | 4:83,864,227 | A/T | — | — |
| rs11934234 | 4:83,864,917 | G/A | downstream gene variant | — |
| rs12499234 | 4:83,865,038 | T/A | — | — |
| rs16999103 | 4:83,886,422 | G/T | — | — |
| rs2547314636 | 4:83,891,523 | G/C | — | uncertain significance |
| rs752980606 | 4:83,891,545 | T/C | — | uncertain significance |
| rs13127052 | 4:83,895,226 | G/A | intron variant | — |
| rs13103322 | 4:83,895,232 | A/G | intron variant | — |
| rs12649662 | 4:83,896,818 | T/A | intron variant | — |
| rs4693066 | 4:83,901,562 | G/A | regulatory region variant | — |
| rs116142917 | 4:83,901,724 | A/G | — | — |
| rs2547334896 | 4:83,905,351 | G/A | — | uncertain significance |
| rs140057831 | 4:83,905,412 | G/T | — | uncertain significance |
| rs2547335808 | 4:83,905,712 | G/A | — | uncertain significance |
| rs1251798169 | 4:83,905,721 | G/T | — | uncertain significance |
| rs769590982 | 4:83,905,886 | T/C | — | uncertain significance |
| rs771716531 | 4:83,905,916 | T/G | — | uncertain significance |
| rs778661311 | 4:83,905,955 | C/T | — | uncertain significance |
| rs2547336845 | 4:83,905,958 | C/G | — | uncertain significance |
| rs781282651 | 4:83,905,969 | C/T | — | uncertain significance |
| rs13111599 | 4:83,917,037 | A/G | intron variant | — |
| rs6535425 | 4:83,923,503 | T/G | — | — |
| rs13111200 | 4:83,925,604 | C/T | downstream gene variant | — |
| rs6823199 | 4:83,925,895 | T/C | downstream gene variant | — |
| rs10009824 | 4:83,926,921 | A/C | downstream gene variant | — |
| rs11099565 | 4:83,935,760 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.