CCDC148
coiled-coil domain containing 148
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs143247186 | 2:159,028,710 | G/T | — | uncertain significance |
| rs140240262 | 2:159,028,721 | T/C | — | likely benign |
| rs760832124 | 2:159,033,040 | T/C | — | uncertain significance |
| rs896283916 | 2:159,033,048 | T/C | — | likely benign |
| rs113178783 | 2:159,033,098 | C/T | — | benign |
| rs1684600933 | 2:159,033,122 | C/T | — | uncertain significance |
| rs764349131 | 2:159,033,182 | G/A | — | likely benign |
| rs1996787 | 2:159,058,096 | C/T | — | — |
| rs1687124052 | 2:159,077,113 | C/G | — | uncertain significance |
| rs35617573 | 2:159,107,374 | T/C | — | benign |
| rs561422515 | 2:159,107,385 | G/A | — | benign |
| rs78384759 | 2:159,113,653 | C/T | intron variant | — |
| rs116466468 | 2:159,137,557 | T/C | intron variant | — |
| rs113692953 | 2:159,145,379 | A/C | intron variant | — |
| rs199997012 | 2:159,151,822 | A/T | — | — |
| rs775799208 | 2:159,166,024 | C/G | — | uncertain significance |
| rs533489653 | 2:159,166,097 | T/C | — | likely benign |
| rs145531516 | 2:159,166,135 | T/A | — | benign |
| rs2467977467 | 2:159,170,277 | C/A | — | uncertain significance |
| rs753549086 | 2:159,170,285 | T/C | — | uncertain significance |
| rs34363253 | 2:159,170,302 | T/C | — | uncertain significance |
| rs368173329 | 2:159,170,307 | C/T | — | uncertain significance |
| rs13411714 | 2:159,176,930 | G/A | intron variant | — |
| rs145834406 | 2:159,187,366 | T/G | intron variant | — |
| rs773020595 | 2:159,195,268 | T/A | — | uncertain significance |
| rs141574148 | 2:159,195,385 | G/A | — | likely benign |
| rs758655252 | 2:159,195,393 | C/G | — | uncertain significance |
| rs1682528441 | 2:159,195,418 | A/T | — | uncertain significance |
| rs185438286 | 2:159,196,789 | G/T | — | likely benign |
| rs148058893 | 2:159,196,848 | T/C | — | conflicting classifications of pathogenicity |
| rs777369798 | 2:159,196,873 | G/C | — | uncertain significance |
| rs80319144 | 2:159,199,835 | C/A | — | — |
| rs4664950 | 2:159,201,754 | C/T | — | benign |
| rs1399061683 | 2:159,201,787 | G/A | — | uncertain significance |
| rs1162626671 | 2:159,201,817 | A/T | — | uncertain significance |
| rs9677434 | 2:159,208,979 | A/G | — | — |
| rs140798767 | 2:159,215,010 | C/T | — | likely benign |
| rs377450369 | 2:159,215,011 | G/A | — | uncertain significance |
| rs150764340 | 2:159,215,032 | G/A | — | uncertain significance |
| rs77276698 | 2:159,250,229 | G/A | intron variant | — |
| rs113330028 | 2:159,273,472 | A/G | upstream gene variant | — |
| rs1408587825 | 2:159,312,942 | C/T | — | uncertain significance |
| rs561533043 | 2:159,312,950 | A/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.