CCDC146
coiled-coil domain containing 146
Summary
Involved in spermatid development. Located in several cellular components, including microtubule organizing center; midbody; and sperm flagellum. Implicated in spermatogenic failure 94. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12540771 | 7:76,762,951 | A/G | intron variant | — |
| rs753129034 | 7:76,763,086 | A/G | — | — |
| rs12667702 | 7:76,772,116 | C/T | intron variant | — |
| rs200517168 | 7:76,797,082 | A/G | — | uncertain significance |
| rs1791360073 | 7:76,797,140 | A/T | — | uncertain significance |
| rs3095473 | 7:76,844,269 | A/G | — | — |
| rs142441315 | 7:76,871,126 | G/A | — | uncertain significance |
| rs758717646 | 7:76,883,845 | A/G | — | uncertain significance |
| rs2484514979 | 7:76,885,653 | A/T | — | uncertain significance |
| rs748802973 | 7:76,885,699 | G/A | — | uncertain significance |
| rs764584639 | 7:76,885,741 | G/A | — | uncertain significance |
| rs767393095 | 7:76,885,780 | A/G | — | uncertain significance |
| rs368986405 | 7:76,885,818 | G/A | — | uncertain significance |
| rs754605585 | 7:76,888,324 | C/A | — | uncertain significance |
| rs946974575 | 7:76,888,361 | T/C | — | uncertain significance |
| rs902726368 | 7:76,888,376 | G/T | — | uncertain significance |
| rs138738765 | 7:76,889,366 | A/G | — | uncertain significance |
| rs775855459 | 7:76,889,414 | A/G | — | likely benign |
| rs766948572 | 7:76,889,453 | G/A | — | uncertain significance |
| rs138325273 | 7:76,889,501 | G/C | — | uncertain significance |
| rs374348160 | 7:76,889,503 | C/T | — | likely benign |
| rs1027523120 | 7:76,891,527 | G/A | — | uncertain significance |
| rs371350411 | 7:76,891,535 | C/G | — | pathogenic |
| rs369894709 | 7:76,903,018 | C/A | — | uncertain significance |
| rs1264059275 | 7:76,903,808 | T/C | — | uncertain significance |
| rs1168304964 | 7:76,903,899 | A/C | — | uncertain significance |
| rs201190001 | 7:76,903,959 | T/C | — | uncertain significance |
| rs73375428 | 7:76,907,550 | C/G | intron variant | — |
| rs753740121 | 7:76,908,070 | A/C | — | uncertain significance |
| rs2484646591 | 7:76,908,085 | T/G | — | uncertain significance |
| rs1793710902 | 7:76,908,303 | A/G | — | uncertain significance |
| rs771660449 | 7:76,909,764 | G/A | — | uncertain significance |
| rs751587535 | 7:76,909,816 | C/T | — | likely benign |
| rs202079778 | 7:76,909,817 | G/C | — | uncertain significance |
| rs778548993 | 7:76,909,840 | G/A | — | uncertain significance |
| rs199901563 | 7:76,909,895 | C/G | — | uncertain significance |
| rs376608993 | 7:76,909,903 | A/G | — | uncertain significance |
| rs140693664 | 7:76,909,915 | G/A | — | uncertain significance |
| rs754555358 | 7:76,909,939 | T/A | — | uncertain significance |
| rs1562861707 | 7:76,911,936 | A/G | — | uncertain significance |
| rs1793784715 | 7:76,911,960 | A/G | — | uncertain significance |
| rs776743914 | 7:76,912,016 | G/A | — | uncertain significance |
| rs370638811 | 7:76,916,170 | A/G | — | uncertain significance |
| rs267601574 | 7:76,916,214 | G/A | — | uncertain significance |
| rs1793868903 | 7:76,916,778 | A/G | — | uncertain significance |
| rs747951990 | 7:76,916,841 | C/T | — | uncertain significance |
| rs1203944582 | 7:76,922,311 | A/C | — | uncertain significance |
| rs1292309704 | 7:76,922,357 | T/C | — | uncertain significance |
| rs1214247942 | 7:76,922,405 | G/C | — | uncertain significance |
| rs1219389100 | 7:76,922,422 | A/G | — | uncertain significance |
| rs143220108 | 7:76,922,426 | G/A | — | uncertain significance |
| rs780741373 | 7:76,922,486 | T/G | — | uncertain significance |
| rs201786512 | 7:76,924,016 | G/A | — | uncertain significance |
| rs746349411 | 7:76,924,041 | G/A | — | uncertain significance |
| rs376647143 | 7:76,924,065 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.