CCDC38
coiled-coil domain containing 38
Summary
Predicted to enable ubiquitin-modified histone reader activity. Predicted to be involved in acrosome assembly and sperm flagellum assembly. Located in centrosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1192340742 | 12:96,260,900 | T/C | — | uncertain significance |
| rs376174026 | 12:96,260,967 | A/G | — | likely benign |
| rs6538678 | 12:96,261,568 | A/G | downstream gene variant | — |
| rs374605974 | 12:96,263,263 | T/C | — | uncertain significance |
| rs767841799 | 12:96,263,278 | C/T | — | uncertain significance |
| rs142050445 | 12:96,266,040 | G/A | — | uncertain significance |
| rs144352390 | 12:96,266,057 | A/T | — | uncertain significance |
| rs375981671 | 12:96,266,090 | A/G | — | uncertain significance |
| rs777275253 | 12:96,266,123 | C/T | — | uncertain significance |
| rs200076553 | 12:96,266,163 | C/T | — | likely benign |
| rs147823377 | 12:96,266,164 | G/T | — | uncertain significance |
| rs1036429 | 12:96,271,428 | T/C | intron variant | — |
| rs772170372 | 12:96,272,014 | A/G | — | uncertain significance |
| rs1443850977 | 12:96,272,024 | G/T | — | uncertain significance |
| rs750316596 | 12:96,272,026 | T/C | — | likely benign |
| rs150365821 | 12:96,272,047 | G/A | — | uncertain significance |
| rs779209048 | 12:96,272,063 | C/T | — | uncertain significance |
| rs199784559 | 12:96,272,087 | T/C | — | uncertain significance |
| rs762948398 | 12:96,272,104 | A/G | — | uncertain significance |
| rs149118920 | 12:96,272,113 | A/G | — | uncertain significance |
| rs759270278 | 12:96,272,115 | G/C | — | uncertain significance |
| rs770198207 | 12:96,273,431 | T/C | — | uncertain significance |
| rs781624197 | 12:96,275,268 | C/G | — | uncertain significance |
| rs118134418 | 12:96,275,271 | C/T | — | uncertain significance |
| rs2499517225 | 12:96,275,291 | A/G | — | uncertain significance |
| rs752095676 | 12:96,275,325 | C/T | — | uncertain significance |
| rs138378399 | 12:96,282,261 | G/T | — | uncertain significance |
| rs747486733 | 12:96,284,648 | A/G | — | uncertain significance |
| rs147138435 | 12:96,284,703 | A/G | — | uncertain significance |
| rs10859974 | 12:96,288,860 | T/C | missense variant | — |
| rs200003296 | 12:96,292,356 | C/T | — | uncertain significance |
| rs1481321217 | 12:96,292,394 | T/A | — | uncertain significance |
| rs1435335025 | 12:96,292,428 | C/T | — | uncertain significance |
| rs775160721 | 12:96,292,445 | C/T | — | uncertain significance |
| rs763269020 | 12:96,292,464 | C/A | — | uncertain significance |
| rs933308342 | 12:96,292,496 | G/A | — | uncertain significance |
| rs2499548293 | 12:96,292,508 | T/C | — | uncertain significance |
| rs370665950 | 12:96,300,211 | G/C | — | uncertain significance |
| rs368457474 | 12:96,300,224 | C/T | — | uncertain significance |
| rs187475866 | 12:96,306,513 | G/A | intron variant | — |
| rs542768194 | 12:96,310,927 | G/A | — | likely benign |
| rs2136718160 | 12:96,310,931 | C/T | — | likely benign |
| rs934044022 | 12:96,310,985 | C/G | — | uncertain significance |
| rs769873402 | 12:96,310,999 | T/G | — | uncertain significance |
| rs141575774 | 12:96,311,005 | T/C | — | likely benign |
| rs780650229 | 12:96,311,051 | T/C | — | uncertain significance |
| rs764916100 | 12:96,311,065 | A/C | — | uncertain significance |
| rs371858893 | 12:96,312,679 | T/C | — | uncertain significance |
| rs746972610 | 12:96,312,709 | A/T | — | uncertain significance |
| rs7954638 | 12:96,314,795 | C/G | — | — |
| rs4762641 | 12:96,321,276 | C/G | — | — |
| rs10859988 | 12:96,326,220 | C/G | — | — |
| rs7955759 | 12:96,337,164 | G/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.