MUCL3
mucin like 3
Summary
Predicted to be located in cytoplasm and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants95 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs915940214 | 6:30,908,847 | C/G | — | uncertain significance |
| rs765315692 | 6:30,908,850 | G/C | — | uncertain significance |
| rs186409480 | 6:30,912,564 | G/A | downstream gene variant | — |
| rs9391637 | 6:30,912,907 | G/A | downstream gene variant | — |
| rs3132581 | 6:30,913,458 | G/A | downstream gene variant | — |
| rs543981699 | 6:30,916,333 | C/T | — | uncertain significance |
| rs559708429 | 6:30,916,494 | C/T | — | uncertain significance |
| rs778584802 | 6:30,916,512 | C/T | — | uncertain significance |
| rs1429732679 | 6:30,916,578 | G/A | — | uncertain significance |
| rs2538775238 | 6:30,916,621 | A/G | — | uncertain significance |
| rs564525731 | 6:30,916,627 | G/T | — | uncertain significance |
| rs371675645 | 6:30,916,644 | C/T | — | uncertain significance |
| rs138097862 | 6:30,916,645 | G/A | — | benign |
| rs746410138 | 6:30,916,672 | A/C | — | uncertain significance |
| rs775587986 | 6:30,916,698 | G/A | — | uncertain significance |
| rs1411098744 | 6:30,916,710 | C/A | — | uncertain significance |
| rs367634528 | 6:30,916,717 | C/T | — | uncertain significance |
| rs572897332 | 6:30,916,747 | G/A | — | likely benign |
| rs1428302600 | 6:30,916,846 | G/A | — | uncertain significance |
| rs1052020126 | 6:30,916,879 | C/T | — | uncertain significance |
| rs970231324 | 6:30,916,962 | G/A | — | uncertain significance |
| rs1562489579 | 6:30,916,991 | A/C | — | uncertain significance |
| rs369773600 | 6:30,917,001 | A/G | — | uncertain significance |
| rs1404961171 | 6:30,917,053 | A/G | — | uncertain significance |
| rs867938809 | 6:30,917,129 | C/A | — | uncertain significance |
| rs2538777475 | 6:30,917,140 | C/A | — | uncertain significance |
| rs747108138 | 6:30,917,181 | G/A | — | uncertain significance |
| rs113216594 | 6:30,917,247 | G/A | — | likely benign |
| rs765335568 | 6:30,917,409 | G/A | — | uncertain significance |
| rs1171008914 | 6:30,917,472 | G/A | — | uncertain significance |
| rs1356799594 | 6:30,917,485 | C/T | — | uncertain significance |
| rs1224686666 | 6:30,917,542 | C/G | — | uncertain significance |
| rs910810625 | 6:30,917,557 | C/T | — | uncertain significance |
| rs1369557920 | 6:30,917,607 | T/G | — | uncertain significance |
| rs1318672356 | 6:30,917,628 | A/G | — | uncertain significance |
| rs769728473 | 6:30,917,638 | C/T | — | uncertain significance |
| rs1480735305 | 6:30,917,671 | T/G | — | uncertain significance |
| rs529934347 | 6:30,917,755 | C/A | — | uncertain significance |
| rs771240132 | 6:30,917,808 | G/A | — | uncertain significance |
| rs2538782176 | 6:30,917,814 | A/G | — | uncertain significance |
| rs760348956 | 6:30,917,906 | C/T | — | likely benign |
| rs954458437 | 6:30,917,913 | G/A | — | uncertain significance |
| rs1222402061 | 6:30,917,950 | A/T | — | uncertain significance |
| rs376915569 | 6:30,917,962 | C/T | — | uncertain significance |
| rs747055496 | 6:30,918,003 | C/T | — | uncertain significance |
| rs749173886 | 6:30,918,042 | C/T | — | likely benign |
| rs1272440115 | 6:30,918,054 | G/A | — | uncertain significance |
| rs1181530169 | 6:30,918,076 | A/G | — | uncertain significance |
| rs1053706397 | 6:30,918,151 | C/A | — | uncertain significance |
| rs1201526684 | 6:30,918,160 | G/A | — | likely benign |
| rs983020909 | 6:30,918,192 | G/A | — | uncertain significance |
| rs763841205 | 6:30,918,237 | A/T | — | uncertain significance |
| rs1479188345 | 6:30,918,271 | C/A | — | uncertain significance |
| rs746584550 | 6:30,918,317 | A/G | — | likely benign |
| rs945338871 | 6:30,918,494 | C/G | — | uncertain significance |
| rs780298487 | 6:30,918,517 | C/T | — | uncertain significance |
| rs900232221 | 6:30,918,562 | C/T | — | uncertain significance |
| rs752489229 | 6:30,918,576 | G/A | — | uncertain significance |
| rs1270958478 | 6:30,918,585 | G/C | — | uncertain significance |
| rs546853626 | 6:30,918,651 | C/T | — | uncertain significance |
| rs775203959 | 6:30,918,665 | T/C | — | likely benign |
| rs1760638707 | 6:30,918,685 | C/T | — | uncertain significance |
| rs367845682 | 6:30,918,980 | G/T | — | uncertain significance |
| rs745439005 | 6:30,918,987 | C/T | — | uncertain significance |
| rs140827661 | 6:30,919,057 | G/A | — | benign |
| rs921801105 | 6:30,919,105 | C/T | — | uncertain significance |
| rs1011726989 | 6:30,919,266 | G/A | — | uncertain significance |
| rs879095920 | 6:30,919,323 | C/G | — | uncertain significance |
| rs1020377932 | 6:30,919,336 | A/C | — | uncertain significance |
| rs1353682758 | 6:30,919,347 | C/G | — | uncertain significance |
| rs986884813 | 6:30,919,366 | C/T | — | uncertain significance |
| rs2538791627 | 6:30,919,401 | A/G | — | uncertain significance |
| rs188928476 | 6:30,919,453 | T/C | — | likely benign |
| rs868580749 | 6:30,919,474 | T/C | — | likely benign |
| rs767368704 | 6:30,919,516 | C/T | — | likely benign |
| rs754526901 | 6:30,919,551 | C/A | — | uncertain significance |
| rs561799201 | 6:30,919,554 | A/G | — | uncertain significance |
| rs1760723827 | 6:30,919,644 | G/C | — | uncertain significance |
| rs2538793489 | 6:30,919,758 | A/G | — | uncertain significance |
| rs73430198 | 6:30,919,846 | C/A | — | benign |
| rs749451042 | 6:30,919,848 | C/G | — | uncertain significance |
| rs139901951 | 6:30,919,911 | G/A | — | uncertain significance |
| rs141271962 | 6:30,919,954 | T/C | — | likely benign |
| rs778816176 | 6:30,920,136 | T/C | — | uncertain significance |
| rs570008856 | 6:30,920,146 | A/C | — | uncertain significance |
| rs140721086 | 6:30,920,172 | G/A | — | uncertain significance |
| rs1254694726 | 6:30,920,187 | G/C | — | uncertain significance |
| rs921505615 | 6:30,920,189 | G/T | — | uncertain significance |
| rs1393110748 | 6:30,920,237 | T/C | — | likely benign |
| rs899900064 | 6:30,920,266 | T/C | — | uncertain significance |
| rs754506455 | 6:30,920,769 | C/T | — | uncertain significance |
| rs373014829 | 6:30,920,770 | G/A | — | uncertain significance |
| rs769541066 | 6:30,920,773 | G/A | — | uncertain significance |
| rs2538797812 | 6:30,920,810 | G/C | — | uncertain significance |
| rs2538797999 | 6:30,920,848 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.