ANKRD30A
ankyrin repeat domain 30A
Summary
This gene encodes a DNA-binding transcription factor that is uniquely expressed in mammary epithelium and the testis. Altered expression levels have been associated with breast cancer progression. [provided by RefSeq, Nov 2016]
Known Variants75 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs376849793 | 10:37,414,920 | C/A | — | uncertain significance |
| rs1041973101 | 10:37,418,836 | G/T | — | uncertain significance |
| rs534812137 | 10:37,418,864 | G/A | — | uncertain significance |
| rs763100757 | 10:37,418,880 | A/G | — | uncertain significance |
| rs750282260 | 10:37,418,895 | T/A | — | uncertain significance |
| rs2538533815 | 10:37,418,898 | A/G | — | uncertain significance |
| rs1211251186 | 10:37,419,253 | T/C | — | uncertain significance |
| rs751991070 | 10:37,421,183 | C/G | — | uncertain significance |
| rs770071345 | 10:37,422,860 | G/T | — | uncertain significance |
| rs753172655 | 10:37,422,915 | A/G | — | uncertain significance |
| rs759133867 | 10:37,430,654 | T/G | — | uncertain significance |
| rs1837144594 | 10:37,430,730 | C/T | — | uncertain significance |
| rs547420743 | 10:37,430,745 | C/A | — | uncertain significance |
| rs761664646 | 10:37,430,753 | G/A | — | uncertain significance |
| rs200193852 | 10:37,430,910 | C/T | — | uncertain significance |
| rs373496322 | 10:37,431,116 | G/T | — | uncertain significance |
| rs372823949 | 10:37,431,226 | G/A | — | likely benign |
| rs759312955 | 10:37,433,950 | A/G | — | uncertain significance |
| rs200164455 | 10:37,433,983 | G/T | — | uncertain significance |
| rs1384271225 | 10:37,436,336 | A/G | — | uncertain significance |
| rs368742296 | 10:37,436,367 | A/G | — | uncertain significance |
| rs1837589389 | 10:37,436,372 | T/G | — | uncertain significance |
| rs201538199 | 10:37,438,587 | A/G | — | likely benign |
| rs1455136326 | 10:37,438,594 | C/T | — | uncertain significance |
| rs750613941 | 10:37,438,597 | C/G | — | uncertain significance |
| rs763274185 | 10:37,438,605 | A/G | — | uncertain significance |
| rs1837981844 | 10:37,440,993 | A/G | — | uncertain significance |
| rs767239968 | 10:37,441,002 | C/G | — | uncertain significance |
| rs765595711 | 10:37,447,328 | A/G | — | uncertain significance |
| rs773598373 | 10:37,447,329 | A/T | — | uncertain significance |
| rs764425571 | 10:37,447,503 | C/A | — | uncertain significance |
| rs1250795090 | 10:37,451,579 | C/A | — | uncertain significance |
| rs376283553 | 10:37,451,603 | G/A | — | uncertain significance |
| rs41276124 | 10:37,451,711 | C/T | — | uncertain significance |
| rs776996853 | 10:37,451,756 | A/C | — | uncertain significance |
| rs200440492 | 10:37,454,022 | A/T | — | likely benign |
| rs762581572 | 10:37,455,558 | A/G | — | uncertain significance |
| rs41276132 | 10:37,455,583 | G/A | — | likely benign |
| rs1343147461 | 10:37,478,410 | G/C | — | uncertain significance |
| rs1299131572 | 10:37,478,434 | C/T | — | uncertain significance |
| rs534800472 | 10:37,478,447 | A/G | — | uncertain significance |
| rs200493214 | 10:37,478,459 | T/C | — | likely benign |
| rs757725579 | 10:37,482,015 | C/A | — | uncertain significance |
| rs746737012 | 10:37,482,019 | A/T | — | uncertain significance |
| rs542212891 | 10:37,486,218 | A/G | — | uncertain significance |
| rs372000133 | 10:37,486,372 | G/A | — | uncertain significance |
| rs376651697 | 10:37,486,387 | A/G | — | uncertain significance |
| rs775101938 | 10:37,488,707 | G/C | — | uncertain significance |
| rs754180463 | 10:37,490,169 | C/T | — | uncertain significance |
| rs751229320 | 10:37,490,174 | G/T | — | uncertain significance |
| rs770642248 | 10:37,490,191 | A/T | — | likely benign |
| rs775115762 | 10:37,505,182 | C/G | — | uncertain significance |
| rs755110014 | 10:37,505,215 | G/A | — | uncertain significance |
| rs2538792715 | 10:37,505,241 | A/C | — | uncertain significance |
| rs757759980 | 10:37,506,683 | T/G | — | uncertain significance |
| rs765402044 | 10:37,507,912 | C/T | — | uncertain significance |
| rs781720953 | 10:37,507,945 | A/T | — | uncertain significance |
| rs995089428 | 10:37,508,154 | A/T | — | uncertain significance |
| rs1842758543 | 10:37,508,199 | G/A | — | likely benign |
| rs754498870 | 10:37,508,200 | A/G | — | uncertain significance |
| rs561896727 | 10:37,508,244 | C/A | — | uncertain significance |
| rs141194244 | 10:37,508,256 | G/C | — | likely benign |
| rs368830038 | 10:37,508,259 | C/A | — | uncertain significance |
| rs779261333 | 10:37,508,317 | C/A | — | uncertain significance |
| rs759239042 | 10:37,508,362 | G/A | — | likely benign |
| rs934222383 | 10:37,508,389 | A/G | — | uncertain significance |
| rs2538801381 | 10:37,508,431 | A/C | — | uncertain significance |
| rs1148259 | 10:37,508,450 | A/C | synonymous variant | — |
| rs367660842 | 10:37,508,501 | C/G | — | uncertain significance |
| rs201865282 | 10:37,508,503 | A/G | — | uncertain significance |
| rs762653177 | 10:37,508,541 | A/G | — | uncertain significance |
| rs746239418 | 10:37,508,620 | A/G | — | uncertain significance |
| rs758109745 | 10:37,508,662 | A/G | — | uncertain significance |
| rs533501860 | 10:37,508,775 | C/T | — | uncertain significance |
| rs764321100 | 10:37,508,799 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.