| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs222975393 | in-del | -/CTCC | | | intron-variant | Trim37 | GRCm38.p3 | 11:87184414 | TCTCTCTCTCTCTCT[-/CTCC]CTCTCCCTCTCCCTC | 68729 |
| rs386922815 | in-del | -/GAGAAGGAAACATTTTTTTTTTTTTTTTTTTTTAAGATTTTGTTTATTTATTATATATAGGTACACTGTCGCTGTCTTCAGACACTCCAGAAGAGGGAGTCAGATTTTGTTACGGATGGTTGTGAGCCACCATGTGGTTGCTGGGATTTGAACTCCGGACCTTCGGAAGAGCAATCGGGTGCTCTAACCCACTGAGCCATCTCACCAGCCCC | | | intron-variant | Trim37 | GRCm38.p3 | 11:87136041 | TAAATATGGTGTATA[lengthTooLong]GAGAAGGAAACATTT | 68729 |
| rs386975103 | in-del | -/TCTTTCTT | | | intron-variant | Trim37 | Mm_Celera | 11:87186972 | CTTTCTTTCTTTCTT[-/TCTTTCTT]CCTTCCTTTCTTTCT | 68729 |
| rs387334222 | in-del | -/T | | | intron-variant | Trim37 | Mm_Celera | 11:87142303 | AAGTTTTTTTTTTTT[-/T]CTTTAGTTTTAGAGG | 68729 |
| rs578411984 | snp | C/T | | | intron-variant | Trim37 | GRCm38.p3 | 11:87186976 | CTTTCTTTCTTTCTT[C/T]CTTCCTTCCTTTCTT | 68729 |