| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs781447072 | snp | A/T | 1.85675e-05 | 0.00304687 | missense, intron-variant | USP17L7, FAM66D | GRCh38.p7 | 8:12133951 | AGCCGAGAAGATGTG[A/T]GTTTTGAAAAGTGAT | 392197 |
| rs781537048 | snp | A/G | 3.71747e-05 | 0.00431115 | synonymous-codon, intron-variant | USP17L7, FAM66D | GRCh38.p7 | 8:12133988 | GCCAGTCACCTCCCA[A/G]ATAGAGTGAGTCGTC | 392197 |
| rs781576213 | snp | C/G | 0.00020447 | 0.0101091 | synonymous-codon, intron-variant | USP17L7, FAM66D | GRCh38.p7 | 8:12133992 | GTCACCTCCCAAATA[C/G]AGTGAGTCGTCTTCC | 392197 |
| rs781684274 | snp | C/G | 1.85882e-05 | 0.00304857 | missense, intron-variant | USP17L7, FAM66D | GRCh38.p7 | 8:12133647 | ACAGAACATGCAGCA[C/G]TTGTGAAGATGACAC | 392197 |
| rs781732977 | snp | C/T | 5.61109e-05 | 0.00529644 | missense, intron-variant | USP17L7, FAM66D | GRCh38.p7 | 8:12133268 | GATAGGCATTCTCTC[C/T]ATTGAGTTCTTTGGG | 392197 |
| rs796561879 | in-del | -/GC | | | downstream-variant-500B, intron-variant | USP17L7, FAM66D | GRCh38.p7 | 8:12132382 | TGTGTGTGTGTGTGT[-/GC]ACCCATCAGTGTGGG | 392197 |
| rs796910244 | in-del | -/GTGTGTGTGTTTG | | | upstream-variant-2KB, intron-variant | USP17L7, FAM66D | GRCh38.p7 | 8:12134461 | TGTGTGTGTGTGTGT[-/GTGTGTGTGTTTG]TGTGTGTGTGTGTGT | 392197 |