SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs781511217 | snp | C/T | | | utr-variant-3-prime | HIC2 | GRCh38.p7 | 22:21448931 | GACACAAAGTCTGTA[C/T]CGCACGGGAAATGTT | 23119 |
rs781520412 | in-del | -/C | 0.000182787 | 0.00955824 | frameshift-variant | HIC2 | GRCh38.p7 | 22:21445369 | ACTGGCATGGGGCGG[-/C]CCCCCCCGCAGCCAG | 23119 |
rs781566367 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon | HIC2 | GRCh38.p7 | 22:21445126 | GTCCCTGGTCCTGCA[C/T]GACAACCTCATCAAC | 23119 |
rs781728707 | snp | A/G | | | utr-variant-3-prime | HIC2 | GRCh38.p7 | 22:21449847 | TACGCGGGGATGGCC[A/G]TCAGTTCTGGCCACA | 23119 |
rs781765159 | snp | A/G | 2.97881e-05 | 0.00385916 | missense | HIC2 | GRCh38.p7 | 22:21446019 | GGGACAGGGTTCCCA[A/G]TGGCATCCTGGCTAG | 23119 |
rs796214396 | snp | A/G | | | intron-variant | HIC2 | GRCh38.p7 | 22:21426321 | GGACCACAGTCATGC[A/G]CCACCACAGCCAGCT | 23119 |
rs796312418 | in-del | AGGAAGA/G | | | utr-variant-3-prime | HIC2 | GRCh38.p7 | 22:21450238 | ATTGCAAAAAAAAAA[AGGAAGA/G]AAAAGATGAACCTTT | 23119 |
rs796354762 | snp | A/G | | | utr-variant-3-prime | HIC2 | GRCh38.p7 | 22:21447832 | TGTGTGGTGTGTGCC[A/G]TATGCATGGGCAGAT | 23119 |
rs796527253 | snp | A/G | | | utr-variant-3-prime | HIC2 | GRCh38.p7 | 22:21447098 | ACGCTGGCCACGGCC[A/G]GGGTGGTGTCGGGAG | 23119 |
rs796621755 | snp | A/G | | | utr-variant-3-prime | HIC2 | GRCh38.p7 | 22:21448021 | AGCAGGGCGCCAAGT[A/G]GCCCAGTGCCTGCAG | 23119 |
rs796951440 | snp | C/T | | | intron-variant, upstream-variant-2KB | HIC2, LOC105377191 | GRCh38.p7 | 22:21422646 | AGCCCATGTGCACTG[C/T]TGGCTTCTCCTGGGA | 23119 |