SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs213580606 | snp | A/C | | | downstream-variant-500B | Gemin5 | GRCm38.p3 | 11:58119828 | GAAAGGGATAATACC[A/C]CCCCTCCCCCCCCCC | 216766 |
rs214929410 | snp | A/C | | | intron-variant | Gemin5 | Mm_Celera | 11:58160225 | TAGCCAGTAACCACC[A/C]CCCCCCCCCCCGCCC | 216766 |
rs218387556 | in-del | -/GAGAGA | | | intron-variant | Gemin5 | GRCm38.p3 | 11:58143487 | CTGACAGAGAGGGGG[-/GAGAGA]GAGAGAGAGAGAGAG | 216766 |
rs218937552 | in-del | -/A | | | intron-variant | Gemin5 | Mm_Celera | 11:58137779 | TGCTAATTTAAAATG[-/A]AAAAAGTCAATGCAG | 216766 |
rs222279217 | in-del | -/ACCA | | | intron-variant | Gemin5 | Mm_Celera | 11:58160222 | AACTAGCCAGTAACC[-/ACCA]CCCCCCCCCCCGCCC | 216766 |
rs223257022 | snp | A/C | | | downstream-variant-500B | Gemin5 | GRCm38.p3 | 11:58119853 | CCCCCCCCCCCCCAC[A/C]CACACACACACACAA | 216766 |
rs249846016 | snp | A/C | | | downstream-variant-500B | Gemin5 | GRCm38.p3 | 11:58119852 | CCCCCCCCCCCCCCA[A/C]ACACACACACACACA | 216766 |
rs255426385 | snp | A/C | | | downstream-variant-500B | Gemin5 | GRCm38.p3 | 11:58119851 | CCCCCCCCCCCCCCC[A/C]CACACACACACACAC | 216766 |
rs260637713 | in-del | -/TTTTT | | | intron-variant | Gemin5 | GRCm38.p3 | 11:58125949 | CATATGCCAGCTCTG[-/TTTTT]TTTTTTTTTTTTTTT | 216766 |
rs387531769 | in-del | -/AAAAAAAAAA | | | intron-variant | Gemin5 | GRCm38.p3 | 11:58167188 | AAAAAAAAAAAAAAA[-/AAAAAAAAAA]GAGTTAGTGACTAGG | 216766 |
rs579897035 | snp | A/G | | | intron-variant | Gemin5 | GRCm38.p3 | 11:58159581 | AAGAAAGAAAGAAAG[A/G]AAGGAAGGAAGGAAG | 216766 |