SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8145037 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | Nop2, Chd4 | Rn_Celera | 4:157645569 | ctttttttttttttt[C/T]CAACTTTATTTTAGC | 117535 |
rs8147390 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | Nop2, Chd4 | Rn_Celera | 4:157645219 | CCTCCCTCCCTGCCC[C/T]CAGTGCGCGCGCAGG | 117535 |
rs8149523 | snp | A/C | | | upstream-variant-2KB, utr-variant-3-prime | Nop2, Chd4 | Rn_Celera | 4:157645153 | AAGGAAGGCAAGGGT[A/C]TCTCTGGCCCACAGG | 117535 |
rs105026145 | snp | G/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157614185 | TTGAAGCTCGCTCTT[G/T]ATCGGATCTATAGAA | 117535 |
rs105203005 | snp | C/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157635295 | GGCATGGAAGCCGCA[C/T]GGCGGCTTTTCATTC | 117535 |
rs105340328 | snp | C/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157629525 | CTGCTGATTATTGGT[C/T]ACTTGGTCCTAGGCA | 117535 |
rs105650560 | snp | G/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157613853 | GGTGCTGGGGGGTGC[G/T]GGGGGAGGTGGAAGC | 117535 |
rs105816208 | snp | C/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157621147 | CTGGAGCTTAGCTGG[C/T]TGGCAGCCAGCAGCA | 117535 |
rs105924642 | snp | A/G | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157623083 | TCTTATATACAAGGG[A/G]CTTGTGTATGTGTGC | 117535 |
rs105996752 | snp | C/G | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157644216 | TGGGATGTAAAAAGG[C/G]AGAGAGGAGATTGTA | 117535 |
rs106806310 | snp | C/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157634098 | CTTTTGTGTTTACAG[C/T]GGGGTGAAGGGTGAG | 117535 |
rs106905003 | snp | A/C | 0 | 0 | missense | Chd4 | Rn_Celera | 4:157636899 | CTGAAGTGGAGGAAA[A/C]CAAAAAAATGTCTCA | 117535 |
rs107026914 | snp | C/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157620744 | GTTTATTGTATAGCT[C/T]GCTTCTTGACTCTTT | 117535 |
rs107027691 | snp | A/G | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157613725 | CCAGGGCAGGAAGGA[A/G]GTGTTTGATCTTTCC | 117535 |
rs107240215 | snp | A/C | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157635239 | TGCTTGCTTAAGGCG[A/C]TAACCTTCTTTTCAG | 117535 |
rs107327797 | snp | C/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157638495 | TATAGGTGCACCTTT[C/T]CCCCCCTTTTTGGTC | 117535 |
rs107332687 | snp | G/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157630918 | TCTCCCAGAGTCTTG[G/T]TTTTTTTTTCTTTTT | 117535 |
rs107341538 | snp | C/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157644340 | GCCACTTGCTGTGAT[C/T]CCAGCGCTTGGGAGG | 117535 |
rs197155222 | snp | A/G | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157619725 | TGCCGCGTAAATGCG[A/G]TTAACTGAAGAGAAG | 117535 |
rs197358533 | snp | A/G | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157631950 | TTGAGATGGTCCTAT[A/G]TATCCCAGGCTGGTC | 117535 |
rs197685805 | snp | G/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157618901 | CCTGTGCTGGGACTC[G/T]CGAATGGCCGGGGAG | 117535 |
rs198156334 | snp | A/G | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157628949 | CTCTCACGTACTGAC[A/G]CATGAATCAGGGAGC | 117535 |
rs198594540 | snp | C/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157620179 | CTTTTTTTTTTTTTT[C/T]TTTCCTTTTTCTTTT | 117535 |
rs198927287 | snp | A/C | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157615507 | AACCTTGGGATCTGA[A/C]TGGCTTCAGACTCAT | 117535 |
rs199158302 | snp | C/T | 0 | 0 | intron-variant | Chd4 | Rn_Celera | 4:157634651 | GTTTTCTTTGAGACA[C/T]GTATGGTCTCGTGTA | 117535 |