SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs14469 | snp | G/T | 0 | 0 | utr-variant-3-prime | CNOT4 | GRCh38.p7 | 7:135362067 | GTCGGAATCTTTTTT[G/T]TTTTACCATAAATTC | 4850 |
rs918874 | snp | G/T | 0 | 0 | intron-variant | CNOT4 | GRCh38.p7 | 7:135406497 | atttttctttttttt[G/T]gtagagatggcgttt | 4850 |
rs918875 | snp | A/C | 0 | 0 | intron-variant | CNOT4 | GRCh38.p7 | 7:135471421 | ACTCATAATAATTGC[A/C]AAATATTCTACAGTT | 4850 |
rs918876 | snp | G/T | 0.433382 | 0.169915 | intron-variant | CNOT4 | GRCh38.p7 | 7:135471381 | TTTTGAGGACCCTCA[G/T]ATTTTATAAGTTTAT | 4850 |
rs918877 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CNOT4 | GRCh38.p7 | 7:135464552 | tcctctccctccttc[C/T]accctccccacttcc | 4850 |
rs997530 | snp | A/G | 0.196149 | 0.244131 | intron-variant | CNOT4 | GRCh38.p7 | 7:135369395 | GACTGCTTCCCGGTA[A/G]GGGTGTATTTATTAT | 4850 |
rs998130 | snp | A/G | 0.093417 | 0.194889 | intron-variant | CNOT4 | GRCh38.p7 | 7:135369406 | GGTCTCTCAGTGACT[A/G]CTTCCCGGTAAGGGT | 4850 |
rs1003226 | snp | C/T | 0.197393 | 0.244402 | utr-variant-3-prime | CNOT4 | GRCh38.p7 | 7:135361800 | ACAACCCAAGTGTCA[C/T]CATCAAGTTTTCTGT | 4850 |
rs1030292 | snp | G/T | 0 | 0 | intron-variant | CNOT4 | GRCh38.p7 | 7:135382550 | TAAATATTCCTAGTT[G/T]GGAAGCAACCTTAGT | 4850 |
rs1030293 | snp | A/T | 0.0391387 | 0.134304 | intron-variant | CNOT4 | GRCh38.p7 | 7:135382453 | AAAGGATAATGCTTC[A/T]AAGTACAAATCATTG | 4850 |
rs1045624 | snp | A/C/T | 1.67801e-05 | 0.00289651 | utr-variant-3-prime, intron-variant | CNOT4 | GRCh38.p7 | 7:135388766 | GAGGAGAGGATTAGA[A/C/T]TCTGGGGTGCTTGCA | 4850 |
rs1266433 | snp | A/C | | | intron-variant | CNOT4 | GRCh38.p7 | 7:135479227 | gcgagactccatctc[A/C]aaaaaaaaaaaaaaa | 4850 |
rs1424551 | snp | A/G | 0.197393 | 0.244402 | intron-variant | CNOT4 | GRCh38.p7 | 7:135368016 | TTGTTTAGAACTGAA[A/G]ATAGTGTTTTGTTGT | 4850 |
rs1424552 | snp | A/G | 0.383632 | 0.211288 | intron-variant | CNOT4 | GRCh38.p7 | 7:135418248 | GTTTAGGCAGAATCT[A/G]GAGTGTTCAAGTTAA | 4850 |
rs1544829 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CNOT4 | GRCh38.p7 | 7:135380211 | CTAAAGATGTGATCT[C/G]CGATTCATCTTTGAA | 4850 |
rs1544830 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | CNOT4 | GRCh38.p7 | 7:135379986 | TAGCCTAGCACTGTT[G/T]CTTAATATAGTGAGA | 4850 |
rs1559535 | snp | C/T | 0.467234 | 0.12373 | intron-variant | CNOT4 | GRCh38.p7 | 7:135459223 | gctgttgagacctac[C/T]gctcagaaaaaaaga | 4850 |
rs1559536 | snp | C/T | 0.44651 | 0.154543 | intron-variant | CNOT4 | GRCh38.p7 | 7:135487468 | aggatcacttgagcc[C/T]aggagttccagacaa | 4850 |
rs1582633 | snp | C/G | 0.170408 | 0.236992 | intron-variant | CNOT4 | GRCh38.p7 | 7:135481956 | CATTAACCAACTTCT[C/G]TTTATCCCCTCTCAC | 4850 |
rs1582634 | snp | A/G | 0.433236 | 0.170072 | intron-variant | CNOT4 | GRCh38.p7 | 7:135481773 | tatgttgctgcaaat[A/G]acatgatttcattct | 4850 |
rs1593209 | snp | A/T | 0.0444908 | 0.142359 | intron-variant | CNOT4 | GRCh38.p7 | 7:135432304 | GGGGTCATGATATAT[A/T]TTTTTTTCCTATGCT | 4850 |
rs1863004 | snp | A/G | 0.338296 | 0.233889 | intron-variant | CNOT4 | GRCh38.p7 | 7:135368886 | AAAGATACCCACTAG[A/G]TGCTATTAATGCTAA | 4850 |
rs1863005 | snp | C/T | 0.494692 | 0.0512434 | intron-variant | CNOT4 | GRCh38.p7 | 7:135368710 | ATACTAAAGATAGTT[C/T]CAACCTGTTGTGAGA | 4850 |
rs1971075 | snp | C/T | 0.24449 | 0.249939 | intron-variant | CNOT4 | GRCh38.p7 | 7:135440780 | AGGCATGTGCCACCA[C/T]GCCCAGCTAATTTTT | 4850 |
rs1997260 | snp | G/T | 0.117188 | 0.211804 | intron-variant | CNOT4 | GRCh38.p7 | 7:135397276 | caggataataaaaca[G/T]aattatgatcaaaac | 4850 |
rs2059366 | snp | A/T | 0.0898077 | 0.191933 | intron-variant | CNOT4 | GRCh38.p7 | 7:135389814 | TTTGTTTTAAAAAAA[A/T]ATTCTGCCAAGTTGT | 4850 |
rs2059367 | snp | C/G | 0.464629 | 0.128197 | intron-variant | CNOT4 | GRCh38.p7 | 7:135363281 | TGTAATCTCTTCTGT[C/G]TTTCCTTTTGGTTTT | 4850 |
rs2178149 | snp | C/T | 0 | 0 | intron-variant | CNOT4 | GRCh38.p7 | 7:135394792 | ATGTATTTATCAAAG[C/T]ACAAATAATTTTGAA | 4850 |
rs2303344 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CNOT4 | GRCh38.p7 | 7:135422473 | TAAGCAGTTAAAACA[C/T]TCTAATAAAGGGAGA | 4850 |
rs2551758 | snp | G/T | 0 | 0 | | | GRCh38.p7 | 7:135406216 | CAGAGAGTAAGCCTT[G/T]GGCTGACTGTCAGTC | 4850 |
rs2551759 | snp | A/G | 0.00914312 | 0.0669923 | | | GRCh38.p7 | 7:135488763 | AGGACTATTAATAAT[A/G]ATACATTCTATAATT | 4850 |
rs2551760 | snp | A/G | 0.434253 | 0.168969 | | | GRCh38.p7 | 7:135484666 | ctgggttcaagtgat[A/G]cttgtgtctcagcct | 4850 |
rs2551761 | snp | A/G | 0.464523 | 0.128375 | | | GRCh38.p7 | 7:135483199 | aggcatgtggcagct[A/G]atttttttttttttt | 4850 |
rs2551762 | snp | A/G | 0.433527 | 0.169758 | | | GRCh38.p7 | 7:135478179 | AATTACCTAACAACT[A/G]GAACAATAAAATATT | 4850 |
rs2551763 | snp | A/G | 0.466618 | 0.124806 | | | GRCh38.p7 | 7:135478149 | TTCATTCAAATAAGA[A/G]TGTGAAATATCATCA | 4850 |
rs2551764 | snp | C/T | 0.0379877 | 0.132479 | | | GRCh38.p7 | 7:135459766 | AAGGATAGGCTGACT[C/T]TTATTAGGGGTTAAT | 4850 |
rs2551765 | snp | A/G | 0.466721 | 0.124627 | | | GRCh38.p7 | 7:135457711 | TTACAATGAAGTTAA[A/G]TAATTTCCCTTTGGG | 4850 |
rs2551766 | snp | A/G | 0.497387 | 0.0360476 | | | GRCh38.p7 | 7:135457372 | TACAGATTTTGACTT[A/G]GCCAAATCATAAAAT | 4850 |
rs2551767 | snp | A/G | 0.487558 | 0.0778863 | | | GRCh38.p7 | 7:135454263 | GAATGAACTAGTTGT[A/G]TGTGGACCAGAGGAC | 4850 |
rs2551768 | snp | A/T | | | | | GRCh38.p7 | 7:135453848 | accAGCtatatatat[A/T]atatatatatatata | 4850 |
rs2551769 | snp | C/T | 0.438526 | 0.164189 | | | GRCh38.p7 | 7:135453583 | TTCTGTCTTACTGTA[C/T]GCTTCCTCCATGTCC | 4850 |
rs2551770 | snp | A/T | 0.0379877 | 0.132479 | | | GRCh38.p7 | 7:135447266 | TTTCACTTAGCACAC[A/T]GTTCATAGCTACTCT | 4850 |
rs2551771 | snp | A/G | 0.0111196 | 0.0737302 | | | GRCh38.p7 | 7:135442052 | TACTTTGTGAAAGAG[A/G]TGAGTCAGTCAACTC | 4850 |
rs2551772 | snp | A/C | 0.104859 | 0.203554 | | | GRCh38.p7 | 7:135436009 | AAAAAAAGGAATGGG[A/C]GTGCTTCAGGATCCT | 4850 |
rs2551773 | snp | C/T | 0.463559 | 0.129972 | | | GRCh38.p7 | 7:135435448 | AAAATGGACACATTA[C/T]AAGAGCAAATTGATA | 4850 |
rs2551774 | snp | C/T | 0.463989 | 0.129263 | | | GRCh38.p7 | 7:135434669 | TGGAGATACAGATTT[C/T]GGTGTCAGTTAGCAT | 4850 |
rs2551775 | snp | G/T | | | | | GRCh38.p7 | 7:135420578 | ttttttttttttttt[G/T]ggagacatggtctca | 4850 |
rs2551776 | snp | A/G | 0.457969 | 0.138741 | | | GRCh38.p7 | 7:135418700 | TAGCTTGTTTGATGA[A/G]CTATGACTTTAAAGA | 4850 |
rs2551777 | snp | A/G | 0.465052 | 0.127485 | | | GRCh38.p7 | 7:135415727 | TAAACAGTGTTATAT[A/G]CAATAGATTTATGAG | 4850 |
rs2551778 | snp | A/G | 0.465263 | 0.127129 | | | GRCh38.p7 | 7:135414900 | ATGTGATAAATAGAT[A/G]AGGATTCGATAGTGA | 4850 |
rs2696877 | snp | A/G | 0.000928336 | 0.0215245 | intron-variant, synonymous-codon | CNOT4 | GRCh38.p7 | 7:135410520 | CAATACTTACGTATC[A/G]TACCTCTGCAGTGGT | 4850 |
rs2696878 | snp | A/T | 0.100231 | 0.200173 | intron-variant | CNOT4 | GRCh38.p7 | 7:135411249 | ACTCTAGACCCAGGG[A/T]CAGCAATTTACAGCC | 4850 |
rs2696879 | snp | G/T | 0.440746 | 0.161604 | intron-variant | CNOT4 | GRCh38.p7 | 7:135418911 | ATACTCAGCACACAT[G/T]TAAGCACTTAAAATT | 4850 |
rs2696880 | snp | A/G | 0.464735 | 0.128019 | intron-variant | CNOT4 | GRCh38.p7 | 7:135430389 | gtgcctataatccca[A/G]cactttaggaggctg | 4850 |
rs2696881 | snp | C/T | 0.465996 | 0.12588 | intron-variant | CNOT4 | GRCh38.p7 | 7:135435083 | GTAAAATGAAAATAC[C/T]GGTATTAATTTTAGT | 4850 |
rs2696882 | snp | A/G/T | 0.0615772 | 0.166367 | intron-variant | CNOT4 | GRCh38.p7 | 7:135469882 | ATGGGCTGAGATTGC[A/G/T]CCACTGCACTCCAGC | 4850 |
rs2696883 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | CNOT4 | GRCh38.p7 | 7:135461555 | CGTGAGCCACTGCGC[C/G]CGGCCTCTGCTTGTT | 4850 |
rs2696884 | snp | A/G | 0.464629 | 0.128197 | intron-variant | CNOT4 | GRCh38.p7 | 7:135459914 | tgtagtcagttgtcc[A/G]gaagatctagctaag | 4850 |
rs2696887 | snp | C/T | 0.485933 | 0.0826777 | intron-variant | CNOT4 | GRCh38.p7 | 7:135482251 | ACTGAATTCATAGTT[C/T]AAAAGCTCCCAATAA | 4850 |
rs2696888 | snp | A/G | 0.464203 | 0.128908 | intron-variant | CNOT4 | GRCh38.p7 | 7:135485700 | gacttccatggatgg[A/G]gaagggaagggggaa | 4850 |
rs2696889 | snp | A/G | 0 | 0 | intron-variant | CNOT4 | GRCh38.p7 | 7:135495690 | aaaaaaaaaaaaaaa[A/G]aaagaaagaaagaaa | 4850 |
rs2718164 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | CNOT4 | GRCh38.p7 | 7:135419888 | TCTCCACTAAAAATC[A/C]AAAAAAAAAAAAAAA | 4850 |
rs2718165 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | CNOT4 | GRCh38.p7 | 7:135439333 | CATACAAGAATAAAT[G/T]CATGAGAATCATTTT | 4850 |
rs2718166 | snp | G/T | 0 | 0 | intron-variant | CNOT4 | GRCh38.p7 | 7:135440148 | AGTAAAAGATACATT[G/T]GCTACATATAATGAA | 4850 |
rs2718167 | snp | C/T | 0.465683 | 0.126415 | intron-variant | CNOT4 | GRCh38.p7 | 7:135408695 | TGTCAATTCACTTAA[C/T]GTGCACAGCTTTGGG | 4850 |
rs2718168 | snp | C/G | 0.464947 | 0.127663 | intron-variant | CNOT4 | GRCh38.p7 | 7:135446601 | ATGTAGCTAGTGCAA[C/G]TCCACTGAATACAGT | 4850 |
rs2718170 | snp | C/G | | | intron-variant | CNOT4 | GRCh38.p7 | 7:135479667 | ctttgggaggcggag[C/G]caggaggatggcttg | 4850 |
rs2840185 | snp | A/G | 0.197703 | 0.244469 | intron-variant | CNOT4 | GRCh38.p7 | 7:135363745 | GCTTTTCACAAAGCC[A/G]CAAGTGTGGAGTGGC | 4850 |
rs3045342 | in-del | -/TAAGAG | 0.0905309 | 0.192535 | intron-variant | CNOT4 | GRCh38.p7 | 7:135385573 | TAATTCCCAGGATGC[-/TAAGAG]TAAGAGACATGAGCT | 4850 |
rs3138785 | microsatellite | (TG)16/17/18/19/20/21/22/23/24/25/26/27 | 0.874166 | 0.0675958 | intron-variant | CNOT4 | GRCh38.p7 | 7:135424042 | TGTTTTAATAAAAAA[lengthTooLong]TTTTGTTTGTTTGTT | 4850 |
rs3750067 | snp | A/G | 0.185791 | 0.241614 | intron-variant | CNOT4 | GRCh38.p7 | 7:135363212 | AAAAGAAAAAAGAGG[A/G]AAAATGGTGAGTTTG | 4850 |
rs3750069 | snp | A/G | 0.39709 | 0.20215 | intron-variant | CNOT4 | GRCh38.p7 | 7:135363494 | TCCTCTGACAGGGAT[A/G]CGTAACAAGACAGCC | 4850 |
rs3750070 | snp | A/G | 0.021333 | 0.101051 | utr-variant-5-prime, upstream-variant-2KB | CNOT4 | GRCh38.p7 | 7:135510069 | GTTCCACAGCCAGAC[A/G]GGCCACCATCTTACA | 4850 |
rs3763425 | snp | C/T | 0.137867 | 0.223442 | upstream-variant-2KB | CNOT4 | GRCh38.p7 | 7:135510572 | GCGCGGGATTTGATC[C/T]AGGGTGAGAATTTGA | 4850 |
rs3793210 | snp | A/G | 0.0225045 | 0.103662 | downstream-variant-500B, intron-variant | CNOT4 | GRCh38.p7 | 7:135386629 | CAAAAGGTGAAGCTT[A/G]CAAGGAAGGTGTAGG | 4850 |
rs3793211 | snp | C/T | 0.0115144 | 0.0749975 | downstream-variant-500B, intron-variant | CNOT4 | GRCh38.p7 | 7:135386846 | CTGATGATTTTTCCA[C/T]GCTGGCTATGAATGA | 4850 |
rs3793212 | snp | C/T | 0.089084 | 0.191327 | intron-variant | CNOT4 | GRCh38.p7 | 7:135400407 | AATAAGGGCTTCAAG[C/T]TGAGAGAAAGAGGTG | 4850 |
rs3812265 | snp | C/T | 0.389842 | 0.20723 | intron-variant, missense | CNOT4 | GRCh38.p7 | 7:135364052 | TATTTAAACTCTCTA[C/T]AGAACTGCTGTTGTC | 4850 |
rs3812268 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | CNOT4 | GRCh38.p7 | 7:135369331 | GCCGTCTTGGAATTC[C/T]TGCCTCTACTTTATT | 4850 |
rs3812271 | snp | C/T | 0.211516 | 0.24702 | intron-variant | CNOT4 | GRCh38.p7 | 7:135369686 | ATTTAGACTTTCAAA[C/T]CTTTGTGCATTTTTA | 4850 |
rs3812272 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | CNOT4 | GRCh38.p7 | 7:135371941 | GGAGGGAAGCATTTA[A/G]GTGAGCACAAAACTG | 4850 |
rs3812273 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | CNOT4 | GRCh38.p7 | 7:135371985 | AACAAAGCCCTGTGA[A/G]GAGATCCAAAGATGG | 4850 |
rs3812274 | snp | C/T | 0.499464 | 0.016365 | intron-variant | CNOT4 | GRCh38.p7 | 7:135376577 | CTTTATGGTTATATA[C/T]CTATTGAAATTCCTA | 4850 |
rs3812275 | snp | A/C | 0.464629 | 0.128197 | intron-variant | CNOT4 | GRCh38.p7 | 7:135380130 | TTGATTGGGGAAAAA[A/C]AAAAAAACAAAAAAA | 4850 |
rs3812276 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | CNOT4 | GRCh38.p7 | 7:135380637 | AGACCTACTGTAATT[A/C]AACTGTAAGACACAA | 4850 |
rs3812277 | snp | C/T | 0.44638 | 0.154709 | intron-variant | CNOT4 | GRCh38.p7 | 7:135382482 | TTTTAAATGTCACAG[C/T]TGATATTTCAGCTGA | 4850 |
rs3812278 | snp | C/T | 0.384593 | 0.210677 | utr-variant-3-prime, intron-variant | CNOT4 | GRCh38.p7 | 7:135387389 | ATAAAGTCATTTAAT[C/T]TGTCACATTATATCT | 4850 |
rs3812279 | snp | G/T | 0.0225045 | 0.103662 | utr-variant-3-prime, intron-variant | CNOT4 | GRCh38.p7 | 7:135387467 | ACTCCAACATGACAT[G/T]AAGTACCATCTCCTA | 4850 |
rs3812280 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CNOT4 | GRCh38.p7 | 7:135392621 | AGGACTGAAAAATGT[C/T]ACTCTGGTTACCTAC | 4850 |
rs3812281 | snp | C/T | 0.467132 | 0.12391 | intron-variant | CNOT4 | GRCh38.p7 | 7:135397999 | AGGGTTAAACTATGC[C/T]CTATATATTCTGGGG | 4850 |
rs3812282 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | CNOT4 | GRCh38.p7 | 7:135404237 | AAAAACCTAGTAATC[C/T]GCTGATTTTAATGTA | 4850 |
rs3812283 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | CNOT4 | GRCh38.p7 | 7:135405430 | CCTACCTAGTTACTA[C/T]TCCTTTCACAGTTGG | 4850 |
rs3812284 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | CNOT4 | GRCh38.p7 | 7:135412185 | CTTTCACTAATATCT[A/G]TGGAAAGCCACAAAG | 4850 |
rs3812286 | snp | C/T | 0.089084 | 0.191327 | intron-variant | CNOT4 | GRCh38.p7 | 7:135416208 | TGTAAAGTATTTCTT[C/T]CCATTCATATTTGAT | 4850 |
rs3812287 | snp | C/T | 0.242488 | 0.249887 | intron-variant | CNOT4 | GRCh38.p7 | 7:135420784 | TGTTGTTCAAGGAAA[C/T]GATCAAAGGTGAGGC | 4850 |
rs3812288 | snp | A/G | 0.381697 | 0.212499 | intron-variant | CNOT4 | GRCh38.p7 | 7:135421199 | AAATTAATTTTTACA[A/G]AAACAGACATTAGAC | 4850 |
rs3812290 | snp | C/T | 0.162909 | 0.23434 | intron-variant | CNOT4 | GRCh38.p7 | 7:135457595 | AATTTTTCCAAAAAT[C/T]TGTAAGTTTCAATGG | 4850 |
rs3812293 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | CNOT4 | GRCh38.p7 | 7:135490120 | CTCAATAAAAATATC[G/T]TTCATTTTCTTCACA | 4850 |
rs3812294 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | CNOT4 | GRCh38.p7 | 7:135490144 | CTTCACAATTTCACA[C/T]ACGATTTCTTCGTTA | 4850 |
rs3812295 | snp | G/T | 0.0681886 | 0.171594 | intron-variant | CNOT4 | GRCh38.p7 | 7:135490176 | ATATTAGTATCAATT[G/T]CCCTTTTGCTATCAT | 4850 |