SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs167664 | snp | G/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043598 | GTGTCTTTCTTACTT[G/T]AGGTGAAATATACCA | 10393 |
rs172784 | snp | A/G | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034031 | ttctggttgtacgaa[A/G]gatagttgtattatg | 10393 |
rs178606 | snp | C/T | 0.0571816 | 0.159126 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038903 | ATTCAACAGATACTT[C/T]TGATGACGAGACATC | 10393 |
rs186487 | snp | C/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038704 | gtgaatgcctgtaat[C/T]tcagctactcaaaag | 10393 |
rs188874 | snp | A/G | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034003 | ctantatttgggttg[A/G]ggattgatgcatttc | 10393 |
rs189782 | snp | G/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033906 | gaaaatatcttcatt[G/T]tatttccttttcctt | 10393 |
rs192933 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043583 | ATCCCTTATCACACA[G/T]TGTCTTTCTTACTTT | 10393 |
rs193403 | snp | A/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043609 | ACTTGAGGTGAAATA[A/T]ACCATCAATTCTTTC | 10393 |
rs224005 | snp | C/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145038982 | agtggcattgtattt[C/T]tcaacatttacaata | 10393 |
rs320488 | snp | C/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145043577 | CGCAAAATCCCTTAT[C/T]ACACATTGTCTTTCT | 10393 |
rs320489 | snp | A/G | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068385 | AAGTTTTGTACCTTA[A/G]GGTTTATTAGTTACT | 10393 |
rs320490 | snp | C/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066799 | agcccagttattaac[C/T]taagtgttatgtttt | 10393 |
rs320491 | snp | C/T | 0.171671 | 0.237412 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066748 | aagaaataaaagttc[C/T]tatttgacaacactg | 10393 |
rs320492 | snp | A/C | 0 | 0 | intron-variant, synonymous-codon | ANAPC10 | GRCh38.p7 | 4:145064359 | ttgaaattttcagac[A/C]tacagaaaaactcaa | 10393 |
rs320493 | snp | A/G | | | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064306 | tatactcacttccta[A/G]attcttcagttggta | 10393 |
rs320494 | snp | G/T | 0 | 0 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064293 | taaattcttcagttg[G/T]taatattttgctata | 10393 |
rs320495 | snp | A/T | 0 | 0 | intron-variant, utr-variant-3-prime | ANAPC10 | GRCh38.p7 | 4:145064180 | accagtgtgATATAT[A/T]GGTAGAGTTATCAAC | 10393 |
rs611235 | snp | C/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034039 | gtacgaaggatagtt[C/G]tattatgttaggcat | 10393 |
rs611236 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034040 | tacgaaggatagttg[G/T]attatgttaggcata | 10393 |
rs628499 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145033971 | agcatttaagtattg[G/T]taacttcatgtatgt | 10393 |
rs687463 | snp | C/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066813 | aggttaataactggc[C/T]taaggtcaaaaagct | 10393 |
rs789340 | snp | C/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973717 | tatcattttatgatc[C/T]ttataatgtctgtag | 10393 |
rs789341 | snp | C/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973672 | gactcctcatcgttc[C/T]tgatattggttattt | 10393 |
rs789342 | snp | A/G | 0.456214 | 0.141336 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007979 | atcatttttcattgc[A/G]tctatttgattcttt | 10393 |
rs789343 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007546 | ggttgttcagtttcc[A/C]tgtagttgagcggtt | 10393 |
rs789344 | snp | C/T | 0.44306 | 0.158832 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144968683 | ATGTTTTCTGCCATA[C/T]CAAAGACAAAAGGAC | 10393 |
rs789345 | snp | A/G | 0.0256215 | 0.110247 | downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:144966629 | GTAAAAGCTAAATAA[A/G]AAATTCCAGCTCAAA | 10393 |
rs789347 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145012757 | tctattctctgtgtt[G/T]gcggaaaatttaggt | 10393 |
rs809830 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144981648 | gggcaatcaggcaag[A/G]gaaagaataaagggt | 10393 |
rs813138 | snp | C/T | 0.444267 | 0.157354 | downstream-variant-500B, intron-variant | ANAPC10 | GRCh38.p7 | 4:144993596 | ACAGATAATGCATTA[C/T]ATTAACAAAGCATAA | 10393 |
rs890179 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144988765 | acagcagatcagtta[C/T]ataggatggggagtg | 10393 |
rs897334 | snp | A/G | 0.444444 | 0.157135 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034545 | tatatatatatatat[A/G]tgtgtgtgtgtgtgt | 10393 |
rs965967 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144971325 | TTCCTGCAGTAGCTA[A/T]AATGTGCATTTACAA | 10393 |
rs968936 | snp | A/G | 0.309894 | 0.242719 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145068961 | TCCGCGAAAACTTTC[A/G]TCTTAGCATCTAGTT | 10393 |
rs1017278 | snp | G/T | 0.0256215 | 0.110247 | downstream-variant-500B, utr-variant-3-prime, intron-variant | ANAPC10 | GRCh38.p7 | 4:144994561 | ATACATGGAAATGTG[G/T]TTTTTTCCATGGTTT | 10393 |
rs1086102 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144973256 | tatttggttttctat[C/G]tctgccttaatttgc | 10393 |
rs1086103 | snp | G/T | 0.0410537 | 0.137264 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998947 | gtttgtatttctgtt[G/T]gttcagtggtgatat | 10393 |
rs1086104 | snp | C/T | 0.409721 | 0.192325 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144998781 | tgtgtctctatctcc[C/T]tcagtcctgctctga | 10393 |
rs1091617 | snp | A/T | 0.490727 | 0.0674567 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145018124 | tatatatatatatat[A/T]ttttttattatactc | 10393 |
rs1349990 | snp | C/T | 0.324382 | 0.238678 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145095845 | AACATAGTATTAATA[C/T]AGAAAGGGTTCAGTA | 10393 |
rs1378315 | snp | C/T | 0.321053 | 0.23969 | intron-variant, upstream-variant-2KB | ABCE1, ANAPC10 | GRCh38.p7 | 4:145100049 | CCCAATTATTGAAAC[C/T]GATACAGAAATTGAA | 10393 |
rs1455135 | snp | C/T | 0.0252325 | 0.109451 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097667 | ATGAATAGGTTCAGT[C/T]ATGAACTAGTTGTCA | 10393 |
rs1455136 | snp | A/G | 0.467911 | 0.122535 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057230 | CAATCTATAAATTTA[A/G]AAACAATTACTCCAA | 10393 |
rs1455137 | snp | A/C | 0.325091 | 0.238456 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145065516 | TGAGAATGCATTAAA[A/C]TACAGTAACACAATC | 10393 |
rs1519406 | snp | A/G | 0.429238 | 0.174281 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144974834 | tcaatctgaggaaaa[A/G]tgatacttttacaat | 10393 |
rs1559699 | snp | C/G | 0.483345 | 0.0897213 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081058 | GTCTCGAACTCCTGG[C/G]CTCAAGCATTCCTCC | 10393 |
rs2007345 | snp | C/T | 0.456685 | 0.140646 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039888 | cgtaagtcactgtac[C/T]cagccaaggtacatt | 10393 |
rs2008536 | snp | A/G | 0.126909 | 0.217598 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034575 | tgtgtgtgtgtgtgt[A/G]tatatatcccacata | 10393 |
rs2056278 | snp | C/G | 0.488545 | 0.074807 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996528 | AAGAAGCTGTGGGGA[C/G]TGTGGTCTTCTCATT | 10393 |
rs2056279 | snp | A/G | 0.490997 | 0.0664859 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144996405 | ACAGCAGCAGCAGCC[A/G]TGTCTCTAGATCTCC | 10393 |
rs2081470 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030347 | gaccccactacatta[C/G]caacaatttatacag | 10393 |
rs2124206 | snp | C/T | 0 | 0 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | ABCE1, ANAPC10 | GRCh38.p7 | 4:145097606 | AAACTTTGGCAAGGC[C/T]TGAGGCTTAAACGCT | 10393 |
rs2162090 | snp | C/T | 0.030665 | 0.119967 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039315 | GTAATGAATAAGATG[C/T]ACAATTCTGACTTCA | 10393 |
rs2162092 | snp | C/T | 0.483126 | 0.0902898 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145076971 | ACCTCGTGATCCACC[C/T]GCGTTGGCCTCCCAA | 10393 |
rs2217010 | snp | A/G | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145066039 | CTTAACTTTTAAAGC[A/G]CATGTAAATAGATTT | 10393 |
rs2219164 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145091465 | AGGAATATTTGATAC[A/G]ATAATGGATATTAAG | 10393 |
rs2354424 | snp | A/G | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034547 | TATATATATATATGT[A/G]TGTGTGTGTGTGTGT | 10393 |
rs2354425 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034573 | tgtgtgtgtgtgtgt[A/G]tgtATATATCCCACA | 10393 |
rs3028842 | in-del | -/ATAG | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980572 | tagatagatagatag[-/ATAG]caaaaattttctccc | 10393 |
rs3028860 | in-del | -/AT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034582 | TGTGTGTGTATATAT[-/AT]CCCACATACATATCC | 10393 |
rs3096531 | snp | A/G | 0.3852 | 0.210288 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145037040 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGCATGCAT | 10393 |
rs3107285 | snp | C/T | 0.429688 | 0.173817 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144979271 | CACACTGGGCACCTA[C/T]AGAGGGGCAGGGGGA | 10393 |
rs3107286 | snp | A/G | 0.455977 | 0.141681 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144976863 | ATTCAAAATAAGAAA[A/G]TTTTCTTTTAAAACT | 10393 |
rs3114078 | snp | A/C | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:144980554 | gatagatagatagat[A/C]gatagatagatagat | 10393 |
rs3836695 | in-del | -/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145071998 | TTTGTGTTTTTTTTG[-/G]TCCTTTCACATTTCT | 10393 |
rs4000806 | snp | C/T | 0.5 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145010387 | TATTGTGAATAGTGC[C/T]GCAATAAACGTATGT | 10393 |
rs4029448 | in-del | -/AT/ATAT/ATATATATATATATGTGTGTGT | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034543 | tatatatatatatat[lengthTooLong]NNNNNNNNNNNNNNN | 10393 |
rs4148230 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant, missense | ABCE1, ANAPC10 | GRCh38.p7 | 4:145098166 | AGATTCTCGGCACCT[C/T]CAGCAGCTGGCTTCG | 10393 |
rs4835200 | snp | C/G | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145020600 | atcaaacaagcgaaa[C/G]aaataaaggacatcc | 10393 |
rs6537325 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145022419 | tcactcaggaacgga[A/G]aaccaaacatcgtat | 10393 |
rs6537326 | snp | C/T | 0.411242 | 0.191052 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034247 | ttaacatctgagtca[C/T]tgggctgagaaaggc | 10393 |
rs6815519 | snp | C/T | 0.409721 | 0.192325 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145081935 | GGCTGGCCTCGAACT[C/T]CCAGCCTCAAGTGAT | 10393 |
rs6818317 | snp | C/G/T | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029224 | tagtggcaacatccc[C/G/T]tccccgacccacact | 10393 |
rs6818401 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027687 | ctcaacatttacgcc[A/G]aaactatgaggcaat | 10393 |
rs6819173 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029662 | tctaataggttattt[C/G]cttggttagctgaaa | 10393 |
rs6819396 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085968 | tcctgggttcaagca[A/G]ttcCCAGAAGTGACT | 10393 |
rs6821761 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B | ANAPC10 | GRCh38.p7 | 4:145032882 | acttaccagatatgg[G/T]tttgcctatcctgca | 10393 |
rs6822486 | snp | G/T | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145027220 | tgttggccaggctag[G/T]cttgaactcttcacc | 10393 |
rs6823268 | snp | A/G | 0.324145 | 0.238752 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061411 | GTACACTTCCCAAAA[A/G]TGCATCAAAGAGTTC | 10393 |
rs6823444 | snp | C/T | 0.409721 | 0.192325 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145085480 | AGGTTTTTTTTCTCC[C/T]CCATTTCACAACTTT | 10393 |
rs6823870 | snp | G/T | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057985 | TACCTGGTCTCTAGG[G/T]GCTCCAGCTCCCCCA | 10393 |
rs6836914 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144985001 | TTTATAGTGGGGAGT[G/T]TTCTAATTATTAGAC | 10393 |
rs6837363 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145032241 | tccctgaaggacagc[A/G]gtgaaaggaaatctt | 10393 |
rs6840411 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145057825 | CAGATGCCCCTTTCT[A/G]CTTATTCAAATCCTA | 10393 |
rs6842499 | snp | A/T | 0.488606 | 0.0746142 | intron-variant | ANAPC10 | GRCh38.p7 | 4:144989134 | atgtttaattttttt[A/T]aaattaccaaactgt | 10393 |
rs6843258 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029198 | agaagaaagagcttc[A/C]ccatccccagtagtg | 10393 |
rs6843696 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145029450 | tccatgaggaggtgc[A/G]ctacaactgaaaaga | 10393 |
rs6848379 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145058653 | CTCTTAAATAATCTA[C/T]AGTATAAGTTTGTGG | 10393 |
rs7349671 | snp | C/T | 0.100588 | 0.200439 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016525 | aggaagaatcaatat[C/T]gtgaaaatggccata | 10393 |
rs7349727 | snp | A/G | 0.100588 | 0.200439 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145016526 | ggaagaatcaatatt[A/G]tgaaaatggccatat | 10393 |
rs7437451 | snp | A/G | 0 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145039983 | gcagagcaagaattc[A/G]aactccagcagatga | 10393 |
rs7438409 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145026957 | tatatgtgtgtgtgt[A/G]tatatatatatatat | 10393 |
rs7441251 | snp | A/G | | | intron-variant | ANAPC10 | GRCh38.p7 | 4:145007684 | tttaaagcagtgtgt[A/G]gagggaaatttatag | 10393 |
rs7660966 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061050 | AGAACTATGGCAGAA[A/T]AGTAGTATGTTCATT | 10393 |
rs7661646 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145030002 | aatcccaaggtggca[C/G]gcgctaagtggcagc | 10393 |
rs7662396 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014726 | aggtgctggtatcca[C/T]ggctgagagacccac | 10393 |
rs7666221 | snp | A/T | 0.10237 | 0.201756 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145061091 | GGAAAACAACTCACA[A/T]TATCACCTGATAATA | 10393 |
rs7670125 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145056050 | GGTATtgtcagaggc[A/G]tgtgaaaccagagca | 10393 |
rs7672532 | snp | A/G | 0.5 | 0 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145034543 | tatatatatatatat[A/G]tgtgtgtgtgtgtgt | 10393 |
rs7680398 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | ANAPC10 | GRCh38.p7 | 4:145014883 | acatccataggaaaa[C/G]ggggagagtgctaca | 10393 |