SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6155758 | snp | A/G | 0.5 | 0 | intron-variant | Kctd2 | Mm_Celera | 11:115424344 | GGCAAGCCCTGGAGA[A/G]CAGAGTCAGATTTAC | 70382 |
rs6157324 | snp | C/T | 0.5 | 0 | intron-variant | Kctd2 | Mm_Celera | 11:115424624 | GTCCAGGCAGctgtc[C/T]gtctgtctgtctgtc | 70382 |
rs6157394 | snp | C/T | 0.5 | 0 | intron-variant | Kctd2 | Mm_Celera | 11:115424668 | GGATGCTCTGCCCTC[C/T]GGGCTGGAGGGCCAG | 70382 |
rs27031542 | snp | A/G | 0.489796 | 0.070696 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Kctd2 | GRCm38.p3 | 11:115430350 | GAATGTAAGCGGACA[A/G]TCTGAAGTTTCAGAA | 70382 |
rs27031543 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Kctd2 | GRCm38.p3 | 11:115428905 | TTGCTTGGTGGCGTA[C/T]CTCAGTGGACACAGG | 70382 |
rs27031544 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Kctd2 | Mm_Celera | 11:115427495 | GCTCACGCAGATGGT[C/T]TCCACTATGTCTGAT | 70382 |
rs29396112 | snp | A/C | 0.375 | 0.216506 | intron-variant | Kctd2 | GRCm38.p3 | 11:115422719 | CAAAGCTTGTACTAG[A/C]AACCCTCATTAGTGA | 70382 |
rs29403237 | snp | A/T | 0.375 | 0.216506 | intron-variant | Kctd2 | GRCm38.p3 | 11:115428568 | AGTGGAGATGTCCTA[A/T]GGGAGAGTGAAGTCT | 70382 |
rs29429026 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Kctd2 | GRCm38.p3 | 11:115430530 | AGACAGTGCGCCTCT[A/G]GCTGCACGGTCCCTT | 70382 |
rs29437245 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Atp5h, Kctd2 | GRCm38.p3 | 11:115418356 | AGGTTCAGCATCAAG[A/G]ATGGGGGCTCCCTCT | 70382 |
rs29438726 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Atp5h, Kctd2 | GRCm38.p3 | 11:115418534 | AGAAAACAAAACAGC[A/G]CCTTTGGAGAGAACC | 70382 |
rs29448194 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kctd2 | Mm_Celera | 11:115425357 | CCTGTGCTCTCTACT[C/T]CTGGCCATCTTCCAT | 70382 |
rs29452409 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Atp5h, Kctd2 | GRCm38.p3 | 11:115419481 | ATAGAGAATGACCAA[C/T]AGTTAATTAGATCAA | 70382 |
rs29452549 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kctd2 | Mm_Celera | 11:115428406 | ATGTAAAAAATTAAA[A/G]TAAAAATAGATGCGT | 70382 |
rs29456678 | snp | A/C | 0.5 | 0 | intron-variant | Kctd2 | GRCm38.p3 | 11:115428654 | TTGCGACAGGAGGAC[A/C]CAGCTTGAGGCTGTG | 70382 |
rs29469029 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Atp5h, Kctd2 | GRCm38.p3 | 11:115418351 | CTTCCAGGTTCAGCA[A/T]CAAGGATGGGGGCTC | 70382 |
rs29470341 | snp | A/G | 0.32 | 0.24 | intron-variant | Kctd2 | Mm_Celera | 11:115422891 | CAGTGCAGTGGTGGC[A/G]CACATCTGTAATCCC | 70382 |
rs29471649 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Atp5h, Kctd2 | Mm_Celera | 11:115419510 | AATCGGTAAACCTCA[C/T]GAGGAATCCTCCATT | 70382 |
rs29472892 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Atp5h, Kctd2 | GRCm38.p3 | 11:115421593 | TGCCAATAGAATGGA[A/G]GTTTTCTCAGAATTA | 70382 |
rs29479484 | snp | A/G | 0.5 | 0 | intron-variant | Kctd2 | GRCm38.p3 | 11:115428656 | GCGACAGGAGGACAC[A/G]GCTTGAGGCTGTGAG | 70382 |
rs46340217 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115423595 | GGTTTTGAAGCCACT[A/G]AACTTTGTCCCCTGG | 70382 |
rs46440067 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Kctd2 | GRCm38.p3 | 11:115431044 | CGTGCTAGATGGACA[G/T]CGGGACTGAGCAGTT | 70382 |
rs46747127 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Kctd2 | GRCm38.p3 | 11:115430975 | TGGTGTCTCTCAGCC[A/G]GGCCCCTCGTAGCCC | 70382 |
rs48456926 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Atp5h, Kctd2 | GRCm38.p3 | 11:115419435 | TTCTCAGACAAATTG[A/G]CCAGCCTGCTCTCAT | 70382 |
rs48464463 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Kctd2 | GRCm38.p3 | 11:115430935 | GCGTGGGAGTTGCTG[C/T]TCCTGGTCCCACGAG | 70382 |
rs48488459 | snp | G/T | | | intron-variant | Kctd2 | GRCm38.p3 | 11:115423717 | AATTCTCAGCCAGGC[G/T]TGGTGGCACACGCCT | 70382 |
rs48697378 | snp | A/G | | | intron-variant | Kctd2 | GRCm38.p3 | 11:115428613 | CAAGGTGTAGATGAG[A/G]AAGGGGAGTGTGGGG | 70382 |
rs48939706 | snp | C/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115423605 | CCACTAAACTTTGTC[C/T]CCTGGGCGCTTCTAC | 70382 |
rs49236738 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Kctd2 | GRCm38.p3 | 11:115430697 | GCTTTTCTAAAAGCC[G/T]GAGCCGAGGAAGAAG | 70382 |
rs49371355 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115426803 | ACAGTGAATTCCAGG[A/G]CATTTTCGACAGACG | 70382 |
rs49610258 | snp | A/G | | | intron-variant | Kctd2 | GRCm38.p3 | 11:115428701 | CACTCGCTCTCTGCC[A/G]GCCTCCTCTGTGTGC | 70382 |
rs50600570 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115426990 | AACAGCTGGCTCAGC[A/G]GGTAAGAGTCCCTGC | 70382 |
rs51440425 | snp | C/G | | | intron-variant | Kctd2 | GRCm38.p3 | 11:115428703 | CTCGCTCTCTGCCGG[C/G]CTCCTCTGTGTGCAC | 70382 |
rs212001485 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115428685 | AGTGCTTACGAGGCT[A/G]CACTCGCTCTCTGCC | 70382 |
rs212317633 | snp | G/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115427087 | ACATCTTCATAGGTC[G/T]TCTACGGACACCCAC | 70382 |
rs212414115 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115426272 | TGTGTTGTAGTCATT[A/G]TCCTCTGGTTTATGG | 70382 |
rs212433451 | snp | G/T | | | intron-variant, upstream-variant-2KB | Atp5h, Kctd2 | Mm_Celera | 11:115418583 | AGAGAAATACAAGTC[G/T]TTAAGAGACGGATCA | 70382 |
rs212533681 | in-del | -/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115426723 | GGCAGGCAGCATGCT[-/G]TAGTCCCAACACATG | 70382 |
rs212557714 | snp | C/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115423095 | TTAATGATCTTTTTA[C/T]GTCTTTAATAAAAAC | 70382 |
rs212622465 | snp | A/G | | | downstream-variant-500B | Kctd2 | Mm_Celera | 11:115431507 | GAGGCCCTCAGCCTG[A/G]AACTCACAACTACAT | 70382 |
rs212711379 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Kctd2 | Mm_Celera | 11:115430850 | ACAGAACAAAGTTGC[C/T]GAAGGACCCACAATC | 70382 |
rs212720620 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Atp5h, Kctd2 | Mm_Celera | 11:115419538 | TCCTCCATTCGAAGG[A/G]AAGGACGTAGAGTTG | 70382 |
rs212855840 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | Atp5h, Kctd2 | Mm_Celera | 11:115421724 | ACAGAATGTGGGTCT[-/AA]ACCCAGTAAATAAAG | 70382 |
rs212923502 | snp | A/G | | | upstream-variant-2KB, intron-variant | Atp5h, Kctd2 | Mm_Celera | 11:115420972 | GTAAAGTGGTATTAA[A/G]CTCGGGGTTTAATGA | 70382 |
rs212968985 | snp | C/T | | | intron-variant, downstream-variant-500B | Kctd2 | Mm_Celera | 11:115429521 | AGCTACGAGCTTCCT[C/T]TCACCACACTCTGCT | 70382 |
rs213358618 | snp | C/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115425921 | TGTTTGCCGTGGTCT[C/T]GTCTCTTCTCTGTCT | 70382 |
rs213501251 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115421957 | TGCTATTTAGAAAAT[A/G]TTGCTTGGCTGTGCT | 70382 |
rs213993510 | snp | C/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115425150 | AAGAGAGAAAAGACT[C/G]TCTTCTTTGTATAAG | 70382 |
rs214364142 | in-del | -/TC | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Atp5h, Kctd2 | Mm_Celera | 11:115419223 | GTTGTCAAATGCCGG[-/TC]TCTCTCCTTCCTTCC | 70382 |
rs214403436 | snp | A/T | | | intron-variant, stop-gained, downstream-variant-500B | Kctd2 | Mm_Celera | 11:115429638 | CTCGTCCCCAAGGGA[A/T]AACAAAAGGAGGTGG | 70382 |
rs214535497 | in-del | -/C | | | intron-variant | Kctd2 | Mm_Celera | 11:115425927 | CGTGGTCTCGTCTCT[-/C]TCTCTGTCTGTCTGT | 70382 |
rs214570016 | snp | A/G | | | intron-variant, upstream-variant-2KB | Atp5h, Kctd2 | Mm_Celera | 11:115418633 | ATATATATGCAACAG[A/G]TGAAAGAATTCGGAT | 70382 |
rs214570113 | snp | A/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115427721 | CTGGGAAGAGGACCG[A/T]GGCTTTTCTGGCTTC | 70382 |
rs214605344 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115427239 | TAACATATAAAAAGT[A/G]ACTTTCCTATTGTCA | 70382 |
rs214640666 | snp | C/G | | | upstream-variant-2KB, intron-variant | Atp5h, Kctd2 | GRCm38.p3 | 11:115420561 | CCATTCCAGGCTGGT[C/G]CTCCGATCTCTGGGA | 70382 |
rs214678111 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Atp5h, Kctd2 | Mm_Celera | 11:115419731 | GGCTCGCCCCGCGGG[A/G]AAGCGAGCAGGGCAA | 70382 |
rs214860221 | snp | G/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115424434 | AAGCCTTGCCTTGCT[G/T]TTCCCCCTGGGCTCA | 70382 |
rs214965986 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115423988 | TTTTCCTAGCTCAGG[A/G]GCAGATATCCCATAA | 70382 |
rs214998776 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115423679 | AACTGTTTGAGGCTA[A/G]ATTTTGAATTCTGTT | 70382 |
rs215264354 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115422886 | TCACGCAGTGCAGTG[A/G]TGGCGCACATCTGTA | 70382 |
rs215601827 | in-del | -/C | | | intron-variant | Kctd2 | Mm_Celera | 11:115425512 | TGTAATCTGAAGCCA[-/C]CCGAATCCTGGAGCC | 70382 |
rs215787229 | snp | A/G | | | downstream-variant-500B | Kctd2 | Mm_Celera | 11:115431621 | GGTAAGGCTGTCTCT[A/G]GATTAACACAGGCCA | 70382 |
rs216665850 | in-del | -/TGT | | | intron-variant | Kctd2 | Mm_Celera | 11:115429184 | TTGGTTTTGTGGGGG[-/TGT]GGGGGTGTTTGTTTG | 70382 |
rs216820997 | snp | C/T | | | upstream-variant-2KB, intron-variant | Atp5h, Kctd2 | Mm_Celera | 11:115420801 | GTCACATTCCCTGCC[C/T]CTCCTGGGGACCACC | 70382 |
rs216856144 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Atp5h, Kctd2 | Mm_Celera | 11:115419794 | AGCTCGAAGGCCCGA[C/T]GTCCTCCGTGGAGCT | 70382 |
rs216926848 | in-del | -/CT | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Atp5h, Kctd2 | Mm_Celera | 11:115419231 | ATGCCGGTCTCTCTC[-/CT]TCCTTCCTTCCTTCC | 70382 |
rs217325812 | in-del | -/ATTCA | | | intron-variant, upstream-variant-2KB | Atp5h, Kctd2 | Mm_Celera | 11:115418985 | ACCACAACCCCGGCC[-/ATTCA]ATTCACTCGAACTGT | 70382 |
rs217355745 | snp | C/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115426213 | CAAAGGGGTTGTCAG[C/T]GGTTTGTCTGTATTT | 70382 |
rs217590873 | snp | C/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115426989 | GAACAGCTGGCTCAG[C/T]AGGTAAGAGTCCCTG | 70382 |
rs217630812 | snp | C/T | | | intron-variant, missense, downstream-variant-500B | Kctd2 | Mm_Celera | 11:115429687 | AGCAAGAGGAGCCGT[C/T]TCCACTCTGGCCGCC | 70382 |
rs218119291 | snp | C/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115422989 | ACACAGAGAAACCCT[C/G]TGTGGAAAAAAAAAA | 70382 |
rs218172990 | snp | C/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115427978 | CTTTCCCTTCCTATG[C/G]CTTGTGCTTAGAATG | 70382 |
rs218174624 | snp | C/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115427808 | TCCTTTTGCTTGTCT[C/T]TGCCTCAGAGATTTC | 70382 |
rs218251692 | in-del | -/GTG | | | upstream-variant-2KB, intron-variant | Atp5h, Kctd2 | Mm_Celera | 11:115421021 | CTGCAGGAAGTGCTT[-/GTG]GTGATACATCCTGTG | 70382 |
rs218357869 | snp | A/C | | | intron-variant | Kctd2 | Mm_Celera | 11:115428642 | GGCACCCCAGCCTTG[A/C]GACAGGAGGACCCGG | 70382 |
rs218396229 | snp | C/T | | | intron-variant, missense, downstream-variant-500B | Kctd2 | Mm_Celera | 11:115429725 | ATGCACACCCACACA[C/T]GTGCACACTTATGCC | 70382 |
rs218725349 | snp | A/C | | | intron-variant | Kctd2 | Mm_Celera | 11:115424064 | ACTGATTGCCCCCCC[A/C]CACACACACACGTTT | 70382 |
rs218920445 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115424963 | GCTTTGGGTTTTTAT[A/G]CCGACTTAGATGTGA | 70382 |
rs218963584 | snp | A/C | | | intron-variant | Kctd2 | Mm_Celera | 11:115428916 | CGTACCTCAGTGGAC[A/C]CAGGCAGTGACTACA | 70382 |
rs219197814 | in-del | -/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115426599 | AACAGGAATATACTG[-/T]TAAACACTGGCAGCT | 70382 |
rs219309047 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | Kctd2 | Mm_Celera | 11:115430791 | GGACCATTCTTCCCT[-/G]GGCAGGGCATTCCGT | 70382 |
rs219323296 | snp | C/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115425542 | CTGAGTGCTCTGCAT[C/T]CCTGGCAATGAGTTG | 70382 |
rs219474092 | in-del | -/GG | | | intron-variant | Kctd2 | Mm_Celera | 11:115429179 | TTGATTTGGTTTTGT[-/GG]GGGGGGGGGGTGTTT | 70382 |
rs219498135 | snp | A/T | | | upstream-variant-2KB | Atp5h, Kctd2 | GRCm38.p3 | 11:115420004 | GGCGGGTCTCATGTC[A/T]CACTTCAGCCAATGA | 70382 |
rs219645294 | in-del | -/TAAATAAATAAATAAATAAA | | | upstream-variant-2KB, intron-variant | Atp5h, Kctd2 | Mm_Celera | 11:115421851 | GCAAAACCGGCTCAG[-/TAAATAAATAAATAAATAAA]TAAATAAATAAATAA | 70382 |
rs219818745 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115423816 | GGAGTGCTATACAGA[A/G]AAACCCTGTCTCAAA | 70382 |
rs219910184 | snp | C/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115424169 | ATATACATGTCTCTA[C/T]CAATCTGTCCTTTTT | 70382 |
rs220013949 | snp | A/G | | | upstream-variant-2KB | Atp5h, Kctd2 | Mm_Celera | 11:115419928 | TGCTCTCTCTCCAGC[A/G]AGCAAGGAACGGAAG | 70382 |
rs220020211 | snp | A/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115428011 | GGTCATTTGAACAGA[A/T]AGCCCCTGAGAATCT | 70382 |
rs220108324 | snp | C/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115426452 | CTCTCCTGGACTCTC[C/T]GCCCTCCTGTTTTAG | 70382 |
rs220108621 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115427605 | CAGTAGCCCCGAGGT[A/G]GGGGTGAGTGAGGTG | 70382 |
rs220179198 | snp | A/C | | | upstream-variant-2KB | Atp5h, Kctd2 | Mm_Celera | 11:115420064 | CGGCGCCTGCGCCGT[A/C]GGGGTCCCTTTTCCC | 70382 |
rs220185379 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115424444 | TTGCTGTTCCCCCTG[A/G]GCTCACACCTCTCTG | 70382 |
rs220201551 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115427372 | TACTCCCAGGCAACT[A/G]TGGGCGGTGGGTCCT | 70382 |
rs220280213 | snp | G/T | | | upstream-variant-2KB, intron-variant | Atp5h, Kctd2 | Mm_Celera | 11:115421066 | CTGGTCCCAGACCTT[G/T]TGTGCCGTAACAGTC | 70382 |
rs220441571 | snp | C/T | | | intron-variant, upstream-variant-2KB | Atp5h, Kctd2 | Mm_Celera | 11:115419035 | CCACAGCACACATAC[C/T]GTGCACTTTCAGAGG | 70382 |
rs220470005 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115423159 | TCGTTGAGCCAGCAA[A/G]GTGACTCACCAGGTA | 70382 |
rs220523504 | in-del | -/GC | | | intron-variant | Kctd2 | Mm_Celera | 11:115423242 | GATAGGAGGAAAGGA[-/GC]AGAACGCAGCAAATT | 70382 |
rs220712202 | snp | A/G | | | intron-variant | Kctd2 | Mm_Celera | 11:115425421 | ATAGAGGTCCTGGAA[A/G]TCTAGCTTTACCCCC | 70382 |
rs220832411 | snp | G/T | | | intron-variant | Kctd2 | Mm_Celera | 11:115422374 | GTGAGTGCCTGAAGC[G/T]CCACGTCTTCGTCAG | 70382 |