SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3653478 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kctd21 | GRCm38.p3 | 7:97338004 | GAAATACTCACTCTC[C/T]GGCCCCTGGCATGGG | 622320 |
rs3654021 | snp | A/G | 0.5 | 0 | intron-variant | Kctd21 | GRCm38.p3 | 7:97338063 | TGAAGATACCTACAG[A/G]GGCAAAGACCTTCAC | 622320 |
rs3654113 | snp | C/T | 0.5 | 0 | intron-variant | Kctd21 | GRCm38.p3 | 7:97338117 | CCCTGCTGGCAGAGT[C/T]GCCTGCACACAGCCT | 622320 |
rs3654198 | snp | G/T | 0.5 | 0 | intron-variant | Kctd21 | GRCm38.p3 | 7:97338149 | CTGATGCTTTGGGCA[G/T]GTTATCTAATCTCCT | 622320 |
rs3696363 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Kctd21, Usp35 | GRCm38.p3 | 7:97333771 | TGCACAGTGGAAGCC[A/T]CCATGGCCTTGGCAG | 622320 |
rs3697480 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Kctd21, Usp35 | GRCm38.p3 | 7:97333964 | ACAAAGttaaaaaaa[A/T]aaaaaaaaaatGTCT | 622320 |
rs3698101 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Kctd21, Usp35 | GRCm38.p3 | 7:97334062 | TCCTACTTAGGTTAA[C/T]TGTGCTAAGTACTGA | 622320 |
rs3710857 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Kctd21, Usp35 | GRCm38.p3 | 7:97331083 | CTTGGCAGCAGAATG[C/T]GTTTTAACTCAGTGT | 622320 |
rs3712100 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Kctd21, Usp35 | GRCm38.p3 | 7:97331263 | AAGATGAAGAGAAGT[C/T]CCCTCTGGGACTGTC | 622320 |
rs3726711 | snp | A/T | 0.5 | 0 | intron-variant | Kctd21 | GRCm38.p3 | 7:97337939 | CATTTGAATAAAATA[A/T]TCTTCAGGAAATGCC | 622320 |
rs4138903 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Kctd21, Usp35 | GRCm38.p3 | 7:97334087 | TACTGAGCATAAAGT[A/G]CTGTGCTAAGTACTG | 622320 |
rs31050916 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kctd21 | Mm_Celera | 7:97342355 | CCTGGCCACGAACAG[A/G]TCTCCATCTCTAGTT | 622320 |
rs31091220 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kctd21 | Mm_Celera | 7:97343971 | AAGAAAGCATTCTTC[C/T]AATGAATTATATCCT | 622320 |
rs31148102 | snp | C/T | 0.5 | 0 | intron-variant | Kctd21 | GRCm38.p3 | 7:97343688 | TGGTAAAGGCTATCC[C/T]GGGAGCTTCGGCAGA | 622320 |
rs31150147 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kctd21 | GRCm38.p3 | 7:97342376 | ATCTCTAGTTTTCCC[C/T]GTCACAATATTATAC | 622320 |
rs31239892 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Kctd21 | GRCm38.p3 | 7:97350294 | AACTGACTCTGTTGC[C/T]TACTGTCAGATCCTG | 622320 |
rs31310194 | snp | C/G | 0.5 | 0 | intron-variant | Kctd21 | GRCm38.p3 | 7:97343500 | ACAGCTGGTGTCAAA[C/G]AGTAATCTTCCACTT | 622320 |
rs31312234 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kctd21 | GRCm38.p3 | 7:97342509 | GTTTGTGTGTAAAAG[C/T]TATATAATGTATAGT | 622320 |
rs31409438 | snp | G/T | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97343737 | ACAGGGAAAAGAGAT[G/T]CGTGGAAGGCTGCCT | 622320 |
rs31439944 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Kctd21 | GRCm38.p3 | 7:97349696 | GGGAAGCCTGGAGCC[C/T]GCATCCACAGGTGGA | 622320 |
rs31466468 | snp | C/G | 0.5 | 0 | intron-variant | Kctd21 | GRCm38.p3 | 7:97344915 | GCCTGGAGTCTCCCG[C/G]CCCTCTCCACCCCTA | 622320 |
rs31605280 | snp | A/C | 0.5 | 0 | intron-variant | Kctd21 | GRCm38.p3 | 7:97344413 | CAGGGCAGGTGGGTG[A/C]GGTGAATGGCAGAGC | 622320 |
rs31696779 | snp | C/T | 0.5 | 0 | intron-variant | Kctd21 | GRCm38.p3 | 7:97343448 | TCTAGACCTTCCTTC[C/T]AGATGGATTGTTTAT | 622320 |
rs31702904 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Kctd21 | Mm_Celera | 7:97349955 | CTCAAATCAACACTG[C/T]CCCCCTCCCCCGAGT | 622320 |
rs31756576 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kctd21 | GRCm38.p3 | 7:97344271 | AGTACGGACCACCAC[A/G]CCCAGTGAGAAGAGA | 622320 |
rs31808044 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kctd21 | GRCm38.p3 | 7:97342375 | CATCTCTAGTTTTCC[C/T]CGTCACAATATTATA | 622320 |
rs31833415 | snp | C/G | 0.444444 | 0.157135 | utr-variant-3-prime | Kctd21 | GRCm38.p3 | 7:97348429 | TTACGGGGGAATCAC[C/G]TGCCCCTAGTCAGTG | 622320 |
rs31916515 | snp | C/G | 0.444444 | 0.157135 | utr-variant-3-prime | Kctd21 | Mm_Celera | 7:97349170 | GTGCTAGGTCTTGTT[C/G]TTAGACCTTCCTCAG | 622320 |
rs31933236 | snp | A/G | 0.5 | 0 | intron-variant | Kctd21 | GRCm38.p3 | 7:97345092 | TAGAAAGGCTGGGTG[A/G]GGGAGAGGGTGACAT | 622320 |
rs31990173 | snp | C/G | 0.5 | 0 | intron-variant | Kctd21 | GRCm38.p3 | 7:97342824 | CTCTAACAGGTAGTG[C/G]TGCTTAATTGTTCTT | 622320 |
rs32115336 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kctd21 | Mm_Celera | 7:97344260 | CTAGAATTCAAAGTA[C/T]GGACCACCACACCCA | 622320 |
rs32120867 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kctd21 | GRCm38.p3 | 7:97342386 | TTCCCCGTCACAATA[G/T]TATACAAATAGAATC | 622320 |
rs32146471 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Kctd21 | GRCm38.p3 | 7:97350378 | CACCGGGCATCTTAA[A/G]AGAGTTGGTTGGAAT | 622320 |
rs32326679 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kctd21 | GRCm38.p3 | 7:97344270 | AAGTACGGACCACCA[C/T]ACCCAGTGAGAAGAG | 622320 |
rs32347989 | snp | C/T | 0.5 | 0 | intron-variant | Kctd21 | Mm_Celera | 7:97344720 | TGGGTCTGGAGCAGA[C/T]CCCATAGAGGGTTCC | 622320 |
rs32370672 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Kctd21 | GRCm38.p3 | 7:97350633 | GTGAGGATGGGTGGC[C/T]CTCCCACATAGCCAC | 622320 |
rs32374458 | snp | A/G | 0.5 | 0 | intron-variant | Kctd21 | Mm_Celera | 7:97342782 | TTTTGTAGACGTACA[A/G]TGGTATTTGTGGTTT | 622320 |
rs32451957 | snp | G/T | 0.375 | 0.216506 | utr-variant-3-prime | Kctd21 | Mm_Celera | 7:97348420 | GCAGTTTTCTTACGG[G/T]GGAATCACGTGCCCC | 622320 |
rs32502475 | snp | A/G | 0.5 | 0 | intron-variant | Kctd21 | Mm_Celera | 7:97344468 | GTGGGGAGAGTGGAC[A/G]GACAAAGTGGTTTAG | 622320 |
rs32527436 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Kctd21 | GRCm38.p3 | 7:97349363 | AGCCTTCCCCACCAG[C/T]ATGGCTCAGCTTGCT | 622320 |
rs36467112 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Kctd21 | GRCm38.p3 | 7:97337959 | CAGGAAATGCCTCAC[A/G]AGGCTCTGAGAATCC | 622320 |
rs36973076 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kctd21 | GRCm38.p3 | 7:97338262 | CCCACAACCAGGTTG[A/G]CTGCACACGACTACC | 622320 |
rs36994738 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Kctd21 | Mm_Celera | 7:97341680 | CGCCACGCCCAGTGC[C/T]CAAACAAATCTTATC | 622320 |
rs37331150 | snp | C/T | 0.277778 | 0.248452 | intron-variant, upstream-variant-2KB | Kctd21, Usp35 | GRCm38.p3 | 7:97333476 | CAAGCAAGGAAATGC[C/T]TCAGGTTGGGTGGTC | 622320 |
rs37468722 | snp | C/G | 0.32 | 0.24 | intron-variant | Kctd21 | GRCm38.p3 | 7:97336909 | CAGTGTGACCATGTG[C/G]CGTGCCACAAACCCT | 622320 |
rs37531419 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Kctd21 | Mm_Celera | 7:97348155 | GCAGCTCATGTCAGC[A/G]AAGGCTCTGAGGAGA | 622320 |
rs37825724 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kctd21 | GRCm38.p3 | 7:97336910 | AGTGTGACCATGTGG[C/T]GTGCCACAAACCCTG | 622320 |
rs38208758 | snp | A/G | 0.46875 | 0.121031 | intron-variant, upstream-variant-2KB | Usp35, Kctd21 | GRCm38.p3 | 7:97330316 | ATTAGGCATAGATGG[A/G]AATTGGAGAAAGGCT | 622320 |
rs38416554 | snp | A/G | 0.408163 | 0.193609 | upstream-variant-2KB, intron-variant | Kctd21, Usp35 | GRCm38.p3 | 7:97331211 | TGACAGGCAAGAACA[A/G]CCCTGTTACTGAAGA | 622320 |
rs38519287 | snp | A/T | 0.46875 | 0.121031 | intron-variant, upstream-variant-2KB | Kctd21, Usp35 | GRCm38.p3 | 7:97332850 | GGAGCTCAGTGCGTC[A/T]CACACATACTCATTC | 622320 |
rs38835085 | snp | A/G | 0.5 | 0 | intron-variant | Kctd21 | Mm_Celera | 7:97346457 | GGCCAAAAACTAAGT[A/G]ATCCGTGATCGTTCT | 622320 |
rs38840620 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kctd21 | GRCm38.p3 | 7:97335967 | TGATCTTTGCCTGAA[C/T]TGCAGCACTGAAGGC | 622320 |
rs38998691 | snp | C/T | 0.489796 | 0.070696 | intron-variant, upstream-variant-2KB | Kctd21, Usp35 | GRCm38.p3 | 7:97334116 | TGAGCATAAAGTGCT[C/T]TGAGTCAAAAAGGAT | 622320 |
rs39473242 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kctd21 | GRCm38.p3 | 7:97339863 | CTTTTTAAGGCTGTT[A/G]CACCTTCTGTTGCTT | 622320 |
rs39817618 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Kctd21 | GRCm38.p3 | 7:97337577 | CAATGTTTGGTCTTT[A/C]CTGATAGCACATAAA | 622320 |
rs40125069 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kctd21 | GRCm38.p3 | 7:97335600 | TTTAGAAGGCAGCTA[G/T]CAGGGGTCTTCATGA | 622320 |
rs45681046 | snp | C/T | | | intron-variant, upstream-variant-2KB | Kctd21, Usp35 | GRCm38.p3 | 7:97334143 | GGATGGTGTGGGTGC[C/T]ACAGGTGAGGCTTGG | 622320 |
rs45698152 | snp | C/T | | | upstream-variant-2KB, intron-variant | Kctd21, Usp35 | GRCm38.p3 | 7:97330810 | TGAACATCTGCGAGA[C/T]ACCTCACAGAGGCCA | 622320 |
rs45713030 | snp | A/G | | | intron-variant | Kctd21 | Mm_Celera | 7:97347256 | GGCATGCGCCACCAC[A/G]CCCGGCTAATAATCA | 622320 |
rs45810312 | snp | A/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97345542 | ATGCACAAAGCATCT[A/G]AGCCTCTTGGTCCAT | 622320 |
rs45817014 | snp | C/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97335925 | CCTCTGCTCCAGACT[C/G]TGTTCCTTCCCTGCC | 622320 |
rs45941874 | snp | G/T | | | downstream-variant-500B | Kctd21 | GRCm38.p3 | 7:97350659 | GCCACTGCCCAGGGG[G/T]GGGAAGGGAGGCGGG | 622320 |
rs45988240 | snp | C/G | | | intron-variant | Kctd21 | Mm_Celera | 7:97344957 | TAACACCTGGAGGTG[C/G]TGATACAGTCTTTGG | 622320 |
rs46072356 | snp | C/T | | | upstream-variant-2KB, intron-variant | Kctd21, Usp35 | GRCm38.p3 | 7:97331478 | CTACTCCAGTTGGGC[C/T]CCCTCTCTTCCTTCC | 622320 |
rs46165443 | snp | C/T | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97339197 | TTGAAGTTTATACAA[C/T]ATCCTGGAGTAGAGA | 622320 |
rs46216780 | snp | A/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97339206 | ATACAACATCCTGGA[A/G]TAGAGAAAGGAAGAA | 622320 |
rs46360001 | snp | A/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97342121 | AATATCACTGCAGTC[A/G]ATGCAACGGGTCACA | 622320 |
rs46412997 | snp | G/T | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97339742 | CACCCAAAGTGAAAG[G/T]AATTAATTAAAATGA | 622320 |
rs46502285 | snp | C/T | | | intron-variant | Kctd21 | Mm_Celera | 7:97346190 | GGGTATTAGATCCTC[C/T]GGGACTGGAGTTTCA | 622320 |
rs46585769 | snp | G/T | | | intron-variant | Kctd21 | Mm_Celera | 7:97345809 | TGGCTGCCCTCCCCC[G/T]ACTCCCACCAGCATA | 622320 |
rs46654576 | snp | A/G | | | intron-variant | Kctd21 | Mm_Celera | 7:97347260 | TGCGCCACCACGCCC[A/G]GCTAATAATCATTTC | 622320 |
rs46791357 | snp | C/T | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97344291 | GTGAGAAGAGAGTTC[C/T]TAACATAGGAATTTG | 622320 |
rs46859717 | snp | A/G | | | intron-variant | Kctd21 | Mm_Celera | 7:97342012 | GTCTCAACCTAGTCT[A/G]TAATTCTGATCTTAA | 622320 |
rs46972289 | snp | A/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97345903 | ATGTTGCTGAGCTCA[A/G]TCTACAGGTTTCCTG | 622320 |
rs46983558 | snp | A/G | | | intron-variant | Kctd21 | Mm_Celera | 7:97346219 | CAGGCAGTTAGCCCC[A/G]ATGAGATTACTGAGA | 622320 |
rs46990968 | snp | A/G | | | intron-variant, upstream-variant-2KB | Kctd21, Usp35 | GRCm38.p3 | 7:97333648 | AGGGGAAGTCTGCAG[A/G]GCTCTGGGCCAAAGC | 622320 |
rs47148908 | snp | C/T | | | synonymous-codon | Kctd21 | GRCm38.p3 | 7:97347600 | GGTACAGCCCCTGAT[C/T]GAGGCCCTGCAGGAA | 622320 |
rs47161780 | snp | A/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97339684 | GACAGCGCAGTGATA[A/G]AATGCCTGCCTAACA | 622320 |
rs47209721 | snp | A/C | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97345047 | GAACTAAATTACTTC[A/C]CAAAGCCTAGGCTTG | 622320 |
rs47290418 | snp | A/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97341247 | ACAACATCGGAAGAT[A/G]CTCCAACACATGTAC | 622320 |
rs47320154 | snp | A/C | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97340050 | TCATGGAGTTACGCC[A/C]AGCCCCCATCTTAGT | 622320 |
rs47393589 | snp | A/T | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97342833 | GTAGTGCTGCTTAAT[A/T]GTTCTTTGTGTTGTT | 622320 |
rs47400146 | snp | A/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97340825 | ATCAGAGGGCCCCAG[A/G]ACCTCCTACCCAGGC | 622320 |
rs47401238 | snp | A/G | | | downstream-variant-500B | Kctd21 | GRCm38.p3 | 7:97350546 | TCCCACAAAGAGCTC[A/G]AGGGGTGGTAGAGAG | 622320 |
rs47420805 | snp | C/T | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97334336 | CAGAGGCAGGCGGAT[C/T]TCTGAGTTTAAAGCC | 622320 |
rs47441196 | snp | C/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97345048 | AACTAAATTACTTCC[C/G]AAAGCCTAGGCTTGA | 622320 |
rs47457891 | snp | C/T | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97334359 | TTAAAGCCAGCCTGG[C/T]CTACAGAGTGAGTTC | 622320 |
rs47495899 | snp | C/T | | | intron-variant | Kctd21 | Mm_Celera | 7:97341311 | ACCCAAAGGAGCTTC[C/T]GGGGCCTTTTCCCGT | 622320 |
rs47498229 | snp | C/T | | | synonymous-codon | Kctd21 | GRCm38.p3 | 7:97347678 | CACCCTGAAGCAGCG[C/T]GTGCAGACGGTCCAC | 622320 |
rs47509716 | snp | A/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97341595 | TGGGGGTGGGGGGGC[A/G]GCTTTCTCTGAAGAT | 622320 |
rs47531216 | snp | A/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97346407 | GCTGGGGGGAGGGGG[A/G]GCAGGGGGATGTCCA | 622320 |
rs47574077 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Kctd21, Usp35 | GRCm38.p3 | 7:97332037 | ACTGCGCGGTCTCAG[A/G]GCTGCGGGACGGAAC | 622320 |
rs47631119 | snp | A/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97339263 | GAATTATGGGGGAGT[A/G]GGGGTGGGGAGGAAG | 622320 |
rs47699483 | snp | C/T | | | intron-variant | Kctd21 | Mm_Celera | 7:97344290 | AGTGAGAAGAGAGTT[C/T]TTAACATAGGAATTT | 622320 |
rs47714728 | snp | C/T | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97338668 | ACTCAGTTTGCATCC[C/T]CATTCATCTTTTAAA | 622320 |
rs47723373 | snp | C/T | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97342046 | AAAGCACTCTGCAGG[C/T]GAGTGTCTCCCTTTG | 622320 |
rs47792382 | snp | A/G | | | intron-variant | Kctd21 | Mm_Celera | 7:97340947 | GGGGAAGAAGTGCAC[A/G]TGGCTGGGTAGGAGA | 622320 |
rs47809390 | snp | C/G | | | intron-variant | Kctd21 | GRCm38.p3 | 7:97345262 | TGACTCAACTGTGAG[C/G]CCAAGCACCCTTCCC | 622320 |
rs47933164 | snp | A/C | | | intron-variant | Kctd21 | Mm_Celera | 7:97339344 | GCTCTTCTGGGTTCT[A/C]ACGAGTTTTCTCTGT | 622320 |
rs47980748 | snp | C/T | | | upstream-variant-2KB, intron-variant | Kctd21, Usp35 | GRCm38.p3 | 7:97330788 | GGACTCTAATATCCA[C/T]GACCCTTGAACATCT | 622320 |