SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs558017229 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477606 | TTTCCGGAACTGGAT[G/T]CTTGCTTCCTGGCGG | 83892 |
rs558087920 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109463015 | GCATTTTCCACAAAT[A/G]AAACAGAGGCTCAGA | 83892 |
rs558173380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468514 | GCCAAGGAATGAAGG[A/C]TGGTACTATTTTTAA | 83892 |
rs558222462 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453481 | TACAGGTGTGAGCCA[C/T]CATGCTCAGTCCTTT | 83892 |
rs558320026 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468394 | CTCCCAAGTCAATGT[A/C]CCTGGAAAGGTAGGG | 83892 |
rs558357091 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470397 | TAGTGCTGCCCAAAA[C/G]AGCAAGATCCCACTA | 83892 |
rs558377981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455792 | CCAGCTTTGTGGAAC[A/G]GCATGGTGGGAGAAG | 83892 |
rs558420570 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463151 | AATTCAACTCAGCTG[C/T]GCAGGGAAGGAACCT | 83892 |
rs558553055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467856 | ATGCTCTGTCCAGTC[A/G]GGGACAGGGGGACAG | 83892 |
rs558612967 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474608 | AGAGCCCACTATTCT[A/G]AAAAGCACTGTACCC | 83892 |
rs558704119 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449033 | AAAACCCTTGATTAC[A/G]ACACACCAAAGCTGT | 83892 |
rs558965025 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448217 | TGTAGGAATTTAACT[C/G]TTGTTTACATCCATT | 83892 |
rs559110562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466352 | GGCCCTGTGGCAAGC[A/G]CTTTCTCATGTCCTC | 83892 |
rs559420248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460898 | TCGGCTCCCTCTACC[C/T]CCCAGCGGAGAGCGG | 83892 |
rs559731402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460498 | CAACCGAAGGAATCG[A/G]GCTCCAGGGCAAACT | 83892 |
rs559757956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472855 | TTTTTTGGCTTTCCA[A/G]TACCTTTTTAAAGAT | 83892 |
rs559793733 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466780 | TTAACCAGCAAGCTG[A/T]ACTGCTGGATTCACT | 83892 |
rs559822978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478505 | GATTATTGAGGCTGG[C/T]CACGGTGGCTCACGC | 83892 |
rs559928896 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467351 | TCGGCTGTGCGTGGT[A/G]GCTCACGCCTGTAAT | 83892 |
rs559986270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471435 | TGTTTTCTCAAGAAA[C/T]AGTTCCTTTTTCATC | 83892 |
rs560068240 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467816 | AGGGATTTAGAAGGT[A/G]AGCAGTCCTGCCAGT | 83892 |
rs560099559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473416 | TAGCTCTGAGTAAAC[A/G]CTCCAAACACTCAAA | 83892 |
rs560188455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464563 | TAAAAAAGCTCAGAC[A/C]AGTCAGACTGGGAGA | 83892 |
rs560200606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470616 | CTGGGGTAGCCCCCA[C/T]GGCTGGCCCTACCAT | 83892 |
rs560431537 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452854 | TCTTTCCTTTTTTTT[A/T]AAAAGATATGGGATC | 83892 |
rs560432985 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451412 | ACGACAGGGGTCATA[C/T]GCCTGGGTCAAGACA | 83892 |
rs560439628 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455598 | ACCGTCGGCCCACAG[A/C]AGACCTGCTGCATGT | 83892 |
rs560445954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459536 | AAAGAAAATAATCAC[C/T]GTACACTCTGTGGCT | 83892 |
rs560470681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458819 | GATTCCTCTTCAGGA[A/G]CACCACCTGCTTCCC | 83892 |
rs560650918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465111 | CAGAGAAACTCCCAC[A/G]CACGGGGAAAGCGTT | 83892 |
rs560746414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459585 | ACACGTCATGACGTA[A/G]ACTCTGAATTTAACC | 83892 |
rs560748352 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452205 | CTAACTTAACCTAGA[G/T]ATCATTCTGTATCAA | 83892 |
rs560996810 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462017 | GTGCCCTGTTCCACG[G/T]CCTCCTCAGACTGGG | 83892 |
rs560999037 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451491 | CAAAAGTATCTCCAG[A/G]CTCCAAGGGAAGCAG | 83892 |
rs561186852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453725 | CAAACCCCCAGCTTT[C/T]TGGCTGGCCGATCAG | 83892 |
rs561249170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458229 | GTGAACTAGATGGGG[A/G]AAGACAGGGAGTTGA | 83892 |
rs561260011 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460448 | ACAGTAGTTAGGTGG[A/C]CTGCTGTTCCAGGGA | 83892 |
rs561338848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459310 | GAAAGAATTAGGAGG[A/T]CAGTCCTGGAGGTCT | 83892 |
rs561743867 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476576 | TGGAAGTTACAGATA[C/G]GTACCCAGGCGCCAG | 83892 |
rs561960568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470508 | GTGAGATTGGTATCC[G/T]GCACATGTGTACTCA | 83892 |
rs562040806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461812 | CTGACAAGCAGGGTG[A/C]CCTCAGGCAAGGGGC | 83892 |
rs562130992 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477810 | CGGTCCGGCCTGCGG[C/G]AGAACTGGGTCGTCA | 83892 |
rs562135992 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454254 | AGCAGCTATTATTAA[C/T]CTGTTCCAGTAAGTA | 83892 |
rs562197872 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456931 | CAGAGAAATGAAAAC[A/G]TAAGTCCACATAGAG | 83892 |
rs562308838 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450379 | GTGCCCCACAAGCAC[A/C]CGTCCCCACCCACAG | 83892 |
rs562424196 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477791 | GGTAGGCCGGTAGGG[C/T]CTGCGGTCCGGCCTG | 83892 |
rs562631428 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463278 | AATGAACAGGCAGAC[C/T]GTGACACTGGGCTCC | 83892 |
rs562645564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462462 | AAGAGGCCTTCCCAG[G/T]CATGGTAAATCACAT | 83892 |
rs562700086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458765 | ATCCCCAAAGGCAGC[C/T]GGCCAGGCCTAGACC | 83892 |
rs562737194 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451539 | GCACAGGATCTGGGT[A/G]TAGCACGGCAGGGAG | 83892 |
rs562762824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465073 | CGTGCCCCATGATGT[A/G]GCAAAGGCTGGGCAG | 83892 |
rs562943247 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471267 | AACAGCAGAAGCAAC[A/G]CGACAGTCATGGACA | 83892 |
rs562981874 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473625 | AGGTCAGTCAACCTA[A/G]TAGTAGGCAAGGCCC | 83892 |
rs563107598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468793 | GAGTAGCTGGGACTA[C/T]AGGCACCCACCACCA | 83892 |
rs563186219 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449374 | AACACTAGCTCATTA[A/G]GCATAGAGGCCACAG | 83892 |
rs563303676 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476229 | GGACCAGAGTTTGAG[A/G]ACCACTGGTTTATGC | 83892 |
rs563420964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455585 | GACAAGAGGCATGAC[C/T]GTCGGCCCACAGCAG | 83892 |
rs563755206 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460937 | GGAGAATGGCAGCCT[-/CA]CCTGCCTACCTGCCC | 83892 |
rs563816577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460977 | CTGAGGAAGCCCCCA[C/T]AGCCTCCAGGCCCTA | 83892 |
rs563960004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468033 | TGGTTCTCAGATAAT[A/G]CCTGCTTCCTCCAGC | 83892 |
rs563974302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467437 | CCAGCCTGGGCAACA[C/T]AGTGAGGCCCCATCT | 83892 |
rs564028160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461518 | GAAACATTCTTGGGG[A/G]TGGGGGCCAGGAAGA | 83892 |
rs564400005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469399 | GATGGTGGGAGTCCC[C/T]AACAAGCTGCCTCCT | 83892 |
rs564473412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468083 | TGATTTCCACAGATA[C/G]TCTCGGGCCATGTGG | 83892 |
rs564510798 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457106 | GATTCATGCTACAAC[A/G]TGGATAAACCTTGAA | 83892 |
rs564557015 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109448907 | ACTGGGGAATGGGGT[C/T]CCCACACAGTGATCG | 83892 |
rs564583137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474882 | ACGTTTTCTATATGC[C/T]TCTCTGTAGAAGTCT | 83892 |
rs564630792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460487 | AGGGGTCACTCCAAC[C/T]GAAGGAATCGGGCTC | 83892 |
rs564701603 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456021 | CAAGCAAAGCATTTT[A/T]AAAGCATTTCCCTCT | 83892 |
rs564762137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453767 | CCAGGGAAGCTTAGA[A/G]AACTGCGGAGAAGAG | 83892 |
rs564765187 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474079 | AGCCACCGCGACTGG[C/T]TAATTTTGTATTTTT | 83892 |
rs564810693 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465667 | ATGCCTGGGCTGAGC[C/T]TGGTGGCACAGGTGA | 83892 |
rs564857740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109454372 | TACAATAACCAACAA[C/T]CTCAAACAAAAACAC | 83892 |
rs565105222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466120 | GGGCATGCTCACTGC[C/T]ACAGTGTCCTTGTCT | 83892 |
rs565236663 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478715 | GAACCTGGGAGGCGG[A/C]GGTTGCAGTGAGCAG | 83892 |
rs565268871 | in-del | -/GACCT | 0.00676609 | 0.0577691 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473321 | AAGGGTTTGGAGTTA[-/GACCT]GTGCATAAGGCCCCA | 83892 |
rs565310422 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476021 | GAATCACACCTATAA[A/G]AGCCCTCTGACTCCC | 83892 |
rs565445881 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473371 | AGCTGTGTCCAGGGC[C/T]AAAAGCCTCACCTCC | 83892 |
rs565481454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479267 | CTTAAGGACAATACA[A/G]TAAAGCTCACTTACA | 83892 |
rs565625121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474344 | TGAGATACTGGCTAC[A/G]GATCTGATTCAATCA | 83892 |
rs565712603 | snp | G/T | 1.6483e-05 | 0.00287076 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460712 | AGCAGCTCCTCGATC[G/T]CCCGGCGGCTCTCGG | 83892 |
rs565717940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468249 | ACCCTGGCCTTCCCC[A/G]GGACACAGAGAGGAA | 83892 |
rs565781730 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109448928 | ACAGTGATCGCCCCA[C/T]GGGAGGGTGACAGAA | 83892 |
rs565841709 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467690 | TGATATGAAGCAGGG[G/T]CTGAGCTCCGGTGAC | 83892 |
rs565961030 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453361 | TGCCCAGCTATTTTT[A/T]AAAAAATTTTTGGTA | 83892 |
rs566166766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471967 | ATACTTGTATAGGAC[A/G]CTTACCATGAATGGA | 83892 |
rs566226197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478765 | CAGCCTGGGCAACAA[A/T]GTGAGACTCCGTCTC | 83892 |
rs566454264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464052 | CCTCCTCCCCGCCCC[A/G]TGAGCATACCATGTG | 83892 |
rs566502378 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451287 | GCAAACAAAAGTTCT[A/C]ACATACACTTCACAC | 83892 |
rs566784899 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457303 | GGGAAAATGGGGAGT[A/G]ACTGCTAACGAATAG | 83892 |
rs566811242 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477325 | AGGAAACACCCAGCT[C/T]ACGCCAGCCGGGGGC | 83892 |
rs566846324 | snp | A/T | | | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460732 | GCGGCTCTCGGGTAA[A/T]GGCACCGCCCCGTCT | 83892 |
rs566871640 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476897 | CACCCCCAAATGTCC[A/G]TTTTCAATTGATATC | 83892 |
rs566926117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470146 | CTGGCTGCACCCTAA[A/G]ACAGCCTAAAGCACT | 83892 |
rs567290884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452551 | AGGTTCTGGGAAAAA[C/T]GGAGCAGGCACACTC | 83892 |
rs567336990 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477041 | TCCCGGATTCCTAAC[C/G]GCCAGGGAGCCTCCC | 83892 |
rs567342549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458947 | GCACAAACAGCTTTC[A/C]GAGTCTCTCATTCCT | 83892 |
rs567433437 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451189 | AACTGCAGGACAACT[C/G]TCAGAATTGTCAAAC | 83892 |
rs567483833 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464658 | AGAAAAAGGCAAATG[G/T]GTAAGTAAGATGCAA | 83892 |
rs567596960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470731 | CCATTCAGTCATCAT[C/G]TCCGGACACAGACAA | 83892 |
rs567657374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470336 | ACTAAACAACAGACA[C/T]GGAAACTTTTGGAAC | 83892 |
rs567939779 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450712 | CCCAGGGAGGGGTAG[C/T]TTATGAGCTATGCCT | 83892 |
rs567989143 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477976 | TCTTTTCACTTTGGG[A/G]ACGGTAGGCCTTTAT | 83892 |
rs568013253 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450100 | AATATAAACTCGTTT[A/T]TGGAATACATGTGTC | 83892 |
rs568034877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469459 | ACTTCTTCAGGGAAG[C/T]CCTCCTTGACCACAT | 83892 |
rs568200709 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475759 | GAGGCTTGTATAAAA[A/C]CTTCCCAAACTGAGG | 83892 |
rs568252695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457235 | AAATTCATCAAGACA[C/G]AAAACAGATTAGTGG | 83892 |
rs568287446 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472356 | GCCTAGCCTACACAG[A/G]GTCAGGATTATCAGT | 83892 |
rs568556241 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455122 | GATGATTCTGGTTCA[C/G]CCCCTGCCCCCGGGA | 83892 |
rs568569861 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472469 | CCTTCTTCTGGGATA[C/G]CTCCAGAAGCACCTG | 83892 |
rs568654613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452976 | CTGTTTCTTGATTCA[C/T]AGACCAGGTTCAGGA | 83892 |
rs568661096 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453579 | CTCTGAGGGAAGGAA[A/C]CTTCTTTTCTGATGA | 83892 |
rs568772657 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451485 | TTGTTACAAAAGTAT[C/T]TCCAGGCTCCAAGGG | 83892 |
rs568805776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457313 | GGAGTGACTGCTAAC[A/G]AATAGAGGGTTTCTT | 83892 |
rs569052854 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451267 | CACCCACAAAAATAA[A/T]TATTGCAAACAAAAG | 83892 |
rs569248979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456502 | AGGATCAGAGAAATT[A/C]GGTAATTGCTCAAGG | 83892 |
rs569306071 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476800 | TCCAAAACGCCAAAC[G/T]CTCCGCCCCAAGGAA | 83892 |
rs569342963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455760 | GCCAGATCTCTAGCA[A/G]CACTATGCAGAGCAA | 83892 |
rs569351705 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478898 | GGTGGTCATTAAACC[C/T]GGTGGCCCAGCTTTT | 83892 |
rs569429318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469090 | TGCCGATGGCCCCAC[A/G]GGGGAGGGTATTGTC | 83892 |
rs569451187 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475992 | CAACCCCACTTTTTT[G/T]GGGAGAAAACTAGGA | 83892 |
rs569477436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461988 | CTGTGCCCTGTTCCA[C/T]TCCTAACAATGCTGT | 83892 |
rs569594234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461240 | GCTTCCTTCAAACTG[C/T]CACATTAACAGAGCC | 83892 |
rs569656581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467798 | AGAAAAACATCTCAT[A/T]GCAGGGATTTAGAAG | 83892 |
rs569894569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475138 | CATTGGGATCAGTGG[C/T]TCCCAACCCTGGCTA | 83892 |
rs569916537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460116 | CTACGAAAACCCAAA[A/G]GGATGCTTCTGATGC | 83892 |
rs570032133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466933 | GACCCAAGGGTGCAT[C/T]TGAGGCAACATGCAG | 83892 |
rs570096018 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476703 | GCTCTCTCGATTTCT[C/T]TCCCTCACTGGGCCG | 83892 |
rs570142918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109466295 | CTCAGAACAAAAGCC[A/G]TAATTGACAGTTCCC | 83892 |
rs570331098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460543 | ACATCTCAGTCAGAC[A/C]GAAACTGCCCCCATT | 83892 |
rs570341876 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456547 | TGGCAGACACGCCCC[C/G]CAAAAGACAGCCCTG | 83892 |
rs570399376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468283 | CCTCACCAGTGGGTA[A/G]CCCAAGCCTCAGCCC | 83892 |
rs570405357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455879 | AGAGTCCAGCCCAGT[A/C]AGGGAGTCAAGCATG | 83892 |
rs570421743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462083 | GCCAGCAAAAGTTGA[C/G]AGCAGCAAACGCATC | 83892 |
rs570498296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474615 | ACTATTCTAAAAAGC[A/G]CTGTACCCCTTATTT | 83892 |
rs570509631 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475193 | AAAACATGATGCCAG[C/G]CCAGGCACAGTGGCT | 83892 |
rs570664695 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109468895 | CTGACCTCGTGATCC[A/G]CCCGCCTCAGCTTCC | 83892 |
rs570808236 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478378 | TTTTGGATATACATG[A/G]ATTCAGATTCAAAAG | 83892 |
rs570889888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461004 | CCTACTGGCTGGACA[C/T]AACCATAACCCCAGG | 83892 |
rs570930285 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109467059 | CAGCCCAGGCCTTCA[C/T]GAGGGCCCCCACCAG | 83892 |
rs570952911 | snp | A/G | 5.13738e-05 | 0.00506797 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460591 | GAGGAAGGCAGGTAG[A/G]CTTGGTGCCTCTCCA | 83892 |
rs571261528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452572 | AGGCACACTCTACCC[C/T]GTCTTCCTCACTGAC | 83892 |
rs571314732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453288 | TTGAACTACTGGGCT[C/T]AAATGATTCTCCCAC | 83892 |
rs571588705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465198 | CAGAATATGGCTCCG[A/G]CAGCGGCTGTATGCT | 83892 |
rs571614359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464815 | AAGGTTGGACAGTGC[C/G]AAGGGTTGGCAAAAA | 83892 |
rs571723203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109472518 | TTTTCACTTAAAAAA[A/G]AAAAGGCAGGTAGGA | 83892 |
rs571758349 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477444 | TAGGGGCCAGTTTTC[C/T]TTCCAGCCTCCCCGG | 83892 |
rs571897325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465682 | CTGGTGGCACAGGTG[A/G]GTTTGTTGTATTATT | 83892 |
rs571985983 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465748 | ACCAAAGAGCATTGT[A/C]ATGGAAGGCAGAAGG | 83892 |
rs572071990 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451440 | ACAATCAATTTGCCT[C/T]GTCAAGCAATACCAA | 83892 |
rs572243825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453687 | GCATGGTTACAGAAA[A/G]TGGGTGGCAAAGGGG | 83892 |
rs572294299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478540 | AATCCTAGCACTTTG[G/T]GAGGCCGAGGCGGGC | 83892 |
rs572406512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452059 | CTTCTTAAAGGTACA[A/G]TTTCTCATCATTTTA | 83892 |
rs572453418 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479303 | CATGCTTTTAGATAT[C/T]CTATATTAATATTTT | 83892 |
rs572489571 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464856 | TGCAGGGAGTAGAAG[C/T]TGCCATAACCACTCC | 83892 |
rs572495464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464337 | CTTAGTTGTAAGAGG[C/T]TGCCCCGCACATTGT | 83892 |
rs572564875 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476906 | ATGTCCGTTTTCAAT[A/T]GATATCTCTTTGTTC | 83892 |
rs572776348 | snp | A/G | 8.41956e-05 | 0.00648774 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451694 | GTCCAGGTGGTGGGA[A/G]CGCCCCGCCGCCCCG | 83892 |
rs572863270 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476044 | TGACTCCCAACTCCT[A/T]TGCCCCTTTCATTAC | 83892 |
rs572892759 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450580 | TGGTGTGAGGGTGTC[C/G]CTGCCTGGATGCCAG | 83892 |
rs572912529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470499 | GCCTGGAAAGTGAGA[C/T]TGGTATCCGGCACAT | 83892 |
rs572977957 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450338 | AGGCGCTGCGCCCAG[C/T]CGGGCTCCAGCAGGG | 83892 |
rs573096712 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477662 | CAAGATGGCGGTAGT[C/G]CGTCGGCTGCTGCCC | 83892 |
rs573201906 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477148 | AATGCCTCTCCACTA[G/T]CGTGACTGCCCCTCA | 83892 |
rs573424227 | in-del | -/TCTT | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453055 | GGGAGTCCAAGGGCC[-/TCTT]TCTTTTCTCTTTTTT | 83892 |
rs573530397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462311 | TTGTTAAAAGAACGG[A/T]CTCCACCCTCCAGCG | 83892 |
rs573548033 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477707 | CTCGGGTGTTTTGGG[C/T]TGAGACAGTGGCAGC | 83892 |
rs573562034 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468087 | TTCCACAGATACTCT[C/T]GGGCCATGTGGGGTG | 83892 |
rs573656078 | snp | C/T | | | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448582 | GGCAGAACGTGGGGG[C/T]CCTGCCTTTGTTGTA | 83892 |
rs573676047 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454881 | TAAATCCCCTTGTTC[C/T]TTATTAAGCTCTAAA | 83892 |
rs573873647 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463281 | GAACAGGCAGACCGT[A/G]ACACTGGGCTCCGGC | 83892 |
rs574075423 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463279 | ATGAACAGGCAGACC[A/G]TGACACTGGGCTCCG | 83892 |
rs574235869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457416 | ATATTGTGAATATAA[C/T]AATAACTGTACACTC | 83892 |
rs574285673 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475555 | AATCAGTATCTCAGA[C/G]ATGCGGAGGGGTGGC | 83892 |
rs574292105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109463594 | GCCTGGGATCCCAGA[C/T]CCATTAGGCAAGGCT | 83892 |
rs574326502 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455922 | CCAGCAAGGTAGGGA[A/G]CTAAAGGAATGCCAG | 83892 |
rs574404352 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449330 | ACTCAAAACTACAAG[G/T]GCAAAGTTGGGTAGA | 83892 |
rs574460385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455462 | TTGCTTTTTGTTCGA[A/G]GTCAGCTACAGAATC | 83892 |
rs574858098 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478472 | AAGTCGTGTTTCCTA[C/T]TCTTTAAATAAAAAT | 83892 |
rs575098937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474650 | TACCATTAACTCCAC[A/G]GTCTTGGCCCAGTGA | 83892 |
rs575150059 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450189 | CATCCATCACCTGAC[A/G]CACATTCACATCTCC | 83892 |
rs575280693 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449400 | CACAGCAAATCAAAT[A/T]GTTCCACAAACTCAT | 83892 |
rs575304347 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477094 | TCTCCACCCAAAGCC[A/C]TTCCCCCACCCCGGG | 83892 |
rs575415880 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476286 | ATTTTGCACAAAATG[A/G]AGCGGACTAGTCAAC | 83892 |
rs575418391 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450710 | ATCCCAGGGAGGGGT[A/G]GTTTATGAGCTATGC | 83892 |
rs575552569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109474847 | TACAGTAGGAAAAAA[C/T]GCACCAAATCCCTGA | 83892 |
rs575658058 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448651 | AAAAGAGCCAGAAAA[C/G]AGAAGCATTTTATGA | 83892 |
rs575864023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109462235 | TGCCAGGAAAGTTTG[A/G]TAACAGGGCCGTTTC | 83892 |
rs575891948 | in-del | -/CATCAGCTT | 0.00557542 | 0.0525036 | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448264 | TCAAGTCTCAGCTTC[-/CATCAGCTT]CAAGAACCTATCGAT | 83892 |
rs575893997 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109475319 | CCACAAAAAAATTAA[A/T]AAAAAAAATTAACCG | 83892 |
rs575903463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460468 | TGTTCCAGGGAGGCC[C/T]CTCAGGGGTCACTCC | 83892 |
rs575964340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473864 | TCAGCTCACCGCAAC[A/G]TCTGCCTCCCAGGTT | 83892 |
rs576128274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455322 | GCTGATGGCCCTTGA[C/T]GTGGCGTGATGGCAC | 83892 |
rs576402088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109461412 | CCAAGACAGACCCCA[C/T]CCTCAGGCAGCTCGG | 83892 |
rs576460495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109459226 | AAATTTTGATAGAAG[G/T]GTTGAAAAGGTGAAA | 83892 |
rs576501132 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458747 | AGCTCCTTCCCCTTC[C/T]AGATCCCCAAAGGCA | 83892 |
rs576516545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460860 | CCTCTTGTGGGAGGC[C/T]CTGAGCAGAGCTGGG | 83892 |
rs576643870 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476513 | ACAGCTGAGAGACAG[A/T]TCTTGAAACATCCTC | 83892 |
rs576651219 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465447 | AATGCTGGTTGCACA[C/T]TAGAATCACCCAGAG | 83892 |
rs576730207 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109455350 | CACAGGGGAAATCAC[C/T]ACACTATAATTCTGT | 83892 |
rs576991764 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449200 | TTCCTTGTATACTCA[A/G]TAACAGAGCTTGGAC | 83892 |
rs577059320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448690 | TTACATGTCGCCAAC[A/G]TTTGTACAACATACA | 83892 |
rs577175530 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479010 | ACAAGAGTCTGAATC[C/G]TGCCTCTTAGTTATT | 83892 |
rs577271843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109452828 | GAGAGGCTGGGAGGA[A/G]ATCCTGGTTTTCTTT | 83892 |
rs577329641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473980 | GAGATGGGGTTTCAC[C/T]ATGTTGGTCAGGCTG | 83892 |
rs577391896 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KCTD10 | GRCh38.p7 | 12:109473380 | CAGGGCCAAAAGCCT[C/T]ACCTCCCTCACAGGG | 83892 |
rs577409448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109453650 | CTTTTTCTATCTTCA[C/T]GCTCCTGGGCCCAAA | 83892 |
rs577524027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471326 | CTGGCCAACTCTCCC[C/T]AACTCCATGGCACCC | 83892 |
rs577550823 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473565 | AATGAGACTACAGAT[G/T]AGGCAACAAAAGCTC | 83892 |
rs577584952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464139 | GAACCTTCACTGACC[C/T]CTCTTTGCCATCCTA | 83892 |
rs577730673 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464981 | AAGATCTTAAAGCCA[C/T]AGCCCTTGAGATGGC | 83892 |
rs577987259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465549 | TGACTCCCTCTGTAG[C/T]CAAGCTTGAGATCCA | 83892 |
rs578031667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109465094 | GGCTGGGCAGCATCG[C/T]ACAGAGAAACTCCCA | 83892 |
rs578036738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD10 | GRCh38.p7 | 12:109470413 | AGCAAGATCCCACTA[C/T]CATCTCCCTGATAGC | 83892 |
rs578058835 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457895 | TTATCAGGCCTCACT[A/C]AGGCAATTATACATG | 83892 |
rs578068691 | snp | G/T | 1.86496e-05 | 0.0030536 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469786 | TGACTGCTTTCAGCC[G/T]GTGGATTCAATCTGG | 83892 |
rs578101080 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD10 | GRCh38.p7 | 12:109451889 | GACTTTAAGCAGGGC[A/C]GCCAGGCTAAATCAG | 83892 |
rs578128186 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458782 | GCCAGGCCTAGACCC[A/G]TCAGGCAGGAGGAGA | 83892 |
rs745326687 | snp | A/G | 0.000186654 | 0.00965879 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464803 | TGCAATAATTAAAAG[A/G]TTGGACAGTGCCAAG | 83892 |
rs745329737 | snp | C/G | 1.76699e-05 | 0.00297231 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451560 | CGGCAGGGAGTGGGG[C/G]CGGTGAGAGGAGGGC | 83892 |
rs745443029 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109456719 | TTTAAAGATCTTGAG[C/T]AACCTGATTAAATCC | 83892 |
rs745469763 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476225 | GGTGGGACCAGAGTT[-/TG]AGAACCACTGGTTTA | 83892 |
rs745556709 | in-del | -/CTCTCCTGAAG | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466693 | TGGATGCCAGGTCCC[-/CTCTCCTGAAG]CAATCACTTTCTTGG | 83892 |
rs745641288 | snp | C/T | 3.3006e-05 | 0.00406226 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457581 | CCTGGCTGGTGTGAG[C/T]GGAGGTTTTCCTAGT | 83892 |
rs745684347 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472915 | TGTACAGTTTGATGT[A/G]TTTTGGTCAATACTT | 83892 |
rs745756189 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462325 | GTCTCCACCCTCCAG[C/T]GGCTTCCACTTCCTA | 83892 |
rs745922438 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452618 | TGGGATGCACACAGC[A/G]GCTAACTGTGGACTC | 83892 |
rs746102887 | snp | A/C | 1.64939e-05 | 0.0028717 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469545 | GCACTTCCATGCGCC[A/C]GCTGAACATGGCCTT | 83892 |
rs746147287 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467528 | ACAGAAGGCTGAGGC[A/G]GGAGGATTGCTTGAA | 83892 |
rs746200845 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468158 | GTGTGAGATGGCAGC[A/T]TTGGGGCTCCAACCT | 83892 |
rs746279267 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457778 | GGCCCTGCCCTGCAT[C/T]AGAAGAGGCAGACAA | 83892 |
rs746290732 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448684 | TTTATTTTACATGTC[A/G]CCAACGTTTGTACAA | 83892 |
rs746409249 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474405 | TCTTCTCTCCATCTC[C/G]CCTGAATATAATGTT | 83892 |
rs746443007 | snp | C/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458046 | TGAGGTGATCACAGG[C/G]ACCTTGCAGAAAGGC | 83892 |
rs746468091 | snp | C/T | 1.69922e-05 | 0.00291476 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451695 | TCCAGGTGGTGGGAG[C/T]GCCCCGCCGCCCCGC | 83892 |
rs746483758 | snp | C/G | | | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475440 | CAAGATAATACCAGT[C/G]CACTCTCCAGCCTGG | 83892 |
rs746503433 | in-del | -/T/TTT/TTTTTTTTTT | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452845 | CCTGGTTTTCTTTCC[-/T/TTT/TTTTTTTTTT]TTTTTTTTTAAAAGA | 83892 |
rs746549022 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449317 | CAGAGAGACAAAGAC[C/T]CAAAACTACAAGTGC | 83892 |
rs746703319 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465092 | AAGGCTGGGCAGCAT[C/T]GCACAGAGAAACTCC | 83892 |
rs746826604 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455321 | AGCTGATGGCCCTTG[A/G]CGTGGCGTGATGGCA | 83892 |
rs746975410 | snp | C/T | 1.65679e-05 | 0.00287814 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469516 | GTGGGTGAGCTTACC[C/T]TCACTGTCGGTGAGC | 83892 |
rs747003080 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471407 | AGAGAAAGAACGGCC[C/T]CCTGGAAAGAAATGT | 83892 |
rs747021710 | snp | A/C/G | 6.6755e-05 | 0.00577699 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451649 | GTGGATCCTCCGCAC[A/C/G]CGCTCGATCCGCTCC | 83892 |
rs747033208 | snp | A/G | 4.94629e-05 | 0.00497283 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469667 | GTGCCCTTGAAGGAA[A/G]TGGTGCGGGTAGCAG | 83892 |
rs747040862 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450659 | ACTTAGAAAGTTAGC[C/G]CAGCTTCATGGGGAA | 83892 |
rs747070010 | in-del | -/CGCCCCGC | 3.368e-05 | 0.00410352 | frameshift-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451694 | TCCAGGTGGTGGGAG[-/CGCCCCGC]CGCCCCGCCGCCCCG | 83892 |
rs747086083 | snp | A/G | 1.67801e-05 | 0.00289651 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469737 | TCTCTTCCTGCCAGT[A/G]GAGAGGATACAGGGT | 83892 |
rs747252985 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456234 | CAATAACATCCTTTA[G/T]GAACAGGACCCTTCC | 83892 |
rs747271863 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451350 | GCCTGGCTCCAAAGA[A/G]TCTCAGATTCTCATG | 83892 |
rs747384843 | snp | C/T | 1.70263e-05 | 0.00291768 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460609 | TGGTGCCTCTCCACC[C/T]ATATGGGAAGAAAGG | 83892 |
rs747613147 | snp | C/G | 3.29658e-05 | 0.00405978 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458068 | CAGAAAGGCTCATAA[C/G]TATCTTTGTTCTGCT | 83892 |
rs747630749 | snp | A/G | | | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448602 | CCTTTGTTGTAAACC[A/G]ATTTTAGGGGCCTGG | 83892 |
rs747810858 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109475333 | AAAAAAAAAATTAAC[C/T]GGTCATGGTGGCACA | 83892 |
rs747887218 | snp | C/T | 1.66394e-05 | 0.00288434 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460644 | TGCCTACTTGTAGGG[C/T]CGCCTGGCACTCTTC | 83892 |
rs747890164 | snp | C/T | 1.65083e-05 | 0.00287296 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469534 | ACTGTCGGTGAGCAC[C/T]TCCATGCGCCCGCTG | 83892 |
rs747919641 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464270 | TTCCTGATCAGAATC[C/G]CTAGGGCAGGGTCTC | 83892 |
rs747941598 | snp | A/G | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469646 | ACGTATTTGGAGCTG[A/G]GGCTCGTGCCCTTGA | 83892 |
rs747989469 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453138 | CAATCATAGCTCACT[A/G]CAGCCTTGAACGCCT | 83892 |
rs748145808 | snp | A/G | 1.91338e-05 | 0.00309298 | intron-variant | KCTD10 | GRCh38.p7 | 12:109451831 | GTGTTCCCACAGTAT[A/G]CAGGGCAGGTAAGTT | 83892 |
rs748153144 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478761 | ACTCCAGCCTGGGCA[A/G]CAAAGTGAGACTCCG | 83892 |
rs748162863 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109460174 | TAAAGGGGTGTTGGC[C/G]ATGTCTAGAAGCATT | 83892 |
rs748196046 | snp | A/G | 9.88321e-05 | 0.00702896 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456250 | GAACAGGACCCTTCC[A/G]TTAAAGCGCAGAGAC | 83892 |
rs748196238 | snp | C/G | 1.69186e-05 | 0.00290844 | upstream-variant-2KB, splice-donor-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477259 | GCACCGCCCTCCCTA[C/G]CATGAAAAGTCGGAG | 83892 |
rs748249164 | snp | A/G | 8.2464e-05 | 0.00642069 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457594 | AGTGGAGGTTTTCCT[A/G]GTAAATGGAGCTGTC | 83892 |
rs748422400 | snp | A/G | 3.29658e-05 | 0.00405978 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460716 | GCTCCTCGATCTCCC[A/G]GCGGCTCTCGGGTAA | 83892 |
rs748430002 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470647 | TCCCATTGAACATCA[A/G]CAGTTTTTCACAGCA | 83892 |
rs748467518 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478336 | GAGCCCTGGATCTTG[A/T]TTGTTTTACTTAGTG | 83892 |
rs748518199 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465203 | TATGGCTCCGGCAGC[A/G]GCTGTATGCTTCTAG | 83892 |
rs748646000 | in-del | -/GAGCATTTGATACGGT | 1.65176e-05 | 0.00287376 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456322 | AGAATTGCTGCAAAA[-/GAGCATTTGATACGGT]GACCACAAGCTGGTA | 83892 |
rs748649242 | in-del | -/GA | 1.70478e-05 | 0.00291952 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477301 | CTCCAAACCCGGACT[-/GA]GAGAGGCAGGAAACA | 83892 |
rs748758257 | snp | C/T | 1.65913e-05 | 0.00288017 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460647 | CTACTTGTAGGGCCG[C/T]CTGGCACTCTTCCAC | 83892 |
rs748826758 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109456870 | GTTTGGCAGGTCCTC[G/T]AATGATTAAACATAG | 83892 |
rs748976724 | in-del | -/A | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458429 | GACTGCAGAGGAATT[-/A]AAAAAAAAAAGCATA | 83892 |
rs749001280 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473067 | GCTGGAAGACAGCTA[C/T]AGTTATTTCCATTTT | 83892 |
rs749023112 | snp | C/T | 1.67013e-05 | 0.0028897 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451751 | AGGTCCCCGGCCATC[C/T]TGGGCCTCATACAGC | 83892 |
rs749074673 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462686 | TCTTCCCACTCCAGC[C/T]AAGAGTGGCCAGGCA | 83892 |
rs749093375 | snp | C/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456180 | CTTCAGCAATCTTCC[C/G]GCCCTGACCATAAAA | 83892 |
rs749336054 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468449 | GAAACAGGAAGGCGG[G/T]GTCAAGGTCAAGCCA | 83892 |
rs749347472 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453733 | CAGCTTTCTGGCTGG[C/T]CGATCAGAGAAGGGG | 83892 |
rs749348647 | snp | G/T | 1.6483e-05 | 0.00287076 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457729 | GTTACTTGGCAGGCA[G/T]ATGCAATGAACTACT | 83892 |
rs749696535 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448776 | TAATGACACACTTAA[C/T]TGTTACAGTGACTTT | 83892 |
rs749754231 | snp | A/G | 1.69582e-05 | 0.00291184 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477272 | TACCATGAAAAGTCG[A/G]AGGACGCAGGAGTCT | 83892 |
rs749794174 | snp | C/G | | | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475572 | TGCGGAGGGGTGGCT[C/G]ATCAGTCACTAGTGT | 83892 |
rs749845957 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477183 | ACCCCCTCCTCTCGG[C/T]CCCTTCTTATACTCT | 83892 |
rs749899539 | snp | G/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478182 | CAGGTTTCACAGAGG[G/T]TGTGAATACGTTTTA | 83892 |
rs749965974 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451218 | ACTGAACCCTTAAGG[A/G]AGTGTCACCCAAAAA | 83892 |
rs750145335 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467167 | ACTAGCCATGGACAG[C/T]AGACAGTAAGAGGCA | 83892 |
rs750166397 | snp | G/T | 3.353e-05 | 0.00409437 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451685 | CTCGTCCTCGTCCAG[G/T]TGGTGGGAGCGCCCC | 83892 |
rs750184408 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471156 | ATTGTCTAGCTTTTC[C/T]AGATTTTCTATAATG | 83892 |
rs750204348 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457686 | CTTCACGGCTGGCTG[C/T]GGGTTGTTTTAAAAG | 83892 |
rs750209617 | snp | A/C | 5.11356e-05 | 0.0050562 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477295 | AGGAGTCTCCAAACC[A/C]GGACTGAGAGAGGCA | 83892 |
rs750216384 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467493 | TGTGTTTGGTGGTGC[A/G]TGCCTGTATTCCCAG | 83892 |
rs750237798 | in-del | -/A | 1.66776e-05 | 0.00288765 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460809 | GAGGATCCAGCCTGC[-/A]AGAGGGAGGAGGCAG | 83892 |
rs750305903 | snp | G/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109457998 | CCAACATACCTTATT[G/T]GAAGTCGCTATAAGT | 83892 |
rs750384217 | snp | C/G | | | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448493 | AGACTTCCTTTTGGT[C/G]TTTGAATTCAAACAA | 83892 |
rs750388118 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473906 | CCTGCCTCACCCTCC[C/T]GAGTAGCTGGGATTA | 83892 |
rs750473933 | in-del | -/TA | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109469015 | GTGTGTGTGTGTGTG[-/TA]TATCTATCTATCTAT | 83892 |
rs750710466 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453667 | CTCCTGGGCCCAAAA[C/T]ACAGGCATGGTTACA | 83892 |
rs750790041 | snp | A/G | 1.6912e-05 | 0.00290787 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451787 | GTTCAGGGTCTCCTC[A/G]TAAATCCGGGCTTCG | 83892 |
rs750890033 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459859 | GAGGGGTATGGTGGT[A/G]TTTTGATGTTAACCT | 83892 |
rs751042686 | snp | A/C | 3.29527e-05 | 0.00405898 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469632 | CCACATTCAGCTTCA[A/C]GTATTTGGAGCTGGG | 83892 |
rs751097809 | snp | A/G | 5.20513e-05 | 0.00510127 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451802 | ATAAATCCGGGCTTC[A/G]GGAAACTCCACCTGT | 83892 |
rs751241555 | snp | C/T | 1.65162e-05 | 0.00287365 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456113 | TGTCCTCTCGAGGCT[C/T]TTACCTTGGTCTGTT | 83892 |
rs751273435 | snp | C/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478098 | TACTGTTCGCTCGCT[C/G]TGTGACCTTGGGTGA | 83892 |
rs751372905 | snp | A/G | 0.000230624 | 0.0107359 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458008 | TTATTTGAAGTCGCT[A/G]TAAGTTTTTGTTCTT | 83892 |
rs751432104 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464388 | TGGCCTCTACTCACT[A/T]GACGCCAGGAGCACC | 83892 |
rs751570168 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109460876 | CTGAGCAGAGCTGGG[A/G]TGTCTCTCGGCTCCC | 83892 |
rs751605030 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472690 | ACACCAGCATCACCA[C/T]GAACACGTAATATGT | 83892 |
rs751657819 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473667 | GTTTTGGCAGCATTC[A/G]TGTCCTTGAGCCCAA | 83892 |
rs751738092 | in-del | -/AAGTCTTTGTCAAGACCCCATCTTGGGAGGACAAGGGTC | 1.64781e-05 | 0.00287033 | cds-indel, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469587 | CTGCTTGGTCAGCGT[lengthTooLong]CTGCATGGTGGTATA | 83892 |
rs751828990 | in-del | -/AT | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472224 | CATAGCTTAAAACAC[-/AT]ATTGCACAGCTGTAC | 83892 |
rs751850161 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109463217 | TGCTTGGGAAGACCC[A/G]GGGCCCTGAAATCAA | 83892 |
rs751886434 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452447 | CTCATTGCCCTTCAG[A/G]GTTAAGGTGTGATGA | 83892 |
rs751940013 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109463870 | AGCACTCAAAAGCAG[C/T]TATGGGTCTTTAACA | 83892 |
rs752121457 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459573 | TCAGCCGTATTTACA[C/T]GTCATGACGTAAACT | 83892 |
rs752171714 | snp | A/C | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456158 | TAGACGATGGAGGTA[A/C]AACAGACTTCAGCAA | 83892 |
rs752173188 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467925 | AAGGCGAGGCCTTTC[A/G]AGGAGAAGAGCCTCA | 83892 |
rs752173846 | snp | C/T | 1.691e-05 | 0.0029077 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477217 | GCTGCCCAGCTCCCT[C/T]GGCCGCCCTCAACCC | 83892 |
rs752277411 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458559 | AGGAGAGGGGGAAAG[A/C]TGAAACCAGTGGGCG | 83892 |
rs752375730 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467730 | GTCACAGTTTGCAGT[A/G]TCAAAATGACACTGT | 83892 |
rs752406823 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449046 | ACGACACACCAAAGC[C/T]GTTCCAATTTGTAAA | 83892 |
rs752560528 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464942 | CTGGGAATAAACTCT[A/G]GGGCTGAGCTCCCAA | 83892 |
rs752611722 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465613 | AGAGGGACAAACAGA[A/G]AAGGCACAAAGGGGC | 83892 |
rs752693063 | snp | A/C/G | 1.6546e-05 | 0.00287624 | synonymous-codon, missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469708 | CGCTGAGCTCACCAC[A/C/G]CTTTCTCCTGACATC | 83892 |
rs752697805 | snp | A/G | 1.67312e-05 | 0.00289229 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451666 | GCTCGATCCGCTCCC[A/G]CTCCTCGTCCTCGTC | 83892 |
rs752750449 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455134 | TCACCCCCTGCCCCC[A/G]GGATCTTTGAAAGCA | 83892 |
rs752981174 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472384 | AGTATCACTGTCCTC[C/T]ACATCCTGTCCCACT | 83892 |
rs753027148 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462040 | AGACTGGGCCCTACT[A/G]ATCCTGGGCCTTGGA | 83892 |
rs753028683 | snp | C/G | 1.64808e-05 | 0.00287057 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457721 | AGAAGAGAGTTACTT[C/G]GCAGGCAGATGCAAT | 83892 |
rs753123537 | snp | A/G | 1.6727e-05 | 0.00289193 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460815 | TCCAGCCTGCAGAGG[A/G]AGGAGGCAGGGGCTG | 83892 |
rs753215007 | snp | A/G | 1.68932e-05 | 0.00290625 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469489 | TAACGCATGGCCAGA[A/G]GCAGGCACATGGTGG | 83892 |
rs753358527 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467298 | ACAGTATCCACCCCT[C/T]GAAGGGTTATGGTGA | 83892 |
rs753366775 | snp | G/T | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109457658 | ATTTGTTGTTACTTC[G/T]GTTGTAGAGCAACTT | 83892 |
rs753554950 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458371 | CCCTTGACGTGGCAG[C/T]AGAAACGTGTTTTAA | 83892 |
rs753585725 | snp | C/T | 1.68932e-05 | 0.00290625 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477226 | CTCCCTCGGCCGCCC[C/T]CAACCCCTAGTCCAT | 83892 |
rs753606280 | snp | A/G | 1.70635e-05 | 0.00292087 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460851 | ATGGGCCCTCCTCTT[A/G]TGGGAGGCCCTGAGC | 83892 |
rs753625590 | snp | C/G | 1.66394e-05 | 0.00288434 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469723 | ACTTTCTCCTGACAT[C/G]TCTTCCTGCCAGTGG | 83892 |
rs753649287 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459390 | GATGAAACAGAACCT[C/G]TGATGTGTCTGAACA | 83892 |
rs753651732 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464129 | CACCTCCAGGGAACC[C/T]TCACTGACCTCTCTT | 83892 |
rs753742129 | in-del | -/ACCCATA | 1.7072e-05 | 0.00292159 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460606 | GCTTGGTGCCTCTCC[-/ACCCATA]TGGGAAGAAAGGGTG | 83892 |
rs753837616 | snp | C/T | 2.03048e-05 | 0.00318622 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456393 | TTCTACACGCAGGGC[C/T]CTACTGAGCCCACTT | 83892 |
rs753877578 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458029 | TTTTGTTCTTCCTTG[A/G]ATGAGGTGATCACAG | 83892 |
rs753892158 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476437 | TCTTTGGTCATCTCT[A/T]CCCAGGGACAATGAG | 83892 |
rs753923878 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454793 | CACTAACTAGCTTTA[C/T]AAACACAAGAACATG | 83892 |
rs754123482 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471184 | ATGAATGGGTACTAC[A/C]ACTATAACTGGTAAA | 83892 |
rs754157928 | snp | C/T | 1.67612e-05 | 0.00289488 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458115 | TCAGCCTAGGAGGCC[C/T]GCCTAGCACTGCATT | 83892 |
rs754222054 | snp | C/T | 1.68468e-05 | 0.00290226 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469495 | ATGGCCAGAGGCAGG[C/T]ACATGGTGGGTGAGC | 83892 |
rs754231823 | snp | A/G | 5.01316e-05 | 0.00500632 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451755 | CCCCGGCCATCCTGG[A/G]CCTCATACAGCAAAA | 83892 |
rs754232358 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109460961 | ACCTGCCCACTAAGG[A/G]CTGAGGAAGCCCCCA | 83892 |
rs754280878 | snp | A/G | | | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475412 | AGGCAGGGAAGGTGA[A/G]GCTTTAGTGAGCCAA | 83892 |
rs754381374 | snp | A/C | 1.75277e-05 | 0.00296033 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451807 | TCCGGGCTTCGGGAA[A/C]CTCCACCTGTGTTCC | 83892 |
rs754461630 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461870 | AGGTGGAAAATGCCA[A/G]TGCGCAGGGCCGTGA | 83892 |
rs754482512 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467633 | TCTCAAAAAAAGAGA[A/C]AAGAATGCCCCATAA | 83892 |
rs754600324 | in-del | -/TTTT | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453068 | CCTCTTTCTTTTCTC[-/TTTT]TTGTTTTGAGAGGGA | 83892 |
rs754649804 | snp | A/G | 4.94303e-05 | 0.00497119 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456142 | TTTCTTCTCAGTGGC[A/G]TAGACGATGGAGGTA | 83892 |
rs754885613 | snp | C/T | 1.65422e-05 | 0.0028759 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469524 | GCTTACCTTCACTGT[C/T]GGTGAGCACTTCCAT | 83892 |
rs754905537 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453812 | AGCCTGTGAAGTTGT[A/G]TATGAACTCCTAGAC | 83892 |
rs754997156 | snp | C/T | 1.72228e-05 | 0.00293447 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451585 | GAGGGCGGCTCGGTC[C/T]CTTGCCTGCTCACTG | 83892 |
rs755004297 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464850 | GACTTCTGCAGGGAG[C/T]AGAAGTTGCCATAAC | 83892 |
rs755040324 | in-del | -/T | 1.93721e-05 | 0.00311219 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469799 | CCTGTGGATTCAATC[-/T]GGCCTCCAGATGTGT | 83892 |
rs755134591 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470162 | ACAGCCTAAAGCACT[A/G]CCCAGGTCTCTTTAC | 83892 |
rs755242121 | in-del | -/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473782 | CTACTGGAATCCTGC[-/T]TTTTTTTTTTTTTTT | 83892 |
rs755275676 | in-del | -/GTG | | | cds-indel, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449665 | CAGGAGGCACAAGTT[-/GTG]GTAAGTGGAGATGGT | 83892 |
rs755281867 | snp | A/G | 1.71346e-05 | 0.00292694 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477310 | CGGACTGAGAGAGGC[A/G]GGAAACACCCAGCTC | 83892 |
rs755427857 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109460966 | CCCACTAAGGGCTGA[A/G]GAAGCCCCCACAGCC | 83892 |
rs755445008 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461936 | CACCTTCCTCCCCAC[C/T]TTGGGAGAAGGGCCA | 83892 |
rs755494746 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451221 | GAACCCTTAAGGGAG[C/T]GTCACCCAAAAAGCC | 83892 |
rs755544851 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450540 | GGGGGTCTGTGTTTA[C/T]AGCAGGGAAGCTCCC | 83892 |
rs755556608 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466150 | TTCTCAGAAAAGCCA[A/T]CCCTTGGGGGTAGTG | 83892 |
rs755564852 | snp | A/G | 9.69904e-05 | 0.00696317 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456386 | TGGGCCCTTCTACAC[A/G]CAGGGCCCTACTGAG | 83892 |
rs755634774 | in-del | -/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464590 | GAGAAGATATTTGCA[-/G]CACTGGACCCCAAAG | 83892 |
rs755723887 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457387 | CTCACAACTTGTGAA[C/T]ATATAAAAACCACAT | 83892 |
rs755802412 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109456763 | CAAGTTCCTGAGTTA[C/G]AGCCACATGTTTTCA | 83892 |
rs755814378 | snp | C/G | 1.6483e-05 | 0.00287076 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460717 | CTCCTCGATCTCCCG[C/G]CGGCTCTCGGGTAAA | 83892 |
rs755875489 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457109 | TCATGCTACAACATG[A/G]ATAAACCTTGAAAAC | 83892 |
rs755931524 | snp | A/C | | | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448515 | TTCAAACAAACACTA[A/C]AGAAACATGACTGTC | 83892 |
rs755939717 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450857 | AAAGTTCTGCTCCTA[C/T]GCAGACATATGGGGT | 83892 |
rs756026927 | snp | C/G | 1.65745e-05 | 0.00287871 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469715 | CTCACCACACTTTCT[C/G]CTGACATCTCTTCCT | 83892 |
rs756045761 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109463349 | TCATACTTTGGACAA[A/G]TAAGGGCAAGGGAGC | 83892 |
rs756436392 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458010 | ATTTGAAGTCGCTAT[A/G]AGTTTTTGTTCTTCC | 83892 |
rs756437155 | snp | C/T | 3.5529e-05 | 0.00421465 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451545 | GATCTGGGTGTAGCA[C/T]GGCAGGGAGTGGGGG | 83892 |
rs756533673 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449329 | GACTCAAAACTACAA[A/G]TGCAAAGTTGGGTAG | 83892 |
rs756566223 | snp | C/T | 5.12711e-05 | 0.0050629 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451591 | GGCTCGGTCTCTTGC[C/T]TGCTCACTGGTGGAG | 83892 |
rs756646835 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109460912 | CTCCCAGCGGAGAGC[A/G]GGACTGCCTGGAGAA | 83892 |
rs756699915 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459868 | GGTGGTGTTTTGATG[C/T]TAACCTTGCAGCACT | 83892 |
rs756840469 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450314 | TCACTGAGAACACCC[A/G]TCCTACATAGGCGCT | 83892 |
rs756885450 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454843 | CTAATCTAGAAACAG[G/T]TGGGATCAGACCATG | 83892 |
rs756894805 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465944 | GGGGGAAGTATTGTA[C/T]GAAGCAACAGGGATG | 83892 |
rs756909261 | in-del | -/TC | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452899 | TAAAATTTTAAGACT[-/TC]TCTCATTTTTAGAGC | 83892 |
rs756933591 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456187 | AATCTTCCGGCCCTG[A/G]CCATAAAAGGACCAG | 83892 |
rs756945408 | snp | A/G | 1.71543e-05 | 0.00292862 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460855 | GCCCTCCTCTTGTGG[A/G]AGGCCCTGAGCAGAG | 83892 |
rs757000390 | snp | A/G | 3.38266e-05 | 0.00411244 | stop-gained, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451600 | TCTTGCCTGCTCACT[A/G]GTGGAGGTGGGCCCG | 83892 |
rs757006162 | snp | A/T | 1.68986e-05 | 0.00290672 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477240 | CTCAACCCCTAGTCC[A/T]TGGGCACCGCCCTCC | 83892 |
rs757204887 | snp | C/T | 2.08305e-05 | 0.0032272 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456398 | CACGCAGGGCCCTAC[C/T]GAGCCCACTTTCTCC | 83892 |
rs757297003 | snp | G/T | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458034 | TTCTTCCTTGGATGA[G/T]GTGATCACAGGGACC | 83892 |
rs757389471 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462275 | CTGATGAAACAGCTC[A/G]GCCTAAAGTTCCTGG | 83892 |
rs757406585 | snp | G/T | 1.71334e-05 | 0.00292684 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460587 | AAATGAGGAAGGCAG[G/T]TAGGCTTGGTGCCTC | 83892 |
rs757428137 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452454 | CCCTTCAGGGTTAAG[G/T]TGTGATGAACAGGAA | 83892 |
rs757635793 | snp | C/T | 5.02079e-05 | 0.00501014 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451676 | CTCCCGCTCCTCGTC[C/T]TCGTCCAGGTGGTGG | 83892 |
rs757663719 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453589 | AGGAACCTTCTTTTC[C/T]GATGAGAAGAGCTGT | 83892 |
rs757712088 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462309 | TTTTGTTAAAAGAAC[A/G]GTCTCCACCCTCCAG | 83892 |
rs757779430 | snp | A/G | 6.66056e-05 | 0.00577047 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469504 | GGCAGGCACATGGTG[A/G]GTGAGCTTACCTTCA | 83892 |
rs757821988 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467983 | CTGAGCCCCTCCAGA[G/T]AGTGGGTAGGGTATG | 83892 |
rs757924866 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449249 | CACTCATGGCTATAA[C/T]GCAGCCGACAGAATT | 83892 |
rs757952804 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109469755 | GAGGATACAGGGTCA[C/T]GACATCAGGCCTGGT | 83892 |
rs757980094 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459581 | ATTTACACGTCATGA[C/T]GTAAACTCTGAATTT | 83892 |
rs758014451 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476530 | CTTGAAACATCCTCC[G/T]CTCCTTAGGCGTGGT | 83892 |
rs758047351 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109475370 | TAGTCCCAGCTACTC[A/G]GGAGACTGCGGTGGG | 83892 |
rs758053864 | snp | C/G | 3.29527e-05 | 0.00405898 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469624 | GGCTCCACCCACATT[C/G]AGCTTCACGTATTTG | 83892 |
rs758107652 | snp | A/G | 1.67897e-05 | 0.00289733 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451690 | CCTCGTCCAGGTGGT[A/G]GGAGCGCCCCGCCGC | 83892 |
rs758151959 | snp | G/T | 1.64808e-05 | 0.00287057 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457701 | TGGGTTGTTTTAAAA[G/T]AAGAAGAAGAGAGTT | 83892 |
rs758161281 | snp | A/C | 1.69663e-05 | 0.00291253 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451790 | CAGGGTCTCCTCATA[A/C]ATCCGGGCTTCGGGA | 83892 |
rs758410649 | snp | A/C/G | 3.2967e-05 | 0.00405988 | missense, synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460708 | TGCTAGCAGCTCCTC[A/C/G]ATCTCCCGGCGGCTC | 83892 |
rs758417143 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455214 | TATTCTTTTAGGATA[C/G]ATTTTGAATGCTTAG | 83892 |
rs758569166 | snp | C/T | 0.000893482 | 0.0211174 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469727 | TCTCCTGACATCTCT[C/T]CCTGCCAGTGGAGAG | 83892 |
rs758663565 | in-del | -/C | 1.70035e-05 | 0.00291572 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451596 | GGTCTCTTGCCTGCT[-/C]ACTGGTGGAGGTGGG | 83892 |
rs758663861 | in-del | -/AT | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109460049 | GGGCCAGACACAGAC[-/AT]GTGGTGTGGGGGAGG | 83892 |
rs758689089 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452351 | AGCAGTCTCTAAAGC[A/T]GTTTTTTGTACAGGG | 83892 |
rs758981532 | snp | A/G | 1.65209e-05 | 0.00287405 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469698 | CCGCTGGCACCGCTG[A/G]GCTCACCACACTTTC | 83892 |
rs759080663 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461770 | TAAAAAGAAGCCAGA[C/G]AGATGAGAGGGTGAA | 83892 |
rs759143048 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459420 | ACACCACTATGAGAC[C/T]GCTGAGAACGTGGGG | 83892 |
rs759152216 | snp | C/G | 1.78306e-05 | 0.00298579 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456369 | AAACTGCCATCATTT[C/G]CTGGGCCCTTCTACA | 83892 |
rs759224713 | in-del | -/AC | 1.6517e-05 | 0.00287372 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456416 | CCCACTTTCTCCACT[-/AC]ACCTCATTTCAACCT | 83892 |
rs759231007 | snp | A/G | 1.69761e-05 | 0.00291337 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477278 | GAAAAGTCGGAGGAC[A/G]CAGGAGTCTCCAAAC | 83892 |
rs759317003 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450089 | AACCGTTTGAAAATA[C/T]AAACTCGTTTTTGGA | 83892 |
rs759348023 | snp | A/C | 1.6666e-05 | 0.00288664 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458107 | ACATGCTTTCAGCCT[A/C]GGAGGCCTGCCTAGC | 83892 |
rs759544181 | snp | A/G | 3.30289e-05 | 0.00406366 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460665 | GGCACTCTTCCACCA[A/G]GCCTTGGACTAGGTA | 83892 |
rs759622898 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457117 | CAACATGGATAAACC[A/T]TGAAAACCTCTTAGG | 83892 |
rs759638320 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465440 | GGTTCTCAATGCTGG[C/T]TGCACACTAGAATCA | 83892 |
rs759754083 | snp | A/G | 1.672e-05 | 0.00289132 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451660 | GCACGCGCTCGATCC[A/G]CTCCCGCTCCTCGTC | 83892 |
rs759897917 | snp | C/T | 8.23961e-05 | 0.00641804 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457622 | GTCTTTCCCGGCTGA[C/T]GCCTTACCTGGTATA | 83892 |
rs760029667 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450357 | GCTCCAGCAGGGGCC[-/G]CCACCTGTGCCCCAC | 83892 |
rs760111726 | in-del | -/A | 1.6489e-05 | 0.00287128 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457734 | TTGGCAGGCAGATGC[-/A]ATGAACTACTAGCTT | 83892 |
rs760120966 | snp | A/G | 1.66963e-05 | 0.00288927 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460811 | AGGATCCAGCCTGCA[A/G]AGGGAGGAGGCAGGG | 83892 |
rs760171800 | snp | A/C/G | 0.000322596 | 0.012697 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477282 | AGTCGGAGGACGCAG[A/C/G]AGTCTCCAAACCCGG | 83892 |
rs760207401 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479069 | GTCTAGACTGGAGTA[A/G]ATGAGATCATGAATG | 83892 |
rs760301309 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452218 | GAGATCATTCTGTAT[C/T]AAGGAATTATAAATA | 83892 |
rs760314553 | snp | G/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109457638 | GCCTTACCTGGTATA[G/T]GAGTATTTGTTGTTA | 83892 |
rs760334274 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460744 | TAAAGGCACCGCCCC[A/G]TCTCGAAGGTAGTTG | 83892 |
rs760361202 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467795 | AGGAGAAAAACATCT[C/T]ATAGCAGGGATTTAG | 83892 |
rs760391344 | snp | A/G | 1.75167e-05 | 0.0029594 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451574 | GGCGGTGAGAGGAGG[A/G]CGGCTCGGTCTCTTG | 83892 |
rs760473254 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109448929 | CAGTGATCGCCCCAC[A/G]GGAGGGTGACAGAAT | 83892 |
rs760563449 | snp | C/T | 1.69006e-05 | 0.00290689 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477221 | CCCAGCTCCCTCGGC[C/T]GCCCTCAACCCCTAG | 83892 |
rs760781352 | snp | G/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476149 | AGAATGTCTGATTCA[G/T]TAGTCTCTGACAGGG | 83892 |
rs760812460 | snp | G/T | 2.27627e-05 | 0.00337355 | intron-variant | KCTD10 | GRCh38.p7 | 12:109451860 | TTATGGCCCACCCCC[G/T]CTGCCAACACCTGGA | 83892 |
rs760856370 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465294 | CACAAGCATAATGCT[A/G]CGTAAGCAAAAGCAA | 83892 |
rs760975776 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477467 | CTCCCCGGCCGGAGT[A/G]GGTTCCAGCTTTTCT | 83892 |
rs761124637 | snp | C/T | 3.29565e-05 | 0.00405921 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469585 | GTCCTGCTTGGTCAG[C/T]GTCTGCATGGTGGTA | 83892 |
rs761232968 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109456966 | TGCATGAATGTTCAT[A/G]ACAGCATTACACACA | 83892 |
rs761285998 | snp | C/T | 1.67388e-05 | 0.00289294 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451670 | GATCCGCTCCCGCTC[C/T]TCGTCCTCGTCCAGG | 83892 |
rs761287595 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471886 | GACAAAAAAGTACAT[A/G]AAGTATACTTCATGT | 83892 |
rs761403775 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462897 | CAGCTTGAGGCCTCT[A/G]TGCTACCCTACACCA | 83892 |
rs761470056 | snp | A/G | 1.6701e-05 | 0.00288968 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451656 | CTCCGCACGCGCTCG[A/G]TCCGCTCCCGCTCCT | 83892 |
rs761677759 | in-del | -/TGC | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466220 | CAGCCTCTCCCGACA[-/TGC]TGCTAAGACCTGCTT | 83892 |
rs761692943 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109457677 | GTAGAGCAACTTCAC[A/G]GCTGGCTGTGGGTTG | 83892 |
rs761980138 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109463918 | TATTGCTGGAAGCAG[A/G]GCAGCAGCGTCCAGA | 83892 |
rs761985355 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475875 | TTATAAGACAGCTAC[C/T]GCCAATTGCAACTTC | 83892 |
rs761992929 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459217 | CAGAAATGAAAATTT[C/T]GATAGAAGGGTTGAA | 83892 |
rs762024584 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448194 | TGTTTTTGTGCCCAG[C/G]AACATGCTGTAGGAA | 83892 |
rs762086331 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474739 | ACTTCACAGCTTCAG[A/G]GCCACAGGGAGGAAG | 83892 |
rs762119644 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464515 | GTAAGTGTAAAAAAG[C/T]GATTTAAACTCTGAG | 83892 |
rs762135350 | snp | C/T | 1.64885e-05 | 0.00287123 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460693 | GTAGTACTTGGCTTC[C/T]GCTAGCAGCTCCTCG | 83892 |
rs762206598 | snp | C/T | 3.29538e-05 | 0.00405904 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469604 | TGCATGGTGGTATAG[C/T]AGAGGGCTCCACCCA | 83892 |
rs762352858 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462346 | CCACTTCCTACTTCC[A/G]CACTGTTCCAATTTC | 83892 |
rs762375727 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471113 | CAGCACATAACTTGT[C/T]TGAACTATTCCCTGA | 83892 |
rs762404760 | snp | C/G | 1.67103e-05 | 0.00289048 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451763 | ATCCTGGGCCTCATA[C/G]AGCAAAATGTTCAGG | 83892 |
rs762404975 | snp | A/G | 4.94972e-05 | 0.00497455 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469674 | TGAAGGAAGTGGTGC[A/G]GGTAGCAGCCGCTGG | 83892 |
rs762453680 | in-del | -/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464196 | GTTCCCAAACACCCC[-/T]GATCATAAATGCCAC | 83892 |
rs762498722 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470735 | TCAGTCATCATGTCC[A/G]GACACAGACAAAAAC | 83892 |
rs762746894 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478022 | GGGTGATTTGTTCCT[A/G]TGGTTGTTGATGCCG | 83892 |
rs763027938 | snp | C/G | 1.65616e-05 | 0.00287759 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458093 | TCTGCTGGAACAAAA[C/G]ATGCTTTCAGCCTAG | 83892 |
rs763115852 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457932 | TTTCAAAAGTTATTC[A/G]GAAGAACCTCCATCA | 83892 |
rs763136379 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109451890 | ACTTTAAGCAGGGCC[G/T]CCAGGCTAAATCAGG | 83892 |
rs763156025 | snp | A/C/G | 8.24768e-05 | 0.00642125 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460766 | AGGTAGTTGAGTATC[A/C/G]TACCAAAGTGCTTCC | 83892 |
rs763169006 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457160 | GCTGAATGAAGGAAT[C/T]TGGTCACAAAAGGCC | 83892 |
rs763199235 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473509 | GCTCTAATGGCAGAC[A/G]GCATGACTAAGAGAT | 83892 |
rs763282619 | snp | A/G | 3.48906e-05 | 0.00417661 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451577 | GGTGAGAGGAGGGCG[A/G]CTCGGTCTCTTGCCT | 83892 |
rs763478676 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474260 | TTTGATTTCATTACC[A/G]ATGAAGCTGGGGAGG | 83892 |
rs763620974 | in-del | -/T | 1.67767e-05 | 0.00289622 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458118 | CCTAGGAGGCCTGCC[-/T]TAGCACTGCATTTTT | 83892 |
rs763639312 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454313 | ACATAGGGAGTCTCA[G/T]CAAGGAGACAGAAAA | 83892 |
rs763652009 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109457641 | TTACCTGGTATATGA[A/G]TATTTGTTGTTACTT | 83892 |
rs763655323 | snp | A/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109478032 | TTCCTGTGGTTGTTG[A/T]TGCCGAGGAAAGACT | 83892 |
rs763960241 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109456910 | ATGACCCAGCAATTC[C/T]GTTCCCAGAGAAATG | 83892 |
rs764002238 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479160 | AATGGGCACTCATTT[A/G]CTTTTTTAAATGATC | 83892 |
rs764021969 | snp | A/G | 1.97709e-05 | 0.00314405 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456389 | GCCCTTCTACACGCA[A/G]GGCCCTACTGAGCCC | 83892 |
rs764057311 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466794 | GTACTGCTGGATTCA[C/T]TGCCTGGCTGAGCTG | 83892 |
rs764228628 | snp | A/G | 1.66743e-05 | 0.00288736 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458109 | ATGCTTTCAGCCTAG[A/G]AGGCCTGCCTAGCAC | 83892 |
rs764310740 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474607 | TAGAGCCCACTATTC[C/T]AAAAAGCACTGTACC | 83892 |
rs764432123 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450727 | TTTATGAGCTATGCC[C/T]GTCACAGGGTCAGAT | 83892 |
rs764455055 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452444 | TTGCTCATTGCCCTT[C/T]AGGGTTAAGGTGTGA | 83892 |
rs764471352 | in-del | -/AAT | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449142 | AGTGCTTACATTATA[-/AAT]AATATTGGTTTTTGC | 83892 |
rs764535090 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453379 | AAAATTTTTGGTAGA[C/G]ACAGGGGTGTTGCTA | 83892 |
rs764652859 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469593 | TGGTCAGCGTCTGCA[C/T]GGTGGTATAGTAGAG | 83892 |
rs764761578 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470617 | TGGGGTAGCCCCCAC[A/G]GCTGGCCCTACCATT | 83892 |
rs764850725 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449026 | AACAAAAAAAACCCT[C/T]GATTACGACACACCA | 83892 |
rs764930666 | snp | A/G | 3.33868e-05 | 0.00408562 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469501 | AGAGGCAGGCACATG[A/G]TGGGTGAGCTTACCT | 83892 |
rs764990817 | snp | A/C | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476469 | TACTCAGGGAACAGA[A/C]CCTTGAGGATCCCAA | 83892 |
rs765086475 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450218 | CCTGGTAACTACTCT[A/T]CCTAGTCTAGTCTCA | 83892 |
rs765097276 | snp | C/T | 1.64757e-05 | 0.00287012 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457982 | TTCCACAAGGGTGCC[C/T]CCAACATACCTTATT | 83892 |
rs765165850 | in-del | -/C | 1.66051e-05 | 0.00288137 | frameshift-variant, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460801 | GCGGTCAATGAGGAT[-/C]CAGCCTGCAGAGGGA | 83892 |
rs765172123 | snp | C/T | 1.70177e-05 | 0.00291694 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477293 | GCAGGAGTCTCCAAA[C/T]CCGGACTGAGAGAGG | 83892 |
rs765177726 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109457680 | GAGCAACTTCACGGC[C/T]GGCTGTGGGTTGTTT | 83892 |
rs765181442 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477944 | CTCCAGGGGCTCTTT[C/T]CGCGGCCCTTTCCAC | 83892 |
rs765225044 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464916 | TAGAAGATGCTGTCC[C/G]AATTCCCCTCCTGGG | 83892 |
rs765276385 | snp | C/G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465485 | CAAAGTCCTACTGCC[C/G/T]GGGCCACACCCTGGC | 83892 |
rs765336618 | snp | C/T | 1.64882e-05 | 0.00287121 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460695 | AGTACTTGGCTTCTG[C/T]TAGCAGCTCCTCGAT | 83892 |
rs765345460 | snp | A/G | 4.94222e-05 | 0.00497078 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456160 | GACGATGGAGGTACA[A/G]CAGACTTCAGCAATC | 83892 |
rs765384728 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450403 | CCCACAGTCACACAT[A/G]TCCCTTAAACAAACA | 83892 |
rs765406416 | snp | C/T | 1.71378e-05 | 0.00292722 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460588 | AATGAGGAAGGCAGG[C/T]AGGCTTGGTGCCTCT | 83892 |
rs765489365 | in-del | -/GA | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448834 | TCCAGAGGGCGGGCT[-/GA]GTGTTGTTCACACTT | 83892 |
rs765578515 | snp | A/G | 1.65083e-05 | 0.00287296 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469676 | AAGGAAGTGGTGCGG[A/G]TAGCAGCCGCTGGCA | 83892 |
rs765581319 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457132 | TTGAAAACCTCTTAG[G/T]TAATCTCATTATGCT | 83892 |
rs765646949 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473289 | CCCTGAAAATAGTCG[A/C]GAGGTAAAGTGTGGC | 83892 |
rs765751345 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477396 | CACTTCCGCCCCGCA[A/G]AGGGCAACGTCTTAA | 83892 |
rs765751713 | snp | A/G | 1.67486e-05 | 0.00289379 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451772 | CTCATACAGCAAAAT[A/G]TTCAGGGTCTCCTCA | 83892 |
rs765804890 | snp | C/T | 1.67638e-05 | 0.0028951 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456088 | GTGTTTCAGAACAGC[C/T]ACTCCAAACTGTCCT | 83892 |
rs765807729 | in-del | -/ACTG | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109469065 | ACACATGCACTGAAT[-/ACTG]ACTATGTGCCGATGG | 83892 |
rs765853312 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469628 | CCACCCACATTCAGC[C/T]TCACGTATTTGGAGC | 83892 |
rs765984159 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453346 | AGGCACACACCACCA[C/T]GCCCAGCTATTTTTT | 83892 |
rs766024562 | snp | A/C | | | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448520 | ACAAACACTACAGAA[A/C]CATGACTGTCTTTTC | 83892 |
rs766033805 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109469359 | ACTTTCTCAAAGTAA[C/T]ATAGCAAATCAACGA | 83892 |
rs766062123 | snp | C/T | 3.30458e-05 | 0.0040647 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456111 | ACTGTCCTCTCGAGG[C/T]TCTTACCTTGGTCTG | 83892 |
rs766097451 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459351 | TAACAGAAACGAGAC[C/G]CAGGGGCATGTCTCC | 83892 |
rs766314551 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467568 | TGGAGGCTGCCGTGA[A/G]CTATGATGGCCCTAG | 83892 |
rs766329850 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458005 | ACCTTATTTGAAGTC[A/G]CTATAAGTTTTTGTT | 83892 |
rs766363071 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109448947 | AGGGTGACAGAATAT[A/G]CCAGGAATTGTCTTG | 83892 |
rs766372705 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109475167 | TACTAGAATCACCTG[C/T]GTGTGCTTAAAAAAC | 83892 |
rs766383123 | snp | A/G | 1.6569e-05 | 0.00287824 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458094 | CTGCTGGAACAAAAC[A/G]TGCTTTCAGCCTAGG | 83892 |
rs766425808 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476227 | TGGGACCAGAGTTTG[A/T]GAACCACTGGTTTAT | 83892 |
rs766427546 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464789 | ATACTCACCAGATTT[A/G]CAATAATTAAAAGGT | 83892 |
rs766540299 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454678 | AGGCTGCATTGAGCT[A/T]TGATTGTGTCACTGT | 83892 |
rs766591958 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465296 | CAAGCATAATGCTAC[A/G]TAAGCAAAAGCAAAA | 83892 |
rs766603420 | snp | C/G | 1.67147e-05 | 0.00289086 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451658 | CCGCACGCGCTCGAT[C/G]CGCTCCCGCTCCTCG | 83892 |
rs766607101 | in-del | -/A | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471196 | ACAACTATAACTGGT[-/A]AAAACACAAACGTTA | 83892 |
rs766624227 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477018 | TACTCCGCAAGCCCA[A/G]ATGTGCTTCCCGGAT | 83892 |
rs766715984 | snp | A/G | 4.9923e-05 | 0.0049959 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456335 | AAGAGCATTTGATAC[A/G]GTGACCACAAGCTGG | 83892 |
rs766756924 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471944 | ATGAAGGATTTTTTT[A/C]TAATGGCATACTTGT | 83892 |
rs766817010 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471149 | AAAAAGAATTGTCTA[A/G]CTTTTCCAGATTTTC | 83892 |
rs766822758 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109475297 | TGAGCAACATAAGAC[C/T]TAATCTCCACAAAAA | 83892 |
rs766978011 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461848 | CACGGCTCCTGCCAC[A/G]CATTACAGGTGGAAA | 83892 |
rs767010189 | snp | C/T | 1.65408e-05 | 0.00287578 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469707 | CCGCTGAGCTCACCA[C/T]ACTTTCTCCTGACAT | 83892 |
rs767065975 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451193 | GCAGGACAACTCTCA[C/G]AATTGTCAAACTGAA | 83892 |
rs767067337 | snp | C/T | 1.69126e-05 | 0.00290792 | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477213 | TGCTGCTGCCCAGCT[C/T]CCTCGGCCGCCCTCA | 83892 |
rs767069643 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462956 | GCAGGGAAAGACCGT[A/C]TTATCTTTCTACCAG | 83892 |
rs767158891 | in-del | -/TC | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472284 | TTCTATAAGCTTTTT[-/TC]TCTTTTTTTACTTTT | 83892 |
rs767302589 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109452164 | GTGGCCCACCACACA[A/G]AGTTGTACATGTCTT | 83892 |
rs767359538 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467727 | CAAGTCACAGTTTGC[A/T]GTGTCAAAATGACAC | 83892 |
rs767401463 | snp | G/T | 1.65064e-05 | 0.00287279 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460670 | TCTTCCACCAGGCCT[G/T]GGACTAGGTAGTACT | 83892 |
rs767460995 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462485 | AATCACATCACCCTG[A/G]CAGTGACCTGCAAAT | 83892 |
rs767466886 | snp | A/G | | | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448490 | CCAAGACTTCCTTTT[A/G]GTGTTTGAATTCAAA | 83892 |
rs767545164 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109475069 | CCCTCAGAGAATGAA[C/T]GTTAAAGCATTTGGC | 83892 |
rs767791545 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477312 | GACTGAGAGAGGCAG[A/G]AAACACCCAGCTCAC | 83892 |
rs767801206 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454342 | AAACCAAATGAGCAC[G/T]TGAGAACTGACAAAT | 83892 |
rs767864164 | snp | C/G | 1.67041e-05 | 0.00288994 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460813 | GATCCAGCCTGCAGA[C/G]GGAGGAGGCAGGGGC | 83892 |
rs768020325 | snp | C/T | 1.71832e-05 | 0.00293109 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451587 | GGGCGGCTCGGTCTC[C/T]TGCCTGCTCACTGGT | 83892 |
rs768092375 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109469761 | ACAGGGTCATGACAT[C/T]AGGCCTGGTTGACTG | 83892 |
rs768324702 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465058 | AAATATGATTGTCTA[C/T]GTGCCCCATGATGTG | 83892 |
rs768341946 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471811 | CAGATCTAATTTTAT[A/G]TAATAAATGCTTGTT | 83892 |
rs768406285 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478760 | CACTCCAGCCTGGGC[-/A]ACAAAGTGAGACTCC | 83892 |
rs768494077 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467581 | GAGCTATGATGGCCC[G/T]AGTGCACTTCAGCCT | 83892 |
rs768562825 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109451936 | TGAAGGCCACCAGTA[C/T]TATTTTTAAATAAAC | 83892 |
rs768637747 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109463436 | GCTTTCAAAGCAGGA[A/G]GTGATCCCTTTGAAA | 83892 |
rs768659247 | snp | A/G | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476504 | ACAAACCCCACAGCT[A/G]AGAGACAGATCTTGA | 83892 |
rs768668021 | in-del | -/TTCCACTCCTAACAACGCTGTGCCCTG | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461956 | GAGAAGGGCCAACAT[-/TTCCACTCCTAACAACGCTGTGCCCTG]TTCCACTCCTAACAA | 83892 |
rs768685869 | snp | A/G | 0.00011832 | 0.00769065 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456069 | AAGGAAGTTCTATAG[A/G]TGTGTGTTTCAGAAC | 83892 |
rs768724195 | in-del | -/A | 1.69286e-05 | 0.0029093 | frameshift-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451788 | TCAGGGTCTCCTCAT[-/A]AAATCCGGGCTTCGG | 83892 |
rs768778274 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468874 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 83892 |
rs768850918 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468559 | GCACGCAAACCCAGC[C/T]AGGTAAGGATGGAGC | 83892 |
rs768897949 | snp | C/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456238 | AACATCCTTTATGAA[C/G]AGGACCCTTCCGTTA | 83892 |
rs768923691 | snp | C/T | 1.69628e-05 | 0.00291224 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469745 | TGCCAGTGGAGAGGA[C/T]ACAGGGTCATGACAT | 83892 |
rs768942926 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458919 | AGCCCAGTGGACAAC[A/G]AGGACCTTCCATGCA | 83892 |
rs769080520 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455842 | TACTGGTTTGGAGAG[A/G]ATGATATAAAAACAC | 83892 |
rs769124539 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477336 | AGCTCACGCCAGCCG[A/G]GGGCGGAGGCGGGGC | 83892 |
rs769175898 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465123 | CACGCACGGGGAAAG[C/T]GTTCAAGGATGTTCA | 83892 |
rs769182893 | in-del | -/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462427 | ATAGCCCTGAGTCAA[-/C]CTCCTGGTTTCAGGG | 83892 |
rs769201470 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449600 | ATGGGCTGATGGGTA[C/T]CTGCAATCCCAGCTA | 83892 |
rs769252164 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455412 | AAAAAAAAAGACTCT[C/G]GTTTCTACTTTGTGA | 83892 |
rs769303357 | snp | C/T | 1.66178e-05 | 0.00288247 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460645 | GCCTACTTGTAGGGC[C/T]GCCTGGCACTCTTCC | 83892 |
rs769396770 | in-del | -/GAGAT | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454418 | CTCAATAACAGAGTG[-/GAGAT]GAGACAGGAGAGGAG | 83892 |
rs769406940 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458070 | GAAAGGCTCATAAGT[A/G]TCTTTGTTCTGCTGG | 83892 |
rs769503356 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471590 | TCTGAAATCAGTCCC[C/T]AGAGACCTCACACTA | 83892 |
rs769562255 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461425 | CACCCTCAGGCAGCT[C/T]GGTAAACATGGGGAG | 83892 |
rs769627108 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478921 | CAGCTTTTCCTACTG[C/T]ACAGGGACAATCCTC | 83892 |
rs769646933 | snp | C/T | 5.04715e-05 | 0.00502327 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451703 | GTGGGAGCGCCCCGC[C/T]GCCCCGCCTGTGGCC | 83892 |
rs769683715 | snp | C/G/T | 0.00065466 | 0.0180826 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451556 | AGCACGGCAGGGAGT[C/G/T]GGGGCGGTGAGAGGA | 83892 |
rs769697984 | snp | A/G | 1.94384e-05 | 0.0031175 | intron-variant | KCTD10 | GRCh38.p7 | 12:109451833 | GTTCCCACAGTATAC[A/G]GGGCAGGTAAGTTAT | 83892 |
rs769707415 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474044 | CCTCGGCATCCCAAA[G/T]TGCTCGGATTACAGG | 83892 |
rs770068287 | snp | C/T | 1.64857e-05 | 0.00287099 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460757 | CCGTCTCGAAGGTAG[C/T]TGAGTATCGTACCAA | 83892 |
rs770073767 | in-del | -/T | 1.65518e-05 | 0.00287674 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456327 | TGCTGCAAAAGAGCA[-/T]TTGATACGGTGACCA | 83892 |
rs770217184 | snp | C/T | 1.69255e-05 | 0.00290903 | upstream-variant-2KB, missense, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477262 | CCGCCCTCCCTACCA[C/T]GAAAAGTCGGAGGAC | 83892 |
rs770251417 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474411 | CTCCATCTCCCCTGA[A/G]TATAATGTTGCTGAT | 83892 |
rs770253131 | in-del | -/AAACACCC | 1.71971e-05 | 0.00293227 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477313 | ACTGAGAGAGGCAGG[-/AAACACCC]AGCTCACGCCAGCCG | 83892 |
rs770276481 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464377 | AGTTGCATCCCTGGC[C/T]TCTACTCACTTGACG | 83892 |
rs770303268 | snp | C/G/T | 3.72955e-05 | 0.00431817 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469788 | ACTGCTTTCAGCCTG[C/G/T]GGATTCAATCTGGCC | 83892 |
rs770346637 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458734 | GATGAGCAACCCCAG[C/G]TCCTTCCCCTTCCAG | 83892 |
rs770507378 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454116 | TATTCAAAATGTTTA[C/G]GATACAATCAAAATT | 83892 |
rs770635100 | snp | A/G | 3.29641e-05 | 0.00405968 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460726 | CTCCCGGCGGCTCTC[A/G]GGTAAAGGCACCGCC | 83892 |
rs770640587 | snp | A/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479301 | TACATGCTTTTAGAT[A/T]TCCTATATTAATATT | 83892 |
rs770694606 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470688 | AGACAAGGCCACTCT[C/G]TGCCCTTGCGACAAG | 83892 |
rs770744225 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449918 | CTAATATAAAAGTTT[C/T]TCACACGACAGTTTA | 83892 |
rs770748741 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471460 | TTCATCAAGAAAAGT[C/T]ACAAGAAAATATGTT | 83892 |
rs770827672 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461152 | ACCTGGGTAAAACAG[A/G]CCCAAATGGCCACAT | 83892 |
rs771006904 | snp | C/T | 1.65312e-05 | 0.00287495 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460658 | GCCGCCTGGCACTCT[C/T]CCACCAGGCCTTGGA | 83892 |
rs771079673 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466603 | TTCTTCTTGGTTTAG[C/G]AGTTACTTGCACACA | 83892 |
rs771156666 | snp | C/T | 1.64996e-05 | 0.0028722 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469541 | GTGAGCACTTCCATG[C/T]GCCCGCTGAACATGG | 83892 |
rs771191233 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477706 | ACTCGGGTGTTTTGG[A/G]CTGAGACAGTGGCAG | 83892 |
rs771286268 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450293 | CAGAGGAGCCTGGGA[G/T]GTAGGTCACTGAGAA | 83892 |
rs771365554 | snp | C/G/T | 3.29675e-05 | 0.00405991 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457731 | TACTTGGCAGGCAGA[C/G/T]GCAATGAACTACTAG | 83892 |
rs771384931 | snp | A/G | 3.3923e-05 | 0.0041183 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477273 | ACCATGAAAAGTCGG[A/G]GGACGCAGGAGTCTC | 83892 |
rs771437976 | snp | C/T | 1.64852e-05 | 0.00287094 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457615 | TGGAGCTGTCTTTCC[C/T]GGCTGACGCCTTACC | 83892 |
rs771482951 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473277 | AAGTACAAAAAGCCC[C/T]GAAAATAGTCGCGAG | 83892 |
rs771675959 | snp | A/C | 1.69812e-05 | 0.00291382 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477279 | AAAAGTCGGAGGACG[A/C]AGGAGTCTCCAAACC | 83892 |
rs771685459 | snp | C/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478762 | CTCCAGCCTGGGCAA[C/G]AAAGTGAGACTCCGT | 83892 |
rs771702608 | in-del | -/AAG | 0.000411851 | 0.0143442 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457699 | TGTGGGTTGTTTTAA[-/AAG]AAGAAGAAGAGAGTT | 83892 |
rs771727289 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457623 | TCTTTCCCGGCTGAC[A/G]CCTTACCTGGTATAT | 83892 |
rs771870540 | snp | C/T | 3.29625e-05 | 0.00405958 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460740 | CGGGTAAAGGCACCG[C/T]CCCGTCTCGAAGGTA | 83892 |
rs771880897 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459302 | ACTAAGAGGAAAGAA[C/T]TAGGAGGTCAGTCCT | 83892 |
rs771968030 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109469089 | GTGCCGATGGCCCCA[C/T]GGGGGAGGGTATTGT | 83892 |
rs772103899 | snp | A/G | 1.64904e-05 | 0.00287139 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469546 | CACTTCCATGCGCCC[A/G]CTGAACATGGCCTTC | 83892 |
rs772146344 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450587 | AGGGTGTCCCTGCCT[A/G]GATGCCAGGCTGGGA | 83892 |
rs772155801 | snp | C/T | 1.7708e-05 | 0.00297552 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451561 | GGCAGGGAGTGGGGG[C/T]GGTGAGAGGAGGGCG | 83892 |
rs772218356 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454037 | AACTGGGTCAATTGC[C/T]TGCTAAAACAAAAAC | 83892 |
rs772252514 | snp | C/T | 3.34443e-05 | 0.00408913 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451727 | TGTGGCCTCCAGGAG[C/T]GCATTGTCAGGTCCC | 83892 |
rs772308812 | snp | C/G | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469655 | GAGCTGGGGCTCGTG[C/G]CCTTGAAGGAAGTGG | 83892 |
rs772353614 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449772 | TTCCTGGCCAACATT[C/T]ACTTCGACTTTCTAA | 83892 |
rs772363564 | snp | C/G | 2.1099e-05 | 0.00324793 | intron-variant | KCTD10 | GRCh38.p7 | 12:109451850 | GGCAGGTAAGTTATG[C/G]CCCACCCCCTCTGCC | 83892 |
rs772395471 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465178 | ACCCTCTACATGATC[A/G]TCAACAGAATATGGC | 83892 |
rs772490436 | snp | C/T | 1.64798e-05 | 0.00287047 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457970 | TAGCAAAAGAAATTC[C/T]ACAAGGGTGCCTCCA | 83892 |
rs772535595 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109456903 | TTACCACATGACCCA[C/G]CAATTCTGTTCCCAG | 83892 |
rs772577045 | snp | C/T | 1.65247e-05 | 0.00287438 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458088 | TTTGTTCTGCTGGAA[C/T]AAAACATGCTTTCAG | 83892 |
rs772763757 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474361 | ATCTGATTCAATCAG[A/G]AGTTTATTCCAGTTA | 83892 |
rs772802417 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459762 | AAGAGCAGCACAGGC[A/G]AATTATGTGGAAACA | 83892 |
rs772814750 | snp | A/G | 1.6601e-05 | 0.00288101 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460646 | CCTACTTGTAGGGCC[A/G]CCTGGCACTCTTCCA | 83892 |
rs772978237 | snp | A/G | 6.73197e-05 | 0.00580132 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451704 | TGGGAGCGCCCCGCC[A/G]CCCCGCCTGTGGCCT | 83892 |
rs772998149 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109468952 | CCACTGTGCCCAGCC[A/G]ATTCTTTGCCTTTTA | 83892 |
rs773016237 | in-del | -/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464142 | CTTCACTGACCTCTC[-/T]TTTGCCATCCTAAGG | 83892 |
rs773048216 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453252 | AGAGATGAGTGTGTT[C/G]CTATGTTGCCCAGGC | 83892 |
rs773076018 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470455 | TCTGTACATCTCAAA[A/G]AAATGGATACAGTGG | 83892 |
rs773118194 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449777 | GGCCAACATTCACTT[C/T]GACTTTCTAAAAAAG | 83892 |
rs773242650 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464656 | TAAGAAAAAGGCAAA[C/T]GTGTAAGTAAGATGC | 83892 |
rs773412685 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450141 | CATGTTAATACCTTT[G/T]GTATAAAACGGTAAC | 83892 |
rs773416414 | snp | C/T | 1.64844e-05 | 0.00287087 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457610 | GTAAATGGAGCTGTC[C/T]TTCCCGGCTGACGCC | 83892 |
rs773419349 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477435 | TTGTGCGCCTAGGGG[A/C]CAGTTTTCTTTCCAG | 83892 |
rs773502748 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466809 | CTGCCTGGCTGAGCT[A/G]CACTTGGCATTTCTG | 83892 |
rs773524441 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455771 | AGCAGCACTATGCAG[A/C]GCAATCCAGCTTTGT | 83892 |
rs773540806 | in-del | -/A | 3.32099e-05 | 0.00407478 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456332 | AAAAGAGCATTTGAT[-/A]ACGGTGACCACAAGC | 83892 |
rs773603315 | snp | C/G | 0.00176053 | 0.029617 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469679 | GAAGTGGTGCGGGTA[C/G]CAGCCGCTGGCACCG | 83892 |
rs773613681 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465281 | TGTGGATTGATCTCA[A/C]AAGCATAATGCTACG | 83892 |
rs773618480 | snp | C/G | | | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448581 | AGGCAGAACGTGGGG[C/G]CCCTGCCTTTGTTGT | 83892 |
rs773738610 | in-del | -/A | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478482 | TCCTATTCTTTAAAT[-/A]AAAATTAGATTATTG | 83892 |
rs773741362 | snp | C/T | 1.66358e-05 | 0.00288402 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456098 | ACAGCCACTCCAAAC[C/T]GTCCTCTCGAGGCTC | 83892 |
rs773966228 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461785 | CAGATGAGAGGGTGA[A/G]GTCGAGGCCTTCTGA | 83892 |
rs773978426 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471864 | GGAAGGTGCCTATCA[C/T]GAAACAGACAAAAAA | 83892 |
rs773993728 | in-del | -/ACATGCTGTAGGAATTTAACTCTTGTTT | | | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448196 | TTTTTGTGCCCAGCA[-/ACATGCTGTAGGAATTTAACTCTTGTTT]ACATCCATTAGCCTC | 83892 |
rs774019754 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109451973 | TTTCAATGGCAACAC[C/T]TACATGTGGTGCTAA | 83892 |
rs774031263 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473191 | GGCTGGCCCAGAGAC[A/C]ATCACACCTAGTAGA | 83892 |
rs774057435 | snp | C/T | 0.000436967 | 0.0147747 | intron-variant | KCTD10 | GRCh38.p7 | 12:109471344 | CTCCATGGCACCCAA[C/T]AGTGGCCTGGATATC | 83892 |
rs774247674 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459523 | AAAGTTATAGAAGAA[A/G]GAAAATAATCACTGT | 83892 |
rs774253064 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459087 | AGAAAGAAAACAAAC[A/T]GAATCATCAGACAGT | 83892 |
rs774280573 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467688 | AATGATATGAAGCAG[A/G]GGCTGAGCTCCGGTG | 83892 |
rs774283682 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109469005 | AAAGAAAAACGTGTG[C/T]GTGTGTGTGTATATC | 83892 |
rs774311462 | snp | A/G | 1.65877e-05 | 0.00287986 | intron-variant | KCTD10 | GRCh38.p7 | 12:109458096 | GCTGGAACAAAACAT[A/G]CTTTCAGCCTAGGAG | 83892 |
rs774364980 | snp | A/G | 1.65252e-05 | 0.00287443 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460661 | GCCTGGCACTCTTCC[A/G]CCAGGCCTTGGACTA | 83892 |
rs774369697 | snp | A/G | 1.6495e-05 | 0.0028718 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469542 | TGAGCACTTCCATGC[A/G]CCCGCTGAACATGGC | 83892 |
rs774428939 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470624 | GCCCCCACGGCTGGC[A/C]CTACCATTCCCATTG | 83892 |
rs774494060 | snp | C/T | 1.67153e-05 | 0.00289091 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451659 | CGCACGCGCTCGATC[C/T]GCTCCCGCTCCTCGT | 83892 |
rs774498936 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458137 | CACTGCATTTTTAAA[A/G]TTGACCGGCTGGACA | 83892 |
rs774528472 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448175 | TTATTTAGAAATTGG[A/G]TGATGTTTTTGTGCC | 83892 |
rs774611520 | snp | A/G | 8.24069e-05 | 0.00641846 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457616 | GGAGCTGTCTTTCCC[A/G]GCTGACGCCTTACCT | 83892 |
rs774679982 | snp | A/G | 3.39219e-05 | 0.00411823 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477275 | CATGAAAAGTCGGAG[A/G]ACGCAGGAGTCTCCA | 83892 |
rs774760238 | snp | A/G | 1.69789e-05 | 0.00291362 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456352 | TGACCACAAGCTGGT[A/G]AAAACTGCCATCATT | 83892 |
rs774784445 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465202 | ATATGGCTCCGGCAG[C/T]GGCTGTATGCTTCTA | 83892 |
rs775000920 | snp | A/C | 3.39512e-05 | 0.00412001 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477280 | AAAGTCGGAGGACGC[A/C]GGAGTCTCCAAACCC | 83892 |
rs775070343 | in-del | -/AGAG | 1.64779e-05 | 0.00287031 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457709 | TTTAAAAGAAGAAGA[-/AGAG]AGTTACTTGGCAGGC | 83892 |
rs775157580 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461440 | CGGTAAACATGGGGA[A/G]ACAGAATCAGCTTTT | 83892 |
rs775215691 | snp | C/T | 4.94385e-05 | 0.0049716 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457969 | GTAGCAAAAGAAATT[C/T]CACAAGGGTGCCTCC | 83892 |
rs775382432 | snp | C/T | 1.64822e-05 | 0.00287068 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460743 | GTAAAGGCACCGCCC[C/T]GTCTCGAAGGTAGTT | 83892 |
rs775460610 | snp | A/T | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469662 | GGCTCGTGCCCTTGA[A/T]GGAAGTGGTGCGGGT | 83892 |
rs775499604 | snp | C/G | 0.000247111 | 0.0111128 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109457632 | GCTGACGCCTTACCT[C/G]GTATATGAGTATTTG | 83892 |
rs775515727 | snp | C/G | 2.26007e-05 | 0.00336152 | intron-variant | KCTD10 | GRCh38.p7 | 12:109451858 | AGTTATGGCCCACCC[C/G]CTCTGCCAACACCTG | 83892 |
rs775619535 | snp | A/G | 1.64811e-05 | 0.00287059 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469562 | CTGAACATGGCCTTC[A/G]GCATGGTGTCCTGCT | 83892 |
rs775672360 | snp | A/G | 1.67128e-05 | 0.00289069 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451733 | CTCCAGGAGCGCATT[A/G]TCAGGTCCCCGGCCA | 83892 |
rs775675655 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457147 | GTAATCTCATTATGC[G/T]GAATGAAGGAATCTG | 83892 |
rs775747239 | snp | C/G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467572 | GGCTGCCGTGAGCTA[C/G/T]GATGGCCCTAGTGCA | 83892 |
rs775790479 | in-del | -/TAGATCAAGGA | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464488 | TGGGCATCACTGAGG[-/TAGATCAAGGA]TGTAAGTGTAAAAAA | 83892 |
rs775817228 | snp | A/G | 1.64789e-05 | 0.0028704 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457973 | CAAAAGAAATTCCAC[A/G]AGGGTGCCTCCAACA | 83892 |
rs775861870 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474504 | ACCTAGGTCCTACCA[C/T]GAAAATTCTGATGTA | 83892 |
rs775908682 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457878 | TTCCCACTGTGAACC[C/T]ATTATCAGGCCTCAC | 83892 |
rs775915235 | snp | A/G | | | intron-variant, upstream-variant-2KB | KCTD10, UBE3B | GRCh38.p7 | 12:109475560 | GTATCTCAGAGATGC[A/G]GAGGGGTGGCTGATC | 83892 |
rs775922344 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109463779 | TTCTCTTCTACAAAC[A/G]ATCTCACAGGGTTGA | 83892 |
rs775945147 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | MYO1H, KCTD10 | GRCh38.p7 | 12:109448735 | AACTTTGAGCATTTT[A/T]TTATGGCGCAAAGAG | 83892 |
rs776032582 | snp | G/T | 0.000461239 | 0.0151792 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457977 | AGAAATTCCACAAGG[G/T]TGCCTCCAACATACC | 83892 |
rs776254924 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461549 | CTCCCTACTCTGCTG[C/T]TCAATGTCCTTTCTA | 83892 |
rs776366346 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473859 | CGATCTCAGCTCACC[A/G]CAACGTCTGCCTCCC | 83892 |
rs776372686 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109460361 | ACCAAGTTTCACACC[A/G]CGGGGTTCTCTGCTG | 83892 |
rs776526778 | snp | A/G | 3.34001e-05 | 0.00408643 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451655 | CCTCCGCACGCGCTC[A/G]ATCCGCTCCCGCTCC | 83892 |
rs776603313 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109449950 | AAAGCATCTGCCCAA[A/T]ACACGATTTTGACAT | 83892 |
rs776603411 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461159 | TAAAACAGGCCCAAA[C/T]GGCCACATACCAAGG | 83892 |
rs776694775 | snp | C/T | 1.69991e-05 | 0.00291535 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477287 | GAGGACGCAGGAGTC[C/T]CCAAACCCGGACTGA | 83892 |
rs776814524 | snp | C/T | | | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109457676 | TGTAGAGCAACTTCA[C/T]GGCTGGCTGTGGGTT | 83892 |
rs776824588 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478193 | GAGGGTGTGAATACG[-/T]TTTAGTACCGTGCCT | 83892 |
rs776887033 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456248 | ATGAACAGGACCCTT[C/T]CGTTAAAGCGCAGAG | 83892 |
rs776935657 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473287 | AGCCCTGAAAATAGT[C/T]GCGAGGTAAAGTGTG | 83892 |
rs777059491 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457018 | CCCAAATGTCCATCA[A/G]CTGATGAATGGGTAA | 83892 |
rs777078858 | in-del | -/A | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464691 | AGCAGTTAAAAGATT[-/A]AAACTCAAAAGAGCA | 83892 |
rs777154696 | snp | G/T | 6.59065e-05 | 0.00574012 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469597 | CAGCGTCTGCATGGT[G/T]GTATAGTAGAGGGCT | 83892 |
rs777187146 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109475394 | CGGTGGGAGGACTGC[A/T]TGAGGCAGGGAAGGT | 83892 |
rs777584837 | snp | A/G | 5.87159e-05 | 0.00541798 | intron-variant | KCTD10 | GRCh38.p7 | 12:109451836 | CCCACAGTATACAGG[A/G]CAGGTAAGTTATGGC | 83892 |
rs777639871 | snp | A/T | 4.94222e-05 | 0.00497078 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109456172 | ACAACAGACTTCAGC[A/T]ATCTTCCGGCCCTGA | 83892 |
rs777655703 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109455314 | GTGCCCAAGCTGATG[A/G]CCCTTGACGTGGCGT | 83892 |
rs777783056 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461097 | AGTACCCTCAAATAT[C/T]CCTTACACAAGGACA | 83892 |
rs777799447 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459007 | CATGTGAAAAGCCTC[C/T]TTAACATGAGAACAA | 83892 |
rs777876976 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109472572 | TAGTAAATACATTAA[A/C]CAGTGATATATCTAT | 83892 |
rs777889874 | snp | A/G | | | splice-donor-variant, intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478110 | GCTGTGTGACCTTGG[A/G]TGAGTTCCCTCACCT | 83892 |
rs777892679 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109456525 | GCTCAAGGCTGAACC[C/T]AATAAATGGCAGACA | 83892 |
rs777984456 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478365 | TGATAAATAACTGTT[C/T]TGGATATACATGGAT | 83892 |
rs777996505 | snp | A/G | 1.77417e-05 | 0.00297834 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451546 | ATCTGGGTGTAGCAC[A/G]GCAGGGAGTGGGGGC | 83892 |
rs778003685 | snp | G/T | 1.64746e-05 | 0.00287002 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458026 | AGTTTTTGTTCTTCC[G/T]TGGATGAGGTGATCA | 83892 |
rs778012755 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462182 | GCCAAGTGCCCTCTC[A/G]TGGTTTTAGGGCATA | 83892 |
rs778043202 | snp | A/G | 1.64817e-05 | 0.00287064 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457725 | GAGAGTTACTTGGCA[A/G]GCAGATGCAATGAAC | 83892 |
rs778097786 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450621 | CAAAGGGTATGGGCC[A/G]CACTGAATTTCTAAG | 83892 |
rs778251130 | snp | C/G | 1.70487e-05 | 0.0029196 | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451593 | CTCGGTCTCTTGCCT[C/G]CTCACTGGTGGAGGT | 83892 |
rs778281997 | snp | A/G | 5.0255e-05 | 0.00501248 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460819 | GCCTGCAGAGGGAGG[A/G]GGCAGGGGCTGGTTA | 83892 |
rs778538260 | snp | C/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109466714 | TGAAGCAATCACTTT[C/G]TTGGGCAACATGACA | 83892 |
rs778556011 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, intron-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109460734 | GGCTCTCGGGTAAAG[A/G]CACCGCCCCGTCTCG | 83892 |
rs778603203 | snp | C/T | 0.000190858 | 0.00976691 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464775 | CAAGGTACCATATCA[C/T]ACTCACCAGATTTGC | 83892 |
rs778622333 | snp | A/C | 0.000453451 | 0.0150506 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456402 | CAGGGCCCTACTGAG[A/C]CCACTTTCTCCACTA | 83892 |
rs778651999 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474142 | CTGGTCTCGAACTCC[C/T]GACCTCAAGTGATCC | 83892 |
rs778658209 | snp | A/G | 1.67365e-05 | 0.00289275 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451615 | GGTGGAGGTGGGCCC[A/G]GTCATCAGGGCGCTT | 83892 |
rs778713247 | snp | A/G | 3.34986e-05 | 0.00409245 | | | GRCh38.p7 | 12:109451679 | CCGCTCCTCGTCCTC[A/G]TCCAGGTGGTGGGAG | 83892 |
rs778757521 | snp | C/T | | | | | GRCh38.p7 | 12:109453902 | CTGCAAGAGATACTG[C/T]CCAGGACAGACGGGC | 83892 |
rs778803211 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464164 | ATCCTAAGGTATTTA[G/T]ACTCTATATTTTTGT | 83892 |
rs778953823 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471244 | GGGAGTAAAGGGAGG[C/T]AGCTTGCAACAGCAG | 83892 |
rs778983119 | snp | A/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109454906 | TCTAAAAATGAGAAG[A/T]CTTAATCTTTTAAAG | 83892 |
rs778989368 | in-del | -/C | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478762 | CTCCAGCCTGGGCAA[-/C]AAAGTGAGACTCCGT | 83892 |
rs778998722 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109460968 | CACTAAGGGCTGAGG[A/G]AGCCCCCACAGCCTC | 83892 |
rs779022938 | in-del | -/A | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109451974 | TCAATGGCAACACTT[-/A]ACATGTGGTGCTAAA | 83892 |
rs779085176 | in-del | -/TTCAG | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459958 | GTAAATGCTGCAACA[-/TTCAG]TTAGGTCTGCAGTGA | 83892 |
rs779243445 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109460173 | ATAAAGGGGTGTTGG[C/T]CATGTCTAGAAGCAT | 83892 |
rs779363694 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450550 | GTTTATAGCAGGGAA[A/G]CTCCCTGGGGCTGGT | 83892 |
rs779418221 | snp | A/G | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478274 | TAGCCCCCACAGGCA[A/G]TCTTGCACTCTCAAC | 83892 |
rs779488577 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109456819 | TGCATATATTGCTGG[C/T]GGGAATGTAAAATGG | 83892 |
rs779530838 | snp | C/T | 1.7074e-05 | 0.00292177 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451793 | GGTCTCCTCATAAAT[C/T]CGGGCTTCGGGAAAC | 83892 |
rs779597264 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451246 | AAAGCCCACATAGGA[A/G]GTCGACACCCACAAA | 83892 |
rs779610402 | snp | C/T | 1.66007e-05 | 0.00288098 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469511 | ACATGGTGGGTGAGC[C/T]TACCTTCACTGTCGG | 83892 |
rs779720359 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109457414 | ACATATTGTGAATAT[A/C]ATAATAACTGTACAC | 83892 |
rs779797472 | snp | C/T | 0.00037679 | 0.0137205 | intron-variant | KCTD10 | GRCh38.p7 | 12:109464886 | CAGAAGGGACTCCTG[C/T]AATATCTAAGGAAGT | 83892 |
rs779903464 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109463401 | TTCAATCAGCGTTTT[G/T]ACTTTAAGATACTGT | 83892 |
rs779931178 | in-del | -/A | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109461250 | AACTGTCACATTAAC[-/A]GAGCCATTTCTAAGA | 83892 |
rs779937701 | snp | A/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109476445 | CATCTCTACCCAGGG[A/T]CAATGAGCTACTCAG | 83892 |
rs779984431 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109473011 | TCGGTGTCCCTTGAC[C/T]ACTGCATTTCTACCA | 83892 |
rs779994341 | snp | A/G | 1.64781e-05 | 0.00287033 | intron-variant | KCTD10 | GRCh38.p7 | 12:109457714 | AAGAAGAAGAAGAGA[A/G]TTACTTGGCAGGCAG | 83892 |
rs780035801 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109464120 | CTCTCCCACCACCTC[C/T]AGGGAACCTTCACTG | 83892 |
rs780122580 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109453730 | CCCCAGCTTTCTGGC[G/T]GGCCGATCAGAGAAG | 83892 |
rs780261673 | snp | C/T | 3.3325e-05 | 0.00408184 | missense, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469728 | CTCCTGACATCTCTT[C/T]CTGCCAGTGGAGAGG | 83892 |
rs780281498 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470031 | ACCCAAAAAGCCTCA[C/T]ACACTGACCCTGCCT | 83892 |
rs780339537 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109462802 | AGGACGGTAAACTAA[C/T]TAAAACAAAACAAAA | 83892 |
rs780346683 | in-del | -/TTTAAAACACTATGCAGCCAGGTGTGGT | 1.66952e-05 | 0.00288917 | frameshift-variant, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451644 | TGATGTGGATCCTCC[-/TTTAAAACACTATGCAGCCAGGTGTGGT]GCACGCGCTCGATCC | 83892 |
rs780436105 | snp | A/G/T | 4.94338e-05 | 0.00497141 | missense, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109458060 | GGACCTTGCAGAAAG[A/G/T]CTCATAAGTATCTTT | 83892 |
rs780436493 | in-del | -/T | 2.00266e-05 | 0.00316432 | intron-variant | KCTD10 | GRCh38.p7 | 12:109469499 | CCAGAGGCAGGCACA[-/T]GGTGGGTGAGCTTAC | 83892 |
rs780486958 | snp | C/G | 1.70525e-05 | 0.00291992 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460607 | CTTGGTGCCTCTCCA[C/G]CCATATGGGAAGAAA | 83892 |
rs780514419 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459904 | ACTTCTTGAAGGATG[C/T]ATGTGCATCACTTTC | 83892 |
rs780530856 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109463411 | GTTTTGACTTTAAGA[C/T]ACTGTGGTTGCTTTC | 83892 |
rs780567163 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458775 | GCAGCCGGCCAGGCC[G/T]AGACCCGTCAGGCAG | 83892 |
rs780693972 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450331 | CCTACATAGGCGCTG[C/T]GCCCAGCCGGGCTCC | 83892 |
rs780724429 | snp | C/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109478151 | CAGTTTCCTTCTGTG[C/T]AAATGGAGTAATTAG | 83892 |
rs780777412 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109465996 | TGCTGAACAGAATGC[A/G]TTGTGAAAGGTGCTA | 83892 |
rs780891216 | snp | A/C | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109456662 | GAGCCCCAAGAGGAG[A/C]AGAATGGCACTGCCC | 83892 |
rs780935876 | snp | C/G | 1.68972e-05 | 0.0029066 | synonymous-codon, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451697 | CAGGTGGTGGGAGCG[C/G]CCCGCCGCCCCGCCT | 83892 |
rs781051114 | snp | A/G | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant, intron-variant | KCTD10 | GRCh38.p7 | 12:109469642 | CTTCACGTATTTGGA[A/G]CTGGGGCTCGTGCCC | 83892 |
rs781077217 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109471472 | AGTCACAAGAAAATA[C/T]GTTTTCAAAAGCTCA | 83892 |
rs781194656 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109451478 | ATCTGGCTTGTTACA[A/G]AAGTATCTCCAGGCT | 83892 |
rs781280361 | in-del | -/A | 5.10412e-05 | 0.00505154 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109477289 | GACGCAGGAGTCTCC[-/A]AAACCCGGACTGAGA | 83892 |
rs781389715 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109460939 | AGAATGGCAGCCTCA[C/T]CTGCCTACCTGCCCA | 83892 |
rs781403079 | snp | A/G | 3.3888e-05 | 0.00411617 | intron-variant | KCTD10 | GRCh38.p7 | 12:109460624 | CATATGGGAAGAAAG[A/G]GTGATGCCTACTTGT | 83892 |
rs781541942 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109459609 | TTTAACCAAAACTGT[A/G]ATGAACTGTACTGGG | 83892 |
rs781554154 | in-del | -/A | 1.67002e-05 | 0.00288961 | intron-variant | KCTD10 | GRCh38.p7 | 12:109456093 | CAGAACAGCCACTCC[-/A]AAACTGTCCTCTCGA | 83892 |
rs781563553 | in-del | -/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109474517 | ATGAAAATTCTGATG[-/T]TAATTGGTCCGGGAT | 83892 |
rs781684149 | snp | G/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109467508 | ATGCCTGTATTCCCA[G/T]CTACACAGAAGGCTG | 83892 |
rs781716767 | snp | A/G | | | downstream-variant-500B | MYO1H, KCTD10 | GRCh38.p7 | 12:109448625 | GGGCCTGGTTATGCC[A/G]GGCATGCCTGAAAAG | 83892 |
rs781722444 | snp | C/T | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109470266 | CTTTATGAAGTTGAA[C/T]GGGATTCCAGCTGGC | 83892 |
rs781745062 | snp | A/G | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458607 | CCCAAATCCATCTCC[A/G]TCCCCATGCAGGCAG | 83892 |
rs796529250 | snp | C/T | | | upstream-variant-2KB, intron-variant | UBE3B, KCTD10 | GRCh38.p7 | 12:109475628 | ATGTGGGACCAGGGC[C/T]TACTGCCACCTAGCT | 83892 |
rs796643185 | in-del | -/TA | | | intron-variant | KCTD10 | GRCh38.p7 | 12:109458492 | AGGTCAGCAGACCAG[-/TA]AAAAAAGTCAAAAAT | 83892 |
rs796811851 | in-del | -/GCC | | | cds-indel, nc-transcript-variant | KCTD10 | GRCh38.p7 | 12:109450357 | GCTCCAGCAGGGGCC[-/GCC]ACCTGTGCCCCACAA | 83892 |
rs796825299 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UBE3B, KCTD10 | GRCh38.p7 | 12:109479279 | ACAATAAAGCTCACT[-/T]ACATGCTACATGCTT | 83892 |