SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs757255917 | snp | A/G | 1.66921e-05 | 0.00288891 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606810 | TGCTTGAAGTCTGGG[A/G]TTTGGGTTGGGGGGA | 4296 |
rs757312458 | snp | A/G | 1.80742e-05 | 0.00300612 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599449 | CTGGCCCACAGGGAT[A/G]CCCAGGTCCAGCAAC | 4296 |
rs757439213 | snp | G/T | 1.67391e-05 | 0.00289297 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613316 | CTCATCGGGGTCCTG[G/T]CGAGCTGCCTTCACA | 4296 |
rs757456029 | snp | C/T | 0.000139718 | 0.00835702 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605992 | AACTGGGACCCCAAG[C/T]CCAGCATGCTCGCCG | 4296 |
rs757520731 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598767 | CCGCCCTTCCTGCTC[C/T]GTGGTGCCTCTGTTT | 4296 |
rs757568452 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611839 | AGGTAGCGGGGGTCC[C/G]TAGATAGTTAGAGCC | 4296 |
rs757605417 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606598 | GCGGGGAGGAAGAGG[A/G]GATAGTGAGTGGGCT | 4296 |
rs757688762 | snp | A/G | 1.6684e-05 | 0.00288821 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607677 | GTCGAAGAGACCCTG[A/G]ATCTCGCGCTTCCAG | 4296 |
rs757705121 | snp | A/G | 1.83501e-05 | 0.00302898 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605719 | CAAGGTGCCCACGGA[A/G]GGAGCTCAGCCAGAT | 4296 |
rs757750590 | snp | A/G | 3.39697e-05 | 0.00412113 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613405 | TCACCTCCTCCAGCC[A/G]CAGCTCCTGGAAGCT | 4296 |
rs757766244 | in-del | -/GCA | 1.88035e-05 | 0.00306617 | cds-indel, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607374 | CGCGGTCCACCTGCT[-/GCA]GCAGCAGCAGCGTCA | 4296 |
rs757791494 | snp | C/G | 0.000107302 | 0.00732389 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616266 | GGCCGGGGGCCGCCC[C/G]CATGAGGGTCCCGGG | 4296 |
rs757793097 | snp | A/G | | | intron-variant, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605595 | CTGTAGGTCAGACCT[A/G]GGTTCCAGGATCGGC | 4296 |
rs757844751 | snp | C/G | 1.85341e-05 | 0.00304413 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605712 | GCCTCCCCAAGGTGC[C/G]CACGGAAGGAGCTCA | 4296 |
rs757879340 | snp | C/G/T | 3.2992e-05 | 0.00406142 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608339 | CCAGGCGTAGGTGCC[C/G/T]GCGGCACTCATTTGT | 4296 |
rs757885090 | snp | C/T | 7.94439e-05 | 0.00630203 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607448 | CTCGCGCCGCCGCAG[C/T]TGCTCCGCCTGTGAC | 4296 |
rs757921400 | snp | G/T | 1.80971e-05 | 0.00300803 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598425 | AGTCCGGGAACAAGG[G/T]CCAGGGTGCTCGGCG | 4296 |
rs757953791 | snp | A/G | 9.93855e-05 | 0.00704861 | synonymous-codon, upstream-variant-2KB | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616323 | GGCCATGGGGTCGCA[A/G]GTGTTGCAGATCCTG | 4296 |
rs758121140 | snp | G/T | 9.15485e-05 | 0.00676505 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599751 | CCTCGGGCTCCAGGC[G/T]AGGCCGCGGGGGGTT | 4296 |
rs758263078 | snp | C/G | 6.75276e-05 | 0.00581027 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606656 | GAATAAGGAGCTGGG[C/G]GGCGGAGAGGGGCAT | 4296 |
rs758317455 | snp | A/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603296 | GCAAGAGTTAGCAAC[A/T]CTGTTGTTTAGGAGA | 4296 |
rs758407931 | snp | A/G/T | 3.30171e-05 | 0.00406296 | missense, synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608420 | CTTGTGCTCCATGTC[A/G/T]TCACTCTCAATGGGC | 4296 |
rs758465671 | snp | G/T | 6.61594e-05 | 0.00575112 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608094 | GAGACAACAGGTCTG[G/T]GTTCCCTTTTCTCTC | 4296 |
rs758480097 | snp | A/G | 0.000138124 | 0.00830921 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605976 | TCCCCAGGCTTGGGG[A/G]AACTGGGACCCCAAG | 4296 |
rs758510182 | snp | C/T | 3.056e-05 | 0.00390885 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599359 | GGGAACCCCCGTCTC[C/T]CATATGTGAAGCAGG | 4296 |
rs758537099 | snp | C/T | 2.00979e-05 | 0.00316994 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598367 | CAGTCCTGGGGGCCC[C/T]CCTGGAAGGGGTTGG | 4296 |
rs758623501 | snp | C/T | 0.000165166 | 0.00908603 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607297 | TGATACGCTCGCCGC[C/T]GTCGCGCGCCCGGAG | 4296 |
rs758655505 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609567 | ATGAGAGAAGTTTTC[A/G]AGGAATAGAAAGAGG | 4296 |
rs758769421 | snp | C/T | 6.69271e-05 | 0.00578438 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613306 | CACTGATGTCCTCAT[C/T]GGGGTCCTGGCGAGC | 4296 |
rs758786939 | snp | G/T | 7.36323e-05 | 0.00606718 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599428 | TCGGGGGCTCTTGGC[G/T]GACCGCTGGCCCACA | 4296 |
rs758797291 | in-del | -/CGA | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610561 | CATTTAGCAAGCCCC[-/CGA]CGACAAGCTCATTCC | 4296 |
rs758811212 | snp | C/T | 3.54943e-05 | 0.00421259 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607412 | CTCGAACACCTCTAG[C/T]TCCCACTGGGCCAGC | 4296 |
rs758869808 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604626 | AGGCCAATACTACTA[C/T]TCCCCTCACAGAACT | 4296 |
rs758902516 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615561 | AATGGCTACTCAACT[A/G]TCTCTTTGGTTCCGC | 4296 |
rs759030384 | snp | C/T | 1.79532e-05 | 0.00299604 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613178 | ACCGGCTGCATACTC[C/T]ATCACCAGGCACAGG | 4296 |
rs759072502 | snp | A/G | 5.46602e-05 | 0.00522754 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599485 | TGCAGGAGTGGGCGG[A/G]GAGTCGGGCGTCTTG | 4296 |
rs759080222 | snp | A/C | 0.000493571 | 0.0157016 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613392 | CCTCCAATGCCGATC[A/C]CCTCCTCCAGCCGCA | 4296 |
rs759098631 | snp | G/T | 1.88106e-05 | 0.00306675 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607558 | TCAGCCTGGCACCAA[G/T]CCCGGCAGCGCCCGC | 4296 |
rs759169271 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608530 | AGCAAACTCATCTGA[C/T]GGACATCCTGGCTGG | 4296 |
rs759227355 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606346 | TGATTCTGGCTCTTC[C/T]ACTTATTAACTGTGT | 4296 |
rs759242610 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603174 | CAAAATGAGAGTGAA[C/G]AGAAGTTCCTGCAGT | 4296 |
rs759296633 | snp | C/G | 1.84514e-05 | 0.00303733 | stop-gained, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598409 | TCCCAGAAGGGGTCT[C/G]AGTCCGGGAACAAGG | 4296 |
rs759341826 | snp | G/T | 3.36808e-05 | 0.00410357 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616303 | GGCGCGGGCAGCAGC[G/T]GCGGGGCCATGGGGT | 4296 |
rs759349343 | snp | A/G | 3.35087e-05 | 0.00409307 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607777 | TGCTGCAGGATGGAG[A/G]CGAAGTCGGGCCTGC | 4296 |
rs759384386 | snp | A/G | 1.7208e-05 | 0.00293321 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598501 | TGACACAAAGCTCCA[A/G]GGATCAATGCGGCTG | 4296 |
rs759420941 | snp | C/G | 9.31113e-05 | 0.00682254 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599808 | AGGGTGTGGCTGGTG[C/G]ATATTCCGGGTGAGG | 4296 |
rs759594907 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610185 | ACCTGATGTCCAGGT[A/G]CCCTCCATGACCACC | 4296 |
rs759751814 | snp | A/G | 6.8271e-05 | 0.00584216 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599696 | AGCTTGGGCGTCCCA[A/G]AGCTGCTACCGCGCT | 4296 |
rs759790465 | snp | A/T | 5.49305e-05 | 0.00524044 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606853 | TTTGTGATGAAGTAG[A/T]GCCAGGACCCCAACC | 4296 |
rs759879182 | snp | A/G | 1.67262e-05 | 0.00289185 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608264 | GCCCCACCAAGGGCC[A/G]CACCTCCAGACGTCA | 4296 |
rs759948264 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599188 | TTTCACAGCAGGCAT[C/T]GCCCCCACCTGCCTG | 4296 |
rs759999704 | snp | A/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611381 | GTTTCCTGCCTGTGC[A/C]CCCCACCAGCCCAGG | 4296 |
rs760075378 | snp | G/T | 2.61969e-05 | 0.00361908 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613750 | AGAGGCTCTTCAAGG[G/T]CTCCATGGCCGGGAG | 4296 |
rs760075424 | snp | A/G | 1.65181e-05 | 0.00287381 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608060 | GCAGTTCCCACAGCA[A/G]CACCCCAAAACTGTG | 4296 |
rs760150188 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605303 | TCTCTTCTTCACCTA[C/T]AGGCTCCCAGAAGGG | 4296 |
rs760151604 | in-del | -/C | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601755 | AGCGAGACTCCGTCT[-/C]AAAAAAAAAAAAAAG | 4296 |
rs760201740 | snp | C/T | 0.000167968 | 0.00916275 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613276 | GGGCCTCCTGGCGAA[C/T]GCTCTCGGCTGTCAC | 4296 |
rs760225912 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611774 | AGGAAAAACAGAAGA[C/T]GGGAGTCCCCTCCCC | 4296 |
rs760321394 | snp | A/G | | | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599480 | AGGGGTGCAGGAGTG[A/G]GCGGGGAGTCGGGCG | 4296 |
rs760421556 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608936 | TTTCACACTCAACCC[C/T]AGCACTCAAAACCAT | 4296 |
rs760451378 | snp | A/G | 1.88956e-05 | 0.00307367 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607538 | AGACAGCGATGGTGG[A/G]GAGGTCAGCCTGGCA | 4296 |
rs760505657 | in-del | -/A | 6.50442e-05 | 0.00570244 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606111 | GATGAAATCGGAGAT[-/A]ATCTTTATTCTCCCT | 4296 |
rs760531669 | snp | A/G | 5.46926e-05 | 0.00522908 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599798 | GGCACAGGTGAGGGT[A/G]TGGCTGGTGCATATT | 4296 |
rs760545908 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614829 | ACTACCGGCGCGTGG[A/C]ACCACGGCCGGCTAA | 4296 |
rs760593585 | in-del | -/C | 4.5753e-05 | 0.00478272 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613802 | GACCTTCTCTGGGTG[-/C]CCGTGGTCCCCACCC | 4296 |
rs760647641 | snp | C/T | 0.000431406 | 0.0146805 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607358 | GCGCACGTGCGGTCG[C/T]TCGCGGTCCACCTGC | 4296 |
rs760824405 | snp | C/T | 1.64885e-05 | 0.00287123 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606742 | CCCCAGGCCCGACCT[C/T]GAAGACGTTTCTCCT | 4296 |
rs760840853 | snp | A/G | 1.75909e-05 | 0.00296566 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606841 | GCAGGGTTCAGGTTT[A/G]TGATGAAGTAGAGCC | 4296 |
rs760944599 | snp | C/T | 3.40686e-05 | 0.00412713 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613646 | GGCATAACCCGCTGC[C/T]TTTGGAGACCCCTCA | 4296 |
rs760960892 | snp | A/G | 6.606e-05 | 0.00574679 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608017 | ACAGCAAGGCAGTCA[A/G]TGCCACGGTATGGCA | 4296 |
rs761019211 | snp | A/G | 1.82061e-05 | 0.00301708 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612972 | AGGTTGGGAGCAGGT[A/G]TGTACCAGAGCCATG | 4296 |
rs761098005 | snp | G/T | 1.68599e-05 | 0.00290338 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607934 | TACCGGCCATAAGCT[G/T]TGCGAAGGGCTCGGG | 4296 |
rs761125108 | snp | A/G | 6.6346e-05 | 0.00575922 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605855 | GCGGGACCTTCTCCT[A/G]GTGATGGGAGGGCAA | 4296 |
rs761168855 | snp | A/G | 1.8085e-05 | 0.00300702 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599446 | CCGCTGGCCCACAGG[A/G]ATACCCAGGTCCAGC | 4296 |
rs761204178 | snp | A/G | 0.000108804 | 0.00737497 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599612 | CCTGGGCCTCCCGGC[A/G]GCTGCAGGTCGCGGC | 4296 |
rs761401595 | snp | A/G | 3.3168e-05 | 0.00407221 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605834 | GTACCATGTGGCTTC[A/G]TCCATGCGGGACCTT | 4296 |
rs761419985 | snp | G/T | 1.67789e-05 | 0.00289641 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605922 | GCAAATGATGCTGGG[G/T]CTGGGGGGCACTCAG | 4296 |
rs761496655 | snp | C/T | 1.85699e-05 | 0.00304707 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606856 | GTGATGAAGTAGAGC[C/T]AGGACCCCAACCTGC | 4296 |
rs761531372 | snp | A/G | 9.21871e-05 | 0.0067886 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599625 | GCGGCTGCAGGTCGC[A/G]GCCAAGGCCCAGCGA | 4296 |
rs761532818 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611484 | CTCAGGGAGGCTGAG[A/G]GCACCTTGCCTGCCC | 4296 |
rs761594078 | snp | C/T | 1.70869e-05 | 0.00292286 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613260 | AGCATGGCGAAGAGC[C/T]GGGCCTCCTGGCGAA | 4296 |
rs761601383 | snp | C/T | 1.70697e-05 | 0.00292139 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607902 | GCTCTGTACCTCACC[C/T]GCCCTCCCCGTCCTC | 4296 |
rs761774934 | snp | C/T | 1.70942e-05 | 0.00292349 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598475 | GGCAGGGGAGAAGGC[C/T]GTGGCCCAGCTGACA | 4296 |
rs761793345 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601416 | CTGCCTGCTTCATCA[C/T]ATGAGGTCAGGGCAG | 4296 |
rs761799177 | snp | A/G | 1.64868e-05 | 0.00287109 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608393 | CAGGCCAAAGTCGGT[A/G]ATCTTCAGGGTCTTG | 4296 |
rs761826276 | in-del | -/G | 4.98409e-05 | 0.00499179 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605874 | ATGGGAGGGCAAGGA[-/G]GGGTGCTTTAGGAAT | 4296 |
rs762001420 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600397 | AGCTGAATGGCATAG[C/G]GGCATTATGTTGTCT | 4296 |
rs762054182 | snp | A/G/T | 3.70846e-05 | 0.00430595 | missense, synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598405 | GGAGTCCCAGAAGGG[A/G/T]TCTGAGTCCGGGAAC | 4296 |
rs762074538 | snp | A/C | 0.000258164 | 0.0113585 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599349 | CTCCCTCCCTGGGAA[A/C]CCCCGTCTCCCATAT | 4296 |
rs762110211 | snp | C/G | 1.68122e-05 | 0.00289928 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613559 | CAGCACCTCCACACG[C/G]TCACCCTTCCTCAGG | 4296 |
rs762116269 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600845 | CAGCAGGTTGGATGT[C/T]GGGAGGGAGAAATAC | 4296 |
rs762174188 | snp | C/T | 1.68937e-05 | 0.0029063 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613496 | CACCTGGCCACCCAC[C/T]TGGCCCGCCCACCAG | 4296 |
rs762256510 | snp | G/T | 1.9847e-05 | 0.00315009 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599537 | GAAGGGGGCGGCTCG[G/T]TCGGGCAGGGCGCGG | 4296 |
rs762294465 | snp | A/G | 1.68403e-05 | 0.0029017 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607815 | GTCCTGCGCCCAGCA[A/G]TCTAGGGGCACGGCG | 4296 |
rs762343923 | snp | A/T | 6.60099e-05 | 0.00574461 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606714 | GCTCGGAACCGGGGA[A/T]AGGTGGGCGAATCCC | 4296 |
rs762371469 | snp | A/G | 1.7065e-05 | 0.00292099 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607885 | GTGTCCTGGGCCAGG[A/G]AGCTCTGTACCTCAC | 4296 |
rs762384860 | in-del | -/G | | | downstream-variant-500B, upstream-variant-2KB | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597263 | GCCTCCCAAAGTGCT[-/G]GGATTACAGGCGTGA | 4296 |
rs762540493 | snp | C/T | 3.37826e-05 | 0.00410977 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605763 | GAAGGCCACTCACCA[C/T]TGAGTGCTGGGGGTG | 4296 |
rs762549751 | snp | C/T | 1.75416e-05 | 0.0029615 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607626 | TCCAACGCTGGGTCC[C/T]TTGATTCCTCGCACC | 4296 |
rs762651199 | snp | C/T | 3.63716e-05 | 0.00426432 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612992 | CCAGAGCCATGCCAC[C/T]CCCAACCATGCCCCC | 4296 |
rs762717646 | snp | A/G/T | 0.000149079 | 0.00863257 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598608 | AGCGTGATGTCCCCG[A/G/T]TGGGGGTGAGACAGT | 4296 |
rs762785903 | in-del | -/A | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608897 | CTGGGATTACAGGCC[-/A]CTGCACCTGGCCGAG | 4296 |
rs762787122 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604419 | GGCCTTCCAGCTCTC[A/G]GTTCAGTCCCTGCAG | 4296 |
rs762840511 | snp | A/G | 1.79383e-05 | 0.0029948 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598512 | TCCAGGGATCAATGC[A/G]GCTGCGAAGGGGCGA | 4296 |
rs762853042 | snp | A/T | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606765 | TTTCTCCTCCGGTCA[A/T]GGCCGGGTGAGGCCT | 4296 |
rs762929665 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612434 | TCGCAGGTCGGGCTT[A/G]CCCAAGCTGTTGAGC | 4296 |
rs762933984 | snp | A/G | 5.87976e-05 | 0.00542175 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613761 | AAGGGCTCCATGGCC[A/G]GGAGCCGGCGCTGGG | 4296 |
rs762995424 | in-del | -/GCGCTCT | | | frameshift-variant, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599706 | CCCAGAGCTGCTACC[-/GCGCTCT]GCGCTCTGCGGGGAC | 4296 |
rs763030681 | snp | A/G | 1.656e-05 | 0.00287745 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608289 | ACGTCACTGCCCTTA[A/G]AGAAGGTGGAGGCCT | 4296 |
rs763092184 | snp | C/T | 0.000185856 | 0.00963813 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598270 | AAGGCAGCTGGAGCT[C/T]GGGGGAGTGGCCTGG | 4296 |
rs763137154 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611672 | ACAGGAAGCCGGCTC[A/G]GGGGCAGCAGGAAAC | 4296 |
rs763179055 | snp | A/G | 3.89325e-05 | 0.00441188 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598376 | GGGCCCCCCTGGAAG[A/G]GGTTGGCAGGTGGGG | 4296 |
rs763182102 | snp | C/T | 1.69398e-05 | 0.00291026 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599708 | CCAGAGCTGCTACCG[C/T]GCTCTGCGGGGACAG | 4296 |
rs763236463 | snp | C/G | 1.96385e-05 | 0.0031335 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599532 | GCGGGGAAGGGGGCG[C/G]CTCGGTCGGGCAGGG | 4296 |
rs763294272 | snp | A/G | 2.07308e-05 | 0.00321946 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606096 | ACTGCAGGGGAAACC[A/G]ATGAAATCGGAGATA | 4296 |
rs763348971 | snp | C/T | 1.8284e-05 | 0.00302352 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599490 | GAGTGGGCGGGGAGT[C/T]GGGCGTCTTGAGCGA | 4296 |
rs763365200 | in-del | -/A | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610553 | ACCTGAGCATTTAGC[-/A]AAGCCCCCGACGACA | 4296 |
rs763432626 | snp | C/T | 0.000119061 | 0.00771468 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613395 | CCAATGCCGATCACC[C/T]CCTCCAGCCGCAGCT | 4296 |
rs763449769 | snp | C/T | 1.68286e-05 | 0.0029007 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605768 | CCACTCACCATTGAG[C/T]GCTGGGGGTGTGGAA | 4296 |
rs763454395 | in-del | -/T | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615407 | GTACGAGGTCCAGCA[-/T]TAAAGGGGGCGGGCC | 4296 |
rs763537644 | snp | A/G | 1.84208e-05 | 0.00303481 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598518 | GATCAATGCGGCTGC[A/G]AAGGGGCGAGGGCCG | 4296 |
rs763549876 | snp | A/G | 2.88604e-05 | 0.0037986 | synonymous-codon, upstream-variant-2KB | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616332 | GTCGCAGGTGTTGCA[A/G]ATCCTGCGCCAGGGG | 4296 |
rs763559569 | snp | G/T | 1.64857e-05 | 0.00287099 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608375 | TTTGTGCCACTCTCG[G/T]GCCAGGCCAAAGTCG | 4296 |
rs763790363 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605206 | CAGTAGGGCAGTTAC[C/T]GTCATGGAGAACAGA | 4296 |
rs763812821 | snp | A/G | 8.44245e-05 | 0.00649655 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613470 | GACACATAGTTGGAC[A/G]GGAAGATGCCCACCT | 4296 |
rs763814509 | snp | C/T | 1.74427e-05 | 0.00295314 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607634 | TGGGTCCCTTGATTC[C/T]TCGCACCTTTTCCTT | 4296 |
rs763902491 | snp | A/G/T | 5.04718e-05 | 0.00502332 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607807 | CGGTGGGGGTCCTGC[A/G/T]CCCAGCAGTCTAGGG | 4296 |
rs763931056 | snp | C/T | 1.65359e-05 | 0.00287536 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606792 | GCCTGCACGGTGATG[C/T]GGTGCTTGAAGTCTG | 4296 |
rs764029799 | snp | C/T | 1.83515e-05 | 0.00302909 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599432 | GGGCTCTTGGCTGAC[C/T]GCTGGCCCACAGGGA | 4296 |
rs764042587 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603323 | GAGAAAGCTGCGTGA[C/T]TATTCTTGACCCAAA | 4296 |
rs764096366 | snp | C/T | 1.81817e-05 | 0.00301504 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612994 | AGAGCCATGCCACCC[C/T]CAACCATGCCCCCAG | 4296 |
rs764134023 | in-del | -/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609300 | CCCACATCACACTGT[-/G]GGCAAGTGCAGCCAC | 4296 |
rs764176941 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612437 | CAGGTCGGGCTTGCC[C/T]AAGCTGTTGAGCTGT | 4296 |
rs764181266 | snp | G/T | 1.65433e-05 | 0.002876 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608294 | ACTGCCCTTAGAGAA[G/T]GTGGAGGCCTTGATA | 4296 |
rs764206080 | snp | A/G | 5.67951e-05 | 0.00532863 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613679 | CCGGCCTCCTCCACC[A/G]CCCCCACCACCCCCG | 4296 |
rs764222517 | snp | C/T | 1.65479e-05 | 0.0028764 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608099 | AACAGGTCTGTGTTC[C/T]CTTTTCTCTCCCAAC | 4296 |
rs764372087 | snp | C/T | 1.97042e-05 | 0.00313875 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599535 | GGGAAGGGGGCGGCT[C/T]GGTCGGGCAGGGCGC | 4296 |
rs764379333 | snp | A/G | 3.0232e-05 | 0.00388781 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613765 | GCTCCATGGCCGGGA[A/G]CCGGCGCTGGGATGT | 4296 |
rs764474783 | snp | A/G | 1.78487e-05 | 0.00298731 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598271 | AGGCAGCTGGAGCTC[A/G]GGGGAGTGGCCTGGC | 4296 |
rs764566604 | snp | C/T | 5.42245e-05 | 0.00520666 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606036 | GAGTCCTCCAGACGT[C/T]GGGGGGACTGGCGGC | 4296 |
rs764602712 | snp | C/T | 3.75686e-05 | 0.00433392 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607561 | GCCTGGCACCAATCC[C/T]GGCAGCGCCCGCCCC | 4296 |
rs764634524 | snp | C/T | | | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612402 | TCCATGGCTGAGGAC[C/T]CGCTGTGGGTTGGGG | 4296 |
rs764656241 | snp | C/G | 2.08574e-05 | 0.00322929 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606099 | GCAGGGGAAACCGAT[C/G]AAATCGGAGATAATC | 4296 |
rs764694994 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600325 | GAGGTTCAGAGGGGT[C/T]AGTACCTTGCCCAAG | 4296 |
rs764792741 | in-del | -/G | 5.07357e-05 | 0.00503639 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606819 | TCTGGGATTTGGGTT[-/G]GGGGGAGCAGGGTTC | 4296 |
rs764800427 | snp | C/T | 8.49322e-05 | 0.00651605 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613393 | CTCCAATGCCGATCA[C/T]CTCCTCCAGCCGCAG | 4296 |
rs764834459 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615619 | CCTGGGTCTACGCAT[C/G]CGCCCAAACGCTTTT | 4296 |
rs764946306 | snp | C/T | 0.000230335 | 0.0107291 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607391 | CAGCAGCAGCGTCAG[C/T]TCGCGCTCGAACACC | 4296 |
rs764953350 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608742 | CCTGCCCCAGCCTCC[C/T]GAGTAGTGGGATTAT | 4296 |
rs764954819 | snp | A/G | 1.75041e-05 | 0.00295833 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598507 | AAAGCTCCAGGGATC[A/G]ATGCGGCTGCGAAGG | 4296 |
rs765006637 | snp | A/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606415 | TAAATTAACAACAAA[A/T]ATAACTACCAAATAG | 4296 |
rs765026571 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603271 | GAATCTGCCTCTAAG[C/T]TTCCTGGCAGCAAGA | 4296 |
rs765085120 | snp | C/T | 4.38548e-05 | 0.00468247 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613796 | GTGGAGGACCTTCTC[C/T]GGGTGCCCGTGGTCC | 4296 |
rs765085231 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601653 | CCCAGATACTCAAGA[A/G]GCTGAGGCAGGAGAA | 4296 |
rs765086066 | snp | A/G | 3.30071e-05 | 0.00406232 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608417 | GGTCTTGTGCTCCAT[A/G]TCGTCACTCTCAATG | 4296 |
rs765123706 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601530 | GGGAGGCCCAGGTGG[A/G]ATGATCACGAGGTCA | 4296 |
rs765139619 | snp | C/T | 0.000157038 | 0.00885969 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599815 | GGCTGGTGCATATTC[C/T]GGGTGAGGGCCCAAG | 4296 |
rs765225812 | snp | C/T | 3.67195e-05 | 0.00428467 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598414 | GAAGGGGTCTGAGTC[C/T]GGGAACAAGGTCCAG | 4296 |
rs765227651 | snp | G/T | 1.73957e-05 | 0.00294916 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605745 | CAGATCCTGCCGGGG[G/T]AGGAAGGCCACTCAC | 4296 |
rs765239856 | snp | A/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610195 | CAGGTGCCCTCCATG[A/T]CCACCTTTACTATCC | 4296 |
rs765260408 | snp | A/G | 1.67536e-05 | 0.00289423 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607947 | CTGTGCGAAGGGCTC[A/G]GGGCAGGTGGATGGG | 4296 |
rs765441333 | snp | A/G | 1.83913e-05 | 0.00303238 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598243 | GTTCCAGTGTATGCT[A/G]TGACTCCTCCTAAGG | 4296 |
rs765456719 | snp | A/C | 1.68199e-05 | 0.00289994 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613610 | GGGCTCGTAGTCGAA[A/C]AGGGCTGTCCACACC | 4296 |
rs765538121 | snp | C/T | 2.59906e-05 | 0.0036048 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599584 | TGTTGTCGGGGACTC[C/T]CCGCGCTCGCGTCCT | 4296 |
rs765625058 | snp | C/T | 1.87131e-05 | 0.00305879 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599622 | CCGGCGGCTGCAGGT[C/T]GCGGCCAAGGCCCAG | 4296 |
rs765660467 | snp | A/G | 5.46961e-05 | 0.00522925 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599488 | AGGAGTGGGCGGGGA[A/G]TCGGGCGTCTTGAGC | 4296 |
rs765724275 | snp | A/G | 3.41863e-05 | 0.00413424 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605957 | TCACCTCCCATTCTG[A/G]GCTTCCCCAGGCTTG | 4296 |
rs765743075 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598091 | GTGAGCTGGGGGGAC[A/C]TACAGGTTTCAGATG | 4296 |
rs765752888 | snp | A/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606153 | GTCAGGCTTCAGAGA[A/T]AAACTTTAGAGTATG | 4296 |
rs765767167 | snp | A/G | 3.35711e-05 | 0.00409688 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613277 | GGCCTCCTGGCGAAC[A/G]CTCTCGGCTGTCACA | 4296 |
rs765837478 | snp | C/T | 0.000224694 | 0.010597 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607265 | CCCCGGGGCCCGGCC[C/T]TCACCGAGTGGCATG | 4296 |
rs765969079 | in-del | -/G | 0.00010169 | 0.00712983 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606653 | AGAGAATAAGGAGCT[-/G]GGGGGCGGAGAGGGG | 4296 |
rs766010610 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609363 | AATGCAGCTGGAAGG[A/G]AAGAGAAAGGGTGGG | 4296 |
rs766019315 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605345 | CACAGTGTGGCTGAC[A/G]CTTGTTTGGCTCCAC | 4296 |
rs766033369 | snp | A/C/G | 3.36622e-05 | 0.00410246 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605930 | TGCTGGGTCTGGGGG[A/C/G]CACTCAGGTACTCAC | 4296 |
rs766037928 | snp | A/G | 1.80331e-05 | 0.00300271 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613139 | AGGCACGCGCCGCCC[A/G]GCCAGAGCTCGGCTG | 4296 |
rs766092829 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612023 | GTCAGCCCAGGCCAG[A/G]AGGCTCAAAATATCC | 4296 |
rs766095232 | snp | G/T | 0.0120675 | 0.0767367 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599806 | TGAGGGTGTGGCTGG[G/T]GCATATTCCGGGTGA | 4296 |
rs766105925 | snp | A/G | 0.000276434 | 0.0117533 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598646 | GTGAGGATATAGGAG[A/G]GGCACAGGGTCAAGC | 4296 |
rs766131413 | snp | C/T | 0.000154907 | 0.00879939 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598306 | TCAAGGCCCCGCTTC[C/T]GGCACCCACGGGGCC | 4296 |
rs766164452 | in-del | -/G | 0.000189036 | 0.0097202 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616283 | ATGAGGGTCCCGGGA[-/G]GGGGGGCGCGGGCAG | 4296 |
rs766221169 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612692 | GAAGATGAGGAGCAC[A/G]AGCTTCCAGAGGACT | 4296 |
rs766321466 | snp | A/G | 3.17839e-05 | 0.00398634 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613771 | TGGCCGGGAGCCGGC[A/G]CTGGGATGTGTGGAG | 4296 |
rs766364469 | snp | C/T | | | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599643 | CAAGGCCCAGCGAGG[C/T]GAGCAGGGCGGTGCC | 4296 |
rs766371770 | snp | G/T | 1.88571e-05 | 0.00307053 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607542 | AGCGATGGTGGAGAG[G/T]TCAGCCTGGCACCAA | 4296 |
rs766392971 | snp | A/G | 4.27469e-05 | 0.00462295 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599620 | TCCCGGCGGCTGCAG[A/G]TCGCGGCCAAGGCCC | 4296 |
rs766486524 | snp | C/T | 1.68935e-05 | 0.00290628 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613513 | GGCCCGCCCACCAGC[C/T]CTCGTCTCCTGAGAT | 4296 |
rs766567022 | snp | C/T | 2.09826e-05 | 0.00323896 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599548 | CTCGGTCGGGCAGGG[C/T]GCGGGCGTTGGCGTG | 4296 |
rs766611917 | snp | A/G | 1.66023e-05 | 0.00288113 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605865 | CTCCTGGTGATGGGA[A/G]GGCAAGGAGGGGTGC | 4296 |
rs766684677 | snp | A/G | 1.82028e-05 | 0.0030168 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612976 | TGGGAGCAGGTGTGT[A/G]CCAGAGCCATGCCAC | 4296 |
rs766705913 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597962 | TGACAGCTGAGGCCG[G/T]CCCCTCTTCCCTGCA | 4296 |
rs766718638 | snp | C/T | 1.65124e-05 | 0.00287331 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608031 | AATGCCACGGTATGG[C/T]ACCTCCCCGGTCAGC | 4296 |
rs766735682 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601500 | GGTGGCTCACATCTG[C/T]AATCCCAGCACTTTG | 4296 |
rs766774276 | snp | C/T | 6.59402e-05 | 0.00574158 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606756 | TCGAAGACGTTTCTC[C/T]TCCGGTCAAGGCCGG | 4296 |
rs766868287 | snp | C/T | 0.00010829 | 0.00735752 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598620 | CCGGTGGGGGTGAGA[C/T]AGTGCCTCCTGTGAG | 4296 |
rs766891617 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609026 | CTTGGCAGAGGTCAT[A/G]CAACAAATACAGCAG | 4296 |
rs767076424 | snp | C/G | 0.000116834 | 0.0076422 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599399 | GGCCACTCACCGCGG[C/G]GCTCCTCCTCACGTC | 4296 |
rs767102152 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609733 | CTGCCCTGTGTGACA[C/T]GGCTGTCATGGGGGC | 4296 |
rs767171001 | snp | C/T | 0.000221117 | 0.0105123 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607352 | GCGGCGGCGCACGTG[C/T]GGTCGCTCGCGGTCC | 4296 |
rs767233839 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599140 | GCTGGGATCACAGGC[A/G]TGCACCACTGCCTGG | 4296 |
rs767385503 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605118 | CTTCACCTCTCAGAG[C/T]CTCAGTTTCCTTATC | 4296 |
rs767433009 | snp | C/T | 1.80445e-05 | 0.00300365 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613134 | TGGGGAGGCACGCGC[C/T]GCCCGGCCAGAGCTC | 4296 |
rs767500994 | in-del | -/G | 6.72625e-05 | 0.00579886 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605924 | AATGATGCTGGGTCT[-/G]GGGGGGCACTCAGGT | 4296 |
rs767587349 | snp | A/C | 6.49878e-05 | 0.00569997 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606111 | GATGAAATCGGAGAT[A/C]ATCTTTATTCTCCCT | 4296 |
rs767622827 | snp | C/T | 1.65244e-05 | 0.00287436 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608303 | AGAGAAGGTGGAGGC[C/T]TTGATAACCTCAGGA | 4296 |
rs767643360 | snp | G/T | 1.83363e-05 | 0.00302784 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606047 | ACGTCGGGGGGACTG[G/T]CGGCCCCATGCCTGG | 4296 |
rs767691892 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601432 | ATGAGGTCAGGGCAG[C/T]GTTTAACATGTTGAT | 4296 |
rs767716906 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608969 | ATGAGCTAAATAATA[G/T]TTTTCATGTTTCACA | 4296 |
rs767785768 | snp | A/C | 6.59533e-05 | 0.00574215 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608399 | AAAGTCGGTGATCTT[A/C]AGGGTCTTGTGCTCC | 4296 |
rs767843052 | snp | A/G/T | 0.000102534 | 0.0071595 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616289 | GTCCCGGGAGGGGGG[A/G/T]CGCGGGCAGCAGCGG | 4296 |
rs767888238 | snp | C/G | 1.67888e-05 | 0.00289726 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613579 | CCTTCCTCAGGGCCA[C/G]CTCATCCTGCCCACT | 4296 |
rs767989362 | snp | C/T | 4.01752e-05 | 0.00448174 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599539 | AGGGGGCGGCTCGGT[C/T]GGGCAGGGCGCGGGC | 4296 |
rs768169186 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610817 | AACAACTCACCCAAA[A/G]TTTCAGGACTTCTTT | 4296 |
rs768235387 | snp | C/G | 1.69458e-05 | 0.00291078 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613638 | ACCGGGTTGGCATAA[C/G]CCGCTGCCTTTGGAG | 4296 |
rs768235592 | snp | C/T | 1.70918e-05 | 0.00292329 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607895 | CCAGGGAGCTCTGTA[C/T]CTCACCTGCCCTCCC | 4296 |
rs768273388 | snp | A/G | 7.9648e-05 | 0.00631012 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599395 | TTCAGGCCACTCACC[A/G]CGGGGCTCCTCCTCA | 4296 |
rs768276539 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612199 | CTGCTTCCATGCCTT[C/T]TCTCTCTAAATGCTG | 4296 |
rs768336877 | snp | A/G | 5.63174e-05 | 0.00530618 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599595 | ACTCCCCGCGCTCGC[A/G]TCCTGGGCCTCCCGG | 4296 |
rs768385255 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609884 | ACAAGCCCTGATCCT[A/G]CTGCTGGCCAGGCCA | 4296 |
rs768524074 | snp | C/T | 1.80049e-05 | 0.00300035 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599458 | AGGGATACCCAGGTC[C/T]AGCAACAGGGGTGCA | 4296 |
rs768531907 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611156 | ACACCTCTTCCGCTT[C/T]CCTCCCGTGGTCCCT | 4296 |
rs768612025 | snp | G/T | 1.65798e-05 | 0.00287917 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605831 | CAGGTACCATGTGGC[G/T]TCGTCCATGCGGGAC | 4296 |
rs768673829 | in-del | -/CAGAA | 0.000199856 | 0.00999441 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613007 | CCCCAACCATGCCCC[-/CAGAA]ACTCACTGTTGTTGG | 4296 |
rs768688511 | snp | C/T | 1.65433e-05 | 0.002876 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607991 | GCTTGTTAACAGCTA[C/T]GCCATAGGCCACAGC | 4296 |
rs768752926 | in-del | -/GGGCTCCTC | 0 | 0 | cds-indel, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599730 | GGGGACAGGCCTCTT[-/GGGCTCCTC]GGGCTCCTCGGGCTC | 4296 |
rs768786864 | in-del | -/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606283 | GCCCTTGGGCTGAAG[-/T]TTGCTGCTTAGTAAT | 4296 |
rs768797212 | snp | A/G | 1.92873e-05 | 0.00310537 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598381 | CCCCTGGAAGGGGTT[A/G]GCAGGTGGGGAGTCC | 4296 |
rs768870857 | snp | A/G | 1.65974e-05 | 0.0028807 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605804 | TCCTAAGGGGGATGA[A/G]TCATCTGAATCCAGG | 4296 |
rs768888767 | snp | A/G | 1.71018e-05 | 0.00292414 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598471 | TGATGGCAGGGGAGA[A/G]GGCCGTGGCCCAGCT | 4296 |
rs768954769 | snp | A/C | 1.65146e-05 | 0.0028735 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606707 | CTGGATGGCTCGGAA[A/C]CGGGGAAAGGTGGGC | 4296 |
rs768976919 | in-del | -/A | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602645 | ATGACACTTCATCTC[-/A]AAAAAAAAAAAAATT | 4296 |
rs769021512 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601279 | CAGTGACCTCTTATG[C/T]ACCATCCAAGACCAA | 4296 |
rs769023854 | in-del | -/TTTTTTTTTTT/TTTTTTTTTTTT | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614681 | TCATTATTTTCTTTC[-/TTTTTTTTTTT/TTTTTTTTTTTT]TTTTTTCTTCTTTTG | 4296 |
rs769028417 | snp | C/G | 2.2567e-05 | 0.00335902 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599565 | CGGGCGTTGGCGTGG[C/G]GGGTGTTGTCGGGGA | 4296 |
rs769042664 | snp | A/G | 3.43324e-05 | 0.00414307 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606825 | ATTTGGGTTGGGGGG[A/G]GCAGGGTTCAGGTTT | 4296 |
rs769076498 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613926 | TGTCTCCCGGCCCCC[C/T]GCATCTCGGGCTTCT | 4296 |
rs769131035 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602421 | GAAGCTGAAGCAGGT[A/G]GCTCACTTGAGGTCA | 4296 |
rs769182471 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615870 | GAGCGCGGAGCCCCA[A/C]GCAAGTGACCTGCGA | 4296 |
rs769298739 | snp | A/G | 1.692e-05 | 0.00290856 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613453 | GCGGGCCGCCACCCC[A/G]AGACACATAGTTGGA | 4296 |
rs769337531 | snp | A/C/G | 0.000135249 | 0.00822242 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599563 | CGCGGGCGTTGGCGT[A/C/G]GGGGGTGTTGTCGGG | 4296 |
rs769482000 | snp | A/G | 1.66724e-05 | 0.0028872 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606676 | GAGAGGGGCATGAGA[A/G]GTGAAGTTTCTTACA | 4296 |
rs769523347 | snp | C/T | 1.65842e-05 | 0.00287955 | stop-gained, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605823 | TCTGAATCCAGGTAC[C/T]ATGTGGCTTCGTCCA | 4296 |
rs769612134 | snp | C/T | 5.63206e-05 | 0.00530633 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598600 | AGGAGCAGAGCGTGA[C/T]GTCCCCGGTGGGGGT | 4296 |
rs769666459 | snp | A/G | 3.3389e-05 | 0.00408575 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605901 | GAATTTCAGGACTTG[A/G]GGAAAGCAAATGATG | 4296 |
rs769675788 | snp | C/T | 8.50984e-05 | 0.00652242 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607875 | GTGGGTGGATGTGTC[C/T]TGGGCCAGGGAGCTC | 4296 |
rs769708799 | snp | C/G | 2.28689e-05 | 0.00338141 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607485 | TCGCGCGCCGCTCGC[C/G]TCAGCTCCTCCTCGC | 4296 |
rs769768283 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608778 | TGTGCCACCACGCCC[A/G]ACTAATTTTGCATTT | 4296 |
rs769831790 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605693 | TGCCTACTAGCCTAT[C/T]GTGGCCTCCCCAAGG | 4296 |
rs769929442 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, KCNK7 | GRCh38.p7 | 11:65597942 | GACTTGGTCAAAAGT[A/G]CTGGTGACAGCTGAG | 4296 |
rs769940928 | snp | C/T | 0.000118008 | 0.0076805 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599706 | TCCCAGAGCTGCTAC[C/T]GCGCTCTGCGGGGAC | 4296 |
rs769979690 | snp | C/G/T | 6.69718e-05 | 0.00578637 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613322 | GGGGTCCTGGCGAGC[C/G/T]GCCTTCACAGCCACC | 4296 |
rs770023643 | snp | C/T | 1.75056e-05 | 0.00295846 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613243 | TGATGTTGGGGTGTG[C/T]CAGCATGGCGAAGAG | 4296 |
rs770038305 | in-del | -/GGT | 2.29387e-05 | 0.00338656 | cds-indel, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599567 | GGCGTTGGCGTGGGG[-/GGT]GTTGTCGGGGACTCC | 4296 |
rs770083831 | snp | G/T | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608353 | CCGCGGCACTCATTT[G/T]TGTGGTTTTGTGCCA | 4296 |
rs770108989 | snp | A/G | 0.000333167 | 0.0129024 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607327 | GCTTGCTGCGCTTGA[A/G]TGTCCCGCGGCGGCG | 4296 |
rs770111161 | snp | C/G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65610941 | TCAACTGTCCCAACT[C/G/T]GAACTGCTGTTCTGG | 4296 |
rs770171700 | snp | A/C | 4.09937e-05 | 0.00452716 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606094 | CCACTGCAGGGGAAA[A/C]CGATGAAATCGGAGA | 4296 |
rs770174212 | snp | C/T | 5.73148e-05 | 0.00535295 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613759 | TCAAGGGCTCCATGG[C/T]CGGGAGCCGGCGCTG | 4296 |
rs770188314 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614791 | CAAGAGATTCTCCTG[-/C]CTCAGCCTCCCGAGT | 4296 |
rs770252416 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613788 | TGGGATGTGTGGAGG[A/G]CCTTCTCTGGGTGCC | 4296 |
rs770259335 | snp | A/G | | | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612404 | CATGGCTGAGGACCC[A/G]CTGTGGGTTGGGGAT | 4296 |
rs770265239 | snp | C/T | 1.75332e-05 | 0.0029608 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598444 | GGGTGCTCGGCGGGG[C/T]GCAGGCTGTGGTGAT | 4296 |
rs770397589 | snp | C/G/T | 9.20683e-05 | 0.00678422 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616283 | ATGAGGGTCCCGGGA[C/G/T]GGGGGGCGCGGGCAG | 4296 |
rs770405733 | snp | C/T | 3.95695e-05 | 0.00444783 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606085 | CTGCAGGCTCCACTG[C/T]AGGGGAAACCGATGA | 4296 |
rs770439390 | snp | A/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600382 | TTTGTGCCAGGCCTG[A/T]GCTGAATGGCATAGG | 4296 |
rs770458398 | snp | C/T | 1.68323e-05 | 0.00290101 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608255 | GCCCGTCCAGCCCCA[C/T]CAAGGGCCGCACCTC | 4296 |
rs770461213 | snp | A/G | 2.07089e-05 | 0.00321776 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598361 | GCCCTGCAGTCCTGG[A/G]GGCCCCCCTGGAAGG | 4296 |
rs770556617 | snp | C/T | 1.7904e-05 | 0.00299193 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606028 | CATTGCTTGAGTCCT[C/T]CAGACGTCGGGGGGA | 4296 |
rs770654079 | snp | A/C | 1.66793e-05 | 0.0028878 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607760 | CCTCCAGCGCCTCCA[A/C]CTGCTGCAGGATGGA | 4296 |
rs770675194 | snp | C/G | 1.64928e-05 | 0.00287161 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608342 | GGCGTAGGTGCCCGC[C/G]GCACTCATTTGTGTG | 4296 |
rs770743812 | snp | A/G | 1.69158e-05 | 0.00290819 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607846 | TGCAGCGGGGACAGA[A/G]TAAGAAGGGGTCCGT | 4296 |
rs770880024 | snp | A/T | 3.36118e-05 | 0.00409936 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613354 | GCTCACCTCGCCAGC[A/T]GCCCCTGTACACCTT | 4296 |
rs771076308 | snp | A/G | 3.55101e-05 | 0.00421352 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606843 | AGGGTTCAGGTTTGT[A/G]ATGAAGTAGAGCCAG | 4296 |
rs771076394 | snp | A/G | 5.36246e-05 | 0.00517778 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613198 | CCAGGCACAGGTTGG[A/G]CTCCTCCAGGCACAC | 4296 |
rs771164223 | snp | C/T | 0.000159426 | 0.00892679 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607318 | GCGCCCGGAGCTTGC[C/T]GCGCTTGAATGTCCC | 4296 |
rs771189864 | snp | G/T | 8.67265e-05 | 0.00658451 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599759 | TCCAGGCTAGGCCGC[G/T]GGGGGTTACCTGCGG | 4296 |
rs771197158 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604123 | GAATTACTTAGAAGT[C/T]TGTCACTGATCTGAA | 4296 |
rs771234053 | snp | G/T | | | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607309 | CGCCGTCGCGCGCCC[G/T]GAGCTTGCTGCGCTT | 4296 |
rs771234612 | snp | C/T | 2.4536e-05 | 0.00350248 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613740 | CTCTTGAGGAAGAGG[C/T]TCTTCAAGGGCTCCA | 4296 |
rs771325830 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604908 | GCCTCACTCAGAGCT[A/G]GGCAGTGTTGAGCTG | 4296 |
rs771344710 | in-del | -/C | 0.000106951 | 0.0073119 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599382 | GAAGCAGGCCGGCTT[-/C]AGGCCACTCACCGCG | 4296 |
rs771346201 | snp | A/T | 5.43001e-05 | 0.00521029 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613110 | TGCACAGCCCAGTTG[A/T]CCAGCACATGGGGAG | 4296 |
rs771434772 | snp | G/T | 1.71905e-05 | 0.00293172 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613653 | CCCGCTGCCTTTGGA[G/T]ACCCCTCAGGCCGGC | 4296 |
rs771511538 | snp | A/G | 8.79701e-05 | 0.00663154 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599673 | CGCGCAGCAGCGCCC[A/G]CTGGATCAGCTTGGG | 4296 |
rs771552529 | snp | A/G | 3.39288e-05 | 0.00411865 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608239 | CTGCAGCCCCGTAGC[A/G]GCCCGTCCAGCCCCA | 4296 |
rs771573042 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604959 | ATGCTGGAGCCCTGC[C/T]TTCTGCCTGACCCTC | 4296 |
rs771640479 | snp | C/T | 1.68165e-05 | 0.00289965 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605924 | AAATGATGCTGGGTC[C/T]GGGGGGCACTCAGGT | 4296 |
rs771676610 | snp | A/G | | | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598522 | AATGCGGCTGCGAAG[A/G]GGCGAGGGCCGAGGT | 4296 |
rs771714616 | snp | C/G | | | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612356 | ATTTCAGGCTAGGCC[C/G]TCTTGGCGATCCAGC | 4296 |
rs771728761 | snp | A/G | 1.77269e-05 | 0.0029771 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606007 | CCCAGCATGCTCGCC[A/G]CTCTCCATTGCTTGA | 4296 |
rs771808903 | snp | A/G | 1.64743e-05 | 0.00287 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613338 | GCCTTCACAGCCACC[A/G]GCTCACCTCGCCAGC | 4296 |
rs771825448 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607832 | CTAGGGGCACGGCGT[A/G]CAGCGGGGACAGAAT | 4296 |
rs771826070 | snp | C/G | 4.47838e-05 | 0.0047318 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613724 | CCATGACCCTAGAGG[C/G]CTCTTGAGGAAGAGG | 4296 |
rs772022239 | snp | G/T | 1.80762e-05 | 0.00300629 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606038 | GTCCTCCAGACGTCG[G/T]GGGGACTGGCGGCCC | 4296 |
rs772163782 | in-del | -/CCCACCTGGCCA | 1.68832e-05 | 0.00290539 | cds-indel, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613479 | TTGGACGGGAAGATG[-/CCCACCTGGCCA]CCCACCTGGCCCGCC | 4296 |
rs772174216 | snp | C/G | 1.80026e-05 | 0.00300016 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599466 | CCAGGTCCAGCAACA[C/G]GGGTGCAGGAGTGGG | 4296 |
rs772229508 | snp | C/T | 1.68411e-05 | 0.00290177 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608477 | GCCAGATTGTGGATG[C/T]TCCAGGATCAGGTGG | 4296 |
rs772335580 | snp | A/G/T | 0.000474599 | 0.0153986 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616285 | GAGGGTCCCGGGAGG[A/G/T]GGGGCGCGGGCAGCA | 4296 |
rs772354978 | snp | C/G | 1.77779e-05 | 0.00298138 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599665 | GGCGGTGCCGCGCAG[C/G]AGCGCCCGCTGGATC | 4296 |
rs772378784 | snp | A/G | 3.41717e-05 | 0.00413336 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598476 | GCAGGGGAGAAGGCC[A/G]TGGCCCAGCTGACAC | 4296 |
rs772414583 | in-del | -/CT | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603941 | CCCTGGGGGCTGCGG[-/CT]CTCTCAGTTTGCAGG | 4296 |
rs772428256 | snp | C/G | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606735 | GGCGAATCCCCAGGC[C/G]CGACCTCGAAGACGT | 4296 |
rs772655083 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603733 | CAGCCAGCCACTGAG[C/T]TGGGCAGCTGACATC | 4296 |
rs772677421 | snp | C/G/T | 3.63341e-05 | 0.00426215 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613077 | TCGCAGTGCAGGTAG[C/G/T]GCATCCCACGGGCAA | 4296 |
rs772694332 | snp | C/T | 3.50342e-05 | 0.0041852 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606839 | GAGCAGGGTTCAGGT[C/T]TGTGATGAAGTAGAG | 4296 |
rs772696603 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607056 | CTTTCGTGAACCCCA[C/T]CCCTTCCCACTCCCA | 4296 |
rs772753565 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598651 | GATATAGGAGGGGCA[C/T]AGGGTCAAGCAACCC | 4296 |
rs772762859 | snp | C/T | 3.38181e-05 | 0.00411192 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608247 | CCGTAGCAGCCCGTC[C/T]AGCCCCACCAAGGGC | 4296 |
rs772848649 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614828 | GACTACCGGCGCGTG[A/G]CACCACGGCCGGCTA | 4296 |
rs772856050 | snp | A/G | 1.65168e-05 | 0.00287369 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608009 | CATAGGCCACAGCAA[A/G]GCAGTCAATGCCACG | 4296 |
rs772898141 | snp | C/T | 1.77209e-05 | 0.0029766 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606016 | CTCGCCGCTCTCCAT[C/T]GCTTGAGTCCTCCAG | 4296 |
rs773041548 | snp | C/G | 1.92832e-05 | 0.00310504 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607521 | AGTAGTTCCTGCGCC[C/G]GAGACAGCGATGGTG | 4296 |
rs773165963 | snp | C/T | 1.67925e-05 | 0.00289758 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613341 | TTCACAGCCACCAGC[C/T]CACCTCGCCAGCTGC | 4296 |
rs773167892 | snp | C/T | 1.98474e-05 | 0.00315013 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607356 | CGGCGCACGTGCGGT[C/T]GCTCGCGGTCCACCT | 4296 |
rs773183989 | snp | A/G | 6.81315e-05 | 0.00583619 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608229 | CCTCTGCCCTCTGCA[A/G]CCCCGTAGCAGCCCG | 4296 |
rs773235826 | in-del | -/CCT | 1.77049e-05 | 0.00297526 | cds-indel, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613668 | GACCCCTCAGGCCGG[-/CCT]CCTCCACCGCCCCCA | 4296 |
rs773277282 | snp | G/T | 1.80273e-05 | 0.00300222 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599470 | GTCCAGCAACAGGGG[G/T]GCAGGAGTGGGCGGG | 4296 |
rs773304406 | snp | C/T | 1.70784e-05 | 0.00292214 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598481 | GGAGAAGGCCGTGGC[C/T]CAGCTGACACAAAGC | 4296 |
rs773390948 | snp | C/T | 3.29832e-05 | 0.00406085 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606736 | GCGAATCCCCAGGCC[C/T]GACCTCGAAGACGTT | 4296 |
rs773418840 | snp | A/G | 1.67871e-05 | 0.00289711 | stop-gained, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613588 | GGGCCAGCTCATCCT[A/G]CCCACTGGGCTCGTA | 4296 |
rs773452677 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614907 | GTCTCAAACCCCTGA[-/C]CTCGTGATCCTCCCG | 4296 |
rs773588472 | snp | G/T | 1.75888e-05 | 0.00296548 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606840 | AGCAGGGTTCAGGTT[G/T]GTGATGAAGTAGAGC | 4296 |
rs773597052 | snp | C/T | 3.61109e-05 | 0.00424901 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599611 | TCCTGGGCCTCCCGG[C/T]GGCTGCAGGTCGCGG | 4296 |
rs773602183 | snp | A/G | 3.45e-05 | 0.00415317 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608500 | TCAGGTGGTGGGGAC[A/G]GGGTAAGAGCTGGGA | 4296 |
rs773635155 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614978 | CCGCGCCCGGCCATT[A/C]TTTTCATATATGATA | 4296 |
rs773685190 | snp | C/G | 1.6989e-05 | 0.00291449 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613642 | GGTTGGCATAACCCG[C/G]TGCCTTTGGAGACCC | 4296 |
rs773754882 | snp | C/G | 2.3448e-05 | 0.00342395 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599573 | GGCGTGGGGGGTGTT[C/G]TCGGGGACTCCCCGC | 4296 |
rs773901002 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603747 | GCTGGGCAGCTGACA[C/T]CCTTTCAGGGCAAGT | 4296 |
rs773986232 | snp | C/G/T | 0.000138172 | 0.00831086 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599608 | GCGTCCTGGGCCTCC[C/G/T]GGCGGCTGCAGGTCG | 4296 |
rs774035099 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599076 | CAGTGTCATGATCAC[C/T]GCTCACTGCAGCCTC | 4296 |
rs774055831 | snp | C/T | 1.65307e-05 | 0.0028749 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607996 | TTAACAGCTACGCCA[C/T]AGGCCACAGCAAGGC | 4296 |
rs774075066 | snp | C/T | 1.73057e-05 | 0.00294152 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613252 | GGTGTGCCAGCATGG[C/T]GAAGAGCCGGGCCTC | 4296 |
rs774092295 | snp | A/G | 3.36344e-05 | 0.00410074 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613558 | ACAGCACCTCCACAC[A/G]GTCACCCTTCCTCAG | 4296 |
rs774094158 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609353 | GATACCTACCAATGC[A/G]GCTGGAAGGGAAGAG | 4296 |
rs774182491 | snp | C/T | 3.41758e-05 | 0.00413361 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607898 | GGGAGCTCTGTACCT[C/T]ACCTGCCCTCCCCGT | 4296 |
rs774220027 | in-del | -/GGGCTCCTC | | | cds-indel, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599731 | GGGGACAGGCCTCTT[-/GGGCTCCTC]GGGCTCCAGGCTAGG | 4296 |
rs774286152 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611332 | CGCCAGGCTTCCTCA[C/T]AAGGCCCCCATTGTC | 4296 |
rs774329524 | snp | A/G | 3.35548e-05 | 0.00409588 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605919 | AAAGCAAATGATGCT[A/G]GGTCTGGGGGGCACT | 4296 |
rs774420703 | snp | A/G | 5.25818e-05 | 0.00512719 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599784 | CTGCGGGCAGAGGCG[A/G]CACAGGTGAGGGTGT | 4296 |
rs774438025 | snp | A/G | 1.70977e-05 | 0.00292379 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598472 | GATGGCAGGGGAGAA[A/G]GCCGTGGCCCAGCTG | 4296 |
rs774440785 | snp | A/G | 1.89313e-05 | 0.00307657 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598390 | GGGGTTGGCAGGTGG[A/G]GAGTCCCAGAAGGGG | 4296 |
rs774500592 | in-del | -/G | 1.67326e-05 | 0.00289241 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613306 | ACTGATGTCCTCATC[-/G]GGGGTCCTGGCGAGC | 4296 |
rs774552032 | snp | A/G | 3.29734e-05 | 0.00406025 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608390 | GGCCAGGCCAAAGTC[A/G]GTGATCTTCAGGGTC | 4296 |
rs774637486 | snp | A/C/T | 8.87404e-05 | 0.00666058 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605740 | TCAGCCAGATCCTGC[A/C/T]GGGGGAGGAAGGCCA | 4296 |
rs774658431 | snp | C/G | 6.72382e-05 | 0.00579781 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608473 | AGGGGCCAGATTGTG[C/G]ATGCTCCAGGATCAG | 4296 |
rs774744644 | snp | G/T | 1.65091e-05 | 0.00287303 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606709 | GGATGGCTCGGAACC[G/T]GGGAAAGGTGGGCGA | 4296 |
rs774745538 | snp | A/G | 2.29771e-05 | 0.0033894 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599567 | GGCGTTGGCGTGGGG[A/G]GTGTTGTCGGGGACT | 4296 |
rs774912406 | snp | C/T | 1.68858e-05 | 0.00290561 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613483 | ACGGGAAGATGCCCA[C/T]CTGGCCACCCACCTG | 4296 |
rs775207886 | snp | A/G | 5.88587e-05 | 0.00542456 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599531 | AGCGGGGAAGGGGGC[A/G]GCTCGGTCGGGCAGG | 4296 |
rs775219665 | snp | C/T | 0.000610025 | 0.0174539 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598606 | AGAGCGTGATGTCCC[C/T]GGTGGGGGTGAGACA | 4296 |
rs775278605 | snp | A/G | 1.72246e-05 | 0.00293462 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605750 | CCTGCCGGGGGAGGA[A/G]GGCCACTCACCATTG | 4296 |
rs775308678 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604354 | CAAGTTCTCCTTTGG[C/T]CCATCTGGCCTGGTA | 4296 |
rs775350789 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608773 | GGGCATGTGCCACCA[C/T]GCCCGACTAATTTTG | 4296 |
rs775403150 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611015 | GAGGAGAATGGGCCA[C/G]AGACCCCGAAACTGG | 4296 |
rs775411017 | snp | C/G | 3.64033e-05 | 0.00426619 | intron-variant, upstream-variant-2KB | MAP3K11, PCNX3 | GRCh38.p7 | 11:65612977 | GGGAGCAGGTGTGTA[C/G]CAGAGCCATGCCACC | 4296 |
rs775506696 | snp | A/C/T | 3.3161e-05 | 0.00407181 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605830 | CCAGGTACCATGTGG[A/C/T]TTCGTCCATGCGGGA | 4296 |
rs775513372 | snp | C/T | 2.02235e-05 | 0.00317983 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607338 | TTGAATGTCCCGCGG[C/T]GGCGGCGCACGTGCG | 4296 |
rs775693055 | snp | C/T | 5.83976e-05 | 0.00540327 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613760 | CAAGGGCTCCATGGC[C/T]GGGAGCCGGCGCTGG | 4296 |
rs775703369 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608867 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 4296 |
rs775735855 | in-del | -/GTC | 2.34351e-05 | 0.00342301 | cds-indel, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599573 | GGCGTGGGGGGTGTT[-/GTC]GGGGACTCCCCGCGC | 4296 |
rs775759325 | snp | A/G | 3.67471e-05 | 0.00428628 | utr-variant-3-prime, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598246 | CCAGTGTATGCTGTG[A/G]CTCCTCCTAAGGCAG | 4296 |
rs775794376 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65601120 | ATGTGCCTTGGCCCC[C/T]GTCCGCAGCCCCAGT | 4296 |
rs775868356 | snp | C/G | 2.05899e-05 | 0.00320851 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606095 | CACTGCAGGGGAAAC[C/G]GATGAAATCGGAGAT | 4296 |
rs775882150 | snp | A/G | 0.000279088 | 0.0118096 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599707 | CCCAGAGCTGCTACC[A/G]CGCTCTGCGGGGACA | 4296 |
rs775906919 | snp | A/G | 1.66153e-05 | 0.00288225 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608276 | GCCGCACCTCCAGAC[A/G]TCACTGCCCTTAGAG | 4296 |
rs775907209 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65600450 | CAGGCTCAGAGAGGT[C/T]GAGGGCTTGTGCGGA | 4296 |
rs775959086 | snp | A/G | 7.56137e-05 | 0.00614826 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599519 | GAGAAGCAGATGAGC[A/G]GGGAAGGGGGCGGCT | 4296 |
rs775996855 | snp | C/T | 3.29707e-05 | 0.00406008 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608369 | TGTGGTTTTGTGCCA[C/T]TCTCGGGCCAGGCCA | 4296 |
rs775998982 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598973 | ACCATCTCGGGAAAG[C/G]CTTGCAAACAGTACT | 4296 |
rs776011306 | snp | C/G/T | 3.59785e-05 | 0.00424125 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606035 | TGAGTCCTCCAGACG[C/G/T]CGGGGGGACTGGCGG | 4296 |
rs776065218 | snp | A/G | 1.69364e-05 | 0.00290997 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613389 | AAGCCTCCAATGCCG[A/G]TCACCTCCTCCAGCC | 4296 |
rs776159436 | snp | A/G | 3.96912e-05 | 0.00445466 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606087 | GCAGGCTCCACTGCA[A/G]GGGAAACCGATGAAA | 4296 |
rs776289394 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606218 | GAGCTTTGGGCAAGA[G/T]AGATGGGTTTGGGTC | 4296 |
rs776334879 | snp | C/T | 3.59273e-05 | 0.0042382 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606033 | CTTGAGTCCTCCAGA[C/T]GTCGGGGGGACTGGC | 4296 |
rs776356733 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | MAP3K11, PCNX3 | GRCh38.p7 | 11:65615386 | GGGAGCGAAATCGGT[C/T]GTGACGTACGAGGTC | 4296 |
rs776484664 | snp | C/G | 1.88457e-05 | 0.00306961 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607544 | CGATGGTGGAGAGGT[C/G]AGCCTGGCACCAATC | 4296 |
rs776563704 | snp | C/T | 3.4024e-05 | 0.00412442 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613444 | CGCAGGGGGGCGGGC[C/T]GCCACCCCGAGACAC | 4296 |
rs776572682 | snp | C/T | 3.34303e-05 | 0.00408828 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607772 | CCAACTGCTGCAGGA[C/T]GGAGGCGAAGTCGGG | 4296 |
rs776649134 | snp | A/C | 3.61454e-05 | 0.00425105 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613127 | CAGCACATGGGGAGG[A/C]ACGCGCCGCCCGGCC | 4296 |
rs776751532 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609723 | CTCAGCTCTCCTGCC[C/T]TGTGTGACACGGCTG | 4296 |
rs776801414 | in-del | -/ACTT | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606397 | TTTCTCATCCATAAA[-/ACTT]AAATTAACAACAAAA | 4296 |
rs776805949 | snp | C/T | 2.04887e-05 | 0.00320061 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599389 | GCCGGCTTCAGGCCA[C/T]TCACCGCGGGGCTCC | 4296 |
rs776817191 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604927 | AGTGTTGAGCTGAGT[A/G]AGCCCTCCTCCCTGC | 4296 |
rs776887296 | snp | A/G | 1.91496e-05 | 0.00309426 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607319 | CGCCCGGAGCTTGCT[A/G]CGCTTGAATGTCCCG | 4296 |
rs776901400 | snp | A/C/T | 8.69386e-05 | 0.00659266 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599621 | CCCGGCGGCTGCAGG[A/C/T]CGCGGCCAAGGCCCA | 4296 |
rs776990175 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611009 | CACCCAGAGGAGAAT[A/G]GGCCAGAGACCCCGA | 4296 |
rs777013875 | snp | A/G | 1.78688e-05 | 0.00298899 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606846 | GTTCAGGTTTGTGAT[A/G]AAGTAGAGCCAGGAC | 4296 |
rs777027213 | snp | C/G | 3.36434e-05 | 0.00410129 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608256 | CCCGTCCAGCCCCAC[C/G]AAGGGCCGCACCTCC | 4296 |
rs777064845 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603100 | AGAATGAGACTCTAT[C/T]TTTAAAAAAATAAAA | 4296 |
rs777153665 | snp | A/G | 5.11705e-05 | 0.00505793 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613747 | GGAAGAGGCTCTTCA[A/G]GGGCTCCATGGCCGG | 4296 |
rs777200800 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602073 | CAGGGCATGGTGGCA[C/T]GCACCTGTAGTCTCA | 4296 |
rs777225955 | snp | C/T | 2.27038e-05 | 0.00336918 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613727 | TGACCCTAGAGGGCT[C/T]TTGAGGAAGAGGCTC | 4296 |
rs777262484 | snp | C/T | 0.00023682 | 0.010879 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599756 | GGCTCCAGGCTAGGC[C/T]GCGGGGGGTTACCTG | 4296 |
rs777274087 | snp | A/G | 1.79638e-05 | 0.00299693 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598430 | GGGAACAAGGTCCAG[A/G]GTGCTCGGCGGGGTG | 4296 |
rs777275564 | snp | C/T | 0.000534902 | 0.0163452 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599689 | CTGGATCAGCTTGGG[C/T]GTCCCAGAGCTGCTA | 4296 |
rs777460184 | snp | A/C | 2.76277e-05 | 0.0037166 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598329 | ACGGGGCCTGGGCAC[A/C]CATGTCTTTGGTCTG | 4296 |
rs777501748 | snp | A/G | 0.000106377 | 0.00729228 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616268 | CCGGGGGCCGCCCCC[A/G]TGAGGGTCCCGGGAG | 4296 |
rs777594989 | snp | A/G | 1.70481e-05 | 0.00291955 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613433 | GCTGGCCACCTCGCA[A/G]GGGGGCGGGCCGCCA | 4296 |
rs777793376 | snp | C/T | 2.98191e-05 | 0.00386118 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65599362 | AACCCCCGTCTCCCA[C/T]ATGTGAAGCAGGCCG | 4296 |
rs777793382 | snp | G/T | 1.73309e-05 | 0.00294366 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605982 | GGCTTGGGGGAACTG[G/T]GACCCCAAGCCCAGC | 4296 |
rs777849778 | snp | A/G | 1.91393e-05 | 0.00309343 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606075 | TGGCCTGGCTCTGCA[A/G]GCTCCACTGCAGGGG | 4296 |
rs777856021 | snp | C/T | 3.37844e-05 | 0.00410987 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606659 | TAAGGAGCTGGGGGG[C/T]GGAGAGGGGCATGAG | 4296 |
rs777957821 | snp | A/C | 1.77363e-05 | 0.00297789 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607416 | AACACCTCTAGCTCC[A/C]ACTGGGCCAGCAGGT | 4296 |
rs777987684 | snp | C/T | 1.66391e-05 | 0.00288431 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605883 | CAAGGAGGGGTGCTT[C/T]AGGAATTTCAGGACT | 4296 |
rs778152793 | snp | A/C | 9.11286e-05 | 0.00674952 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599668 | GGTGCCGCGCAGCAG[A/C]GCCCGCTGGATCAGC | 4296 |
rs778191074 | in-del | -/G | 5.67789e-05 | 0.00532787 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65598642 | TCCTGTGAGGATATA[-/G]GAGGGGCACAGGGTC | 4296 |
rs778215901 | snp | C/T | | | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599672 | CCGCGCAGCAGCGCC[C/T]GCTGGATCAGCTTGG | 4296 |
rs778257735 | snp | A/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607079 | CACTCCCAGACCGAC[A/T]TGCAAATACTTCCGC | 4296 |
rs778355372 | snp | A/G | 1.89881e-05 | 0.00308119 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607305 | TCGCCGCCGTCGCGC[A/G]CCCGGAGCTTGCTGC | 4296 |
rs778356085 | snp | C/T | 3.55942e-05 | 0.00421851 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599737 | AGGCCTCTTGGGCTC[C/T]TCGGGCTCCAGGCTA | 4296 |
rs778412136 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612214 | CTCTCTCTAAATGCT[A/G]CGTGCACCAGGAAAC | 4296 |
rs778418004 | snp | C/T | 3.80815e-05 | 0.0043634 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607291 | GCATGCTGATACGCT[C/T]GCCGCCGTCGCGCGC | 4296 |
rs778437377 | snp | A/G | 5.01945e-05 | 0.00500946 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613307 | ACTGATGTCCTCATC[A/G]GGGTCCTGGCGAGCT | 4296 |
rs778465179 | snp | C/G | 1.69582e-05 | 0.00291184 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613639 | CCGGGTTGGCATAAC[C/G]CGCTGCCTTTGGAGA | 4296 |
rs778522527 | snp | A/C | 1.80016e-05 | 0.00300008 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599461 | GATACCCAGGTCCAG[A/C]AACAGGGGTGCAGGA | 4296 |
rs778534983 | snp | A/G | 1.99603e-05 | 0.00315907 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613697 | CCCACCACCCCCGCT[A/G]CCACTGCCATTCCAT | 4296 |
rs778644098 | in-del | -/GGGGCCTGGGCACCCAT | | | frameshift-variant, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598316 | GCTTCCGGCACCCAC[-/GGGGCCTGGGCACCCAT]GTCTTTGGTCTGTGC | 4296 |
rs778801240 | snp | C/G | 1.8941e-05 | 0.00307736 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606070 | ATGCCTGGCCTGGCT[C/G]TGCAGGCTCCACTGC | 4296 |
rs778810390 | snp | A/G | 4.98575e-05 | 0.00499262 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65605796 | GAAGGAGATCCTAAG[A/G]GGGATGAGTCATCTG | 4296 |
rs778997363 | snp | A/C/G | 1.76421e-05 | 0.00296998 | missense, stop-gained, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606004 | AAGCCCAGCATGCTC[A/C/G]CCGCTCTCCATTGCT | 4296 |
rs779034724 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65614002 | CCCCGGGGCCTCCGG[C/G]GCCTCACCATGGCTA | 4296 |
rs779098350 | snp | G/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65609480 | GCTTTAACCCAAATG[G/T]GGCCACCGTACTTGG | 4296 |
rs779151955 | snp | C/T | 4.98608e-05 | 0.00499279 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607734 | CCGCGGCATTTCCCG[C/T]AGGACCTGTGCCTCC | 4296 |
rs779187339 | snp | A/G | 1.79751e-05 | 0.00299787 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613166 | GCTGAGGGGCCCACC[A/G]GCTGCATACTCCATC | 4296 |
rs779258727 | snp | A/G | 3.55297e-05 | 0.00421468 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598579 | ACGTGGGGTGCCTGG[A/G]GTGCCAGGAGCAGAG | 4296 |
rs779269688 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603630 | TCTTAGCTGGGTTTC[A/G]GGGGGTGGCTGTGAG | 4296 |
rs779313978 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604255 | CAGGCCCCTTGTGCC[C/G]CTGCTTCTGGGAGCT | 4296 |
rs779376387 | snp | C/G | 1.72531e-05 | 0.00293705 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606830 | GGTTGGGGGGAGCAG[C/G]GTTCAGGTTTGTGAT | 4296 |
rs779414471 | snp | A/G | | | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606777 | TCAAGGCCGGGTGAG[A/G]CCTGCACGGTGATGC | 4296 |
rs779497729 | snp | C/T | 5.45063e-05 | 0.00522017 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613063 | CGGGCACCAGGGCCT[C/T]GCAGTGCAGGTAGTG | 4296 |
rs779565351 | snp | C/G/T | 0.000112967 | 0.00751482 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599594 | GACTCCCCGCGCTCG[C/G/T]GTCCTGGGCCTCCCG | 4296 |
rs779681234 | snp | C/G | 1.65507e-05 | 0.00287664 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65606695 | AAGTTTCTTACACTG[C/G]ATGGCTCGGAACCGG | 4296 |
rs779725688 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603850 | ACCATGGTTTCCAGT[A/G]CTTTCATGAAACCTC | 4296 |
rs779823760 | snp | A/G | 8.14498e-05 | 0.00638109 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599649 | CCAGCGAGGCGAGCA[A/G]GGCGGTGCCGCGCAG | 4296 |
rs779943838 | snp | A/G | 1.70752e-05 | 0.00292187 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608219 | TAGGCAGCCACCTCT[A/G]CCCTCTGCAGCCCCG | 4296 |
rs780040675 | snp | C/G | 1.66535e-05 | 0.00288556 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607744 | TCCCGTAGGACCTGT[C/G]CCTCCAGCGCCTCCA | 4296 |
rs780088161 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65612029 | CCAGGCCAGGAGGCT[C/T]AAAATATCCACGTTG | 4296 |
rs780164933 | snp | A/C | 4.13736e-05 | 0.00454809 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613688 | TCCACCGCCCCCACC[A/C]CCCCCGCTGCCACTG | 4296 |
rs780182695 | in-del | -/TG | 4.95724e-05 | 0.00497833 | splice-acceptor-variant | MAP3K11 | GRCh38.p7 | 11:65608072 | GCAGCACCCCAAAAC[-/TG]TGGGCGAGACAACAG | 4296 |
rs780448440 | snp | A/G | 1.66643e-05 | 0.0028865 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65608457 | AGCAAAACTAGAGAA[A/G]AGGGGCCAGATTGTG | 4296 |
rs780599035 | snp | A/C | 0.000101447 | 0.00712133 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607829 | AGTCTAGGGGCACGG[A/C]GTGCAGCGGGGACAG | 4296 |
rs780659088 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603762 | TCCTTTCAGGGCAAG[C/T]GGCAATCCATTTCTT | 4296 |
rs780700147 | snp | A/C/T | 8.97971e-05 | 0.00670011 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65605735 | GGAGCTCAGCCAGAT[A/C/T]CTGCCGGGGGAGGAA | 4296 |
rs780709591 | snp | A/T | 1.67091e-05 | 0.00289038 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606673 | GCGGAGAGGGGCATG[A/T]GAGGTGAAGTTTCTT | 4296 |
rs780716514 | snp | C/G | 3.45459e-05 | 0.00415593 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598455 | GGGGTGCAGGCTGTG[C/G]TGATGGCAGGGGAGA | 4296 |
rs780818081 | snp | A/G | 2.68258e-05 | 0.00366227 | synonymous-codon, upstream-variant-2KB | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616338 | GGTGTTGCAGATCCT[A/G]CGCCAGGGGGTGTGG | 4296 |
rs780818114 | snp | A/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65603404 | ACAGCCACGTAGTTA[A/T]TGGCTCTAAGGCAAC | 4296 |
rs780832462 | snp | C/T | 1.65332e-05 | 0.00287512 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65608431 | TGTCGTCACTCTCAA[C/T]GGGCTGCAGCAGCAA | 4296 |
rs780873268 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602332 | GCCTGGCCAACATGG[C/T]CAAACCCTGTCTCTA | 4296 |
rs780952481 | snp | C/T | 2.16284e-05 | 0.00328842 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598538 | GGCGAGGGCCGAGGT[C/T]GGCTGATGAGGCCCA | 4296 |
rs780966245 | snp | C/G/T | 3.37361e-05 | 0.00410696 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65606817 | AGTCTGGGATTTGGG[C/G/T]TGGGGGGAGCAGGGT | 4296 |
rs781004018 | snp | A/G | 8.4702e-05 | 0.00650721 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607853 | GGGACAGAATAAGAA[A/G]GGGTCCGTGGGTGGA | 4296 |
rs781013413 | snp | C/T | 5.06598e-05 | 0.00503263 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613534 | CTCCTGAGATGGCTG[C/T]GTCCCGGGACAGCAC | 4296 |
rs781052493 | snp | C/G/T | 0.00016071 | 0.00896289 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599588 | GTCGGGGACTCCCCG[C/G/T]GCTCGCGTCCTGGGC | 4296 |
rs781068365 | snp | C/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65611977 | ATATCTGGGGCTCAG[C/G]ACTCTGTTTCCTGCA | 4296 |
rs781077171 | snp | A/C | 3.37189e-05 | 0.00410588 | missense, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613624 | ACAGGGCTGTCCACA[A/C]CGGGTTGGCATAACC | 4296 |
rs781205052 | snp | A/T | 1.84551e-05 | 0.00303763 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599501 | GAGTCGGGCGTCTTG[A/T]GCGAGAAGCAGATGA | 4296 |
rs781295291 | snp | A/G | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65604986 | CCTCTGGCTTCCTAA[A/G]CAGTCTATACGTGAG | 4296 |
rs781495861 | snp | C/G | 1.76993e-05 | 0.00297478 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613220 | CAGGCACACAGCCTT[C/G]AGGGCAATGATGTTG | 4296 |
rs781551410 | in-del | -/GCGGGGAGTCGGGCGTCTTGAGCGAGAAGCAGATGA | 0.000289742 | 0.0120328 | cds-indel, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599481 | GGGGTGCAGGAGTGG[lengthTooLong]GCGGGGAAGGGGGCG | 4296 |
rs781581951 | snp | C/G | 2.13924e-05 | 0.00327044 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65598356 | TCTGTGCCCTGCAGT[C/G]CTGGGGGCCCCCCTG | 4296 |
rs781581998 | snp | G/T | 3.4635e-05 | 0.00416129 | upstream-variant-2KB, utr-variant-5-prime | PCNX3, MAP3K11 | GRCh38.p7 | 11:65616279 | CCCCATGAGGGTCCC[G/T]GGAGGGGGGGCGCGG | 4296 |
rs781635640 | in-del | -/A | 1.91184e-05 | 0.00309174 | intron-variant | MAP3K11 | GRCh38.p7 | 11:65607527 | TCCTGCGCCCGAGAC[-/A]GCGATGGTGGAGAGG | 4296 |
rs781713464 | snp | A/G | 1.69902e-05 | 0.00291458 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | MAP3K11, PCNX3 | GRCh38.p7 | 11:65613415 | CAGCCGCAGCTCCTG[A/G]AAGCTGGCCACCTCG | 4296 |
rs781760357 | snp | C/T | 6.01993e-05 | 0.00548598 | missense, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607458 | CGCAGCTGCTCCGCC[C/T]GTGACCGCTGCTCGC | 4296 |
rs781768921 | snp | C/T | 3.32834e-05 | 0.00407929 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65607686 | ACCCTGGATCTCGCG[C/T]TTCCAGCCTTCCTGC | 4296 |
rs781769081 | snp | A/G | 2.81551e-05 | 0.0037519 | synonymous-codon, nc-transcript-variant | MAP3K11 | GRCh38.p7 | 11:65599764 | GCTAGGCCGCGGGGG[A/G]TTACCTGCGGGCAGA | 4296 |
rs796081723 | snp | C/T | | | intron-variant | MAP3K11 | GRCh38.p7 | 11:65602383 | GGGCATGGTGGTTCA[C/T]GCTTGTAATCCCAGC | 4296 |