ING3
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs13881snpC/T0.3472530.230308downstream-variant-500BING3GRCh38.p77:120975956TTATGGGTGTTTTGA[C/T]TGGAGGCAATGTAGC54556
rs2074576snpC/G0.3505460.22889intron-variantING3GRCh38.p77:120970578GATTACTTTAGCTTA[C/G]ACTTTAATTTATACA54556
rs2074577snpA/G0.4891420.0728777intron-variantING3GRCh38.p77:120971109CTAAACATTTTTGGT[A/G]TACCACTACCATATA54556
rs2189544snpA/G0.02367460.106192intron-variantING3GRCh38.p77:120974361CTTTATGAGACAGCA[A/G]ATAAGGCTGACTATT54556
rs2248890snpA/G0.4874320.0782705intron-variantING3GRCh38.p77:120957939ATTTATACCTTACTG[A/G]AGGGTTTGCATTAGA54556
rs2402552snpC/T00intron-variantING3GRCh38.p77:120953838ATTTAAGAAAGCCTT[C/T]TAGTTTAAACTCTAA54556
rs2525711snpC/T0.3505460.22889intron-variantING3GRCh38.p77:120960348CTTAGTCTAAAGCGG[C/T]GGGAAGCCAGTGAAG54556
rs2525712snpG/T0.4890830.0730708intron-variantING3GRCh38.p77:120960413AAGAGATTTTGTGTA[G/T]GTATGCCTTTGCTTA54556
rs2525713snpA/G0.4868550.0799975intron-variantING3GRCh38.p77:120960915AAAGTTGATTTATAC[A/G]TACCCTGATAAAATT54556
rs2525714snpA/G0.3501090.229081intron-variantING3GRCh38.p77:120961383AACTTACTGCTGTCT[A/G]TTTCAACTTAGAATG54556
rs2525715snpC/T0.2396140.249784intron-variantING3GRCh38.p77:120961536TCCATTAGTGATACA[C/T]TTTAAATGTGAATAT54556
rs2525716snpC/T0.358090.225425intron-variantING3GRCh38.p77:120962766ACAATCCATCTTCAC[C/T]GTCTTAATTCGTACC54556
rs2525717snpA/G0.3576640.225629intron-variantING3GRCh38.p77:120962777TCACCGTCTTAATTC[A/G]TACCTCCTTCGTGTC54556
rs2525718snpC/T0.3507640.228794intron-variantING3GRCh38.p77:120964228TGTTTACAAGCATTA[C/T]GATTCACTCTCATGC54556
rs2525719snpG/T0.4868550.0799975intron-variantING3GRCh38.p77:120964473TAATTTTCATGTCCT[G/T]ACTTCTGAAAATGGA54556
rs2525720snpA/G0.3503270.228986intron-variantING3GRCh38.p77:120964976ATAGCTTGGACCCTA[A/G]CAGTTGGAAATGTTT54556
rs2525721snpC/T0.06521440.168387intron-variantING3GRCh38.p77:120965604AAACTTACAAACCTT[C/T]TTTTTCTTGGTGCAT54556
rs2525722snpA/C0.3503270.228986intron-variantING3GRCh38.p77:120966384GAGTATGCCTTGAGC[A/C]ATTTTGTACTTAAGA54556
rs2525723snpG/T0.3503270.228986intron-variantING3GRCh38.p77:120968618GATAGGCCGAGGCAG[G/T]TGGATCACTTGAGGT54556
rs2525724snpA/G0.352070.228214intron-variantING3GRCh38.p77:120969889CCTTAAAGAACGATC[A/G]ATATGAAATAACCAC54556
rs2525725snpC/T0.2956750.245792synonymous-codon, nc-transcript-variantING3GRCh38.p77:120970847TGATTGGACTTACGA[C/T]CCAAATGAACCTCGA54556
rs2525726snpA/G0.352070.228214intron-variantING3GRCh38.p77:120973396AATATTCCTCTTCAA[A/G]ATAGGGTAGTGTCCC54556
rs2721350snpC/T0.2404780.249819intron-variantING3GRCh38.p77:120962958TGATTCTCTTCCATT[C/T]TTCATATATCCTCCA54556
rs2721351snpA/G0.358090.225425intron-variantING3GRCh38.p77:120964044TTTTTGTTAGTTTGA[A/G]GTGTCATATAATTTT54556
rs2721354snpA/G0.4867250.0803809intron-variantING3GRCh38.p77:120951953TTCTTAGCTGCAGCA[A/G]GTGGTCCCTGAGCCA54556
rs2721368snpC/T0.3503270.228986intron-variantING3GRCh38.p77:120973483AATTTTCATACAACA[C/T]AACACTTCTGAGACA54556
rs2721369snpC/T0.001596170.0282053intron-variantING3GRCh38.p77:120973365CTAGCATTAGCATAA[C/T]ATAACTAATATACCT54556
rs2721370snpC/T0.2427750.249896intron-variantING3GRCh38.p77:120972185AAGCCCTTCTAAGTA[C/T]ATAATCCATGGCTTG54556
rs2721372snpC/T0.4869840.079614intron-variantING3GRCh38.p77:120969339CTATAAAATGAAAAC[C/T]GCATGTCTCCCTACC54556
rs2721373snpC/T0.004780850.0486577intron-variantING3GRCh38.p77:120967290ATAACCCAAGATACA[C/T]CATGGGCTCACATAC54556
rs3180313snpA/G00missense, nc-transcript-variantING3GRCh38.p77:120967637CAGATGCCTCTAAGG[A/G]AAATACACTAGGTAA54556
rs3214197in-del-/C0.2899420.246789intron-variantING3GRCh38.p77:120954899GAACTTTAACAAAAA[-/C]TTTTTTAATGGAATG54556
rs3216951in-del-/CTAintron-variant, downstream-variant-500BING3GRCh38.p77:120957208accccatctctacta[-/CTA]aaaatacaaaaatat54556
rs3757556snpC/G0.4071580.194426upstream-variant-2KBING3GRCh38.p77:120950028CATGAATTACGGATG[C/G]AGCCTTGATTTCTAA54556
rs3837125in-del-/TA0.2515780.249995intron-variantING3GRCh38.p77:120973481TTTTCATACAACATA[-/TA]ACACTTCTGAGACAA54556
rs3891287snpA/Gintron-variantING3GRCh38.p77:120953555TAAAAATCCCTATCT[A/G]AAGCTCTAAACCACA54556
rs4440563snpA/G0.003976130.0444101missense, nc-transcript-variantING3GRCh38.p77:120950912ATGTTGTACCTAGAA[A/G]ACTATCTGGAAAGTG54556
rs4523189snpA/C/G1.65304e-050.00287488utr-variant-5-prime, nc-transcript-variantING3GRCh38.p77:120950882CCCCTTGTTCCCTCA[A/C/G]CTCTAAGGGCCGCGA54556
rs5887003in-del-/Cintron-variantING3GRCh38.p77:120974333GTCTTTAATTACAAT[-/C]CAGCTTATTCTACTT54556
rs6964344snpA/G0.4071580.194426intron-variantING3GRCh38.p77:120951882AGCTTGGTAGTCTCT[A/G]GGACTTTTTCCCCAA54556
rs6971619snpA/G0.3024350.244439intron-variantING3GRCh38.p77:120963790ATTATTTAATTCTAA[A/G]CCTTACTTAAAATGT54556
rs10216200snpA/C0.01316610.0800605intron-variantING3GRCh38.p77:120955661ACTGTGCCATAAGTA[A/C]TTGAATAACAGATTA54556
rs10269373snpA/G0.05510130.156571intron-variantING3GRCh38.p77:120954145AGGATCAACTAAGAg[A/G]cctggcgtggtggct54556
rs10272601snpC/G0.4081880.193589intron-variantING3GRCh38.p77:120954539GGGAAGATTGTTTCT[C/G]TTAGGAAAAAAAAAA54556
rs10281679snpC/T0.05773440.159793intron-variant, downstream-variant-500BING3GRCh38.p77:120957093AAGTAAATACTAggc[C/T]gggcgcagtggctca54556
rs10464522snpA/G0.2842090.247648intron-variantING3GRCh38.p77:120969729TATGAAAACCTAATA[A/G]CATTTATCACTGTCT54556
rs10464661snpA/G0.0003992810.0141238intron-variantING3GRCh38.p77:120968701aatacaaaaaaatta[A/G]ctgggtgcctggtgg54556
rs10464662snpA/G0.003587790.0422022intron-variantING3GRCh38.p77:120968739taatcccagctactc[A/G]gtaggctatggcagg54556
rs11408222in-del-/G00upstream-variant-2KBING3GRCh38.p77:120950732AGTGAGGCAAGCGCC[-/G]TCAGGCGCCAAAGTG54556
rs11548053snpA/G/T1.65636e-050.00287776synonymous-codon, nc-transcript-variantING3GRCh38.p77:120951192TCCTATGGATCTGCG[A/G/T]GACCGCTTCACGGAA54556
rs11770991snpC/G00upstream-variant-2KBING3GRCh38.p77:120949043TCTGAAGAAATAGCA[C/G]TAAAAGGCCCATAAA54556
rs12531744snpC/T0.05886050.161139upstream-variant-2KBING3GRCh38.p77:120949600CGAAGTAAGGTTCCG[C/T]TGAGATTCATCATGA54556
rs12533095snpC/T0.1094610.206758intron-variantING3GRCh38.p77:120966234TAATGTCCCCCATCA[C/T]GTAGAACTTCAGAAT54556
rs12539365snpA/G0.05886050.161139upstream-variant-2KBING3GRCh38.p77:120949468AGaagaaggaaggat[A/G]ggaaacgaagaaagg54556
rs12706299snpC/T0.01663250.0896639intron-variantING3GRCh38.p77:120962699AAGCATACTGTTTGT[C/T]TTTCTGTCTCTACAT54556
rs13230872snpC/Tintron-variantING3GRCh38.p77:120959736ctgcaagctccgcct[C/T]ttgggttcatgccat54556
rs13232488snpG/Tintron-variantING3GRCh38.p77:120968799tgcagcgagccaaaa[G/T]cgtgccactagactc54556
rs13238968snpG/T00intron-variantING3GRCh38.p77:120954645TATATCCACATCCCA[G/T]AGTCACTAATCATTT54556
rs13245078snpA/Tintron-variantING3GRCh38.p77:120968809caaaatcgtgccact[A/T]gactccagcccaagc54556
rs13245182snpA/C/T0.02523250.109451intron-variantING3GRCh38.p77:120968800gcagcgagccaaaat[A/C/T]gtgccactagactcc54556
rs17143067snpC/T0.05246040.153226intron-variantING3GRCh38.p77:120965195TATACACTTAAGCTT[C/T]GAGGAAAGTTGTTAG54556
rs17533951snpC/T0.07189190.175435intron-variantING3GRCh38.p77:120968397CATAGTTCTTCGTTC[C/T]TTCTGCCAGTTCCAA54556
rs28366865snpA/T0.05886050.161139intron-variantING3GRCh38.p77:120973868TTTAGTAGTGACAGG[A/T]TCCTAAGATTAACAA54556
rs28582920snpA/G0.05397040.155153intron-variantING3GRCh38.p77:120968231ATTTCACGATATGTG[A/G]TATTTTATTTAATGA54556
rs28627810snpA/G0.05547790.157039upstream-variant-2KBING3GRCh38.p77:120949348CCCCTCAAATCCTAA[A/G]CATAATTTTAAAATT54556
rs33947704in-del-/Gupstream-variant-2KBING3GRCh38.p77:120950733GTGAGGCAAGCGCCT[-/G]CAGGCGCCAAAGTGG54556
rs34088681in-del-/Cintron-variantING3GRCh38.p77:120952060TTTTCCGGTAAGTTT[-/C]CAGGTGGCACATAAT54556
rs34121165in-del-/Aintron-variantING3GRCh38.p77:120958495CTTCAGTCGCCACAG[-/A]ACTGAACCTGATCAT54556
rs34314625in-del-/Tupstream-variant-2KBING3GRCh38.p77:120950748CAGGCGCCAAAGTGG[-/T]TTTTTTTTTTTTTCT54556
rs34400070in-del-/Cintron-variantING3GRCh38.p77:120961935TCAGTACCCTCTTTA[-/C]CTATTGTAAATCAGT54556
rs34461894in-del-/Gdownstream-variant-500BING3GRCh38.p77:120975944GAAAATAATGGTTAT[-/G]GGGTGTTTTGACTGG54556
rs34591238in-del-/Aintron-variantING3GRCh38.p77:120961845TTGACATTAACTGGG[-/A]AAAAAAGAAATAATT54556
rs34679146in-del-/Cintron-variantING3GRCh38.p77:120955919CTTTATTTTACTAAT[-/C]CCTTGTCTTCTTAAG54556
rs34775399in-del-/Aintron-variantING3GRCh38.p77:120963445TGAAGAATGTTTTTC[-/A]AAAAAAAAAACAGTT54556
rs34826982in-del-/Aintron-variantING3GRCh38.p77:120958287GAACATTATATCCTT[-/A]AATATAAAAAATCCC54556
rs34894193in-del-/Cutr-variant-3-prime, nc-transcript-variantING3GRCh38.p77:120975065GCTATGAATATTATT[-/C]CCAGTTAGCCTTGGA54556
rs34926686snpG/Tintron-variantING3GRCh38.p77:120952453TTTTATATTTTATTG[G/T]TTAAAATTTTAAATT54556
rs35223362in-del-/Aintron-variantING3GRCh38.p77:120958323TTCAGACTTAGTGAT[-/A]AATCATCTCAGTTAC54556
rs35698124in-del-/Gintron-variantING3GRCh38.p77:120954408ACAGCCTGGGCAACA[-/G]GAGTGACAGAGTGAG54556
rs35749576in-del-/Tintron-variantING3GRCh38.p77:120952506ATACATATTACAGGC[-/T]TTTTTAAACGTGCAT54556
rs35872651in-del-/Aintron-variant, downstream-variant-500BING3GRCh38.p77:120957372GAGCGACTCTGTCTT[-/A]AAAAAAAAAAAAAAA54556
rs35989015in-del-/Cintron-variantING3GRCh38.p77:120958847AGCTAGTGTAGTCTT[-/C]CCTTAATTTCTCATT54556
rs56288063snpA/Tintron-variantING3GRCh38.p77:120971189TTAAACAACAGAAAA[A/T]AATTTTCTCACAGGT54556
rs57319324snpA/Tintron-variantING3GRCh38.p77:120971188CTTAAACAACAGAAA[A/T]TAATTTTCTCACAGG54556
rs58433173snpA/C0.003985640.0444627intron-variantING3GRCh38.p77:120967741TGAATCATACAGTTT[A/C]TTTACCTGGTTAAAG54556
rs58515942snpG/T0.01032950.0711199intron-variantING3GRCh38.p77:120960227ACCAAGAGAGAGGCC[G/T]GGGTGGTTGGTCTGT54556
rs60615553snpA/G0.1586320.232706intron-variantING3GRCh38.p77:120970204GGCGGGGTGGCTCAT[A/G]CCTATAATCCCAGCA54556
rs61088337snpC/G0.1446320.226711intron-variantING3GRCh38.p77:120951564AAATGTTGAGATGTC[C/G]TCTTGAGCCTTTTCG54556
rs61553827in-del-/A/AAutr-variant-3-prime, nc-transcript-variantING3GRCh38.p77:120975290CAAAAAAAAAAAAAA[-/A/AA]GTCAGTGCTTCTAAA54556
rs61612657snpA/Tintron-variantING3GRCh38.p77:120956059AGAATCATTTGAATC[A/T]GTGTTTATGTGAGTG54556
rs62469957snpA/T0.50utr-variant-3-prime, nc-transcript-variantING3GRCh38.p77:120975292AAAAAAAAAAAAAAG[A/T]CAGTGCTTCTAAAAA54556
rs71530050in-del-/A0.50intron-variantING3GRCh38.p77:120954204CTGAGGCGGGTGGAT[-/A]CACCTGAGGTCAGGA54556
rs71569050snpA/C0.50intron-variantING3GRCh38.p77:120957963CATTAGAATACATAC[A/C]ATGCTATTAGTTTGG54556
rs71569051snpA/C0.50utr-variant-3-prime, nc-transcript-variantING3GRCh38.p77:120974930GAAGAGAAAGAAGAA[A/C]CAATGCATTTCCAGG54556
rs73221221snpG/T0.0003992810.0141238intron-variantING3GRCh38.p77:120957519GTTGAATATTAAGGG[G/T]TGTCTACTGAAAAAC54556
rs73221223snpC/T0.0003992810.0141238intron-variantING3GRCh38.p77:120963653TTCAAAAGATCAGAT[C/T]GAGGGCTAGAAAAGA54556
rs73221224snpA/G0.01387990.0821421intron-variantING3GRCh38.p77:120974073AAACAATATTGCCCA[A/G]CCATTTCAAGAACAT54556
rs73429864snpA/T0.1037940.20279intron-variantING3GRCh38.p77:120961492ATCATGTAGAGACTT[A/T]AAAAAAGCTGTATTT54556
rs73429874snpA/G0.0306650.119967intron-variantING3GRCh38.p77:120962788ATTCGTACCTCCTTC[A/G]TGTCTACCAGTGTTA54556
rs73429893snpA/G0.0306650.119967intron-variantING3GRCh38.p77:120971358CTTATAAGGGCACCA[A/G]CCTTGTCAGAGTAGG54556
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