SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13881 | snp | C/T | 0.347253 | 0.230308 | downstream-variant-500B | ING3 | GRCh38.p7 | 7:120975956 | TTATGGGTGTTTTGA[C/T]TGGAGGCAATGTAGC | 54556 |
rs2074576 | snp | C/G | 0.350546 | 0.22889 | intron-variant | ING3 | GRCh38.p7 | 7:120970578 | GATTACTTTAGCTTA[C/G]ACTTTAATTTATACA | 54556 |
rs2074577 | snp | A/G | 0.489142 | 0.0728777 | intron-variant | ING3 | GRCh38.p7 | 7:120971109 | CTAAACATTTTTGGT[A/G]TACCACTACCATATA | 54556 |
rs2189544 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | ING3 | GRCh38.p7 | 7:120974361 | CTTTATGAGACAGCA[A/G]ATAAGGCTGACTATT | 54556 |
rs2248890 | snp | A/G | 0.487432 | 0.0782705 | intron-variant | ING3 | GRCh38.p7 | 7:120957939 | ATTTATACCTTACTG[A/G]AGGGTTTGCATTAGA | 54556 |
rs2402552 | snp | C/T | 0 | 0 | intron-variant | ING3 | GRCh38.p7 | 7:120953838 | ATTTAAGAAAGCCTT[C/T]TAGTTTAAACTCTAA | 54556 |
rs2525711 | snp | C/T | 0.350546 | 0.22889 | intron-variant | ING3 | GRCh38.p7 | 7:120960348 | CTTAGTCTAAAGCGG[C/T]GGGAAGCCAGTGAAG | 54556 |
rs2525712 | snp | G/T | 0.489083 | 0.0730708 | intron-variant | ING3 | GRCh38.p7 | 7:120960413 | AAGAGATTTTGTGTA[G/T]GTATGCCTTTGCTTA | 54556 |
rs2525713 | snp | A/G | 0.486855 | 0.0799975 | intron-variant | ING3 | GRCh38.p7 | 7:120960915 | AAAGTTGATTTATAC[A/G]TACCCTGATAAAATT | 54556 |
rs2525714 | snp | A/G | 0.350109 | 0.229081 | intron-variant | ING3 | GRCh38.p7 | 7:120961383 | AACTTACTGCTGTCT[A/G]TTTCAACTTAGAATG | 54556 |
rs2525715 | snp | C/T | 0.239614 | 0.249784 | intron-variant | ING3 | GRCh38.p7 | 7:120961536 | TCCATTAGTGATACA[C/T]TTTAAATGTGAATAT | 54556 |
rs2525716 | snp | C/T | 0.35809 | 0.225425 | intron-variant | ING3 | GRCh38.p7 | 7:120962766 | ACAATCCATCTTCAC[C/T]GTCTTAATTCGTACC | 54556 |
rs2525717 | snp | A/G | 0.357664 | 0.225629 | intron-variant | ING3 | GRCh38.p7 | 7:120962777 | TCACCGTCTTAATTC[A/G]TACCTCCTTCGTGTC | 54556 |
rs2525718 | snp | C/T | 0.350764 | 0.228794 | intron-variant | ING3 | GRCh38.p7 | 7:120964228 | TGTTTACAAGCATTA[C/T]GATTCACTCTCATGC | 54556 |
rs2525719 | snp | G/T | 0.486855 | 0.0799975 | intron-variant | ING3 | GRCh38.p7 | 7:120964473 | TAATTTTCATGTCCT[G/T]ACTTCTGAAAATGGA | 54556 |
rs2525720 | snp | A/G | 0.350327 | 0.228986 | intron-variant | ING3 | GRCh38.p7 | 7:120964976 | ATAGCTTGGACCCTA[A/G]CAGTTGGAAATGTTT | 54556 |
rs2525721 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | ING3 | GRCh38.p7 | 7:120965604 | AAACTTACAAACCTT[C/T]TTTTTCTTGGTGCAT | 54556 |
rs2525722 | snp | A/C | 0.350327 | 0.228986 | intron-variant | ING3 | GRCh38.p7 | 7:120966384 | GAGTATGCCTTGAGC[A/C]ATTTTGTACTTAAGA | 54556 |
rs2525723 | snp | G/T | 0.350327 | 0.228986 | intron-variant | ING3 | GRCh38.p7 | 7:120968618 | GATAGGCCGAGGCAG[G/T]TGGATCACTTGAGGT | 54556 |
rs2525724 | snp | A/G | 0.35207 | 0.228214 | intron-variant | ING3 | GRCh38.p7 | 7:120969889 | CCTTAAAGAACGATC[A/G]ATATGAAATAACCAC | 54556 |
rs2525725 | snp | C/T | 0.295675 | 0.245792 | synonymous-codon, nc-transcript-variant | ING3 | GRCh38.p7 | 7:120970847 | TGATTGGACTTACGA[C/T]CCAAATGAACCTCGA | 54556 |
rs2525726 | snp | A/G | 0.35207 | 0.228214 | intron-variant | ING3 | GRCh38.p7 | 7:120973396 | AATATTCCTCTTCAA[A/G]ATAGGGTAGTGTCCC | 54556 |
rs2721350 | snp | C/T | 0.240478 | 0.249819 | intron-variant | ING3 | GRCh38.p7 | 7:120962958 | TGATTCTCTTCCATT[C/T]TTCATATATCCTCCA | 54556 |
rs2721351 | snp | A/G | 0.35809 | 0.225425 | intron-variant | ING3 | GRCh38.p7 | 7:120964044 | TTTTTGTTAGTTTGA[A/G]GTGTCATATAATTTT | 54556 |
rs2721354 | snp | A/G | 0.486725 | 0.0803809 | intron-variant | ING3 | GRCh38.p7 | 7:120951953 | TTCTTAGCTGCAGCA[A/G]GTGGTCCCTGAGCCA | 54556 |
rs2721368 | snp | C/T | 0.350327 | 0.228986 | intron-variant | ING3 | GRCh38.p7 | 7:120973483 | AATTTTCATACAACA[C/T]AACACTTCTGAGACA | 54556 |
rs2721369 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ING3 | GRCh38.p7 | 7:120973365 | CTAGCATTAGCATAA[C/T]ATAACTAATATACCT | 54556 |
rs2721370 | snp | C/T | 0.242775 | 0.249896 | intron-variant | ING3 | GRCh38.p7 | 7:120972185 | AAGCCCTTCTAAGTA[C/T]ATAATCCATGGCTTG | 54556 |
rs2721372 | snp | C/T | 0.486984 | 0.079614 | intron-variant | ING3 | GRCh38.p7 | 7:120969339 | CTATAAAATGAAAAC[C/T]GCATGTCTCCCTACC | 54556 |
rs2721373 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ING3 | GRCh38.p7 | 7:120967290 | ATAACCCAAGATACA[C/T]CATGGGCTCACATAC | 54556 |
rs3180313 | snp | A/G | 0 | 0 | missense, nc-transcript-variant | ING3 | GRCh38.p7 | 7:120967637 | CAGATGCCTCTAAGG[A/G]AAATACACTAGGTAA | 54556 |
rs3214197 | in-del | -/C | 0.289942 | 0.246789 | intron-variant | ING3 | GRCh38.p7 | 7:120954899 | GAACTTTAACAAAAA[-/C]TTTTTTAATGGAATG | 54556 |
rs3216951 | in-del | -/CTA | | | intron-variant, downstream-variant-500B | ING3 | GRCh38.p7 | 7:120957208 | accccatctctacta[-/CTA]aaaatacaaaaatat | 54556 |
rs3757556 | snp | C/G | 0.407158 | 0.194426 | upstream-variant-2KB | ING3 | GRCh38.p7 | 7:120950028 | CATGAATTACGGATG[C/G]AGCCTTGATTTCTAA | 54556 |
rs3837125 | in-del | -/TA | 0.251578 | 0.249995 | intron-variant | ING3 | GRCh38.p7 | 7:120973481 | TTTTCATACAACATA[-/TA]ACACTTCTGAGACAA | 54556 |
rs3891287 | snp | A/G | | | intron-variant | ING3 | GRCh38.p7 | 7:120953555 | TAAAAATCCCTATCT[A/G]AAGCTCTAAACCACA | 54556 |
rs4440563 | snp | A/G | 0.00397613 | 0.0444101 | missense, nc-transcript-variant | ING3 | GRCh38.p7 | 7:120950912 | ATGTTGTACCTAGAA[A/G]ACTATCTGGAAAGTG | 54556 |
rs4523189 | snp | A/C/G | 1.65304e-05 | 0.00287488 | utr-variant-5-prime, nc-transcript-variant | ING3 | GRCh38.p7 | 7:120950882 | CCCCTTGTTCCCTCA[A/C/G]CTCTAAGGGCCGCGA | 54556 |
rs5887003 | in-del | -/C | | | intron-variant | ING3 | GRCh38.p7 | 7:120974333 | GTCTTTAATTACAAT[-/C]CAGCTTATTCTACTT | 54556 |
rs6964344 | snp | A/G | 0.407158 | 0.194426 | intron-variant | ING3 | GRCh38.p7 | 7:120951882 | AGCTTGGTAGTCTCT[A/G]GGACTTTTTCCCCAA | 54556 |
rs6971619 | snp | A/G | 0.302435 | 0.244439 | intron-variant | ING3 | GRCh38.p7 | 7:120963790 | ATTATTTAATTCTAA[A/G]CCTTACTTAAAATGT | 54556 |
rs10216200 | snp | A/C | 0.0131661 | 0.0800605 | intron-variant | ING3 | GRCh38.p7 | 7:120955661 | ACTGTGCCATAAGTA[A/C]TTGAATAACAGATTA | 54556 |
rs10269373 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | ING3 | GRCh38.p7 | 7:120954145 | AGGATCAACTAAGAg[A/G]cctggcgtggtggct | 54556 |
rs10272601 | snp | C/G | 0.408188 | 0.193589 | intron-variant | ING3 | GRCh38.p7 | 7:120954539 | GGGAAGATTGTTTCT[C/G]TTAGGAAAAAAAAAA | 54556 |
rs10281679 | snp | C/T | 0.0577344 | 0.159793 | intron-variant, downstream-variant-500B | ING3 | GRCh38.p7 | 7:120957093 | AAGTAAATACTAggc[C/T]gggcgcagtggctca | 54556 |
rs10464522 | snp | A/G | 0.284209 | 0.247648 | intron-variant | ING3 | GRCh38.p7 | 7:120969729 | TATGAAAACCTAATA[A/G]CATTTATCACTGTCT | 54556 |
rs10464661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ING3 | GRCh38.p7 | 7:120968701 | aatacaaaaaaatta[A/G]ctgggtgcctggtgg | 54556 |
rs10464662 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ING3 | GRCh38.p7 | 7:120968739 | taatcccagctactc[A/G]gtaggctatggcagg | 54556 |
rs11408222 | in-del | -/G | 0 | 0 | upstream-variant-2KB | ING3 | GRCh38.p7 | 7:120950732 | AGTGAGGCAAGCGCC[-/G]TCAGGCGCCAAAGTG | 54556 |
rs11548053 | snp | A/G/T | 1.65636e-05 | 0.00287776 | synonymous-codon, nc-transcript-variant | ING3 | GRCh38.p7 | 7:120951192 | TCCTATGGATCTGCG[A/G/T]GACCGCTTCACGGAA | 54556 |
rs11770991 | snp | C/G | 0 | 0 | upstream-variant-2KB | ING3 | GRCh38.p7 | 7:120949043 | TCTGAAGAAATAGCA[C/G]TAAAAGGCCCATAAA | 54556 |
rs12531744 | snp | C/T | 0.0588605 | 0.161139 | upstream-variant-2KB | ING3 | GRCh38.p7 | 7:120949600 | CGAAGTAAGGTTCCG[C/T]TGAGATTCATCATGA | 54556 |
rs12533095 | snp | C/T | 0.109461 | 0.206758 | intron-variant | ING3 | GRCh38.p7 | 7:120966234 | TAATGTCCCCCATCA[C/T]GTAGAACTTCAGAAT | 54556 |
rs12539365 | snp | A/G | 0.0588605 | 0.161139 | upstream-variant-2KB | ING3 | GRCh38.p7 | 7:120949468 | AGaagaaggaaggat[A/G]ggaaacgaagaaagg | 54556 |
rs12706299 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | ING3 | GRCh38.p7 | 7:120962699 | AAGCATACTGTTTGT[C/T]TTTCTGTCTCTACAT | 54556 |
rs13230872 | snp | C/T | | | intron-variant | ING3 | GRCh38.p7 | 7:120959736 | ctgcaagctccgcct[C/T]ttgggttcatgccat | 54556 |
rs13232488 | snp | G/T | | | intron-variant | ING3 | GRCh38.p7 | 7:120968799 | tgcagcgagccaaaa[G/T]cgtgccactagactc | 54556 |
rs13238968 | snp | G/T | 0 | 0 | intron-variant | ING3 | GRCh38.p7 | 7:120954645 | TATATCCACATCCCA[G/T]AGTCACTAATCATTT | 54556 |
rs13245078 | snp | A/T | | | intron-variant | ING3 | GRCh38.p7 | 7:120968809 | caaaatcgtgccact[A/T]gactccagcccaagc | 54556 |
rs13245182 | snp | A/C/T | 0.0252325 | 0.109451 | intron-variant | ING3 | GRCh38.p7 | 7:120968800 | gcagcgagccaaaat[A/C/T]gtgccactagactcc | 54556 |
rs17143067 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | ING3 | GRCh38.p7 | 7:120965195 | TATACACTTAAGCTT[C/T]GAGGAAAGTTGTTAG | 54556 |
rs17533951 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | ING3 | GRCh38.p7 | 7:120968397 | CATAGTTCTTCGTTC[C/T]TTCTGCCAGTTCCAA | 54556 |
rs28366865 | snp | A/T | 0.0588605 | 0.161139 | intron-variant | ING3 | GRCh38.p7 | 7:120973868 | TTTAGTAGTGACAGG[A/T]TCCTAAGATTAACAA | 54556 |
rs28582920 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | ING3 | GRCh38.p7 | 7:120968231 | ATTTCACGATATGTG[A/G]TATTTTATTTAATGA | 54556 |
rs28627810 | snp | A/G | 0.0554779 | 0.157039 | upstream-variant-2KB | ING3 | GRCh38.p7 | 7:120949348 | CCCCTCAAATCCTAA[A/G]CATAATTTTAAAATT | 54556 |
rs33947704 | in-del | -/G | | | upstream-variant-2KB | ING3 | GRCh38.p7 | 7:120950733 | GTGAGGCAAGCGCCT[-/G]CAGGCGCCAAAGTGG | 54556 |
rs34088681 | in-del | -/C | | | intron-variant | ING3 | GRCh38.p7 | 7:120952060 | TTTTCCGGTAAGTTT[-/C]CAGGTGGCACATAAT | 54556 |
rs34121165 | in-del | -/A | | | intron-variant | ING3 | GRCh38.p7 | 7:120958495 | CTTCAGTCGCCACAG[-/A]ACTGAACCTGATCAT | 54556 |
rs34314625 | in-del | -/T | | | upstream-variant-2KB | ING3 | GRCh38.p7 | 7:120950748 | CAGGCGCCAAAGTGG[-/T]TTTTTTTTTTTTTCT | 54556 |
rs34400070 | in-del | -/C | | | intron-variant | ING3 | GRCh38.p7 | 7:120961935 | TCAGTACCCTCTTTA[-/C]CTATTGTAAATCAGT | 54556 |
rs34461894 | in-del | -/G | | | downstream-variant-500B | ING3 | GRCh38.p7 | 7:120975944 | GAAAATAATGGTTAT[-/G]GGGTGTTTTGACTGG | 54556 |
rs34591238 | in-del | -/A | | | intron-variant | ING3 | GRCh38.p7 | 7:120961845 | TTGACATTAACTGGG[-/A]AAAAAAGAAATAATT | 54556 |
rs34679146 | in-del | -/C | | | intron-variant | ING3 | GRCh38.p7 | 7:120955919 | CTTTATTTTACTAAT[-/C]CCTTGTCTTCTTAAG | 54556 |
rs34775399 | in-del | -/A | | | intron-variant | ING3 | GRCh38.p7 | 7:120963445 | TGAAGAATGTTTTTC[-/A]AAAAAAAAAACAGTT | 54556 |
rs34826982 | in-del | -/A | | | intron-variant | ING3 | GRCh38.p7 | 7:120958287 | GAACATTATATCCTT[-/A]AATATAAAAAATCCC | 54556 |
rs34894193 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | ING3 | GRCh38.p7 | 7:120975065 | GCTATGAATATTATT[-/C]CCAGTTAGCCTTGGA | 54556 |
rs34926686 | snp | G/T | | | intron-variant | ING3 | GRCh38.p7 | 7:120952453 | TTTTATATTTTATTG[G/T]TTAAAATTTTAAATT | 54556 |
rs35223362 | in-del | -/A | | | intron-variant | ING3 | GRCh38.p7 | 7:120958323 | TTCAGACTTAGTGAT[-/A]AATCATCTCAGTTAC | 54556 |
rs35698124 | in-del | -/G | | | intron-variant | ING3 | GRCh38.p7 | 7:120954408 | ACAGCCTGGGCAACA[-/G]GAGTGACAGAGTGAG | 54556 |
rs35749576 | in-del | -/T | | | intron-variant | ING3 | GRCh38.p7 | 7:120952506 | ATACATATTACAGGC[-/T]TTTTTAAACGTGCAT | 54556 |
rs35872651 | in-del | -/A | | | intron-variant, downstream-variant-500B | ING3 | GRCh38.p7 | 7:120957372 | GAGCGACTCTGTCTT[-/A]AAAAAAAAAAAAAAA | 54556 |
rs35989015 | in-del | -/C | | | intron-variant | ING3 | GRCh38.p7 | 7:120958847 | AGCTAGTGTAGTCTT[-/C]CCTTAATTTCTCATT | 54556 |
rs56288063 | snp | A/T | | | intron-variant | ING3 | GRCh38.p7 | 7:120971189 | TTAAACAACAGAAAA[A/T]AATTTTCTCACAGGT | 54556 |
rs57319324 | snp | A/T | | | intron-variant | ING3 | GRCh38.p7 | 7:120971188 | CTTAAACAACAGAAA[A/T]TAATTTTCTCACAGG | 54556 |
rs58433173 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ING3 | GRCh38.p7 | 7:120967741 | TGAATCATACAGTTT[A/C]TTTACCTGGTTAAAG | 54556 |
rs58515942 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | ING3 | GRCh38.p7 | 7:120960227 | ACCAAGAGAGAGGCC[G/T]GGGTGGTTGGTCTGT | 54556 |
rs60615553 | snp | A/G | 0.158632 | 0.232706 | intron-variant | ING3 | GRCh38.p7 | 7:120970204 | GGCGGGGTGGCTCAT[A/G]CCTATAATCCCAGCA | 54556 |
rs61088337 | snp | C/G | 0.144632 | 0.226711 | intron-variant | ING3 | GRCh38.p7 | 7:120951564 | AAATGTTGAGATGTC[C/G]TCTTGAGCCTTTTCG | 54556 |
rs61553827 | in-del | -/A/AA | | | utr-variant-3-prime, nc-transcript-variant | ING3 | GRCh38.p7 | 7:120975290 | CAAAAAAAAAAAAAA[-/A/AA]GTCAGTGCTTCTAAA | 54556 |
rs61612657 | snp | A/T | | | intron-variant | ING3 | GRCh38.p7 | 7:120956059 | AGAATCATTTGAATC[A/T]GTGTTTATGTGAGTG | 54556 |
rs62469957 | snp | A/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | ING3 | GRCh38.p7 | 7:120975292 | AAAAAAAAAAAAAAG[A/T]CAGTGCTTCTAAAAA | 54556 |
rs71530050 | in-del | -/A | 0.5 | 0 | intron-variant | ING3 | GRCh38.p7 | 7:120954204 | CTGAGGCGGGTGGAT[-/A]CACCTGAGGTCAGGA | 54556 |
rs71569050 | snp | A/C | 0.5 | 0 | intron-variant | ING3 | GRCh38.p7 | 7:120957963 | CATTAGAATACATAC[A/C]ATGCTATTAGTTTGG | 54556 |
rs71569051 | snp | A/C | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | ING3 | GRCh38.p7 | 7:120974930 | GAAGAGAAAGAAGAA[A/C]CAATGCATTTCCAGG | 54556 |
rs73221221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ING3 | GRCh38.p7 | 7:120957519 | GTTGAATATTAAGGG[G/T]TGTCTACTGAAAAAC | 54556 |
rs73221223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ING3 | GRCh38.p7 | 7:120963653 | TTCAAAAGATCAGAT[C/T]GAGGGCTAGAAAAGA | 54556 |
rs73221224 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | ING3 | GRCh38.p7 | 7:120974073 | AAACAATATTGCCCA[A/G]CCATTTCAAGAACAT | 54556 |
rs73429864 | snp | A/T | 0.103794 | 0.20279 | intron-variant | ING3 | GRCh38.p7 | 7:120961492 | ATCATGTAGAGACTT[A/T]AAAAAAGCTGTATTT | 54556 |
rs73429874 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ING3 | GRCh38.p7 | 7:120962788 | ATTCGTACCTCCTTC[A/G]TGTCTACCAGTGTTA | 54556 |
rs73429893 | snp | A/G | 0.030665 | 0.119967 | intron-variant | ING3 | GRCh38.p7 | 7:120971358 | CTTATAAGGGCACCA[A/G]CCTTGTCAGAGTAGG | 54556 |