SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4223260 | snp | A/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B, upstream-variant-2KB | Ambra1, Chrm4 | Mm_Celera | 2:91918983 | TTGGGCTAATGGGTC[A/T]CAAGAGGATGCCATT | 228361 |
rs4223261 | snp | A/G | 0.21875 | 0.248039 | intron-variant, downstream-variant-500B, upstream-variant-2KB | Ambra1, Chrm4 | GRCm38.p3 | 2:91918858 | CGGCAGAAATAAGCA[A/G]GAGCCTGGTGAGGGG | 228361 |
rs4223262 | snp | A/C | 0.277778 | 0.248452 | intron-variant, downstream-variant-500B, upstream-variant-2KB | Ambra1, Chrm4 | GRCm38.p3 | 2:91918854 | AGAAATAAGCAGGAG[A/C]CTGGTGAGGGGCGTG | 228361 |
rs4223263 | snp | C/G | 0.21875 | 0.248039 | splice-donor-variant, downstream-variant-500B, upstream-variant-2KB | Ambra1, Chrm4 | Mm_Celera | 2:91918851 | AATAAGCAGGAGCCT[C/G]GTGAGGGGCGTGTCA | 228361 |
rs4223264 | snp | A/G | 0.21875 | 0.248039 | utr-variant-3-prime, upstream-variant-2KB | Ambra1, Chrm4 | GRCm38.p3 | 2:91918841 | AGCCTGGTGAGGGGC[A/G]TGTCATCATTTTAAT | 228361 |
rs6179972 | snp | A/T | 0.5 | 0 | intron-variant | Ambra1 | Mm_Celera | 2:91738994 | TTTTTTTCCattttt[A/T]aaatttatgtattat | 228361 |
rs6184998 | snp | G/T | 0.5 | 0 | intron-variant | Ambra1 | Mm_Celera | 2:91733319 | gaagagggagtcaga[G/T]cccgctacagatggt | 228361 |
rs6185161 | snp | C/T | 0.5 | 0 | intron-variant | Ambra1 | Mm_Celera | 2:91896523 | ggctgtacagcaagg[C/T]caaacccaTCTCAAA | 228361 |
rs6185206 | snp | A/C | 0.5 | 0 | intron-variant | Ambra1 | Mm_Celera | 2:91896552 | AAAGAAAAAAGAAAA[A/C]AATAGTAATAGTGTG | 228361 |
rs6185500 | snp | C/T | 0.5 | 0 | intron-variant | Ambra1 | Mm_Celera | 2:91733378 | cgaactctggacctt[C/T]ggaagagcagtcggg | 228361 |
rs6196800 | snp | C/T | 0.5 | 0 | intron-variant | Ambra1 | GRCm38.p3 | 2:91779842 | CTTTTGAAATGTCTT[C/T]TTTTTTTTTTTtttt | 228361 |
rs6262715 | snp | C/T | 0.5 | 0 | intron-variant | Ambra1 | Mm_Celera | 2:91789395 | cttagttgcttatag[C/T]tntttgtgtagtgtt | 228361 |
rs6262718 | snp | A/C | 0.5 | 0 | intron-variant | Ambra1 | Mm_Celera | 2:91789397 | tagttgcttatagnt[A/C]tttgtgtagtgttgT | 228361 |
rs6262756 | snp | A/C | 0.5 | 0 | intron-variant | Ambra1 | Mm_Celera | 2:91789423 | gttgTTAGGATCCCA[A/C]ATNTAGGCTatctcc | 228361 |
rs6262776 | snp | A/G | 0.5 | 0 | intron-variant | Ambra1 | Mm_Celera | 2:91789426 | gTTAGGATCCCANAT[A/G]TAGGCTatctcctta | 228361 |
rs6263344 | snp | C/T | 0.5 | 0 | intron-variant | Ambra1 | Mm_Celera | 2:91789515 | cttttgcttctgctt[C/T]ataactataattttg | 228361 |
rs6399553 | snp | G/T | 0.5 | 0 | intron-variant | Ambra1 | Mm_Celera | 2:91881725 | CTTTTTCTTTGGCTA[G/T]TTGGTTGGTTGAGGT | 228361 |
rs27368539 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B, upstream-variant-2KB | Ambra1, Chrm4 | Mm_Celera | 2:91919071 | TGGAGAGAGTCATCC[A/G]TATTGCTTCCTGCCA | 228361 |
rs27368540 | snp | A/G | 0.297521 | 0.245442 | utr-variant-3-prime, upstream-variant-2KB | Ambra1, Chrm4 | Mm_Celera | 2:91918407 | ACCTGTGGAGTGAAG[A/G]AAATAGCCTGCTTGC | 228361 |
rs27368541 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, upstream-variant-2KB | Ambra1, Chrm4 | GRCm38.p3 | 2:91918320 | CCAGCCTCTCTCATC[C/T]TCTTAGCCCACAGAG | 228361 |
rs27368542 | snp | A/G | 0.197531 | 0.244432 | utr-variant-3-prime, upstream-variant-2KB | Ambra1, Chrm4 | Mm_Celera | 2:91918135 | CTAGGGGACTCAAAC[A/G]ACCCTGGGCAGAAGC | 228361 |
rs27368543 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Ambra1 | Mm_Celera | 2:91916714 | CTCTCCAGGAAATGT[A/G]GTATCAGGCATACAG | 228361 |
rs27368544 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Ambra1 | Mm_Celera | 2:91916414 | GTAGTGAAAGGAGAC[A/G]AATCAACACTCTGAT | 228361 |
rs27368545 | snp | A/G | 0.32 | 0.24 | intron-variant | Ambra1 | Mm_Celera | 2:91915739 | TGAACAGACAGAATT[A/G]TCATGATGGGTTCAA | 228361 |
rs27368546 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91914552 | ACCAACAGCACTAAA[A/C]CAGTCTCCTGTTTTT | 228361 |
rs27368547 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ambra1 | Mm_Celera | 2:91914283 | AACAGCATTCACAGT[C/T]CAGGCCTCAGGCTAG | 228361 |
rs27368548 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91914039 | GTTACCCTGCCACAC[A/G]CTGCCCTACTCTCTG | 228361 |
rs27368549 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91914013 | GGAGCCGCTGTGGGA[C/T]GTGAATGTGAGTTAC | 228361 |
rs27368550 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ambra1 | Mm_Celera | 2:91913763 | TGTAGCCAGCCACTC[C/T]TTAAATTATATAAAC | 228361 |
rs27368551 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91913420 | TCCACGAATAATAGC[C/T]CATTTCAAAAACTAG | 228361 |
rs27368552 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91913309 | AATCCTGGCAGAACC[C/G]GAAGCTTCTGTCCTC | 228361 |
rs27368553 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ambra1 | Mm_Celera | 2:91913027 | TAAAGTACAGCGGTG[A/G]CTGTGAGCAGAATTT | 228361 |
rs27368554 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91912821 | CTGAGTAATAGTTAG[A/G]CAGAATGTGCTGGCA | 228361 |
rs27368555 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91912495 | AGGGATTTATGGACT[C/T]TGAGCCACCCTGGAA | 228361 |
rs27368556 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ambra1 | Mm_Celera | 2:91911354 | GAATTGGTATGGAAT[C/T]CAAGACTTCTGGAAA | 228361 |
rs27368557 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91911270 | TCAACCTACCAGGCT[C/T]TTTTTTCATGGCTCC | 228361 |
rs27368558 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91911147 | TGGAACTCAGCTGTC[C/T]TGCCTGTCCTAGGCT | 228361 |
rs27368559 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91911069 | TCTAGGGACTGCAGA[C/G]TACAGCTAGAAAAAT | 228361 |
rs27368560 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91910876 | TGAGGAGTGGAGTAT[C/T]GCTTTAAGATGACTA | 228361 |
rs27368561 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ambra1 | Mm_Celera | 2:91910841 | GCCCTGTGAAATCTG[C/T]TCATTTGCCCAAGGA | 228361 |
rs27368562 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91910458 | CCATAGCAGCCTTTC[A/C]TTGATCTGTTACCTG | 228361 |
rs27368563 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91910428 | GTGTTTGAGGGTCTC[C/T]GGATGTTTGCTCAAC | 228361 |
rs27368564 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91910403 | GGGTAAGCTAAAGTC[A/G]GAAAGTCCTGTGTTT | 228361 |
rs27368565 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91909961 | ATCCTTCTGACAGCT[A/G]TCCATGGCACATTTC | 228361 |
rs27368566 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91909945 | TCTGAGGACTGAGTT[A/C]ATCCTTCTGACAGCT | 228361 |
rs27368567 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91909879 | AGGTGCTTCTGTTCT[C/T]TCTCTCGGCCTCTTA | 228361 |
rs27384468 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91909845 | TCCAGCCATTCATCT[C/G]GGGTACATAAGGTTG | 228361 |
rs27384469 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91909763 | CCTGGGGAACACAGC[A/G]GGTAGAGCACTGCAG | 228361 |
rs27384470 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Ambra1 | Mm_Celera | 2:91909496 | CAGTATAGTTAGTTA[A/C]CATTCTGCCTGGCTA | 228361 |
rs27384471 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91909441 | GCCTAGACTAGCCTG[A/G]AATTCTCAATCTTTC | 228361 |
rs27384472 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91907434 | CCTCAAAACCTTCAC[A/G]TGCCTGCCATACCAT | 228361 |
rs27384473 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91906782 | GCCCAACCTTCCACT[A/G]TAGTCCTTGCTCATT | 228361 |
rs27384474 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ambra1 | Mm_Celera | 2:91906636 | TTCAGTGAGCATGAG[A/G]TATACAAGCATGTAA | 228361 |
rs27384475 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91906114 | ATTACACACCCAGTT[A/G]TGACGTCTTCCGTAA | 228361 |
rs27384476 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91905930 | TACCAGAAAAGGTCT[A/C]ATCAACTCTGATCCT | 228361 |
rs27384477 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Ambra1 | Mm_Celera | 2:91905861 | AGTCCCAAGAAAGAA[A/C]GAGCTGGCTGAAAAT | 228361 |
rs27384478 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ambra1 | GRCm38.p3 | 2:91905836 | AACAGTGTCTCAATC[A/G]TCCTTACCAAGTCCC | 228361 |
rs27384479 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91905772 | ACACTGCTTCTTGTA[A/G]ACCTTCTCAGTCTTT | 228361 |
rs27384480 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91905514 | CTGCTAGTCGTCCTG[A/G]AAGCAGTCATCAGAG | 228361 |
rs27384481 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91905455 | GGCTAGCCAGGAGAG[C/T]CAGGTGCCAGGACTT | 228361 |
rs27384482 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91905400 | AGGCATAATTTGGAA[C/T]GAAAAAGGGAGCCAG | 228361 |
rs27384483 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ambra1 | Mm_Celera | 2:91905326 | GCCTCAGTTCAGTCA[A/G]GGGGAGCTACCTGTG | 228361 |
rs27384484 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Ambra1 | Mm_Celera | 2:91904867 | CAGGCAGCTGCACTG[C/T]ATTTTGTGCTCTCAG | 228361 |
rs27384485 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Ambra1 | Mm_Celera | 2:91904542 | GAACACACCCATGCT[C/T]TTATAATTCCCTAAG | 228361 |
rs27384486 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91904313 | TTTAAGCCTTTTCTC[A/T]TTAAAAATCCTTCTA | 228361 |
rs27384487 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ambra1 | Mm_Celera | 2:91904148 | CTCCCCAATCACAGG[C/T]ACTTTCCACTATACT | 228361 |
rs27384488 | snp | C/G | 0.188366 | 0.242283 | intron-variant | Ambra1 | Mm_Celera | 2:91903052 | TGATTGACCCTATCA[C/G]CTCTCAGCTGAGTTG | 228361 |
rs27384489 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ambra1 | Mm_Celera | 2:91902619 | CTTCTAGAGTGTTGT[A/G]CAGGCCCGAGTGCTT | 228361 |
rs27384490 | snp | A/G | 0.32 | 0.24 | intron-variant | Ambra1 | Mm_Celera | 2:91902285 | GCAGCAGACTGAAAA[A/G]CTCAGTGTAAAGTCA | 228361 |
rs27384491 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91901202 | CCTAGACACTTCAGT[A/G]GTTGCTTTCTTGAAT | 228361 |
rs27384492 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Ambra1 | Mm_Celera | 2:91900618 | ACCAACAAAGGAGAC[C/T]TGGTGATCTGCCGAC | 228361 |
rs27384493 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ambra1 | Mm_Celera | 2:91900386 | TGAGTTGAAAGTCAG[C/T]CCATTCCAGCCTAAA | 228361 |
rs27384494 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91900275 | GATGAGGTGAGGGGT[A/T]CTGAGAGGCTAAGAT | 228361 |
rs27384495 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ambra1 | Mm_Celera | 2:91899974 | TAGAAGGTTCCTCTC[A/T]GCTCTGCTCCCCACA | 228361 |
rs27384496 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ambra1 | Mm_Celera | 2:91899787 | GAAAGGATTCTCAGG[C/T]AGAGACCTTGTAGCT | 228361 |
rs27384497 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ambra1 | GRCm38.p3 | 2:91899305 | ATTTTTATGTCCCTC[C/T]GTGCCCAAGTTTCTC | 228361 |
rs27384498 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91899194 | TGAGTCTCCATTCCT[A/G]TCCCTTCACAGACCC | 228361 |
rs27384499 | snp | C/T | 0.32 | 0.24 | intron-variant | Ambra1 | Mm_Celera | 2:91898303 | TGAAGGCCTTTCTAG[C/T]TGATACACAAAGCAC | 228361 |
rs27384500 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91898238 | CTGATAATCAGGATT[C/G]TGTCTGTGTGGCAAT | 228361 |
rs27384501 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ambra1 | Mm_Celera | 2:91897949 | GATCATTCATGTTTC[A/G]CAGTAGCTGGAGCTA | 228361 |
rs27384502 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ambra1 | Mm_Celera | 2:91897605 | TTTGTATCCAACCTT[C/G]CGTAGAGTCCCCAGG | 228361 |
rs27384503 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91897435 | TGTTCGTTTTAGCGT[A/G]CTGATTCTCATTTCC | 228361 |
rs27384504 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91897177 | CCCAGATTTCTCTGC[A/G]TTTTAAAGGTTTTCC | 228361 |
rs27384505 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91897102 | GCACAAGCAAGCCTC[A/G]GATTTGGAATCTTCT | 228361 |
rs27384506 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Ambra1 | Mm_Celera | 2:91896891 | TACATAAAAGCAACA[C/T]AGGTTTTTTTCTCCT | 228361 |
rs27384507 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91896875 | AGTTTCACTGATGTT[A/G]TACATAAAAGCAACA | 228361 |
rs27384508 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ambra1 | Mm_Celera | 2:91896821 | GGTAACATAGACCCA[C/T]CAACTGCATTAGACC | 228361 |
rs27384509 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91896681 | TCCCATCTAATGACA[A/C]TTGGTTTTCTTCTAT | 228361 |
rs27384510 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ambra1 | Mm_Celera | 2:91896624 | TTTGATTAAGACACC[C/T]ATCTATCCAGTGTTT | 228361 |
rs27384511 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91894159 | AATATGCATTCAGGA[A/G]TGTGAGAGAGGGTCT | 228361 |
rs27384512 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91893270 | TATTTTTATCTATTG[C/G]AAGGATACCATTTCT | 228361 |
rs27384513 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91893230 | GGCTTTGAGTGCGGA[A/G]TTGATACTGAAATTA | 228361 |
rs27384514 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ambra1 | Mm_Celera | 2:91893148 | GTGATCCAAACTCTG[A/G]CTTGGTGAAGAACAC | 228361 |
rs27384515 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ambra1 | Mm_Celera | 2:91892319 | GCTGAGAAATTGATG[A/G]GTATTCCATGTCCTA | 228361 |
rs27384516 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ambra1 | Mm_Celera | 2:91892093 | TGTCCTGGTTAGCCA[C/T]GTGGAAGATGTATTA | 228361 |
rs27384517 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Ambra1 | GRCm38.p3 | 2:91892051 | TGGTTTGTTTATGCA[A/C/G]TAAAGCTGAATTTAA | 228361 |
rs27384518 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Ambra1 | GRCm38.p3 | 2:91891569 | ACCAAGTTGCTCCTT[C/G]AGTTTGTGTGTATAA | 228361 |
rs27384519 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ambra1 | Mm_Celera | 2:91891398 | CTGTGTTCCCGCTCA[A/G]CTTTCATTTTCTAAT | 228361 |
rs27384520 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ambra1 | Mm_Celera | 2:91891251 | AGACTCTATAACTCA[A/G]TCACCTTTGCTGTTG | 228361 |
rs27384521 | snp | A/C | 0.32 | 0.24 | intron-variant | Ambra1 | Mm_Celera | 2:91890647 | GTTTCCACCAAACTC[A/C]GCTTCCCCCAGGGTC | 228361 |