| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs256992470 | snp | A/C | | | intron-variant | Nedd1 | Mm_Celera | 10:92714406 | TAAAACCCATACTTA[A/C]GATTAGCTTACCTTG | 17997 |
| rs257024490 | in-del | -/GGCT | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92721247 | TCACTCTGTAGACCA[-/GGCT]GGCTGGCCTTGAACT | 17997 |
| rs257026960 | in-del | -/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92693753 | AAACTGAGGCACAAA[-/G]ATTAAGCCTTTTCCT | 17997 |
| rs257077053 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | Mm_Celera | 10:92723217 | GGAGAGGAAATTGTG[A/G]CAGGAGTGGGAGAAG | 17997 |
| rs257078768 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92707253 | AACATTTCTGCCATG[C/T]CAGAAATAGAACCCA | 17997 |
| rs257118508 | in-del | -/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92703224 | ACTCACTCAAGATGG[-/T]TTTTTTTTTCTAGTT | 17997 |
| rs257168809 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | Mm_Celera | 10:92723463 | AATGTATTTCATGGT[A/G]GAAAGGGGCCAATGA | 17997 |
| rs257332523 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92720859 | AATTTATCCTATTGC[C/T]TGTCTGAAGACATTA | 17997 |
| rs257392877 | snp | A/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92712469 | TCTATCACAGCACAA[A/T]TGCCTGAGGGGAAAA | 17997 |
| rs257584196 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92718829 | CCAGGAGAGACCCCA[C/T]AACACTGAATCGCCA | 17997 |
| rs257613251 | snp | A/G | | | synonymous-codon | Nedd1 | Mm_Celera | 10:92689772 | CACTCCAGCAGTGAC[A/G]GAGGATGCTGCCTTT | 17997 |
| rs257648398 | in-del | -/AAA | | | intron-variant | Nedd1 | Mm_Celera | 10:92701817 | CAAAATCTGTAGGGC[-/AAA]AAAAAAAGTCAAACA | 17997 |
| rs257747929 | in-del | -/C | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92696500 | AGAACTGAAAGGTGG[-/C]CCGGCAGACCCCACA | 17997 |
| rs257776343 | in-del | -/A | | | intron-variant | Nedd1 | Mm_Celera | 10:92718745 | CATTTGGATCAGCAC[-/A]ACTAGGAGTTACAGG | 17997 |
| rs257822470 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92693067 | TTCCCTCTCCCAAGA[A/G]GGCAGAGACTGACAC | 17997 |
| rs257944128 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92706007 | CTAATCTCACAGGGA[C/T]GCGCATGGCTTTGGA | 17997 |
| rs258053653 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92701512 | TAAACACTAATCCCC[A/G]CCAGAAGATAGGCTT | 17997 |
| rs258186237 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92695768 | CTGTACATTATAAAA[A/G]GAGTTTGACTTGACA | 17997 |
| rs258263312 | snp | A/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92687314 | ATATAACACACATGA[A/T]CAACTTATGGAGGTT | 17997 |
| rs258272286 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | Mm_Celera | 10:92723489 | AATGAACTGAGTTTT[-/C]CCAACATTCCTGCTA | 17997 |
| rs258308335 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92718481 | TAAAAACACTTAATA[C/T]GTTTGTTCATAAATC | 17997 |
| rs258312966 | snp | A/C | | | intron-variant | Nedd1 | Mm_Celera | 10:92703840 | ATAGTTGGTAAAAAT[A/C]TTTTCCCATTCTCTA | 17997 |
| rs258360900 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92693033 | AAAAAAAAGAAGCTG[A/G]GGCAACTTGGGCTTG | 17997 |
| rs258388478 | in-del | -/CTCAAAACAAGTC | | | intron-variant | Nedd1 | Mm_Celera | 10:92700697 | TAGGTACGGTCCTGT[-/CTCAAAACAAGTC]CTCATGACAATGTCA | 17997 |
| rs258442877 | snp | C/G | | | upstream-variant-2KB | Nedd1 | Mm_Celera | 10:92724231 | TAGAAAATCTTATTT[C/G]AGTGGCTTATAGGCT | 17997 |
| rs258697157 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92722247 | CGCCCAACGCAGGAC[C/T]GAAGAGGCTGACCTC | 17997 |
| rs258763406 | snp | C/T | | | downstream-variant-500B | Nedd1 | Mm_Celera | 10:92684495 | TTCATCTACAAATAA[C/T]ACACTGTGTGGTTTC | 17997 |
| rs258798628 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92689525 | TTTTCTGTTTTTGTG[A/G]TCCTCACAACCTAGA | 17997 |
| rs258914154 | snp | A/C | | | intron-variant | Nedd1 | Mm_Celera | 10:92690197 | ACAAATGGAGAAACG[A/C]CTCTCTGTGAAGAGA | 17997 |
| rs258966273 | in-del | -/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92719409 | GTAGCCACACAAATA[-/T]TTTTTTTTATGGGCC | 17997 |
| rs258993725 | snp | A/C | | | intron-variant | Nedd1 | Mm_Celera | 10:92686929 | TTGCTGTGTGACTGG[A/C]AGTACAGTGATTCCT | 17997 |
| rs259024039 | in-del | -/TTC | | | intron-variant | Nedd1 | Mm_Celera | 10:92716752 | ATGAATATATTATTA[-/TTC]ATGAATATTATAGAG | 17997 |
| rs259143114 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92712706 | ATGGATGGGGAAATA[C/T]GACTTAAAATAGACA | 17997 |
| rs259355760 | in-del | -/ATAT | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92708445 | CGCACACACACACAC[-/ATAT]ACACACACATACACA | 17997 |
| rs259436870 | in-del | -/TTTTTG | | | intron-variant | Nedd1 | Mm_Celera | 10:92719336 | TATTTTTATCAGTGT[-/TTTTTG]TTTTTTGTTTTGTTT | 17997 |
| rs259513082 | in-del | -/TT | | | upstream-variant-2KB | Nedd1 | GRCm38.p3 | 10:92723808 | GGTGTTATTAGCTGA[-/TT]TTTTTTTTCCTGGAA | 17997 |
| rs259515361 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92692248 | CTGGAGTGTGGTAAG[C/T]CTTTGAAAAACCATG | 17997 |
| rs259548633 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92701640 | GTCCAGATTTCTATT[A/G]GCATCATAATTAACT | 17997 |
| rs259621534 | in-del | -/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92694795 | CACAAAAGACCCTAA[-/G]TGGCTCCCCTTTTGA | 17997 |
| rs259648084 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | Mm_Celera | 10:92722612 | GGTGTGCACTTACTG[G/T]GTTTAGCTTGAAGGG | 17997 |
| rs259648105 | snp | A/C | | | intron-variant | Nedd1 | Mm_Celera | 10:92713036 | TTGACATCTAACTCG[A/C]ATGAGAATGTTTGCT | 17997 |
| rs259712056 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92713586 | ACTTTCCTGAGATGA[A/G]TATGTTTATTTTTTG | 17997 |
| rs259777141 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92714365 | TGCCAGCTGTCACAG[A/G]TATAATTATTGTTAA | 17997 |
| rs259807242 | in-del | -/AGA | | | upstream-variant-2KB, cds-indel | Nedd1 | Mm_Celera | 10:92722885 | TGAACAAAACAAAAC[-/AGA]AGAATAAAAGATGGG | 17997 |
| rs259825716 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92708269 | TTAAGATCTAGAACG[A/G]ATCTTTCTAAGAGGC | 17997 |
| rs259869722 | in-del | -/CAGT | | | intron-variant | Nedd1 | Mm_Celera | 10:92709649 | ATCTAAATAAAACCC[-/CAGT]CAGAACTAAGCATGA | 17997 |
| rs259870801 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92699103 | AGCAGGACCTGTAAA[A/G]AATGAACATCCCACC | 17997 |
| rs259915779 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92712165 | CCAAGACAATCTCCA[A/G]GGCCCTTGGCCCTCC | 17997 |
| rs260109831 | snp | C/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92693905 | AATCCCAGCACTCAG[C/G]AGGCAGAGGCAGGTG | 17997 |
| rs260193501 | in-del | -/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92706053 | TTGCTTTTTCTTGGA[-/G]TTGGGGGTGGGGGAG | 17997 |
| rs260299619 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92708145 | CAATTCTGGTAATGA[C/T]AGGTAAACAGCAGTT | 17997 |
| rs260328171 | in-del | -/GGCTGGG | | | intron-variant | Nedd1 | Mm_Celera | 10:92715788 | TCCAGCCTTAAGGAA[-/GGCTGGG]GCACATCCTTGAGTG | 17997 |
| rs260352683 | snp | A/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92716575 | GCAACAAACAGAAAT[A/T]ATAATCAGCTTTTTC | 17997 |
| rs260573091 | in-del | -/TTCCCTCC | | | downstream-variant-500B | Nedd1 | GRCm38.p3 | 10:92684697 | GAGGGAAGGTTAAAT[-/TTCCCTCC]TGTTACTCCATTTCA | 17997 |
| rs260612301 | snp | A/C/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92710904 | CTGTATCAGAAATGC[A/C/G]TTTTAGAATTGTGCT | 17997 |
| rs260644755 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92703435 | GAAACGGTTTTTGGG[C/T]ATGTGCCTGAGAATG | 17997 |
| rs260763772 | snp | A/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92688193 | AATCTAGGGAGAAAC[A/T]AACTCTAAGAAACCC | 17997 |
| rs261090434 | snp | A/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92713307 | AAACCAAATGTCTGG[A/T]ATATCCTACAAACAG | 17997 |
| rs261120131 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92706097 | GCAGCACAGAAGCAG[C/T]TAAAGGCCCCTGAGC | 17997 |
| rs261214207 | in-del | -/ATCACT | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92688266 | TGAAAACTCTGAAAG[-/ATCACT]ATTCATGCCATCTCT | 17997 |
| rs261309553 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92720129 | CCTTTATCAGCAGCT[A/G]CCCTATATTCTAGCA | 17997 |
| rs261470505 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92709607 | GTCACGCACTAGGAC[A/G]GGTGAGAAGCACTGC | 17997 |
| rs261546685 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92716835 | AAATTTGAATTATTT[C/T]CAGTTAATCTTAAAA | 17997 |
| rs261632306 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92715042 | TAAAGCAAAAATAGA[A/G]TCGGAAGTATCAAAG | 17997 |
| rs261736707 | in-del | -/CA | | | intron-variant | Nedd1 | Mm_Celera | 10:92708432 | ACATGCATGCATTCG[-/CA]CACACACACACATAT | 17997 |
| rs261780257 | snp | A/G/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92714693 | ATTCTAAAAATATTT[A/G/T]AAAATAAGTAGGATG | 17997 |
| rs261852337 | snp | C/T | | | downstream-variant-500B | Nedd1 | Mm_Celera | 10:92684509 | ATACACTGTGTGGTT[C/T]CCTCAATTTTAAAGG | 17997 |
| rs261978431 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | Mm_Celera | 10:92722473 | AGCGCTCAGCCCGCG[C/G]GGGTGCTGGGTGGCC | 17997 |
| rs262018676 | in-del | -/A | | | intron-variant | Nedd1 | Mm_Celera | 10:92718152 | ACAAAGATAAGCAGG[-/A]AAAAAAAAACAAAAA | 17997 |
| rs262147510 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92712082 | TACAGATGAGGCACA[C/T]GAGACATGAAAGCAT | 17997 |
| rs262295222 | snp | A/C | | | intron-variant | Nedd1 | Mm_Celera | 10:92693988 | aaaacaaaaacaaaa[A/C]aaaaacaaaaacaaa | 17997 |
| rs262306173 | snp | A/C | | | intron-variant | Nedd1 | Mm_Celera | 10:92721444 | GGCCAACAGTGGTCA[A/C]AGACACGCCCCCACA | 17997 |
| rs262335718 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92712928 | CCCTCTAAGCAGTGT[A/G]AATTCACATAGTGCA | 17997 |
| rs262473016 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92711370 | TTTTGATGAAAAGAG[C/T]ATGGCTGTTAATCAA | 17997 |
| rs262522946 | in-del | -/A | | | intron-variant | Nedd1 | Mm_Celera | 10:92707109 | TATTAAGGAAATGTT[-/A]ATCGTGCCAAATATT | 17997 |
| rs262557488 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92715057 | ATCGGAAGTATCAAA[A/G]TACAAAGTATACTAC | 17997 |
| rs262770882 | in-del | -/AG | | | intron-variant | Nedd1 | Mm_Celera | 10:92715957 | GACAAAAGGGGAAAC[-/AG]AGAGAGTCCCTTCCT | 17997 |
| rs262938878 | in-del | -/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92704674 | CTGAAGGTTAACACA[-/T]TATCATTCTGCAAAG | 17997 |
| rs262966644 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | Mm_Celera | 10:92723004 | GGTTGGTTTAGGAGA[G/T]GATTACTTGAGAGGA | 17997 |
| rs262972314 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92717227 | ACATTGTGCAGAGTA[C/T]CCTGGTATTTTATGA | 17997 |
| rs263010932 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | Mm_Celera | 10:92722648 | AGGTCAGTCAACACG[C/T]AGGTTCCCTAGCCTG | 17997 |
| rs263161554 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92704066 | AGTCTATGATGCACA[C/T]AGAGTTGAGCTTTGT | 17997 |
| rs263191533 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92693377 | AAGAATATTTTACCA[A/G]TATTACAATGTTATA | 17997 |
| rs263243337 | in-del | -/GT | | | intron-variant | Nedd1 | Mm_Celera | 10:92696757 | CACACACACACACAC[-/GT]ACACACACGTACACA | 17997 |
| rs263277302 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92695516 | CTTCTTCCGTTAATA[A/G]TGGGAGCTTAACTTT | 17997 |
| rs263386526 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92692705 | TAGCCAATTCCTTAA[C/T]TGAAGCATCAAGAAA | 17997 |
| rs263458938 | in-del | -/AAAC | | | intron-variant | Nedd1 | Mm_Celera | 10:92718163 | CAGGAAAAAAAAACA[-/AAAC]AAAAAACATCCTATT | 17997 |
| rs263535582 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92720203 | TCCCATAACAATGCC[C/T]GCCTCCTCACACAGG | 17997 |
| rs263707187 | snp | G/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92702171 | CTATGCTTAGAAGGC[G/T]ATGTTTTTTTGTTGT | 17997 |
| rs263726324 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92690962 | GCACCTTAAACATAA[C/T]GTGAATTTTCGAAAA | 17997 |
| rs263937789 | snp | C/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92701446 | ATGGGTTCCTCCACA[C/G]TGGAATGGGCTAAAC | 17997 |
| rs264148566 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92708443 | TTCGCACACACACAC[A/G]CATATACACACACAT | 17997 |
| rs264178848 | in-del | -/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92709561 | ATTCTATGGTTGGGG[-/G]TCACCACAATATGAG | 17997 |
| rs264329286 | snp | A/C | | | intron-variant | Nedd1 | Mm_Celera | 10:92712570 | AGCACTGTCTTCCCA[A/C]TTTCCATTGTGGAAA | 17997 |
| rs264335334 | in-del | -/C | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92694778 | AGAGCACTTGCTTAA[-/C]ACACAAAAGACCCTA | 17997 |
| rs264426460 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92696285 | TCTCAAAATAAGTCA[A/G]CATCATGGTTATGAC | 17997 |
| rs264481590 | snp | A/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92712108 | AGCATAAGAGACTGG[A/T]GCATCTCACATATGT | 17997 |
| rs264553743 | in-del | -/ACACACAC | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92696759 | CACACACACACACGT[-/ACACACAC]GTACACACACGTACA | 17997 |
| rs264668690 | in-del | -/ACGGGT | | | intron-variant | Nedd1 | Mm_Celera | 10:92710409 | CACACGGGAGGGCAG[-/ACGGGT]AAGAAGAGGCTATAA | 17997 |
| rs264724116 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92717581 | ATCTTCATAAGAACC[A/G]AGTCCAATTCTCTGG | 17997 |
| rs264737911 | in-del | -/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92709557 | AAGAATTCTATGGTT[-/G]GGGGTCACCACAATA | 17997 |
| rs264740944 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92709902 | GTATCCACAGTTCTC[C/T]CCTGTGAGCCATAGT | 17997 |
| rs264803363 | snp | G/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92708260 | TGGACTTTCTTAAGA[G/T]CTAGAACGGATCTTT | 17997 |
| rs264911599 | in-del | -/AT | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92716006 | AACTGCTCTCCTAAA[-/AT]TCATTATAATCTCAC | 17997 |
| rs264992173 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92721499 | TCTGGGTTCCAGAGG[A/G]CAAACTAAAAAGCAT | 17997 |
| rs265021387 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92720273 | GGGAAATAAACTAAG[C/T]AATGTTCTCATATTT | 17997 |
| rs265152174 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92692826 | GGAGCTGGGTAAGTA[C/T]TACAGAGCAGCAACA | 17997 |
| rs265231761 | in-del | -/T | | | upstream-variant-2KB | Nedd1 | GRCm38.p3 | 10:92724545 | TTCCTTGGTGATGAA[-/T]TAGCAGTATGGAAGT | 17997 |
| rs265295458 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92688397 | TCTTGGGAGAAGAGG[C/T]CCAAGATTCTGGACT | 17997 |
| rs265432654 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | Mm_Celera | 10:92723385 | ATCCGCAGCTTCACA[C/T]GCTGCTGTTCAGGTA | 17997 |
| rs265565735 | snp | A/C | | | intron-variant | Nedd1 | Mm_Celera | 10:92696024 | AGGGACTGGGCTGGA[A/C]GCACATCACGTGGGG | 17997 |
| rs265588259 | snp | C/T | | | utr-variant-3-prime | Nedd1 | Mm_Celera | 10:92685297 | TATCAAAGTGTAGGT[C/T]CCAGCAGGCAGATGA | 17997 |
| rs265648077 | in-del | -/GAC | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92719024 | ATGTGGATGACACAC[-/GAC]GACTTCTGAATCTCC | 17997 |
| rs265712448 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92721201 | GTTTTTTGAGACAGG[A/G]TTTCTCTGTATAGTC | 17997 |
| rs265816933 | snp | G/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92691434 | ATAAACACATCCCCA[G/T]TGTTTTAGCTTTGTT | 17997 |
| rs265847343 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92708992 | TTCTGATGCAAACTA[A/G]TCAATTAAAATTCTT | 17997 |
| rs265934546 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92697541 | AGGATCAAGGCCTTG[A/G]CTGGCAAAGTCAAGT | 17997 |
| rs265997171 | in-del | -/GCATTGGAACA | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92717251 | TTATGACTAGATCAC[-/GCATTGGAACA]AAGTTTTGGGGGGCT | 17997 |
| rs266047107 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92714373 | GTCACAGGTATAATT[A/G]TTGTTAAGGGTTCAG | 17997 |
| rs266099249 | snp | A/G | | | downstream-variant-500B | Nedd1 | GRCm38.p3 | 10:92684595 | AGAGGGAGGGGAGGA[A/G]AGATGGGGGGGGGGA | 17997 |
| rs266136362 | in-del | -/TT | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92719467 | ACAAAAAGTGATTAC[-/TT]TTTTTTTTAAAGGAT | 17997 |
| rs266153109 | snp | C/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92711437 | CTGAGCTGATTAGGA[C/T]ACCACAGAATCCACA | 17997 |
| rs266212051 | snp | A/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92705351 | TCTCAAGGCTTCTGG[A/G]CAAGCCCTTCCATTA | 17997 |
| rs386869602 | in-del | -/CGGAAGTATCAAAGT | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92715044 | AAGCAAAAATAGAAT[-/CGGAAGTATCAAAGT]ACAAAGTATACTACT | 17997 |
| rs386914441 | in-del | -/AAAAG | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92713895 | ACATAAAAAATAAAG[-/AAAAG]GCAACATGAATCAAC | 17997 |
| rs386930079 | in-del | -/A | | | intron-variant | Nedd1 | Mm_Celera | 10:92701778 | AACCCCACAAAAAAA[-/A]CTGTAACTCATAATA | 17997 |
| rs386950662 | in-del | -/TGGC | | | intron-variant | Nedd1 | Mm_Celera | 10:92721254 | GTAGACCAGGCTGGC[-/TGGC]CTTGAACTCAGAAAT | 17997 |
| rs386975487 | in-del | -/CCCTCCTT | | | downstream-variant-500B | Nedd1 | GRCm38.p3 | 10:92684698 | AGGGAAGGTTAAATT[-/CCCTCCTT]GTTACTCCATTTCAG | 17997 |
| rs386984390 | in-del | -/TT | | | intron-variant | Nedd1 | Mm_Celera | 10:92719469 | AAAAAGTGATTACTT[-/TT]TTTTTTAAAGGATAC | 17997 |
| rs386986507 | in-del | -/ATTTAA | | | intron-variant | Nedd1 | Mm_Celera | 10:92687375 | AATGCTTGCAGAAAA[-/ATTTAA]GTCTTCTGAATATTA | 17997 |
| rs386992059 | in-del | -/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92704675 | TGAAGGTTAACACAT[-/T]ATCATTCTGCAAAGG | 17997 |
| rs386993377 | in-del | -/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92709056 | GATTTTAAGGTTTTT[-/T]CTTTTCATTTGAGAA | 17997 |
| rs387015121 | in-del | -/TT | | | intron-variant | Nedd1 | Mm_Celera | 10:92719475 | TGATTACTTTTTTTT[-/TT]AAAGGATACTATTGC | 17997 |
| rs387051893 | in-del | -/CACACA | | | intron-variant | Nedd1 | Mm_Celera | 10:92708457 | ACATATACACACACA[-/CACACA]TACACACACACACAC | 17997 |
| rs387085087 | in-del | -/TCAGAC | | | intron-variant | Nedd1 | Mm_Celera | 10:92689427 | CCACATTCTGAAGAC[-/TCAGAC]AAAGTCTGTGCTGCA | 17997 |
| rs387118962 | in-del | -/ATC | | | intron-variant | Nedd1 | Mm_Celera | 10:92715851 | TGCAGAACCAGACCC[-/ATC]TGCTGCTGCTGCTGC | 17997 |
| rs387119879 | in-del | -/CAAATGG | | | intron-variant | Nedd1 | Mm_Celera | 10:92711659 | GCTCCAAAATGACAG[-/CAAATGG]TAAATGAAGAGTGGC | 17997 |
| rs387126468 | in-del | -/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92699979 | TTTAAAACAAAACTG[-/G]ATTTTTGTTGGTTTG | 17997 |
| rs387147470 | in-del | -/AA | | | intron-variant | Nedd1 | Mm_Celera | 10:92701826 | AGGGCAAAAAAAAAA[-/AA]GTCAAACAAAAGTAA | 17997 |
| rs387192673 | in-del | -/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92695897 | GCTAAAAACCCACGG[-/G]TCTGAGTATCATAAC | 17997 |
| rs387200444 | in-del | -/GGCATA | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92712906 | TCCCTATACAAAATA[-/GGCATA]TCCCTCTAAGCAGTG | 17997 |
| rs387221507 | in-del | -/C | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92709734 | GCCTATGGCCACTGC[-/C]CTTTGGTGCCTTCCA | 17997 |
| rs387237945 | in-del | -/T | | | upstream-variant-2KB | Nedd1 | GRCm38.p3 | 10:92724546 | TCCTTGGTGATGAAT[-/T]AGCAGTATGGAAGTG | 17997 |
| rs387277073 | in-del | -/A | | | utr-variant-3-prime | Nedd1 | Mm_Celera | 10:92685481 | TTGTGAGGGAAAAAA[-/A]TGGCAACAATATTCT | 17997 |
| rs387292234 | in-del | -/A | | | intron-variant | Nedd1 | Mm_Celera | 10:92702561 | ATGGAGTGGGCCTTA[-/A]CGTCCCCTCAGGTAC | 17997 |
| rs387307334 | in-del | -/AAAACAAAAAAACA | | | intron-variant | Nedd1 | Mm_Celera | 10:92718171 | AAAAACAAAAAAACA[-/AAAACAAAAAAACA]TCCTATTAAGAACTG | 17997 |
| rs387308056 | in-del | -/AAATGAATGAATGAATGAATGAAT | | | intron-variant | Nedd1 | Mm_Celera | 10:92715536 | TTAAGTTTACCAAAT[-/AAATGAATGAATGAATGAATGAAT]GAATGAATGAATAAG | 17997 |
| rs387356668 | in-del | -/CAAACAAA | | | intron-variant | Nedd1 | Mm_Celera | 10:92714215 | AAACAAACAAACAAA[-/CAAACAAA]ATTAGCCTAACAGAG | 17997 |
| rs387366122 | in-del | -/CACTAT | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92688268 | AAAACTCTGAAAGAT[-/CACTAT]TCATGCCATCTCTCA | 17997 |
| rs387374447 | in-del | -/TCGA | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92709101 | ACCCCAAGGCATTGA[-/TCGA]GTGTCTTATCTGCCA | 17997 |
| rs387393904 | in-del | -/C | | | intron-variant | Nedd1 | Mm_Celera | 10:92696502 | AACTGAAAGGTGGCC[-/C]GGCAGACCCCACAAG | 17997 |
| rs387437140 | in-del | -/CTAAT | | | intron-variant | Nedd1 | Mm_Celera | 10:92721486 | GCATCATACATATCT[-/CTAAT]GGGTTCCAGAGGACA | 17997 |
| rs387442441 | in-del | -/TTT | | | intron-variant | Nedd1 | Mm_Celera | 10:92720292 | TTCTCATATTTTTTT[-/TTT]AATGTGCTATAATCT | 17997 |
| rs387487712 | in-del | -/C | | | intron-variant | Nedd1 | Mm_Celera | 10:92709735 | CCTATGGCCACTGCC[-/C]TTTGGTGCCTTCCAA | 17997 |
| rs387499328 | in-del | -/GTCTTGAT | | | intron-variant | Nedd1 | Mm_Celera | 10:92708744 | GGAAAGTAATGTAAT[-/GTCTTGAT]CTAATGAATTGTTAA | 17997 |
| rs387510686 | in-del | -/ATGACTACAGAGGTGG | | | intron-variant | Nedd1 | Mm_Celera | 10:92713334 | CAGTCCAACGACGGG[-/ATGACTACAGAGGTGG]TGAGGACACAGATGA | 17997 |
| rs387543050 | in-del | -/ACA | | | intron-variant | Nedd1 | Mm_Celera | 10:92711656 | TCAGCTCCAAAATGA[-/ACA]TAAATGAAGAGTGGC | 17997 |
| rs387544442 | in-del | -/A | | | intron-variant | Nedd1 | Mm_Celera | 10:92690186 | CTTCGACTTTAACAA[-/A]TGGAGAAACGCCTCT | 17997 |
| rs387555263 | in-del | -/GGCTAC | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92708856 | GTCCTACAGAGGTGC[-/GGCTAC]CCAAGGAGGAGGCAG | 17997 |
| rs387574741 | in-del | -/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92689482 | AAGTGACTCTCCACA[-/G]CGTAGTACGAAAAGG | 17997 |
| rs387584995 | in-del | -/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92686654 | ATGGATCATTTTTTT[-/T]CATGGATTCTTTTTC | 17997 |
| rs387590199 | in-del | -/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92712228 | TCTACTCTGAGGGAT[-/T]AAAAAGACTTACAAG | 17997 |
| rs387609733 | in-del | -/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92719417 | ACAAATATTTTTTTT[-/T]ATGGGCCAACAGTTT | 17997 |
| rs387633004 | in-del | -/AC | | | intron-variant | Nedd1 | Mm_Celera | 10:92702696 | AGAACACTAACACAC[-/AC]GCACACACAATTTAG | 17997 |
| rs387633760 | in-del | -/A | | | intron-variant | Nedd1 | Mm_Celera | 10:92702041 | TATCAACTGGAGATA[-/A]TGTCTGGGCTAGAGA | 17997 |
| rs387639657 | in-del | -/GCTGGGG | | | intron-variant | Nedd1 | Mm_Celera | 10:92715789 | CCAGCCTTAAGGAAG[-/GCTGGGG]CACATCCTTGAGTGC | 17997 |
| rs387648268 | in-del | -/G | | | intron-variant | Nedd1 | Mm_Celera | 10:92712676 | AAAGAACTCAGGGCG[-/G]AAAAAAAAAGTCTCA | 17997 |
| rs387654650 | in-del | -/A | | | intron-variant | Nedd1 | Mm_Celera | 10:92714844 | CCTTTATTAAAAAAA[-/A]CTGCTTGCAAAAAGC | 17997 |
| rs387682063 | in-del | -/TGAATGA | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92697129 | GGTCTTCATTTGCTA[-/TGAATGA]ATGAGAGTGGTCATC | 17997 |
| rs387692651 | in-del | -/C | | | intron-variant | Nedd1 | Mm_Celera | 10:92700597 | TGTGGTGACATCCAC[-/C]TGTAATTCCATCATT | 17997 |
| rs387731304 | in-del | -/GG | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92703222 | AACTCACTCAAGATG[-/GG]TTTTTTTTTCTAGTT | 17997 |
| rs387795252 | in-del | -/GTTT | | | upstream-variant-2KB | Nedd1 | GRCm38.p3 | 10:92724157 | TTTGTTTTGTTTTTT[-/GTTT]TGTTTTGTTTTGTTT | 17997 |
| rs387813069 | in-del | -/CACACACACACACACACACATA | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92709353 | ACACACACACACACA[-/CACACACACACACACACACATA]AAGTTATACTTGAGG | 17997 |
| rs387818558 | in-del | -/T | | | intron-variant | Nedd1 | Mm_Celera | 10:92705463 | TAAATCAGTGATTTT[-/T]CAACTTTCCTAATGC | 17997 |
| rs387826061 | in-del | -/TT | | | downstream-variant-500B | Nedd1 | Mm_Celera | 10:92684341 | TTTCACCAATTGATT[-/TT]GTTTTCCACTGCATG | 17997 |
| rs387836977 | in-del | -/CT | | | intron-variant | Nedd1 | Mm_Celera | 10:92688926 | ACATCTTAATATTCT[-/CT]GAGTGAAAAAAATCT | 17997 |
| rs387859063 | in-del | -/GCTAATTTACTAAGCA | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92690978 | GTGAATTTTCGAAAA[-/GCTAATTTACTAAGCA]CTTGTTGACAACAGG | 17997 |
| rs387883467 | in-del | -/A | | | intron-variant | Nedd1 | Mm_Celera | 10:92720803 | AACAGCAACAAAAAA[-/A]GAGTACTATACTACT | 17997 |
| rs387892335 | in-del | -/AGAAAGACTAAAATCCTAGT | | | intron-variant | Nedd1 | Mm_Celera | 10:92710905 | GTATCAGAAATGCAT[-/AGAAAGACTAAAATCCTAGT]TTTAGAATTGTGCTA | 17997 |
| rs578388883 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92708474 | ACACACACACACACA[C/T]ACACGCATAATCACT | 17997 |
| rs578405096 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92716010 | TGCTCTCCTAAATCA[C/T]TATAATCTCACCTAT | 17997 |
| rs578433233 | snp | A/C | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92695954 | CAGCCTGGCAGTGAC[A/C]CAGCTGGAAGGGAGG | 17997 |
| rs578810127 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92718749 | TGGATCAGCACAACT[A/G]GGAGTTACAGGCTCT | 17997 |
| rs578975738 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92701833 | AAAAAAAAAGTCAAA[C/T]AAAAGTAAAAGTAAA | 17997 |
| rs579097365 | snp | C/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92710683 | TTCCATAAAGATTTC[C/G]ATACTAACCTGAAAA | 17997 |
| rs579218608 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92705635 | CTGCTTTAAATGTTA[A/G]TCCTTTGCTGATTTT | 17997 |
| rs579571421 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | GRCm38.p3 | 10:92722878 | TCTGTCTTGAACAAA[A/C]CAAAACAGAAGAATA | 17997 |
| rs579982603 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | GRCm38.p3 | 10:92723585 | TCCTTTGTCCCAGGT[A/G]CACACCGGATGTGTT | 17997 |
| rs580111911 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92710404 | AGCACCACACGGGAG[A/G]GCAGACGGGTAAGAA | 17997 |
| rs580120470 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92700073 | GTATAGCCCTGGCTG[C/T]CCTGGAACTCACTCT | 17997 |
| rs580217868 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92721312 | GGATTAAAGGTGTGC[A/G]CCACCACGCCCTACT | 17997 |
| rs580581156 | snp | A/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92712220 | GCACAGCATCTACTC[A/T]GAGGGATTAAAAAGA | 17997 |
| rs580675941 | snp | A/G | | | downstream-variant-500B | Nedd1 | GRCm38.p3 | 10:92684434 | AAACTGAGGTCACTA[A/G]TTTTAGGGGTCTTTC | 17997 |
| rs580892761 | snp | A/C | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92700693 | TTTGCTAGGTACGGT[A/C]CTGTCTCATGACAAT | 17997 |
| rs580954257 | snp | A/T | | | utr-variant-3-prime | Nedd1 | GRCm38.p3 | 10:92685577 | GATTTTGCACATAGT[A/T]AATTCATTAGACAAT | 17997 |
| rs581067721 | snp | G/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92701758 | CACTTGATTGTACAT[G/T]CAAGAACCCCACAAA | 17997 |
| rs581240915 | snp | A/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92702546 | GTCTGACCCTTTCTC[A/T]TGGAGTGGGCCTTAA | 17997 |
| rs581298415 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92716850 | TCAGTTAATCTTAAA[A/G]CTTTTATTTTACTCT | 17997 |
| rs581857193 | snp | A/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92696557 | CGGCAATGGTGAGGC[A/T]GAGGTGGTAAAGGGA | 17997 |
| rs582766126 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92694807 | TAAGTGGCTCCCCTT[C/T]TGACAGGGGCGGGGA | 17997 |
| rs582790399 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92708433 | CATGCATGCATTCGC[A/G]CACACACACACATAT | 17997 |
| rs582998030 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | GRCm38.p3 | 10:92723567 | TCCTATGGAAAGTGT[C/T]GCTCCTTTGTCCCAG | 17997 |
| rs583227802 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92712328 | AGTTACAAGGGTGGC[A/G]TTTTTGTTTTGTTTT | 17997 |
| rs583238669 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92701347 | CCTACAGCCCTTAGG[C/T]TCTGGGATGCATTGT | 17997 |
| rs583430706 | snp | G/T | | | upstream-variant-2KB | Nedd1 | GRCm38.p3 | 10:92724130 | AACAAAAGTTGTTTT[G/T]TTTTGTTTTGTTTTG | 17997 |
| rs584009673 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92711694 | AGGGAACACAAGGAG[A/G]AAACAGACATCACTG | 17997 |
| rs584361237 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92716851 | CAGTTAATCTTAAAA[C/T]TTTTATTTTACTCTA | 17997 |
| rs584533910 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92701808 | ATACACATGCAAAAT[C/T]TGTAGGGCAAAAAAA | 17997 |
| rs584699732 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92689435 | CTGAAGACAAAGTCT[A/G]TGCTGCACACTAGAT | 17997 |
| rs585033555 | snp | C/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92712658 | AGGGATAAGAGCGTA[C/G]ATAAAGAACTCAGGG | 17997 |
| rs585202687 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92700584 | GCACATAATGTAGGT[A/G]TGGTGACATCCACTG | 17997 |
| rs585298869 | snp | G/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92705448 | AAGAAAGGAATGTTT[G/T]AAATCAGTGATTTTT | 17997 |
| rs585592810 | snp | A/C | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92710394 | AACAGACTTTAGCAC[A/C]ACACGGGAGGGCAGA | 17997 |
| rs585666851 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92708441 | CATTCGCACACACAC[A/G]CACATATACACACAC | 17997 |
| rs585807788 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92699685 | AATGACCTTAGCATA[A/G]GATCTATAAATTATT | 17997 |
| rs585924669 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92698438 | ATATTTTATAAGTGC[C/T]GCACAAAATTAAAAA | 17997 |
| rs586194616 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime | Nedd1 | GRCm38.p3 | 10:92723577 | AGTGTTGCTCCTTTG[G/T]CCCAGGTGCACACCG | 17997 |
| rs586212732 | snp | G/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92721275 | ACTCAGAAATCCGCC[G/T]GCCTCTGCCTCCCGA | 17997 |
| rs586318170 | snp | A/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92695902 | AAAACCCACGGTCTG[A/T]GTATCATAACCCTGA | 17997 |
| rs586402705 | snp | A/G | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92712008 | TGCTCCCACTGGGGC[A/G]TCACACACTAACTAG | 17997 |
| rs586594505 | snp | A/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92701470 | GCTAAACCTCCTGTC[A/T]GCCTGAAGGCAGCAC | 17997 |
| rs586837389 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92712335 | AGGGTGGCATTTTTG[C/T]TTTGTTTTTTTAACA | 17997 |
| rs587296910 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92712688 | GCGGAAAAAAAAAGT[C/T]TCATGGATGGGGAAA | 17997 |
| rs587337910 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92700689 | CGCCTTTGCTAGGTA[C/T]GGTCCTGTCTCATGA | 17997 |
| rs587440871 | snp | C/T | | | upstream-variant-2KB | Nedd1 | GRCm38.p3 | 10:92724581 | CCGAATAAACCCTTT[C/T]CTCCCCAACTTGCTT | 17997 |
| rs864286043 | snp | A/T | | | utr-variant-3-prime | Nedd1 | GRCm38.p3 | 10:92684772 | GTGAAAATTTATTGT[A/T]CTCAGTGCTTAAATC | 17997 |
| rs864308936 | in-del | -/A | | | utr-variant-3-prime | Nedd1 | GRCm38.p3 | 10:92684857 | TATATACACCTATAG[-/A]AAAAAAGGAAATAGG | 17997 |
| rs864311900 | snp | C/T | | | intron-variant | Nedd1 | GRCm38.p3 | 10:92708442 | ATTCGCACACACACA[C/T]ACATATACACACACA | 17997 |