SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs27386937 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91265050 | CGGGTCCAGCAGGAA[C/T]TCGTGAGGAAGTTTG | 80708 |
rs27386938 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91264826 | CAATCTGGACTGGAA[A/G]GGACTTGGTGATCAA | 80708 |
rs27386939 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, utr-variant-3-prime | Arfgap2, Pacsin3 | Mm_Celera | 2:91264494 | GGAATGATGGAGGGT[C/T]GAGAGGTGCCCGAGC | 80708 |
rs27386940 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, synonymous-codon | Arfgap2, Pacsin3 | Mm_Celera | 2:91264300 | CGTAGAATGTGTGGG[C/T]GCCTGAGTGCCCTGA | 80708 |
rs27386941 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263956 | GAGCAGGGCTGTAGA[C/T]GAAGAAAGCCAGGGA | 80708 |
rs29575679 | snp | A/C | 0.5 | 0 | intron-variant | Pacsin3 | GRCm38.p3 | 2:91261443 | CTCAGAGGAGGCAGG[A/C]ACTTTCCAGGTCTAC | 80708 |
rs29672443 | snp | C/T | 0.5 | 0 | intron-variant | Pacsin3 | GRCm38.p3 | 2:91261429 | CCGGAGCAGTGCTTC[C/T]CAGAGGAGGCAGGAA | 80708 |
rs33614421 | snp | C/T | 0.5 | 0 | intron-variant | Pacsin3 | GRCm38.p3 | 2:91261446 | AGAGGAGGCAGGAAC[C/T]TTCCAGGTCTACGCG | 80708 |
rs45711965 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91256638 | TCTGGTAGCCTCGCT[A/G]CACCTCCTTAGACTA | 80708 |
rs46747206 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260814 | GGGTAGGAAGATCCT[A/G]GGCATTACAGAGCTT | 80708 |
rs47500845 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91256970 | GCACGGCGGCGGCAT[C/G]GTGGCTCTAGCTTGC | 80708 |
rs48389341 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261008 | GATCGCTCATGTCAG[A/G]GCAGAGTAGGGAATT | 80708 |
rs49753924 | snp | C/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260780 | GAAAAGCTAAATGTG[C/G]AGTGTAGGTCTTTTA | 80708 |
rs49989284 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260645 | GAGGCTTTGTGGGGC[C/T]TGGGGATGGAATTTA | 80708 |
rs50604399 | snp | C/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260703 | AGCTATCTTCCTACT[C/G]CACCTGTTTTCTAGA | 80708 |
rs212269701 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91256996 | CTTGCTCTTTGGTCC[C/T]TCGACTCCTGAAGTT | 80708 |
rs212347482 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91259826 | GGACACTGGAAGCTC[C/T]CAATCTTTACTCCCT | 80708 |
rs212741769 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258487 | CTCAAGAGGAAACAA[A/G]GTGGAGAGCTAGTGG | 80708 |
rs212743967 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91264721 | TGCTGGTGGGAGGCA[C/G]GGGGTCGGCCCGTGG | 80708 |
rs212808125 | snp | C/T | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263679 | CTCCTCCCTGCCCGC[C/T]GCCAAGCAGCCAAGC | 80708 |
rs212920675 | in-del | -/AC | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91255658 | TCTACTGAGCAAAGA[-/AC]ACACGTCAGTGATTC | 80708 |
rs213070650 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261846 | CCTGGATTACATAGA[A/G]GCTACTAGCCCTGTC | 80708 |
rs213318817 | snp | A/C | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91254869 | CTGGGATTCTGAGCC[A/C]GTGTCTGTTTCCTTT | 80708 |
rs213337318 | snp | C/T | | | synonymous-codon | Pacsin3 | Mm_Celera | 2:91261211 | GGCCTGGCATGCCTT[C/T]TTCACTGCGGCTGAG | 80708 |
rs213455899 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91256625 | AAGCTCACAGCTCTC[C/T]GGTAGCCTCGCTGCA | 80708 |
rs214645508 | in-del | -/TA | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262343 | TTTTATTTTTTTATT[-/TA]TTTATTTTATTTTTT | 80708 |
rs214656892 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260040 | TAGCCTTCTGCTGCT[C/T]GGCCATTCCTCCGGT | 80708 |
rs214721751 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258619 | AAGTCAGCTTAGACC[A/G]GGCTTTTCTCAGGGC | 80708 |
rs215239071 | snp | C/T | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263498 | TTCTTCCTGCTTTCC[C/T]ATCACATCAGTGCCC | 80708 |
rs215299242 | snp | G/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261973 | TGAGGAGATAGCTTG[G/T]TTGGTGAAGTGCTGG | 80708 |
rs215596045 | snp | C/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258216 | TGAAGCCGGGGTGCC[C/G]GGCCTGCCTGTGCCT | 80708 |
rs215643602 | snp | A/G | | | intron-variant, upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91256943 | TGAGTGCTTTGGAGG[A/G]GGAGCTGGGGGGCAC | 80708 |
rs217934027 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262410 | TGGAGACTTAGTTAC[C/T]TGGAATCGGTTCTCA | 80708 |
rs217999114 | snp | C/T | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263575 | CCATGGTCCGGTGTC[C/T]CTCGAAGTTTGGCTG | 80708 |
rs218336779 | snp | A/C | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260296 | GTCCGGAGTGGCAGC[A/C]AACTGTCCCTTTCTT | 80708 |
rs218353658 | snp | C/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261497 | GGATTCTGAGTTGTT[C/G]TCATGGTCGTTAGGT | 80708 |
rs218467821 | snp | G/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262495 | TTCTGAGGGGTGGCA[G/T]TTCTATAACACCTCC | 80708 |
rs218500800 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261124 | GGGGAGGGGAAGGTC[A/G]TATTTAAGTTAGCAA | 80708 |
rs218758519 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Pacsin3, Gm31054 | Mm_Celera | 2:91254349 | ACACCCTATTGCTCC[C/T]GCCTAGAATACCTCT | 80708 |
rs219776060 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91265033 | GCGGTACGTAGGGTA[C/G]CCGGGTCCAGCAGGA | 80708 |
rs220065905 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91256116 | AGAGGCTGGGGGTGG[A/G]GCAGTGAAGAAGGGA | 80708 |
rs220086687 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91259036 | ACCTAACTGTCCCAA[C/T]GGCCTTGGGCTATCT | 80708 |
rs220195378 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91257168 | CTCTCAGGGTGCCTA[A/G]AGGGTCCCCAACTGC | 80708 |
rs220400989 | in-del | -/A | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91255724 | TTAAAGTTGTCTTTT[-/A]AAAAAATCCGCGCGC | 80708 |
rs220434753 | snp | C/T | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263897 | AGCAGGTATGCTGGG[C/T]CCTTTCATGGTCCTT | 80708 |
rs220476565 | snp | C/T | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91255922 | CCAGAGGCCTGGGAC[C/T]CCGCTGGCCCGCGTT | 80708 |
rs220489090 | snp | G/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262707 | CTATGCTCAGAGAAT[G/T]CTGGTGCGGGCCTGA | 80708 |
rs220813762 | in-del | -/TGTGGTAGGA | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258091 | TCTCTGACCTCTTGC[-/TGTGGTAGGA]TGTGTTCACTCAGAT | 80708 |
rs221725337 | snp | G/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260345 | TCCAGGAGTAGCCTA[G/T]CTATCAGCCCCAGCT | 80708 |
rs222207037 | in-del | -/AACA | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261911 | ATGAGACCCTGTCTC[-/AACA]AACAAACAAACAAAC | 80708 |
rs222234784 | snp | A/G | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91255681 | CAGTGATTCCTTCCA[A/G]ATTTAGAAACAACAC | 80708 |
rs224015642 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260916 | TGTTTGTTTTGCTTT[A/G]TTGTTGTTTATTTTT | 80708 |
rs224188181 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91264756 | GCCATGTGTTATGGA[A/G]CTGGGATTGGGCAGG | 80708 |
rs225147656 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91265100 | GCCCGCTCGGGCTGC[A/G]GATTGGCCAGGCGCA | 80708 |
rs225334036 | in-del | -/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258507 | GAGCTAGTGGAACTT[-/G]GGGGGGCAGTTTGTT | 80708 |
rs225670071 | snp | G/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261453 | GCAGGCACCTTCCAG[G/T]TCTACGCGGGACCAG | 80708 |
rs225800654 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261886 | TTTCAGGCCAACAAA[A/G]GCTACTGTAATGAGA | 80708 |
rs225801483 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258912 | GGGAGCCCTGAGGAA[A/G]ACAGAGTCAAATTTG | 80708 |
rs225948635 | snp | A/T | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263484 | TTGCTTGTTACCACT[A/T]CTTCCTGCTTTCCTA | 80708 |
rs225963942 | in-del | -/CCT | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262506 | GGCAGTTCTATAACA[-/CCT]CCTCCTCCAGGGAGC | 80708 |
rs226082925 | snp | A/G | | | upstream-variant-2KB, synonymous-codon | Arfgap2, Pacsin3 | Mm_Celera | 2:91264204 | AGGGGAAGAGTTGCT[A/G]AAGATGAGCGAGGAG | 80708 |
rs226314423 | snp | A/T | | | intron-variant, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91257533 | TGTGATTTGGTGTGG[A/T]GGTTAGGAGTGCGTC | 80708 |
rs226348857 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91257985 | AGTTCAGCACTAGCG[A/G]CTGGGAAGAGACCCT | 80708 |
rs226473863 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91259354 | GCAAGTGTCTCCTTA[C/T]AAATGACGGGTCTTT | 80708 |
rs226819118 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91264942 | TATGAGCACTTGGGA[A/G]ATTGTTAATCATTAC | 80708 |
rs227051041 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261020 | CAGAGCAGAGTAGGG[A/G]ATTCTAACACAGGAC | 80708 |
rs227133769 | in-del | -/AACAAACAAACAAACA | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261910 | ATGAGACCCTGTCTC[-/AACAAACAAACAAACA]AACAAACAAACAAAC | 80708 |
rs227163495 | snp | A/G | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263984 | GGACTCCATCCTCAC[A/G]GGCTGCTCAGGGTCC | 80708 |
rs227172360 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261685 | CAGTCCCCTGGCAGA[A/G]CTTCCTGGATGCCTT | 80708 |
rs227417813 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Pacsin3, Gm31054 | Mm_Celera | 2:91254166 | CCACAGCTTTATCTC[C/T]TCAGCAACTGTGGGC | 80708 |
rs227475955 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91257766 | CAGGCTGACTGGGAG[A/G]GGCTGCTGGGGAAGC | 80708 |
rs227546791 | snp | A/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91256398 | AGATCTTGGGCAGAT[A/T]ACCGCTGAAGGTATC | 80708 |
rs227596008 | in-del | -/CA | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263606 | TATAACAGTCCTGTG[-/CA]CAGAGATAGACCTGT | 80708 |
rs228032713 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91256552 | CCTAATGATTAGTGT[A/G]CAAGTTCCCGCTCAT | 80708 |
rs228334090 | snp | G/T | | | utr-variant-5-prime, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91265147 | CAGGCCCGTGGTGGA[G/T]CTCCCGGCTGCTAAC | 80708 |
rs229669404 | snp | A/C | | | intron-variant, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91259865 | TTGTTAACATCAAGA[A/C]AGGCTCATAGTGGCA | 80708 |
rs230560074 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260391 | AAAGCCATCTCTCTT[C/T]TCTGTGTTCCAGGCT | 80708 |
rs231205978 | snp | A/C | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263745 | GCCCTGAGTTGTGCC[A/C]CTTGTGTTCCCCTCT | 80708 |
rs231331642 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91264727 | TGGGAGGCACGGGGT[A/C]GGCCCGTGGGCGTGC | 80708 |
rs231866734 | snp | C/G | | | synonymous-codon | Pacsin3 | Mm_Celera | 2:91261220 | TGCCTTCTTCACTGC[C/G]GCTGAGAGGCTGAGC | 80708 |
rs232428420 | snp | C/T | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91255011 | CCAGATGTTTTCCAC[C/T]GCACATCCTTTCCTC | 80708 |
rs232480055 | snp | A/C | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263520 | TCAGTGCCCGACGGC[A/C]ATCTTGGGAGAGTTA | 80708 |
rs232788485 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91259632 | TTGTCATCCAAGGGG[C/T]CTAGCTAGGCAAGAG | 80708 |
rs233003897 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258797 | ATTCTAGTGCCCGGG[A/G]GTAACGTGAACCAAA | 80708 |
rs233123813 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260130 | TCCTAGTCCCCAAAC[A/G]GCAGGTCTCACTTTT | 80708 |
rs233149135 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | Arfgap2, Pacsin3 | Mm_Celera | 2:91264410 | TGTGCTGCTGCTGTC[C/T]CTCTTTTCCCACAGG | 80708 |
rs233591468 | in-del | -/GTTC | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91254801 | GTAATTAAGGGGTCT[-/GTTC]GTTCCTAGGGCACAG | 80708 |
rs233714811 | snp | A/C | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258430 | TTACTGCTCCCCACC[A/C]CCCTATCTGGCTGGC | 80708 |
rs233839913 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | Arfgap2, Pacsin3 | Mm_Celera | 2:91264438 | AGGAGGAAGTCTCAG[A/G]GCCCATGAAGGGCAG | 80708 |
rs233871125 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262025 | AAGGCAGCTGGAGTG[A/G]TAAAGGGGAGTTGTC | 80708 |
rs234161876 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261796 | TCTGCACTCAGGAAG[C/T]AGAGGCAGGTGGATT | 80708 |
rs234439375 | snp | A/G | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91254530 | GTCCCAAAACCTGGG[A/G]TAGGGTTTAGCATAA | 80708 |
rs235025869 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91264979 | ATCACAGAGTCTGTT[A/G]CCATGGCTCTCTGCC | 80708 |
rs235227209 | in-del | -/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258532 | TTTGTTCTGTGTCTA[-/G]GGATCTTCGTTGACT | 80708 |
rs235255050 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262975 | GAGAGAGGCTCCCCT[A/G]ACCTCCTCTGGGTTC | 80708 |
rs235633579 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258521 | TTGGGGGGCAGTTTG[C/T]TCTGTGTCTAGGGAT | 80708 |
rs235780332 | in-del | -/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262353 | TTTATTTTTATTTTA[-/T]TTTTTTTTACCCAAG | 80708 |
rs237195904 | snp | A/C | | | synonymous-codon | Pacsin3 | Mm_Celera | 2:91261645 | GGAGCGGGTGGGCCG[A/C]TGCACCAAGGAGGCA | 80708 |
rs237343741 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262574 | ACCCTGTCTTGCACT[C/T]CATCCAGATTCTTCT | 80708 |
rs237485076 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91257035 | GACGGACTCCCGCGC[C/T]GGAGACCCCGGCCAT | 80708 |
rs238084255 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91259129 | CCTTGCCTGGAGGCA[A/G]GAGGCTGCATGTCAC | 80708 |
rs239258423 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91257299 | CGCCCCTTCCCCGCT[A/G]CAGTAACCAGCTGGC | 80708 |
rs239321864 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Pacsin3 | Mm_Celera | 2:91256225 | AGATATGTTGAGATA[C/G]AAAATCTGAAACCGT | 80708 |
rs239865255 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91256969 | GGCACGGCGGCGGCA[C/T]GGTGGCTCTAGCTTG | 80708 |
rs240206981 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262450 | CTCTGTCGCCTGCCC[A/G]GAGTGTCCTTCTCTC | 80708 |
rs240279866 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91259424 | TAGCATGGACACTGA[C/T]CAGGTGGGGGAATTT | 80708 |
rs240341856 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260305 | GGCAGCAAACTGTCC[C/T]TTTCTTGATGGGCTC | 80708 |
rs240512051 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91264904 | GCTGAGCTGGAGCCC[C/T]GCCAATGCCTTCCGG | 80708 |
rs241555783 | snp | A/G | | | missense | Pacsin3 | Mm_Celera | 2:91263090 | CGAGACCTGCAGCAG[A/G]GCATTGAGGCTGCCA | 80708 |
rs242266159 | snp | A/G | | | utr-variant-5-prime, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91265160 | GAGCTCCCGGCTGCT[A/G]ACGTCATGTTTCAGC | 80708 |
rs242359780 | snp | A/G | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91255791 | GGGTTGGAAATGTGC[A/G]TGCTGGATAGAGAGC | 80708 |
rs242374188 | snp | G/T | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91255929 | CCTGGGACCCCGCTG[G/T]CCCGCGTTCCCTCCT | 80708 |
rs242854939 | snp | A/C | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263580 | GTCCGGTGTCTCTCG[A/C]AGTTTGGCTGTATAA | 80708 |
rs243251755 | snp | A/C | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261140 | TATTTAAGTTAGCAA[A/C]CCCGCCTGGCCCAAG | 80708 |
rs243952786 | in-del | -/TGG | | | intron-variant | Pacsin3 | Mm_Celera | 2:91257821 | GACACAGGACTGGGC[-/TGG]GCAGGATAGCTTTGC | 80708 |
rs244157878 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260935 | TTGTTTATTTTTGCC[C/T]GGTCCACGTTAGCAA | 80708 |
rs244217438 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260003 | CATCTTTGCCTTTCT[C/T]CTGGCTCCTCCTGGG | 80708 |
rs244336811 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91264732 | GGCACGGGGTCGGCC[C/T]GTGGGCGTGCCATGT | 80708 |
rs244545822 | snp | A/G | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91264028 | CAGTTGCCTCCCTGG[A/G]GTCTAAGGTTGGGTG | 80708 |
rs244898169 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91257905 | ATGTGTAAGAAAGGA[A/G]CAAGGCAGAAACCTT | 80708 |
rs245799237 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261964 | ACTTGGGCCTGAGGA[A/G]ATAGCTTGGTTGGTG | 80708 |
rs245916733 | snp | A/T | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263493 | ACCACTTCTTCCTGC[A/T]TTCCTATCACATCAG | 80708 |
rs245979659 | snp | C/T | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263935 | CAGCCCCCGTCCTAC[C/T]TGCTAGAGCAGGGCT | 80708 |
rs246113775 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260291 | ACTGGGTCCGGAGTG[A/G]CAGCAAACTGTCCCT | 80708 |
rs246166420 | snp | C/G | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91256914 | ACCCACCGAGGGCCC[C/G]TGAGAGGACACGGTG | 80708 |
rs246230875 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261108 | ACTCAGAGCAGTATG[C/T]GGGGAGGGGAAGGTC | 80708 |
rs246289785 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258199 | CCACCCCAAGAGCTC[A/G]ATGAAGCCGGGGTGC | 80708 |
rs247401385 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91257675 | TCCTTCCAAAAGACT[A/G]TGCCAGTCTCTTGAT | 80708 |
rs248164287 | snp | G/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260876 | ACAAGTTAACCTGAC[G/T]TCTCTAGGTTTAGTT | 80708 |
rs249302669 | snp | A/C | | | synonymous-codon | Pacsin3 | Mm_Celera | 2:91261184 | AGGCCCACAGTACGG[A/C]ACCCTGGAGAAGGCC | 80708 |
rs249591456 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262726 | GTGCGGGCCTGAGTG[A/G]AAGGCAGTCTGTCCT | 80708 |
rs249643913 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91256574 | CCCGCTCATTCCCAC[A/C]GGCCTCCTAGTCTCT | 80708 |
rs249841336 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91257162 | AATCATCTCTCAGGG[C/T]GCCTAGAGGGTCCCC | 80708 |
rs249980933 | snp | A/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258598 | CCTCCTGCCAGCAGA[A/T]GTAGGAAGTCAGCTT | 80708 |
rs250166393 | snp | C/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262660 | GGTAGGAAGTGAGTT[C/G]CAGGTCTGACTGCTT | 80708 |
rs250295577 | snp | A/T | | | upstream-variant-2KB, synonymous-codon | Arfgap2, Pacsin3 | Mm_Celera | 2:91263813 | GAGTCCCCGGAAAGT[A/T]GCCACTGGGGTGAGG | 80708 |
rs250426334 | snp | A/G | | | utr-variant-5-prime, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91265120 | GGCCAGGCGCAGCGC[A/G]GCGTTCACTCTCAGG | 80708 |
rs250851603 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91264997 | ATGGCTCTCTGCCTG[A/C]CGCCTACAGCCAGTG | 80708 |
rs250899571 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261461 | CTTCCAGGTCTACGC[A/G]GGACCAGGGTGTGGC | 80708 |
rs251170905 | snp | A/G | | | synonymous-codon | Pacsin3 | Mm_Celera | 2:91261373 | GGATGGTTTCCGTAA[A/G]GCTCAGAAGCCCTGG | 80708 |
rs251221862 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260619 | GGGTGGGACCCTCAG[A/G]GCAGCTTCCTGAGGC | 80708 |
rs251459425 | snp | A/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258959 | TAGAGGTTTCCCAGT[A/T]TAGAGAGCACTGTGT | 80708 |
rs252005481 | snp | A/G | | | intron-variant, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91257329 | CCCCACCTCCCCACC[A/G]AGACCAAGTTCAACA | 80708 |
rs252129672 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258886 | GTGGGACTGAGAGCA[C/T]AGGGGCTATAGGGAG | 80708 |
rs252906608 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261813 | GAGGCAGGTGGATTT[C/T]TATAGGTTCAAGGCC | 80708 |
rs253193121 | snp | C/T | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91255335 | CCAGTGGTAGGTCAG[C/T]TGGGTTACCTGTCAG | 80708 |
rs253566368 | snp | C/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261733 | TCCTGCTCTACTCCC[C/G]GATGCCACTGGAACT | 80708 |
rs253814206 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Pacsin3, Gm31054 | Mm_Celera | 2:91254175 | TATCTCTTCAGCAAC[C/T]GTGGGCATTTGCACC | 80708 |
rs253894607 | snp | C/T | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91254726 | TTTGGCCCTCTGGGC[C/T]TGGGCATTTCATTTT | 80708 |
rs253995528 | snp | G/T | | | upstream-variant-2KB, utr-variant-3-prime | Arfgap2, Pacsin3 | Mm_Celera | 2:91264415 | TGCTGCTGTCTCTCT[G/T]TTCCCACAGGAGGAA | 80708 |
rs254051432 | in-del | -/A | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262333 | CATTTTTTACTTTTT[-/A]TTTTTTTATTTTTAT | 80708 |
rs255044006 | snp | A/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258434 | TGCTCCCCACCACCC[A/T]ATCTGGCTGGCAAGC | 80708 |
rs255315628 | in-del | -/AA | | | upstream-variant-2KB, downstream-variant-500B | Pacsin3, Gm31054 | Mm_Celera | 2:91254109 | ATGAAATGTTTAATT[-/AA]AAAAAAAAATGTTTC | 80708 |
rs255381046 | snp | A/G | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263582 | CCGGTGTCTCTCGAA[A/G]TTTGGCTGTATAACA | 80708 |
rs256688494 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261671 | AGGCAGAGAAGGTAC[A/G]GTCCCCTGGCAGAAC | 80708 |
rs256858120 | in-del | -/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258331 | GAGAAGGAACGGGTT[-/G]GGGGGCAGCTCTCCT | 80708 |
rs256896386 | snp | A/G | | | upstream-variant-2KB, synonymous-codon | Arfgap2, Pacsin3 | Mm_Celera | 2:91263295 | TCCACAGGAATGGTC[A/G]TTAGACACACAGAGA | 80708 |
rs257026860 | snp | C/T | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91264047 | TAAGGTTGGGTGGCT[C/T]TTCCTGGCTGTGTCC | 80708 |
rs257149735 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Pacsin3 | Mm_Celera | 2:91256331 | GCTAAAGCTGCAAGC[A/G]GAGCTGCTCTAGGTA | 80708 |
rs257216787 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | Pacsin3, Gm31054 | Mm_Celera | 2:91254120 | AATTAAAAAAAAAAA[A/T]GTTTCCCCTGTTCTG | 80708 |
rs257281423 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91257907 | GTGTAAGAAAGGAAC[A/G]AGGCAGAAACCTTTG | 80708 |
rs257417127 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91259277 | TTGAAGGCAGAATGG[A/G]ATTGTTACCTTAGGA | 80708 |
rs258184434 | snp | A/G | | | upstream-variant-2KB, intron-variant | Arfgap2, Pacsin3 | Mm_Celera | 2:91263544 | AGAGTTAATTTCACC[A/G]AGGTTTAGATTTGCT | 80708 |
rs259221412 | snp | A/C | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91256429 | TCTAACCCTCATTCA[A/C]GGTTACAAGGAGTGG | 80708 |
rs259253394 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91265054 | TCCAGCAGGAACTCG[C/T]GAGGAAGTTTGGGCC | 80708 |
rs259317625 | snp | A/C | | | upstream-variant-2KB, utr-variant-3-prime | Arfgap2, Pacsin3 | Mm_Celera | 2:91264320 | GAGTGCCCTGACAGC[A/C]CTACCAAGGCGTCTC | 80708 |
rs259478377 | snp | A/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262358 | TTTTATTTTATTTTT[A/T]TTTACCCAAGAGAGA | 80708 |
rs259786124 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91259677 | AAAGTAGGAGTGTGG[A/G]GCTTTCTGCCCACCA | 80708 |
rs259935297 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91264929 | TTCCGGATGGGGCTA[G/T]GAGCACTTGGGAGAT | 80708 |
rs260675399 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262480 | CTAGCATTTCATCCT[C/T]TCTGAGGGGTGGCAG | 80708 |
rs260837124 | snp | C/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91258966 | TTCCCAGTTTAGAGA[C/G]CACTGTGTCAGAGTC | 80708 |
rs260950803 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260326 | TGATGGGCTCAGCCA[C/T]CTGTCCAGGAGTAGC | 80708 |
rs261098370 | snp | A/T | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91255799 | AATGTGCGTGCTGGA[A/T]AGAGAGCAGCTAGGC | 80708 |
rs261348710 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261488 | TGGCGGCTAGGATTC[C/T]GAGTTGTTCTCATGG | 80708 |
rs263080048 | in-del | -/T | | | upstream-variant-2KB, downstream-variant-500B | Pacsin3, Gm31054 | Mm_Celera | 2:91254204 | CCTCATTCTCTTGGA[-/T]TTTTGAATAGTGCTA | 80708 |
rs263654538 | in-del | -/ACACACACACACACAC | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262158 | GACATTCTGCCTCCA[-/ACACACACACACACAC]ACACACACACACACA | 80708 |
rs264223053 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262949 | GTAGCGACAAGTATG[A/G]CGGCGCGCTGGAGAG | 80708 |
rs264358847 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Pacsin3 | Mm_Celera | 2:91256482 | GTAGCTAACCTCTAA[C/T]TTTCTAGGTGCTCTC | 80708 |
rs264370215 | in-del | -/TGTT | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91254800 | TGTAATTAAGGGGTC[-/TGTT]CGTTCCTAGGGCACA | 80708 |
rs264459216 | snp | A/C | | | utr-variant-5-prime, downstream-variant-500B | Arfgap2, Pacsin3 | Mm_Celera | 2:91265138 | GTTCACTCTCAGGCC[A/C]GTGGTGGAGCTCCCG | 80708 |
rs264484156 | snp | C/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91260902 | TAGTTTTTTGTTGTT[C/G]TTTGTTTTGCTTTGT | 80708 |
rs265125337 | snp | C/T | | | upstream-variant-2KB | Pacsin3 | Mm_Celera | 2:91255970 | TCAGGGGCACCGCTG[C/T]GGGGTCACCCGGCTC | 80708 |
rs265661695 | snp | A/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91259491 | AAGGCACAGTTGTCC[A/T]AAAACTTCCTGGTCA | 80708 |
rs265994169 | snp | C/T | | | intron-variant | Pacsin3 | Mm_Celera | 2:91261736 | TGCTCTACTCCCGGA[C/T]GCCACTGGAACTTGG | 80708 |
rs266090931 | in-del | -/TTT | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Pacsin3 | Mm_Celera | 2:91256265 | GGGGAGGAGTTCGTG[-/TTT]TTTTTTTGTCCCACT | 80708 |
rs266138701 | snp | A/G | | | intron-variant | Pacsin3 | Mm_Celera | 2:91257689 | TGTGCCAGTCTCTTG[A/G]TTTTAAGCGCCCCTC | 80708 |
rs266172930 | snp | C/G | | | upstream-variant-2KB, utr-variant-3-prime | Arfgap2, Pacsin3 | Mm_Celera | 2:91264437 | CAGGAGGAAGTCTCA[C/G]GGCCCATGAAGGGCA | 80708 |
rs387824025 | in-del | -/ACACACACACACAC | | | intron-variant | Pacsin3 | Mm_Celera | 2:91262158 | GACATTCTGCCTCCA[-/ACACACACACACAC]ACACACACACACACA | 80708 |
rs579411579 | snp | A/G | | | intron-variant | Pacsin3 | GRCm38.p3 | 2:91259208 | AGAGAGAGAGAGAGA[A/G]AGAGAGAGAGAGAGA | 80708 |
rs581728366 | snp | A/T | | | intron-variant | Pacsin3 | GRCm38.p3 | 2:91262337 | TTTTACTTTTTATTT[A/T]TTTATTTTTATTTTA | 80708 |
rs582569862 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | Pacsin3, Gm31054 | GRCm38.p3 | 2:91254191 | GTGGGCATTTGCACC[G/T]CATTCTCTTGGATTT | 80708 |
rs586358228 | snp | C/G | | | upstream-variant-2KB | Pacsin3 | GRCm38.p3 | 2:91254786 | CTGTCCATGCACTGT[C/G]TAATTAAGGGGTCTG | 80708 |