SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8157407 | snp | G/T | 0.438594 | 0.164111 | downstream-variant-500B, utr-variant-3-prime | Arhgap10 | Rn_Celera | 19:34402648 | GCAGGTGTGTGGACA[G/T]CGAGGTCGCCAATGA | 688429 |
rs13452939 | snp | A/G | | | intron-variant | Arhgap10 | Rn_Celera | 19:34230779 | GTTTCCCAGTCAAAC[A/G]GTTAACACCGATCTG | 688429 |
rs13452940 | snp | C/T | | | intron-variant | Arhgap10 | Rn_Celera | 19:34230918 | CAGGTTCGGGAACTC[C/T]TCTCCCATGTATATA | 688429 |
rs13452941 | snp | C/T | | | intron-variant | Arhgap10 | Rn_Celera | 19:34231134 | GTGGCACACGCTTCC[C/T]GAGTGGAGACAGCCA | 688429 |
rs64175459 | snp | G/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34352070 | ACAATTTTTGTCATA[G/T]ATGAACAAATGACAT | 688429 |
rs64292377 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34174919 | TGGTGAGAAGTGGAT[A/G]CAAAGAGGGAGGAAG | 688429 |
rs64337376 | snp | G/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34226782 | CATCATGCCAGGCCT[G/T]CGAGCAGGTCATAGC | 688429 |
rs64737021 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34175107 | GACAAAGCTCTGTGT[A/G]ATTTTCTCTGCCTTT | 688429 |
rs65032913 | snp | A/C | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34226332 | GCCTTAGGTTACAGT[A/C]GGCACTTACCTGGCC | 688429 |
rs65665479 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34352168 | AAACAAGTGTGGTAT[C/T]TAGATCTCGTAACTA | 688429 |
rs104901845 | snp | C/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34302048 | TGCACTTCCCAGCCT[C/G]GATGAGGTTCGAGCA | 688429 |
rs104904698 | snp | G/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34326396 | AAAAATAAGTCTACT[G/T]TTTTTTTTGTAATTT | 688429 |
rs104919398 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34265410 | TAAGTAGTCTTTTCT[C/T]TCCAGAACATACAGA | 688429 |
rs104919594 | snp | A/C | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34377710 | CTTAAAACAAACAAA[A/C]AAAAAAAGCGAAAAG | 688429 |
rs104935409 | snp | A/C | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34160652 | GGTAGTGGTCGCAGA[A/C]GCCTTTGATCCTAGC | 688429 |
rs104936931 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34320686 | TGAGAAAACCAAAAG[A/G]TCAGGTGGTTTTCAG | 688429 |
rs104939903 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34282127 | CGGGCAAGAGGCGAC[A/G]TCTGACAGGAAAACG | 688429 |
rs104941317 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34244352 | CAGGACCTTGGGCAC[C/T]TGGTACATGCGTGTG | 688429 |
rs104942776 | snp | C/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34243906 | CAGCAGTCTCCTGGG[C/G]CTTTGGTCAGCCGGT | 688429 |
rs104945904 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34303599 | TGGCATGCTGAAACC[C/T]GTTGATCTATTGATG | 688429 |
rs104949336 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34313569 | AGTTCATAATTATGC[C/T]TCTCCTCTTACCCTA | 688429 |
rs104954475 | snp | C/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34190441 | TGGCAAAAAGCTTTC[C/G]TCCTCCTTCTTCCCA | 688429 |
rs104954664 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34376732 | CGGCGAGGTGACGGG[C/T]GACTTCATTGCCAGC | 688429 |
rs104965334 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34257952 | TCTTTTTGAGGAAAT[A/G]TGCACATGCCACATG | 688429 |
rs104979942 | snp | A/C | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34324705 | CACGACCATCCGTAA[A/C]CACATTTCTGGAGGA | 688429 |
rs104990938 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34276425 | GTGGCTCACGGGATG[A/G]GGTGCTGCTCTGTAT | 688429 |
rs104994101 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34156673 | TGAAGATGCCGACCT[C/T]ACTGGCTTCTTTCTC | 688429 |
rs104994369 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34260314 | TATTTCAGCAAACAG[C/T]GTGCCACTCGTTTAA | 688429 |
rs104994892 | snp | G/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34160647 | GGCTAGGTAGTGGTC[G/T]CAGACGCCTTTGATC | 688429 |
rs104997148 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34380204 | ATTCAGAATGACACG[C/T]CGCAGGCAGACAGCG | 688429 |
rs105006125 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34326173 | GCTCCAAACTACACG[C/T]AGTACGCAAAGACCC | 688429 |
rs105011632 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34275067 | TCCCAAGGCAGATTG[C/T]CACCATGCCAGACAT | 688429 |
rs105019718 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34326773 | AAGAAACAGTGTCTA[C/T]CACACACAGAATCTG | 688429 |
rs105025523 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34260666 | CTTGGGTTGTAGAGA[C/T]GCCTAGGGTTTGTGA | 688429 |
rs105026250 | snp | G/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34191168 | TGATGTGGATTGAAA[G/T]CACATTCCTTTGCCC | 688429 |
rs105030667 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34391947 | AAGACTCCATTCACT[C/T]ACCTCTTCAATATTT | 688429 |
rs105050608 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34356830 | GATTTTCATCTACCA[C/T]AATACCTAGGATTGT | 688429 |
rs105070232 | snp | A/C | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34383778 | CTGGCCTCCTCTGCA[A/C]GCCTTGCTGTTTGGG | 688429 |
rs105070341 | snp | G/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34310183 | CTGTCCCTCCTTCCC[G/T]TTATGCCCTGCCTCA | 688429 |
rs105089204 | snp | C/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34250972 | CACGTGGGCTGGAGC[C/G]TGTGTGGGGTTAGGG | 688429 |
rs105093381 | snp | G/T | 0 | 0 | intron-variant | Arhgap10 | Rnor_6.0 | 19:34224808 | TTGTTGGAAGACGAG[G/T]CCCTTCTCCCTGTGT | 688429 |
rs105094970 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34238130 | TTGAGTGTGTTTTGT[C/T]CACAGAGACCCGGGT | 688429 |
rs105095025 | snp | A/G | 0.5 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34225752 | TCCTCTCCTGTGTGT[A/G]TGTTGTTGGAAGACG | 688429 |
rs105124863 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34155910 | GTCAGAAGTGCTTTG[C/T]GCGTCCACGGAGTTG | 688429 |
rs105144054 | snp | C/T | 0 | 0 | missense | Arhgap10 | Rn_Celera | 19:34372737 | ATTCACTGTCCACTC[C/T]GTCTCCTACAACTTC | 688429 |
rs105144290 | snp | A/C | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34142571 | GTTGGTTGGGTCACG[A/C]TGTTCTTGCCATGTT | 688429 |
rs105145350 | snp | C/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34326981 | TCGGCTCTAACCGCT[C/G]GGTCTCTTTGGAATG | 688429 |
rs105150933 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34188702 | CTCTTCTAGGAGATG[A/G]ACTTAACACTACCGT | 688429 |
rs105156386 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34267119 | GTGTGTGTGTGTGTG[C/T]GCGCGCGTGCGCCCA | 688429 |
rs105168106 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34352350 | TCGCTTTGCTTGGCT[C/T]TGCTTGGTGCTTTTC | 688429 |
rs105168891 | snp | A/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34359327 | AGTGAAGCCTATGTG[A/T]CTGATCCTTCACGAC | 688429 |
rs105178195 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34317381 | GGGCCTGACATTCCC[A/G]AAACACTCCTCAGAC | 688429 |
rs105180758 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34185841 | CCCCCTACATGAACC[A/G]ATTCATATTTAGTGT | 688429 |
rs105182920 | snp | C/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34298269 | TTCCCTGGAGCTGCC[C/G]TGTTGAAATGCCTTA | 688429 |
rs105191120 | snp | A/C | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34330709 | AAGGGATATATCTGG[A/C]TGCCTCGTTTTTTTT | 688429 |
rs105192829 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34261655 | TAAAAATATGTAGAT[C/T]GGATAAGTAGATACT | 688429 |
rs105200784 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34269512 | AACTTAGCCAATCCC[A/G]TTGACCTTTATAGAT | 688429 |
rs105201443 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rnor_6.0 | 19:34224754 | GTTGGAAGACGAGGC[C/T]CTTCTCCCTGTGTGG | 688429 |
rs105206165 | snp | A/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34258784 | TGCCATACGGGTTTT[A/T]AAATGATCATAAGCA | 688429 |
rs105208888 | snp | A/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34293952 | TCTAATTGTTTCTTT[A/T]AAAAAAAAAAGTCAC | 688429 |
rs105211865 | snp | C/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34222863 | GTCTCTGGGCAGGTC[C/G]CATGGTGCTAAACGT | 688429 |
rs105217386 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34155958 | GAAGACAGACTGAAG[C/T]GATGCTGGTCATAGT | 688429 |
rs105224148 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | Arhgap10 | Rn_Celera | 19:34218945 | GGTGTGGGCTGCAGC[C/T]GGGAATGGCGGCAGG | 688429 |
rs105228974 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34299611 | AGGGCAAATGTAGTG[C/T]GCAGAAACAATTGTA | 688429 |
rs105229223 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34240803 | TAGGAAGCGCAAGGC[C/T]CTGGGTTCGGTCCCC | 688429 |
rs105234010 | snp | G/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34304980 | ACATGTGACATGGAT[G/T]GAAGTTCAGCGTCAT | 688429 |
rs105269062 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34269401 | CTCAAGGAAGCTGTG[C/T]GTAGGGCTGGTTGTA | 688429 |
rs105275575 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34155318 | CCTCCCCCCTGACCC[A/G]TGCAGTGTGGCTCAG | 688429 |
rs105279550 | snp | A/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34258068 | AGTGTCCGTGAGGAA[A/T]AGCAACTGTTGGTCA | 688429 |
rs105281017 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34299363 | AGTTTGCTTGTTGAG[A/G]TTTTAAAGCCATTTT | 688429 |
rs105306215 | snp | A/C | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34371093 | AAACACACTGGAATC[A/C]CAGTGTCTCCTCAGG | 688429 |
rs105318832 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34309423 | GAGAGCGCACGAGCG[C/T]GAGTGAGCTTGGTTT | 688429 |
rs105319525 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34185888 | GTGCGAGTGTGTGTG[C/T]GCGCGCGCGTGTGTA | 688429 |
rs105336497 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34285788 | GGCTCAGTTTCTGAT[A/G]AGGGTATCTGTGTAT | 688429 |
rs105340203 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34179310 | TACATATGAGCAAAA[C/T]ACTCATATACATAAG | 688429 |
rs105342044 | snp | C/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34309658 | TGCCAGGGTAGGCTC[C/G]GAAGCCAGCAGTTTT | 688429 |
rs105356169 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34146493 | AATGTAAAGCACATC[A/G]ATACTTCCTGGATAT | 688429 |
rs105359217 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34330750 | TGATACATTGTGAGG[A/G]CCTAATTTTGGCTTT | 688429 |
rs105366577 | snp | G/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34339174 | ATATGCATGTATGAC[G/T]GTTCTTAAATTTCAA | 688429 |
rs105369901 | snp | G/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34327757 | CAGAAGAGGGCGTCA[G/T]ACACCCTAGGGGTGG | 688429 |
rs105376397 | snp | A/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34397828 | CACATACACTCACAC[A/T]CACACTCACACACAC | 688429 |
rs105392208 | snp | A/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34251361 | GAGAGAGAGAGAGAG[A/T]GAGTGTGTGTGTGTG | 688429 |
rs105393855 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34243584 | TTATGGGATTGATGT[A/G]TAATGAGAACAGAAC | 688429 |
rs105395421 | snp | A/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34140458 | TGGAGGAATAGGCGA[A/T]TCCATAGGGCATAAG | 688429 |
rs105409038 | snp | G/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34377730 | AAAGCGAAAAGCCAT[G/T]AAGTCCCATGTGCGT | 688429 |
rs105409681 | snp | C/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34304824 | TGTGTGCATGTGCAC[C/G]TGTGCTTCTGTATGT | 688429 |
rs105419218 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34152112 | GGGTCAAGGCGAGGT[A/G]AGGTCTCAGTTCCTG | 688429 |
rs105420038 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34302184 | CAGCATTTTACTCCT[C/T]CGTGAGAGACCTGGC | 688429 |
rs105423820 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34363753 | GTTTATTTGGTGGTT[A/G]GCTTCTTGTGTTCTT | 688429 |
rs105424180 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34281125 | ATAGAGAGGCATATC[A/G]GAACAGAAGGTGCTG | 688429 |
rs105429888 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34380763 | GAGTGGGTTTACCCG[A/G]CCGGGTGGATTCAGA | 688429 |
rs105431151 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34380523 | TTAATGGTCACAGTT[A/G]AATACTGATTGTTTT | 688429 |
rs105435215 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34192921 | CTGGGGAAAGGAGAC[A/G]TCAACTGAGAAACTG | 688429 |
rs105445778 | snp | A/G | 0 | 0 | missense | Arhgap10 | Rn_Celera | 19:34372823 | AACTGTGGAGACGCC[A/G]CTGCCACTACGTAAG | 688429 |
rs105447581 | snp | A/C | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34145666 | TTCTGATTAGAATCC[A/C]CTAGCACAGGGCATT | 688429 |
rs105471866 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34278439 | CCGAGGGCAAATTCC[A/G]TGTGCGCCATCTCTG | 688429 |
rs105477448 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34324956 | TAGCTTGTAACATCC[A/G]TTTTCCTTTTTTTTT | 688429 |
rs105483497 | snp | C/T | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34252662 | CAGTTCTAATGCTCT[C/T]ACGGAGGGTGACACT | 688429 |
rs105493542 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34156610 | AGGGACTCTGTTGTA[A/G]GACTAGACTATCTAT | 688429 |
rs105493624 | snp | A/G | 0 | 0 | intron-variant | Arhgap10 | Rn_Celera | 19:34381307 | TACCTGGTTGGTTCC[A/G]TCATTATCTAGCACC | 688429 |