SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs28211671 | snp | C/T | 0.142012 | 0.225474 | downstream-variant-500B, upstream-variant-2KB | Ssh2, Coro6 | Mm_Celera | 11:77460478 | TGGGAACTTGGCTGG[C/T]CAAAGAGTCACTCAC | 216961 |
rs52652695 | snp | A/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461673 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 216961 |
rs211877290 | snp | G/T | | | intron-variant | Coro6 | Mm_Celera | 11:77467056 | ATAACCCTCAAGCGT[G/T]GCTTATCCCAGCTGG | 216961 |
rs212381803 | in-del | -/GAGGA | | | upstream-variant-2KB, intron-variant | Coro6 | Mm_Celera | 11:77462904 | CGGACAGCGGCTGGC[-/GAGGA]GAGGAGACACCTAGT | 216961 |
rs212381992 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77469371 | TTCTGTCTCCCACAT[A/G]CCAGCAGCAGCACAC | 216961 |
rs212658393 | snp | C/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461237 | GAGAACCAAGCCCAG[C/T]GGCTTCTTTGCCTGA | 216961 |
rs212709962 | snp | C/G | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77462202 | TTGCCCTGGGTCAAC[C/G]TAGACCCTCATCAAG | 216961 |
rs212920239 | snp | C/G | | | intron-variant | Coro6 | Mm_Celera | 11:77464305 | CTGTGCGCCCGATCT[C/G]TAGGCCACAGAGCAC | 216961 |
rs213288202 | snp | C/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77462079 | CTGCCTGGCTTAAGC[C/T]GTGGCTCATAGAACC | 216961 |
rs213308367 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77465290 | GAGACCTTAACTTGA[A/G]TCTGGGTTCCGTGTC | 216961 |
rs213444672 | in-del | -/AGAAGCCGAAGTCG | | | upstream-variant-2KB, intron-variant | Coro6 | Mm_Celera | 11:77463116 | TAAGCTCCTAGCTCC[-/AGAAGCCGAAGTCG]TAGAACCAGAAAGAG | 216961 |
rs213493555 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | Coro6 | Mm_Celera | 11:77463860 | TCCACAGCTCGCAGG[A/G]TTAAGGACCAACGTG | 216961 |
rs213547817 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | Coro6 | Mm_Celera | 11:77462426 | CCTGTATGCGAGGGA[C/T]GGTGGCAGACACGAG | 216961 |
rs213746736 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77466336 | GCAGGTCTGGGGTGG[A/G]GCTAAGGAGGGTCCC | 216961 |
rs214027504 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77465368 | TCCTAATACAAAGGC[A/G]TTCACACTGTGCATC | 216961 |
rs214050239 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | Ssh2, Coro6 | Mm_Celera | 11:77460461 | AAATCAGGTGACCAG[A/G]CTGGGAACTTGGCTG | 216961 |
rs214271319 | snp | C/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77460991 | CAAGTGAGTGGCGCA[C/T]TGCTATTCTCCAGTG | 216961 |
rs214482462 | in-del | -/CCC | | | upstream-variant-2KB, intron-variant | Coro6 | GRCm38.p3 | 11:77462827 | GGGCAGAGGTCTGCG[-/CCC]CCCCCCCCCCCCCCC | 216961 |
rs214611482 | snp | C/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461287 | TTGTGTGTGTGGAAA[C/T]TTTTCCTGCATGTTG | 216961 |
rs214884162 | snp | C/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461219 | CCACTGACAGTTCTA[C/T]GGGAGAACCAAGCCC | 216961 |
rs215123596 | snp | G/T | | | upstream-variant-2KB, intron-variant | Coro6 | Mm_Celera | 11:77463090 | CCCTTGGGAAAAGTA[G/T]CAAGCATTGCTAAGC | 216961 |
rs215195806 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | Ssh2, Coro6 | Mm_Celera | 11:77460498 | GAGTCACTCACAGAA[A/G]CTGTCACCTGAATGT | 216961 |
rs215623923 | snp | G/T | | | missense, nc-transcript-variant | Coro6 | Mm_Celera | 11:77469426 | AAAGGCCCTCCGAGA[G/T]CGAGTGCAGGCCCAA | 216961 |
rs215770212 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Coro6 | Mm_Celera | 11:77462518 | GCCCGCCGGACTTTC[C/G]CGCGCTGGACAGGGC | 216961 |
rs216052747 | in-del | -/GA | | | intron-variant | Coro6 | Mm_Celera | 11:77468691 | GTGCTGTTCTTTGGG[-/GA]AAAAAGAAAGGAGCC | 216961 |
rs216436760 | snp | C/T | | | intron-variant | Coro6 | Mm_Celera | 11:77464253 | TGTCTTTGCCAAACC[C/T]ACAAAGAATGGTGGA | 216961 |
rs216454842 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Ankrd13b, Coro6 | GRCm38.p3 | 11:77470947 | CCTTGCCCAAACTAG[A/G]GGGCACCTTAGGCAC | 216961 |
rs217674194 | snp | A/T | | | intron-variant | Coro6 | Mm_Celera | 11:77465637 | CACGAATGACAGTGA[A/T]CCCATATCACCCTCT | 216961 |
rs217685040 | snp | C/G | | | intron-variant | Coro6 | Mm_Celera | 11:77465109 | GGGCTAAGCCACTGC[C/G]GTCAGAGTCACTCAC | 216961 |
rs217743337 | in-del | -/C | | | upstream-variant-2KB, intron-variant | Coro6 | Mm_Celera | 11:77463295 | ACCATAGCCAGGACT[-/C]CCCCCACCCCACCCC | 216961 |
rs219381142 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Coro6 | Mm_Celera | 11:77466428 | GACAGGGGGTGATAA[C/T]GTGATCATCATCTGG | 216961 |
rs219802447 | snp | G/T | | | intron-variant | Coro6 | Mm_Celera | 11:77464765 | AAGACCTCACAAGTG[G/T]TGGGGTCAGGACAGG | 216961 |
rs219812813 | snp | C/T | | | upstream-variant-2KB, intron-variant | Coro6 | Mm_Celera | 11:77463394 | CACCGGAGGAATCTT[C/T]TAAAAAGAGTAGGAA | 216961 |
rs219817260 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Coro6 | Mm_Celera | 11:77469134 | TGATGAGTGGCTATC[A/G]GGTCAGGATGCAGAA | 216961 |
rs220091855 | snp | A/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77460821 | ATACAAATGCACATT[A/T]AAAAAATAAACACTT | 216961 |
rs220172251 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Coro6 | Mm_Celera | 11:77469929 | AATTTCCAATATTTC[C/T]CCTAATAAGCAGCAC | 216961 |
rs220933618 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | Ssh2, Coro6 | Mm_Celera | 11:77460648 | TAACACAGAGCAAAC[A/G]AGTTTTCATCACAGT | 216961 |
rs221186614 | snp | A/C | | | intron-variant | Coro6 | Mm_Celera | 11:77467421 | GAGTGGTGGCCCAAC[A/C]CAAGAGGCCCAAGTG | 216961 |
rs221435294 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77465854 | CTCACCTGTGCTGGG[A/G]AAGATAATAGAAGGG | 216961 |
rs221598504 | snp | A/G | | | upstream-variant-2KB, intron-variant | Coro6 | Mm_Celera | 11:77462964 | GCTGGAGGAGGGGGC[A/G]AGTAGGCCGGCCTTC | 216961 |
rs221980200 | snp | A/G | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461509 | TATGCACACATAGAA[A/G]CCACAAATCTTCTGT | 216961 |
rs222013953 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77465860 | TGTGCTGGGGAAGAT[A/G]ATAGAAGGGGTAGAG | 216961 |
rs222740930 | snp | C/G | | | intron-variant | Coro6 | Mm_Celera | 11:77464834 | CACCATCCAGAGACA[C/G]CATCCCAAGGGCTCA | 216961 |
rs222847348 | in-del | -/T | | | intron-variant | Coro6 | Mm_Celera | 11:77468892 | AGCAGGAATGTTGAA[-/T]TTCCCCCTCCCTCAT | 216961 |
rs224276128 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77466146 | AATAGCACTAAGTGT[A/G]TGAGCCATCTCTGAA | 216961 |
rs224307023 | snp | A/G | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461367 | TTCCCCAGAACTGGC[A/G]TTAGAGATGGTTGTA | 216961 |
rs224358996 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77468137 | GAAAGGGAAAGATGC[A/G]TCTAGAAGAGCCTGT | 216961 |
rs225343032 | in-del | -/AG | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Coro6 | Mm_Celera | 11:77469619 | CGTGGGGTTGGAATC[-/AG]GGGAGGGATCAGAAA | 216961 |
rs225418249 | snp | A/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461196 | CCTCATGGATTGCAG[A/T]ACAGGACCCACTGAC | 216961 |
rs225510066 | snp | A/G | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461917 | GTCTTGGGGGTGAGG[A/G]ATTCTGCCCTAAAAT | 216961 |
rs225761971 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Coro6 | Mm_Celera | 11:77469573 | CCGACTGGCAGCACC[A/G]GCTTTTGGTCTGGAA | 216961 |
rs226032810 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77467613 | CCTGCCACTGACCTC[A/G]GAGAAGCTGAGTTCT | 216961 |
rs226400720 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Ankrd13b, Coro6 | Mm_Celera | 11:77470486 | TAAGTAGAAATGCAT[C/T]TGGTTTGAAACCGCT | 216961 |
rs226910391 | snp | A/C | | | intron-variant | Coro6 | Mm_Celera | 11:77464864 | ACATTTCAGCCCGAG[A/C]CACCTCCTCCCCCAG | 216961 |
rs227049518 | snp | C/T | | | intron-variant | Coro6 | Mm_Celera | 11:77465500 | AATCTACTGCCCACT[C/T]CAAAACCACATACAG | 216961 |
rs227080431 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | Ssh2, Coro6 | Mm_Celera | 11:77460403 | CTTTCACAAAAGACT[A/G]CGAAGGAAACAGAGT | 216961 |
rs227450705 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | Coro6 | Mm_Celera | 11:77463882 | ACCAACGTGCCTCTA[C/G]ACTCTGATACTCCCT | 216961 |
rs228079363 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Coro6 | Mm_Celera | 11:77463690 | CCCTGTGTCAGCCTC[C/T]GCTATCCCGGCTAGC | 216961 |
rs228289498 | snp | A/T | | | intron-variant | Coro6 | Mm_Celera | 11:77466353 | CTAAGGAGGGTCCCT[A/T]CTGTAGATGAGGGTG | 216961 |
rs228406055 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | Ssh2, Coro6 | Mm_Celera | 11:77460442 | GTTGCAGACAATGAG[A/G]CTCAAATCAGGTGAC | 216961 |
rs229585751 | snp | A/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461091 | AAATATGTTCAGTCT[A/T]GGCTTTGTAGCCAAA | 216961 |
rs229991313 | snp | C/G | | | intron-variant | Coro6 | Mm_Celera | 11:77465311 | GTTCCGTGTCCTGCT[C/G]TGGGTACTTTGTTAG | 216961 |
rs230096791 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Coro6 | Mm_Celera | 11:77462834 | GGTCTGCGCCCCCCC[-/A]CCCCCCCCGCCGCTA | 216961 |
rs230185671 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77464630 | TTCCCTCCCCTGCAC[A/G]TGAGGGAAAGGGCCA | 216961 |
rs230470052 | in-del | -/CACACACACA | | | intron-variant | Coro6 | Mm_Celera | 11:77465604 | CCAGCGGTGCTTGTG[-/CACACACACA]CACACACACACGAAT | 216961 |
rs231116104 | snp | A/G | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461255 | CTTCTTTGCCTGACT[A/G]GTGTtttgttttaac | 216961 |
rs231463332 | snp | A/C | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461308 | CTGCATGTTGGTGCA[A/C]CACATGTGTGTCTGG | 216961 |
rs231820908 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77467122 | CCTCCTTCTAACCTG[A/G]GAAGTCGGGTGCCTG | 216961 |
rs231898673 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Coro6 | Mm_Celera | 11:77469408 | GACATTGCTGGAGGA[A/G]ATAAAGGCCCTCCGA | 216961 |
rs232146255 | in-del | -/AGA | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461341 | CCATGGAAGCTATTG[-/AGA]AGATATTGGATTCCC | 216961 |
rs232453099 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Coro6 | Mm_Celera | 11:77468949 | GTGTGAACCCATCAT[C/T]ATGACTGTACCGCGA | 216961 |
rs233007428 | snp | C/T | | | intron-variant | Coro6 | Mm_Celera | 11:77465908 | GTCCTGCCCAGTTCC[C/T]AGATTATTTTTAGTT | 216961 |
rs233120747 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Coro6 | Mm_Celera | 11:77463838 | CCTACTCACTCACTC[-/A]CTCCCTTCCACAGCT | 216961 |
rs233178661 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Ankrd13b, Coro6 | Mm_Celera | 11:77470266 | ATATGCTGCCCCCAT[C/T]CCCCAAGGCACCATG | 216961 |
rs233438801 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Ankrd13b, Coro6 | Mm_Celera | 11:77470308 | CCTTGCCCAAACTAG[A/G]GGGCACCTCAGTCCT | 216961 |
rs233553617 | snp | C/T | | | upstream-variant-2KB, intron-variant | Coro6 | Mm_Celera | 11:77463514 | AGGGCTGCAGTCCTA[C/T]CTAGCCTTGAGCTAC | 216961 |
rs234389567 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Coro6 | Mm_Celera | 11:77469203 | CAAACACCGTGAGCT[C/T]CGGGTCACCAAACGC | 216961 |
rs234599867 | snp | C/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77462055 | TGCTGGGAGTTAGTT[C/T]ACTTTTCTCTGCCTG | 216961 |
rs234737804 | snp | A/G | | | upstream-variant-2KB, intron-variant | Coro6 | Mm_Celera | 11:77463451 | CTTGGCCAAGCTGTA[A/G]AAAAAGACACACCGG | 216961 |
rs235052143 | snp | C/G | | | intron-variant | Coro6 | Mm_Celera | 11:77465396 | ATCTCCAGCAAAGTT[C/G]AAAGAGTAGACTGAG | 216961 |
rs235115256 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77465221 | TGGGTTCACGCCCAT[A/G]AGCCCAGCACTGGGA | 216961 |
rs235559419 | snp | G/T | | | downstream-variant-500B, upstream-variant-2KB | Ssh2, Coro6 | Mm_Celera | 11:77460695 | GGGAGAGGGCTCAGT[G/T]GTTAAGAGCACTGGC | 216961 |
rs236135655 | snp | G/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461257 | TCTTTGCCTGACTGG[G/T]GTTTTGTTTTAACTT | 216961 |
rs237595331 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Coro6 | Mm_Celera | 11:77469495 | GCTGGTGGACGGCAC[A/G]GACTAGCACTGCCTA | 216961 |
rs237660993 | snp | A/G | | | upstream-variant-2KB, intron-variant | Coro6 | Mm_Celera | 11:77463085 | GTGTCCCCTTGGGAA[A/G]AGTAGCAAGCATTGC | 216961 |
rs237698744 | snp | C/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77460964 | CGCCAACCTACTTCT[C/T]TCTGAGTCGGCCAAG | 216961 |
rs238035771 | in-del | -/AAGGTATATA | | | downstream-variant-500B, upstream-variant-2KB | Ssh2, Coro6 | Mm_Celera | 11:77460385 | GCATGTATATAACCT[-/AAGGTATATA]ACCTTTCACAAAAGA | 216961 |
rs238099877 | snp | C/T | | | intron-variant | Coro6 | Mm_Celera | 11:77465642 | ATGACAGTGAACCCA[C/T]ATCACCCTCTCTGAC | 216961 |
rs238308743 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77465152 | CTCCAGGGGCTTGCC[A/G]AAGGTCCTCCAACTT | 216961 |
rs239544533 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Ankrd13b, Coro6 | Mm_Celera | 11:77470950 | TGCCCAAACTAGGGG[G/T]CACCTTAGGCACACT | 216961 |
rs239818576 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Coro6 | Mm_Celera | 11:77466461 | TGTGGGCACTGGGGA[A/G]GTACTGCTGAGCCTG | 216961 |
rs239842946 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | Ankrd13b, Coro6 | Mm_Celera | 11:77470021 | GCTCTTCCCATCTTC[C/T]CACTTCCAAAGACGG | 216961 |
rs239910426 | snp | C/T | | | intron-variant | Coro6 | Mm_Celera | 11:77468199 | GGGATTTGGGGTGGC[C/T]ATAAAGCGAATTCTG | 216961 |
rs240052274 | in-del | -/AGAC | | | intron-variant | Coro6 | Mm_Celera | 11:77464478 | CACACACAGAAACAG[-/AGAC]AGAGAGACAGAGATA | 216961 |
rs240253050 | snp | A/G | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461222 | CTGACAGTTCTATGG[A/G]AGAACCAAGCCCAGT | 216961 |
rs240373412 | snp | A/G | | | intron-variant | Coro6 | Mm_Celera | 11:77464267 | CCACAAAGAATGGTG[A/G]AGAACAGCAACATCA | 216961 |
rs240947526 | snp | C/T | | | intron-variant | Coro6 | Mm_Celera | 11:77465045 | TCAGCACCAAGACTG[C/T]GTGCTGCCTATGACT | 216961 |
rs241034395 | snp | A/G | | | upstream-variant-2KB, intron-variant | Coro6 | Mm_Celera | 11:77463396 | CCGGAGGAATCTTTT[A/G]AAAAGAGTAGGAAGC | 216961 |
rs241090553 | snp | A/T | | | upstream-variant-2KB | Coro6 | Mm_Celera | 11:77461918 | TCTTGGGGGTGAGGA[A/T]TTCTGCCCTAAAATA | 216961 |
rs241768388 | snp | A/C | | | intron-variant | Coro6 | Mm_Celera | 11:77465504 | TACTGCCCACTTCAA[A/C]ACCACATACAGGAGA | 216961 |