SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4159540 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp7 | Mm_Celera | 16:8691550 | CCCAGCCCTTTCAAC[G/T]CTTACCTGGTGTATC | 252870 |
rs4159541 | snp | C/T | 0.362812 | 0.2231 | synonymous-codon | Usp7 | Mm_Celera | 16:8691568 | TACCTGGTGTATCCT[C/T]AGCAAAAATGGAATT | 252870 |
rs4159542 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8692305 | GAATGGGTGCTACGG[C/T]GGCACCCATCCCAGC | 252870 |
rs4159543 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8692310 | GGTGCTACGGTGGCA[C/G]CCATCCCAGCACAAG | 252870 |
rs4159544 | snp | C/G/T | 0.375 | 0.216506 | intron-variant | Usp7 | GRCm38.p3 | 16:8692314 | CTACGGTGGCACCCA[C/G/T]CCCAGCACAAGACAG | 252870 |
rs4159545 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp7 | Mm_Celera | 16:8692579 | CCAGGTGACAGCACC[A/G]CACCCGGGTGCATAT | 252870 |
rs4159546 | snp | A/G | 0.2688 | 0.249292 | intron-variant | Usp7 | Mm_Celera | 16:8692747 | CTTTGACATCCCTAG[A/G]AAAACCATAGGAATA | 252870 |
rs4159547 | snp | A/G | 0.42344 | 0.180051 | intron-variant | Usp7 | Mm_Celera | 16:8695265 | ACTGTGCTTACCAGA[A/G]GCTACAGGAGCCTGC | 252870 |
rs4159548 | snp | C/T | 0.287335 | 0.247197 | intron-variant | Usp7 | Mm_Celera | 16:8695375 | CAGAGGCCCTAACAG[C/T]CATATGGTGCCTGCA | 252870 |
rs4159549 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp7 | Mm_Celera | 16:8695575 | CCTACAGACATTCCT[C/T]GGACATCAGAGAACT | 252870 |
rs4159550 | snp | C/T | 0.340265 | 0.233136 | intron-variant | Usp7 | Mm_Celera | 16:8695704 | TGCAGGTGCTCGCCA[C/T]CGTATCACTAAGAGA | 252870 |
rs4159551 | snp | A/G | 0.30839 | 0.243086 | intron-variant | Usp7 | Mm_Celera | 16:8696109 | TTAGGTTGGCCCTGG[A/G]TGCCAGCCTTAGCCT | 252870 |
rs4159552 | snp | G/T | 0.32 | 0.24 | intron-variant | Usp7 | Mm_Celera | 16:8696367 | AGCCTCAATCTTTTA[G/T]CATTATCTGAGGCAC | 252870 |
rs4159553 | snp | C/T | 0.2688 | 0.249292 | intron-variant | Usp7 | Mm_Celera | 16:8696380 | TAGCATTATCTGAGG[C/T]ACTTTCTCAATAAAA | 252870 |
rs4159554 | snp | A/G | 0.453686 | 0.144955 | intron-variant | Usp7 | Mm_Celera | 16:8696634 | CCACCTCCCTCCCAA[A/G]CAGAAATGGTGTAGT | 252870 |
rs4159555 | snp | A/G/T | 0.433884 | 0.169371 | intron-variant | Usp7 | Mm_Celera | 16:8697143 | GTGTTAACAAGTGAG[A/G/T]CTGACTACTGGACTA | 252870 |
rs4159556 | snp | C/T | 0.471655 | 0.115624 | intron-variant | Usp7 | Mm_Celera | 16:8697317 | ACATAGGCCATGTGG[C/T]TTAAGGAGAAGCATC | 252870 |
rs4159557 | snp | C/T | 0.287335 | 0.247197 | intron-variant | Usp7 | Mm_Celera | 16:8699441 | ATTTCCAACTTTGGA[C/T]CAATCATTCACACAG | 252870 |
rs4159558 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp7 | Mm_Celera | 16:8700251 | TTACTTTTAAAATCA[A/G]TATTGATTTGCATGT | 252870 |
rs4159559 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp7 | Mm_Celera | 16:8700618 | TTTTACAAAGGTACT[A/G]TATTTGACAGTCCTA | 252870 |
rs4159560 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8700745 | CTGGACAGCGTGCAG[A/G]AGACCATAAGCTCTT | 252870 |
rs4159561 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp7 | Mm_Celera | 16:8702080 | CTGCCTCCTGGAAGT[A/G]GAGAAGAAATGGTAA | 252870 |
rs4159562 | snp | C/T | 0.287335 | 0.247197 | intron-variant | Usp7 | Mm_Celera | 16:8703069 | AGCACATTTCACCTA[C/T]TCTGCTAGTTCTGTC | 252870 |
rs4159563 | snp | C/T | 0.2688 | 0.249292 | intron-variant | Usp7 | Mm_Celera | 16:8703916 | CAGAGCAACAACTAA[C/T]ACAATGACATCACTA | 252870 |
rs4159564 | snp | A/G | 0.287335 | 0.247197 | intron-variant | Usp7 | Mm_Celera | 16:8704476 | GTATCAGTCCACACC[A/G]CGAGATAAATGATGC | 252870 |
rs4159565 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Usp7 | Mm_Celera | 16:8706508 | GCCCTGGGGCCAGCC[C/G]TGAGCCTGCCTGAGC | 252870 |
rs4159566 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Usp7 | Mm_Celera | 16:8707971 | TCACTGCCATAGACA[C/T]TCACACTCAATTTCA | 252870 |
rs4159567 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Usp7 | Mm_Celera | 16:8708415 | GAGAGAAATCTACTG[C/G]TAAACAGAAAACTAC | 252870 |
rs4159568 | snp | C/G | 0.385633 | 0.210009 | intron-variant | Usp7 | Mm_Celera | 16:8709693 | GCCATGCCTGAGGAG[C/G]CAGTGAGATGACACA | 252870 |
rs4159569 | snp | C/T | 0.235537 | 0.249581 | intron-variant | Usp7 | Mm_Celera | 16:8709771 | AATCCACAGAACCCA[C/T]ACAAATGGACCACAC | 252870 |
rs4159570 | snp | A/T | 0.5 | 0 | intron-variant | Usp7 | Mm_Celera | 16:8710423 | TGAGAGCTAAGATTA[A/T]GGTGCATACCATGAC | 252870 |
rs4159571 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Usp7 | Mm_Celera | 16:8710501 | TGGCACATCAGCCTT[A/T]GGTTTTATGCACTGT | 252870 |
rs4159572 | snp | A/G | 0.30839 | 0.243086 | intron-variant | Usp7 | Mm_Celera | 16:8711046 | TTGTACTGGGCAACT[A/G]TTTACCGCTGCACCA | 252870 |
rs4159573 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Usp7 | Mm_Celera | 16:8711285 | TGTCACACTAAGAGG[A/C]GTTTACTACTGACAG | 252870 |
rs4159574 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Usp7 | Mm_Celera | 16:8711301 | GTTTACTACTGACAG[C/T]GAGGATGTGTACTGA | 252870 |
rs4159575 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp7 | Mm_Celera | 16:8711311 | GACAGTGAGGATGTG[G/T]ACTGAAAGGAGAACC | 252870 |
rs4159576 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Usp7 | Mm_Celera | 16:8712255 | AGCATATCAACACTG[C/G]AGTAACTGCTCTACA | 252870 |
rs4159577 | snp | A/G | 0.433884 | 0.169371 | intron-variant | Usp7 | Mm_Celera | 16:8712309 | TGATGCCTCAGGGAA[A/G]TGAGAGTGGCTTTTC | 252870 |
rs4159578 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8712567 | GCCATCCGTTGTGCT[A/G]GGAGCACAGTAGAGC | 252870 |
rs4159579 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Usp7 | Mm_Celera | 16:8712737 | GCCTCTGCTCAGAGG[C/T]TTAGTGTCTCAATCA | 252870 |
rs4159580 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Usp7 | Mm_Celera | 16:8712848 | GAATGCCTTACTGTT[G/T]GCTTCTCAAGCCATA | 252870 |
rs4159581 | snp | C/G | 0.30839 | 0.243086 | intron-variant | Usp7 | Mm_Celera | 16:8713370 | CCGAAGTCTGTCAAT[C/G]TTCCCTCACCCCGTT | 252870 |
rs4159582 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Usp7 | Mm_Celera | 16:8713691 | AGACGCCAAGGACAG[A/G]GGCAGTGCACACTAC | 252870 |
rs4159583 | snp | C/T | 0.433884 | 0.169371 | intron-variant | Usp7 | Mm_Celera | 16:8714725 | AGCTACCCAAGTTCT[C/T]ACACGAGAGACGCCT | 252870 |
rs4159584 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Usp7 | Mm_Celera | 16:8714738 | CTCACACGAGAGACG[C/G]CTCTAAGAACCCTGA | 252870 |
rs4159585 | snp | A/T | 0.265928 | 0.249492 | intron-variant | Usp7 | Mm_Celera | 16:8715118 | GCCCAGGCCTTGCTG[A/T]AGACACTTCCAACTG | 252870 |
rs4159586 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8719008 | CCTATTCCTAGTTGA[C/T]CCTGGTCATCTGGAA | 252870 |
rs4159587 | snp | A/C | 0.5 | 0 | intron-variant | Usp7 | Mm_Celera | 16:8720289 | TGAAGAGTCATGTAG[A/C]CAACAATGACAGTCC | 252870 |
rs4159588 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Usp7 | Mm_Celera | 16:8721408 | CGCCTTTAATCCCAG[C/G]ACCCGGGAGGCAGAG | 252870 |
rs4159589 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Usp7 | Mm_Celera | 16:8722254 | AACTAAAGGAAAAAA[A/T]AAATATCAAGGGTTA | 252870 |
rs4159590 | snp | G/T | 0.2688 | 0.249292 | intron-variant, upstream-variant-2KB | Usp7 | Mm_Celera | 16:8722488 | TACTAGAAGGGACCG[G/T]GTGCCTGTGAGGTAC | 252870 |
rs4159591 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp7 | Mm_Celera | 16:8725879 | AGGTTACCCCCCAAT[A/G]ATCGTCAAAGCCAAA | 252870 |
rs4159592 | snp | A/G | 0.2688 | 0.249292 | intron-variant | Usp7 | Mm_Celera | 16:8726014 | ACTCAGAAAGCAGAA[A/G]TAGTTAAATCAAGGC | 252870 |
rs4159593 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Usp7 | Mm_Celera | 16:8727299 | CTGCCAAAGTTGATC[C/T]GTATAATGCAAAACT | 252870 |
rs4159594 | snp | C/T | 0.30839 | 0.243086 | intron-variant | Usp7 | Mm_Celera | 16:8728726 | AGATGTGAATGAACA[C/T]AGATATGCACGTGGA | 252870 |
rs4159595 | snp | A/G | 0.471655 | 0.115624 | intron-variant | Usp7 | Mm_Celera | 16:8730321 | GCTACCAACATTTGA[A/G]AAATCTCCAATTTCC | 252870 |
rs4159596 | snp | A/T | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8730690 | CAGCACAGGGGGAAG[A/T]TGGACACTCACCGTA | 252870 |
rs4159597 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8730694 | ACAGGGGGAAGTTGG[A/G]CACTCACCGTAAGAC | 252870 |
rs4159598 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp7 | Mm_Celera | 16:8730972 | CCGCCACATGGGCGC[C/T]ACAGTATGCATGCTC | 252870 |
rs4159599 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Usp7 | Mm_Celera | 16:8731428 | GCCCACAGCCAATTT[C/T]TAGAGGGTTGTTAGA | 252870 |
rs4159600 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp7 | Mm_Celera | 16:8732593 | TCTGTAAAAAAAAAA[A/G]AAAAAAGAAGCTTCA | 252870 |
rs4159601 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Usp7 | Mm_Celera | 16:8732594 | CTGTAAAAAAAAAAA[A/C]AAAAAGAAGCTTCAA | 252870 |
rs4159602 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp7 | Mm_Celera | 16:8732596 | GTAAAAAAAAAAAAA[A/G]AAAGAAGCTTCAATT | 252870 |
rs4159603 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Usp7 | Mm_Celera | 16:8732597 | TAAAAAAAAAAAAAA[A/T]AAGAAGCTTCAATTC | 252870 |
rs4159604 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Usp7 | Mm_Celera | 16:8732653 | TGGCTAACAATGTCA[A/T]CTATCTAACTCCCTG | 252870 |
rs4159605 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8733940 | GCGGGCAGTGGTGGC[A/G]CACACCTTCAATCCT | 252870 |
rs4159606 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8734092 | AGAGAGAGAGAGAGA[C/G]AGACAGAGACAGAGA | 252870 |
rs4159607 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8734096 | AGAGAGAGAGACAGA[C/G]AGAGACAGAGACAGA | 252870 |
rs4159608 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8734675 | GGTGTAACTCAGTCA[A/G]ACTGTGTGGCTTGCA | 252870 |
rs4159609 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Usp7 | Mm_Celera | 16:8736404 | GCTATTCTGGACTTT[A/G]GAAGAAGTTATCAAC | 252870 |
rs4159610 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8737413 | AAGCCAGAGTCCCTC[C/G]ACTGCGCTTTCACAG | 252870 |
rs4159611 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Usp7 | Mm_Celera | 16:8740145 | GCATGCTGCAAAAGC[A/G]CACACACTCAAATAA | 252870 |
rs4159612 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp7 | Mm_Celera | 16:8740861 | GAGTGAGTTCCAGGA[C/T]AGCCAGGGCTACACA | 252870 |
rs4159613 | snp | A/C | 0.32 | 0.24 | intron-variant | Usp7 | Mm_Celera | 16:8743021 | CTCTCTTGCCCCTCA[A/C]CCCCCAACCTGGTCA | 252870 |
rs4159614 | snp | A/C/G | 0.408163 | 0.193609 | intron-variant | Usp7 | Mm_Celera | 16:8744582 | TGTAAGAGAGTTGAA[A/C/G]GGCCCAGTGTATCTC | 252870 |
rs4159615 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp7 | Mm_Celera | 16:8745070 | CATTCAGAGGGCAGC[A/G]GCAAGCAGGCTTCTG | 252870 |
rs4159616 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Usp7 | Mm_Celera | 16:8747660 | AGGGTCAGCATCAAC[A/C]CAGGCTACAGGTCAA | 252870 |
rs4159617 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8747716 | CACTCAAGGTCAAAA[C/T]AAACAGAGCCAGCAG | 252870 |
rs4159618 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp7 | Mm_Celera | 16:8749620 | AATACTTAGAACTAA[A/G]CCCTAAAACAGCTGC | 252870 |
rs4159619 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8749803 | GAGAGATGGCTCAGC[A/G]GTTAAGAGCACTGAC | 252870 |
rs4159620 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8749942 | TACTCATATACATAA[A/G]TAAATAAATCTTAAA | 252870 |
rs4159621 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Usp7 | Mm_Celera | 16:8750074 | CTCTGCATGCGAATG[A/G]TGCATCTATACATAT | 252870 |
rs4159622 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Usp7 | Mm_Celera | 16:8750149 | ATGTAGCTCAGTGGC[A/G]GAACTCCTGCCCCGA | 252870 |
rs4159623 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8750350 | TGGTGTGAATGCATC[A/G]GTCAGAGCACAGTTT | 252870 |
rs4159624 | snp | A/C | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8750563 | CCAAACCAAACCAAA[A/C]CAAAACAAAAAAAAC | 252870 |
rs4159625 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Usp7 | Mm_Celera | 16:8751025 | AATTCTCCAAGTTTT[G/T]GGGGTTTTTAAGATC | 252870 |
rs4159626 | snp | G/T | 0.5 | 0 | intron-variant | Usp7 | Mm_Celera | 16:8751787 | AGAGATTATGCTACC[G/T]TAGCCTGGGGCCAGG | 252870 |
rs4159627 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8752600 | CATGATGATAATGGA[C/T]TCAACCTCTGAACCC | 252870 |
rs4159628 | snp | A/C | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8752675 | TGGTTATGGTGACTG[A/C]TCACAGAAGTAAAAC | 252870 |
rs4159629 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp7 | Mm_Celera | 16:8753240 | CACACAATAAATAAA[C/T]GTGATTTGAAAGTAA | 252870 |
rs4159630 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp7 | Mm_Celera | 16:8753600 | AAAAGTTCCAGGCCG[G/T]CTAGGGTTATGTAGT | 252870 |
rs4159631 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp7 | Mm_Celera | 16:8755331 | TGTTTGGTTTTGAAA[C/T]AGGATCTCACTCTGG | 252870 |
rs4159632 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp7 | Mm_Celera | 16:8755362 | AGCCACAGATGGCCT[C/T]GGGTTCACAATAGAC | 252870 |
rs4159633 | snp | A/C | 0.287335 | 0.247197 | upstream-variant-2KB | Usp7 | Mm_Celera | 16:8757115 | ACCTATGTCTCTCCG[A/C]TCCAGACTCCTACAC | 252870 |
rs4159634 | snp | A/G | 0.287335 | 0.247197 | upstream-variant-2KB | Usp7 | Mm_Celera | 16:8757418 | AGGGCTGGAAAGATC[A/G]CCTGTCTGCCCAAGC | 252870 |
rs4159635 | snp | A/G | 0.30839 | 0.243086 | upstream-variant-2KB | Usp7 | Mm_Celera | 16:8757655 | TATGTTATGTTAATG[A/G]CTGACTAAACAAATA | 252870 |
rs4159636 | snp | C/T | 0.46281 | 0.131194 | upstream-variant-2KB | Usp7 | Mm_Celera | 16:8757735 | TAAGGATCCCTTGGA[C/T]ATTGTGAAATCTGAA | 252870 |
rs4159637 | snp | A/G/T | 0.408163 | 0.193609 | upstream-variant-2KB | Usp7 | Mm_Celera | 16:8757847 | ACTTCAGGCGGGGAC[A/G/T]CACGCCTTTAATCCC | 252870 |
rs4159638 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB | Usp7 | Mm_Celera | 16:8758200 | AAACCCTGTCTCAAA[A/C]AAACAAACAAACAAA | 252870 |
rs4159639 | snp | A/G | 0.30839 | 0.243086 | upstream-variant-2KB | Usp7 | Mm_Celera | 16:8758268 | CAGGTACTAGGTTCC[A/G]TTCTCAGCAGAACAA | 252870 |