SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs30274964 | snp | A/G | 0.32 | 0.24 | intron-variant | Fchsd1 | Mm_Celera | 18:37960285 | CACTAGAATATTTTA[A/G]AAATGCTGAGTATTG | 319262 |
rs31752254 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fchsd1 | Mm_Celera | 18:37968128 | TCTACCTTCAGCTCA[C/T]GTGCCTTCCCCTGCT | 319262 |
rs31752255 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37967290 | GGCTTGACCTAATCT[C/T]TTACTTTTATGCCAC | 319262 |
rs31752256 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37967277 | AATCTGTATACTTGG[C/T]TTGACCTAATCTCTT | 319262 |
rs31752257 | snp | C/T | 0.124444 | 0.216185 | missense, upstream-variant-2KB, nc-transcript-variant | Fchsd1 | Mm_Celera | 18:37966452 | TGGCCTTGAGCAGTG[C/T]TGGCAATTCCTCTTG | 319262 |
rs31752258 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37966128 | TGGGGCCCGGACATG[A/C]AGGATAGGGAAGAGA | 319262 |
rs31752259 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fchsd1 | Mm_Celera | 18:37965569 | TCATCAAATCAATAC[C/T]GGGATGGGAACAATG | 319262 |
rs31752260 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fchsd1 | Mm_Celera | 18:37965465 | GGGTGGATGAAGAGA[A/G]CAGGACTGACTTCCA | 319262 |
rs31752261 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fchsd1 | Mm_Celera | 18:37965442 | ACACAGGCCCAGGAA[C/T]GGGATCAGGGTGGAT | 319262 |
rs31752262 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, missense, nc-transcript-variant | Fchsd1 | Mm_Celera | 18:37964803 | CACCCGATGCCCGTG[A/G]TGCTGGATCTTGTAG | 319262 |
rs31752263 | snp | G/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Fchsd1 | Mm_Celera | 18:37964352 | TCACTTCCTGTAGCC[G/T]CTGTTCTACGCCTGG | 319262 |
rs31752914 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Fchsd1 | Mm_Celera | 18:37964237 | TGCTTCCCTCTTTTT[C/T]CCTCCCATGGTGAAG | 319262 |
rs31752915 | snp | C/T | 0.32 | 0.24 | intron-variant | Fchsd1 | Mm_Celera | 18:37964196 | CAAAAGAGAGTAGTA[C/T]GTCCTGGCTAGTTGG | 319262 |
rs31752916 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fchsd1 | Mm_Celera | 18:37963954 | TCTGGCTTCTAACAA[A/G]GAATTTTAGCTTCCC | 319262 |
rs31752917 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fchsd1 | Mm_Celera | 18:37963922 | GAATTAGACACTGTG[C/G]TTCCCATTTTAGGGG | 319262 |
rs31752918 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fchsd1 | Mm_Celera | 18:37963504 | CTCTACGGGACACTG[G/T]GAATCTCCTTCAAGA | 319262 |
rs31752919 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fchsd1 | Mm_Celera | 18:37963494 | CCTATCTTAACTCTA[C/T]GGGACACTGTGAATC | 319262 |
rs31752920 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Fchsd1 | GRCm38.p3 | 18:37963392 | AGCTTCCTCACATTC[A/G]TCGAAGTCAGAAAGC | 319262 |
rs31752921 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon, nc-transcript-variant | Fchsd1 | Mm_Celera | 18:37963197 | TGTGATGGTCAGCTC[A/G]TCCTCACGTCCTGCC | 319262 |
rs31752922 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fchsd1 | Mm_Celera | 18:37963070 | GTGAACAGGTTATCA[A/G]ACTTGCTTAGCACTC | 319262 |
rs31752923 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon, nc-transcript-variant | Fchsd1 | Mm_Celera | 18:37963014 | CTCAGGGACAAAGCC[C/T]GCTTCACCGTGCTGG | 319262 |
rs31753664 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Fchsd1 | Mm_Celera | 18:37962987 | GGAGAGATCCGGGAA[A/G]TTGAGATATCGCTCA | 319262 |
rs31753665 | snp | C/T | 0.142012 | 0.225474 | intron-variant, downstream-variant-500B | Fchsd1 | Mm_Celera | 18:37962852 | TGTACACCAGCGCCA[C/T]GACACCCCAGAACCA | 319262 |
rs31753666 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Fchsd1 | Mm_Celera | 18:37962503 | CTCTAATGTTAATAC[A/G]GAGCGTCGCTGAGGT | 319262 |
rs31753667 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fchsd1 | Mm_Celera | 18:37962430 | TTTTCTCTTTCCAAC[C/G]AAAGCACACAGAGAG | 319262 |
rs31753668 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Fchsd1 | Mm_Celera | 18:37961218 | TTACCGCTGCTGATG[C/T]TCCCCAGCCTCGGCT | 319262 |
rs31753669 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fchsd1 | Mm_Celera | 18:37961188 | GCAGGCGAAGGCGGA[A/G]TCCAAGCCTCTTCCT | 319262 |
rs31753670 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Fchsd1 | Mm_Celera | 18:37961184 | CAGGGCAGGCGAAGG[C/T]GGAGTCCAAGCCTCT | 319262 |
rs31753671 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Fchsd1 | Mm_Celera | 18:37961164 | TGCAAGTGCACAAGG[A/G]CACACAGGGCAGGCG | 319262 |
rs31753672 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fchsd1 | Mm_Celera | 18:37961024 | GGATAACAACACAAA[A/G]CATGGACCAAGGACC | 319262 |
rs31753673 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fchsd1 | Mm_Celera | 18:37960364 | TATGTATGTGTGCCT[C/G]GCATGAACATGATCC | 319262 |
rs31754514 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Fchsd1 | Mm_Celera | 18:37960289 | AGAATATTTTAGAAA[G/T]GCTGAGTATTGGATG | 319262 |
rs31754515 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fchsd1 | Mm_Celera | 18:37960265 | GGTGACTGAGAAGGT[A/G]GGCACACTAGAATAT | 319262 |
rs31754516 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fchsd1 | Mm_Celera | 18:37960227 | ATGCTAGAAGAGATG[A/G]TGGTGCCCCTGAAGT | 319262 |
rs31754517 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fchsd1 | Mm_Celera | 18:37960089 | AAATGCCTATTGAGA[A/G]TCCCATAATATCACA | 319262 |
rs31754518 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Fchsd1 | Mm_Celera | 18:37960056 | AAGAAATGGAGTGAC[C/G]TGCAAATCTGCCCCT | 319262 |
rs31754519 | snp | A/G | 0.32 | 0.24 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Rell2, Fchsd1 | GRCm38.p3 | 18:37959553 | AGCGTGGAGACAGGG[A/G]CAGCAGCATCACTGG | 319262 |
rs31754520 | snp | A/G | 0.132653 | 0.220748 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Rell2, Fchsd1 | Mm_Celera | 18:37959480 | TGAGAACGGACATCG[A/G]GAAAGATTGCAGCTT | 319262 |
rs31754521 | snp | A/G | 0.142012 | 0.225474 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Rell2, Fchsd1 | Mm_Celera | 18:37959304 | AGATGAGCCAGAGCC[A/G]TGCAAGGCTTTGGGA | 319262 |
rs31754522 | snp | A/T | 0.260355 | 0.249785 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Rell2, Fchsd1 | Mm_Celera | 18:37959219 | TCCAAGGTCTGCTCC[A/T]CTCCTGGCCCCAGGC | 319262 |
rs31754523 | snp | C/G | 0.260355 | 0.249785 | utr-variant-3-prime, downstream-variant-500B | Rell2, Fchsd1 | Mm_Celera | 18:37958899 | GAGATACATGGTCCC[C/G]GGCTGAGAGCCCTCA | 319262 |
rs31755314 | snp | A/G | 0.336735 | 0.234472 | utr-variant-3-prime, downstream-variant-500B | Rell2, Fchsd1 | Mm_Celera | 18:37958868 | TCAGTTGAGGGACCA[A/G]CTCTACTTCCATCTG | 319262 |
rs31755315 | snp | C/T | 0.32 | 0.24 | intron-variant, utr-variant-3-prime, downstream-variant-500B | Rell2, Fchsd1 | GRCm38.p3 | 18:37958735 | GACTAGGCAACAACA[C/T]TGCTTCCCTTCCTTT | 319262 |
rs31755316 | snp | A/G | 0.336735 | 0.234472 | intron-variant, downstream-variant-500B | Rell2, Fchsd1 | Mm_Celera | 18:37957288 | CTAACTGATCTATGA[A/G]AGAAGTTTTGTAGCA | 319262 |
rs31755317 | snp | C/T | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Rell2, Fchsd1 | Mm_Celera | 18:37957190 | TGACTTAGCTTACCT[C/T]GGAGTACCGTCTCCT | 319262 |
rs31755318 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, synonymous-codon, downstream-variant-500B | Hdac3, Rell2, Fchsd1 | Mm_Celera | 18:37956954 | TGACGTGAATGAGGA[C/T]ACAGTAGAGCGGATT | 319262 |
rs31757429 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37971791 | ACTCAGGAAACTCAA[A/G]AGCCACCGGAATTGC | 319262 |
rs31757430 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37971768 | TGATAAAAGAAATAC[A/G]TGTGGCGACTCAGGA | 319262 |
rs31757431 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37971724 | AAAGCCATTACATTG[A/C]GAAAAAGGGTTTCCT | 319262 |
rs31757432 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37971378 | AGAAAATTCAATCAG[A/G]AGAAAGTGAGACAAA | 319262 |
rs31757433 | snp | A/G | 0.426035 | 0.177515 | upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37970548 | CTAGCCCCTCAGTGT[A/G]CATTTTATTTTATCC | 319262 |
rs31758204 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37970232 | TTCGCAGAAACGAGT[C/T]CAGAGGAAAAAGACG | 319262 |
rs31758205 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37970069 | TGCTTATCACCAGTC[C/T]CTACACTAAACGCAG | 319262 |
rs31758206 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37969862 | GCGGAAGAACACAGG[A/G]GCAGCAGCAGTGGAA | 319262 |
rs31758207 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Fchsd1 | Mm_Celera | 18:37969509 | CCCCACTCCTGCGGC[A/G]TGGGGACCTACAAAA | 319262 |
rs31758208 | snp | A/C | 0.48 | 0.0979796 | synonymous-codon, nc-transcript-variant | Fchsd1 | GRCm38.p3 | 18:37969432 | CAAAAAGCGAAGTTT[A/C]ACCTCCTGGGCTGGC | 319262 |
rs31758209 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fchsd1 | Mm_Celera | 18:37969283 | CCCAACCCTGACAGA[A/T]GTATATTGAGGAAAG | 319262 |
rs31758210 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fchsd1 | Mm_Celera | 18:37969150 | AGGAGAGAGTGGTGT[A/G]AAGTCAAGTGGTTTG | 319262 |
rs31758211 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fchsd1 | Mm_Celera | 18:37969076 | CTAATACCTGGCTCC[A/G]TCACTTCCAACAGGT | 319262 |
rs31758212 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fchsd1 | Mm_Celera | 18:37968848 | TTGGCTACTGTTTTT[C/T]CACACTCAAGTCTCT | 319262 |
rs31758213 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Fchsd1 | Mm_Celera | 18:37968768 | GCCATACTCCCGTTC[A/G]ATGGCTGCCCTTTGC | 319262 |
rs31759014 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fchsd1 | Mm_Celera | 18:37968733 | AAGGAGGCTAGAACA[C/G]GAGAGGAGTCCCATA | 319262 |
rs31759015 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Fchsd1 | Mm_Celera | 18:37968165 | GTCCTTGTCCCCACA[C/G]ATCTCTAGGGGCTGA | 319262 |
rs46336660 | snp | C/T | | | intron-variant | Fchsd1 | Mm_Celera | 18:37960853 | GCCAACTCCCTAGCC[C/T]CTGATAACAATTCAA | 319262 |
rs50470732 | snp | C/T | | | intron-variant | Fchsd1 | Mm_Celera | 18:37961581 | CCTCTTCTGGTGTGT[C/T]TGAAGACAGCTACCG | 319262 |
rs211745039 | snp | A/G | | | intron-variant, utr-variant-3-prime | Rell2, Fchsd1 | Mm_Celera | 18:37957789 | GGTGGGGATATAGTA[A/G]TCCAAGAAAAGGGAG | 319262 |
rs211839946 | snp | G/T | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Fchsd1 | Mm_Celera | 18:37966522 | TAGCAGGTACTCATT[G/T]CGGGCTGCTCTCAGC | 319262 |
rs212117680 | snp | C/G | | | intron-variant | Fchsd1 | Mm_Celera | 18:37969633 | CCCTGTGACCCACCC[C/G]GAGTCGAGAGCCCAC | 319262 |
rs212158904 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Rell2, Fchsd1 | Mm_Celera | 18:37959010 | CAAAACCTCGCTCCA[C/T]ATGCTAGAGCGTGGC | 319262 |
rs212227184 | snp | A/C | | | intron-variant, upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37967094 | TGTTCTCACTGTATC[A/C]CCGGGGTGGAACACT | 319262 |
rs212652746 | snp | A/G | | | intron-variant | Fchsd1 | Mm_Celera | 18:37960058 | GAAATGGAGTGACGT[A/G]CAAATCTGCCCCTCA | 319262 |
rs212774981 | snp | A/G | | | upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37971078 | AAGACAGGCTACAAT[A/G]ATATGAAGGGTGGGC | 319262 |
rs212949918 | snp | G/T | | | intron-variant, downstream-variant-500B | Fchsd1 | Mm_Celera | 18:37962565 | AGAGAAAATGAAGCT[G/T]CACCTACCTGTTCAG | 319262 |
rs213167533 | snp | C/T | | | intron-variant | Fchsd1 | Mm_Celera | 18:37961649 | CAGAGCAAGCTGGAG[C/T]GAGCAAAGGTCCTAA | 319262 |
rs213755928 | snp | A/G | | | upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37969882 | CAGCAGTGGAACTCA[A/G]CCTGTTATTGCTTTG | 319262 |
rs213832817 | snp | G/T | | | intron-variant | Fchsd1 | Mm_Celera | 18:37961561 | CCTGTAATGAGATCT[G/T]ACACCCTCTTCCAGT | 319262 |
rs214096954 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37965840 | TAGAACTGCATGTCA[-/G]GGGGGGGTGGGGGGG | 319262 |
rs214122379 | snp | G/T | | | upstream-variant-2KB | Fchsd1 | GRCm38.p3 | 18:37970932 | GGCTCACAACCATCC[G/T]TAATGAGATCTGATG | 319262 |
rs214587638 | snp | A/G | | | intron-variant | Fchsd1 | Mm_Celera | 18:37965324 | CCTTTGTAAGAACAA[A/G]TGCTTAACCACTGAG | 319262 |
rs214676242 | snp | A/C | | | intron-variant | Fchsd1 | Mm_Celera | 18:37963545 | CAACCAATTATAATG[A/C]ATCATAACCAAAACC | 319262 |
rs214829232 | snp | C/T | | | intron-variant, downstream-variant-500B | Fchsd1 | Mm_Celera | 18:37962880 | CCACCCAGTAACCTG[C/T]ATACCCCTGGTCTCT | 319262 |
rs215042994 | snp | A/G | | | synonymous-codon, downstream-variant-500B | Fchsd1 | GRCm38.p3 | 18:37962780 | GTAGCTGTACAGAGC[A/G]CGTGCCAAGAATGCT | 319262 |
rs215100640 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B | Rell2, Fchsd1 | Mm_Celera | 18:37958852 | TGGACAGCTCTGCCC[C/G]TCAGTTGAGGGACCA | 319262 |
rs215653835 | snp | C/T | | | intron-variant | Fchsd1 | Mm_Celera | 18:37964747 | AATGGTCCCTATCAC[C/T]CAGCTTTTCTTACCC | 319262 |
rs215673764 | snp | A/G | | | intron-variant | Fchsd1 | Mm_Celera | 18:37964939 | GGAATGCTTGAGGGG[A/G]AAAAAAAAACAACAA | 319262 |
rs215993010 | snp | A/G | | | intron-variant | Fchsd1 | Mm_Celera | 18:37965495 | ATCTGAGATGTGCTT[A/G]TGTTCAGAGGGGAGG | 319262 |
rs216226247 | snp | C/T | | | missense, utr-variant-3-prime, downstream-variant-500B | Rell2, Fchsd1 | Mm_Celera | 18:37958336 | CCAAGCCCAGGGCTG[C/T]CTAGTCAAGAAGCAA | 319262 |
rs216424948 | snp | G/T | | | intron-variant | Fchsd1 | Mm_Celera | 18:37964628 | ACTCACAAGCAACAG[G/T]AGAGACTACAAACCC | 319262 |
rs216481813 | snp | A/G | | | intron-variant | Fchsd1 | Mm_Celera | 18:37963593 | TACTAAATAATAGCG[A/G]TTACAACAACTAGGT | 319262 |
rs216510278 | in-del | -/AG | | | intron-variant | Fchsd1 | GRCm38.p3 | 18:37960138 | AACACACACACACAC[-/AG]AGAGAGAGAGAGAGA | 319262 |
rs216740767 | snp | C/T | | | intron-variant | Fchsd1 | Mm_Celera | 18:37961060 | AGTTAAGTCTCCCAC[C/T]TCAAGTCATACAGCA | 319262 |
rs216909051 | snp | C/T | | | intron-variant, upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37966982 | ACCTGTTCAGGGAGG[C/T]CTCCCTTCTCACTGG | 319262 |
rs216964510 | snp | C/T | | | intron-variant | Fchsd1 | Mm_Celera | 18:37965555 | CCAAGGCTGAACAGT[C/T]ATCAAATCAATACCG | 319262 |
rs216986843 | snp | C/G | | | intron-variant, utr-variant-3-prime | Rell2, Fchsd1 | Mm_Celera | 18:37957874 | TCCTCTGAATTTCCT[C/G]TAGGCAACTACAGCA | 319262 |
rs217144209 | snp | C/T | | | intron-variant, utr-variant-3-prime, downstream-variant-500B | Rell2, Fchsd1 | Mm_Celera | 18:37958733 | TTGACTAGGCAACAA[C/T]ACTGCTTCCCTTCCT | 319262 |
rs217358016 | snp | A/C | | | intron-variant | Fchsd1 | Mm_Celera | 18:37960123 | AGACAGACAGACACA[A/C]ACACACACACACACA | 319262 |
rs217358046 | snp | A/G | | | upstream-variant-2KB | Fchsd1 | Mm_Celera | 18:37970701 | GTTCTCAAGGCTAAC[A/G]TTCAGCCTTCTTGCT | 319262 |
rs217401354 | snp | A/T | | | intron-variant | Fchsd1 | Mm_Celera | 18:37969657 | AGCCCACGGCCTCCC[A/T]CCGCTCCCCTAGACC | 319262 |
rs217417735 | snp | C/T | | | intron-variant | Fchsd1 | Mm_Celera | 18:37960985 | AGTGCTCGTTCAAGG[C/T]TAGCCCTAGCTCCAA | 319262 |
rs217528405 | snp | A/G | | | intron-variant | Fchsd1 | Mm_Celera | 18:37968693 | GGTGGTTGGGGTTGG[A/G]TGGGGTGGATCTGCT | 319262 |