| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs584902541 | snp | A/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128255587 | CCTTTGATACTAACA[A/G]CTGGGAGGCAGAAGC | 67812 |
| rs585112333 | snp | C/T | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128252797 | TGGATCTCGTGGAGG[C/T]ATTTCCCCAACTGAA | 67812 |
| rs585127136 | snp | C/T | | | utr-variant-3-prime | Ubxn4 | GRCm38.p3 | 1:128279049 | GGGCGTGGTGGCGCA[C/T]GCCTTTAATCCCAGC | 67812 |
| rs585133314 | snp | C/T | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128252653 | CATGGAGGGATGTTA[C/T]TTATTGGCTTGCTTC | 67812 |
| rs585227032 | snp | A/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128260071 | TTGTAATCCTACCCT[A/G]AAACCTCTTAATATT | 67812 |
| rs585277298 | snp | A/C | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128268289 | TCGGAAAAAAAAAAT[A/C]ATTTGTATAGCTCAG | 67812 |
| rs585570689 | snp | A/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128255637 | CCTGGTCTATAGCAC[A/G]AGTTCCAGGACAGCC | 67812 |
| rs585582869 | snp | C/T | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128248218 | AACTTAACCGCCAGG[C/T]GTGGTGGTGCACGCC | 67812 |
| rs585650480 | snp | A/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128255839 | TATCTGAAGAACAGT[A/G]TAGAGTAGTTTACTG | 67812 |
| rs585654279 | snp | A/C | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128255634 | TCACCTGGTCTATAG[A/C]ACAAGTTCCAGGACA | 67812 |
| rs585690155 | snp | C/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128266133 | AGAGAAACCCTGTCT[C/G]GAAAAACAAACAAAA | 67812 |
| rs585830361 | snp | A/C | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128266054 | GGAGGCAGAGGCAGG[A/C]GGATTTCTGAGTTCG | 67812 |
| rs585836250 | snp | A/T | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128263557 | CTGTCTCGAAAAAAA[A/T]AAATAAATAAAATAA | 67812 |
| rs586107268 | snp | A/C | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128252736 | ATGGCACCACCCACA[A/C]GGGGCCTTTCCCCCA | 67812 |
| rs586188951 | snp | C/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128254540 | CTTTTCCTTTCCTTT[C/G]TCTTCTTTTCTTTTC | 67812 |
| rs586242439 | snp | C/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128262629 | CTCTTACCCACTGAG[C/G]CATCTCACCAGCCCC | 67812 |
| rs586348835 | snp | C/T | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128252878 | CCAATACAAGCCGGG[C/T]GTGGTGGTGCACGCC | 67812 |
| rs586586996 | snp | A/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128264012 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTTATATA | 67812 |
| rs586590857 | snp | A/C | | | upstream-variant-2KB | Ubxn4 | GRCm38.p3 | 1:128242079 | TGGTGTATGCCTTTA[A/C]TCCCAGCACTTGGGA | 67812 |
| rs586760765 | snp | A/G | | | missense | Ubxn4 | GRCm38.p3 | 1:128258973 | TGTGAGACACCAGCT[A/G]CCTCTGACACAAAGT | 67812 |
| rs586824425 | snp | A/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128256879 | ACAGGGTTTCTCTGT[A/G]TAGCCCTGGCTGTCC | 67812 |
| rs586928500 | snp | C/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128274248 | AAGTGTCTGAAGATA[C/G]CTATAGTGTCCTGAC | 67812 |
| rs586941270 | snp | A/T | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128251973 | CTCACAACTGTCATA[A/T]CCCCATTTCCAGGGG | 67812 |
| rs586990031 | snp | A/G | | | upstream-variant-2KB | Ubxn4, LOC105246702 | GRCm38.p3 | 1:128243669 | TTGGGGTTTTTGGTA[A/G]GTTGGTTGGTTGGTT | 67812 |
| rs587174554 | snp | C/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128261334 | ACTTTGGAGAGCAGT[C/G]AGTGCTCTTAACTGC | 67812 |
| rs587276238 | snp | A/C | | | synonymous-codon | Ubxn4 | GRCm38.p3 | 1:128269917 | TGGTTCTTCCTTTAC[A/C]AACCAGTTTCCTTCT | 67812 |
| rs587282974 | snp | C/T | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128248717 | ACACAGGCCCACACA[C/T]ACATAAAATATTTTT | 67812 |
| rs587340456 | snp | A/T | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128253662 | TCAGTCCTCTCTCCC[A/T]TCCCTGACCAGAAAA | 67812 |
| rs587373979 | snp | A/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128264899 | GTGAGCCTTCATGTG[A/G]TTATTGGGAATTGAA | 67812 |
| rs587423243 | snp | A/G | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128265061 | GTCTTCAGACACACC[A/G]GGAGAGGGAGTCAGA | 67812 |
| rs587429476 | snp | A/T | | | intron-variant, splice-acceptor-variant | Ubxn4, LOC105246702 | GRCm38.p3 | 1:128244761 | TTTTTTTTTTTTATA[A/T]GGCTCCAGGCTTGCT | 67812 |
| rs864256883 | snp | A/T | | | intron-variant | Ubxn4 | GRCm38.p3 | 1:128276914 | AACAGCTTTGCGTGG[A/T]TTGTATTTTATGTCA | 67812 |