SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346432145 | snp | C/T | | | missense | EDM2 | TAIR10 | 5:22451893 | TTCTTTGCTCTTTCA[C/T]GAAGACCTTCTGCTC | 835632 |
rs346484143 | snp | G/T | | | intron-variant | EDM2 | TAIR10 | 5:22449921 | CTATTTCAATGACAC[G/T]GGAGCTTACACAAAG | 835632 |
rs346494133 | snp | A/T | | | missense | EDM2 | TAIR10 | 5:22449791 | ATCTTTGGGCGGAAC[A/T]CAAGAGCCTTGGTAA | 835632 |
rs346495792 | snp | A/G | | | synonymous-codon | EDM2 | TAIR10 | 5:22452450 | AAAGTAGCCACAGGT[A/G]GCTGACACGCATTGG | 835632 |
rs346511688 | snp | A/G | | | intron-variant | EDM2 | TAIR10 | 5:22449958 | CTAAAGGAAATTTGT[A/G]TCTTACCAGCTTTGA | 835632 |
rs346518278 | snp | A/G | | | intron-variant | EDM2 | TAIR10 | 5:22452707 | CCATAAACAGCATTA[A/G]CATAGACTCCATGCC | 835632 |
rs346524125 | snp | A/G | | | intron-variant | EDM2 | TAIR10 | 5:22450691 | ACATCCTACATTTTA[A/G]GAGTCATCTCTCCTT | 835632 |
rs346547492 | snp | A/G | | | missense | EDM2 | TAIR10 | 5:22448564 | TCCGGTAGGAAAGGA[A/G]GATCCGGCATTCTAT | 835632 |
rs346617974 | snp | G/T | | | missense | EDM2 | TAIR10 | 5:22451557 | ACAACCTCTCACCCA[G/T]TGAAATCTTGCTTTT | 835632 |
rs346655254 | snp | A/T | | | intron-variant | EDM2 | TAIR10 | 5:22453507 | AGTACTCAAGTGGGA[A/T]AAAAGATTCGAACCT | 835632 |
rs346693451 | snp | C/G | | | missense | EDM2 | TAIR10 | 5:22448174 | TTAATCCAACCGCCA[C/G]ATCGACTCATATAAG | 835632 |
rs346700914 | snp | A/G | | | utr-variant-5-prime | EDM2 | TAIR10 | 5:22454789 | AATTGAGGAAAAAAA[A/G]AGAGTAAGAATCGTC | 835632 |
rs346701960 | snp | A/C | | | missense | EDM2 | TAIR10 | 5:22451060 | TGCTTTTGCATCCTC[A/C]ATGTTTCCTCCTTCC | 835632 |
rs346705560 | snp | C/G | | | missense | EDM2 | TAIR10 | 5:22452419 | GTAGCCGTCTTGTGA[C/G]ACAGTGAGGATGGTA | 835632 |
rs346747654 | snp | C/G | | | intron-variant | EDM2 | TAIR10 | 5:22453148 | ACACTAAATGTAAAA[C/G]CAAACGCTGGCATAA | 835632 |
rs346785607 | snp | A/G | | | synonymous-codon | EDM2 | TAIR10 | 5:22449172 | AGTTTCTACTGTGTC[A/G]ATTTTCTCAGAGACT | 835632 |
rs346797202 | snp | G/T | | | missense | EDM2 | TAIR10 | 5:22452312 | CTTAACCTCTCCGTT[G/T]TCACAGACACTGCAT | 835632 |
rs346840836 | snp | A/C | | | intron-variant | EDM2 | TAIR10 | 5:22450167 | TAGTAGGCACACACA[A/C]ACAAGTCATTACCTT | 835632 |
rs346852557 | snp | A/C | | | missense | EDM2 | TAIR10 | 5:22448475 | GATATTCTCTTTGAC[A/C]AATCCCTCTATCAAG | 835632 |
rs346913494 | snp | A/G | | | missense | EDM2 | TAIR10 | 5:22451808 | GAAGCTTTTCCACAA[A/G]TATCTTGTAAGGCAG | 835632 |
rs346927218 | snp | C/T | | | missense | EDM2 | TAIR10 | 5:22454368 | TAATTGGAAGCTGAT[C/T]GAGGAACAGAGAAGT | 835632 |
rs346949544 | snp | A/T | | | missense | EDM2 | TAIR10 | 5:22450879 | GTGCACCATGGAGAA[A/T]AGGAGCAAGATAAAC | 835632 |
rs346959853 | snp | C/T | | | missense | EDM2 | TAIR10 | 5:22454411 | CATCGTCAACGAACG[C/T]CATTCAATCCCAAAA | 835632 |
rs346988735 | snp | A/C | | | utr-variant-3-prime | EDM2 | TAIR10 | 5:22447971 | TCAAAAGTTTAAGAC[A/C]ATAGAAGCTGGCTTC | 835632 |
rs347006199 | snp | A/T | | | missense | EDM2 | TAIR10 | 5:22452066 | CTTACTGGCAATATA[A/T]GAGTACACGGTTGTG | 835632 |
rs347079079 | snp | G/T | | | intron-variant | EDM2 | TAIR10 | 5:22452934 | GGAATAATAACAGTG[G/T]ATCTTTAGAACCTTT | 835632 |
rs347095727 | snp | A/C | | | intron-variant | EDM2 | TAIR10 | 5:22452749 | ACCAAGACGCCCAGA[A/C]ATATTCAGAACTAAT | 835632 |
rs347139690 | snp | A/G | | | missense | EDM2 | TAIR10 | 5:22451623 | TTTTGCCAGCTTCAC[A/G]GGAGTCTTCCATCAT | 835632 |
rs347140563 | snp | C/T | | | intron-variant | EDM2 | TAIR10 | 5:22450771 | GTAACATACAGGATG[C/T]TTAGACCTAAATCTT | 835632 |
rs347146085 | snp | A/G | | | intron-variant | EDM2 | TAIR10 | 5:22453630 | GAATCAGGGTAAGAA[A/G]ATGATACATATACAG | 835632 |
rs347203617 | snp | A/G | | | synonymous-codon | EDM2 | TAIR10 | 5:22448236 | CCTTGGACTCATTTC[A/G]AAGTCACTAGGTGGT | 835632 |
rs347229830 | snp | A/T | | | intron-variant | EDM2 | TAIR10 | 5:22449898 | TAAACAGTCAGATAC[A/T]ACTCAAACTATTTCA | 835632 |
rs347270037 | snp | C/T | | | missense | EDM2 | TAIR10 | 5:22448832 | TACTTTTTGTCCTTG[C/T]TATTGCAGGCAGAGA | 835632 |
rs347273440 | snp | C/T | | | missense | EDM2 | TAIR10 | 5:22449015 | ACTCTCCTTGATCCT[C/T]TTCCATGTCATTGCT | 835632 |
rs347287392 | snp | A/T | | | missense | EDM2 | TAIR10 | 5:22449437 | TTCCAGTCTTCCAAT[A/T]GCTTGTCTTCTTCAT | 835632 |
rs347362949 | snp | A/G | | | missense | EDM2 | TAIR10 | 5:22449803 | AACTCAAGAGCCTTG[A/G]TAATAAACTTGTTTG | 835632 |
rs347389590 | snp | A/T | | | missense | EDM2 | TAIR10 | 5:22448290 | AGGATTTAAGAGATT[A/T]TGTCCGCTAGGTTGC | 835632 |
rs347399857 | snp | C/T | | | missense | EDM2 | TAIR10 | 5:22451598 | CGGGCTTCTTTTACT[C/T]CCAGCTTGTTTTTGC | 835632 |
rs347412733 | snp | C/T | | | missense | EDM2 | TAIR10 | 5:22449344 | TCCCTAGACAAATGG[C/T]AATGCTTCTCCGCTA | 835632 |
rs347485550 | snp | A/G | | | intron-variant | EDM2 | TAIR10 | 5:22453251 | CAAACTACAAGATCA[A/G]TATCCAGCAAGGAAA | 835632 |