F10G7.10
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs193325626snpA/T0.2500260.25missense?WS195II:4713847TGTGAATTCGTCATA[A/T]TGAACCATTGTGGAA173813
rs193325627snpC/G0.009950.0698283intron-variant, missense?WS195II:4717505TTGCAAAGAATTTGA[C/G]TGATTATATCAATGA173813
rs193325628snpA/T0.02969620.118179intron-variant?WS195II:4718143ATGTTGCTCGAATTC[A/T]TTAGTTTTTTTGTGG173813
rs193325629snpA/C0.01989850.097741missense?WS195II:4721068TCGCTGCTTTCTTCA[A/C]AGGATCCATTGGTGC173813
rs193325630snpG/T0.01980.0975088synonymous-codon?WS195II:4722824GCTCACATTCCACTG[G/T]GAATAGATTAGAGCG173813
rs193325631snpC/T0.01980.0975088synonymous-codon?WS195II:4722833CCACTGGGAATAGAT[C/T]AGAGCGGACATCTTG173813
rs193325632snpC/G0.01980.0975088synonymous-codon?WS195II:4722839GGAATAGATTAGAGC[C/G]GACATCTTGGCTTGT173813
rs193325633snpA/G0.01980.0975088synonymous-codon?WS195II:4722866TTGTGCACCATTTCT[A/G]ACCCACATATTGCAG173813
rs193325634snpA/G0.01980.0975088synonymous-codon?WS195II:4722875ATTTCTAACCCACAT[A/G]TTGCAGTTGATTTCG173813
rs193325635snpA/G0.01980.0975088synonymous-codon?WS195II:4722935GACGAGAAGAAGACG[A/G]ATCAGTGTCTCGTCA173813
rs193325636snpA/C0.01980.0975088missense?WS195II:4722974ATTCGATCGAATGTG[A/C]TCATAGAAGCCGTCG173813
rs193325637snpA/T0.4640770.129116intron-variant?WS195II:4723040TCTGGAAAGTTGGAA[A/T]TTGGAAAAAAAGGAG173813
rs193325638snpG/T0.4677710.122784intron-variant?WS195II:4723042TGGAAAGTTGGAAAT[G/T]GGAAAAAAAGGAGAA173813
rs193325639snpA/G0.4693910.119865intron-variant?WS195II:4723044GAAAGTTGGAAATTG[A/G]AAAAAAAGGAGAATA173813
rs193325640snpA/C0.05876950.161031intron-variant?WS195II:4723096GGTAAATTTGGTCCA[A/C]AAGTTGCGGCAAATT173813
rs193325641snpG/T0.01980.0975088synonymous-codon?WS195II:4723448TTCCTGTTGAATCGC[G/T]GCGACGATGTTGAAA173813
rs193325642snpA/G0.01980.0975088synonymous-codon?WS195II:4723454TTGAATCGCTGCGAC[A/G]ATGTTGAAAAGTGTG173813
rs193325643snpA/G0.01980.0975088synonymous-codon?WS195II:4723472GTTGAAAAGTGTGAC[A/G]GCTAGGGTTTCGAAT173813
rs193586508snpA/Gintron-variant?WS195II:4725030AATCCTTAAAAAAGT[A/G]AAATATTCTTACCCA173813
rs193586509snpC/Tintron-variant?WS195II:4725512TACAAAATTTTTGAC[C/T]AAAGTTTTGGTAAAT173813
rs353130777snpA/Tutr-variant-3-prime, intron-variant?WS195II:4718494ACTATTATTAAAATT[A/T]AAATTTAAATAAAAA173813
rs353131293snpA/Gintron-variant, missense?WS195II:4717370GATTTCAGACGAATG[A/G]GCATCTACAACCATC173813
rs353151852in-del-/Tintron-variant?WS195II:4715450CTGGGCTTCTCTTTA[-/T]TTTTTTTTGCACGAC173813
rs353162847snpA/Tintron-variant?WS195II:4726038TAACATATTTCATAA[A/T]GTTTGTTGAAACAAC173813
rs353166209snpA/Cintron-variant?WS195II:4724262CACTTGTTGGGAATA[A/C]AGTGACCACAAACTA173813
Full records
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