SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346424703 | snp | G/T | | | intron-variant | HAF01 | TAIR10 | 1:11855915 | GGTCATGAGCTAGCC[G/T]AAATGCACCAAACAC | 840169 |
rs346484635 | snp | A/T | | | intron-variant | HAF01 | TAIR10 | 1:11855763 | CCATTCTCTTCGTCA[A/T]CTAAGATCCTACAAA | 840169 |
rs346495324 | snp | A/G | | | missense | HAF01 | TAIR10 | 1:11853206 | TTCCTAGCTTCGTAA[A/G]TTCTCTTGATTCTGG | 840169 |
rs346496335 | snp | G/T | | | intron-variant | HAF01 | TAIR10 | 1:11853589 | GAATACACAGATCTA[G/T]CACATTCTTGCCAAA | 840169 |
rs346529930 | snp | G/T | | | intron-variant | HAF01 | TAIR10 | 1:11853640 | AGGAAAAGGTCTTTT[G/T]GTTTCAACACTTAGC | 840169 |
rs346532864 | snp | A/G | | | utr-variant-5-prime | HAF01 | TAIR10 | 1:11856663 | AAACCAGCTCAATCG[A/G]ACGAGACGGTACGAT | 840169 |
rs346627022 | snp | A/G | | | utr-variant-5-prime | HAF01 | TAIR10 | 1:11856643 | GTAAGCTTCGCCGGA[A/G]AGGTAAACCAGCTCA | 840169 |
rs346644478 | snp | C/G | | | missense | HAF01 | TAIR10 | 1:11852874 | TCTTGAGCCAAAAGA[C/G]TCCAACAGATTGGCA | 840169 |
rs346664559 | snp | A/G | | | synonymous-codon | HAF01 | TAIR10 | 1:11848972 | ATTTTCCAGATCTCC[A/G]GCAAAGGAGTCCAAG | 840169 |
rs346679637 | snp | C/T | | | missense | HAF01 | TAIR10 | 1:11847708 | TTGAGTTTGCTGATC[C/T]TAGATGTGGACTTAA | 840169 |
rs346685822 | snp | A/T | | | intron-variant | HAF01 | TAIR10 | 1:11846815 | ATATGAAAGCATGCT[A/T]CGTGGCTATAGAGCA | 840169 |
rs346687524 | snp | A/G | | | intron-variant | HAF01 | TAIR10 | 1:11853470 | AAAAAAAAAAAAAAG[A/G]AATGCTGAGACAACA | 840169 |
rs346688091 | snp | A/G | | | synonymous-codon | HAF01 | TAIR10 | 1:11848004 | CATATCTATGCCTTC[A/G]GGTTGTGATTCTGTA | 840169 |
rs346709429 | snp | A/G | | | utr-variant-5-prime | HAF01 | TAIR10 | 1:11856295 | AATGGTGACAATCGG[A/G]AGACGACAAGGCAAT | 840169 |
rs346717278 | snp | G/T | | | intron-variant | HAF01 | TAIR10 | 1:11848428 | AAGACATGCAAGACA[G/T]CATGGTTTGACACAA | 840169 |
rs346765091 | snp | A/G | | | intron-variant | HAF01 | TAIR10 | 1:11846817 | ATGAAAGCATGCTAC[A/G]TGGCTATAGAGCATT | 840169 |
rs346808128 | snp | A/G | | | intron-variant | HAF01 | TAIR10 | 1:11846792 | ACAAAGGTTGAGGTT[A/G]TGTAGACATATGAAA | 840169 |
rs346847389 | snp | A/T | | | synonymous-codon | HAF01 | TAIR10 | 1:11849122 | AGACATTCTCTGGCC[A/T]CGAGCATACTTGCCT | 840169 |
rs346897130 | snp | C/T | | | utr-variant-3-prime | ?, HAF01 | TAIR10 | 1:11846311 | GCTATTCGTACAAAA[C/T]AGTTAACTAAGCTAA | 840169 |
rs346910185 | snp | A/C | | | intron-variant | HAF01 | TAIR10 | 1:11849826 | CAAGAATAAACACGA[A/C]ACGACTTTTACGGAT | 840169 |
rs346944459 | snp | A/C | | | intron-variant | HAF01 | TAIR10 | 1:11849638 | ATGTGAGTATTGAAC[A/C]GGCCAAGTACAAAAG | 840169 |
rs346949759 | snp | C/T | | | intron-variant | HAF01 | TAIR10 | 1:11853956 | TCCTCCTGAATGTTT[C/T]GATGAGATCACTAAC | 840169 |
rs346966859 | snp | G/T | | | missense | HAF01 | TAIR10 | 1:11852721 | GCGCCCAAGGGCGTC[G/T]TTTTCAAGTCGCTTA | 840169 |
rs346978010 | snp | A/G | | | intron-variant | HAF01 | TAIR10 | 1:11849662 | ACAAAAGCATGAGCG[A/G]TGACTGATCAGAAGT | 840169 |
rs346991967 | snp | G/T | | | intron-variant | HAF01 | TAIR10 | 1:11849661 | TACAAAAGCATGAGC[G/T]ATGACTGATCAGAAG | 840169 |
rs347009382 | snp | A/C | | | intron-variant | HAF01 | TAIR10 | 1:11850233 | AACAGAGTGGTGTAT[A/C]AACCAATGAAATGAA | 840169 |
rs347048374 | snp | A/G | | | intron-variant | HAF01 | TAIR10 | 1:11854286 | AATTTGAGTGATGAG[A/G]TAACACAACAAAAGT | 840169 |
rs347051740 | snp | A/G | | | missense | HAF01 | TAIR10 | 1:11847265 | GTCTCCGCTCCAGAG[A/G]ATTCTCTGACAATCT | 840169 |
rs347095491 | snp | C/G | | | intron-variant | HAF01 | TAIR10 | 1:11854666 | CCAGGATTTGGTAGT[C/G]TAAATAGTGTCAGTA | 840169 |
rs347129450 | snp | A/G | | | intron-variant | HAF01 | TAIR10 | 1:11853469 | AAAAAAAAAAAAAAA[A/G]GAATGCTGAGACAAC | 840169 |
rs347133282 | snp | A/G | | | intron-variant | HAF01 | TAIR10 | 1:11855262 | TTAGCATTGGCACAG[A/G]TATGCTTGGTGGAGA | 840169 |
rs347147913 | snp | A/T | | | intron-variant | HAF01 | TAIR10 | 1:11851560 | AAAAACTAAACAAAG[A/T]TTCCAATTTGACTCT | 840169 |
rs347177291 | snp | A/G | | | synonymous-codon | HAF01 | TAIR10 | 1:11847578 | GGGTTGTCCAGAGAC[A/G]GAAGGCTTGTGTGAT | 840169 |
rs347246598 | snp | C/T | | | synonymous-codon | HAF01 | TAIR10 | 1:11850644 | GTTCACTAAATAAGT[C/T]TGTAGATTCTTTGAT | 840169 |
rs347272287 | snp | A/G | | | intron-variant | HAF01 | TAIR10 | 1:11855657 | GTTAACACTCTTGTT[A/G]AACTGCTAAATCCAA | 840169 |
rs347277825 | snp | A/C | | | intron-variant | HAF01 | TAIR10 | 1:11855384 | AACAAGGTCATCATA[A/C]TGAAAGCGTAAAACA | 840169 |
rs347304058 | snp | C/T | | | intron-variant | HAF01 | TAIR10 | 1:11855281 | GCTTGGTGGAGAATT[C/T]GCAACTCATAGTTAA | 840169 |
rs347333484 | snp | A/G | | | intron-variant | HAF01 | TAIR10 | 1:11851847 | ATCTGCAAAACAATT[A/G]TAGCAAGTGAGCTTC | 840169 |
rs347356094 | snp | C/T | | | intron-variant | HAF01 | TAIR10 | 1:11854347 | AAGAAACGGAAATTT[C/T]GAAATGCAAACCTGG | 840169 |
rs347370255 | snp | A/G | | | intron-variant | HAF01 | TAIR10 | 1:11850168 | ACCTAGGACAACAAA[A/G]TAGAGAATATTATGC | 840169 |
rs347425242 | snp | G/T | | | intron-variant | HAF01 | TAIR10 | 1:11855270 | GGCACAGGTATGCTT[G/T]GTGGAGAATTTGCAA | 840169 |
rs347441657 | snp | A/G | | | synonymous-codon | HAF01 | TAIR10 | 1:11851125 | GCAAACCTGTTGTCC[A/G]ACAACAACTATCTTG | 840169 |
rs347459112 | snp | C/G | | | synonymous-codon | HAF01 | TAIR10 | 1:11852394 | ATTAGTATTTGCCTG[C/G]AGTTGCTGAGAGCTT | 840169 |
rs347483763 | snp | A/G | | | utr-variant-5-prime | HAF01 | TAIR10 | 1:11856718 | CAAACTCTCAAATCG[A/G]AGGAAAAAAAAAAGT | 840169 |
rs347485371 | snp | C/T | | | missense | HAF01 | TAIR10 | 1:11855479 | CCAAGGTTAAAACCC[C/T]TGCTGTTGTCCTCAT | 840169 |