17 variations found. LOC_Os08g40690 (glycosyl hydrolase; putative; expressed), ranging from 25,762,456 bp to 25,763,824 bp (including 0 kb upstream and 0 kb downstream of the gene).
Color | Explain | Details |
---|---|---|
red | High impact variants defined by snpEff | 'STOP_LOST', 'START_LOST', 'STOP_GAINED', 'FRAME_SHIFT' et. al., the details can be found at http://snpef f.sourceforge.net/SnpEff_manual.html#eff. |
purple | 'Damaging' or 'probably damaging' non-synonymous SNPs defined by PolyPhen-2 | This is a qualitative result of nonsynonymous SNP annotation, where 'damaging' or 'probably damaging' means that the variant is more likely to affect protein function. Details can be found here. |
Var ID | Chrom | Position | Primary Allele | Secondary Allele | Primary Allele Frequency | DEL Frequency | Var | GWAS Results | Effect |
---|---|---|---|---|---|---|---|---|---|
vg0825762457 (J) | chr08 | 25762457 | AC | CC | 87.10% | 2.52% | AC -> CC,ACCCCCC ,ACCCCCCC, A,ACCCCCCC CC | NA |
LOC_Os08g40690.1 Alt: ACCCCCC| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g40680.1 Alt: ACCCCCC| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: ACCCCCC| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) N Alt: DEL/silent_mutation(CooVar) LOC_Os08g40690.1 Alt: ACCCCCCCCC| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40680.1 Alt: ACCCCCCCCC| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: ACCCCCCCCC| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40690.1 Alt: CC| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40680.1 Alt: CC| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: CC| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40690.1 Alt: A| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40680.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40690.1 Alt: ACCCCCCC| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40680.1 Alt: ACCCCCCC| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: ACCCCCCC| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) The average chromatin accessibility score: 75.556; most accessible tissue: Callus, score: 94.222 |
vg0825762464 (J) | chr08 | 25762464 | A | C | 94.90% | 2.56% | A -> C | NA |
LOC_Os08g40690.1 Alt: C| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g40680.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) N Alt: DEL/silent_mutation(CooVar) The average chromatin accessibility score: 76.144; most accessible tissue: Callus, score: 94.222 |
vg0825762465 (J) | chr08 | 25762465 | A | C | 94.90% | 2.62% | A -> C | NA |
LOC_Os08g40690.1 Alt: C| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g40680.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) N Alt: DEL/silent_mutation(CooVar) The average chromatin accessibility score: 76.241; most accessible tissue: Callus, score: 94.222 |
vg0825762467 (J) | chr08 | 25762467 | A | C | 97.80% | 0.95% | A -> C | NA |
LOC_Os08g40690.1 Alt: C| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g40680.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) N Alt: DEL/silent_mutation(CooVar) The average chromatin accessibility score: 76.097; most accessible tissue: Callus, score: 94.222 |
vg0825762477 (J) | chr08 | 25762477 | T | A | 69.70% | 0.00% | T -> A | NA |
LOC_Os08g40690.1 Alt: A| 5_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g40680.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: A| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) The average chromatin accessibility score: 77.110; most accessible tissue: Callus, score: 94.222 |
vg0825762523 (J) | chr08 | 25762523 | G | C | 98.80% | 0.00% | G -> C | NA |
LOC_Os08g40690.1 Alt: C| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 76.006; most accessible tissue: Callus, score: 94.222 |
vg0825762827 (J) | chr08 | 25762827 | C | A | 93.80% | 0.00% | C -> A |
mr1073 (All); LR P-value: 5.06E-06;
mr1113 (All); LR P-value: 4.38E-15; mr1114 (All); LR P-value: 2.98E-18; mr1117 (All); LR P-value: 2.45E-20; mr1119 (All); LR P-value: 3.52E-18; mr1123 (All); LR P-value: 1.41E-23; mr1126 (All); LR P-value: 2.30E-06; mr1153 (All); LR P-value: 9.29E-06; mr1240 (All); LR P-value: 2.78E-17; mr1262 (All); LR P-value: 2.10E-08; mr1348 (All); LR P-value: 1.60E-09; mr1365 (All); LR P-value: 3.80E-07; mr1409 (All); LR P-value: 1.86E-11; mr1417 (All); LR P-value: 1.43E-06; mr1496 (All); LR P-value: 5.97E-15; mr1522 (All); LR P-value: 4.75E-12; mr1549 (All); LR P-value: 9.29E-41; mr1550 (All); LR P-value: 1.20E-53; mr1757 (All); LR P-value: 4.20E-43; mr1762 (All); LR P-value: 4.42E-07; mr1774 (All); LR P-value: 6.21E-06; mr1931 (All); LR P-value: 4.33E-08; mr1961 (All); LR P-value: 2.23E-20; mr1549_2 (All); LR P-value: 4.38E-37; mr1550_2 (All); LR P-value: 6.01E-56; mr1757_2 (All); LR P-value: 1.41E-30 |
LOC_Os08g40690.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 74.874; most accessible tissue: Minghui63 panicle, score: 91.227 |
vg0825762961 (J) | chr08 | 25762961 | T | C | 98.80% | 0.00% | T -> C | NA |
LOC_Os08g40690.1 Alt: C| missense_variant MODERATE(snpEff)/nonsynonymous_codon(CooVar)
The average chromatin accessibility score: 77.062; most accessible tissue: Minghui63 panicle, score: 91.586 |
vg0825762997 (J) | chr08 | 25762997 | C | G | 99.90% | 0.00% | C -> G | NA |
LOC_Os08g40690.1 Alt: G| missense_variant MODERATE(snpEff)
LOC_Os08g40680.1 Alt: G| upstream_gene_variant MODIFIER(snpEff) LOC_Os08g40700.1 Alt: G| upstream_gene_variant MODIFIER(snpEff) LOC_Os08g40710.1 Alt: G| downstream_gene_variant MODIFIER(snpEff) The average chromatin accessibility score: 77.558; most accessible tissue: Minghui63 panicle, score: 91.227 |
vg0825763134 (J) | chr08 | 25763134 | A | C | 99.40% | 0.00% | A -> C | NA |
LOC_Os08g40690.1 Alt: C| missense_variant MODERATE(snpEff)
LOC_Os08g40680.1 Alt: C| upstream_gene_variant MODIFIER(snpEff) LOC_Os08g40700.1 Alt: C| upstream_gene_variant MODIFIER(snpEff) LOC_Os08g40710.1 Alt: C| downstream_gene_variant MODIFIER(snpEff) The average chromatin accessibility score: 74.735; most accessible tissue: Minghui63 panicle, score: 89.702 |
vg0825763345 (J) | chr08 | 25763345 | C | T | 99.70% | 0.00% | C -> T | NA |
LOC_Os08g40690.1 Alt: T| missense_variant MODERATE(snpEff)
LOC_Os08g40680.1 Alt: T| upstream_gene_variant MODIFIER(snpEff) LOC_Os08g40700.1 Alt: T| upstream_gene_variant MODIFIER(snpEff) LOC_Os08g40710.1 Alt: T| downstream_gene_variant MODIFIER(snpEff) The average chromatin accessibility score: 71.382; most accessible tissue: Minghui63 panicle, score: 86.012 |
vg0825763424 (J) | chr08 | 25763424 | G | A | 78.20% | 0.00% | G -> A |
LOC_Os08g40690.1 Alt: A| synonymous_variant LOW(snpEff)/synonymous_codon(CooVar)
The average chromatin accessibility score: 68.702; most accessible tissue: Minghui63 panicle, score: 87.238 |
|
vg0825763579 (J) | chr08 | 25763579 | T | C | 98.00% | 0.00% | T -> C | NA |
LOC_Os08g40690.1 Alt: C| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g40680.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: C| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40710.1 Alt: C| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) The average chromatin accessibility score: 66.716; most accessible tissue: Minghui63 panicle, score: 88.595 |
vg0825763600 (J) | chr08 | 25763600 | GT | G | 99.10% | 0.00% | GT -> G,GTT | NA |
LOC_Os08g40690.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g40680.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40710.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40690.1 Alt: GTT| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40680.1 Alt: GTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: GTT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40710.1 Alt: GTT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) The average chromatin accessibility score: 67.329; most accessible tissue: Minghui63 panicle, score: 89.949 |
vg0825763614 (J) | chr08 | 25763614 | T | G | 99.60% | 0.00% | T -> G | NA |
LOC_Os08g40690.1 Alt: G| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g40680.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: G| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40710.1 Alt: G| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) The average chromatin accessibility score: 67.046; most accessible tissue: Minghui63 panicle, score: 89.949 |
vg0825763675 (J) | chr08 | 25763675 | C | CT | 98.80% | 0.00% | C -> CT | NA |
LOC_Os08g40690.1 Alt: CT| 3_prime_UTR_variant MODIFIER(snpEff)/silent_mutation(CooVar)
LOC_Os08g40680.1 Alt: CT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40700.1 Alt: CT| upstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) LOC_Os08g40710.1 Alt: CT| downstream_gene_variant MODIFIER(snpEff)/silent_mutation(CooVar) The average chromatin accessibility score: 63.417; most accessible tissue: Callus, score: 91.712 |
STR0825763675 (J) | chr08 | 25763675 | C | CT | 98.40% | 0.00% | C -> CT | NA |
|