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Mutant Information |
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Mutant Name | FN760-S [Download] |
Generation | M2 |
Genus Species | Oryza Sativa |
Cultivar | Kitaake |
Alignment File (BAM File) | Download FN760-S Alignment File |
Seed Availability | Yes [Order Seeds] |
Mapping (Hover to Zoom-In) | ![]() |
Variant Information |
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Single base substitutions: 34
Variant Type | Chromosome | Position | Change | Genotype | Effect | Gene Affected |
---|---|---|---|---|---|---|
SBS | Chr1 | 11378199 | A-G | HOMO | INTERGENIC | |
SBS | Chr1 | 15412690 | C-A | HOMO | INTERGENIC | |
SBS | Chr1 | 24414941 | G-A | HET | INTERGENIC | |
SBS | Chr1 | 30997343 | G-C | HOMO | INTERGENIC | |
SBS | Chr1 | 31678330 | A-G | HOMO | UTR_3_PRIME | |
SBS | Chr1 | 40928325 | T-C | HOMO | INTRON | |
SBS | Chr10 | 11679274 | C-T | HET | NON_SYNONYMOUS_CODING | LOC_Os10g22540 |
SBS | Chr10 | 20816287 | C-T | HET | INTERGENIC | |
SBS | Chr10 | 8225787 | C-T | HET | NON_SYNONYMOUS_CODING | LOC_Os10g16490 |
SBS | Chr11 | 14449195 | A-T | HET | INTRON | |
SBS | Chr11 | 20097264 | A-T | HET | INTERGENIC | |
SBS | Chr11 | 20117249 | C-A | HET | INTERGENIC | |
SBS | Chr11 | 8487238 | T-G | HET | INTRON | |
SBS | Chr12 | 11942789 | C-T | HET | NON_SYNONYMOUS_CODING | LOC_Os12g20450 |
SBS | Chr12 | 16712311 | T-A | HET | NON_SYNONYMOUS_CODING | LOC_Os12g28270 |
SBS | Chr2 | 115824 | A-T | HOMO | INTERGENIC | |
SBS | Chr2 | 14682026 | C-G | HET | NON_SYNONYMOUS_CODING | LOC_Os02g25230 |
SBS | Chr3 | 10924591 | A-G | HET | INTRON | |
SBS | Chr3 | 12141160 | T-G | HOMO | INTERGENIC | |
SBS | Chr3 | 18059351 | G-A | HOMO | INTERGENIC | |
SBS | Chr3 | 3195715 | T-C | HET | UTR_3_PRIME | |
SBS | Chr4 | 13215787 | G-A | HOMO | INTRON | |
SBS | Chr4 | 22948944 | G-A | HET | INTRON | |
SBS | Chr4 | 3182909 | C-T | HET | NON_SYNONYMOUS_CODING | LOC_Os04g06120 |
SBS | Chr5 | 102459 | A-G | HET | INTRON | |
SBS | Chr5 | 7758900 | G-A | HOMO | INTERGENIC | |
SBS | Chr5 | 7758901 | T-A | HOMO | INTERGENIC | |
SBS | Chr5 | 8051638 | A-T | HOMO | INTERGENIC | |
SBS | Chr6 | 5056931 | A-T | HOMO | INTERGENIC | |
SBS | Chr7 | 10207958 | A-C | HOMO | INTRON | |
SBS | Chr7 | 2054911 | T-G | HET | NON_SYNONYMOUS_CODING | LOC_Os07g04630 |
SBS | Chr8 | 18591928 | G-A | HOMO | INTERGENIC | |
SBS | Chr8 | 19440631 | C-T | HOMO | INTERGENIC | |
SBS | Chr9 | 12662477 | T-C | HET | INTERGENIC |
Deletions: 17
Variant Type | Chromosome | Start | End | Size (bp) | Number of Genes |
---|---|---|---|---|---|
Deletion | Chr6 | 2579903 | 2579923 | 20 | |
Deletion | Chr5 | 8052514 | 8052527 | 13 | |
Deletion | Chr11 | 9250359 | 9250450 | 91 | |
Deletion | Chr11 | 10418339 | 10418350 | 11 | |
Deletion | Chr11 | 10637017 | 10637019 | 2 | |
Deletion | Chr7 | 10786108 | 10786121 | 13 | LOC_Os07g18190 |
Deletion | Chr2 | 16539718 | 16539720 | 2 | |
Deletion | Chr11 | 17483221 | 17494110 | 10889 | 2 |
Deletion | Chr7 | 18051001 | 18146000 | 95000 | 15 |
Deletion | Chr8 | 18170795 | 18170807 | 12 | LOC_Os08g29615 |
Deletion | Chr11 | 20063350 | 20063636 | 286 | |
Deletion | Chr1 | 23201492 | 23201493 | 1 | LOC_Os01g40990 |
Deletion | Chr3 | 24366088 | 24366094 | 6 | |
Deletion | Chr2 | 30348052 | 30353218 | 5166 | LOC_Os02g49670 |
Deletion | Chr2 | 31698028 | 31698030 | 2 | |
Deletion | Chr3 | 32090847 | 32090861 | 14 | LOC_Os03g56290 |
Deletion | Chr3 | 33623326 | 33623415 | 89 |
Insertions: 2
Variant Type | Chromosome | Start | End | Size (bp) | Number of Genes |
---|---|---|---|---|---|
Insertion | Chr6 | 700093 | 700094 | 2 | |
Insertion | Chr7 | 11351622 | 11351624 | 3 |
Inversions: 6
Variant Type | Chromosome | Position 1 | Position 2 | Number of Genes |
---|---|---|---|---|
Inversion | Chr8 | 5099380 | 5330986 | 2 |
Inversion | Chr1 | 12512538 | 12955842 | 2 |
Inversion | Chr6 | 14990002 | 15279183 | LOC_Os06g25650 |
Inversion | Chr6 | 14990020 | 15279191 | LOC_Os06g25650 |
Inversion | Chr3 | 25159161 | 25288755 | |
Inversion | Chr3 | 25159186 | 25288757 |
Translocations: 3
Variant Type | Chromosome | Position 1 | Chromosome | Position 2 | Number of Genes |
---|---|---|---|---|---|
Translocation | Chr5 | 1214099 | Chr1 | 9504062 | LOC_Os01g16740 |
Translocation | Chr11 | 7064789 | Chr1 | 7099386 | |
Translocation | Chr11 | 7065023 | Chr1 | 7099216 |