Search Results
Mutant Information |
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Mutant Name | FN1412-S [Download] |
Generation | M2 |
Genus Species | Oryza Sativa |
Cultivar | Kitaake |
Alignment File (BAM File) | Download FN1412-S Alignment File |
Seed Availability | Yes [Order Seeds] |
Phenotype |
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Mapping (Hover to Zoom-In) |
Variant Information |
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Single base substitutions: 35
Variant Type | Chromosome | Position | Change | Genotype | Effect | Gene Affected |
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SBS | Chr1 | 9796394 | G-A | HET | INTRON | |
SBS | Chr1 | 20917991 | T-G | HOMO | INTERGENIC | |
SBS | Chr2 | 6897894 | C-T | HOMO | INTERGENIC | |
SBS | Chr2 | 11722189 | C-T | HOMO | INTRON | |
SBS | Chr2 | 22596542 | G-A | HET | INTRON | |
SBS | Chr2 | 31577900 | G-A | HOMO | INTERGENIC | |
SBS | Chr3 | 4637996 | T-C | HET | INTERGENIC | |
SBS | Chr3 | 11817977 | C-G | HET | SYNONYMOUS_CODING | |
SBS | Chr3 | 16224567 | A-G | HET | INTERGENIC | |
SBS | Chr3 | 23685594 | T-C | HET | INTERGENIC | |
SBS | Chr4 | 10892113 | A-G | HET | NON_SYNONYMOUS_CODING | LOC_Os04g19570 |
SBS | Chr4 | 14911052 | G-C | HET | INTERGENIC | |
SBS | Chr4 | 24420115 | C-T | HOMO | INTERGENIC | |
SBS | Chr4 | 34890346 | C-G | HOMO | INTERGENIC | |
SBS | Chr5 | 5536199 | G-T | HET | INTERGENIC | |
SBS | Chr5 | 11214221 | C-T | HET | INTERGENIC | |
SBS | Chr5 | 16726495 | G-A | HET | INTRON | |
SBS | Chr5 | 17137151 | C-T | HET | INTERGENIC | |
SBS | Chr6 | 3454478 | C-T | HOMO | SYNONYMOUS_CODING | |
SBS | Chr6 | 16466193 | C-T | HOMO | INTERGENIC | |
SBS | Chr8 | 1959960 | A-C | HET | NON_SYNONYMOUS_CODING | LOC_Os08g04040 |
SBS | Chr8 | 6479761 | T-C | HET | SYNONYMOUS_CODING | |
SBS | Chr9 | 6268373 | G-A | HET | INTERGENIC | |
SBS | Chr9 | 19600251 | T-A | HOMO | INTRON | |
SBS | Chr10 | 17129265 | C-T | HOMO | INTERGENIC | |
SBS | Chr11 | 5954613 | G-A | HET | INTERGENIC | |
SBS | Chr11 | 8238788 | T-G | HET | INTERGENIC | |
SBS | Chr11 | 8285193 | T-C | HET | INTERGENIC | |
SBS | Chr11 | 12682719 | G-A | HET | NON_SYNONYMOUS_CODING | LOC_Os11g22070 |
SBS | Chr11 | 12755388 | C-T | HET | INTERGENIC | |
SBS | Chr11 | 16159965 | A-G | HET | INTRON | |
SBS | Chr12 | 9453348 | G-T | HET | INTERGENIC | |
SBS | Chr12 | 15168109 | G-A | HET | INTERGENIC | |
SBS | Chr12 | 21947235 | T-G | HOMO | INTERGENIC | |
SBS | Chr12 | 27446979 | G-A | HOMO | NON_SYNONYMOUS_CODING | LOC_Os12g44280 |
Deletions: 23
Variant Type | Chromosome | Start | End | Size (bp) | Number of Genes |
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Deletion | Chr10 | 988371 | 988376 | 5 | |
Deletion | Chr11 | 1522262 | 1522673 | 411 | LOC_Os11g03840 |
Deletion | Chr3 | 1578417 | 1578433 | 16 | |
Deletion | Chr7 | 3013001 | 3105000 | 92000 | 17 |
Deletion | Chr3 | 3177086 | 3177112 | 26 | |
Deletion | Chr7 | 3406211 | 3406215 | 4 | |
Deletion | Chr9 | 4223122 | 4223123 | 1 | |
Deletion | Chr9 | 5809344 | 5809346 | 2 | |
Deletion | Chr1 | 7873162 | 7873163 | 1 | |
Deletion | Chr2 | 7974871 | 7974884 | 13 | |
Deletion | Chr9 | 9106258 | 9106265 | 7 | |
Deletion | Chr11 | 18430645 | 18430650 | 5 | LOC_Os11g31540 |
Deletion | Chr3 | 20509329 | 20509334 | 5 | |
Deletion | Chr12 | 21247509 | 21247511 | 2 | |
Deletion | Chr12 | 25109690 | 25109694 | 4 | |
Deletion | Chr5 | 26128785 | 26128791 | 6 | |
Deletion | Chr1 | 27538098 | 27538110 | 12 | |
Deletion | Chr3 | 29475381 | 29475385 | 4 | LOC_Os03g51520 |
Deletion | Chr5 | 29700920 | 29700924 | 4 | |
Deletion | Chr1 | 29985900 | 29985901 | 1 | |
Deletion | Chr6 | 31134340 | 31134348 | 8 | |
Deletion | Chr3 | 35002688 | 35002689 | 1 | LOC_Os03g61740 |
Deletion | Chr1 | 37684213 | 37684217 | 4 |
Insertions: 3
Variant Type | Chromosome | Start | End | Size (bp) | Number of Genes |
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Insertion | Chr9 | 19656411 | 19656411 | 1 | |
Insertion | Chr4 | 31804115 | 31804115 | 1 | |
Insertion | Chr8 | 26530008 | 26530008 | 1 |
Inversions: 3
Variant Type | Chromosome | Position 1 | Position 2 | Number of Genes |
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Inversion | Chr2 | 20397 | 822082 | LOC_Os02g02390 |
Inversion | Chr6 | 5817251 | 6641621 | |
Inversion | Chr3 | 12180203 | 12426432 | 2 |
Translocations: 2
Variant Type | Chromosome | Position 1 | Chromosome | Position 2 | Number of Genes |
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Translocation | Chr3 | 12180206 | Chr2 | 2813657 | 2 |
Translocation | Chr3 | 12426435 | Chr2 | 2821755 | 2 |