Search Nipponbare
Mutant Information |
---|
Mutant Name | FN2608-S [Download] |
Generation | M2 |
Genus Species | Oryza Sativa |
Cultivar | Kitaake |
Alignment File (BAM File) | Download FN2608-S Alignment File |
Seed Availability | Yes [Order Seeds] |
Mapping (Hover to Zoom-In) | ![]() |
Variant Information |
---|
Single base substitutions: 49
Variant Type | Chromosome | Position | Change | Genotype | Effect | Gene Affected |
---|---|---|---|---|---|---|
SBS | Chr1 | 17696677 | G-A | HET | ||
SBS | Chr1 | 18004915 | C-T | HET | ||
SBS | Chr1 | 1966096 | T-A | Homo | ||
SBS | Chr1 | 28693861 | A-T | Homo | ||
SBS | Chr1 | 9990953 | C-T | Homo | ||
SBS | Chr10 | 17399453 | A-T | HET | ||
SBS | Chr10 | 385422 | C-A | HET | ||
SBS | Chr11 | 10490921 | G-A | HET | NON_SYNONYMOUS_CODING | LOC_Os11g18580 |
SBS | Chr11 | 13313335 | A-G | HET | ||
SBS | Chr11 | 15313311 | G-C | HET | ||
SBS | Chr11 | 17223772 | A-T | HET | ||
SBS | Chr11 | 1802593 | G-A | HET | ||
SBS | Chr12 | 10022136 | C-T | HET | ||
SBS | Chr12 | 10173780 | C-A | HET | ||
SBS | Chr12 | 12099665 | T-A | HET | NON_SYNONYMOUS_CODING | LOC_Os12g21510 |
SBS | Chr12 | 19955582 | C-T | HET | ||
SBS | Chr2 | 14829933 | G-T | HET | ||
SBS | Chr2 | 14886690 | G-T | HET | ||
SBS | Chr2 | 14886691 | A-T | HET | ||
SBS | Chr2 | 17321643 | A-G | HET | ||
SBS | Chr2 | 2496646 | C-A | HET | ||
SBS | Chr2 | 34410052 | G-A | HET | ||
SBS | Chr2 | 35372097 | C-T | HET | ||
SBS | Chr2 | 7135924 | A-G | HET | ||
SBS | Chr2 | 9684690 | G-A | HET | NON_SYNONYMOUS_CODING | LOC_Os02g16970 |
SBS | Chr3 | 11703825 | C-T | HET | NON_SYNONYMOUS_CODING | LOC_Os03g20690 |
SBS | Chr3 | 12109152 | A-T | HET | ||
SBS | Chr3 | 28220534 | G-A | HET | NON_SYNONYMOUS_CODING | LOC_Os03g49550 |
SBS | Chr3 | 31636102 | T-C | HET | ||
SBS | Chr4 | 10724103 | C-T | HET | ||
SBS | Chr4 | 12576139 | A-G | HET | ||
SBS | Chr4 | 21634026 | C-G | Homo | ||
SBS | Chr4 | 23205270 | C-T | Homo | ||
SBS | Chr5 | 13399735 | T-A | HET | ||
SBS | Chr5 | 13399737 | T-A | HET | ||
SBS | Chr5 | 24256340 | G-T | HET | NON_SYNONYMOUS_CODING | LOC_Os05g41420 |
SBS | Chr5 | 28639847 | T-C | Homo | ||
SBS | Chr5 | 29685310 | G-A | HET | ||
SBS | Chr5 | 7539250 | C-T | HET | ||
SBS | Chr6 | 12061260 | T-C | Homo | ||
SBS | Chr6 | 13568548 | G-A | Homo | ||
SBS | Chr6 | 26285946 | G-C | HET | ||
SBS | Chr7 | 15155478 | T-G | HET | ||
SBS | Chr7 | 17934104 | G-A | HET | ||
SBS | Chr7 | 6132430 | A-G | HET | ||
SBS | Chr8 | 14025765 | A-G | HET | ||
SBS | Chr8 | 18445961 | A-G | HET | ||
SBS | Chr8 | 27780237 | C-T | HET | ||
SBS | Chr9 | 12619793 | A-T | Homo |
Deletions: 8
Variant Type | Chromosome | Start | End | Size (bp) | Number of Genes |
---|---|---|---|---|---|
Deletion | Chr12 | 1827771 | 1827772 | 1 | LOC_Os12g04310 |
Deletion | Chr9 | 5584050 | 5584078 | 28 | |
Deletion | Chr8 | 8949570 | 8949572 | 2 | |
Deletion | Chr2 | 13341930 | 13341931 | 1 | |
Deletion | Chr8 | 16470222 | 16470223 | 1 | |
Deletion | Chr5 | 22089731 | 22089732 | 1 | |
Deletion | Chr4 | 33170658 | 33170664 | 6 | LOC_Os04g55730 |
Deletion | Chr1 | 34921719 | 34921720 | 1 |
Insertions: 4
Variant Type | Chromosome | Start | End | Size (bp) | Number of Genes |
---|---|---|---|---|---|
Insertion | Chr1 | 29173556 | 29173556 | 1 | |
Insertion | Chr12 | 8548657 | 8548658 | 2 | |
Insertion | Chr3 | 15138760 | 15138777 | 18 | LOC_Os03g26510![]() |
Insertion | Chr5 | 9992062 | 9992063 | 2 |
No Inversion
Translocations: 9
Variant Type | Chromosome | Position 1 | Chromosome | Position 2 | Number of Genes |
---|---|---|---|---|---|
Translocation | Chr12 | 3174873 | Chr5 | 19834064 | 2 |
Translocation | Chr11 | 9323567 | Chr6 | 23180839 | |
Translocation | Chr7 | 11638243 | Chr6 | 15056095 | 2 |
Translocation | Chr10 | 11725800 | Chr2 | 20278275 | LOC_Os10g22590 |
Translocation | Chr10 | 11758920 | Chr2 | 20278272 | LOC_Os10g22630 |
Translocation | Chr11 | 17770759 | Chr5 | 19949319 | |
Translocation | Chr9 | 18185184 | Chr1 | 10304409 | LOC_Os09g29910 |
Translocation | Chr10 | 18620383 | Chr2 | 16598646 | 2 |
Translocation | Chr12 | 20276070 | Chr7 | 15549639 |