Table 6.
Chr. | Gene annotation | Locus ID | SNP ID | Nucleotide change | Impact |
---|---|---|---|---|---|
1 | OsACA6 | LOC_Os01g71240 | na | na | na |
3 | OsANK | LOC_Os03g47640 | vg03_26984941 | C>T | Arg355* |
3 | OsANK | LOC_Os03g47686 | vg03_27020751 | C>G | Tyr518* |
3 | OsANK | LOC_Os03g47693 | vg03_27022097 | G>A | Trp56* |
3 | OsANK | LOC_Os03g47720 | vg03_27044642 | CAA>CAAA | Glu86fs |
3 | OsGST3 | LOC_Os03g50130 | vg03_28595867 | A>G | start_lost;Met1? |
7 | OsWAK38 | LOC_Os04g29680 | na | na | na |
4 | OsWAK40 | LOC_Os04g29790 | vg04_17752550 | A>AAC | Ile158fsa |
vg04_17752554 | TTG>T | Lys157fsa | |||
6 | OsRLK-803 | LOC_Os06g04370 | vg06-01867369 | A>T | Ser529Cys |
6 | Transferase | LOC_Os06g04380 | vg06_01875711 | A>AC | Ser56fs |
6 | OsNAPL2 | LOC_Os06g05660 | vg06_02560533 | G>T | Gly126Cys |
6 | Transferase | LOC_Os06g05790 | vg06_02633463 | T>TA | Leu483fs |
6 | OsFBL27 | LOC_Os06g06050 | vg06_02780806 | A>AGAG | Glu6dup |
vg06_02781107 | TGCGGCGGCGGCG>TGCGGCGGCGGCGGCG | Glu110dup | |||
6 | Esterase | LOC_Os06g06080 | vg06_02803110 | TCC>T | Arg25fs |
6 | OsMPK6 | LOC_Os06g06090 | vg06_02812762 | GCCC>G | Gly29delb |
6 | OsFKBP13 | LOC_Os06g45340 | vg06_27403638 | CGG>N/C | Ala4fs (if C) |
6 | CYP59A | LOC_Os06g45900 | vg06_27783122 | C>CGGGG | Leu43fs |
vg06_27791008 | T>C | Ter549Argext*? | |||
6 | OsNAC011 | LOC_Os06g46270 | vg06_28037986 | GCGGGCGGCG>C | Ala38_Ala50del |
6 | Hydrolase | LOC_Os06g46284 | vg06_28057827 | A>T | Tyr74* |
8 | RF6 | LOC_Os08g01870 | vg08_00538004 | T>C | Cys484Arg |
8 | OsbHLH070 | LOC_Os08g08160 | vg08_04647095 | T>TAA | Ile333fs |
vg08_04648125 | CT>C | Splice variant | |||
8 | LTPL130 | LOC_Os08g27674 | vg08_16869517 | TG>T | Thr61fs |
8 | OsRLCK253 | LOC_Os08g28710 | vg08_17559305 | T>TCGC | Ala256 dup |
11 | OsPDIL1-1 | LOC_Os11g09280 | vg11_04974896 | C>CG | Gly35fs |
vg11_04974890 | GCATC>G | Asp36fs | |||
11 | OsFBX398 | LOC_Os11g09360 | vg11_05026584 | G>A | Splice variant |
na, not available; ext*?, stop codon lost, reading frame extended; fs, frameshift.
*Premature stop codon.
Variant in Krasnodarskij 3352; Carolino 164 same as the Nipponbare reference genome.
Total of 233 variants between Krasnodarskij 3352 and Carolino 164.