| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID | 
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g42690 | A07 | 36907152 | G | A | missense_variant | MODERATE | c.6041C>T|p.Ser2014Leu | S223 | 
| 2 | BAA07g42690 | A07 | 36907197 | G | A | missense_variant | MODERATE | c.5996C>T|p.Ala1999Val | S137 | 
| 3 | BAA07g42690 | A07 | 36907294 | G | A | missense_variant | MODERATE | c.5899C>T|p.Pro1967Ser | S269 | 
| 4 | BAA07g42690 | A07 | 36907302 | G | A | missense_variant | MODERATE | c.5891C>T|p.Ser1964Phe | S13 S140 S278 | 
| 5 | BAA07g42690 | A07 | 36908162 | C | T | synonymous_variant | LOW | c.5031G>A|p.Gln1677Gln | S210 S225 | 
| 6 | BAA07g42690 | A07 | 36909298 | G | A | missense_variant | MODERATE | c.4319C>T|p.Ser1440Phe | S110 | 
| 7 | BAA07g42690 | A07 | 36909553 | C | T | synonymous_variant | LOW | c.4170G>A|p.Lys1390Lys | S252 | 
| 8 | BAA07g42690 | A07 | 36910050 | C | T | missense_variant | MODERATE | c.4081G>A|p.Val1361Ile | S260 | 
| 9 | BAA07g42690 | A07 | 36910196 | C | T | missense_variant | MODERATE | c.4003G>A|p.Asp1335Asn | S37 | 
| 10 | BAA07g42690 | A07 | 36910312 | C | T | missense_variant | MODERATE | c.3887G>A|p.Arg1296His | S148 S210 S30 S31 | 
| 11 | BAA07g42690 | A07 | 36910748 | C | T | synonymous_variant | LOW | c.3723G>A|p.Arg1241Arg | S252 | 
| 12 | BAA07g42690 | A07 | 36911178 | G | A | synonymous_variant | LOW | c.3547C>T|p.Leu1183Leu | S298 | 
| 13 | BAA07g42690 | A07 | 36912508 | C | T | synonymous_variant | LOW | c.2961G>A|p.Glu987Glu | S173 | 
| 14 | BAA07g42690 | A07 | 36913464 | G | A | intron_variant | MODIFIER | c.2721+126C>T| | S51 | 
| 15 | BAA07g42690 | A07 | 36914286 | C | T | splice_donor_variant&intron_variant | HIGH | c.2346+1G>A| | S68 | 
| 16 | BAA07g42690 | A07 | 36914892 | G | A | intron_variant | MODIFIER | c.1991-71C>T| | S76 | 
| 17 | BAA07g42690 | A07 | 36916577 | C | T | missense_variant | MODERATE | c.1357G>A|p.Glu453Lys | S260 | 
| 18 | BAA07g42690 | A07 | 36917077 | G | A | missense_variant | MODERATE | c.1159C>T|p.His387Tyr | S308 | 
| 19 | BAA07g42690 | A07 | 36918533 | C | T | missense_variant&splice_region_variant | MODERATE | c.778G>A|p.Glu260Lys | S140 | 
| 20 | BAA07g42690 | A07 | 36919097 | G | A | splice_region_variant&synonymous_variant | LOW | c.456C>T|p.Ile152Ile | S87 | 
| 21 | BAA07g42690 | A07 | 36919150 | C | T | missense_variant | MODERATE | c.403G>A|p.Asp135Asn | S140 | 
| 22 | BAA07g42690 | A07 | 36919421 | G | A | missense_variant | MODERATE | c.211C>T|p.Leu71Phe | S262 | 
| 23 | BAA07g42690 | A07 | 36919481 | C | T | missense_variant | MODERATE | c.151G>A|p.Glu51Lys | S48 | 
| 24 | BAA07g42690 | A07 | 36920225 | G | A | upstream_gene_variant | MODIFIER | c.-594C>T| | S280 | 
| 25 | BAA07g42690 | A07 | 36922283 | G | A | upstream_gene_variant | MODIFIER | c.-2652C>T| | S238 |