| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 170201 | BAA02g14960 | A02 | 7124101 | C | T | upstream_gene_variant | MODIFIER | c.-1076G>A| |
S18 |
| 170202 | BAA02g14960 | A02 | 7125014 | G | A | upstream_gene_variant | MODIFIER | c.-1989C>T| |
S298 |
| 170203 | BAA02g14960 | A02 | 7125287 | C | T | upstream_gene_variant | MODIFIER | c.-2262G>A| |
S238 |
| 170204 | BAA02g14960 | A02 | 7125699 | C | T | upstream_gene_variant | MODIFIER | c.-2674G>A| |
S185 |
| 170205 | BAA02g14960 | A02 | 7126388 | G | A | upstream_gene_variant | MODIFIER | c.-3363C>T| |
S45 |
| 170206 | BAA02g14960 | A02 | 7126447 | G | A | upstream_gene_variant | MODIFIER | c.-3422C>T| |
S79 S91 |
| 170207 | BAA02g14960 | A02 | 7127168 | C | T | upstream_gene_variant | MODIFIER | c.-4143G>A| |
S162 |
| 170208 | BAA02g14970 | A02 | 7129183 | C | T | downstream_gene_variant | MODIFIER | c.*68G>A| |
S263 |
| 170209 | BAA02g14970 | A02 | 7129484 | C | T | missense_variant | MODERATE | c.6334G>A|p.Glu2112Lys |
S55 |
| 170210 | BAA02g14970 | A02 | 7129577 | C | T | missense_variant | MODERATE | c.6241G>A|p.Glu2081Lys |
S206 S26 |
| 170211 | BAA02g14970 | A02 | 7130071 | C | T | missense_variant | MODERATE | c.5747G>A|p.Arg1916Lys |
S192 |
| 170212 | BAA02g14970 | A02 | 7131012 | C | T | synonymous_variant | LOW | c.4806G>A|p.Lys1602Lys |
S270 S63 |
| 170213 | BAA02g14970 | A02 | 7131709 | G | A | missense_variant | MODERATE | c.4109C>T|p.Thr1370Ile |
S95 |
| 170214 | BAA02g14970 | A02 | 7131914 | C | T | missense_variant | MODERATE | c.3904G>A|p.Asp1302Asn |
S174 S27 |
| 170215 | BAA02g14970 | A02 | 7132073 | G | A | missense_variant | MODERATE | c.3745C>T|p.Pro1249Ser |
S34 |
| 170216 | BAA02g14970 | A02 | 7132423 | C | T | missense_variant | MODERATE | c.3395G>A|p.Gly1132Glu |
S189 |
| 170217 | BAA02g14970 | A02 | 7132509 | G | A | intron_variant | MODIFIER | c.3346-37C>T| |
S50 |
| 170218 | BAA02g14970 | A02 | 7134991 | G | A | synonymous_variant | LOW | c.2050C>T|p.Leu684Leu |
S10 |
| 170219 | BAA02g14970 | A02 | 7135266 | C | T | missense_variant | MODERATE | c.1775G>A|p.Gly592Glu |
S216 |
| 170220 | BAA02g14970 | A02 | 7135361 | G | A | synonymous_variant | LOW | c.1680C>T|p.Leu560Leu |
S146 |
| 170221 | BAA02g14970 | A02 | 7136515 | G | A | stop_gained | HIGH | c.526C>T|p.Gln176* |
S197 |
| 170222 | BAA02g14970 | A02 | 7136898 | C | T | missense_variant | MODERATE | c.143G>A|p.Gly48Glu |
S302 |
| 170223 | BAA02g14970 | A02 | 7137968 | C | T | upstream_gene_variant | MODIFIER | c.-928G>A| |
S178 |
| 170224 | BAA02g14970 | A02 | 7137994 | G | A | upstream_gene_variant | MODIFIER | c.-954C>T| |
S256 |
| 170225 | BAA02g14980 | A02 | 7140002 | G | A | synonymous_variant | LOW | c.840C>T|p.Ser280Ser |
S139 |