| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 93251 | BAA10g02730 | A10 | 1311683 | C | T | missense_variant | MODERATE | c.95G>A|p.Arg32Lys |
S54 |
| 93252 | BAA10g02740 | A10 | 1312733 | G | A | missense_variant | MODERATE | c.196G>A|p.Asp66Asn |
S262 |
| 93253 | BAA10g02730 | A10 | 1313830 | C | T | upstream_gene_variant | MODIFIER | c.-2053G>A| |
S226 |
| 93254 | BAA10g02740 | A10 | 1314629 | G | A | missense_variant | MODERATE | c.931G>A|p.Ala311Thr |
S12 |
| 93255 | BAA10g02730 | A10 | 1315154 | C | T | upstream_gene_variant | MODIFIER | c.-3377G>A| |
S1 S228 S289 S90 |
| 93256 | BAA10g02740 | A10 | 1315763 | G | A | splice_region_variant&intron_variant | LOW | c.1399-4G>A| |
S55 |
| 93257 | BAA10g02740 | A10 | 1315827 | G | A | missense_variant | MODERATE | c.1459G>A|p.Glu487Lys |
S187 |
| 93258 | BAA10g02740 | A10 | 1316116 | C | T | missense_variant | MODERATE | c.1630C>T|p.Pro544Ser |
S269 |
| 93259 | BAA10g02750 | A10 | 1317076 | C | T | upstream_gene_variant | MODIFIER | c.-443C>T| |
S255 |
| 93260 | BAA10g02750 | A10 | 1317232 | G | A | upstream_gene_variant | MODIFIER | c.-287G>A| |
S284 |
| 93261 | BAA10g02750 | A10 | 1317631 | C | T | splice_region_variant&intron_variant | LOW | c.106+7C>T| |
S63 |
| 93262 | BAA10g02750 | A10 | 1319732 | C | T | synonymous_variant | LOW | c.1443C>T|p.Gly481Gly |
S177 |
| 93263 | BAA10g02760 | A10 | 1320507 | G | A | missense_variant | MODERATE | c.121G>A|p.Asp41Asn |
S242 |
| 93264 | BAA10g02760 | A10 | 1320625 | C | T | missense_variant | MODERATE | c.239C>T|p.Ser80Phe |
S287 |
| 93265 | BAA10g02760 | A10 | 1321132 | C | T | missense_variant | MODERATE | c.502C>T|p.Leu168Phe |
S185 |
| 93266 | BAA10g02770 | A10 | 1322502 | C | T | synonymous_variant | LOW | c.1806G>A|p.Pro602Pro |
S247 |
| 93267 | BAA10g02770 | A10 | 1323903 | G | A | synonymous_variant | LOW | c.405C>T|p.Ser135Ser |
S284 |
| 93268 | BAA10g02770 | A10 | 1324244 | C | T | missense_variant | MODERATE | c.64G>A|p.Glu22Lys |
S54 |
| 93269 | BAA10g02770 | A10 | 1324978 | G | A | upstream_gene_variant | MODIFIER | c.-671C>T| |
S76 |
| 93270 | BAA10g02770 | A10 | 1324992 | G | T | upstream_gene_variant | MODIFIER | c.-685C>A| |
S284 |
| 93271 | BAA10g02770 | A10 | 1325397 | G | A | upstream_gene_variant | MODIFIER | c.-1090C>T| |
S284 |
| 93272 | BAA10g02780 | A10 | 1325690 | G | A | missense_variant | MODERATE | c.139G>A|p.Glu47Lys |
S150 |
| 93273 | BAA10g02780 | A10 | 1325751 | T | C | missense_variant | MODERATE | c.200T>C|p.Val67Ala |
S226 |
| 93274 | BAA10g02770 | A10 | 1325955 | C | T | upstream_gene_variant | MODIFIER | c.-1648G>A| |
S122 |
| 93275 | BAA10g02770 | A10 | 1326377 | G | A | upstream_gene_variant | MODIFIER | c.-2070C>T| |
S176 S39 |