| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 123151 | BAA10g13170 | A10 | 14403365 | C | T | upstream_gene_variant | MODIFIER | c.-1073G>A| |
S191 |
| 123152 | BAA10g13170 | A10 | 14403441 | G | A | upstream_gene_variant | MODIFIER | c.-1149C>T| |
S262 |
| 123153 | BAA10g13180 | A10 | 14403556 | C | T | synonymous_variant | LOW | c.25C>T|p.Leu9Leu |
S196 |
| 123154 | BAA10g13180 | A10 | 14403885 | G | A | synonymous_variant | LOW | c.354G>A|p.Ser118Ser |
S136 |
| 123155 | BAA10g13190 | A10 | 14411310 | G | A | missense_variant | MODERATE | c.1552C>T|p.Leu518Phe |
S240 S287 |
| 123156 | BAA10g13190 | A10 | 14411404 | C | T | synonymous_variant | LOW | c.1458G>A|p.Arg486Arg |
S12 |
| 123157 | BAA10g13190 | A10 | 14411664 | C | T | missense_variant | MODERATE | c.1198G>A|p.Ala400Thr |
S86 |
| 123158 | BAA10g13190 | A10 | 14411769 | C | T | missense_variant | MODERATE | c.1093G>A|p.Ala365Thr |
S96 |
| 123159 | BAA10g13190 | A10 | 14411867 | G | A | missense_variant | MODERATE | c.995C>T|p.Ala332Val |
S221 |
| 123160 | BAA10g13190 | A10 | 14412268 | G | A | synonymous_variant | LOW | c.670C>T|p.Leu224Leu |
S280 |
| 123161 | BAA10g13190 | A10 | 14412487 | C | T | missense_variant | MODERATE | c.451G>A|p.Glu151Lys |
S131 |
| 123162 | BAA10g13190 | A10 | 14412751 | C | T | missense_variant | MODERATE | c.187G>A|p.Gly63Arg |
S185 |
| 123163 | BAA10g13190 | A10 | 14412958 | C | T | upstream_gene_variant | MODIFIER | c.-21G>A| |
S75 S81 |
| 123164 | BAA10g13190 | A10 | 14413976 | C | T | upstream_gene_variant | MODIFIER | c.-1039G>A| |
S68 |
| 123165 | BAA10g13190 | A10 | 14414328 | C | T | upstream_gene_variant | MODIFIER | c.-1391G>A| |
S44 |
| 123166 | BAA10g13200 | A10 | 14415305 | G | A | synonymous_variant | LOW | c.108G>A|p.Gln36Gln |
S186 |
| 123167 | BAA10g13200 | A10 | 14415369 | G | A | missense_variant | MODERATE | c.172G>A|p.Val58Ile |
S240 |
| 123168 | BAA10g13210 | A10 | 14415871 | C | T | missense_variant | MODERATE | c.92C>T|p.Thr31Ile |
S233 |
| 123169 | BAA10g13190 | A10 | 14416870 | G | A | upstream_gene_variant | MODIFIER | c.-3933C>T| |
S279 |
| 123170 | BAA10g13190 | A10 | 14417388 | C | T | upstream_gene_variant | MODIFIER | c.-4451G>A| |
S46 |
| 123171 | BAA10g13230 | A10 | 14417987 | C | T | upstream_gene_variant | MODIFIER | c.-2505C>T| |
S281 |
| 123172 | BAA10g13220 | A10 | 14418560 | G | A | upstream_gene_variant | MODIFIER | c.-132C>T| |
S280 |
| 123173 | BAA10g13220 | A10 | 14418971 | G | A | upstream_gene_variant | MODIFIER | c.-543C>T| |
S230 |
| 123174 | BAA10g13230 | A10 | 14420614 | C | T | synonymous_variant | LOW | c.123C>T|p.Ser41Ser |
S242 |
| 123175 | BAA10g13230 | A10 | 14420624 | G | A | missense_variant | MODERATE | c.133G>A|p.Val45Ile |
S198 |