| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 123401 | BAA10g13350 | A10 | 14492177 | G | A | upstream_gene_variant | MODIFIER | c.-1395G>A| |
S287 |
| 123402 | BAA10g13350 | A10 | 14492295 | G | A | upstream_gene_variant | MODIFIER | c.-1277G>A| |
S271 |
| 123403 | BAA10g13370 | A10 | 14495048 | G | A | upstream_gene_variant | MODIFIER | c.-4158G>A| |
S263 |
| 123404 | BAA10g13360 | A10 | 14495990 | C | T | missense_variant | MODERATE | c.1708G>A|p.Glu570Lys |
S242 |
| 123405 | BAA10g13360 | A10 | 14496147 | G | A | synonymous_variant | LOW | c.1551C>T|p.Asp517Asp |
S250 |
| 123406 | BAA10g13370 | A10 | 14496269 | G | A | upstream_gene_variant | MODIFIER | c.-2937G>A| |
S207 |
| 123407 | BAA10g13370 | A10 | 14496592 | C | T | upstream_gene_variant | MODIFIER | c.-2614C>T| |
S206 S26 |
| 123408 | BAA10g13360 | A10 | 14498798 | G | A | upstream_gene_variant | MODIFIER | c.-571C>T| |
S166 S167 S236 S262 |
| 123409 | BAA10g13360 | A10 | 14498857 | G | A | upstream_gene_variant | MODIFIER | c.-630C>T| |
S197 |
| 123410 | BAA10g13360 | A10 | 14499456 | C | T | upstream_gene_variant | MODIFIER | c.-1229G>A| |
S180 |
| 123411 | BAA10g13370 | A10 | 14499692 | G | A | missense_variant | MODERATE | c.205G>A|p.Ala69Thr |
S283 |
| 123412 | BAA10g13370 | A10 | 14499764 | G | A | missense_variant | MODERATE | c.277G>A|p.Val93Ile |
S240 |
| 123413 | BAA10g13370 | A10 | 14500270 | G | A | missense_variant | MODERATE | c.614G>A|p.Arg205Lys |
S145 S32 |
| 123414 | BAA10g13360 | A10 | 14500373 | C | T | upstream_gene_variant | MODIFIER | c.-2146G>A| |
S87 |
| 123415 | BAA10g13360 | A10 | 14500388 | C | T | upstream_gene_variant | MODIFIER | c.-2161G>A| |
S156 |
| 123416 | BAA10g13360 | A10 | 14500397 | G | A | upstream_gene_variant | MODIFIER | c.-2170C>T| |
S17 |
| 123417 | BAA10g13380 | A10 | 14501403 | C | T | stop_gained | HIGH | c.1920G>A|p.Trp640* |
S302 |
| 123418 | BAA10g13380 | A10 | 14501504 | G | A | synonymous_variant | LOW | c.1819C>T|p.Leu607Leu |
S262 |
| 123419 | BAA10g13380 | A10 | 14502024 | C | T | missense_variant | MODERATE | c.1369G>A|p.Asp457Asn |
S142 |
| 123420 | BAA10g13380 | A10 | 14502258 | G | A | missense_variant | MODERATE | c.1135C>T|p.Leu379Phe |
S139 |
| 123421 | BAA10g13380 | A10 | 14502336 | G | A | synonymous_variant | LOW | c.1057C>T|p.Leu353Leu |
S136 |
| 123422 | BAA10g13380 | A10 | 14502727 | C | T | missense_variant | MODERATE | c.758G>A|p.Arg253Gln |
S302 |
| 123423 | BAA10g13380 | A10 | 14502873 | C | T | synonymous_variant | LOW | c.612G>A|p.Thr204Thr |
S47 |
| 123424 | BAA10g13380 | A10 | 14502874 | G | A | missense_variant | MODERATE | c.611C>T|p.Thr204Met |
S15 S3 |
| 123425 | BAA10g13390 | A10 | 14503338 | G | A | upstream_gene_variant | MODIFIER | c.-1275G>A| |
S241 |