| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 96651 | BAA10g04770 | A10 | 2447747 | C | T | upstream_gene_variant | MODIFIER | c.-1002C>T| |
S281 |
| 96652 | BAA10g04760 | A10 | 2448105 | G | A | missense_variant | MODERATE | c.3514G>A|p.Gly1172Arg |
S65 |
| 96653 | BAA10g04760 | A10 | 2448126 | C | T | missense_variant | MODERATE | c.3535C>T|p.Pro1179Ser |
S202 |
| 96654 | BAA10g04770 | A10 | 2448368 | C | T | upstream_gene_variant | MODIFIER | c.-381C>T| |
S193 |
| 96655 | BAA10g04770 | A10 | 2448740 | G | A | upstream_gene_variant | MODIFIER | c.-9G>A| |
S219 S72 |
| 96656 | BAA10g04770 | A10 | 2448764 | G | A | missense_variant | MODERATE | c.16G>A|p.Asp6Asn |
S242 |
| 96657 | BAA10g04770 | A10 | 2448905 | C | T | missense_variant | MODERATE | c.157C>T|p.Pro53Ser |
S165 |
| 96658 | BAA10g04770 | A10 | 2449317 | C | T | missense_variant | MODERATE | c.569C>T|p.Ala190Val |
S146 |
| 96659 | BAA10g04760 | A10 | 2452340 | G | A | downstream_gene_variant | MODIFIER | c.*4155G>A| |
S215 |
| 96660 | BAA10g04780 | A10 | 2453457 | C | T | synonymous_variant | LOW | c.921G>A|p.Gln307Gln |
S282 |
| 96661 | BAA10g04780 | A10 | 2453495 | C | T | missense_variant | MODERATE | c.883G>A|p.Glu295Lys |
S35 |
| 96662 | BAA10g04780 | A10 | 2453567 | C | T | missense_variant | MODERATE | c.811G>A|p.Glu271Lys |
S117 |
| 96663 | BAA10g04800 | A10 | 2454891 | G | A | upstream_gene_variant | MODIFIER | c.-2797G>A| |
S245 |
| 96664 | BAA10g04780 | A10 | 2455148 | C | T | upstream_gene_variant | MODIFIER | c.-58G>A| |
S194 |
| 96665 | BAA10g04780 | A10 | 2456101 | C | T | upstream_gene_variant | MODIFIER | c.-1011G>A| |
S260 |
| 96666 | BAA10g04780 | A10 | 2457075 | C | T | upstream_gene_variant | MODIFIER | c.-1985G>A| |
S132 S137 S215 S89 |
| 96667 | BAA10g04780 | A10 | 2457282 | G | A | upstream_gene_variant | MODIFIER | c.-2192C>T| |
S70 |
| 96668 | BAA10g04780 | A10 | 2457626 | G | A | upstream_gene_variant | MODIFIER | c.-2536C>T| |
S20 |
| 96669 | BAA10g04780 | A10 | 2458234 | C | T | upstream_gene_variant | MODIFIER | c.-3144G>A| |
S2 |
| 96670 | BAA10g04780 | A10 | 2458297 | G | A | upstream_gene_variant | MODIFIER | c.-3207C>T| |
S278 |
| 96671 | BAA10g04780 | A10 | 2458364 | C | T | upstream_gene_variant | MODIFIER | c.-3274G>A| |
S110 |
| 96672 | BAA10g04840 | A10 | 2461896 | C | T | upstream_gene_variant | MODIFIER | c.-4765C>T| |
S58 |
| 96673 | BAA10g04810 | A10 | 2462006 | C | T | missense_variant | MODERATE | c.782C>T|p.Thr261Ile |
S35 |
| 96674 | BAA10g04810 | A10 | 2462201 | G | A | missense_variant | MODERATE | c.896G>A|p.Gly299Glu |
S82 S92 |
| 96675 | BAA10g04840 | A10 | 2462454 | G | A | upstream_gene_variant | MODIFIER | c.-4207G>A| |
S172 S217 |