Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03250 | A10 | 1572275 | C | T | missense_variant | MODERATE | c.3554G>A|p.Cys1185Tyr |
S169 |
2 | BAA10g03250 | A10 | 1572477 | C | T | synonymous_variant | LOW | c.3426G>A|p.Ala1142Ala |
S166 |
3 | BAA10g03250 | A10 | 1572937 | G | A | synonymous_variant | LOW | c.3027C>T|p.Ile1009Ile |
S283 |
4 | BAA10g03250 | A10 | 1573283 | C | T | missense_variant | MODERATE | c.2681G>A|p.Gly894Asp |
S233 |
5 | BAA10g03250 | A10 | 1575741 | C | T | missense_variant | MODERATE | c.797G>A|p.Gly266Asp |
S63 |
6 | BAA10g03250 | A10 | 1575794 | G | A | synonymous_variant | LOW | c.744C>T|p.Asn248Asn |
S251 |
7 | BAA10g03250 | A10 | 1575860 | C | T | synonymous_variant | LOW | c.678G>A|p.Gln226Gln |
S63 |
8 | BAA10g03250 | A10 | 1577470 | C | T | upstream_gene_variant | MODIFIER | c.-524G>A| |
S185 |
9 | BAA10g03250 | A10 | 1577585 | G | A | upstream_gene_variant | MODIFIER | c.-639C>T| |
S234 |
10 | BAA10g03250 | A10 | 1578670 | G | A | upstream_gene_variant | MODIFIER | c.-1724C>T| |
S178 |
11 | BAA10g03250 | A10 | 1579198 | G | A | upstream_gene_variant | MODIFIER | c.-2252C>T| |
S71 |
12 | BAA10g03250 | A10 | 1580485 | C | T | upstream_gene_variant | MODIFIER | c.-3539G>A| |
S135 |
13 | BAA10g03250 | A10 | 1580637 | G | A | upstream_gene_variant | MODIFIER | c.-3691C>T| |
S1 S90 |
14 | BAA10g03250 | A10 | 1580751 | G | A | upstream_gene_variant | MODIFIER | c.-3805C>T| |
S167 |
15 | BAA10g03250 | A10 | 1580806 | G | A | upstream_gene_variant | MODIFIER | c.-3860C>T| |
S180 |
16 | BAA10g03250 | A10 | 1581470 | G | A | upstream_gene_variant | MODIFIER | c.-4524C>T| |
S180 |