Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g32590 | A07 | 31968089 | G | A | missense_variant | MODERATE | c.3110C>T|p.Ser1037Phe |
S239 |
2 | BAA07g32590 | A07 | 31968272 | G | A | missense_variant | MODERATE | c.3013C>T|p.His1005Tyr |
S268 |
3 | BAA07g32590 | A07 | 31968751 | G | A | missense_variant | MODERATE | c.2629C>T|p.Arg877Cys |
S37 |
4 | BAA07g32590 | A07 | 31968921 | G | A | missense_variant | MODERATE | c.2459C>T|p.Ser820Leu |
S87 |
5 | BAA07g32590 | A07 | 31969501 | C | T | missense_variant | MODERATE | c.1879G>A|p.Glu627Lys |
S66 |
6 | BAA07g32590 | A07 | 31969964 | C | T | synonymous_variant | LOW | c.1416G>A|p.Glu472Glu |
S243 |
7 | BAA07g32590 | A07 | 31970059 | G | A | missense_variant | MODERATE | c.1321C>T|p.Leu441Phe |
S110 |
8 | BAA07g32590 | A07 | 31970383 | C | T | missense_variant | MODERATE | c.997G>A|p.Asp333Asn |
S35 |
9 | BAA07g32590 | A07 | 31970941 | C | T | missense_variant | MODERATE | c.695G>A|p.Gly232Glu |
S35 |
10 | BAA07g32590 | A07 | 31972120 | C | T | synonymous_variant | LOW | c.81G>A|p.Ser27Ser |
S207 |
11 | BAA07g32590 | A07 | 31972740 | G | A | upstream_gene_variant | MODIFIER | c.-540C>T| |
S206 S26 |
12 | BAA07g32590 | A07 | 31975924 | G | A | upstream_gene_variant | MODIFIER | c.-3724C>T| |
S5 |
13 | BAA07g32590 | A07 | 31977168 | C | T | upstream_gene_variant | MODIFIER | c.-4968G>A| |
S28 |