Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
4651 | BAA01g03720 | A01 | 1696100 | C | T | missense_variant | MODERATE | c.3416C>T|p.Ala1139Val |
S262 |
4652 | BAA01g03720 | A01 | 1696674 | C | T | synonymous_variant | LOW | c.3810C>T|p.Asn1270Asn |
S168 |
4653 | BAA01g03720 | A01 | 1697641 | G | A | downstream_gene_variant | MODIFIER | c.*623G>A| |
S289 S290 |
4654 | BAA01g03720 | A01 | 1697898 | G | A | downstream_gene_variant | MODIFIER | c.*880G>A| |
S308 |
4655 | BAA01g03730 | A01 | 1698333 | C | T | synonymous_variant | LOW | c.588G>A|p.Ser196Ser |
S100 |
4656 | BAA01g03720 | A01 | 1698664 | C | T | downstream_gene_variant | MODIFIER | c.*1646C>T| |
S11 |
4657 | BAA01g03730 | A01 | 1699031 | G | A | synonymous_variant | LOW | c.267C>T|p.Ile89Ile |
S288 |
4658 | BAA01g03730 | A01 | 1699150 | C | T | missense_variant | MODERATE | c.148G>A|p.Glu50Lys |
S1 S90 |
4659 | BAA01g03730 | A01 | 1699163 | G | A | synonymous_variant | LOW | c.135C>T|p.Leu45Leu |
S216 |
4660 | BAA01g03730 | A01 | 1699234 | C | T | missense_variant | MODERATE | c.64G>A|p.Glu22Lys |
S57 |
4661 | BAA01g03730 | A01 | 1700333 | C | T | upstream_gene_variant | MODIFIER | c.-1036G>A| |
S268 |
4662 | BAA01g03740 | A01 | 1700665 | G | A | synonymous_variant | LOW | c.276C>T|p.Asp92Asp |
S262 |
4663 | BAA01g03740 | A01 | 1700832 | G | A | missense_variant | MODERATE | c.109C>T|p.Arg37Cys |
S191 |
4664 | BAA01g03730 | A01 | 1700971 | G | A | upstream_gene_variant | MODIFIER | c.-1674C>T| |
S280 |
4665 | BAA01g03730 | A01 | 1701223 | G | A | upstream_gene_variant | MODIFIER | c.-1926C>T| |
S296 |
4666 | BAA01g03730 | A01 | 1701608 | G | A | upstream_gene_variant | MODIFIER | c.-2311C>T| |
S28 |
4667 | BAA01g03730 | A01 | 1703398 | G | A | upstream_gene_variant | MODIFIER | c.-4101C>T| |
S274 |
4668 | BAA01g03750 | A01 | 1703836 | G | A | synonymous_variant | LOW | c.135G>A|p.Leu45Leu |
S181 |
4669 | BAA01g03750 | A01 | 1703885 | C | T | missense_variant | MODERATE | c.184C>T|p.Leu62Phe |
S164 |
4670 | BAA01g03750 | A01 | 1704036 | G | A | missense_variant | MODERATE | c.335G>A|p.Arg112Lys |
S296 |
4671 | BAA01g03750 | A01 | 1705407 | G | A | missense_variant | MODERATE | c.1486G>A|p.Ala496Thr |
S263 |
4672 | BAA01g03760 | A01 | 1705932 | C | T | missense_variant | MODERATE | c.1105G>A|p.Glu369Lys |
S249 |
4673 | BAA01g03760 | A01 | 1706382 | G | A | synonymous_variant | LOW | c.741C>T|p.Asn247Asn |
S156 |
4674 | BAA01g03760 | A01 | 1706470 | C | T | missense_variant | MODERATE | c.653G>A|p.Gly218Asp |
S223 |
4675 | BAA01g03760 | A01 | 1706754 | G | A | synonymous_variant | LOW | c.369C>T|p.Ile123Ile |
S250 |