Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03770 | A10 | 1825776 | C | T | upstream_gene_variant | MODIFIER | c.-3295C>T| |
S47 |
2 | BAA10g03770 | A10 | 1826376 | C | T | upstream_gene_variant | MODIFIER | c.-2695C>T| |
S225 S73 |
3 | BAA10g03770 | A10 | 1826597 | C | T | upstream_gene_variant | MODIFIER | c.-2474C>T| |
S47 |
4 | BAA10g03770 | A10 | 1827288 | C | T | upstream_gene_variant | MODIFIER | c.-1783C>T| |
S226 |
5 | BAA10g03770 | A10 | 1827550 | C | T | upstream_gene_variant | MODIFIER | c.-1521C>T| |
S121 |
6 | BAA10g03770 | A10 | 1827602 | C | T | upstream_gene_variant | MODIFIER | c.-1469C>T| |
S226 |
7 | BAA10g03770 | A10 | 1827797 | C | T | upstream_gene_variant | MODIFIER | c.-1274C>T| |
S298 |
8 | BAA10g03770 | A10 | 1827919 | G | A | upstream_gene_variant | MODIFIER | c.-1152G>A| |
S36 |
9 | BAA10g03770 | A10 | 1828735 | G | A | upstream_gene_variant | MODIFIER | c.-336G>A| |
S245 |
10 | BAA10g03770 | A10 | 1829291 | C | T | missense_variant | MODERATE | c.221C>T|p.Pro74Leu |
S61 |
11 | BAA10g03770 | A10 | 1829412 | G | A | splice_region_variant&intron_variant | LOW | c.267-7G>A| |
S303 |
12 | BAA10g03770 | A10 | 1829488 | C | T | synonymous_variant | LOW | c.336C>T|p.Phe112Phe |
S224 |