Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01640 | A10 | 793916 | C | T | downstream_gene_variant | MODIFIER | c.*1698G>A| |
S35 |
2 | BAA10g01640 | A10 | 794102 | C | T | downstream_gene_variant | MODIFIER | c.*1512G>A| |
S276 |
3 | BAA10g01640 | A10 | 796932 | C | T | missense_variant | MODERATE | c.2942G>A|p.Gly981Glu |
S162 |
4 | BAA10g01640 | A10 | 797172 | G | A | missense_variant | MODERATE | c.2791C>T|p.Pro931Ser |
S230 |
5 | BAA10g01640 | A10 | 797718 | C | T | missense_variant | MODERATE | c.2510G>A|p.Arg837His |
S95 |
6 | BAA10g01640 | A10 | 798440 | G | A | missense_variant | MODERATE | c.2158C>T|p.Leu720Phe |
S133 |
7 | BAA10g01640 | A10 | 801345 | C | T | splice_region_variant&intron_variant | LOW | c.292+6G>A| |
S204 |
8 | BAA10g01640 | A10 | 801435 | C | T | missense_variant | MODERATE | c.208G>A|p.Asp70Asn |
S200 |
9 | BAA10g01640 | A10 | 801667 | G | A | missense_variant | MODERATE | c.67C>T|p.Arg23Cys |
S240 |
10 | BAA10g01640 | A10 | 801740 | C | T | upstream_gene_variant | MODIFIER | c.-7G>A| |
S294 |
11 | BAA10g01640 | A10 | 801859 | G | A | upstream_gene_variant | MODIFIER | c.-126C>T| |
S241 |
12 | BAA10g01640 | A10 | 804257 | T | C | upstream_gene_variant | MODIFIER | c.-2524A>G| |
S218 |
13 | BAA10g01640 | A10 | 804916 | G | A | upstream_gene_variant | MODIFIER | c.-3183C>T| |
S125 |
14 | BAA10g01640 | A10 | 805355 | G | A | upstream_gene_variant | MODIFIER | c.-3622C>T| |
S157 S163 |
15 | BAA10g01640 | A10 | 806047 | G | A | upstream_gene_variant | MODIFIER | c.-4314C>T| |
S38 |