Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g25490 | A01 | 13849391 | C | T | downstream_gene_variant | MODIFIER | c.*3136G>A| |
S136 |
2 | BAA01g25490 | A01 | 13849535 | C | T | downstream_gene_variant | MODIFIER | c.*2992G>A| |
S120 |
3 | BAA01g25490 | A01 | 13849568 | C | T | downstream_gene_variant | MODIFIER | c.*2959G>A| |
S198 |
4 | BAA01g25490 | A01 | 13850319 | C | T | downstream_gene_variant | MODIFIER | c.*2208G>A| |
S146 |
5 | BAA01g25490 | A01 | 13850553 | C | T | downstream_gene_variant | MODIFIER | c.*1974G>A| |
S270 |
6 | BAA01g25490 | A01 | 13850701 | G | A | downstream_gene_variant | MODIFIER | c.*1826C>T| |
S203 |
7 | BAA01g25490 | A01 | 13851146 | G | A | downstream_gene_variant | MODIFIER | c.*1381C>T| |
S217 |
8 | BAA01g25490 | A01 | 13851396 | C | T | downstream_gene_variant | MODIFIER | c.*1131G>A| |
S167 |
9 | BAA01g25490 | A01 | 13851755 | G | A | downstream_gene_variant | MODIFIER | c.*772C>T| |
S262 |
10 | BAA01g25490 | A01 | 13851830 | G | A | downstream_gene_variant | MODIFIER | c.*697C>T| |
S156 |
11 | BAA01g25490 | A01 | 13852936 | C | T | missense_variant | MODERATE | c.641G>A|p.Ser214Asn |
S280 |
12 | BAA01g25490 | A01 | 13853501 | C | T | intron_variant | MODIFIER | c.412-249G>A| |
S136 |
13 | BAA01g25490 | A01 | 13853932 | G | A | missense_variant | MODERATE | c.335C>T|p.Ala112Val |
S12 |
14 | BAA01g25490 | A01 | 13854952 | G | A | synonymous_variant | LOW | c.111C>T|p.Cys37Cys |
S91 |
15 | BAA01g25490 | A01 | 13854958 | A | C | missense_variant | MODERATE | c.105T>G|p.Ser35Arg |
S147 S91 |
16 | BAA01g25490 | A01 | 13854961 | G | A | synonymous_variant | LOW | c.102C>T|p.Asp34Asp |
S147 S91 |
17 | BAA01g25490 | A01 | 13854979 | A | G | synonymous_variant | LOW | c.84T>C|p.Leu28Leu |
S147 S91 |
18 | BAA01g25490 | A01 | 13854982 | C | T | synonymous_variant | LOW | c.81G>A|p.Gln27Gln |
S147 S15 S91 |
19 | BAA01g25490 | A01 | 13854989 | T | G | missense_variant | MODERATE | c.74A>C|p.Asp25Ala |
S147 S91 |
20 | BAA01g25490 | A01 | 13854996 | G | A | synonymous_variant | LOW | c.67C>T|p.Leu23Leu |
S147 S91 |
21 | BAA01g25490 | A01 | 13855000 | C | T | synonymous_variant | LOW | c.63G>A|p.Ala21Ala |
S147 S91 |
22 | BAA01g25490 | A01 | 13855004 | C | T | missense_variant | MODERATE | c.59G>A|p.Arg20His |
S147 S91 |
23 | BAA01g25490 | A01 | 13858205 | C | T | upstream_gene_variant | MODIFIER | c.-3143G>A| |
S88 |
24 | BAA01g25490 | A01 | 13858862 | C | T | upstream_gene_variant | MODIFIER | c.-3800G>A| |
S250 |
25 | BAA01g25490 | A01 | 13859287 | C | T | upstream_gene_variant | MODIFIER | c.-4225G>A| |
S242 |