Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29610 | A10 | 22213267 | G | A | downstream_gene_variant | MODIFIER | c.*4969C>T| |
S212 |
2 | BAA10g29610 | A10 | 22213981 | C | T | downstream_gene_variant | MODIFIER | c.*4255G>A| |
S42 |
3 | BAA10g29610 | A10 | 22214123 | G | A | downstream_gene_variant | MODIFIER | c.*4113C>T| |
S16 |
4 | BAA10g29610 | A10 | 22214241 | G | A | downstream_gene_variant | MODIFIER | c.*3995C>T| |
S1 S90 |
5 | BAA10g29610 | A10 | 22214940 | C | T | downstream_gene_variant | MODIFIER | c.*3296G>A| |
S247 |
6 | BAA10g29610 | A10 | 22215021 | T | G | downstream_gene_variant | MODIFIER | c.*3215A>C| |
S86 |
7 | BAA10g29610 | A10 | 22215328 | C | T | downstream_gene_variant | MODIFIER | c.*2908G>A| |
S155 S211 |
8 | BAA10g29610 | A10 | 22215535 | C | T | downstream_gene_variant | MODIFIER | c.*2701G>A| |
S230 |
9 | BAA10g29610 | A10 | 22218447 | G | A | missense_variant | MODERATE | c.929C>T|p.Ala310Val |
S192 |
10 | BAA10g29610 | A10 | 22218823 | C | T | missense_variant | MODERATE | c.553G>A|p.Asp185Asn |
S9 |
11 | BAA10g29610 | A10 | 22219239 | G | A | missense_variant | MODERATE | c.137C>T|p.Thr46Ile |
S273 |
12 | BAA10g29610 | A10 | 22219423 | C | T | upstream_gene_variant | MODIFIER | c.-48G>A| |
S105 |
13 | BAA10g29610 | A10 | 22219490 | C | T | upstream_gene_variant | MODIFIER | c.-115G>A| |
S38 |
14 | BAA10g29610 | A10 | 22220088 | C | T | upstream_gene_variant | MODIFIER | c.-713G>A| |
S188 |
15 | BAA10g29610 | A10 | 22220598 | C | T | upstream_gene_variant | MODIFIER | c.-1223G>A| |
S306 S308 |