Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03690 | A10 | 1773761 | T | G | stop_lost&splice_region_variant | HIGH | c.1623A>C|p.Ter541Tyrext*? |
S199 |
2 | BAA10g03690 | A10 | 1773762 | T | G | stop_lost&splice_region_variant | HIGH | c.1622A>C|p.Ter541Serext*? |
S199 |
3 | BAA10g03690 | A10 | 1775750 | G | A | missense_variant | MODERATE | c.736C>T|p.Pro246Ser |
S134 |
4 | BAA10g03690 | A10 | 1776599 | G | A | missense_variant | MODERATE | c.346C>T|p.Leu116Phe |
S59 |
5 | BAA10g03690 | A10 | 1777282 | C | T | missense_variant | MODERATE | c.70G>A|p.Glu24Lys |
S247 |
6 | BAA10g03690 | A10 | 1777315 | C | T | missense_variant | MODERATE | c.37G>A|p.Ala13Thr |
S2 |
7 | BAA10g03690 | A10 | 1777721 | G | A | upstream_gene_variant | MODIFIER | c.-370C>T| |
S60 |
8 | BAA10g03690 | A10 | 1777884 | G | A | upstream_gene_variant | MODIFIER | c.-533C>T| |
S81 |
9 | BAA10g03690 | A10 | 1779534 | G | A | upstream_gene_variant | MODIFIER | c.-2183C>T| |
S17 S176 |
10 | BAA10g03690 | A10 | 1780212 | G | A | upstream_gene_variant | MODIFIER | c.-2861C>T| |
S83 S88 |