Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04770 | A10 | 2445718 | C | T | upstream_gene_variant | MODIFIER | c.-3031C>T| |
S23 |
2 | BAA10g04770 | A10 | 2445983 | C | T | upstream_gene_variant | MODIFIER | c.-2766C>T| |
S171 |
3 | BAA10g04770 | A10 | 2446756 | C | T | upstream_gene_variant | MODIFIER | c.-1993C>T| |
S142 |
4 | BAA10g04770 | A10 | 2447747 | C | T | upstream_gene_variant | MODIFIER | c.-1002C>T| |
S281 |
5 | BAA10g04770 | A10 | 2448368 | C | T | upstream_gene_variant | MODIFIER | c.-381C>T| |
S193 |
6 | BAA10g04770 | A10 | 2448740 | G | A | upstream_gene_variant | MODIFIER | c.-9G>A| |
S219 S72 |
7 | BAA10g04770 | A10 | 2448764 | G | A | missense_variant | MODERATE | c.16G>A|p.Asp6Asn |
S242 |
8 | BAA10g04770 | A10 | 2448905 | C | T | missense_variant | MODERATE | c.157C>T|p.Pro53Ser |
S165 |
9 | BAA10g04770 | A10 | 2449317 | C | T | missense_variant | MODERATE | c.569C>T|p.Ala190Val |
S146 |