Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g03800 | A05 | 1902478 | G | A | stop_gained | HIGH | c.2059C>T|p.Gln687* |
S293 |
2 | BAA05g03800 | A05 | 1902783 | C | T | missense_variant | MODERATE | c.1899G>A|p.Met633Ile |
S174 S27 |
3 | BAA05g03800 | A05 | 1903257 | C | T | missense_variant&splice_region_variant | MODERATE | c.1425G>A|p.Met475Ile |
S83 S88 |
4 | BAA05g03800 | A05 | 1904110 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1010-1G>A| |
S162 |
5 | BAA05g03800 | A05 | 1904231 | C | T | missense_variant | MODERATE | c.955G>A|p.Gly319Arg |
S36 |
6 | BAA05g03800 | A05 | 1904324 | C | T | missense_variant | MODERATE | c.862G>A|p.Glu288Lys |
S280 |
7 | BAA05g03800 | A05 | 1904723 | C | T | missense_variant | MODERATE | c.463G>A|p.Val155Ile |
S71 |
8 | BAA05g03800 | A05 | 1905480 | C | T | upstream_gene_variant | MODIFIER | c.-9G>A| |
S2 |
9 | BAA05g03800 | A05 | 1906417 | C | T | upstream_gene_variant | MODIFIER | c.-946G>A| |
S20 |
10 | BAA05g03800 | A05 | 1906522 | C | T | upstream_gene_variant | MODIFIER | c.-1051G>A| |
S42 |
11 | BAA05g03800 | A05 | 1906607 | C | T | upstream_gene_variant | MODIFIER | c.-1136G>A| |
S240 |
12 | BAA05g03800 | A05 | 1907181 | G | A | upstream_gene_variant | MODIFIER | c.-1710C>T| |
S125 |
13 | BAA05g03800 | A05 | 1907849 | C | T | upstream_gene_variant | MODIFIER | c.-2378G>A| |
S191 |