Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02790 | A10 | 1330539 | C | T | missense_variant | MODERATE | c.4189G>A|p.Asp1397Asn |
S2 |
2 | BAA10g02790 | A10 | 1330759 | C | T | missense_variant | MODERATE | c.4052G>A|p.Gly1351Glu |
S249 |
3 | BAA10g02790 | A10 | 1331006 | C | T | missense_variant&splice_region_variant | MODERATE | c.3805G>A|p.Val1269Ile |
S56 |
4 | BAA10g02790 | A10 | 1331792 | G | A | synonymous_variant | LOW | c.3177C>T|p.Leu1059Leu |
S129 |
5 | BAA10g02790 | A10 | 1333161 | C | T | synonymous_variant | LOW | c.2157G>A|p.Lys719Lys |
S170 |
6 | BAA10g02790 | A10 | 1334007 | C | T | missense_variant | MODERATE | c.1390G>A|p.Glu464Lys |
S23 |
7 | BAA10g02790 | A10 | 1334444 | G | A | missense_variant | MODERATE | c.953C>T|p.Pro318Leu |
S51 |
8 | BAA10g02790 | A10 | 1334552 | G | A | missense_variant | MODERATE | c.845C>T|p.Ser282Phe |
S164 |
9 | BAA10g02790 | A10 | 1334561 | C | T | missense_variant | MODERATE | c.836G>A|p.Arg279Lys |
S260 |
10 | BAA10g02790 | A10 | 1334609 | C | T | missense_variant | MODERATE | c.788G>A|p.Arg263Lys |
S177 |
11 | BAA10g02790 | A10 | 1335287 | G | A | missense_variant | MODERATE | c.110C>T|p.Ser37Phe |
S17 |
12 | BAA10g02790 | A10 | 1335355 | G | A | synonymous_variant | LOW | c.42C>T|p.Leu14Leu |
S71 |
13 | BAA10g02790 | A10 | 1335652 | G | A | upstream_gene_variant | MODIFIER | c.-256C>T| |
S149 S170 |
14 | BAA10g02790 | A10 | 1336763 | G | A | upstream_gene_variant | MODIFIER | c.-1367C>T| |
S48 |
15 | BAA10g02790 | A10 | 1338039 | G | A | upstream_gene_variant | MODIFIER | c.-2643C>T| |
S48 |
16 | BAA10g02790 | A10 | 1338165 | C | T | upstream_gene_variant | MODIFIER | c.-2769G>A| |
S226 |
17 | BAA10g02790 | A10 | 1338204 | C | T | upstream_gene_variant | MODIFIER | c.-2808G>A| |
S193 |
18 | BAA10g02790 | A10 | 1339281 | G | A | upstream_gene_variant | MODIFIER | c.-3885C>T| |
S234 |
19 | BAA10g02790 | A10 | 1339543 | G | A | upstream_gene_variant | MODIFIER | c.-4147C>T| |
S295 |
20 | BAA10g02790 | A10 | 1339997 | G | A | upstream_gene_variant | MODIFIER | c.-4601C>T| |
S13 |