Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19240 | A09 | 11685327 | G | A | upstream_gene_variant | MODIFIER | c.-2043G>A| |
S201 |
2 | BAA09g19240 | A09 | 11685334 | C | T | upstream_gene_variant | MODIFIER | c.-2036C>T| |
S148 |
3 | BAA09g19240 | A09 | 11686776 | C | T | upstream_gene_variant | MODIFIER | c.-594C>T| |
S211 S227 |
4 | BAA09g19240 | A09 | 11687339 | G | A | upstream_gene_variant | MODIFIER | c.-31G>A| |
S1 |
5 | BAA09g19240 | A09 | 11687766 | C | T | intron_variant | MODIFIER | c.183+90C>T| |
S143 |
6 | BAA09g19240 | A09 | 11688048 | G | A | intron_variant | MODIFIER | c.184-138G>A| |
S229 |
7 | BAA09g19240 | A09 | 11688130 | G | A | intron_variant | MODIFIER | c.184-56G>A| |
S245 |
8 | BAA09g19240 | A09 | 11688438 | G | A | missense_variant | MODERATE | c.436G>A|p.Asp146Asn |
S226 |
9 | BAA09g19240 | A09 | 11688748 | C | T | missense_variant | MODERATE | c.638C>T|p.Ser213Phe |
S168 |
10 | BAA09g19240 | A09 | 11688861 | G | A | intron_variant | MODIFIER | c.713+38G>A| |
S208 |
11 | BAA09g19240 | A09 | 11689173 | C | T | missense_variant | MODERATE | c.925C>T|p.Pro309Ser |
S305 |
12 | BAA09g19240 | A09 | 11690437 | G | A | missense_variant | MODERATE | c.1531G>A|p.Asp511Asn |
S81 |
13 | BAA09g19240 | A09 | 11690596 | G | A | missense_variant | MODERATE | c.1690G>A|p.Val564Met |
S301 S304 |
14 | BAA09g19240 | A09 | 11690905 | C | T | missense_variant | MODERATE | c.1999C>T|p.Arg667Cys |
S96 |
15 | BAA09g19240 | A09 | 11691076 | C | T | missense_variant | MODERATE | c.2170C>T|p.Pro724Ser |
S62 |
16 | BAA09g19240 | A09 | 11691363 | G | A | synonymous_variant | LOW | c.2457G>A|p.Lys819Lys |
S42 |
17 | BAA09g19240 | A09 | 11691777 | G | A | synonymous_variant | LOW | c.2871G>A|p.Lys957Lys |
S28 |
18 | BAA09g19240 | A09 | 11691964 | C | T | missense_variant | MODERATE | c.3058C>T|p.Pro1020Ser |
S87 |
19 | BAA09g19240 | A09 | 11692009 | C | T | missense_variant | MODERATE | c.3103C>T|p.Leu1035Phe |
S263 |
20 | BAA09g19240 | A09 | 11692724 | G | A | synonymous_variant | LOW | c.3642G>A|p.Lys1214Lys |
S25 S264 S293 |
21 | BAA09g19240 | A09 | 11692748 | C | T | synonymous_variant | LOW | c.3666C>T|p.His1222His |
S263 |
22 | BAA09g19240 | A09 | 11694523 | G | A | intron_variant | MODIFIER | c.5360-59G>A| |
S20 |
23 | BAA09g19240 | A09 | 11694575 | G | A | splice_region_variant&intron_variant | LOW | c.5360-7G>A| |
S251 |
24 | BAA09g19240 | A09 | 11694671 | G | A | missense_variant | MODERATE | c.5449G>A|p.Asp1817Asn |
S183 S198 |
25 | BAA09g19240 | A09 | 11695474 | C | T | synonymous_variant | LOW | c.5902C>T|p.Leu1968Leu |
S9 |