Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00380 | A09 | 442474 | C | T | upstream_gene_variant | MODIFIER | c.-4338C>T| |
S19 |
2 | BAA09g00380 | A09 | 445633 | G | A | upstream_gene_variant | MODIFIER | c.-1179G>A| |
S266 |
3 | BAA09g00380 | A09 | 445757 | C | T | upstream_gene_variant | MODIFIER | c.-1055C>T| |
S297 |
4 | BAA09g00380 | A09 | 447251 | C | T | missense_variant | MODERATE | c.196C>T|p.His66Tyr |
S62 |
5 | BAA09g00380 | A09 | 449035 | G | A | missense_variant | MODERATE | c.1139G>A|p.Gly380Asp |
S13 |
6 | BAA09g00380 | A09 | 449476 | G | A | missense_variant | MODERATE | c.1580G>A|p.Gly527Glu |
S81 S85 |
7 | BAA09g00380 | A09 | 449502 | G | A | missense_variant | MODERATE | c.1606G>A|p.Glu536Lys |
S266 |
8 | BAA09g00380 | A09 | 449715 | G | A | missense_variant | MODERATE | c.1819G>A|p.Glu607Lys |
S240 |
9 | BAA09g00380 | A09 | 449800 | G | A | missense_variant | MODERATE | c.1904G>A|p.Ser635Asn |
S42 |
10 | BAA09g00380 | A09 | 450341 | C | T | synonymous_variant | LOW | c.2445C>T|p.Pro815Pro |
S297 |
11 | BAA09g00380 | A09 | 450845 | G | A | synonymous_variant | LOW | c.2949G>A|p.Gln983Gln |
S36 |
12 | BAA09g00380 | A09 | 451377 | C | T | missense_variant | MODERATE | c.3377C>T|p.Ala1126Val |
S64 |
13 | BAA09g00380 | A09 | 451380 | C | T | missense_variant | MODERATE | c.3380C>T|p.Ala1127Val |
S203 |
14 | BAA09g00380 | A09 | 451434 | C | T | missense_variant | MODERATE | c.3434C>T|p.Ala1145Val |
S192 |
15 | BAA09g00380 | A09 | 451601 | G | A | missense_variant | MODERATE | c.3601G>A|p.Asp1201Asn |
S201 |
16 | BAA09g00380 | A09 | 451682 | G | A | missense_variant | MODERATE | c.3682G>A|p.Glu1228Lys |
S1 |
17 | BAA09g00380 | A09 | 451732 | C | T | synonymous_variant | LOW | c.3732C>T|p.Ala1244Ala |
S115 |
18 | BAA09g00380 | A09 | 452058 | C | T | missense_variant | MODERATE | c.4058C>T|p.Ser1353Phe |
S45 |
19 | BAA09g00380 | A09 | 452924 | G | A | missense_variant | MODERATE | c.4924G>A|p.Gly1642Arg |
S130 |
20 | BAA09g00380 | A09 | 453625 | G | A | synonymous_variant | LOW | c.5625G>A|p.Glu1875Glu |
S275 |
21 | BAA09g00380 | A09 | 453771 | C | T | missense_variant | MODERATE | c.5771C>T|p.Pro1924Leu |
S249 |
22 | BAA09g00380 | A09 | 454005 | C | T | splice_region_variant&intron_variant | LOW | c.5907-8C>T| |
S172 S217 |
23 | BAA09g00380 | A09 | 456853 | C | T | downstream_gene_variant | MODIFIER | c.*1993C>T| |
S202 |