Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g16510 | A04 | 20889528 | C | T | upstream_gene_variant | MODIFIER | c.-2890C>T| |
S252 |
2 | BAA04g16510 | A04 | 20889534 | C | T | upstream_gene_variant | MODIFIER | c.-2884C>T| |
S197 |
3 | BAA04g16510 | A04 | 20890951 | C | T | upstream_gene_variant | MODIFIER | c.-1467C>T| |
S221 |
4 | BAA04g16510 | A04 | 20892177 | C | T | upstream_gene_variant | MODIFIER | c.-241C>T| |
S95 |
5 | BAA04g16510 | A04 | 20892452 | G | A | missense_variant | MODERATE | c.35G>A|p.Ser12Asn |
S12 |
6 | BAA04g16510 | A04 | 20892523 | G | A | missense_variant | MODERATE | c.106G>A|p.Asp36Asn |
S35 |
7 | BAA04g16510 | A04 | 20892644 | C | T | missense_variant | MODERATE | c.227C>T|p.Ser76Phe |
S107 |
8 | BAA04g16510 | A04 | 20892757 | G | A | missense_variant | MODERATE | c.340G>A|p.Ala114Thr |
S251 S303 |
9 | BAA04g16510 | A04 | 20892882 | C | T | synonymous_variant | LOW | c.465C>T|p.Leu155Leu |
S197 |
10 | BAA04g16510 | A04 | 20893072 | G | A | missense_variant | MODERATE | c.655G>A|p.Glu219Lys |
S153 |
11 | BAA04g16510 | A04 | 20893168 | G | A | missense_variant | MODERATE | c.751G>A|p.Asp251Asn |
S94 |
12 | BAA04g16510 | A04 | 20893295 | C | T | missense_variant | MODERATE | c.878C>T|p.Ser293Phe |
S53 |
13 | BAA04g16510 | A04 | 20893378 | G | A | missense_variant | MODERATE | c.961G>A|p.Val321Ile |
S250 |
14 | BAA04g16510 | A04 | 20893381 | G | A | missense_variant | MODERATE | c.964G>A|p.Glu322Lys |
S109 |
15 | BAA04g16510 | A04 | 20894044 | G | A | missense_variant | MODERATE | c.1553G>A|p.Gly518Asp |
S165 |
16 | BAA04g16510 | A04 | 20894139 | G | A | missense_variant | MODERATE | c.1648G>A|p.Asp550Asn |
S13 S33 |
17 | BAA04g16510 | A04 | 20894412 | C | T | intron_variant | MODIFIER | c.1863-47C>T| |
S247 |
18 | BAA04g16510 | A04 | 20894603 | G | A | synonymous_variant | LOW | c.2007G>A|p.Leu669Leu |
S71 |
19 | BAA04g16510 | A04 | 20894633 | C | T | synonymous_variant | LOW | c.2037C>T|p.Tyr679Tyr |
S68 |
20 | BAA04g16510 | A04 | 20895049 | G | A | missense_variant | MODERATE | c.2453G>A|p.Gly818Glu |
S282 |
21 | BAA04g16510 | A04 | 20896130 | G | A | intron_variant | MODIFIER | c.2941-504G>A| |
S277 |
22 | BAA04g16510 | A04 | 20896140 | C | T | intron_variant | MODIFIER | c.2941-494C>T| |
S110 |
23 | BAA04g16510 | A04 | 20896409 | G | A | intron_variant | MODIFIER | c.2941-225G>A| |
S130 |
24 | BAA04g16510 | A04 | 20896488 | G | A | intron_variant | MODIFIER | c.2941-146G>A| |
S79 S91 |
25 | BAA04g16510 | A04 | 20896995 | C | T | missense_variant | MODERATE | c.3302C>T|p.Ser1101Phe |
S247 |