Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g26900 | A04 | 27275463 | C | T | missense_variant | MODERATE | c.584C>T|p.Ser195Phe |
S1 S90 |
2 | BAA04g26900 | A04 | 27275752 | G | A | intron_variant | MODIFIER | c.727+146G>A| |
S262 |
3 | BAA04g26900 | A04 | 27276096 | C | T | intron_variant | MODIFIER | c.804+21C>T| |
S83 S88 |
4 | BAA04g26900 | A04 | 27276631 | G | A | missense_variant | MODERATE | c.1198G>A|p.Glu400Lys |
S38 |
5 | BAA04g26900 | A04 | 27276921 | C | T | missense_variant | MODERATE | c.1424C>T|p.Ser475Phe |
S100 |
6 | BAA04g26900 | A04 | 27278124 | G | C | missense_variant | MODERATE | c.2137G>C|p.Glu713Gln |
S155 |
7 | BAA04g26900 | A04 | 27278875 | C | T | missense_variant | MODERATE | c.2666C>T|p.Ala889Val |
S46 |
8 | BAA04g26900 | A04 | 27278970 | C | T | missense_variant | MODERATE | c.2761C>T|p.Pro921Ser |
S200 |
9 | BAA04g26900 | A04 | 27279109 | G | A | missense_variant | MODERATE | c.2824G>A|p.Glu942Lys |
S56 |
10 | BAA04g26900 | A04 | 27279933 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.3163-1G>A| |
S165 |
11 | BAA04g26900 | A04 | 27279998 | C | T | missense_variant | MODERATE | c.3227C>T|p.Thr1076Ile |
S272 |
12 | BAA04g26900 | A04 | 27280716 | G | A | missense_variant | MODERATE | c.3557G>A|p.Gly1186Glu |
S38 |
13 | BAA04g26900 | A04 | 27280834 | C | T | synonymous_variant | LOW | c.3675C>T|p.Ala1225Ala |
S215 |
14 | BAA04g26900 | A04 | 27281105 | C | T | synonymous_variant | LOW | c.3946C>T|p.Leu1316Leu |
S140 |
15 | BAA04g26900 | A04 | 27281325 | G | A | missense_variant | MODERATE | c.4081G>A|p.Ala1361Thr |
S158 |