Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g10800 | A09 | 5930997 | T | A | missense_variant | MODERATE | c.592T>A|p.Ser198Thr |
S113 S275 |
2 | BAA09g10800 | A09 | 5931004 | C | T | missense_variant | MODERATE | c.599C>T|p.Ser200Phe |
S56 |
3 | BAA09g10800 | A09 | 5931603 | G | A | missense_variant | MODERATE | c.1198G>A|p.Asp400Asn |
S56 |
4 | BAA09g10800 | A09 | 5931611 | G | A | synonymous_variant | LOW | c.1206G>A|p.Lys402Lys |
S129 |
5 | BAA09g10800 | A09 | 5931667 | G | A | missense_variant | MODERATE | c.1262G>A|p.Gly421Glu |
S262 |
6 | BAA09g10800 | A09 | 5931756 | G | A | missense_variant | MODERATE | c.1351G>A|p.Asp451Asn |
S233 |
7 | BAA09g10800 | A09 | 5932207 | C | T | missense_variant | MODERATE | c.1802C>T|p.Ser601Leu |
S208 S219 |
8 | BAA09g10800 | A09 | 5932384 | G | A | missense_variant | MODERATE | c.1979G>A|p.Arg660His |
S219 S72 |
9 | BAA09g10800 | A09 | 5932651 | C | T | missense_variant | MODERATE | c.2246C>T|p.Thr749Ile |
S298 |
10 | BAA09g10800 | A09 | 5934513 | G | A | splice_region_variant&intron_variant | LOW | c.2584-8G>A| |
S192 |
11 | BAA09g10800 | A09 | 5934728 | C | T | intron_variant | MODIFIER | c.2782+9C>T| |
S204 |
12 | BAA09g10800 | A09 | 5935054 | G | A | missense_variant | MODERATE | c.2897G>A|p.Ser966Asn |
S192 |
13 | BAA09g10800 | A09 | 5935199 | A | T | intron_variant | MODIFIER | c.3005+37A>T| |
S206 |
14 | BAA09g10800 | A09 | 5935590 | G | A | splice_region_variant&intron_variant | LOW | c.3213+3G>A| |
S205 |
15 | BAA09g10800 | A09 | 5935966 | G | A | synonymous_variant | LOW | c.3366G>A|p.Arg1122Arg |
S115 |
16 | BAA09g10800 | A09 | 5936199 | G | A | missense_variant | MODERATE | c.3415G>A|p.Asp1139Asn |
S30 S31 |
17 | BAA09g10800 | A09 | 5937553 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.4151-1G>A| |
S45 |
18 | BAA09g10800 | A09 | 5938066 | C | T | intron_variant | MODIFIER | c.4434+141C>T| |
S64 |
19 | BAA09g10800 | A09 | 5939209 | G | A | missense_variant | MODERATE | c.4907G>A|p.Arg1636Lys |
S66 |
20 | BAA09g10800 | A09 | 5939841 | C | T | intron_variant | MODIFIER | c.5232-122C>T| |
S107 |
21 | BAA09g10800 | A09 | 5940665 | G | A | missense_variant | MODERATE | c.5489G>A|p.Gly1830Glu |
S245 |
22 | BAA09g10800 | A09 | 5942614 | C | T | synonymous_variant | LOW | c.6507C>T|p.Asp2169Asp |
S183 S198 |
23 | BAA09g10800 | A09 | 5944188 | G | A | synonymous_variant | LOW | c.7695G>A|p.Lys2565Lys |
S245 |
24 | BAA09g10800 | A09 | 5944435 | G | A | missense_variant | MODERATE | c.7942G>A|p.Val2648Met |
S200 |
25 | BAA09g10800 | A09 | 5944673 | C | T | missense_variant | MODERATE | c.8180C>T|p.Ser2727Phe |
S236 |