Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g40690 | A07 | 35966437 | C | T | missense_variant | MODERATE | c.482C>T|p.Pro161Leu |
S8 |
2 | BAA07g40690 | A07 | 35966525 | G | A | synonymous_variant | LOW | c.570G>A|p.Arg190Arg |
S209 |
3 | BAA07g40690 | A07 | 35967491 | G | A | synonymous_variant | LOW | c.1536G>A|p.Glu512Glu |
S205 |
4 | BAA07g40690 | A07 | 35968979 | G | A | missense_variant | MODERATE | c.2833G>A|p.Glu945Lys |
S287 |
5 | BAA07g40690 | A07 | 35969221 | C | T | splice_region_variant&intron_variant | LOW | c.3067+8C>T| |
S7 |
6 | BAA07g40690 | A07 | 35969480 | C | T | missense_variant | MODERATE | c.3247C>T|p.Pro1083Ser |
S249 |
7 | BAA07g40690 | A07 | 35969563 | G | A | synonymous_variant | LOW | c.3330G>A|p.Ala1110Ala |
S40 S49 |
8 | BAA07g40690 | A07 | 35969630 | C | T | missense_variant | MODERATE | c.3397C>T|p.His1133Tyr |
S122 |
9 | BAA07g40690 | A07 | 35969641 | G | A | synonymous_variant | LOW | c.3408G>A|p.Glu1136Glu |
S44 |
10 | BAA07g40690 | A07 | 35969879 | G | A | missense_variant | MODERATE | c.3646G>A|p.Val1216Ile |
S142 |
11 | BAA07g40690 | A07 | 35969942 | G | A | missense_variant | MODERATE | c.3709G>A|p.Asp1237Asn |
S60 |
12 | BAA07g40690 | A07 | 35970431 | G | A | missense_variant | MODERATE | c.4198G>A|p.Glu1400Lys |
S79 S84 |
13 | BAA07g40690 | A07 | 35970700 | C | T | synonymous_variant | LOW | c.4467C>T|p.Ala1489Ala |
S63 |
14 | BAA07g40690 | A07 | 35970949 | G | A | synonymous_variant | LOW | c.4716G>A|p.Glu1572Glu |
S269 |
15 | BAA07g40690 | A07 | 35972456 | G | A | splice_region_variant&intron_variant | LOW | c.5713+5G>A| |
S296 |