Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g32550 | A07 | 31939960 | G | A | missense_variant | MODERATE | c.6407C>T|p.Ser2136Phe |
S299 |
2 | BAA07g32550 | A07 | 31941020 | C | T | synonymous_variant | LOW | c.5556G>A|p.Ser1852Ser |
S2 |
3 | BAA07g32550 | A07 | 31941953 | C | T | synonymous_variant | LOW | c.4980G>A|p.Lys1660Lys |
S244 |
4 | BAA07g32550 | A07 | 31943203 | C | T | missense_variant | MODERATE | c.4616G>A|p.Arg1539Lys |
S127 |
5 | BAA07g32550 | A07 | 31944196 | G | A | synonymous_variant | LOW | c.3871C>T|p.Leu1291Leu |
S298 |
6 | BAA07g32550 | A07 | 31945101 | C | T | intron_variant | MODIFIER | c.3542+165G>A| |
S96 |
7 | BAA07g32550 | A07 | 31945476 | C | T | intron_variant | MODIFIER | c.3358-26G>A| |
S192 |
8 | BAA07g32550 | A07 | 31946639 | C | T | missense_variant | MODERATE | c.2984G>A|p.Cys995Tyr |
S162 |
9 | BAA07g32550 | A07 | 31947175 | G | A | missense_variant | MODERATE | c.2752C>T|p.Pro918Ser |
S97 |
10 | BAA07g32550 | A07 | 31948186 | C | T | intron_variant | MODIFIER | c.2419-114G>A| |
S216 |
11 | BAA07g32550 | A07 | 31948716 | C | T | missense_variant | MODERATE | c.2251G>A|p.Val751Met |
S159 S243 |
12 | BAA07g32550 | A07 | 31949630 | C | T | missense_variant | MODERATE | c.1834G>A|p.Glu612Lys |
S15 S3 |
13 | BAA07g32550 | A07 | 31949677 | G | A | missense_variant | MODERATE | c.1787C>T|p.Ala596Val |
S270 |
14 | BAA07g32550 | A07 | 31949969 | G | A | intron_variant | MODIFIER | c.1775+9C>T| |
S267 |
15 | BAA07g32550 | A07 | 31955539 | C | T | upstream_gene_variant | MODIFIER | c.-180G>A| |
S75 S81 |
16 | BAA07g32550 | A07 | 31956701 | C | T | upstream_gene_variant | MODIFIER | c.-1342G>A| |
S293 |
17 | BAA07g32550 | A07 | 31957391 | G | A | upstream_gene_variant | MODIFIER | c.-2032C>T| |
S246 |
18 | BAA07g32550 | A07 | 31958689 | C | T | upstream_gene_variant | MODIFIER | c.-3330G>A| |
S180 |
19 | BAA07g32550 | A07 | 31959649 | G | A | upstream_gene_variant | MODIFIER | c.-4290C>T| |
S227 |