Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g15930 | A06 | 7878607 | G | A | stop_gained | HIGH | c.2623C>T|p.Gln875* |
S185 |
2 | BAA06g15930 | A06 | 7878820 | G | A | synonymous_variant | LOW | c.2410C>T|p.Leu804Leu |
S229 |
3 | BAA06g15930 | A06 | 7878854 | C | T | stop_gained | HIGH | c.2376G>A|p.Trp792* |
S158 |
4 | BAA06g15930 | A06 | 7878938 | C | T | synonymous_variant | LOW | c.2292G>A|p.Ser764Ser |
S237 |
5 | BAA06g15930 | A06 | 7879021 | C | T | missense_variant | MODERATE | c.2209G>A|p.Gly737Arg |
S10 |
6 | BAA06g15930 | A06 | 7879643 | G | A | missense_variant | MODERATE | c.1679C>T|p.Ser560Phe |
S182 |
7 | BAA06g15930 | A06 | 7879829 | C | T | missense_variant | MODERATE | c.1493G>A|p.Arg498Gln |
S60 |
8 | BAA06g15930 | A06 | 7880126 | C | T | missense_variant | MODERATE | c.1196G>A|p.Ser399Asn |
S257 |
9 | BAA06g15930 | A06 | 7880816 | C | T | missense_variant | MODERATE | c.506G>A|p.Arg169Gln |
S255 |
10 | BAA06g15930 | A06 | 7880871 | C | T | missense_variant | MODERATE | c.451G>A|p.Asp151Asn |
S4 |
11 | BAA06g15930 | A06 | 7881111 | C | T | missense_variant | MODERATE | c.211G>A|p.Asp71Asn |
S16 |
12 | BAA06g15930 | A06 | 7881981 | C | T | upstream_gene_variant | MODIFIER | c.-660G>A| |
S245 |
13 | BAA06g15930 | A06 | 7883323 | G | A | upstream_gene_variant | MODIFIER | c.-2002C>T| |
S70 |
14 | BAA06g15930 | A06 | 7883900 | C | T | upstream_gene_variant | MODIFIER | c.-2579G>A| |
S116 |
15 | BAA06g15930 | A06 | 7884861 | G | A | upstream_gene_variant | MODIFIER | c.-3540C>T| |
S186 |
16 | BAA06g15930 | A06 | 7885740 | C | T | upstream_gene_variant | MODIFIER | c.-4419G>A| |
S279 |