Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g16350 | A07 | 23154198 | C | T | missense_variant&splice_region_variant | MODERATE | c.4189G>A|p.Val1397Met |
S153 |
2 | BAA07g16350 | A07 | 23155344 | G | A | missense_variant | MODERATE | c.3560C>T|p.Thr1187Ile |
S210 |
3 | BAA07g16350 | A07 | 23155387 | C | T | missense_variant | MODERATE | c.3517G>A|p.Gly1173Arg |
S109 |
4 | BAA07g16350 | A07 | 23157199 | C | T | missense_variant | MODERATE | c.2839G>A|p.Gly947Arg |
S36 |
5 | BAA07g16350 | A07 | 23157230 | G | A | synonymous_variant | LOW | c.2808C>T|p.Ile936Ile |
S246 |
6 | BAA07g16350 | A07 | 23159889 | C | T | synonymous_variant | LOW | c.1431G>A|p.Lys477Lys |
S164 |
7 | BAA07g16350 | A07 | 23161042 | C | T | missense_variant | MODERATE | c.541G>A|p.Asp181Asn |
S293 |
8 | BAA07g16350 | A07 | 23161211 | C | T | synonymous_variant | LOW | c.372G>A|p.Lys124Lys |
S266 |
9 | BAA07g16350 | A07 | 23161226 | C | T | synonymous_variant | LOW | c.357G>A|p.Gly119Gly |
S166 |
10 | BAA07g16350 | A07 | 23161476 | C | T | missense_variant | MODERATE | c.107G>A|p.Gly36Glu |
S262 |
11 | BAA07g16350 | A07 | 23161577 | G | A | synonymous_variant | LOW | c.6C>T|p.Ser2Ser |
S244 |
12 | BAA07g16350 | A07 | 23161896 | C | T | upstream_gene_variant | MODIFIER | c.-314G>A| |
S104 |
13 | BAA07g16350 | A07 | 23162210 | G | A | upstream_gene_variant | MODIFIER | c.-628C>T| |
S225 S73 |
14 | BAA07g16350 | A07 | 23162288 | G | A | upstream_gene_variant | MODIFIER | c.-706C>T| |
S217 S248 |
15 | BAA07g16350 | A07 | 23164630 | C | T | upstream_gene_variant | MODIFIER | c.-3048G>A| |
S144 |
16 | BAA07g16350 | A07 | 23165286 | G | A | upstream_gene_variant | MODIFIER | c.-3704C>T| |
S226 |
17 | BAA07g16350 | A07 | 23165379 | C | A | upstream_gene_variant | MODIFIER | c.-3797G>T| |
S217 S248 |