Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g32620 | A07 | 31992978 | G | A | downstream_gene_variant | MODIFIER | c.*4920C>T| |
S72 S78 |
2 | BAA07g32620 | A07 | 31995584 | G | A | downstream_gene_variant | MODIFIER | c.*2314C>T| |
S270 |
3 | BAA07g32620 | A07 | 31998161 | G | A | splice_region_variant&intron_variant | LOW | c.1643-5C>T| |
S36 |
4 | BAA07g32620 | A07 | 31998704 | C | T | missense_variant | MODERATE | c.1336G>A|p.Glu446Lys |
S174 S216 S241 S27 S39 |
5 | BAA07g32620 | A07 | 31998846 | G | A | missense_variant | MODERATE | c.1270C>T|p.Leu424Phe |
S195 |
6 | BAA07g32620 | A07 | 31998936 | G | A | missense_variant | MODERATE | c.1180C>T|p.Pro394Ser |
S135 |
7 | BAA07g32620 | A07 | 31999889 | C | T | missense_variant&splice_region_variant | MODERATE | c.640G>A|p.Asp214Asn |
S25 |
8 | BAA07g32620 | A07 | 32000154 | C | T | splice_region_variant&intron_variant | LOW | c.532+7G>A| |
S197 |
9 | BAA07g32620 | A07 | 32000311 | C | T | missense_variant | MODERATE | c.472G>A|p.Ala158Thr |
S262 |
10 | BAA07g32620 | A07 | 32001274 | G | A | upstream_gene_variant | MODIFIER | c.-43C>T| |
S205 |
11 | BAA07g32620 | A07 | 32003006 | G | A | upstream_gene_variant | MODIFIER | c.-1775C>T| |
S97 |
12 | BAA07g32620 | A07 | 32004228 | C | T | upstream_gene_variant | MODIFIER | c.-2997G>A| |
S221 |
13 | BAA07g32620 | A07 | 32004917 | C | T | upstream_gene_variant | MODIFIER | c.-3686G>A| |
S56 |
14 | BAA07g32620 | A07 | 32004938 | G | A | upstream_gene_variant | MODIFIER | c.-3707C>T| |
S273 |