Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00870 | A10 | 404376 | C | T | upstream_gene_variant | MODIFIER | c.-481C>T| |
S143 |
2 | BAA10g00870 | A10 | 404887 | G | A | missense_variant | MODERATE | c.31G>A|p.Glu11Lys |
S134 S193 |
3 | BAA10g00870 | A10 | 405247 | C | T | missense_variant | MODERATE | c.391C>T|p.Pro131Ser |
S63 |
4 | BAA10g00870 | A10 | 405518 | G | A | intron_variant | MODIFIER | c.624+38G>A| |
S176 |
5 | BAA10g00870 | A10 | 405608 | G | A | intron_variant | MODIFIER | c.624+128G>A| |
S43 |
6 | BAA10g00870 | A10 | 405882 | G | A | intron_variant | MODIFIER | c.624+402G>A| |
S157 S163 |
7 | BAA10g00870 | A10 | 406626 | G | A | intron_variant | MODIFIER | c.625-635G>A| |
S125 |
8 | BAA10g00870 | A10 | 407457 | G | A | splice_region_variant&synonymous_variant | LOW | c.648G>A|p.Arg216Arg |
S234 |
9 | BAA10g00870 | A10 | 407894 | G | A | missense_variant | MODERATE | c.1085G>A|p.Arg362Gln |
S176 |
10 | BAA10g00870 | A10 | 408297 | G | A | missense_variant | MODERATE | c.1213G>A|p.Asp405Asn |
S180 |
11 | BAA10g00870 | A10 | 408874 | G | A | missense_variant | MODERATE | c.1595G>A|p.Ser532Asn |
S148 S210 S30 |
12 | BAA10g00870 | A10 | 408897 | G | A | missense_variant | MODERATE | c.1618G>A|p.Asp540Asn |
S256 |
13 | BAA10g00870 | A10 | 409667 | C | T | missense_variant | MODERATE | c.2105C>T|p.Ser702Phe |
S23 |