Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21100 | A10 | 18682934 | C | T | missense_variant | MODERATE | c.1001G>A|p.Ser334Asn |
S255 |
2 | BAA10g21100 | A10 | 18683012 | G | A | missense_variant | MODERATE | c.923C>T|p.Ala308Val |
S303 |
3 | BAA10g21100 | A10 | 18683468 | G | A | synonymous_variant | LOW | c.757C>T|p.Leu253Leu |
S267 |
4 | BAA10g21100 | A10 | 18684178 | G | A | missense_variant | MODERATE | c.490C>T|p.Pro164Ser |
S64 |
5 | BAA10g21100 | A10 | 18684489 | C | T | synonymous_variant | LOW | c.324G>A|p.Glu108Glu |
S121 |
6 | BAA10g21100 | A10 | 18684566 | G | A | splice_region_variant&intron_variant | LOW | c.318+4C>T| |
S82 S92 |
7 | BAA10g21100 | A10 | 18684913 | G | A | missense_variant | MODERATE | c.143C>T|p.Ser48Phe |
S279 |
8 | BAA10g21100 | A10 | 18685129 | G | A | missense_variant | MODERATE | c.70C>T|p.Pro24Ser |
S287 |
9 | BAA10g21100 | A10 | 18686659 | C | T | upstream_gene_variant | MODIFIER | c.-639G>A| |
S144 |
10 | BAA10g21100 | A10 | 18687199 | C | T | upstream_gene_variant | MODIFIER | c.-1179G>A| |
S216 |
11 | BAA10g21100 | A10 | 18687612 | C | T | upstream_gene_variant | MODIFIER | c.-1592G>A| |
S87 |
12 | BAA10g21100 | A10 | 18690865 | G | A | upstream_gene_variant | MODIFIER | c.-4845C>T| |
S182 |