Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13380 | A10 | 14501403 | C | T | stop_gained | HIGH | c.1920G>A|p.Trp640* |
S302 |
2 | BAA10g13380 | A10 | 14501504 | G | A | synonymous_variant | LOW | c.1819C>T|p.Leu607Leu |
S262 |
3 | BAA10g13380 | A10 | 14502024 | C | T | missense_variant | MODERATE | c.1369G>A|p.Asp457Asn |
S142 |
4 | BAA10g13380 | A10 | 14502258 | G | A | missense_variant | MODERATE | c.1135C>T|p.Leu379Phe |
S139 |
5 | BAA10g13380 | A10 | 14502336 | G | A | synonymous_variant | LOW | c.1057C>T|p.Leu353Leu |
S136 |
6 | BAA10g13380 | A10 | 14502727 | C | T | missense_variant | MODERATE | c.758G>A|p.Arg253Gln |
S302 |
7 | BAA10g13380 | A10 | 14502873 | C | T | synonymous_variant | LOW | c.612G>A|p.Thr204Thr |
S47 |
8 | BAA10g13380 | A10 | 14502874 | G | A | missense_variant | MODERATE | c.611C>T|p.Thr204Met |
S15 S3 |
9 | BAA10g13380 | A10 | 14503967 | C | T | missense_variant | MODERATE | c.10G>A|p.Glu4Lys |
S84 S93 |
10 | BAA10g13380 | A10 | 14505482 | G | A | upstream_gene_variant | MODIFIER | c.-1506C>T| |
S261 |
11 | BAA10g13380 | A10 | 14506290 | G | A | upstream_gene_variant | MODIFIER | c.-2314C>T| |
S245 |
12 | BAA10g13380 | A10 | 14506584 | C | T | upstream_gene_variant | MODIFIER | c.-2608G>A| |
S269 |
13 | BAA10g13380 | A10 | 14506838 | C | T | upstream_gene_variant | MODIFIER | c.-2862G>A| |
S45 |
14 | BAA10g13380 | A10 | 14506948 | C | T | upstream_gene_variant | MODIFIER | c.-2972G>A| |
S119 |
15 | BAA10g13380 | A10 | 14508134 | C | T | upstream_gene_variant | MODIFIER | c.-4158G>A| |
S238 |
16 | BAA10g13380 | A10 | 14508451 | C | T | upstream_gene_variant | MODIFIER | c.-4475G>A| |
S121 |