Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12760 | A10 | 14101083 | G | A | missense_variant | MODERATE | c.2156C>T|p.Ala719Val |
S69 |
2 | BAA10g12760 | A10 | 14104057 | C | T | missense_variant | MODERATE | c.1862G>A|p.Gly621Glu |
S87 |
3 | BAA10g12760 | A10 | 14104443 | G | A | synonymous_variant | LOW | c.1476C>T|p.Arg492Arg |
S192 |
4 | BAA10g12760 | A10 | 14104899 | G | A | synonymous_variant | LOW | c.1170C>T|p.Leu390Leu |
S289 |
5 | BAA10g12760 | A10 | 14105053 | G | A | missense_variant | MODERATE | c.1016C>T|p.Ser339Phe |
S261 |
6 | BAA10g12760 | A10 | 14105087 | C | T | missense_variant | MODERATE | c.982G>A|p.Asp328Asn |
S305 |
7 | BAA10g12760 | A10 | 14106429 | C | T | intron_variant | MODIFIER | c.785+709G>A| |
S180 |
8 | BAA10g12760 | A10 | 14107550 | C | T | missense_variant | MODERATE | c.460G>A|p.Val154Ile |
S12 |
9 | BAA10g12760 | A10 | 14108052 | G | A | upstream_gene_variant | MODIFIER | c.-43C>T| |
S59 |
10 | BAA10g12760 | A10 | 14108200 | G | A | upstream_gene_variant | MODIFIER | c.-191C>T| |
S218 |
11 | BAA10g12760 | A10 | 14108830 | G | A | upstream_gene_variant | MODIFIER | c.-821C>T| |
S35 |
12 | BAA10g12760 | A10 | 14109289 | G | A | upstream_gene_variant | MODIFIER | c.-1280C>T| |
S261 |
13 | BAA10g12760 | A10 | 14109632 | G | A | upstream_gene_variant | MODIFIER | c.-1623C>T| |
S217 |
14 | BAA10g12760 | A10 | 14110204 | C | T | upstream_gene_variant | MODIFIER | c.-2195G>A| |
S224 |
15 | BAA10g12760 | A10 | 14110474 | G | A | upstream_gene_variant | MODIFIER | c.-2465C>T| |
S1 S90 |
16 | BAA10g12760 | A10 | 14111509 | G | A | upstream_gene_variant | MODIFIER | c.-3500C>T| |
S1 S90 |
17 | BAA10g12760 | A10 | 14112189 | G | A | upstream_gene_variant | MODIFIER | c.-4180C>T| |
S150 |
18 | BAA10g12760 | A10 | 14112624 | G | A | upstream_gene_variant | MODIFIER | c.-4615C>T| |
S129 |