| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 128051 | BAA10g16360 | A10 | 16205268 | C | T | missense_variant | MODERATE | c.1021G>A|p.Glu341Lys |
S142 |
| 128052 | BAA10g16360 | A10 | 16205352 | G | A | missense_variant | MODERATE | c.937C>T|p.Leu313Phe |
S262 |
| 128053 | BAA10g16360 | A10 | 16205367 | C | T | missense_variant | MODERATE | c.922G>A|p.Glu308Lys |
S133 |
| 128054 | BAA10g16360 | A10 | 16206148 | G | A | synonymous_variant | LOW | c.141C>T|p.Ala47Ala |
S18 |
| 128055 | BAA10g16360 | A10 | 16206532 | G | A | upstream_gene_variant | MODIFIER | c.-244C>T| |
S153 S213 S80 |
| 128056 | BAA10g16360 | A10 | 16208254 | G | A | upstream_gene_variant | MODIFIER | c.-1966C>T| |
S267 |
| 128057 | BAA10g16360 | A10 | 16208550 | C | T | upstream_gene_variant | MODIFIER | c.-2262G>A| |
S246 |
| 128058 | BAA10g16370 | A10 | 16209293 | G | A | missense_variant | MODERATE | c.563C>T|p.Ser188Phe |
S290 |
| 128059 | BAA10g16370 | A10 | 16209606 | G | A | missense_variant | MODERATE | c.250C>T|p.His84Tyr |
S250 |
| 128060 | BAA10g16360 | A10 | 16209923 | G | A | upstream_gene_variant | MODIFIER | c.-3635C>T| |
S176 |
| 128061 | BAA10g16360 | A10 | 16209946 | C | T | upstream_gene_variant | MODIFIER | c.-3658G>A| |
S73 |
| 128062 | BAA10g16360 | A10 | 16210633 | G | A | upstream_gene_variant | MODIFIER | c.-4345C>T| |
S286 |
| 128063 | BAA10g16370 | A10 | 16211743 | C | T | upstream_gene_variant | MODIFIER | c.-1888G>A| |
S246 |
| 128064 | BAA10g16370 | A10 | 16213106 | G | A | upstream_gene_variant | MODIFIER | c.-3251C>T| |
S252 |
| 128065 | BAA10g16370 | A10 | 16214268 | A | T | upstream_gene_variant | MODIFIER | c.-4413T>A| |
S13 S140 S219 S279 S64 |
| 128066 | BAA10g16380 | A10 | 16215781 | G | A | synonymous_variant | LOW | c.663C>T|p.Ile221Ile |
S198 |
| 128067 | BAA10g16390 | A10 | 16218033 | G | A | missense_variant | MODERATE | c.3239C>T|p.Pro1080Leu |
S132 S137 S215 |
| 128068 | BAA10g16390 | A10 | 16218082 | C | T | missense_variant | MODERATE | c.3190G>A|p.Val1064Ile |
S60 |
| 128069 | BAA10g16390 | A10 | 16219914 | C | T | synonymous_variant | LOW | c.2061G>A|p.Lys687Lys |
S169 |
| 128070 | BAA10g16390 | A10 | 16220171 | G | A | missense_variant | MODERATE | c.1804C>T|p.Leu602Phe |
S59 |
| 128071 | BAA10g16390 | A10 | 16220197 | G | A | missense_variant | MODERATE | c.1778C>T|p.Ser593Phe |
S213 |
| 128072 | BAA10g16390 | A10 | 16220352 | G | A | synonymous_variant | LOW | c.1623C>T|p.Asn541Asn |
S125 |
| 128073 | BAA10g16390 | A10 | 16221217 | C | T | missense_variant | MODERATE | c.758G>A|p.Arg253Lys |
S144 |
| 128074 | BAA10g16390 | A10 | 16221389 | G | A | missense_variant | MODERATE | c.586C>T|p.Pro196Ser |
S166 |
| 128075 | BAA10g16390 | A10 | 16221423 | C | T | synonymous_variant | LOW | c.552G>A|p.Glu184Glu |
S116 |