| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 126001 | BAA10g14930 | A10 | 15496331 | C | T | missense_variant | MODERATE | c.410G>A|p.Arg137Gln |
S37 |
| 126002 | BAA10g14940 | A10 | 15496369 | G | A | upstream_gene_variant | MODIFIER | c.-1145G>A| |
S1 S90 |
| 126003 | BAA10g14930 | A10 | 15496679 | C | T | missense_variant | MODERATE | c.359G>A|p.Gly120Asp |
S193 |
| 126004 | BAA10g14930 | A10 | 15496807 | C | T | missense_variant | MODERATE | c.317G>A|p.Arg106Lys |
S92 |
| 126005 | BAA10g14930 | A10 | 15496873 | C | T | missense_variant | MODERATE | c.251G>A|p.Arg84His |
S8 |
| 126006 | BAA10g14930 | A10 | 15496963 | C | T | missense_variant | MODERATE | c.161G>A|p.Ser54Asn |
S87 |
| 126007 | BAA10g14930 | A10 | 15497948 | C | T | upstream_gene_variant | MODIFIER | c.-825G>A| |
S150 |
| 126008 | BAA10g14940 | A10 | 15498028 | C | T | synonymous_variant | LOW | c.348C>T|p.Ala116Ala |
S196 |
| 126009 | BAA10g14940 | A10 | 15498712 | G | A | missense_variant | MODERATE | c.715G>A|p.Ala239Thr |
S219 S72 |
| 126010 | BAA10g14940 | A10 | 15498849 | G | A | missense_variant | MODERATE | c.784G>A|p.Gly262Ser |
S172 S217 |
| 126011 | BAA10g14940 | A10 | 15499343 | G | A | missense_variant | MODERATE | c.1124G>A|p.Gly375Asp |
S111 |
| 126012 | BAA10g14930 | A10 | 15499802 | C | T | upstream_gene_variant | MODIFIER | c.-2679G>A| |
S68 |
| 126013 | BAA10g14930 | A10 | 15500174 | C | T | upstream_gene_variant | MODIFIER | c.-3051G>A| |
S305 |
| 126014 | BAA10g14930 | A10 | 15500453 | C | T | upstream_gene_variant | MODIFIER | c.-3330G>A| |
S87 |
| 126015 | BAA10g14930 | A10 | 15501122 | G | A | upstream_gene_variant | MODIFIER | c.-3999C>T| |
S201 |
| 126016 | BAA10g14950 | A10 | 15502508 | G | A | missense_variant | MODERATE | c.326G>A|p.Gly109Asp |
S180 |
| 126017 | BAA10g14950 | A10 | 15502660 | C | T | missense_variant | MODERATE | c.478C>T|p.Pro160Ser |
S12 |
| 126018 | BAA10g14950 | A10 | 15502760 | C | T | missense_variant | MODERATE | c.578C>T|p.Ser193Phe |
S168 |
| 126019 | BAA10g14940 | A10 | 15502901 | C | T | downstream_gene_variant | MODIFIER | c.*3449C>T| |
S70 |
| 126020 | BAA10g14940 | A10 | 15503764 | C | T | downstream_gene_variant | MODIFIER | c.*4312C>T| |
S170 |
| 126021 | BAA10g14940 | A10 | 15504057 | C | T | downstream_gene_variant | MODIFIER | c.*4605C>T| |
S135 S256 |
| 126022 | BAA10g14950 | A10 | 15505673 | C | T | downstream_gene_variant | MODIFIER | c.*2840C>T| |
S249 |
| 126023 | BAA10g14950-BAA10g14960 | A10 | 15509214 | G | T | intergenic_region | MODIFIER | n.15509214G>T| |
S290 |
| 126024 | BAA10g14950-BAA10g14960 | A10 | 15509639 | C | T | intergenic_region | MODIFIER | n.15509639C>T| |
S297 |
| 126025 | BAA10g14960 | A10 | 15512264 | C | T | downstream_gene_variant | MODIFIER | c.*4349G>A| |
S84 S93 |