| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 93001 | BAA10g02590 | A10 | 1246666 | G | A | synonymous_variant | LOW | c.234C>T|p.Thr78Thr |
S157 S163 |
| 93002 | BAA10g02580 | A10 | 1247924 | G | A | upstream_gene_variant | MODIFIER | c.-3484C>T| |
S228 |
| 93003 | BAA10g02580 | A10 | 1248286 | G | A | upstream_gene_variant | MODIFIER | c.-3846C>T| |
S179 |
| 93004 | BAA10g02580 | A10 | 1248707 | C | T | upstream_gene_variant | MODIFIER | c.-4267G>A| |
S42 |
| 93005 | BAA10g02580 | A10 | 1248756 | A | C | upstream_gene_variant | MODIFIER | c.-4316T>G| |
S119 S54 |
| 93006 | BAA10g02590 | A10 | 1250088 | C | T | upstream_gene_variant | MODIFIER | c.-3189G>A| |
S177 S68 |
| 93007 | BAA10g02600 | A10 | 1251339 | G | A | synonymous_variant | LOW | c.1035G>A|p.Ala345Ala |
S118 |
| 93008 | BAA10g02600 | A10 | 1251680 | T | G | missense_variant | MODERATE | c.1376T>G|p.Met459Arg |
S257 S26 |
| 93009 | BAA10g02610 | A10 | 1252510 | C | T | missense_variant | MODERATE | c.1435G>A|p.Glu479Lys |
S35 |
| 93010 | BAA10g02620 | A10 | 1252975 | C | T | upstream_gene_variant | MODIFIER | c.-2701C>T| |
S142 |
| 93011 | BAA10g02610 | A10 | 1253445 | G | A | missense_variant | MODERATE | c.791C>T|p.Ser264Phe |
S217 S248 |
| 93012 | BAA10g02610 | A10 | 1253658 | G | A | missense_variant | MODERATE | c.673C>T|p.Arg225Trp |
S16 |
| 93013 | BAA10g02610 | A10 | 1253835 | C | T | missense_variant | MODERATE | c.496G>A|p.Ala166Thr |
S294 |
| 93014 | BAA10g02620 | A10 | 1254606 | C | T | upstream_gene_variant | MODIFIER | c.-1070C>T| |
S123 |
| 93015 | BAA10g02610 | A10 | 1255585 | C | T | upstream_gene_variant | MODIFIER | c.-817G>A| |
S139 |
| 93016 | BAA10g02620 | A10 | 1255775 | G | A | missense_variant | MODERATE | c.100G>A|p.Gly34Ser |
S95 |
| 93017 | BAA10g02620 | A10 | 1255956 | C | T | missense_variant | MODERATE | c.281C>T|p.Ser94Leu |
S139 |
| 93018 | BAA10g02610 | A10 | 1256407 | G | A | upstream_gene_variant | MODIFIER | c.-1639C>T| |
S5 |
| 93019 | BAA10g02610 | A10 | 1256472 | C | T | upstream_gene_variant | MODIFIER | c.-1704G>A| |
S35 |
| 93020 | BAA10g02620 | A10 | 1257165 | C | T | missense_variant | MODERATE | c.769C>T|p.Pro257Ser |
S35 |
| 93021 | BAA10g02610 | A10 | 1257387 | C | T | upstream_gene_variant | MODIFIER | c.-2619G>A| |
S277 |
| 93022 | BAA10g02610 | A10 | 1257697 | G | A | upstream_gene_variant | MODIFIER | c.-2929C>T| |
S107 |
| 93023 | BAA10g02610 | A10 | 1257698 | G | A | upstream_gene_variant | MODIFIER | c.-2930C>T| |
S112 |
| 93024 | BAA10g02630 | A10 | 1258871 | G | A | synonymous_variant | LOW | c.60G>A|p.Arg20Arg |
S164 |
| 93025 | BAA10g02630 | A10 | 1259194 | C | T | splice_region_variant&intron_variant | LOW | c.298-8C>T| |
S186 |