| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 135901 | BAA10g21640 | A10 | 18966062 | G | A | downstream_gene_variant | MODIFIER | c.*3489G>A| |
S207 |
| 135902 | BAA10g21660 | A10 | 18967352 | C | T | upstream_gene_variant | MODIFIER | c.-3946C>T| |
S19 |
| 135903 | BAA10g21660 | A10 | 18968064 | C | T | upstream_gene_variant | MODIFIER | c.-3234C>T| |
S18 |
| 135904 | BAA10g21660 | A10 | 18968128 | C | T | upstream_gene_variant | MODIFIER | c.-3170C>T| |
S61 |
| 135905 | BAA10g21660 | A10 | 18969213 | G | A | upstream_gene_variant | MODIFIER | c.-2085G>A| |
S120 |
| 135906 | BAA10g21670 | A10 | 18971704 | G | A | downstream_gene_variant | MODIFIER | c.*4156C>T| |
S178 |
| 135907 | BAA10g21660 | A10 | 18972474 | G | A | missense_variant | MODERATE | c.670G>A|p.Val224Ile |
S18 |
| 135908 | BAA10g21660 | A10 | 18972861 | C | T | synonymous_variant | LOW | c.972C>T|p.Arg324Arg |
S18 S251 |
| 135909 | BAA10g21660 | A10 | 18973031 | C | T | missense_variant | MODERATE | c.1142C>T|p.Ala381Val |
S249 |
| 135910 | BAA10g21660 | A10 | 18973926 | G | A | downstream_gene_variant | MODIFIER | c.*837G>A| |
S239 |
| 135911 | BAA10g21660 | A10 | 18973980 | C | T | downstream_gene_variant | MODIFIER | c.*891C>T| |
S10 |
| 135912 | BAA10g21660 | A10 | 18975051 | G | A | downstream_gene_variant | MODIFIER | c.*1962G>A| |
S166 |
| 135913 | BAA10g21660 | A10 | 18975092 | C | T | downstream_gene_variant | MODIFIER | c.*2003C>T| |
S161 |
| 135914 | BAA10g21670 | A10 | 18976293 | C | T | missense_variant | MODERATE | c.1178G>A|p.Arg393Lys |
S37 |
| 135915 | BAA10g21670 | A10 | 18977851 | G | A | upstream_gene_variant | MODIFIER | c.-124C>T| |
S1 S90 |
| 135916 | BAA10g21670 | A10 | 18979156 | G | A | upstream_gene_variant | MODIFIER | c.-1429C>T| |
S205 |
| 135917 | BAA10g21670 | A10 | 18979228 | C | T | upstream_gene_variant | MODIFIER | c.-1501G>A| |
S34 |
| 135918 | BAA10g21670 | A10 | 18980323 | C | T | upstream_gene_variant | MODIFIER | c.-2596G>A| |
S195 |
| 135919 | BAA10g21670 | A10 | 18980391 | G | A | upstream_gene_variant | MODIFIER | c.-2664C>T| |
S278 |
| 135920 | BAA10g21670 | A10 | 18982447 | C | T | upstream_gene_variant | MODIFIER | c.-4720G>A| |
S186 |
| 135921 | BAA10g21680 | A10 | 18983590 | C | T | synonymous_variant | LOW | c.726C>T|p.Phe242Phe |
S173 |
| 135922 | BAA10g21680 | A10 | 18983861 | G | A | missense_variant | MODERATE | c.997G>A|p.Asp333Asn |
S298 |
| 135923 | BAA10g21680 | A10 | 18984221 | C | T | downstream_gene_variant | MODIFIER | c.*118C>T| |
S247 |
| 135924 | BAA10g21680 | A10 | 18984902 | G | A | downstream_gene_variant | MODIFIER | c.*799G>A| |
S272 |
| 135925 | BAA10g21690 | A10 | 18985107 | C | T | splice_region_variant&synonymous_variant | LOW | c.474G>A|p.Glu158Glu |
S156 |