| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 95951 | BAA10g04420 | A10 | 2228379 | C | T | upstream_gene_variant | MODIFIER | c.-218G>A| |
S169 |
| 95952 | BAA10g04420 | A10 | 2230810 | G | A | upstream_gene_variant | MODIFIER | c.-2649C>T| |
S198 |
| 95953 | BAA10g04420 | A10 | 2231021 | G | A | upstream_gene_variant | MODIFIER | c.-2860C>T| |
S301 S304 |
| 95954 | BAA10g04430 | A10 | 2231675 | C | T | missense_variant | MODERATE | c.4513G>A|p.Gly1505Arg |
S37 |
| 95955 | BAA10g04430 | A10 | 2232021 | C | T | synonymous_variant | LOW | c.4167G>A|p.Glu1389Glu |
S212 |
| 95956 | BAA10g04430 | A10 | 2232316 | C | T | missense_variant | MODERATE | c.3872G>A|p.Gly1291Asp |
S286 |
| 95957 | BAA10g04430 | A10 | 2232645 | G | A | synonymous_variant | LOW | c.3543C>T|p.Leu1181Leu |
S277 |
| 95958 | BAA10g04430 | A10 | 2234285 | C | T | synonymous_variant | LOW | c.2088G>A|p.Glu696Glu |
S6 |
| 95959 | BAA10g04430 | A10 | 2235377 | C | T | synonymous_variant | LOW | c.996G>A|p.Lys332Lys |
S56 |
| 95960 | BAA10g04430 | A10 | 2235650 | C | T | synonymous_variant | LOW | c.723G>A|p.Gln241Gln |
S10 |
| 95961 | BAA10g04430 | A10 | 2235911 | C | T | synonymous_variant | LOW | c.462G>A|p.Glu154Glu |
S104 S52 |
| 95962 | BAA10g04430 | A10 | 2236105 | C | T | missense_variant | MODERATE | c.268G>A|p.Asp90Asn |
S196 |
| 95963 | BAA10g04440 | A10 | 2238142 | C | T | missense_variant | MODERATE | c.86C>T|p.Ser29Phe |
S96 |
| 95964 | BAA10g04440 | A10 | 2239144 | G | A | missense_variant | MODERATE | c.424G>A|p.Glu142Lys |
S100 |
| 95965 | BAA10g04430 | A10 | 2240044 | C | T | upstream_gene_variant | MODIFIER | c.-3672G>A| |
S124 |
| 95966 | BAA10g04430 | A10 | 2240291 | A | G | upstream_gene_variant | MODIFIER | c.-3919T>C| |
S260 |
| 95967 | BAA10g04440 | A10 | 2240470 | G | A | missense_variant | MODERATE | c.769G>A|p.Glu257Lys |
S85 |
| 95968 | BAA10g04440 | A10 | 2240508 | G | A | synonymous_variant | LOW | c.807G>A|p.Val269Val |
S53 |
| 95969 | BAA10g04440 | A10 | 2240822 | G | A | missense_variant | MODERATE | c.1039G>A|p.Ala347Thr |
S295 |
| 95970 | BAA10g04440 | A10 | 2241696 | C | T | synonymous_variant | LOW | c.1602C>T|p.Phe534Phe |
S206 S26 |
| 95971 | BAA10g04460 | A10 | 2243377 | G | A | upstream_gene_variant | MODIFIER | c.-4210G>A| |
S109 |
| 95972 | BAA10g04460 | A10 | 2245739 | C | T | upstream_gene_variant | MODIFIER | c.-1848C>T| |
S35 |
| 95973 | BAA10g04460 | A10 | 2246085 | C | T | upstream_gene_variant | MODIFIER | c.-1502C>T| |
S8 |
| 95974 | BAA10g04460 | A10 | 2246147 | C | T | upstream_gene_variant | MODIFIER | c.-1440C>T| |
S203 |
| 95975 | BAA10g04460 | A10 | 2246533 | G | A | upstream_gene_variant | MODIFIER | c.-1054G>A| |
S92 |