| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 93051 | BAA10g02640 | A10 | 1260709 | C | T | upstream_gene_variant | MODIFIER | c.-3706C>T| |
S221 |
| 93052 | BAA10g02630 | A10 | 1261362 | G | A | missense_variant | MODERATE | c.1036G>A|p.Glu346Lys |
S7 |
| 93053 | BAA10g02640 | A10 | 1261495 | G | A | upstream_gene_variant | MODIFIER | c.-2920G>A| |
S64 |
| 93054 | BAA10g02640 | A10 | 1261504 | G | A | upstream_gene_variant | MODIFIER | c.-2911G>A| |
S151 S263 |
| 93055 | BAA10g02630 | A10 | 1261562 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1147-1G>A| |
S105 S106 |
| 93056 | BAA10g02630 | A10 | 1262086 | G | A | missense_variant | MODERATE | c.1576G>A|p.Asp526Asn |
S241 |
| 93057 | BAA10g02630 | A10 | 1262360 | C | T | synonymous_variant | LOW | c.1770C>T|p.Ile590Ile |
S208 S93 |
| 93058 | BAA10g02630 | A10 | 1262567 | G | A | missense_variant | MODERATE | c.1895G>A|p.Arg632Gln |
S125 |
| 93059 | BAA10g02640 | A10 | 1263269 | C | T | upstream_gene_variant | MODIFIER | c.-1146C>T| |
S233 |
| 93060 | BAA10g02640 | A10 | 1263387 | G | A | upstream_gene_variant | MODIFIER | c.-1028G>A| |
S286 |
| 93061 | BAA10g02640 | A10 | 1264121 | G | A | upstream_gene_variant | MODIFIER | c.-294G>A| |
S212 |
| 93062 | BAA10g02640 | A10 | 1264206 | C | T | upstream_gene_variant | MODIFIER | c.-209C>T| |
S25 |
| 93063 | BAA10g02640 | A10 | 1264409 | G | A | upstream_gene_variant | MODIFIER | c.-6G>A| |
S38 |
| 93064 | BAA10g02640 | A10 | 1264642 | G | A | synonymous_variant | LOW | c.228G>A|p.Ala76Ala |
S303 |
| 93065 | BAA10g02640 | A10 | 1265515 | G | A | missense_variant | MODERATE | c.860G>A|p.Gly287Glu |
S178 |
| 93066 | BAA10g02640 | A10 | 1265566 | G | A | missense_variant | MODERATE | c.911G>A|p.Gly304Glu |
S286 |
| 93067 | BAA10g02640 | A10 | 1267836 | G | A | missense_variant | MODERATE | c.1063G>A|p.Gly355Arg |
S218 |
| 93068 | BAA10g02640 | A10 | 1268242 | G | A | splice_region_variant&synonymous_variant | LOW | c.1293G>A|p.Lys431Lys |
S289 |
| 93069 | BAA10g02650 | A10 | 1268702 | C | T | downstream_gene_variant | MODIFIER | c.*1178G>A| |
S241 S39 |
| 93070 | BAA10g02650 | A10 | 1269108 | C | T | downstream_gene_variant | MODIFIER | c.*772G>A| |
S193 |
| 93071 | BAA10g02650 | A10 | 1269179 | T | C | downstream_gene_variant | MODIFIER | c.*701A>G| |
S8 |
| 93072 | BAA10g02650 | A10 | 1270664 | G | A | missense_variant | MODERATE | c.1160C>T|p.Pro387Leu |
S68 |
| 93073 | BAA10g02650 | A10 | 1271146 | C | T | synonymous_variant | LOW | c.678G>A|p.Gln226Gln |
S174 |
| 93074 | BAA10g02650 | A10 | 1271683 | G | A | synonymous_variant | LOW | c.141C>T|p.Leu47Leu |
S99 |
| 93075 | BAA10g02650 | A10 | 1271894 | G | A | upstream_gene_variant | MODIFIER | c.-71C>T| |
S278 |