| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 150201 | BAA10g34290 | A10 | 24143514 | C | T | upstream_gene_variant | MODIFIER | c.-1970G>A| |
S221 |
| 150202 | BAA10g34290 | A10 | 24143797 | G | A | upstream_gene_variant | MODIFIER | c.-2253C>T| |
S265 |
| 150203 | BAA10g34290 | A10 | 24144574 | G | A | upstream_gene_variant | MODIFIER | c.-3030C>T| |
S260 S263 |
| 150204 | BAA10g34290 | A10 | 24144891 | C | T | upstream_gene_variant | MODIFIER | c.-3347G>A| |
S182 |
| 150205 | BAA10g34290 | A10 | 24145696 | G | A | upstream_gene_variant | MODIFIER | c.-4152C>T| |
S62 |
| 150206 | BAA10g34300 | A10 | 24147050 | G | A | upstream_gene_variant | MODIFIER | c.-4463G>A| |
S139 |
| 150207 | BAA10g34300 | A10 | 24147728 | C | T | upstream_gene_variant | MODIFIER | c.-3785C>T| |
S234 |
| 150208 | BAA10g34300 | A10 | 24148326 | G | A | upstream_gene_variant | MODIFIER | c.-3187G>A| |
S288 |
| 150209 | BAA10g34300 | A10 | 24149250 | G | A | upstream_gene_variant | MODIFIER | c.-2263G>A| |
S268 |
| 150210 | BAA10g34300 | A10 | 24149516 | C | T | upstream_gene_variant | MODIFIER | c.-1997C>T| |
S44 |
| 150211 | BAA10g34300 | A10 | 24150626 | C | T | upstream_gene_variant | MODIFIER | c.-887C>T| |
S229 |
| 150212 | BAA10g34300 | A10 | 24150811 | C | T | upstream_gene_variant | MODIFIER | c.-702C>T| |
S174 |
| 150213 | BAA10g34300 | A10 | 24151393 | G | A | upstream_gene_variant | MODIFIER | c.-120G>A| |
S194 S276 |
| 150214 | BAA10g34300 | A10 | 24151776 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.169-1G>A| |
S261 |
| 150215 | BAA10g34300 | A10 | 24152206 | G | A | missense_variant | MODERATE | c.463G>A|p.Asp155Asn |
S256 |
| 150216 | BAA10g34310 | A10 | 24153926 | G | A | missense_variant | MODERATE | c.682G>A|p.Glu228Lys |
S273 |
| 150217 | BAA10g34310 | A10 | 24154145 | G | A | missense_variant | MODERATE | c.832G>A|p.Glu278Lys |
S270 |
| 150218 | BAA10g34310 | A10 | 24154180 | C | T | synonymous_variant | LOW | c.867C>T|p.Val289Val |
S269 |
| 150219 | BAA10g34310 | A10 | 24155789 | G | A | stop_gained | HIGH | c.1668G>A|p.Trp556* |
S250 |
| 150220 | BAA10g34320 | A10 | 24157574 | C | T | missense_variant | MODERATE | c.1816G>A|p.Glu606Lys |
S268 |
| 150221 | BAA10g34320 | A10 | 24157970 | G | A | missense_variant | MODERATE | c.1420C>T|p.Pro474Ser |
S9 |
| 150222 | BAA10g34320 | A10 | 24158003 | C | T | missense_variant | MODERATE | c.1387G>A|p.Gly463Arg |
S13 |
| 150223 | BAA10g34320 | A10 | 24158018 | C | T | missense_variant | MODERATE | c.1372G>A|p.Asp458Asn |
S118 |
| 150224 | BAA10g34320 | A10 | 24158369 | C | T | missense_variant | MODERATE | c.1021G>A|p.Val341Ile |
S80 |
| 150225 | BAA10g34320 | A10 | 24158604 | G | A | synonymous_variant | LOW | c.786C>T|p.Asn262Asn |
S127 |