| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 129901 | BAA10g17630 | A10 | 16888333 | C | T | upstream_gene_variant | MODIFIER | c.-714C>T| |
S124 |
| 129902 | BAA10g17630 | A10 | 16890020 | G | A | downstream_gene_variant | MODIFIER | c.*605G>A| |
S84 S93 |
| 129903 | BAA10g17630 | A10 | 16890250 | C | T | downstream_gene_variant | MODIFIER | c.*835C>T| |
S193 |
| 129904 | BAA10g17640 | A10 | 16890409 | C | T | missense_variant | MODERATE | c.175G>A|p.Gly59Ser |
S105 S106 |
| 129905 | BAA10g17640 | A10 | 16890657 | G | A | missense_variant | MODERATE | c.19C>T|p.Leu7Phe |
S219 S72 |
| 129906 | BAA10g17640 | A10 | 16892124 | C | T | upstream_gene_variant | MODIFIER | c.-1449G>A| |
S140 |
| 129907 | BAA10g17640 | A10 | 16892408 | C | T | upstream_gene_variant | MODIFIER | c.-1733G>A| |
S103 |
| 129908 | BAA10g17640 | A10 | 16892540 | G | A | upstream_gene_variant | MODIFIER | c.-1865C>T| |
S165 |
| 129909 | BAA10g17640 | A10 | 16893545 | G | A | upstream_gene_variant | MODIFIER | c.-2870C>T| |
S240 |
| 129910 | BAA10g17640 | A10 | 16894511 | G | A | upstream_gene_variant | MODIFIER | c.-3836C>T| |
S180 |
| 129911 | BAA10g17650 | A10 | 16896143 | G | A | upstream_gene_variant | MODIFIER | c.-3869C>T| |
S72 S78 |
| 129912 | BAA10g17650 | A10 | 16896602 | C | T | upstream_gene_variant | MODIFIER | c.-4328G>A| |
S162 |
| 129913 | BAA10g17650 | A10 | 16896632 | C | T | upstream_gene_variant | MODIFIER | c.-4358G>A| |
S174 S216 S241 S265 |
| 129914 | BAA10g17680 | A10 | 16898382 | C | T | missense_variant | MODERATE | c.2251G>A|p.Asp751Asn |
S283 |
| 129915 | BAA10g17680 | A10 | 16898540 | C | A | missense_variant | MODERATE | c.2093G>T|p.Gly698Val |
S96 |
| 129916 | BAA10g17680 | A10 | 16898634 | C | T | missense_variant | MODERATE | c.1999G>A|p.Glu667Lys |
S148 S210 S30 S31 |
| 129917 | BAA10g17680 | A10 | 16899053 | T | A | missense_variant | MODERATE | c.1580A>T|p.Glu527Val |
S281 |
| 129918 | BAA10g17680 | A10 | 16899113 | G | A | missense_variant | MODERATE | c.1520C>T|p.Thr507Met |
S159 S243 |
| 129919 | BAA10g17680 | A10 | 16900518 | C | T | missense_variant | MODERATE | c.115G>A|p.Val39Ile |
S117 |
| 129920 | BAA10g17680 | A10 | 16901837 | G | A | upstream_gene_variant | MODIFIER | c.-1205C>T| |
S241 |
| 129921 | BAA10g17700 | A10 | 16902206 | C | T | missense_variant | MODERATE | c.8C>T|p.Pro3Leu |
S47 |
| 129922 | BAA10g17680 | A10 | 16902399 | G | A | upstream_gene_variant | MODIFIER | c.-1767C>T| |
S9 |
| 129923 | BAA10g17680 | A10 | 16902612 | C | T | upstream_gene_variant | MODIFIER | c.-1980G>A| |
S70 |
| 129924 | BAA10g17680 | A10 | 16902896 | C | T | upstream_gene_variant | MODIFIER | c.-2264G>A| |
S130 |
| 129925 | BAA10g17710 | A10 | 16903888 | C | T | missense_variant | MODERATE | c.58C>T|p.Arg20Cys |
S302 |