| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 90051 | BAA10g00170 | A10 | 80528 | C | T | missense_variant | MODERATE | c.1682G>A|p.Gly561Glu |
S181 |
| 90052 | BAA10g00170 | A10 | 80598 | G | A | missense_variant | MODERATE | c.1612C>T|p.His538Tyr |
S255 |
| 90053 | BAA10g00170 | A10 | 81407 | G | A | synonymous_variant | LOW | c.987C>T|p.Pro329Pro |
S263 S288 |
| 90054 | BAA10g00170 | A10 | 82729 | C | T | upstream_gene_variant | MODIFIER | c.-336G>A| |
S108 |
| 90055 | BAA10g00170 | A10 | 82938 | C | T | upstream_gene_variant | MODIFIER | c.-545G>A| |
S27 |
| 90056 | BAA10g00180 | A10 | 83829 | C | T | missense_variant | MODERATE | c.2156G>A|p.Ser719Asn |
S135 |
| 90057 | BAA10g00180 | A10 | 83999 | C | T | synonymous_variant | LOW | c.1986G>A|p.Val662Val |
S23 |
| 90058 | BAA10g00180 | A10 | 84159 | C | T | missense_variant | MODERATE | c.1826G>A|p.Arg609Lys |
S162 |
| 90059 | BAA10g00180 | A10 | 86085 | G | A | synonymous_variant | LOW | c.156C>T|p.Ile52Ile |
S99 |
| 90060 | BAA10g00170 | A10 | 87157 | C | T | upstream_gene_variant | MODIFIER | c.-4764G>A| |
S161 S228 S244 S290 |
| 90061 | BAA10g00180 | A10 | 88114 | G | A | upstream_gene_variant | MODIFIER | c.-1874C>T| |
S198 |
| 90062 | BAA10g00190 | A10 | 88855 | C | T | synonymous_variant | LOW | c.318G>A|p.Lys106Lys |
S79 S91 |
| 90063 | BAA10g00190 | A10 | 91770 | C | T | upstream_gene_variant | MODIFIER | c.-2598G>A| |
S75 S81 |
| 90064 | BAA10g00190 | A10 | 91837 | G | A | upstream_gene_variant | MODIFIER | c.-2665C>T| |
S136 |
| 90065 | BAA10g00190 | A10 | 92113 | G | A | upstream_gene_variant | MODIFIER | c.-2941C>T| |
S16 |
| 90066 | BAA10g00190 | A10 | 92243 | C | T | upstream_gene_variant | MODIFIER | c.-3071G>A| |
S114 |
| 90067 | BAA10g00200 | A10 | 93474 | G | A | missense_variant | MODERATE | c.992G>A|p.Arg331Lys |
S209 |
| 90068 | BAA10g00200 | A10 | 93550 | C | T | synonymous_variant | LOW | c.1068C>T|p.Leu356Leu |
S269 |
| 90069 | BAA10g00210 | A10 | 94405 | G | A | missense_variant | MODERATE | c.878C>T|p.Ser293Phe |
S228 |
| 90070 | BAA10g00210 | A10 | 94452 | G | A | synonymous_variant | LOW | c.831C>T|p.Val277Val |
S242 |
| 90071 | BAA10g00210 | A10 | 94875 | G | A | missense_variant | MODERATE | c.491C>T|p.Ser164Phe |
S267 |
| 90072 | BAA10g00210 | A10 | 95581 | C | T | synonymous_variant | LOW | c.117G>A|p.Lys39Lys |
S193 |
| 90073 | BAA10g00210 | A10 | 97382 | C | T | upstream_gene_variant | MODIFIER | c.-1588G>A| |
S116 |
| 90074 | BAA10g00220 | A10 | 97623 | C | T | missense_variant | MODERATE | c.2794G>A|p.Asp932Asn |
S73 S91 |
| 90075 | BAA10g00210 | A10 | 98372 | C | T | upstream_gene_variant | MODIFIER | c.-2578G>A| |
S146 |