Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
7601 | BAA01g06100 | A01 | 2741755 | G | A | upstream_gene_variant | MODIFIER | c.-2170C>T| |
S159 S243 |
7602 | BAA01g06100 | A01 | 2741954 | C | T | upstream_gene_variant | MODIFIER | c.-2369G>A| |
S174 S27 |
7603 | BAA01g06100 | A01 | 2742956 | C | T | upstream_gene_variant | MODIFIER | c.-3371G>A| |
S139 |
7604 | BAA01g06120 | A01 | 2743239 | G | A | missense_variant | MODERATE | c.1022C>T|p.Ser341Phe |
S87 |
7605 | BAA01g06100 | A01 | 2743838 | C | T | upstream_gene_variant | MODIFIER | c.-4253G>A| |
S260 |
7606 | BAA01g06100 | A01 | 2744184 | G | A | upstream_gene_variant | MODIFIER | c.-4599C>T| |
S15 S3 |
7607 | BAA01g06120 | A01 | 2744911 | G | A | synonymous_variant | LOW | c.39C>T|p.Asp13Asp |
S33 |
7608 | BAA01g06120 | A01 | 2745949 | C | T | upstream_gene_variant | MODIFIER | c.-1000G>A| |
S19 |
7609 | BAA01g06120 | A01 | 2746043 | G | A | upstream_gene_variant | MODIFIER | c.-1094C>T| |
S208 S219 |
7610 | BAA01g06120 | A01 | 2746397 | G | A | upstream_gene_variant | MODIFIER | c.-1448C>T| |
S286 |
7611 | BAA01g06120 | A01 | 2747506 | G | A | upstream_gene_variant | MODIFIER | c.-2557C>T| |
S124 |
7612 | BAA01g06120 | A01 | 2747540 | C | T | upstream_gene_variant | MODIFIER | c.-2591G>A| |
S4 |
7613 | BAA01g06120 | A01 | 2748558 | C | T | upstream_gene_variant | MODIFIER | c.-3609G>A| |
S296 |
7614 | BAA01g06130 | A01 | 2749423 | G | A | synonymous_variant | LOW | c.1920C>T|p.Phe640Phe |
S11 |
7615 | BAA01g06130 | A01 | 2749812 | G | A | stop_gained | HIGH | c.1531C>T|p.Gln511* |
S83 S88 |
7616 | BAA01g06130 | A01 | 2750210 | C | T | missense_variant | MODERATE | c.1133G>A|p.Cys378Tyr |
S208 S93 |
7617 | BAA01g06130 | A01 | 2750769 | C | T | missense_variant | MODERATE | c.574G>A|p.Gly192Arg |
S18 |
7618 | BAA01g06130 | A01 | 2751009 | C | T | missense_variant | MODERATE | c.334G>A|p.Glu112Lys |
S263 |
7619 | BAA01g06130 | A01 | 2751277 | G | A | synonymous_variant | LOW | c.66C>T|p.Ala22Ala |
S107 |
7620 | BAA01g06130 | A01 | 2751753 | C | T | upstream_gene_variant | MODIFIER | c.-411G>A| |
S164 |
7621 | BAA01g06130 | A01 | 2751760 | G | A | upstream_gene_variant | MODIFIER | c.-418C>T| |
S48 |
7622 | BAA01g06140 | A01 | 2752024 | C | T | missense_variant | MODERATE | c.2335G>A|p.Gly779Arg |
S242 |
7623 | BAA01g06140 | A01 | 2752273 | C | T | missense_variant | MODERATE | c.2086G>A|p.Val696Met |
S176 |
7624 | BAA01g06140 | A01 | 2752475 | G | A | synonymous_variant | LOW | c.1884C>T|p.Ile628Ile |
S83 S88 |
7625 | BAA01g06140 | A01 | 2752516 | C | A | missense_variant | MODERATE | c.1843G>T|p.Gly615Cys |
S68 |