Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
8651 | BAA01g06990 | A01 | 3089310 | G | A | missense_variant | MODERATE | c.232C>T|p.Pro78Ser |
S295 |
8652 | BAA01g06970 | A01 | 3090055 | C | T | upstream_gene_variant | MODIFIER | c.-4870G>A| |
S48 |
8653 | BAA01g06970 | A01 | 3090084 | G | A | upstream_gene_variant | MODIFIER | c.-4899C>T| |
S257 |
8654 | BAA01g06990 | A01 | 3093976 | C | T | upstream_gene_variant | MODIFIER | c.-4435G>A| |
S249 |
8655 | BAA01g07000 | A01 | 3095719 | G | A | downstream_gene_variant | MODIFIER | c.*3313C>T| |
S32 |
8656 | BAA01g07000 | A01 | 3098538 | G | A | downstream_gene_variant | MODIFIER | c.*494C>T| |
S83 |
8657 | BAA01g07000 | A01 | 3098578 | G | A | downstream_gene_variant | MODIFIER | c.*454C>T| |
S174 S216 S27 S39 |
8658 | BAA01g07010 | A01 | 3100465 | G | A | downstream_gene_variant | MODIFIER | c.*4270C>T| |
S282 |
8659 | BAA01g07000 | A01 | 3101200 | G | A | synonymous_variant | LOW | c.840C>T|p.Ala280Ala |
S153 |
8660 | BAA01g07000 | A01 | 3101879 | C | T | synonymous_variant | LOW | c.396G>A|p.Glu132Glu |
S270 |
8661 | BAA01g07000 | A01 | 3103590 | C | T | upstream_gene_variant | MODIFIER | c.-1231G>A| |
S19 |
8662 | BAA01g07000 | A01 | 3104038 | C | T | upstream_gene_variant | MODIFIER | c.-1679G>A| |
S59 |
8663 | BAA01g07000 | A01 | 3104610 | A | T | upstream_gene_variant | MODIFIER | c.-2251T>A| |
S233 |
8664 | BAA01g07010 | A01 | 3105038 | G | A | synonymous_variant | LOW | c.72C>T|p.Ser24Ser |
S95 |
8665 | BAA01g07010 | A01 | 3105089 | G | A | synonymous_variant | LOW | c.21C>T|p.Phe7Phe |
S175 |
8666 | BAA01g07000 | A01 | 3105440 | G | A | upstream_gene_variant | MODIFIER | c.-3081C>T| |
S133 |
8667 | BAA01g07020 | A01 | 3106462 | G | A | missense_variant | MODERATE | c.667C>T|p.Pro223Ser |
S142 |
8668 | BAA01g07020 | A01 | 3106773 | C | T | missense_variant | MODERATE | c.356G>A|p.Ser119Asn |
S266 |
8669 | BAA01g07020 | A01 | 3106897 | G | A | missense_variant | MODERATE | c.232C>T|p.Pro78Ser |
S74 |
8670 | BAA01g07000 | A01 | 3107196 | G | A | upstream_gene_variant | MODIFIER | c.-4837C>T| |
S271 |
8671 | BAA01g07000 | A01 | 3107336 | G | A | upstream_gene_variant | MODIFIER | c.-4977C>T| |
S209 |
8672 | BAA01g07030 | A01 | 3113054 | G | A | upstream_gene_variant | MODIFIER | c.-3360G>A| |
S195 |
8673 | BAA01g07030 | A01 | 3113139 | C | T | upstream_gene_variant | MODIFIER | c.-3275C>T| |
S249 |
8674 | BAA01g07030 | A01 | 3114673 | G | A | upstream_gene_variant | MODIFIER | c.-1741G>A| |
S146 |
8675 | BAA01g07030 | A01 | 3116248 | C | T | upstream_gene_variant | MODIFIER | c.-166C>T| |
S4 |