Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
7351 | BAA01g05960 | A01 | 2678596 | C | T | missense_variant | MODERATE | c.688G>A|p.Asp230Asn |
S168 |
7352 | BAA01g05960 | A01 | 2678776 | C | T | missense_variant | MODERATE | c.508G>A|p.Ala170Thr |
S240 |
7353 | BAA01g05970 | A01 | 2678873 | G | A | upstream_gene_variant | MODIFIER | c.-1325G>A| |
S142 |
7354 | BAA01g05960 | A01 | 2679103 | C | T | stop_gained | HIGH | c.417G>A|p.Trp139* |
S48 |
7355 | BAA01g05960 | A01 | 2679697 | C | T | upstream_gene_variant | MODIFIER | c.-178G>A| |
S200 |
7356 | BAA01g05960 | A01 | 2680334 | C | T | upstream_gene_variant | MODIFIER | c.-815G>A| |
S18 |
7357 | BAA01g05960 | A01 | 2680633 | G | A | upstream_gene_variant | MODIFIER | c.-1114C>T| |
S104 S52 |
7358 | BAA01g05960 | A01 | 2680863 | G | A | upstream_gene_variant | MODIFIER | c.-1344C>T| |
S149 |
7359 | BAA01g05960 | A01 | 2681657 | C | T | upstream_gene_variant | MODIFIER | c.-2138G>A| |
S273 |
7360 | BAA01g05960 | A01 | 2682106 | G | A | upstream_gene_variant | MODIFIER | c.-2587C>T| |
S257 |
7361 | BAA01g05980 | A01 | 2682450 | C | T | missense_variant | MODERATE | c.77C>T|p.Pro26Leu |
S4 |
7362 | BAA01g05980 | A01 | 2682556 | G | A | synonymous_variant | LOW | c.183G>A|p.Ala61Ala |
S281 |
7363 | BAA01g05960 | A01 | 2682943 | C | T | upstream_gene_variant | MODIFIER | c.-3424G>A| |
S18 |
7364 | BAA01g05980 | A01 | 2683102 | C | T | missense_variant | MODERATE | c.560C>T|p.Ala187Val |
S267 |
7365 | BAA01g05980 | A01 | 2683218 | G | A | missense_variant | MODERATE | c.595G>A|p.Asp199Asn |
S156 |
7366 | BAA01g05980 | A01 | 2683935 | C | T | stop_gained&splice_region_variant | HIGH | c.1045C>T|p.Gln349* |
S265 |
7367 | BAA01g05980 | A01 | 2684083 | G | A | synonymous_variant | LOW | c.1104G>A|p.Gln368Gln |
S116 |
7368 | BAA01g05990 | A01 | 2685433 | C | T | upstream_gene_variant | MODIFIER | c.-185C>T| |
S221 |
7369 | BAA01g05990 | A01 | 2687275 | C | T | missense_variant | MODERATE | c.1084C>T|p.Pro362Ser |
S67 |
7370 | BAA01g05990 | A01 | 2687633 | G | A | missense_variant | MODERATE | c.1366G>A|p.Asp456Asn |
S308 |
7371 | BAA01g05990 | A01 | 2687727 | G | A | missense_variant | MODERATE | c.1460G>A|p.Arg487Lys |
S156 |
7372 | BAA01g05990 | A01 | 2687851 | C | T | splice_region_variant&intron_variant | LOW | c.1580+4C>T| |
S1 S90 |
7373 | BAA01g06000 | A01 | 2689981 | G | A | missense_variant | MODERATE | c.1865C>T|p.Ser622Phe |
S13 |
7374 | BAA01g06010 | A01 | 2690814 | C | T | upstream_gene_variant | MODIFIER | c.-3284C>T| |
S67 |
7375 | BAA01g06000 | A01 | 2691372 | G | A | missense_variant | MODERATE | c.1021C>T|p.Pro341Ser |
S180 |