Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
7501 | BAA01g06070 | A01 | 2721879 | C | T | missense_variant | MODERATE | c.424C>T|p.Leu142Phe |
S242 |
7502 | BAA01g06070 | A01 | 2722136 | C | T | synonymous_variant | LOW | c.525C>T|p.Ala175Ala |
S155 S211 |
7503 | BAA01g06060 | A01 | 2722211 | G | A | downstream_gene_variant | MODIFIER | c.*2318G>A| |
S306 S308 |
7504 | BAA01g06070 | A01 | 2722730 | C | T | missense_variant | MODERATE | c.944C>T|p.Ser315Phe |
S148 S210 S30 S31 |
7505 | BAA01g06070 | A01 | 2722994 | C | T | missense_variant | MODERATE | c.1094C>T|p.Pro365Leu |
S69 |
7506 | BAA01g06070 | A01 | 2723174 | G | A | missense_variant | MODERATE | c.1274G>A|p.Arg425Lys |
S279 |
7507 | BAA01g06070 | A01 | 2723378 | G | A | synonymous_variant | LOW | c.1386G>A|p.Val462Val |
S289 S290 |
7508 | BAA01g06070 | A01 | 2723836 | C | T | splice_region_variant&synonymous_variant | LOW | c.1629C>T|p.Ile543Ile |
S223 |
7509 | BAA01g06070 | A01 | 2723953 | C | T | synonymous_variant | LOW | c.1746C>T|p.Tyr582Tyr |
S170 |
7510 | BAA01g06060 | A01 | 2724071 | C | T | downstream_gene_variant | MODIFIER | c.*4178C>T| |
S277 |
7511 | BAA01g06060 | A01 | 2724141 | G | A | downstream_gene_variant | MODIFIER | c.*4248G>A| |
S10 |
7512 | BAA01g06070 | A01 | 2724584 | C | T | missense_variant | MODERATE | c.2192C>T|p.Thr731Met |
S48 |
7513 | BAA01g06070 | A01 | 2724940 | G | A | missense_variant | MODERATE | c.2470G>A|p.Gly824Arg |
S279 |
7514 | BAA01g06070 | A01 | 2725103 | C | T | missense_variant | MODERATE | c.2633C>T|p.Thr878Ile |
S252 |
7515 | BAA01g06080 | A01 | 2725183 | C | T | downstream_gene_variant | MODIFIER | c.*1135G>A| |
S302 |
7516 | BAA01g06070 | A01 | 2725221 | G | A | missense_variant | MODERATE | c.2660G>A|p.Ser887Asn |
S172 S217 |
7517 | BAA01g06070 | A01 | 2725794 | G | A | missense_variant | MODERATE | c.3233G>A|p.Gly1078Asp |
S107 |
7518 | BAA01g06070 | A01 | 2726056 | C | T | downstream_gene_variant | MODIFIER | c.*252C>T| |
S76 |
7519 | BAA01g06070 | A01 | 2726213 | C | T | downstream_gene_variant | MODIFIER | c.*409C>T| |
S170 |
7520 | BAA01g06080 | A01 | 2726562 | C | T | missense_variant | MODERATE | c.905G>A|p.Ser302Asn |
S25 S264 |
7521 | BAA01g06080 | A01 | 2726704 | G | A | missense_variant | MODERATE | c.763C>T|p.Leu255Phe |
S119 |
7522 | BAA01g06080 | A01 | 2726728 | G | A | missense_variant | MODERATE | c.739C>T|p.Leu247Phe |
S178 |
7523 | BAA01g06070 | A01 | 2726877 | C | T | downstream_gene_variant | MODIFIER | c.*1073C>T| |
S50 |
7524 | BAA01g06080 | A01 | 2727327 | G | A | missense_variant | MODERATE | c.493C>T|p.Pro165Ser |
S162 |
7525 | BAA01g06080 | A01 | 2729635 | C | T | upstream_gene_variant | MODIFIER | c.-1816G>A| |
S212 |