Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g10560 | A07 | 19417506 | G | A | upstream_gene_variant | MODIFIER | c.-2935G>A| |
S63 |
2 | BAA07g10560 | A07 | 19417642 | C | T | upstream_gene_variant | MODIFIER | c.-2799C>T| |
S35 |
3 | BAA07g10560 | A07 | 19418351 | T | G | upstream_gene_variant | MODIFIER | c.-2090T>G| |
S41 |
4 | BAA07g10560 | A07 | 19418407 | G | A | upstream_gene_variant | MODIFIER | c.-2034G>A| |
S193 |
5 | BAA07g10560 | A07 | 19418460 | G | A | upstream_gene_variant | MODIFIER | c.-1981G>A| |
S157 S163 |
6 | BAA07g10560 | A07 | 19418516 | C | T | upstream_gene_variant | MODIFIER | c.-1925C>T| |
S226 |
7 | BAA07g10560 | A07 | 19425026 | C | T | intron_variant | MODIFIER | c.725+35C>T| |
S249 |
8 | BAA07g10560 | A07 | 19426366 | G | A | missense_variant | MODERATE | c.1007G>A|p.Gly336Glu |
S13 |
9 | BAA07g10560 | A07 | 19427277 | G | A | missense_variant | MODERATE | c.1486G>A|p.Ala496Thr |
S62 |
10 | BAA07g10560 | A07 | 19429068 | G | A | missense_variant | MODERATE | c.2608G>A|p.Val870Ile |
S87 |
11 | BAA07g10560 | A07 | 19429340 | C | T | missense_variant | MODERATE | c.2807C>T|p.Pro936Leu |
S286 |
12 | BAA07g10560 | A07 | 19429430 | G | A | missense_variant | MODERATE | c.2897G>A|p.Ser966Asn |
S115 |
13 | BAA07g10560 | A07 | 19429463 | G | A | missense_variant | MODERATE | c.2930G>A|p.Gly977Glu |
S219 S72 |
14 | BAA07g10560 | A07 | 19430974 | G | A | downstream_gene_variant | MODIFIER | c.*1372G>A| |
S183 |
15 | BAA07g10560 | A07 | 19430991 | G | A | downstream_gene_variant | MODIFIER | c.*1389G>A| |
S236 |
16 | BAA07g10560 | A07 | 19431641 | G | A | downstream_gene_variant | MODIFIER | c.*2039G>A| |
S89 |
17 | BAA07g10560 | A07 | 19431903 | C | T | downstream_gene_variant | MODIFIER | c.*2301C>T| |
S53 |
18 | BAA07g10560 | A07 | 19434241 | C | T | downstream_gene_variant | MODIFIER | c.*4639C>T| |
S224 |