Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20870 | A10 | 18573724 | G | A | upstream_gene_variant | MODIFIER | c.-2237G>A| |
S138 |
2 | BAA10g20870 | A10 | 18573993 | C | T | upstream_gene_variant | MODIFIER | c.-1968C>T| |
S117 |
3 | BAA10g20870 | A10 | 18575170 | G | A | upstream_gene_variant | MODIFIER | c.-791G>A| |
S240 |
4 | BAA10g20870 | A10 | 18576331 | C | T | missense_variant | MODERATE | c.371C>T|p.Ser124Phe |
S200 |
5 | BAA10g20870 | A10 | 18576349 | C | T | missense_variant | MODERATE | c.389C>T|p.Thr130Ile |
S87 |
6 | BAA10g20870 | A10 | 18576528 | G | A | intron_variant | MODIFIER | c.486+82G>A| |
S175 |
7 | BAA10g20870 | A10 | 18576640 | G | A | missense_variant | MODERATE | c.499G>A|p.Asp167Asn |
S134 |
8 | BAA10g20870 | A10 | 18576893 | C | T | missense_variant | MODERATE | c.752C>T|p.Ser251Phe |
S289 S290 |
9 | BAA10g20870 | A10 | 18577938 | C | T | missense_variant | MODERATE | c.1672C>T|p.Leu558Phe |
S135 |
10 | BAA10g20870 | A10 | 18578352 | A | C | missense_variant | MODERATE | c.2086A>C|p.Met696Leu |
S241 |
11 | BAA10g20870 | A10 | 18578591 | C | T | synonymous_variant | LOW | c.2325C>T|p.Phe775Phe |
S84 S93 |
12 | BAA10g20870 | A10 | 18578900 | C | T | synonymous_variant | LOW | c.2634C>T|p.Phe878Phe |
S294 |
13 | BAA10g20870 | A10 | 18579111 | G | A | missense_variant | MODERATE | c.2845G>A|p.Glu949Lys |
S264 |
14 | BAA10g20870 | A10 | 18579258 | G | A | missense_variant | MODERATE | c.2992G>A|p.Glu998Lys |
S202 |
15 | BAA10g20870 | A10 | 18579437 | C | T | synonymous_variant | LOW | c.3171C>T|p.Asp1057Asp |
S99 |
16 | BAA10g20870 | A10 | 18580145 | G | A | synonymous_variant | LOW | c.3879G>A|p.Arg1293Arg |
S203 |
17 | BAA10g20870 | A10 | 18580308 | C | T | missense_variant | MODERATE | c.4042C>T|p.Leu1348Phe |
S183 |