Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g34320 | A10 | 24157574 | C | T | missense_variant | MODERATE | c.1816G>A|p.Glu606Lys |
S268 |
2 | BAA10g34320 | A10 | 24157970 | G | A | missense_variant | MODERATE | c.1420C>T|p.Pro474Ser |
S9 |
3 | BAA10g34320 | A10 | 24158003 | C | T | missense_variant | MODERATE | c.1387G>A|p.Gly463Arg |
S13 |
4 | BAA10g34320 | A10 | 24158018 | C | T | missense_variant | MODERATE | c.1372G>A|p.Asp458Asn |
S118 |
5 | BAA10g34320 | A10 | 24158369 | C | T | missense_variant | MODERATE | c.1021G>A|p.Val341Ile |
S80 |
6 | BAA10g34320 | A10 | 24158604 | G | A | synonymous_variant | LOW | c.786C>T|p.Asn262Asn |
S127 |
7 | BAA10g34320 | A10 | 24158642 | C | T | missense_variant | MODERATE | c.748G>A|p.Glu250Lys |
S187 |
8 | BAA10g34320 | A10 | 24158693 | G | A | missense_variant | MODERATE | c.697C>T|p.His233Tyr |
S183 S198 |
9 | BAA10g34320 | A10 | 24158724 | G | A | synonymous_variant | LOW | c.666C>T|p.Ile222Ile |
S194 S69 |
10 | BAA10g34320 | A10 | 24158800 | C | T | missense_variant | MODERATE | c.590G>A|p.Gly197Glu |
S23 |
11 | BAA10g34320 | A10 | 24159006 | G | A | synonymous_variant | LOW | c.384C>T|p.Leu128Leu |
S264 |
12 | BAA10g34320 | A10 | 24159147 | G | A | synonymous_variant | LOW | c.243C>T|p.Phe81Phe |
S157 S163 |
13 | BAA10g34320 | A10 | 24159608 | C | T | synonymous_variant | LOW | c.117G>A|p.Arg39Arg |
S296 |
14 | BAA10g34320 | A10 | 24159857 | G | A | upstream_gene_variant | MODIFIER | c.-133C>T| |
S75 S81 |
15 | BAA10g34320 | A10 | 24161215 | C | T | upstream_gene_variant | MODIFIER | c.-1491G>A| |
S218 |
16 | BAA10g34320 | A10 | 24164329 | G | A | upstream_gene_variant | MODIFIER | c.-4605C>T| |
S160 |
17 | BAA10g34320 | A10 | 24164626 | C | T | upstream_gene_variant | MODIFIER | c.-4902G>A| |
S236 |