Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g11630 | A06 | 5887435 | G | A | missense_variant | MODERATE | c.4048C>T|p.Pro1350Ser |
S149 |
2 | BAA06g11630 | A06 | 5889939 | C | T | synonymous_variant | LOW | c.2622G>A|p.Glu874Glu |
S295 |
3 | BAA06g11630 | A06 | 5890279 | G | A | missense_variant | MODERATE | c.2377C>T|p.Leu793Phe |
S35 |
4 | BAA06g11630 | A06 | 5890504 | C | T | missense_variant | MODERATE | c.2246G>A|p.Gly749Glu |
S10 |
5 | BAA06g11630 | A06 | 5891047 | C | T | missense_variant | MODERATE | c.1703G>A|p.Gly568Glu |
S103 |
6 | BAA06g11630 | A06 | 5891284 | G | A | missense_variant | MODERATE | c.1466C>T|p.Ser489Leu |
S209 |
7 | BAA06g11630 | A06 | 5891443 | C | T | missense_variant | MODERATE | c.1307G>A|p.Ser436Asn |
S91 |
8 | BAA06g11630 | A06 | 5891486 | G | A | missense_variant | MODERATE | c.1264C>T|p.Pro422Ser |
S128 |
9 | BAA06g11630 | A06 | 5891495 | C | T | missense_variant | MODERATE | c.1255G>A|p.Asp419Asn |
S278 |
10 | BAA06g11630 | A06 | 5891707 | G | A | missense_variant | MODERATE | c.1043C>T|p.Thr348Ile |
S180 |
11 | BAA06g11630 | A06 | 5892186 | G | A | missense_variant | MODERATE | c.716C>T|p.Ser239Leu |
S45 |
12 | BAA06g11630 | A06 | 5893248 | G | A | upstream_gene_variant | MODIFIER | c.-28C>T| |
S139 |
13 | BAA06g11630 | A06 | 5893379 | G | A | upstream_gene_variant | MODIFIER | c.-159C>T| |
S32 |
14 | BAA06g11630 | A06 | 5896075 | C | T | upstream_gene_variant | MODIFIER | c.-2855G>A| |
S265 |
15 | BAA06g11630 | A06 | 5896180 | C | T | upstream_gene_variant | MODIFIER | c.-2960G>A| |
S20 |