Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g00590 | A06 | 455904 | G | A | missense_variant | MODERATE | c.5258C>T|p.Pro1753Leu |
S118 |
2 | BAA06g00590 | A06 | 457949 | G | A | missense_variant | MODERATE | c.3485C>T|p.Ser1162Phe |
S138 |
3 | BAA06g00590 | A06 | 458028 | G | A | synonymous_variant | LOW | c.3406C>T|p.Leu1136Leu |
S128 |
4 | BAA06g00590 | A06 | 458894 | G | A | missense_variant | MODERATE | c.2990C>T|p.Ser997Phe |
S267 |
5 | BAA06g00590 | A06 | 459608 | C | T | synonymous_variant | LOW | c.2394G>A|p.Glu798Glu |
S247 |
6 | BAA06g00590 | A06 | 460428 | G | A | missense_variant | MODERATE | c.1574C>T|p.Pro525Leu |
S87 |
7 | BAA06g00590 | A06 | 461040 | G | A | missense_variant | MODERATE | c.1307C>T|p.Pro436Leu |
S81 S85 |
8 | BAA06g00590 | A06 | 461854 | C | T | missense_variant | MODERATE | c.943G>A|p.Asp315Asn |
S15 S3 |
9 | BAA06g00590 | A06 | 462033 | C | T | missense_variant | MODERATE | c.764G>A|p.Gly255Asp |
S289 S290 |
10 | BAA06g00590 | A06 | 463774 | C | T | missense_variant | MODERATE | c.28G>A|p.Gly10Ser |
S206 S26 |
11 | BAA06g00590 | A06 | 463923 | C | T | missense_variant | MODERATE | c.20G>A|p.Arg7Lys |
S265 |
12 | BAA06g00590 | A06 | 464032 | C | T | upstream_gene_variant | MODIFIER | c.-90G>A| |
S170 |
13 | BAA06g00590 | A06 | 465098 | G | A | upstream_gene_variant | MODIFIER | c.-1156C>T| |
S115 |
14 | BAA06g00590 | A06 | 465261 | C | T | upstream_gene_variant | MODIFIER | c.-1319G>A| |
S92 |
15 | BAA06g00590 | A06 | 465526 | C | T | upstream_gene_variant | MODIFIER | c.-1584G>A| |
S306 |
16 | BAA06g00590 | A06 | 467427 | C | T | upstream_gene_variant | MODIFIER | c.-3485G>A| |
S202 |
17 | BAA06g00590 | A06 | 467489 | C | T | upstream_gene_variant | MODIFIER | c.-3547G>A| |
S260 |