Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g36660 | A07 | 34129974 | C | T | missense_variant | MODERATE | c.412C>T|p.Arg138Cys |
S121 |
2 | BAA07g36660 | A07 | 34129975 | G | A | missense_variant | MODERATE | c.413G>A|p.Arg138His |
S171 |
3 | BAA07g36660 | A07 | 34130170 | G | A | missense_variant | MODERATE | c.608G>A|p.Arg203Gln |
S263 |
4 | BAA07g36660 | A07 | 34130970 | A | C | synonymous_variant | LOW | c.1408A>C|p.Arg470Arg |
S152 S288 |
5 | BAA07g36660 | A07 | 34131041 | G | A | synonymous_variant | LOW | c.1479G>A|p.Glu493Glu |
S276 |
6 | BAA07g36660 | A07 | 34131198 | C | T | missense_variant | MODERATE | c.1636C>T|p.Leu546Phe |
S144 |
7 | BAA07g36660 | A07 | 34131273 | C | T | stop_gained | HIGH | c.1711C>T|p.Gln571* |
S295 |
8 | BAA07g36660 | A07 | 34132309 | G | A | missense_variant | MODERATE | c.2747G>A|p.Gly916Asp |
S60 |
9 | BAA07g36660 | A07 | 34133352 | G | A | missense_variant | MODERATE | c.3790G>A|p.Val1264Ile |
S48 |
10 | BAA07g36660 | A07 | 34133370 | C | T | stop_gained | HIGH | c.3808C>T|p.Gln1270* |
S32 |
11 | BAA07g36660 | A07 | 34133468 | C | T | synonymous_variant | LOW | c.3906C>T|p.Ser1302Ser |
S96 |
12 | BAA07g36660 | A07 | 34134297 | G | A | missense_variant | MODERATE | c.4735G>A|p.Val1579Ile |
S143 |
13 | BAA07g36660 | A07 | 34134329 | G | A | synonymous_variant | LOW | c.4767G>A|p.Gln1589Gln |
S120 |