Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18550 | A08 | 14816644 | G | A | missense_variant | MODERATE | c.2362C>T|p.Pro788Ser |
S200 |
2 | BAA08g18550 | A08 | 14817312 | C | T | missense_variant | MODERATE | c.1951G>A|p.Asp651Asn |
S157 S163 |
3 | BAA08g18550 | A08 | 14817376 | G | A | splice_region_variant&intron_variant | LOW | c.1895-8C>T| |
S41 |
4 | BAA08g18550 | A08 | 14818521 | C | T | missense_variant | MODERATE | c.1253G>A|p.Gly418Glu |
S223 |
5 | BAA08g18550 | A08 | 14818600 | C | T | missense_variant | MODERATE | c.1174G>A|p.Gly392Arg |
S134 |
6 | BAA08g18550 | A08 | 14819477 | G | A | synonymous_variant | LOW | c.636C>T|p.Thr212Thr |
S116 |
7 | BAA08g18550 | A08 | 14819800 | C | T | missense_variant | MODERATE | c.382G>A|p.Gly128Arg |
S295 |
8 | BAA08g18550 | A08 | 14820263 | C | T | synonymous_variant | LOW | c.81G>A|p.Glu27Glu |
S250 |
9 | BAA08g18550 | A08 | 14820394 | G | A | missense_variant | MODERATE | c.44C>T|p.Ala15Val |
S289 S290 |
10 | BAA08g18550 | A08 | 14820484 | C | T | upstream_gene_variant | MODIFIER | c.-47G>A| |
S197 |
11 | BAA08g18550 | A08 | 14821047 | C | T | upstream_gene_variant | MODIFIER | c.-610G>A| |
S112 |
12 | BAA08g18550 | A08 | 14822715 | G | A | upstream_gene_variant | MODIFIER | c.-2278C>T| |
S86 |
13 | BAA08g18550 | A08 | 14823176 | G | A | upstream_gene_variant | MODIFIER | c.-2739C>T| |
S33 |
14 | BAA08g18550 | A08 | 14824143 | C | T | upstream_gene_variant | MODIFIER | c.-3706G>A| |
S180 |
15 | BAA08g18550 | A08 | 14824335 | C | T | upstream_gene_variant | MODIFIER | c.-3898G>A| |
S122 |
16 | BAA08g18550 | A08 | 14824914 | G | A | upstream_gene_variant | MODIFIER | c.-4477C>T| |
S292 |