Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g07090 | A08 | 5890736 | G | A | missense_variant | MODERATE | c.1840C>T|p.Pro614Ser |
S281 |
2 | BAA08g07090 | A08 | 5893722 | G | A | synonymous_variant | LOW | c.1134C>T|p.Ile378Ile |
S108 |
3 | BAA08g07090 | A08 | 5893760 | C | T | missense_variant | MODERATE | c.1096G>A|p.Glu366Lys |
S243 S299 |
4 | BAA08g07090 | A08 | 5893913 | C | T | missense_variant | MODERATE | c.943G>A|p.Asp315Asn |
S248 S77 |
5 | BAA08g07090 | A08 | 5893949 | C | T | missense_variant&splice_region_variant | MODERATE | c.907G>A|p.Gly303Arg |
S230 |
6 | BAA08g07090 | A08 | 5893950 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.907-1G>A| |
S162 |
7 | BAA08g07090 | A08 | 5894031 | C | T | splice_region_variant&intron_variant | LOW | c.906+8G>A| |
S308 |
8 | BAA08g07090 | A08 | 5894540 | C | T | synonymous_variant | LOW | c.405G>A|p.Glu135Glu |
S157 S163 |
9 | BAA08g07090 | A08 | 5894565 | C | T | missense_variant | MODERATE | c.380G>A|p.Ser127Asn |
S135 |
10 | BAA08g07090 | A08 | 5894778 | C | T | missense_variant | MODERATE | c.167G>A|p.Ser56Asn |
S245 |
11 | BAA08g07090 | A08 | 5894868 | C | T | missense_variant | MODERATE | c.77G>A|p.Arg26Lys |
S219 S72 |
12 | BAA08g07090 | A08 | 5895064 | C | T | upstream_gene_variant | MODIFIER | c.-120G>A| |
S219 S72 |
13 | BAA08g07090 | A08 | 5895957 | C | T | upstream_gene_variant | MODIFIER | c.-1013G>A| |
S149 |
14 | BAA08g07090 | A08 | 5896182 | C | T | upstream_gene_variant | MODIFIER | c.-1238G>A| |
S201 |
15 | BAA08g07090 | A08 | 5896665 | C | T | upstream_gene_variant | MODIFIER | c.-1721G>A| |
S42 |
16 | BAA08g07090 | A08 | 5897281 | C | T | upstream_gene_variant | MODIFIER | c.-2337G>A| |
S295 |
17 | BAA08g07090 | A08 | 5898797 | G | A | upstream_gene_variant | MODIFIER | c.-3853C>T| |
S298 |
18 | BAA08g07090 | A08 | 5898955 | C | T | upstream_gene_variant | MODIFIER | c.-4011G>A| |
S142 |