Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11520 | A10 | 13130752 | G | A | upstream_gene_variant | MODIFIER | c.-3758G>A| |
S159 |
2 | BAA10g11520 | A10 | 13135090 | G | A | missense_variant | MODERATE | c.581G>A|p.Arg194His |
S165 |
3 | BAA10g11520 | A10 | 13135869 | C | T | missense_variant | MODERATE | c.1147C>T|p.Pro383Ser |
S225 S73 |
4 | BAA10g11520 | A10 | 13135929 | C | T | intron_variant | MODIFIER | c.1182+25C>T| |
S84 S93 |
5 | BAA10g11520 | A10 | 13136400 | C | T | missense_variant | MODERATE | c.1409C>T|p.Ser470Phe |
S243 S299 |
6 | BAA10g11520 | A10 | 13136401 | C | T | splice_region_variant&synonymous_variant | LOW | c.1410C>T|p.Ser470Ser |
S274 |
7 | BAA10g11520 | A10 | 13138400 | G | A | missense_variant | MODERATE | c.2431G>A|p.Glu811Lys |
S264 |
8 | BAA10g11520 | A10 | 13138936 | G | A | stop_gained | HIGH | c.2699G>A|p.Trp900* |
S202 |
9 | BAA10g11520 | A10 | 13139448 | G | A | missense_variant | MODERATE | c.2941G>A|p.Asp981Asn |
S184 |