Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g16870 | A06 | 8451548 | C | T | missense_variant | MODERATE | c.2230G>A|p.Asp744Asn |
S142 |
2 | BAA06g16870 | A06 | 8451697 | C | T | missense_variant | MODERATE | c.2081G>A|p.Gly694Glu |
S184 |
3 | BAA06g16870 | A06 | 8451751 | C | T | missense_variant | MODERATE | c.2027G>A|p.Gly676Glu |
S15 S3 |
4 | BAA06g16870 | A06 | 8451940 | G | A | missense_variant | MODERATE | c.1838C>T|p.Ala613Val |
S295 |
5 | BAA06g16870 | A06 | 8452247 | C | T | missense_variant | MODERATE | c.1604G>A|p.Gly535Asp |
S17 |
6 | BAA06g16870 | A06 | 8452262 | C | T | missense_variant | MODERATE | c.1589G>A|p.Ser530Asn |
S17 |
7 | BAA06g16870 | A06 | 8453709 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.558-1G>A| |
S96 |
8 | BAA06g16870 | A06 | 8453792 | C | T | splice_donor_variant&intron_variant | HIGH | c.557+1G>A| |
S294 |
9 | BAA06g16870 | A06 | 8454082 | C | T | missense_variant | MODERATE | c.346G>A|p.Asp116Asn |
S163 |
10 | BAA06g16870 | A06 | 8454369 | G | A | synonymous_variant | LOW | c.144C>T|p.Ala48Ala |
S53 |
11 | BAA06g16870 | A06 | 8455840 | C | T | upstream_gene_variant | MODIFIER | c.-1328G>A| |
S189 |
12 | BAA06g16870 | A06 | 8455849 | C | T | upstream_gene_variant | MODIFIER | c.-1337G>A| |
S192 |
13 | BAA06g16870 | A06 | 8455865 | G | A | upstream_gene_variant | MODIFIER | c.-1353C>T| |
S278 |
14 | BAA06g16870 | A06 | 8456210 | G | A | upstream_gene_variant | MODIFIER | c.-1698C>T| |
S88 |
15 | BAA06g16870 | A06 | 8457354 | C | T | upstream_gene_variant | MODIFIER | c.-2842G>A| |
S103 |
16 | BAA06g16870 | A06 | 8458578 | C | T | upstream_gene_variant | MODIFIER | c.-4066G>A| |
S109 |