Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g35190 | A07 | 33371628 | C | T | upstream_gene_variant | MODIFIER | c.-2161C>T| |
S107 |
2 | BAA07g35190 | A07 | 33371876 | C | T | upstream_gene_variant | MODIFIER | c.-1913C>T| |
S68 |
3 | BAA07g35190 | A07 | 33373431 | G | A | upstream_gene_variant | MODIFIER | c.-358G>A| |
S70 |
4 | BAA07g35190 | A07 | 33373826 | C | T | missense_variant | MODERATE | c.38C>T|p.Thr13Ile |
S4 |
5 | BAA07g35190 | A07 | 33373834 | G | A | missense_variant | MODERATE | c.46G>A|p.Asp16Asn |
S48 |
6 | BAA07g35190 | A07 | 33373906 | G | A | missense_variant | MODERATE | c.118G>A|p.Glu40Lys |
S298 |
7 | BAA07g35190 | A07 | 33374599 | C | T | synonymous_variant | LOW | c.579C>T|p.Thr193Thr |
S25 |
8 | BAA07g35190 | A07 | 33374771 | C | T | synonymous_variant | LOW | c.678C>T|p.Asp226Asp |
S167 |
9 | BAA07g35190 | A07 | 33375724 | G | A | missense_variant | MODERATE | c.1313G>A|p.Cys438Tyr |
S83 S88 |
10 | BAA07g35190 | A07 | 33375747 | C | T | missense_variant | MODERATE | c.1336C>T|p.Pro446Ser |
S57 |
11 | BAA07g35190 | A07 | 33377018 | C | T | missense_variant | MODERATE | c.2288C>T|p.Ala763Val |
S9 |
12 | BAA07g35190 | A07 | 33377173 | C | T | splice_region_variant&intron_variant | LOW | c.2437+6C>T| |
S279 |
13 | BAA07g35190 | A07 | 33377282 | C | T | missense_variant | MODERATE | c.2456C>T|p.Pro819Leu |
S190 |
14 | BAA07g35190 | A07 | 33377695 | G | A | missense_variant | MODERATE | c.2869G>A|p.Glu957Lys |
S40 S49 |
15 | BAA07g35190 | A07 | 33378428 | C | T | missense_variant | MODERATE | c.3383C>T|p.Ser1128Phe |
S241 |
16 | BAA07g35190 | A07 | 33379051 | G | A | synonymous_variant | LOW | c.3771G>A|p.Lys1257Lys |
S139 |