Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g14250 | A06 | 7044985 | C | T | upstream_gene_variant | MODIFIER | c.-2125C>T| |
S111 |
2 | BAA06g14250 | A06 | 7045464 | C | T | upstream_gene_variant | MODIFIER | c.-1646C>T| |
S184 |
3 | BAA06g14250 | A06 | 7046404 | G | A | upstream_gene_variant | MODIFIER | c.-706G>A| |
S292 |
4 | BAA06g14250 | A06 | 7047104 | G | A | upstream_gene_variant | MODIFIER | c.-6G>A| |
S19 |
5 | BAA06g14250 | A06 | 7047724 | C | T | synonymous_variant | LOW | c.351C>T|p.Ile117Ile |
S2 S3 |
6 | BAA06g14250 | A06 | 7048536 | C | T | missense_variant | MODERATE | c.616C>T|p.Leu206Phe |
S295 |
7 | BAA06g14250 | A06 | 7049345 | G | A | missense_variant | MODERATE | c.985G>A|p.Val329Met |
S190 |
8 | BAA06g14250 | A06 | 7049609 | G | A | intron_variant | MODIFIER | c.1167+82G>A| |
S201 |
9 | BAA06g14250 | A06 | 7049759 | G | A | intron_variant | MODIFIER | c.1168-83G>A| |
S127 |
10 | BAA06g14250 | A06 | 7049935 | C | T | missense_variant | MODERATE | c.1261C>T|p.His421Tyr |
S259 |
11 | BAA06g14250 | A06 | 7050075 | G | A | missense_variant&splice_region_variant | MODERATE | c.1309G>A|p.Asp437Asn |
S182 |
12 | BAA06g14250 | A06 | 7050096 | G | A | missense_variant | MODERATE | c.1330G>A|p.Val444Ile |
S228 |
13 | BAA06g14250 | A06 | 7050519 | G | A | intron_variant | MODIFIER | c.1391-239G>A| |
S70 |
14 | BAA06g14250 | A06 | 7050776 | A | T | missense_variant | MODERATE | c.1409A>T|p.Asp470Val |
S19 |
15 | BAA06g14250 | A06 | 7052424 | G | A | splice_region_variant&intron_variant | LOW | c.2141+8G>A| |
S213 |
16 | BAA06g14250 | A06 | 7056795 | C | T | downstream_gene_variant | MODIFIER | c.*3645C>T| |
S171 |
17 | BAA06g14250 | A06 | 7057083 | G | A | downstream_gene_variant | MODIFIER | c.*3933G>A| |
S126 |