Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g31270 | A06 | 21275298 | C | T | upstream_gene_variant | MODIFIER | c.-2762C>T| |
S171 |
2 | BAA06g31270 | A06 | 21277842 | C | T | upstream_gene_variant | MODIFIER | c.-218C>T| |
S87 |
3 | BAA06g31270 | A06 | 21277885 | G | A | upstream_gene_variant | MODIFIER | c.-175G>A| |
S138 |
4 | BAA06g31270 | A06 | 21279429 | C | T | intron_variant | MODIFIER | c.996-53C>T| |
S181 |
5 | BAA06g31270 | A06 | 21279498 | G | A | missense_variant | MODERATE | c.1012G>A|p.Gly338Arg |
S255 |
6 | BAA06g31270 | A06 | 21279539 | C | T | synonymous_variant | LOW | c.1053C>T|p.Ser351Ser |
S283 |
7 | BAA06g31270 | A06 | 21280006 | G | A | splice_donor_variant&intron_variant | HIGH | c.1263+1G>A| |
S88 |
8 | BAA06g31270 | A06 | 21280705 | C | T | intron_variant | MODIFIER | c.1474+24C>T| |
S83 S88 |
9 | BAA06g31270 | A06 | 21280953 | G | A | synonymous_variant | LOW | c.1572G>A|p.Gln524Gln |
S37 |
10 | BAA06g31270 | A06 | 21281012 | G | A | intron_variant | MODIFIER | c.1599+32G>A| |
S130 |
11 | BAA06g31270 | A06 | 21281850 | C | T | missense_variant | MODERATE | c.2402C>T|p.Ser801Phe |
S112 |
12 | BAA06g31270 | A06 | 21282017 | C | T | missense_variant | MODERATE | c.2569C>T|p.Leu857Phe |
S279 |
13 | BAA06g31270 | A06 | 21282194 | G | A | missense_variant | MODERATE | c.2746G>A|p.Val916Met |
S183 S198 |
14 | BAA06g31270 | A06 | 21282471 | C | T | missense_variant | MODERATE | c.2903C>T|p.Thr968Ile |
S176 |
15 | BAA06g31270 | A06 | 21282595 | C | T | synonymous_variant | LOW | c.3027C>T|p.Ser1009Ser |
S174 S27 |
16 | BAA06g31270 | A06 | 21283804 | G | A | missense_variant | MODERATE | c.4144G>A|p.Glu1382Lys |
S226 |
17 | BAA06g31270 | A06 | 21284951 | C | T | missense_variant | MODERATE | c.4942C>T|p.Arg1648Cys |
S221 |
18 | BAA06g31270 | A06 | 21284953 | C | T | synonymous_variant | LOW | c.4944C>T|p.Arg1648Arg |
S182 |
19 | BAA06g31270 | A06 | 21285063 | C | T | intron_variant | MODIFIER | c.5031+23C>T| |
S249 |
20 | BAA06g31270 | A06 | 21285086 | G | A | intron_variant | MODIFIER | c.5031+46G>A| |
S284 |
21 | BAA06g31270 | A06 | 21285159 | G | A | missense_variant | MODERATE | c.5042G>A|p.Ser1681Asn |
S117 |
22 | BAA06g31270 | A06 | 21285746 | C | T | intron_variant | MODIFIER | c.5404-67C>T| |
S180 S217 |
23 | BAA06g31270 | A06 | 21287869 | G | A | intron_variant | MODIFIER | c.6885+38G>A| |
S117 |
24 | BAA06g31270 | A06 | 21287899 | G | A | intron_variant | MODIFIER | c.6885+68G>A| |
S132 S137 S215 S89 |
25 | BAA06g31270 | A06 | 21288840 | A | C | synonymous_variant | LOW | c.7437A>C|p.Ser2479Ser |
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