Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g33350 | A06 | 22547695 | G | A | downstream_gene_variant | MODIFIER | c.*4377C>T| |
S209 |
2 | BAA06g33350 | A06 | 22548475 | C | T | downstream_gene_variant | MODIFIER | c.*3597G>A| |
S96 |
3 | BAA06g33350 | A06 | 22548857 | C | T | downstream_gene_variant | MODIFIER | c.*3215G>A| |
S302 |
4 | BAA06g33350 | A06 | 22549058 | G | A | downstream_gene_variant | MODIFIER | c.*3014C>T| |
S273 |
5 | BAA06g33350 | A06 | 22551517 | G | A | downstream_gene_variant | MODIFIER | c.*555C>T| |
S219 |
6 | BAA06g33350 | A06 | 22551800 | G | A | downstream_gene_variant | MODIFIER | c.*272C>T| |
S298 |
7 | BAA06g33350 | A06 | 22552014 | C | T | downstream_gene_variant | MODIFIER | c.*58G>A| |
S112 |
8 | BAA06g33350 | A06 | 22552164 | C | T | missense_variant | MODERATE | c.10270G>A|p.Glu3424Lys |
S286 |
9 | BAA06g33350 | A06 | 22552270 | C | T | synonymous_variant | LOW | c.10164G>A|p.Gln3388Gln |
S288 |
10 | BAA06g33350 | A06 | 22552293 | C | T | missense_variant | MODERATE | c.10141G>A|p.Asp3381Asn |
S82 S92 |
11 | BAA06g33350 | A06 | 22552331 | C | T | missense_variant | MODERATE | c.10103G>A|p.Cys3368Tyr |
S62 |
12 | BAA06g33350 | A06 | 22552592 | G | A | missense_variant | MODERATE | c.9842C>T|p.Pro3281Leu |
S20 |
13 | BAA06g33350 | A06 | 22553249 | G | A | intron_variant | MODIFIER | c.9496-39C>T| |
S305 |
14 | BAA06g33350 | A06 | 22553356 | G | A | synonymous_variant | LOW | c.9432C>T|p.Leu3144Leu |
S284 |
15 | BAA06g33350 | A06 | 22553402 | C | T | missense_variant&splice_region_variant | MODERATE | c.9386G>A|p.Ser3129Asn |
S6 |
16 | BAA06g33350 | A06 | 22554042 | G | A | intron_variant | MODIFIER | c.9132+189C>T| |
S233 |
17 | BAA06g33350 | A06 | 22554631 | G | A | synonymous_variant | LOW | c.8820C>T|p.Leu2940Leu |
S37 |
18 | BAA06g33350 | A06 | 22556110 | G | A | missense_variant | MODERATE | c.8042C>T|p.Thr2681Met |
S268 |
19 | BAA06g33350 | A06 | 22557857 | G | A | synonymous_variant | LOW | c.7017C>T|p.Ser2339Ser |
S185 |
20 | BAA06g33350 | A06 | 22558537 | G | A | missense_variant | MODERATE | c.6523C>T|p.Pro2175Ser |
S125 S268 |
21 | BAA06g33350 | A06 | 22558854 | G | A | intron_variant | MODIFIER | c.6286-80C>T| |
S2 |
22 | BAA06g33350 | A06 | 22559180 | G | A | missense_variant | MODERATE | c.6230C>T|p.Ser2077Phe |
S273 |
23 | BAA06g33350 | A06 | 22559269 | C | T | intron_variant | MODIFIER | c.6213+9G>A| |
S116 |
24 | BAA06g33350 | A06 | 22559997 | C | T | missense_variant | MODERATE | c.5579G>A|p.Gly1860Glu |
S112 |
25 | BAA06g33350 | A06 | 22560751 | G | A | intron_variant | MODIFIER | c.5361+27C>T| |
S256 |