Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g06310 | A08 | 5053660 | C | T | synonymous_variant | LOW | c.8067G>A|p.Lys2689Lys |
S15 S156 S3 S34 S6 |
2 | BAA08g06310 | A08 | 5054247 | C | T | missense_variant | MODERATE | c.7480G>A|p.Glu2494Lys |
S276 |
3 | BAA08g06310 | A08 | 5055135 | C | T | missense_variant | MODERATE | c.6892G>A|p.Asp2298Asn |
S293 |
4 | BAA08g06310 | A08 | 5055370 | G | A | intron_variant | MODIFIER | c.6855+48C>T| |
S86 |
5 | BAA08g06310 | A08 | 5056169 | C | T | missense_variant | MODERATE | c.6193G>A|p.Ala2065Thr |
S152 |
6 | BAA08g06310 | A08 | 5056769 | C | T | missense_variant | MODERATE | c.6100G>A|p.Glu2034Lys |
S192 |
7 | BAA08g06310 | A08 | 5057426 | C | T | missense_variant | MODERATE | c.5731G>A|p.Glu1911Lys |
S170 |
8 | BAA08g06310 | A08 | 5057502 | G | A | synonymous_variant | LOW | c.5655C>T|p.Tyr1885Tyr |
S100 |
9 | BAA08g06310 | A08 | 5057892 | C | T | synonymous_variant | LOW | c.5265G>A|p.Lys1755Lys |
S161 |
10 | BAA08g06310 | A08 | 5058394 | G | A | missense_variant | MODERATE | c.4763C>T|p.Ser1588Leu |
S122 |
11 | BAA08g06310 | A08 | 5059659 | G | A | stop_gained | HIGH | c.3724C>T|p.Arg1242* |
S103 S162 |
12 | BAA08g06310 | A08 | 5059737 | G | A | stop_gained | HIGH | c.3646C>T|p.Gln1216* |
S202 |
13 | BAA08g06310 | A08 | 5060678 | C | T | missense_variant | MODERATE | c.3065G>A|p.Arg1022Lys |
S177 |
14 | BAA08g06310 | A08 | 5060844 | C | T | missense_variant | MODERATE | c.2899G>A|p.Asp967Asn |
S279 |
15 | BAA08g06310 | A08 | 5060907 | C | T | missense_variant | MODERATE | c.2836G>A|p.Asp946Asn |
S308 |
16 | BAA08g06310 | A08 | 5061239 | C | T | missense_variant | MODERATE | c.2504G>A|p.Arg835Lys |
S36 |
17 | BAA08g06310 | A08 | 5061444 | C | T | missense_variant | MODERATE | c.2299G>A|p.Glu767Lys |
S176 |
18 | BAA08g06310 | A08 | 5062661 | G | A | intron_variant | MODIFIER | c.1732-368C>T| |
S108 |
19 | BAA08g06310 | A08 | 5063557 | C | T | missense_variant | MODERATE | c.1715G>A|p.Gly572Glu |
S252 |
20 | BAA08g06310 | A08 | 5063838 | C | T | synonymous_variant | LOW | c.1593G>A|p.Lys531Lys |
S206 S26 |
21 | BAA08g06310 | A08 | 5064346 | G | A | missense_variant | MODERATE | c.1085C>T|p.Ala362Val |
S229 |
22 | BAA08g06310 | A08 | 5065123 | G | A | missense_variant | MODERATE | c.884C>T|p.Ser295Phe |
S197 |
23 | BAA08g06310 | A08 | 5065534 | C | T | missense_variant | MODERATE | c.569G>A|p.Arg190His |
S114 |
24 | BAA08g06310 | A08 | 5065793 | G | A | missense_variant | MODERATE | c.310C>T|p.Pro104Ser |
S40 S49 |
25 | BAA08g06310 | A08 | 5068218 | G | A | upstream_gene_variant | MODIFIER | c.-2116C>T| |
S181 S293 |