Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g12110 | A08 | 10585246 | C | T | synonymous_variant | LOW | c.11715G>A|p.Gln3905Gln |
S185 |
2 | BAA08g12110 | A08 | 10586471 | G | A | synonymous_variant | LOW | c.10921C>T|p.Leu3641Leu |
S109 |
3 | BAA08g12110 | A08 | 10587880 | G | A | intron_variant | MODIFIER | c.10391+40C>T| |
S97 |
4 | BAA08g12110 | A08 | 10587914 | G | A | splice_region_variant&intron_variant | LOW | c.10391+6C>T| |
S109 |
5 | BAA08g12110 | A08 | 10589327 | C | T | missense_variant | MODERATE | c.9476G>A|p.Gly3159Glu |
S6 |
6 | BAA08g12110 | A08 | 10589592 | C | T | missense_variant | MODERATE | c.9310G>A|p.Asp3104Asn |
S233 |
7 | BAA08g12110 | A08 | 10589905 | G | A | missense_variant | MODERATE | c.9080C>T|p.Ser3027Phe |
S32 |
8 | BAA08g12110 | A08 | 10590470 | C | T | missense_variant | MODERATE | c.8620G>A|p.Glu2874Lys |
S121 |
9 | BAA08g12110 | A08 | 10591230 | C | T | missense_variant&splice_region_variant | MODERATE | c.8009G>A|p.Gly2670Asp |
S88 |
10 | BAA08g12110 | A08 | 10591287 | G | A | intron_variant | MODIFIER | c.8008+31C>T| |
S265 |
11 | BAA08g12110 | A08 | 10592481 | G | A | intron_variant | MODIFIER | c.7500+33C>T| |
S34 |
12 | BAA08g12110 | A08 | 10593561 | G | A | missense_variant | MODERATE | c.6694C>T|p.Pro2232Ser |
S8 |
13 | BAA08g12110 | A08 | 10593693 | C | T | synonymous_variant | LOW | c.6651G>A|p.Gly2217Gly |
S63 |
14 | BAA08g12110 | A08 | 10594384 | C | T | intron_variant | MODIFIER | c.6320+29G>A| |
S34 |
15 | BAA08g12110 | A08 | 10594682 | C | T | synonymous_variant | LOW | c.6051G>A|p.Leu2017Leu |
S149 |
16 | BAA08g12110 | A08 | 10595077 | C | T | synonymous_variant | LOW | c.5814G>A|p.Leu1938Leu |
S47 |
17 | BAA08g12110 | A08 | 10595792 | G | A | splice_region_variant&intron_variant | LOW | c.5335-4C>T| |
S20 |
18 | BAA08g12110 | A08 | 10595819 | C | T | intron_variant | MODIFIER | c.5335-31G>A| |
S113 |
19 | BAA08g12110 | A08 | 10596201 | G | A | synonymous_variant | LOW | c.5020C>T|p.Leu1674Leu |
S40 S49 |
20 | BAA08g12110 | A08 | 10596650 | C | T | intron_variant | MODIFIER | c.4690-119G>A| |
S171 |
21 | BAA08g12110 | A08 | 10596809 | C | T | intron_variant | MODIFIER | c.4689+238G>A| |
S111 |
22 | BAA08g12110 | A08 | 10596898 | C | T | intron_variant | MODIFIER | c.4689+149G>A| |
S74 |
23 | BAA08g12110 | A08 | 10597106 | G | A | synonymous_variant | LOW | c.4630C>T|p.Leu1544Leu |
S158 |
24 | BAA08g12110 | A08 | 10597628 | G | A | intron_variant | MODIFIER | c.4260+57C>T| |
S48 |
25 | BAA08g12110 | A08 | 10597912 | G | A | intron_variant | MODIFIER | c.4151+40C>T| |
S263 |