| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 96601 | BAA10g04750 | A10 | 2436402 | G | A | upstream_gene_variant | MODIFIER | c.-676G>A| |
S77 S82 |
| 96602 | BAA10g04750 | A10 | 2437330 | C | T | intron_variant | MODIFIER | c.177+76C>T| |
S259 |
| 96603 | BAA10g04750 | A10 | 2437388 | C | T | intron_variant | MODIFIER | c.177+134C>T| |
S146 |
| 96604 | BAA10g04750 | A10 | 2438317 | G | A | synonymous_variant | LOW | c.342G>A|p.Glu114Glu |
S178 |
| 96605 | BAA10g04760 | A10 | 2438405 | G | A | upstream_gene_variant | MODIFIER | c.-4369G>A| |
S219 S72 |
| 96606 | BAA10g04750 | A10 | 2438575 | G | A | splice_region_variant&intron_variant | LOW | c.499+5G>A| |
S164 |
| 96607 | BAA10g04750 | A10 | 2438813 | C | T | missense_variant | MODERATE | c.575C>T|p.Ala192Val |
S206 S26 |
| 96608 | BAA10g04750 | A10 | 2439413 | C | T | missense_variant | MODERATE | c.851C>T|p.Ser284Phe |
S166 |
| 96609 | BAA10g04750 | A10 | 2439626 | G | A | missense_variant | MODERATE | c.926G>A|p.Gly309Glu |
S171 |
| 96610 | BAA10g04760 | A10 | 2440610 | G | A | upstream_gene_variant | MODIFIER | c.-2164G>A| |
S111 |
| 96611 | BAA10g04760 | A10 | 2440662 | G | A | upstream_gene_variant | MODIFIER | c.-2112G>A| |
S241 |
| 96612 | BAA10g04750 | A10 | 2440831 | G | A | splice_region_variant&synonymous_variant | LOW | c.1275G>A|p.Gln425Gln |
S234 |
| 96613 | BAA10g04760 | A10 | 2442832 | G | A | missense_variant | MODERATE | c.59G>A|p.Ser20Asn |
S179 |
| 96614 | BAA10g04760 | A10 | 2443378 | C | T | missense_variant | MODERATE | c.299C>T|p.Ser100Phe |
S63 |
| 96615 | BAA10g04760 | A10 | 2443921 | C | T | missense_variant | MODERATE | c.754C>T|p.Pro252Ser |
S41 |
| 96616 | BAA10g04760 | A10 | 2443926 | G | A | synonymous_variant | LOW | c.759G>A|p.Arg253Arg |
S15 |
| 96617 | BAA10g04760 | A10 | 2444307 | G | A | synonymous_variant | LOW | c.1140G>A|p.Gly380Gly |
S240 |
| 96618 | BAA10g04760 | A10 | 2444390 | C | T | missense_variant | MODERATE | c.1223C>T|p.Thr408Ile |
S116 |
| 96619 | BAA10g04760 | A10 | 2444816 | G | A | missense_variant | MODERATE | c.1649G>A|p.Gly550Asp |
S18 |
| 96620 | BAA10g04760 | A10 | 2445523 | G | A | synonymous_variant | LOW | c.2274G>A|p.Arg758Arg |
S153 S213 |
| 96621 | BAA10g04770 | A10 | 2445718 | C | T | upstream_gene_variant | MODIFIER | c.-3031C>T| |
S23 |
| 96622 | BAA10g04770 | A10 | 2445983 | C | T | upstream_gene_variant | MODIFIER | c.-2766C>T| |
S171 |
| 96623 | BAA10g04770 | A10 | 2446756 | C | T | upstream_gene_variant | MODIFIER | c.-1993C>T| |
S142 |
| 96624 | BAA10g04760 | A10 | 2447272 | G | A | missense_variant | MODERATE | c.2903G>A|p.Gly968Glu |
S160 |
| 96625 | BAA10g04760 | A10 | 2447677 | G | A | missense_variant | MODERATE | c.3196G>A|p.Ala1066Thr |
S16 |