| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 146951 | BAA10g31380 | A10 | 22918429 | C | T | upstream_gene_variant | MODIFIER | c.-1819G>A| |
S176 |
| 146952 | BAA10g31380 | A10 | 22920023 | T | A | upstream_gene_variant | MODIFIER | c.-3413A>T| |
S82 S92 |
| 146953 | BAA10g31390 | A10 | 22920371 | G | A | synonymous_variant | LOW | c.1407C>T|p.Asn469Asn |
S64 |
| 146954 | BAA10g31390 | A10 | 22922024 | C | T | missense_variant | MODERATE | c.70G>A|p.Val24Ile |
S12 |
| 146955 | BAA10g31390 | A10 | 22922063 | C | T | missense_variant | MODERATE | c.31G>A|p.Ala11Thr |
S37 |
| 146956 | BAA10g31390 | A10 | 22922082 | G | A | synonymous_variant | LOW | c.12C>T|p.Leu4Leu |
S128 |
| 146957 | BAA10g31390 | A10 | 22922306 | G | A | upstream_gene_variant | MODIFIER | c.-213C>T| |
S175 S177 |
| 146958 | BAA10g31400 | A10 | 22923026 | G | A | missense_variant | MODERATE | c.14G>A|p.Gly5Glu |
S278 |
| 146959 | BAA10g31400 | A10 | 22923113 | G | A | missense_variant | MODERATE | c.101G>A|p.Cys34Tyr |
S205 |
| 146960 | BAA10g31390 | A10 | 22923344 | G | A | upstream_gene_variant | MODIFIER | c.-1251C>T| |
S65 |
| 146961 | BAA10g31390 | A10 | 22925064 | T | G | upstream_gene_variant | MODIFIER | c.-2971A>C| |
S140 S211 S244 S48 |
| 146962 | BAA10g31410 | A10 | 22925145 | C | T | synonymous_variant | LOW | c.69C>T|p.Pro23Pro |
S296 |
| 146963 | BAA10g31410 | A10 | 22926671 | C | T | missense_variant | MODERATE | c.557C>T|p.Thr186Ile |
S255 |
| 146964 | BAA10g31410 | A10 | 22927027 | G | A | synonymous_variant | LOW | c.783G>A|p.Gln261Gln |
S83 S88 |
| 146965 | BAA10g31410 | A10 | 22927158 | G | A | missense_variant | MODERATE | c.829G>A|p.Asp277Asn |
S178 |
| 146966 | BAA10g31410 | A10 | 22927175 | G | A | synonymous_variant | LOW | c.846G>A|p.Val282Val |
S81 S85 |
| 146967 | BAA10g31410 | A10 | 22927309 | C | T | synonymous_variant | LOW | c.864C>T|p.Thr288Thr |
S292 |
| 146968 | BAA10g31410 | A10 | 22927759 | G | A | missense_variant | MODERATE | c.1150G>A|p.Gly384Ser |
S42 |
| 146969 | BAA10g31420 | A10 | 22928407 | C | T | upstream_gene_variant | MODIFIER | c.-2C>T| |
S286 |
| 146970 | BAA10g31420 | A10 | 22928559 | G | A | missense_variant | MODERATE | c.11G>A|p.Arg4Lys |
S217 |
| 146971 | BAA10g31430 | A10 | 22930050 | C | T | missense_variant | MODERATE | c.826G>A|p.Glu276Lys |
S187 |
| 146972 | BAA10g31430 | A10 | 22930360 | C | T | stop_gained | HIGH | c.516G>A|p.Trp172* |
S295 |
| 146973 | BAA10g31430 | A10 | 22930514 | G | A | missense_variant | MODERATE | c.362C>T|p.Pro121Leu |
S278 |
| 146974 | BAA10g31430 | A10 | 22930590 | G | A | synonymous_variant | LOW | c.286C>T|p.Leu96Leu |
S57 |
| 146975 | BAA10g31430 | A10 | 22930622 | G | A | missense_variant | MODERATE | c.254C>T|p.Ala85Val |
S219 S72 |