Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26170 | A10 | 20861387 | C | T | upstream_gene_variant | MODIFIER | c.-4512C>T| |
S296 |
2 | BAA10g26170 | A10 | 20861666 | C | T | upstream_gene_variant | MODIFIER | c.-4233C>T| |
S281 |
3 | BAA10g26170 | A10 | 20863700 | G | A | upstream_gene_variant | MODIFIER | c.-2199G>A| |
S1 S90 |
4 | BAA10g26170 | A10 | 20864182 | C | T | upstream_gene_variant | MODIFIER | c.-1717C>T| |
S166 |
5 | BAA10g26170 | A10 | 20866485 | C | T | missense_variant | MODERATE | c.587C>T|p.Pro196Leu |
S200 |
6 | BAA10g26170 | A10 | 20866519 | G | A | synonymous_variant | LOW | c.621G>A|p.Lys207Lys |
S233 |
7 | BAA10g26170 | A10 | 20866543 | C | T | synonymous_variant | LOW | c.645C>T|p.Ser215Ser |
S144 |
8 | BAA10g26170 | A10 | 20866646 | G | A | missense_variant | MODERATE | c.748G>A|p.Asp250Asn |
S303 |
9 | BAA10g26170 | A10 | 20866666 | G | A | stop_gained | HIGH | c.768G>A|p.Trp256* |
S75 S81 |
10 | BAA10g26170 | A10 | 20866772 | C | T | stop_gained | HIGH | c.874C>T|p.Gln292* |
S204 |
11 | BAA10g26170 | A10 | 20866897 | C | T | synonymous_variant | LOW | c.999C>T|p.Phe333Phe |
S98 |
12 | BAA10g26170 | A10 | 20866901 | G | A | missense_variant | MODERATE | c.1003G>A|p.Asp335Asn |
S63 |
13 | BAA10g26170 | A10 | 20866995 | G | A | missense_variant | MODERATE | c.1097G>A|p.Gly366Glu |
S136 |
14 | BAA10g26170 | A10 | 20867094 | G | A | missense_variant | MODERATE | c.1196G>A|p.Arg399His |
S192 |
15 | BAA10g26170 | A10 | 20867334 | C | T | missense_variant | MODERATE | c.1436C>T|p.Ser479Phe |
S20 |
16 | BAA10g26170 | A10 | 20867689 | C | T | synonymous_variant | LOW | c.1791C>T|p.Phe597Phe |
S203 |
17 | BAA10g26170 | A10 | 20869949 | C | T | downstream_gene_variant | MODIFIER | c.*2122C>T| |
S13 |
18 | BAA10g26170 | A10 | 20872005 | C | T | downstream_gene_variant | MODIFIER | c.*4178C>T| |
S39 |