| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 91601 | BAA10g01500 | A10 | 754583 | C | T | missense_variant | MODERATE | c.877G>A|p.Gly293Arg |
S151 S166 S262 S263 |
| 91602 | BAA10g01500 | A10 | 754686 | G | A | synonymous_variant | LOW | c.774C>T|p.Arg258Arg |
S171 |
| 91603 | BAA10g01500 | A10 | 755058 | C | T | synonymous_variant | LOW | c.402G>A|p.Gly134Gly |
S123 |
| 91604 | BAA10g01500 | A10 | 755693 | G | A | upstream_gene_variant | MODIFIER | c.-234C>T| |
S230 |
| 91605 | BAA10g01500 | A10 | 756081 | G | A | upstream_gene_variant | MODIFIER | c.-622C>T| |
S192 |
| 91606 | BAA10g01510 | A10 | 756999 | G | A | missense_variant | MODERATE | c.4G>A|p.Asp2Asn |
S293 |
| 91607 | BAA10g01510 | A10 | 757065 | G | A | missense_variant | MODERATE | c.70G>A|p.Ala24Thr |
S257 |
| 91608 | BAA10g01500 | A10 | 758114 | C | T | upstream_gene_variant | MODIFIER | c.-2655G>A| |
S104 S52 |
| 91609 | BAA10g01520 | A10 | 759070 | C | T | missense_variant&splice_region_variant | MODERATE | c.551G>A|p.Gly184Asp |
S54 |
| 91610 | BAA10g01520 | A10 | 760903 | C | T | upstream_gene_variant | MODIFIER | c.-745G>A| |
S157 |
| 91611 | BAA10g01520 | A10 | 761460 | G | A | upstream_gene_variant | MODIFIER | c.-1302C>T| |
S267 |
| 91612 | BAA10g01520 | A10 | 764233 | C | T | upstream_gene_variant | MODIFIER | c.-4075G>A| |
S117 |
| 91613 | BAA10g01520 | A10 | 764561 | C | T | upstream_gene_variant | MODIFIER | c.-4403G>A| |
S272 |
| 91614 | BAA10g01540 | A10 | 765471 | C | T | missense_variant | MODERATE | c.611C>T|p.Ser204Phe |
S125 |
| 91615 | BAA10g01540 | A10 | 765503 | C | T | synonymous_variant | LOW | c.643C>T|p.Leu215Leu |
S206 S26 |
| 91616 | BAA10g01540 | A10 | 766501 | G | A | synonymous_variant | LOW | c.1347G>A|p.Gln449Gln |
S76 |
| 91617 | BAA10g01550 | A10 | 767292 | G | A | missense_variant | MODERATE | c.211G>A|p.Val71Ile |
S103 |
| 91618 | BAA10g01550 | A10 | 767315 | G | A | synonymous_variant | LOW | c.234G>A|p.Ser78Ser |
S19 |
| 91619 | BAA10g01560 | A10 | 768993 | C | T | missense_variant | MODERATE | c.494C>T|p.Ser165Leu |
S205 |
| 91620 | BAA10g01590 | A10 | 769075 | G | A | upstream_gene_variant | MODIFIER | c.-4332G>A| |
S289 |
| 91621 | BAA10g01590 | A10 | 769148 | C | T | upstream_gene_variant | MODIFIER | c.-4259C>T| |
S202 |
| 91622 | BAA10g01590 | A10 | 769816 | C | T | upstream_gene_variant | MODIFIER | c.-3591C>T| |
S270 |
| 91623 | BAA10g01590 | A10 | 770273 | C | T | upstream_gene_variant | MODIFIER | c.-3134C>T| |
S113 |
| 91624 | BAA10g01590 | A10 | 770939 | G | A | upstream_gene_variant | MODIFIER | c.-2468G>A| |
S121 |
| 91625 | BAA10g01570 | A10 | 772033 | C | T | upstream_gene_variant | MODIFIER | c.-337G>A| |
S175 |