view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5251): Show |
intron_variant | MODIFIER | HG02040.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0226 | 1 | 25 | 0.0400 | 5258 | c.274 others(5277): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5251): Show |
intron_variant | MODIFIER | NA18991.hp2 NA18994.hp2 |
a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0137 a0001c0002t0004g0145 |
2 | 26 | 0.0769 | 5258 | c.274 others(5277): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5251): Show |
intron_variant | MODIFIER | NA19079.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0154 | 1 | 25 | 0.0400 | 5258 | c.274 others(5277): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
GOLGA8A_chr15_34374068_34442808 | 34376058 | A | AAATGTCA others(5252): Show |
downstream_gene_variant | MODIFIER | HG02572.hp2 NA18906.hp1 |
a0009 | a0009c0009 | a0009c0009t0013a0009c0009t0051 | a0009c0009t0013g0234 a0009c0009t0051g0235 |
2 | 27 | 0.0741 | 5259 | c.*53 others(5270): Show |
GOLGA8A | ENSG00000175265.19 | transcript | ENST00000359187.5 | protein_coding | 3009 | chr15 | TogoVar | |||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5252): Show |
intron_variant | MODIFIER | HG01168.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0089 | 1 | 25 | 0.0400 | 5259 | c.274 others(5278): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5252): Show |
intron_variant | MODIFIER | HG01109.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0281 | 1 | 25 | 0.0400 | 5259 | c.274 others(5278): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5252): Show |
intron_variant | MODIFIER | HG02109.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0282 a0001c0001t0001g0286 a0001c0001t0001g0287 others(4): Show |
7 | 31 | 0.2258 | 5259 | c.274 others(5278): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5252): Show |
intron_variant | MODIFIER | HG00639.hp2 HG01069.hp2 HG01884.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0016 | a0001c0001t0001g0001 a0001c0001t0001g0255 a0001c0001t0001g0256 others(11): Show |
16 | 40 | 0.4000 | 5259 | c.274 others(5278): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5252): Show |
intron_variant | MODIFIER | HG03239.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0227 | 1 | 25 | 0.0400 | 5259 | c.274 others(5278): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
GOLGA8A_chr15_34374068_34442808 | 34376058 | A | AAATGTCA others(5253): Show |
downstream_gene_variant | MODIFIER | HG02976.hp2 HG03486.hp1 |
a0031a0033 | a0031c0034a0033c0033 | a0031c0034t0021a0033c0033t0021 | a0031c0034t0021g0149 a0033c0033t0021g0148 |
2 | 27 | 0.0741 | 5260 | c.*53 others(5271): Show |
GOLGA8A | ENSG00000175265.19 | transcript | ENST00000359187.5 | protein_coding | 3009 | chr15 | TogoVar | |||||||
GOLGA8A_chr15_34374068_34442808 | 34376058 | A | AAATGTCA others(5253): Show |
downstream_gene_variant | MODIFIER | HG02630.hp1 HG03209.hp2 NA20129.hp2 |
a0019a0028 | a0019c0023a0028c0036 | a0019c0023t0026a0028c0036t0038 | a0019c0023t0026g0236 a0019c0023t0026g0237 a0028c0036t0038g0015 |
3 | 28 | 0.1071 | 5260 | c.*53 others(5271): Show |
GOLGA8A | ENSG00000175265.19 | transcript | ENST00000359187.5 | protein_coding | 3009 | chr15 | TogoVar | |||||||
GOLGA8A_chr15_34374068_34442808 | 34376058 | A | AAATGTCA others(5253): Show |
downstream_gene_variant | MODIFIER | HG02486.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
a0005a0027 | a0005c0005a0027c0035 | a0005c0005t0008a0027c0035t0031 | a0005c0005t0008g0004 a0005c0005t0008g0139 a0005c0005t0008g0141 others(2): Show |
6 | 31 | 0.1935 | 5260 | c.*53 others(5271): Show |
GOLGA8A | ENSG00000175265.19 | transcript | ENST00000359187.5 | protein_coding | 3009 | chr15 | TogoVar | |||||||
GOLGA8A_chr15_34374068_34442808 | 34376058 | A | AAATGTCA others(5253): Show |
downstream_gene_variant | MODIFIER | HG01109.hp1 HG02559.hp2 HG02896.hp2 others(1): Show |
a0008 | a0008c0008 | a0008c0008t0012a0008c0008t0054 | a0008c0008t0012g0220 a0008c0008t0012g0222 a0008c0008t0012g0224 others(1): Show |
4 | 29 | 0.1379 | 5260 | c.*53 others(5271): Show |
GOLGA8A | ENSG00000175265.19 | transcript | ENST00000359187.5 | protein_coding | 3009 | chr15 | TogoVar | |||||||
GOLGA8A_chr15_34374068_34442808 | 34376058 | A | AAATGTCA others(5253): Show |
downstream_gene_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(2): Show |
a0005 | a0005c0005 | a0005c0005t0009 | a0005c0005t0009g0010 a0005c0005t0009g0011 a0005c0005t0009g0012 others(2): Show |
5 | 30 | 0.1667 | 5260 | c.*53 others(5271): Show |
GOLGA8A | ENSG00000175265.19 | transcript | ENST00000359187.5 | protein_coding | 3009 | chr15 | TogoVar | |||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5253): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0279 | 1 | 25 | 0.0400 | 5260 | c.274 others(5279): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5253): Show |
intron_variant | MODIFIER | HG03516.hp1 NA18999.hp2 NA19060.hp1 |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0002a0001c0001t0003a0004c0005t0002 | a0001c0001t0002g0060 a0001c0001t0003g0029 a0004c0005t0002g0048 |
3 | 27 | 0.1111 | 5260 | c.274 others(5279): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5253): Show |
intron_variant | MODIFIER | HG00408.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0108 | 1 | 25 | 0.0400 | 5260 | c.274 others(5279): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5253): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0285 | 1 | 25 | 0.0400 | 5260 | c.274 others(5279): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5254): Show |
intron_variant | MODIFIER | NA18956.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0138 | 1 | 25 | 0.0400 | 5261 | c.274 others(5280): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5254): Show |
intron_variant | MODIFIER | HG01433.hp1 HG02129.hp2 HG02165.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0007 | a0001c0001t0002g0112 a0001c0001t0002g0251 a0001c0001t0002g0252 others(4): Show |
7 | 31 | 0.2258 | 5261 | c.274 others(5280): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5254): Show |
intron_variant | MODIFIER | NA18955.hp1 NA18962.hp1 NA19091.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0008 | a0001c0001t0002g0111 a0001c0001t0002g0113 a0001c0001t0008g0115 |
3 | 27 | 0.1111 | 5261 | c.274 others(5280): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5254): Show |
intron_variant | MODIFIER | HG03490.hp2 HG03492.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | 26 | 0.0769 | 5261 | c.274 others(5280): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5254): Show |
intron_variant | MODIFIER | NA19080.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0098 | 1 | 25 | 0.0400 | 5261 | c.274 others(5280): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5255): Show |
intron_variant | MODIFIER | HG02735.hp2 | a0001 | a0001c0002 | a0001c0002t0013 | a0001c0002t0013g0133 | 1 | 25 | 0.0400 | 5262 | c.274 others(5281): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5255): Show |
intron_variant | MODIFIER | HG02080.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0059 | 1 | 25 | 0.0400 | 5262 | c.274 others(5281): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5255): Show |
intron_variant | MODIFIER | NA18952.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0044 | 1 | 25 | 0.0400 | 5262 | c.274 others(5281): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5255): Show |
intron_variant | MODIFIER | NA18947.hp1 NA18978.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0056 a0001c0001t0002g0066 |
2 | 26 | 0.0769 | 5262 | c.274 others(5281): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5255): Show |
intron_variant | MODIFIER | NA18953.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0078 | 1 | 25 | 0.0400 | 5262 | c.274 others(5281): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5255): Show |
intron_variant | MODIFIER | NA18985.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0253 | 1 | 25 | 0.0400 | 5262 | c.274 others(5281): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5255): Show |
intron_variant | MODIFIER | NA18612.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0114 | 1 | 25 | 0.0400 | 5262 | c.274 others(5281): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5255): Show |
intron_variant | MODIFIER | HG02451.hp1 HG02647.hp1 HG03209.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | 27 | 0.1111 | 5262 | c.274 others(5281): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
EYS_chr6_63714980_65712226 | 64295511 | A | AAGAAGAA others(5256): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0014 | a0014c0003 | a0014c0003t0001 | a0014c0003t0001g0016 | 1 | 12 | 0.0833 | 5263 | c.619 others(5284): Show |
EYS | ENSG00000188107.15 | transcript | ENST00000503581.6 | protein_coding | 30/42 | chr6 | TogoVar | |||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5256): Show |
intron_variant | MODIFIER | HG04228.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0125 | 1 | 25 | 0.0400 | 5263 | c.274 others(5282): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5256): Show |
intron_variant | MODIFIER | NA18967.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0097 | 1 | 25 | 0.0400 | 5263 | c.274 others(5282): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5256): Show |
intron_variant | MODIFIER | HG03654.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0070 | 1 | 25 | 0.0400 | 5263 | c.274 others(5282): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5256): Show |
intron_variant | MODIFIER | NA18988.hp1 NA19079.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | 26 | 0.0769 | 5263 | c.274 others(5282): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5256): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0021 a0001c0001t0002g0092 a0001c0001t0002g0093 others(8): Show |
11 | 35 | 0.3143 | 5263 | c.274 others(5282): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5256): Show |
intron_variant | MODIFIER | HG02055.hp2 HG02602.hp1 HG03579.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0077 a0001c0001t0002g0080 a0001c0001t0002g0082 others(1): Show |
4 | 28 | 0.1429 | 5263 | c.274 others(5282): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
IFNAR1_chr21_33319970_33364864 | 33323057 | A | ATACATGG others(5257): Show |
upstream_gene_variant | MODIFIER | NA18944.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0001 | 1 | 317 | 0.0032 | 5264 | c.-19 others(5275): Show |
IFNAR1 | ENSG00000142166.15 | transcript | ENST00000270139.8 | protein_coding | 1912 | chr21 | TogoVar | |||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(5257): Show |
upstream_gene_variant | MODIFIER | NA18971.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0013 | 1 | 8 | 0.1250 | 5264 | c.-45 others(5273): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(5257): Show |
upstream_gene_variant | MODIFIER | NA18970.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0135 | 1 | 8 | 0.1250 | 5264 | c.-45 others(5273): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5257): Show |
intron_variant | MODIFIER | HG01192.hp2 HG03209.hp2 HG04199.hp2 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0104 a0001c0001t0003g0106 a0001c0001t0003g0123 |
3 | 27 | 0.1111 | 5264 | c.274 others(5283): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5257): Show |
intron_variant | MODIFIER | HG00438.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0102 | 1 | 25 | 0.0400 | 5264 | c.274 others(5283): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5257): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0085 | 1 | 25 | 0.0400 | 5264 | c.274 others(5283): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5257): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0105 | 1 | 25 | 0.0400 | 5264 | c.274 others(5283): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5257): Show |
intron_variant | MODIFIER | HG00673.hp1 HG01496.hp1 HG01943.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0008a0001c0001t0015others(1): Show | a0001c0001t0002g0019 a0001c0001t0002g0024 a0001c0001t0002g0026 others(13): Show |
16 | 40 | 0.4000 | 5264 | c.274 others(5283): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5258): Show |
intron_variant | MODIFIER | NA18969.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0031 | 1 | 25 | 0.0400 | 5265 | c.274 others(5284): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5258): Show |
intron_variant | MODIFIER | HG00438.hp2 NA19000.hp1 NA19056.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0030 a0001c0001t0002g0035 a0001c0001t0002g0049 |
3 | 27 | 0.1111 | 5265 | c.274 others(5284): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5258): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0122 | 1 | 25 | 0.0400 | 5265 | c.274 others(5284): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
PBX3_chr9_125742373_125972377 | 125814025 | A | ATGGTGGG others(5258): Show |
intron_variant | MODIFIER | NA18971.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0040 | 1 | 25 | 0.0400 | 5265 | c.274 others(5284): Show |
PBX3 | ENSG00000167081.18 | transcript | ENST00000373489.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar |