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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6090): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(2): Show |
a0001a0007 | a0001c0001a0007c0014 | a0001c0001t0001a0001c0001t0009a0007c0014t0001 | a0001c0001t0001g0221 a0001c0001t0001g0227 a0001c0001t0001g0228 others(2): Show |
5 | 256 | 0.0195 | 6097 | c.120 others(6114): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6090): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0066 | 1 | 252 | 0.0040 | 6097 | c.120 others(6114): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6090): Show |
intron_variant | MODIFIER | HG03669.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0261 | 1 | 252 | 0.0040 | 6097 | c.120 others(6114): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6090): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0130 | 1 | 252 | 0.0040 | 6097 | c.120 others(6114): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6090): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0127 | 1 | 252 | 0.0040 | 6097 | c.120 others(6114): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6090): Show |
intron_variant | MODIFIER | NA19062.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0111 | 1 | 252 | 0.0040 | 6097 | c.120 others(6114): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
OR1S1_chr11_58207720_58221084 | 58217924 | T | TTAAAGAA others(6090): Show |
downstream_gene_variant | MODIFIER | HG00738.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 456 | 0.0022 | 6097 | c.*22 others(6108): Show |
OR1S1 | ENSG00000280204.4 | transcript | ENST00000641544.1 | protein_coding | 1841 | chr11 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 147098431 | G | GTTCCTGT others(6091): Show |
intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0019 | a0001c0019t0006 | a0001c0019t0006g0015 | 1 | 40 | 0.0250 | 6098 | c.551 others(6115): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6091): Show |
intron_variant | MODIFIER | HG02809.hp1 NA21309.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0166 a0001c0001t0001g0170 |
2 | 109 | 0.0183 | 6098 | c.829 others(6117): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6091): Show |
intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141 | 1 | 108 | 0.0093 | 6098 | c.829 others(6117): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
MAP3K9_chr14_70717526_70814513 | 70731059 | T | TAAGAATA others(6091): Show |
intron_variant | MODIFIER | NA19064.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0103 | 1 | 318 | 0.0031 | 6098 | c.283 others(6115): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6091): Show |
intron_variant | MODIFIER | HG02055.hp1 HG03209.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0094 a0001c0001t0001g0168 |
2 | 253 | 0.0079 | 6098 | c.120 others(6115): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6091): Show |
intron_variant | MODIFIER | NA20805.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0182 | 1 | 252 | 0.0040 | 6098 | c.120 others(6115): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6091): Show |
intron_variant | MODIFIER | HG01123.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0214 | 1 | 252 | 0.0040 | 6098 | c.120 others(6115): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
TAF3_chr10_7813505_8021631 | 7983008 | C | CAAACCGT others(6091): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0251 | 1 | 341 | 0.0029 | 6098 | c.231 others(6117): Show |
TAF3 | ENSG00000165632.9 | transcript | ENST00000344293.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6091): Show |
intron_variant | MODIFIER | NA18951.hp1 NA18999.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0281 a0001c0001t0001g0306 |
2 | 285 | 0.0070 | 6098 | c.831 others(6117): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6091): Show |
intron_variant | MODIFIER | NA19065.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0310 | 1 | 284 | 0.0035 | 6098 | c.831 others(6117): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ZMAT4_chr8_40525590_40902826 | 40575656 | A | AGGAAAAA others(6091): Show |
intron_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0124 | 1 | 205 | 0.0049 | 6098 | c.674 others(6115): Show |
ZMAT4 | ENSG00000165061.15 | transcript | ENST00000297737.11 | protein_coding | 6/6 | chr8 | TogoVar | |||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6092): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0137 | 1 | 108 | 0.0093 | 6099 | c.829 others(6118): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
GPHN_chr14_66503147_67186803 | 66953146 | A | ACACCTTT others(6092): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0234 | 1 | 108 | 0.0093 | 6099 | c.829 others(6118): Show |
GPHN | ENSG00000171723.16 | transcript | ENST00000478722.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
LAMA2_chr6_128878138_129521566 | 128982982 | T | TGTGCCAC others(6092): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0008 | a0008c0005 | a0008c0005t0003 | a0008c0005t0003g0034 | 1 | 82 | 0.0122 | 6099 | c.113 others(6118): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 1/64 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
MAP3K9_chr14_70717526_70814513 | 70731059 | T | TAAGAATA others(6092): Show |
intron_variant | MODIFIER | HG02080.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0089 | 1 | 318 | 0.0031 | 6099 | c.283 others(6116): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | TogoVar | |||||||
PGPEP1L_chr15_98963229_99012792 | 98976342 | T | TAAATCAT others(6092): Show |
intron_variant | MODIFIER | NA18967.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0266 | 1 | 396 | 0.0025 | 6099 | c.-14 others(6118): Show |
PGPEP1L | ENSG00000183571.11 | transcript | ENST00000535714.2 | protein_coding | 2/4 | chr15 | TogoVar | |||||||
SDK1_chr7_3296252_4274000 | 3851601 | T | TGAGGATG others(6092): Show |
intron_variant | MODIFIER | HG02717.hp2 HG02723.hp1 |
a0001a0022 | a0001c0095a0022c0094 | a0001c0095t0029a0022c0094t0025 | a0001c0095t0029g0050 a0022c0094t0025g0049 |
2 | 115 | 0.0174 | 6099 | c.847 others(6118): Show |
SDK1 | ENSG00000146555.20 | transcript | ENST00000404826.7 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6092): Show |
intron_variant | MODIFIER | NA18965.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0299 | 1 | 284 | 0.0035 | 6099 | c.831 others(6118): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6092): Show |
intron_variant | MODIFIER | HG02015.hp1 HG02735.hp1 NA18967.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0352 |
3 | 286 | 0.0105 | 6099 | c.831 others(6118): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6092): Show |
intron_variant | MODIFIER | HG00140.hp1 HG01069.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0188 a0001c0001t0001g0197 |
2 | 285 | 0.0070 | 6099 | c.831 others(6118): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6092): Show |
intron_variant | MODIFIER | HG03017.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0309 | 1 | 284 | 0.0035 | 6099 | c.831 others(6118): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6092): Show |
intron_variant | MODIFIER | NA20905.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0344 | 1 | 284 | 0.0035 | 6099 | c.831 others(6118): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6092): Show |
intron_variant | MODIFIER | HG02976.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0311 | 1 | 284 | 0.0035 | 6099 | c.831 others(6118): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6092): Show |
intron_variant | MODIFIER | HG01952.hp1 HG02523.hp1 NA18747.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0282 a0001c0001t0001g0292 a0001c0001t0001g0293 others(8): Show |
11 | 294 | 0.0374 | 6099 | c.831 others(6118): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6092): Show |
intron_variant | MODIFIER | HG02293.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0353 | 1 | 284 | 0.0035 | 6099 | c.831 others(6118): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6092): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0189 | 1 | 284 | 0.0035 | 6099 | c.831 others(6118): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6092): Show |
intron_variant | MODIFIER | HG02738.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0196 | 1 | 284 | 0.0035 | 6099 | c.831 others(6118): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6092): Show |
intron_variant | MODIFIER | HG03491.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0318 | 1 | 284 | 0.0035 | 6099 | c.831 others(6118): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
AKAP6_chr14_32324298_32842684 | 32649427 | G | GAGAAATG others(6093): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0003 | a0003c0002 | a0003c0002t0042 | a0003c0002t0042g0030 | 1 | 152 | 0.0066 | 6100 | c.273 others(6121): Show |
AKAP6 | ENSG00000151320.11 | transcript | ENST00000280979.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
DNAH8_chr6_38710311_39035792 | 38756890 | T | TGTGCCAC others(6093): Show |
intron_variant | MODIFIER | NA18522.hp1 | a0026 | a0026c0092 | a0026c0092t0001 | a0026c0092t0001g0009 | 1 | 282 | 0.0035 | 6100 | c.151 others(6117): Show |
DNAH8 | ENSG00000124721.18 | transcript | ENST00000327475.11 | protein_coding | 10/92 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
LAMA2_chr6_128878138_129521566 | 128982982 | T | TGTGCCAC others(6093): Show |
intron_variant | MODIFIER | HG01192.hp1 | a0002 | a0002c0056 | a0002c0056t0003 | a0002c0056t0003g0078 | 1 | 82 | 0.0122 | 6100 | c.113 others(6119): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 1/64 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
MAP3K9_chr14_70717526_70814513 | 70731059 | T | TAAGAATA others(6093): Show |
intron_variant | MODIFIER | NA18940.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0176 | 1 | 318 | 0.0031 | 6100 | c.283 others(6117): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 11/11 | chr14 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6093): Show |
intron_variant | MODIFIER | NA18971.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0115 | 1 | 252 | 0.0040 | 6100 | c.120 others(6117): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
RIMS1_chr6_71881550_72408145 | 72089796 | T | TAAGAAAA others(6093): Show |
intron_variant | MODIFIER | HG00733.hp2 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0055 | 1 | 109 | 0.0092 | 6100 | c.246 others(6117): Show |
RIMS1 | ENSG00000079841.20 | transcript | ENST00000521978.6 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
RUNX2_chr6_45323330_45556082 | 45358082 | T | TAAAAAAG others(6093): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0034 | 1 | 174 | 0.0057 | 6100 | c.58+ others(6117): Show |
RUNX2 | ENSG00000124813.23 | transcript | ENST00000647337.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
SUPT3H_chr6_44821726_45382934 | 45358082 | T | TAAAAAAG others(6093): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0164 | 1 | 260 | 0.0038 | 6100 | c.101 others(6117): Show |
SUPT3H | ENSG00000196284.18 | transcript | ENST00000371459.6 | protein_coding | 2/10 | chr6 | TogoVar | |||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6093): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0319 | 1 | 284 | 0.0035 | 6100 | c.831 others(6119): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6093): Show |
intron_variant | MODIFIER | HG02135.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0294 | 1 | 284 | 0.0035 | 6100 | c.831 others(6119): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6093): Show |
intron_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0320 | 1 | 284 | 0.0035 | 6100 | c.831 others(6119): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6093): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(30): Show |
a0001a0013 | a0001c0001a0013c0020 | a0001c0001t0001a0013c0020t0001 | a0001c0001t0001g0012 a0001c0001t0001g0280 a0001c0001t0001g0283 others(29): Show |
33 | 316 | 0.1044 | 6100 | c.831 others(6119): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6093): Show |
intron_variant | MODIFIER | NA18946.hp1 NA19011.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0361 a0001c0001t0001g0362 |
2 | 285 | 0.0070 | 6100 | c.831 others(6119): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6093): Show |
intron_variant | MODIFIER | HG01071.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(4): Show |
7 | 290 | 0.0241 | 6100 | c.831 others(6119): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6093): Show |
intron_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0019 | a0001c0019t0001 | a0001c0019t0001g0334 | 1 | 284 | 0.0035 | 6100 | c.831 others(6119): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar |