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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TDRD5_chr1_179586832_179696272 | 179606226 | T | TCTGGTAT others(6091): Show |
intron_variant | MODIFIER | NA18951.hp1 NA18999.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0285 a0001c0001t0001g0312 |
2 | 382 | 0.0052 | 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 | a0001c0001t0001g0316 | 1 | 382 | 0.0026 | 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 | 228 | 0.0044 | 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 | 234 | 0.0043 | 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 | 234 | 0.0043 | 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 | 88 | 0.0114 | 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 | a0001c0002t0001g0088 | 1 | 374 | 0.0027 | 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 | 398 | 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 |
a0001a0024 | a0001c0096a0024c0095 | a0001c0096t0029a0024c0095t0025 | a0001c0096t0029g0050 a0024c0095t0025g0049 |
2 | 116 | 0.0172 | 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 | a0001c0001t0001g0303 | 1 | 382 | 0.0026 | 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 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0357 |
3 | 382 | 0.0079 | 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 | a0001c0001t0001g0189 a0001c0001t0001g0198 |
2 | 382 | 0.0052 | 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 | a0001c0001t0001g0315 | 1 | 382 | 0.0026 | 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 | a0001c0001t0001g0349 | 1 | 382 | 0.0026 | 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 | a0001c0001t0001g0280 | 1 | 382 | 0.0026 | 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 | a0001c0001t0001g0286 a0001c0001t0001g0296 a0001c0001t0001g0297 others(8): Show |
11 | 382 | 0.0288 | 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 | a0001c0001t0001g0358 | 1 | 382 | 0.0026 | 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 | a0001c0001t0001g0190 | 1 | 382 | 0.0026 | 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 | a0001c0001t0001g0197 | 1 | 382 | 0.0026 | 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 | a0001c0001t0001g0323 | 1 | 382 | 0.0026 | 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 | 154 | 0.0065 | 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 | a0026c0092t0001g0157 | 1 | 284 | 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 | a0002c0056t0003g0077 | 1 | 88 | 0.0114 | 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 | a0001c0002t0001g0177 | 1 | 374 | 0.0027 | 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 | a0001c0001t0001g0118 | 1 | 344 | 0.0029 | 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 | a0001c0002t0006 | a0001c0002t0006g0055 | 1 | 140 | 0.0071 | 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 | a0001c0001t0007g0036 | 1 | 178 | 0.0056 | 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 | 262 | 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 | a0001c0001t0001g0324 | 1 | 382 | 0.0026 | 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 | a0001c0001t0001g0298 | 1 | 382 | 0.0026 | 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 | a0001c0001t0001g0325 | 1 | 382 | 0.0026 | 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 | a0001c0001a0013c0021 | a0001c0001t0001a0013c0021t0001 | a0001c0001t0001g0284 a0001c0001t0001g0287 a0001c0001t0001g0288 others(30): Show |
33 | 382 | 0.0864 | 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 | a0001c0001t0001g0366 a0001c0001t0001g0367 |
2 | 382 | 0.0052 | 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 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(4): Show |
7 | 382 | 0.0183 | 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 | a0001c0020 | a0001c0020t0001 | a0001c0020t0001g0339 | 1 | 382 | 0.0026 | 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 | NA18939.hp1 | a0015 | a0015c0022 | a0015c0022t0001 | a0015c0022t0001g0340 | 1 | 382 | 0.0026 | 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 | NA19074.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0302 | 1 | 382 | 0.0026 | 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 | HG04199.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0341 | 1 | 382 | 0.0026 | 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 | HG01081.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0342 | 1 | 382 | 0.0026 | 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 | HG02040.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0304 | 1 | 382 | 0.0026 | 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 | NA18964.hp2 NA19002.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | 382 | 0.0052 | 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 | NA18980.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0307 | 1 | 382 | 0.0026 | 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 | HG03942.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0359 | 1 | 382 | 0.0026 | 6100 | c.831 others(6119): Show |
TDRD5 | ENSG00000162782.16 | transcript | ENST00000444136.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
KSR2_chr12_117448012_117973990 | 117786317 | T | TTATTTTT others(6094): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0003 | a0001c0003t0068 | a0001c0003t0068g0046 | 1 | 196 | 0.0051 | 6101 | c.473 others(6120): Show |
KSR2 | ENSG00000171435.15 | transcript | ENST00000339824.7 | protein_coding | 3/19 | chr12 | TogoVar | |||||||
NEDD4_chr15_55821922_55998612 | 55958936 | T | TAAAACTT others(6094): Show |
intron_variant | MODIFIER | NA18987.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119 | 1 | 344 | 0.0029 | 6101 | c.120 others(6118): Show |
NEDD4 | ENSG00000069869.17 | transcript | ENST00000435532.8 | protein_coding | 2/28 | chr15 | TogoVar | |||||||
RALYL_chr8_84178274_84926844 | 84516373 | T | TTAAAAGC others(6094): Show |
intron_variant | MODIFIER | NA18950.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0037 | 1 | 82 | 0.0122 | 6101 | c.-23 others(6120): Show |
RALYL | ENSG00000184672.12 | transcript | ENST00000521268.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
RALYL_chr8_84178274_84926844 | 84516373 | T | TTAAAAGC others(6094): Show |
intron_variant | MODIFIER | HG01071.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0070 | 1 | 82 | 0.0122 | 6101 | c.-23 others(6120): Show |
RALYL | ENSG00000184672.12 | transcript | ENST00000521268.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
RALYL_chr8_84178274_84926844 | 84516373 | T | TTAAAAGC others(6094): Show |
intron_variant | MODIFIER | NA18964.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0034 | 1 | 82 | 0.0122 | 6101 | c.-23 others(6120): Show |
RALYL | ENSG00000184672.12 | transcript | ENST00000521268.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
RIMS1_chr6_71881550_72408145 | 72089796 | T | TAAGAAAA others(6094): Show |
intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0016 | 1 | 140 | 0.0071 | 6101 | c.246 others(6118): Show |
RIMS1 | ENSG00000079841.20 | transcript | ENST00000521978.6 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
RIMS1_chr6_71881550_72408145 | 72089796 | T | TAAGAAAA others(6094): Show |
intron_variant | MODIFIER | NA20805.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0036 | 1 | 140 | 0.0071 | 6101 | c.246 others(6118): Show |
RIMS1 | ENSG00000079841.20 | transcript | ENST00000521978.6 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar |