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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2613): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0042 | a0001c0001t0042g0257 | 1 | 388 | 0.0026 | 2620 | c.114 others(2639): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2613): Show |
intron_variant | MODIFIER | HG01106.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0063 | 1 | 388 | 0.0026 | 2620 | c.114 others(2639): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
MED16_chr19_862963_898187 | 879404 | T | TCCCTGGT others(2613): Show |
intron_variant | MODIFIER | HG03239.hp2 NA18970.hp2 |
a0001 | a0001c0004 | a0001c0004t0001a0001c0004t0008 | a0001c0004t0001g0016 a0001c0004t0008g0054 |
2 | 56 | 0.0357 | 2620 | c.135 others(2637): Show |
MED16 | ENSG00000175221.16 | transcript | ENST00000325464.6 | protein_coding | 8/15 | chr19 | TogoVar | |||||||
MEGF6_chr1_3482951_3616508 | 3502017 | G | GCCTCACA others(2613): Show |
intron_variant | MODIFIER | HG04199.hp2 | a0002 | a0002c0033 | a0002c0033t0001 | a0002c0033t0001g0140 | 1 | 292 | 0.0034 | 2620 | c.218 others(2635): Show |
MEGF6 | ENSG00000162591.17 | transcript | ENST00000356575.9 | protein_coding | 17/36 | chr1 | TogoVar | |||||||
MEGF6_chr1_3482951_3616508 | 3502017 | G | GCCTCACA others(2613): Show |
intron_variant | MODIFIER | HG02074.hp1 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0194 | 1 | 292 | 0.0034 | 2620 | c.218 others(2635): Show |
MEGF6 | ENSG00000162591.17 | transcript | ENST00000356575.9 | protein_coding | 17/36 | chr1 | TogoVar | |||||||
PDGFA_chr7_492258_524846 | 494651 | T | TGGGGGAT others(2613): Show |
downstream_gene_variant | MODIFIER | NA19012.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0067 | 1 | 302 | 0.0033 | 2620 | c.*39 others(2631): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2606 | chr7 | TogoVar | |||||||
PDGFA_chr7_492258_524846 | 494651 | T | TGGGGGAT others(2613): Show |
downstream_gene_variant | MODIFIER | NA18952.hp2 | a0001 | a0001c0002 | a0001c0002t0006 | a0001c0002t0006g0031 | 1 | 302 | 0.0033 | 2620 | c.*39 others(2631): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2606 | chr7 | TogoVar | |||||||
PDGFA_chr7_492258_524846 | 494651 | T | TGGGGGAT others(2613): Show |
downstream_gene_variant | MODIFIER | NA19057.hp1 | a0014 | a0014c0007 | a0014c0007t0008 | a0014c0007t0008g0027 | 1 | 302 | 0.0033 | 2620 | c.*39 others(2631): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2606 | chr7 | TogoVar | |||||||
RPEL1_chr10_103240887_103253016 | 103251133 | A | AACACCAC others(2613): Show |
downstream_gene_variant | MODIFIER | NA18948.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0000 | 1 | 375 | 0.0027 | 2620 | c.*44 others(2631): Show |
RPEL1 | ENSG00000235376.5 | transcript | ENST00000441178.2 | protein_coding | 3118 | chr10 | TogoVar | |||||||
SPIC_chr12_101470336_101491997 | 101484138 | A | AGAAAGCT others(2613): Show |
intron_variant | MODIFIER | NA19080.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0129 | 1 | 398 | 0.0025 | 2620 | c.319 others(2637): Show |
SPIC | ENSG00000166211.8 | transcript | ENST00000551346.2 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3477303 | G | GTCACCCC others(2614): Show |
intron_variant | MODIFIER | NA18967.hp2 NA19007.hp2 |
a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0015 | 2 | 334 | 0.0060 | 2621 | c.147 others(2638): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2614): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0104 | 1 | 388 | 0.0026 | 2621 | c.114 others(2640): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2614): Show |
intron_variant | MODIFIER | NA18969.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0060 | 1 | 388 | 0.0026 | 2621 | c.114 others(2640): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2614): Show |
intron_variant | MODIFIER | HG00423.hp2 HG01258.hp1 HG01361.hp2 others(25): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(14): Show | a0001c0001t0003g0009 a0001c0001t0003g0028 a0001c0001t0003g0029 others(24): Show |
28 | 388 | 0.0722 | 2621 | c.114 others(2640): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2614): Show |
intron_variant | MODIFIER | NA19085.hp2 NA19088.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0019 | a0001c0001t0003g0099 a0001c0001t0019g0098 |
2 | 388 | 0.0052 | 2621 | c.114 others(2640): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2614): Show |
intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0112 | 1 | 388 | 0.0026 | 2621 | c.114 others(2640): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2614): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0001 | a0001c0001t0146 | a0001c0001t0146g0056 | 1 | 388 | 0.0026 | 2621 | c.114 others(2640): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2614): Show |
intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0001 | a0001c0001t0029 | a0001c0001t0029g0140 | 1 | 388 | 0.0026 | 2621 | c.114 others(2640): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2614): Show |
intron_variant | MODIFIER | NA19010.hp1 | a0001 | a0001c0001 | a0001c0001t0050 | a0001c0001t0050g0102 | 1 | 388 | 0.0026 | 2621 | c.114 others(2640): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2614): Show |
intron_variant | MODIFIER | NA19077.hp1 | a0003 | a0003c0003 | a0003c0003t0010 | a0003c0003t0010g0078 | 1 | 388 | 0.0026 | 2621 | c.114 others(2640): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2614): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0121 | a0001c0001t0121g0258 | 1 | 388 | 0.0026 | 2621 | c.114 others(2640): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2614): Show |
intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 |
a0001 | a0001c0001 | a0001c0001t0049 | a0001c0001t0049g0079 a0001c0001t0049g0090 |
2 | 388 | 0.0052 | 2621 | c.114 others(2640): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
EIF3B_chr7_2349827_2385745 | 2378317 | C | CCTGGGAT others(2614): Show |
intron_variant | MODIFIER | NA19070.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037 | 1 | 384 | 0.0026 | 2621 | c.215 others(2638): Show |
EIF3B | ENSG00000106263.19 | transcript | ENST00000360876.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
GLCE_chr15_69155635_69277207 | 69202819 | T | TCCCAAAT others(2614): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0056 | 1 | 342 | 0.0029 | 2621 | c.-10 others(2640): Show |
GLCE | ENSG00000138604.10 | transcript | ENST00000261858.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
KREMEN1_chr22_29068035_29151820 | 29120383 | A | GATGGAAA others(2614): Show |
intron_variant | MODIFIER | HG02738.hp2 HG03239.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0057 | a0001c0001t0004g0176 a0001c0001t0057g0017 |
2 | 368 | 0.0054 | 2621 | c.353 others(2636): Show |
KREMEN1 | ENSG00000183762.13 | transcript | ENST00000400335.9 | protein_coding | 3/8 | chr22 | TogoVar | |||||||
MARS1_chr12_57483068_57521652 | 57491746 | A | ACTAAGAT others(2614): Show |
intron_variant | MODIFIER | HG00639.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0142 | 1 | 288 | 0.0035 | 2621 | c.770 others(2638): Show |
MARS1 | ENSG00000166986.15 | transcript | ENST00000262027.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
MTG1_chr10_133389157_133427520 | 133397401 | T | TACCGGTC others(2614): Show |
intron_variant | MODIFIER | HG00140.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0241 | 1 | 428 | 0.0023 | 2621 | c.283 others(2638): Show |
MTG1 | ENSG00000148824.19 | transcript | ENST00000317502.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(2614): Show |
intron_variant | MODIFIER | HG02109.hp1 | a0055 | a0055c0076 | a0055c0076t0024 | a0055c0076t0024g0280 | 1 | 282 | 0.0036 | 2621 | c.299 others(2636): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
ARHGEF16_chr1_3449665_3486113 | 3477303 | G | GTCACCCC others(2615): Show |
intron_variant | MODIFIER | NA18977.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0223 | 1 | 334 | 0.0030 | 2622 | c.147 others(2639): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2615): Show |
intron_variant | MODIFIER | HG01099.hp2 | a0001 | a0001c0001 | a0001c0001t0046 | a0001c0001t0046g0068 | 1 | 388 | 0.0026 | 2622 | c.114 others(2641): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2615): Show |
intron_variant | MODIFIER | HG00673.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0108 | 1 | 388 | 0.0026 | 2622 | c.114 others(2641): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2615): Show |
intron_variant | MODIFIER | NA19074.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0072 | 1 | 388 | 0.0026 | 2622 | c.114 others(2641): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2615): Show |
intron_variant | MODIFIER | NA18961.hp2 NA18988.hp1 NA19084.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0018a0001c0001t0154 | a0001c0001t0003g0055 a0001c0001t0018g0073 a0001c0001t0154g0093 |
3 | 388 | 0.0077 | 2622 | c.114 others(2641): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2615): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0148 | a0001c0001t0148g0134 | 1 | 388 | 0.0026 | 2622 | c.114 others(2641): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2615): Show |
intron_variant | MODIFIER | NA18941.hp2 NA18962.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0150 | a0001c0001t0003g0089 a0001c0001t0150g0091 |
2 | 388 | 0.0052 | 2622 | c.114 others(2641): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2615): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00558.hp1 HG01433.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(5): Show | a0001c0001t0003g0025 a0001c0001t0003g0107 a0001c0001t0004g0025 others(9): Show |
12 | 388 | 0.0309 | 2622 | c.114 others(2641): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2615): Show |
intron_variant | MODIFIER | HG01081.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0114 | 1 | 388 | 0.0026 | 2622 | c.114 others(2641): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2615): Show |
intron_variant | MODIFIER | NA19066.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0097 | 1 | 388 | 0.0026 | 2622 | c.114 others(2641): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
DNAH10_chr12_123757301_123940714 | 123911549 | G | GGGGGTCT others(2615): Show |
intron_variant | MODIFIER | HG01099.hp1 | a0008 | a0008c0009 | a0008c0009t0002 | a0008c0009t0002g0032 | 1 | 170 | 0.0059 | 2622 | c.101 others(2641): Show |
DNAH10 | ENSG00000197653.16 | transcript | ENST00000673944.1 | protein_coding | 59/78 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
DOCK8_chr9_209865_470255 | 400506 | T | TCACCACC others(2615): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0067 | a0001c0067t0001 | a0001c0067t0001g0006 | 1 | 256 | 0.0039 | 2622 | c.323 others(2641): Show |
DOCK8 | ENSG00000107099.18 | transcript | ENST00000432829.7 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
HPCAL1_chr2_10297904_10432604 | 10399271 | C | CCACCACC others(2615): Show |
intron_variant | MODIFIER | NA18995.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0018 | 1 | 314 | 0.0032 | 2622 | c.-25 others(2639): Show |
HPCAL1 | ENSG00000115756.13 | transcript | ENST00000307845.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
RPH3AL_chr17_207389_357807 | 304067 | A | AGCAGTGA others(2615): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0003 | a0003c0016 | a0003c0016t0001 | a0003c0016t0001g0075 | 1 | 133 | 0.0075 | 2622 | c.351 others(2641): Show |
RPH3AL | ENSG00000181031.16 | transcript | ENST00000331302.12 | protein_coding | 5/9 | chr17 | TogoVar | |||||||
SLC6A3_chr5_1387794_1450440 | 1414424 | A | AGAAGGCA others(2615): Show |
intron_variant | MODIFIER | NA19065.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0222 | 1 | 373 | 0.0027 | 2622 | c.115 others(2639): Show |
SLC6A3 | ENSG00000142319.18 | transcript | ENST00000270349.12 | protein_coding | 8/14 | chr5 | TogoVar | |||||||
SLC6A3_chr5_1387794_1450440 | 1414431 | A | ACTGGGTG others(2615): Show |
intron_variant | MODIFIER | HG00609.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0211 | 1 | 373 | 0.0027 | 2622 | c.115 others(2639): Show |
SLC6A3 | ENSG00000142319.18 | transcript | ENST00000270349.12 | protein_coding | 8/14 | chr5 | TogoVar | |||||||
SLC6A3_chr5_1387794_1450440 | 1414484 | T | TGGAGGGG others(2615): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0196 | 1 | 373 | 0.0027 | 2622 | c.115 others(2639): Show |
SLC6A3 | ENSG00000142319.18 | transcript | ENST00000270349.12 | protein_coding | 8/14 | chr5 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1844397 | T | TGACAGAG others(2616): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0003 | a0003c0039 | a0003c0039t0065 | a0003c0039t0065g0181 | 1 | 363 | 0.0028 | 2623 | c.37+ others(2636): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2616): Show |
intron_variant | MODIFIER | NA19000.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0057 | 1 | 388 | 0.0026 | 2623 | c.114 others(2642): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2616): Show |
intron_variant | MODIFIER | HG02135.hp1 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0094 | 1 | 388 | 0.0026 | 2623 | c.114 others(2642): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2616): Show |
intron_variant | MODIFIER | NA19001.hp1 | a0001 | a0001c0001 | a0001c0001t0158 | a0001c0001t0158g0069 | 1 | 388 | 0.0026 | 2623 | c.114 others(2642): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
CPSF2_chr14_92116969_92177145 | 92153061 | T | TCAAATTT others(2616): Show |
intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0001 | a0001c0001t0155 | a0001c0001t0155g0075 | 1 | 388 | 0.0026 | 2623 | c.114 others(2642): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar |