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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NACAD_chr7_45075437_45093969 | 45078842 | T | TGGGACAT others(92): Show |
downstream_gene_variant | MODIFIER | HG02145.hp1 | a0013 | a0013c0014 | a0013c0014t0001 | a0013c0014t0001g0070 | 1 | 408 | 0.0025 | 99 | c.*16 others(110): Show |
NACAD | ENSG00000136274.9 | transcript | ENST00000490531.3 | protein_coding | 1594 | chr7 | TogoVar | |||||||
NBAS_chr2_15161916_15566334 | 15481512 | C | CTGGCACC others(92): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02055.hp1 HG02723.hp2 others(7): Show |
a0001a0014a0028others(2): Show | a0001c0003a0014c0028a0028c0024others(2): Show | a0001c0003t0001a0014c0028t0001a0028c0024t0001others(2): Show | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0014 others(7): Show |
10 | 204 | 0.0490 | 99 | c.108 others(118): Show |
NBAS | ENSG00000151779.14 | transcript | ENST00000281513.10 | protein_coding | 12/51 | chr2 | TogoVar | |||||||
NCAM2_chr21_20993409_21548329 | 21331558 | A | ATATATAT others(92): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00741.hp2 HG02293.hp2 |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0035a0002c0002t0037 | a0002c0002t0003g0020 a0002c0002t0035g0052 a0002c0002t0037g0063 |
3 | 122 | 0.0246 | 99 | c.738 others(116): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 6/17 | chr21 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667329 | G | GCTCCTTA others(92): Show |
intron_variant | MODIFIER | HG02145.hp1 HG02698.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0360 a0001c0001t0001g0366 |
2 | 123 | 0.0163 | 99 | c.148 others(118): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCOA3_chr20_47496887_47661872 | 47525870 | G | GCGGCTGG others(92): Show |
intron_variant | MODIFIER | HG02818.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0001 | 1 | 13 | 0.0769 | 99 | c.-99 others(118): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
NCOA3_chr20_47496887_47661872 | 47525870 | G | GCGGCTGG others(92): Show |
intron_variant | MODIFIER | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(33): Show |
a0001a0002a0007others(2): Show | a0001c0003a0001c0021a0002c0002others(3): Show | a0001c0003t0005a0001c0003t0011a0001c0003t0012others(8): Show | a0001c0003t0005g0019 a0001c0003t0005g0049 a0001c0003t0005g0050 others(33): Show |
36 | 48 | 0.7500 | 99 | c.-99 others(118): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
NCOA3_chr20_47496887_47661872 | 47525870 | G | GCGGCTGG others(92): Show |
intron_variant | MODIFIER | HG02109.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
a0001a0009 | a0001c0003a0009c0011 | a0001c0003t0016a0009c0011t0016 | a0001c0003t0016g0020 a0001c0003t0016g0067 a0009c0011t0016g0021 others(1): Show |
4 | 16 | 0.2500 | 99 | c.-99 others(118): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
NCOR1_chr17_16024157_16220534 | 16095667 | G | GGGGGTCA others(92): Show |
intron_variant | MODIFIER | HG01168.hp1 HG01169.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0264 a0001c0001t0003g0265 |
2 | 154 | 0.0130 | 99 | c.282 others(118): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 21/45 | chr17 | TogoVar | |||||||
NDUFV3_chr21_42888309_42918299 | 42894351 | A | AATATATA others(92): Show |
intron_variant | MODIFIER | HG01167.hp2 HG01257.hp2 HG01258.hp1 others(15): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0021a0002c0002t0081others(1): Show | a0002c0002t0002g0008 a0002c0002t0002g0010 a0002c0002t0002g0020 others(9): Show |
18 | 294 | 0.0612 | 99 | c.48+ others(112): Show |
NDUFV3 | ENSG00000160194.18 | transcript | ENST00000354250.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NDUFV3_chr21_42888309_42918299 | 42894351 | A | AATATATA others(92): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0168 | 1 | 277 | 0.0036 | 99 | c.48+ others(112): Show |
NDUFV3 | ENSG00000160194.18 | transcript | ENST00000354250.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NF1_chr17_31089977_31382675 | 31335274 | T | TTATATAT others(92): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01943.hp2 HG03831.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0004 | a0001c0001t0001g0049 a0001c0001t0001g0071 a0001c0001t0001g0106 others(1): Show |
4 | 108 | 0.0370 | 99 | c.600 others(116): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 40/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
NF1_chr17_31089977_31382675 | 31335274 | T | TTTTATAT others(92): Show |
intron_variant | MODIFIER | HG01516.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0064 | 1 | 105 | 0.0095 | 99 | c.600 others(116): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 40/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(92): Show |
intron_variant | MODIFIER | HG02976.hp1 HG03942.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0006a0001c0005t0011 | a0001c0001t0006g0105 a0001c0005t0011g0137 |
2 | 82 | 0.0244 | 99 | c.127 others(116): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(92): Show |
intron_variant | MODIFIER | HG03239.hp1 | a0001 | a0001c0053 | a0001c0053t0003 | a0001c0053t0003g0183 | 1 | 81 | 0.0123 | 99 | c.127 others(116): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400832 | A | ACCCCTCC others(92): Show |
intron_variant | MODIFIER | HG00408.hp1 HG01243.hp2 HG01891.hp2 others(11): Show |
a0001a0002a0012 | a0001c0001a0001c0004a0001c0005others(4): Show | a0001c0001t0006a0001c0001t0012a0001c0004t0004others(8): Show | a0001c0001t0006g0005 a0001c0001t0006g0100 a0001c0001t0006g0104 others(11): Show |
14 | 94 | 0.1489 | 99 | c.127 others(116): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NGEF_chr2_232873701_233018256 | 232995016 | T | TATGCACA others(92): Show |
intron_variant | MODIFIER | NA18942.hp2 | a0001 | a0001c0002 | a0001c0002t0012 | a0001c0002t0012g0125 | 1 | 354 | 0.0028 | 99 | c.-75 others(118): Show |
NGEF | ENSG00000066248.15 | transcript | ENST00000264051.8 | protein_coding | 1/14 | chr2 | TogoVar | |||||||
NIBAN2_chr9_127500343_127574073 | 127509772 | C | CCCCTCCT others(92): Show |
intron_variant | MODIFIER | HG01109.hp1 HG03139.hp1 |
a0001a0007 | a0001c0006a0007c0011 | a0001c0006t0007a0007c0011t0007 | a0001c0006t0007g0305 a0007c0011t0007g0197 |
2 | 316 | 0.0063 | 99 | c.116 others(116): Show |
NIBAN2 | ENSG00000136830.12 | transcript | ENST00000373312.4 | protein_coding | 9/13 | chr9 | TogoVar | |||||||
NLGN4X_chrX_5885042_6233867 | 6160960 | A | AATAAAAT others(92): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(23): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(4): Show | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0057 others(23): Show |
26 | 122 | 0.2131 | 99 | c.-30 others(118): Show |
NLGN4X | ENSG00000146938.16 | transcript | ENST00000381095.8 | protein_coding | 1/5 | chrX | TogoVar | |||||||
NLRP13_chr19_55890945_55937336 | 55931710 | A | AAAGAAAG others(92): Show |
intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0099 | 1 | 250 | 0.0040 | 99 | c.319 others(114): Show |
NLRP13 | ENSG00000173572.12 | transcript | ENST00000342929.4 | protein_coding | 1/10 | chr19 | TogoVar | |||||||
NLRP13_chr19_55890945_55937336 | 55931712 | A | AGAAAGAA others(92): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01433.hp1 |
a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0147 a0001c0004t0001g0148 |
2 | 434 | 0.0046 | 99 | c.319 others(114): Show |
NLRP13 | ENSG00000173572.12 | transcript | ENST00000342929.4 | protein_coding | 1/10 | chr19 | TogoVar | |||||||
NLRP4_chr19_55831540_55886855 | 55851526 | T | TGTCCGAG others(92): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0037 | a0001c0037t0005 | a0001c0037t0005g0382 | 1 | 392 | 0.0026 | 99 | c.-65 others(114): Show |
NLRP4 | ENSG00000160505.16 | transcript | ENST00000301295.11 | protein_coding | 1/9 | chr19 | TogoVar | |||||||
NLRP4_chr19_55831540_55886855 | 55851526 | T | TGTCCGTG others(92): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0005 | a0001c0005t0013 | a0001c0005t0013g0220 | 1 | 392 | 0.0026 | 99 | c.-65 others(114): Show |
NLRP4 | ENSG00000160505.16 | transcript | ENST00000301295.11 | protein_coding | 1/9 | chr19 | TogoVar | |||||||
NLRP4_chr19_55831540_55886855 | 55851526 | T | TGTCCGTG others(92): Show |
intron_variant | MODIFIER | HG00099.hp1 HG01516.hp2 HG01517.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0005a0001c0011others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(4): Show | a0001c0001t0001g0082 a0001c0001t0002g0391 a0001c0001t0002g0392 others(5): Show |
8 | 399 | 0.0201 | 99 | c.-65 others(114): Show |
NLRP4 | ENSG00000160505.16 | transcript | ENST00000301295.11 | protein_coding | 1/9 | chr19 | TogoVar | |||||||
NME8_chr7_37843597_37905397 | 37848245 | G | GAAGAAAA others(92): Show |
upstream_gene_variant | MODIFIER | NA18977.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0192 | 1 | 294 | 0.0034 | 99 | c.-72 others(108): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 351 | chr7 | TogoVar | |||||||
NOB1_chr16_69736871_69759926 | 69738410 | C | CTTGCTCT others(92): Show |
downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0005others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(10): Show | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(103): Show |
318 | 448 | 0.7098 | 99 | c.*39 others(110): Show |
NOB1 | ENSG00000141101.13 | transcript | ENST00000268802.10 | protein_coding | 3460 | chr16 | TogoVar | |||||||
NOS3_chr7_150986017_151019588 | 150995819 | G | GTCCCACC others(92): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02615.hp1 HG02723.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0044 a0001c0002t0001g0045 a0001c0002t0001g0046 |
3 | 375 | 0.0080 | 99 | c.270 others(114): Show |
NOS3 | ENSG00000164867.11 | transcript | ENST00000297494.8 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
NOTCH1_chr9_136489433_136551048 | 136535783 | A | AGGGGAGC others(92): Show |
intron_variant | MODIFIER | HG02602.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
a0001a0009 | a0001c0003a0001c0014a0009c0022 | a0001c0003t0008a0001c0014t0002a0009c0022t0008 | a0001c0003t0008g0010 a0001c0014t0002g0096 a0009c0022t0008g0024 others(1): Show |
4 | 240 | 0.0167 | 99 | c.140 others(116): Show |
NOTCH1 | ENSG00000148400.13 | transcript | ENST00000651671.1 | protein_coding | 2/33 | chr9 | TogoVar | |||||||
NOTCH1_chr9_136489433_136551048 | 136535783 | A | AGGGGAGC others(92): Show |
intron_variant | MODIFIER | HG01952.hp1 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0160 | 1 | 237 | 0.0042 | 99 | c.140 others(116): Show |
NOTCH1 | ENSG00000148400.13 | transcript | ENST00000651671.1 | protein_coding | 2/33 | chr9 | TogoVar | |||||||
NOX1_chrX_100838324_100879359 | 100853333 | T | TTTCTTTC others(92): Show |
intron_variant | MODIFIER | HG01168.hp1 HG01169.hp2 HG03017.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 a0001c0001t0001g0149 |
3 | 292 | 0.0103 | 99 | c.805 others(116): Show |
NOX1 | ENSG00000007952.18 | transcript | ENST00000372966.8 | protein_coding | 7/12 | chrX | TogoVar | |||||||
NPBWR2_chr20_64098802_64112565 | 64105553 | G | GGGTGGGG others(92): Show |
3_prime_UTR_variant | MODIFIER | HG01258.hp2 | a0001 | a0001c0001 | a0001c0001t0077 | a0001c0001t0077g0086 | 1 | 350 | 0.0029 | 99 | c.*27 others(108): Show |
NPBWR2 | ENSG00000125522.4 | transcript | ENST00000684052.1 | protein_coding | 2/2 | 276 | chr20 | TogoVar | ||||||
NRCAM_chr7_108142649_108461436 | 108299114 | A | AAAAAAAA others(92): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0002 | a0002c0013 | a0002c0013t0006 | a0002c0013t0006g0151 | 1 | 35 | 0.0286 | 99 | c.-10 others(120): Show |
NRCAM | ENSG00000091129.22 | transcript | ENST00000379028.8 | protein_coding | 3/32 | chr7 | TogoVar | |||||||
NRG3_chr10_81870194_82992178 | 82046482 | G | GTTTTCTA others(92): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02280.hp1 HG02818.hp2 others(4): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(2): Show | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0005g0044 others(4): Show |
7 | 66 | 0.1061 | 99 | c.823 others(120): Show |
NRG3 | ENSG00000185737.13 | transcript | ENST00000372141.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
NTN5_chr19_48656407_48678017 | 48669498 | C | CCACCACC others(92): Show |
intron_variant | MODIFIER | HG00544.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 | 1 | 311 | 0.0032 | 99 | c.631 others(114): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | TogoVar | |||||||
NTRK2_chr9_84664729_85032054 | 85004039 | A | AAGAAAGA others(92): Show |
intron_variant | MODIFIER | HG01106.hp2 HG01975.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0048 a0001c0002t0001g0037 |
2 | 49 | 0.0408 | 99 | c.217 others(120): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
NTRK2_chr9_84664729_85032054 | 85004039 | A | AAGAAAGA others(92): Show |
intron_variant | MODIFIER | HG02293.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0087 | 1 | 48 | 0.0208 | 99 | c.217 others(120): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
NTRK2_chr9_84664729_85032054 | 85004039 | A | AAGAAAGA others(92): Show |
intron_variant | MODIFIER | HG02717.hp2 HG03225.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016 a0001c0001t0001g0131 |
2 | 49 | 0.0408 | 99 | c.217 others(120): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
NTRK2_chr9_84664729_85032054 | 85004039 | A | AAGAAAGA others(92): Show |
intron_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0081 | 1 | 48 | 0.0208 | 99 | c.217 others(120): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
NTRK2_chr9_84664729_85032054 | 85004039 | A | AAGAAAGA others(92): Show |
intron_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0125 | 1 | 48 | 0.0208 | 99 | c.217 others(120): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
NTRK2_chr9_84664729_85032054 | 85004039 | A | AAGAAAGA others(92): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0001 | a0001c0001t0038 | a0001c0001t0038g0158 | 1 | 48 | 0.0208 | 99 | c.217 others(120): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
NUP93_chr16_56725129_56855286 | 56739951 | C | CATCCCCA others(92): Show |
intron_variant | MODIFIER | HG02738.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0194 | 1 | 374 | 0.0027 | 99 | c.-14 others(116): Show |
NUP93 | ENSG00000102900.13 | transcript | ENST00000308159.10 | protein_coding | 1/21 | chr16 | TogoVar | |||||||
OBI1_chr13_78609289_78664155 | 78659312 | A | AAAAAAAA others(92): Show |
upstream_gene_variant | MODIFIER | HG02080.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061 | 1 | 33 | 0.0303 | 99 | c.-19 others(108): Show |
OBI1 | ENSG00000152193.8 | transcript | ENST00000282003.7 | protein_coding | 158 | chr13 | TogoVar | |||||||
OCLN_chr5_69487790_69563104 | 69515528 | C | CGGGGGGC others(92): Show |
intron_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0007 | 1 | 284 | 0.0035 | 99 | c.891 others(116): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
OCLN_chr5_69487790_69563104 | 69515539 | C | CCCCCCCC others(92): Show |
intron_variant | MODIFIER | HG01070.hp2 HG01071.hp2 HG01934.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0012 a0001c0001t0001g0157 a0001c0001t0001g0168 others(4): Show |
8 | 34 | 0.2353 | 99 | c.891 others(116): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
OCLN_chr5_69487790_69563104 | 69515539 | C | CCCCCCCC others(92): Show |
intron_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0230 | 1 | 27 | 0.0370 | 99 | c.891 others(116): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
OCLN_chr5_69487790_69563104 | 69515539 | C | CCCCCCCC others(92): Show |
intron_variant | MODIFIER | HG02074.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0032 | 1 | 27 | 0.0370 | 99 | c.891 others(116): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
OCLN_chr5_69487790_69563104 | 69515539 | C | CCCCCCCC others(92): Show |
intron_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0243 | 1 | 27 | 0.0370 | 99 | c.891 others(116): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
OCLN_chr5_69487790_69563104 | 69515539 | C | CCCCCCCC others(92): Show |
intron_variant | MODIFIER | HG01175.hp2 | a0001 | a0001c0002 | a0001c0002t0031 | a0001c0002t0031g0174 | 1 | 27 | 0.0370 | 99 | c.891 others(116): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
OCLN_chr5_69487790_69563104 | 69515539 | C | CCCCCCCC others(92): Show |
intron_variant | MODIFIER | HG01175.hp1 HG01891.hp2 HG02280.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(2): Show | a0001c0001t0001g0147 a0001c0001t0010g0148 a0001c0001t0011g0177 others(4): Show |
7 | 33 | 0.2121 | 99 | c.891 others(116): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
OCLN_chr5_69487790_69563104 | 69515539 | C | CCCCCCCC others(92): Show |
intron_variant | MODIFIER | HG00438.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0231 a0001c0001t0002g0004 a0001c0001t0002g0064 others(7): Show |
11 | 37 | 0.2973 | 99 | c.891 others(116): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
OCLN_chr5_69487790_69563104 | 69515539 | C | CCCCCCCC others(92): Show |
intron_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0001 | 1 | 27 | 0.0370 | 99 | c.891 others(116): Show |
OCLN | ENSG00000197822.12 | transcript | ENST00000396442.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |