regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
STK3_chr8_98449633_98830688 | 98751549 | GGAGGTGA others(4381): Show |
G | intron_variant | MODIFIER | HG02080.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0021 | 1 | 170 | 0.0059 | -4388 | c.237 others(17): Show |
STK3 | ENSG00000104375.17 | transcript | ENST00000419617.7 | protein_coding | 3/10 | chr8 | TogoVar | ||||||
PCBP3_chr21_45638725_45947450 | 45652689 | CGCCTCGG others(4371): Show |
C | intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0108 | 1 | 292 | 0.0034 | -4378 | c.-27 others(20): Show |
PCBP3 | ENSG00000183570.17 | transcript | ENST00000681687.1 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
ANKRD36_chr2_97108153_97269521 | 97152093 | AGTGATTC others(4367): Show |
A | exon_loss_variant | HIGH | HG01070.hp2 HG01361.hp2 HG03654.hp1 others(1): Show |
a0017a0027 | a0017c0017a0027c0028 | a0017c0017t0001a0027c0028t0001 | a0017c0017t0001g0145a0017c0017t0001g0169a0017c0017t0001g0170others(1): Show | 4 | 212 | 0.0189 | -4374 | c.116 others(18): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/76 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NBPF10_chr1_146059711_146149804 | 146095500 | GGTTGAAA others(4365): Show |
G | exon_loss_variant | HIGH | HG00597.hp1 | a0100 | a0100c0112 | a0100c0112t0002 | a0100c0112t0002g0109 | 1 | 283 | 0.0035 | -4372 | c.596 others(17): Show |
NBPF10 | ENSG00000271425.9 | transcript | ENST00000583866.9 | protein_coding | 53/90 | chr1 | TogoVar | ||||||
RIPOR3_chr20_50581108_50696542 | 50663978 | GTGCAATG others(4364): Show |
G | intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0122 | 1 | 280 | 0.0036 | -4371 | c.3+2 others(15): Show |
RIPOR3 | ENSG00000042062.13 | transcript | ENST00000327979.8 | protein_coding | 1/21 | chr20 | TogoVar | ||||||
NBPF10_chr1_146059711_146149804 | 146104940 | GGTTGAAA others(4361): Show |
G | exon_loss_variant | HIGH | HG01934.hp1 | a0211 | a0211c0088 | a0211c0088t0002 | a0211c0088t0002g0089 | 1 | 283 | 0.0035 | -4368 | c.450 others(17): Show |
NBPF10 | ENSG00000271425.9 | transcript | ENST00000583866.9 | protein_coding | 41/90 | chr1 | TogoVar | ||||||
NBPF10_chr1_146059711_146149804 | 146104940 | GGTTGAAA others(4357): Show |
G | exon_loss_variant | HIGH | HG02293.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
a0012a0111 | a0012c0008a0111c0123 | a0012c0008t0002a0111c0123t0002 | a0012c0008t0002g0003a0012c0008t0002g0105a0111c0123t0002g0137 | 4 | 283 | 0.0141 | -4364 | c.450 others(17): Show |
NBPF10 | ENSG00000271425.9 | transcript | ENST00000583866.9 | protein_coding | 41/90 | chr1 | TogoVar | ||||||
LRRC31_chr3_169834172_169874935 | 169869027 | TGCTCTTT others(4356): Show |
T | exon_loss_variant others(1): Show |
HIGH | HG02602.hp1 HG02738.hp2 HG03927.hp2 |
a0006a0007 | a0006c0010a0007c0017 | a0006c0010t0003a0007c0017t0003 | a0006c0010t0003g0026a0006c0010t0003g0028a0007c0017t0003g0027 | 3 | 322 | 0.0093 | -4363 | c.-35 others(13): Show |
LRRC31 | ENSG00000114248.10 | transcript | ENST00000316428.10 | protein_coding | 1/9 | chr3 | TogoVar | ||||||
RHNO1_chr12_2872223_2894524 | 2878302 | GATCTGAT others(4349): Show |
G | intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0303 | 1 | 426 | 0.0024 | -4356 | c.-85 others(17): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM11_chr17_21192954_21219161 | 21203874 | ATCACCAG others(4344): Show |
A | intron_variant | MODIFIER | HG00099.hp2 HG00735.hp1 HG01069.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015 | 5 | 422 | 0.0119 | -4351 | c.62+ others(15): Show |
TMEM11 | ENSG00000178307.10 | transcript | ENST00000317635.6 | protein_coding | 1/1 | chr17 | TogoVar | ||||||
NSD3_chr8_38264704_38387271 | 38365706 | CAAGTGCT others(4341): Show |
C | intron_variant | MODIFIER | NA18965.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0067 | 1 | 226 | 0.0044 | -4348 | c.-45 others(19): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | TogoVar | ||||||
STK17A_chr7_43578108_43632379 | 43585274 | ATTACAAA others(4340): Show |
A | intron_variant | MODIFIER | HG01257.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0221 | 1 | 392 | 0.0026 | -4347 | c.206 others(17): Show |
STK17A | ENSG00000164543.7 | transcript | ENST00000319357.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
MREG_chr2_215937584_216018551 | 215970483 | GAGCCATC others(4339): Show |
G | intron_variant | MODIFIER | NA19065.hp1 | a0001 | a0001c0001 | a0001c0001t0027 | a0001c0001t0027g0391 | 1 | 416 | 0.0024 | -4346 | c.255 others(19): Show |
MREG | ENSG00000118242.17 | transcript | ENST00000263268.11 | protein_coding | 2/4 | chr2 | TogoVar | ||||||
SLC35G4_chr18_11604596_11615612 | 11611275 | GCAAGTAA others(4330): Show |
G | downstream_gene_variant | MODIFIER | HG04115.hp2 | a0001 | a0001c0001 | a0001c0001t0000 | a0001c0001t0000g0000 | 1 | 444 | 0.0023 | -4337 | c.*66 others(10): Show |
SLC35G4 | ENSG00000236396.8 | transcript | ENST00000588001.2 | protein_coding | 664 | chr18 | TogoVar | ||||||
ADPRHL1_chr13_113394611_113458488 | 113395851 | TCCAGGCT others(4328): Show |
T | splice_region_variant | LOW | HG02135.hp2 | a0045 | a0045c0060 | a0045c0060t0112 | a0045c0060t0112g0179 | 1 | 262 | 0.0038 | -4335 | c.*31 others(11): Show |
ADPRHL1 | ENSG00000153531.15 | transcript | ENST00000612156.3 | protein_coding | 8/8 | chr13 | TogoVar | ||||||
SAYSD1_chr6_39099063_39120186 | 39100787 | ACCATAGC others(4328): Show |
A | splice_region_variant | LOW | HG00639.hp2 HG02615.hp2 NA21309.hp1 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0017a0003c0003t0011 | a0001c0001t0017g0155a0003c0003t0011g0035 | 3 | 460 | 0.0065 | -4335 | c.*31 others(10): Show |
SAYSD1 | ENSG00000112167.11 | transcript | ENST00000229903.5 | protein_coding | 2/2 | chr6 | TogoVar | ||||||
SCN8A_chr12_51586233_51817864 | 51707763 | CCAAACTC others(4320): Show |
C | intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0161 | 1 | 202 | 0.0050 | -4327 | c.163 others(19): Show |
SCN8A | ENSG00000196876.19 | transcript | ENST00000354534.11 | protein_coding | 11/26 | chr12 | TogoVar | ||||||
TENT2_chr5_79607441_79693246 | 79629603 | GGATCACG others(4319): Show |
G | intron_variant | MODIFIER | NA19085.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0286 | 1 | 344 | 0.0029 | -4326 | c.465 others(17): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
DHRSX_chrX_2214506_2505976 | 2277392 | AGAGGGAG others(4317): Show |
A | intron_variant | MODIFIER | HG02486.hp2 | a0002 | a0002c0005 | a0002c0005t0004 | a0002c0005t0004g0004 | 1 | 50 | 0.0200 | -4324 | c.388 others(18): Show |
DHRSX | ENSG00000169084.15 | transcript | ENST00000334651.11 | protein_coding | 4/6 | chrX | TogoVar | ||||||
DHRSX_chrX_2214506_2505976 | 2277972 | AAGAGAGA others(4317): Show |
A | intron_variant | MODIFIER | HG03130.hp1 NA19066.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | 50 | 0.0400 | -4324 | c.388 others(18): Show |
DHRSX | ENSG00000169084.15 | transcript | ENST00000334651.11 | protein_coding | 4/6 | chrX | TogoVar | ||||||
HMGCLL1_chr6_55429373_55584192 | 55548779 | AGAGAATA others(4305): Show |
A | intron_variant | MODIFIER | HG01358.hp1 HG02559.hp2 HG02622.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0144a0001c0001t0001g0209a0001c0001t0006g0152 | 3 | 334 | 0.0090 | -4312 | c.109 others(18): Show |
HMGCLL1 | ENSG00000146151.14 | transcript | ENST00000274901.9 | protein_coding | 1/8 | chr6 | TogoVar | ||||||
RAVER2_chr1_64740075_64838232 | 64749458 | GCCTCGGC others(4304): Show |
G | intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0322 | 1 | 364 | 0.0028 | -4311 | c.249 others(17): Show |
RAVER2 | ENSG00000162437.15 | transcript | ENST00000294428.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CDC42BPA_chr1_226984865_227323492 | 227257297 | TGCCACTG others(4302): Show |
T | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp2 HG02109.hp1 others(10): Show |
a0001a0008a0011 | a0001c0006a0008c0014a0011c0028 | a0001c0006t0012a0001c0006t0027a0008c0014t0012others(2): Show | a0001c0006t0012g0323a0001c0006t0012g0325a0001c0006t0012g0326others(10): Show | 13 | 352 | 0.0369 | -4309 | c.179 others(17): Show |
CDC42BPA | ENSG00000143776.20 | transcript | ENST00000366766.8 | protein_coding | 1/36 | chr1 | TogoVar | ||||||
NUBPL_chr14_31556404_31866224 | 31793809 | TTTGTGCC others(4302): Show |
T | intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(4): Show |
a0001 | a0001c0002a0001c0003a0001c0005 | a0001c0002t0002a0001c0003t0021a0001c0003t0027others(1): Show | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0004others(4): Show | 7 | 268 | 0.0261 | -4309 | c.607 others(18): Show |
NUBPL | ENSG00000151413.17 | transcript | ENST00000281081.12 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
DLGAP2_chr8_732628_1713476 | 1393895 | GTCCTCCT others(4294): Show |
G | intron_variant | MODIFIER | HG00639.hp1 HG01361.hp1 |
a0001a0002 | a0001c0002a0002c0001 | a0001c0002t0001a0002c0001t0001 | a0001c0002t0001g0019a0002c0001t0001g0018 | 2 | 40 | 0.0500 | -4301 | c.107 others(21): Show |
DLGAP2 | ENSG00000198010.13 | transcript | ENST00000637795.2 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ZNF586_chr19_57764676_57785616 | 57774856 | ACTACCTC others(4286): Show |
A | exon_loss_variant | HIGH | HG00639.hp2 | a0003 | a0003c0004 | a0003c0004t0014 | a0003c0004t0014g0181 | 1 | 410 | 0.0024 | -4293 | c.37- others(11): Show |
ZNF586 | ENSG00000083828.16 | transcript | ENST00000396154.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
NCOA7_chr6_125785960_125937034 | 125861898 | GTGGTGGC others(4285): Show |
G | intron_variant | MODIFIER | HG00280.hp2 HG01106.hp2 HG01175.hp1 others(59): Show |
a0002a0003a0006others(2): Show | a0002c0002a0002c0004a0003c0003others(3): Show | a0002c0002t0001a0002c0002t0002a0002c0002t0004others(11): Show | a0002c0002t0001g0059a0002c0002t0001g0131a0002c0002t0001g0135others(59): Show | 62 | 270 | 0.2296 | -4292 | c.271 others(17): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
GALNTL6_chr4_171808404_173046559 | 172067488 | ATCTACTT others(4284): Show |
A | intron_variant | MODIFIER | HG02015.hp1 HG02015.hp2 HG02145.hp1 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(5): Show | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(16): Show | 19 | 40 | 0.4750 | -4291 | c.139 others(21): Show |
GALNTL6 | ENSG00000174473.17 | transcript | ENST00000506823.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PDS5B_chr13_32581452_32783019 | 32633394 | TCTGTCTT others(4284): Show |
T | intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0316 | 1 | 334 | 0.0030 | -4291 | c.-19 others(19): Show |
PDS5B | ENSG00000083642.19 | transcript | ENST00000315596.15 | protein_coding | 1/34 | chr13 | TogoVar | ||||||
TEPSIN_chr17_81223277_81244055 | 81238942 | GAGGAGCC others(4283): Show |
G | exon_loss_variant others(1): Show |
HIGH | NA18994.hp2 | a0018 | a0018c0030 | a0018c0030t0013 | a0018c0030t0013g0040 | 1 | 366 | 0.0027 | -4290 | c.-41 others(11): Show |
TEPSIN | ENSG00000167302.11 | transcript | ENST00000637944.2 | protein_coding | 1/13 | chr17 | TogoVar | ||||||
EDDM13_chr19_56267748_56315454 | 56290059 | GTGGTTTC others(4278): Show |
G | exon_loss_variant others(4): Show |
HIGH | NA19004.hp2 | a0005 | a0005c0006 | a0005c0006t0001 | a0005c0006t0001g0097 | 1 | 396 | 0.0025 | -4285 | c.227 others(16): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
RAI14_chr5_34651328_34837612 | 34700132 | ACATTTTT others(4278): Show |
A | intron_variant | MODIFIER | HG03927.hp1 | a0002 | a0002c0008 | a0002c0008t0005 | a0002c0008t0005g0032 | 1 | 254 | 0.0039 | -4285 | c.36+ others(17): Show |
RAI14 | ENSG00000039560.14 | transcript | ENST00000265109.8 | protein_coding | 2/17 | chr5 | TogoVar | ||||||
PHC2_chr1_33318626_33436095 | 33406643 | TAGTCCAT others(4273): Show |
T | intron_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0098 | 1 | 370 | 0.0027 | -4280 | c.-55 others(19): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | TogoVar | ||||||
GNAL_chr18_11684264_11890685 | 11825628 | GGCTGAGG others(4272): Show |
G | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 |
a0001 | a0001c0001 | a0001c0001t0032 | a0001c0001t0032g0033a0001c0001t0032g0034 | 2 | 248 | 0.0081 | -4279 | c.722 others(16): Show |
GNAL | ENSG00000141404.17 | transcript | ENST00000334049.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
GNAL_chr18_11747085_11890685 | 11825628 | GGCTGAGG others(4272): Show |
G | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 |
a0001 | a0001c0001 | a0001c0001t0036 | a0001c0001t0036g0184a0001c0001t0036g0185 | 2 | 284 | 0.0070 | -4279 | c.491 others(16): Show |
GNAL | ENSG00000141404.17 | transcript | ENST00000423027.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ASMT_chrX_1610059_1648081 | 1636913 | CTGTGTGT others(4270): Show |
C | intron_variant | MODIFIER | HG01081.hp1 HG03927.hp1 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0078a0002c0002t0001g0088 | 2 | 223 | 0.0090 | -4277 | c.910 others(16): Show |
ASMT | ENSG00000196433.13 | transcript | ENST00000381241.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ADGRB3_chr6_68630282_69394506 | 69304218 | ATTGCAGG others(4269): Show |
A | intron_variant | MODIFIER | HG02970.hp2 NA18906.hp1 |
a0001a0002 | a0001c0002a0002c0005 | a0001c0002t0001a0002c0005t0001 | a0001c0002t0001g0024a0002c0005t0001g0005 | 2 | 120 | 0.0167 | -4276 | c.281 others(21): Show |
ADGRB3 | ENSG00000135298.15 | transcript | ENST00000370598.6 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
SCN8A_chr12_51586233_51817864 | 51663297 | AGACTTCT others(4268): Show |
A | intron_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0001 | a0001c0001t0028 | a0001c0001t0028g0006 | 1 | 202 | 0.0050 | -4275 | c.276 others(16): Show |
SCN8A | ENSG00000196876.19 | transcript | ENST00000354534.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TCP10L_chr21_32568721_32590523 | 32571358 | TTTTCAGT others(4262): Show |
T | splice_region_variant | LOW | HG03927.hp1 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0035 | 2 | 396 | 0.0051 | -4269 | c.*11 others(11): Show |
TCP10L | ENSG00000242220.9 | transcript | ENST00000300258.8 | protein_coding | 5/5 | chr21 | TogoVar | ||||||
IQGAP2_chr5_76398285_76713132 | 76416471 | ATCTGAGG others(4258): Show |
A | intron_variant | MODIFIER | HG02056.hp1 | a0027 | a0027c0035 | a0027c0035t0002 | a0027c0035t0002g0186 | 1 | 222 | 0.0045 | -4265 | c.46+ others(17): Show |
IQGAP2 | ENSG00000145703.17 | transcript | ENST00000274364.11 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CLEC17A_chr19_14578084_14617035 | 14585489 | TGACTCAG others(4256): Show |
T | exon_loss_variant others(4): Show |
HIGH | NA19063.hp1 | a0005 | a0005c0008 | a0005c0008t0003 | a0005c0008t0003g0123 | 1 | 364 | 0.0028 | -4263 | c.122 others(17): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
CLEC17A_chr19_14578084_14617035 | 14585083 | TCCTTTCA others(4254): Show |
T | exon_loss_variant others(4): Show |
HIGH | HG02109.hp2 | a0009 | a0009c0004 | a0009c0004t0002 | a0009c0004t0002g0084 | 1 | 364 | 0.0028 | -4261 | c.121 others(17): Show |
CLEC17A | ENSG00000187912.12 | transcript | ENST00000417570.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
GOLGA6L22_chr15_22453903_22474226 | 22463592 | GGTGAGCT others(4254): Show |
G | exon_loss_variant | HIGH | HG03669.hp2 | a0000 | a0000c0029 | a0000c0029t0013 | a0000c0029t0013g0021 | 1 | 226 | 0.0044 | -4261 | c.562 others(12): Show |
GOLGA6L22 | ENSG00000277865.6 | transcript | ENST00000622895.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
TTN_chr2_178520989_178812423 | 178656457 | TACTACCA others(4254): Show |
T | exon_loss_variant | HIGH | HG02922.hp2 | a0157 | a0157c0107 | a0157c0107t0001 | a0157c0107t0001g0145 | 1 | 242 | 0.0041 | -4261 | c.372 others(21): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/363 | chr2 | TogoVar | ||||||
VRK2_chr2_58041806_58164871 | 58091566 | AAAATGTA others(4254): Show |
A | intron_variant | MODIFIER | HG02698.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0276 | 1 | 340 | 0.0029 | -4261 | c.543 others(17): Show |
VRK2 | ENSG00000028116.18 | transcript | ENST00000340157.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TTN_chr2_178520989_178812423 | 178655278 | ATATCTCA others(4253): Show |
A | exon_loss_variant | HIGH | HG01099.hp1 HG01978.hp2 HG02300.hp2 others(4): Show |
a0085a0100a0102others(4): Show | a0085c0049a0100c0133a0102c0130others(4): Show | a0085c0049t0001a0100c0133t0002a0102c0130t0002others(4): Show | a0085c0049t0001g0131a0100c0133t0002g0233a0102c0130t0002g0103others(4): Show | 7 | 242 | 0.0289 | -4260 | c.372 others(19): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000589042.5 | protein_coding | 189/363 | chr2 | TogoVar | ||||||
GRIN2B_chr12_13532337_13986602 | 13923741 | AGCTCCTT others(4244): Show |
A | intron_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0066 | 1 | 194 | 0.0052 | -4251 | c.-19 others(19): Show |
GRIN2B | ENSG00000273079.7 | transcript | ENST00000609686.4 | protein_coding | 2/13 | chr12 | TogoVar | ||||||
ADARB2_chr10_1172313_1742525 | 1235685 | CCCCTCTG others(4240): Show |
C | intron_variant | MODIFIER | NA21309.hp1 | a0007 | a0007c0011 | a0007c0011t0034 | a0007c0011t0034g0076 | 1 | 106 | 0.0094 | -4247 | c.136 others(19): Show |
ADARB2 | ENSG00000185736.16 | transcript | ENST00000381312.6 | protein_coding | 5/9 | chr10 | TogoVar | ||||||
ZNF677_chr19_53230381_53259873 | 53231017 | CAGAAAAC others(4240): Show |
C | downstream_gene_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0069 | 1 | 406 | 0.0025 | -4247 | c.*17 others(11): Show |
ZNF677 | ENSG00000197928.11 | transcript | ENST00000598513.6 | protein_coding | 4363 | chr19 | TogoVar | ||||||
ALMS1_chr2_73380836_73614916 | 73481578 | ATGAACTT others(4239): Show |
A | intron_variant | MODIFIER | HG03579.hp2 | a0002 | a0002c0004 | a0002c0004t0001 | a0002c0004t0001g0031 | 1 | 248 | 0.0040 | -4246 | c.767 others(19): Show |
ALMS1 | ENSG00000116127.20 | transcript | ENST00000613296.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |