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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NAV3_chr12_77825894_78218010 | 78091795 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG00621.hp1 HG03831.hp2 NA18974.hp1 others(2): Show |
a0001a0006 | a0001c0019a0001c0044a0001c0050others(2): Show | a0001c0019t0067a0001c0044t0003a0001c0050t0001others(2): Show | a0001c0019t0067g0180 a0001c0044t0003g0136 a0001c0050t0001g0124 others(2): Show |
5 | 186 | 0.0269 | 17 | c.263 others(38): Show |
NAV3 | ENSG00000067798.16 | transcript | ENST00000397909.7 | protein_coding | 12/39 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NBEAL1_chr2_203009875_203230194 | 203119424 | C | CTTTTTTT others(10): Show |
intron_variant | MODIFIER | HG02109.hp2 | a0012 | a0012c0027 | a0012c0027t0007 | a0012c0027t0007g0053 | 1 | 292 | 0.0034 | 17 | c.259 others(36): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NBEAL1_chr2_203009875_203230194 | 203141363 | A | ATTTTTTT others(10): Show |
intron_variant | MODIFIER | HG02132.hp2 NA18991.hp2 NA19078.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0018 | a0001c0001t0002g0103 a0001c0001t0002g0149 a0001c0001t0018g0144 |
3 | 292 | 0.0103 | 17 | c.484 others(36): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NBEAL1_chr2_203009875_203230194 | 203141366 | A | ATTATTAT others(10): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0048 | 1 | 292 | 0.0034 | 17 | c.484 others(36): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NBEAL1_chr2_203009875_203230194 | 203141366 | A | ATTATTTT others(10): Show |
intron_variant | MODIFIER | HG00323.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0105 | 1 | 292 | 0.0034 | 17 | c.484 others(36): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NBEAL1_chr2_203009875_203230194 | 203141366 | A | ATTTTTTT others(10): Show |
intron_variant | MODIFIER | HG00438.hp2 HG04115.hp1 NA18940.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006 | a0001c0001t0002g0098 a0001c0001t0002g0162 a0001c0001t0006g0254 |
3 | 292 | 0.0103 | 17 | c.484 others(36): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NBEAL1_chr2_203009875_203230194 | 203141367 | T | TTATTATT others(10): Show |
intron_variant | MODIFIER | NA18977.hp2 | a0004 | a0004c0005 | a0004c0005t0009 | a0004c0005t0009g0176 | 1 | 292 | 0.0034 | 17 | c.484 others(36): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NBEAL1_chr2_203009875_203230194 | 203180933 | A | ATTTTTTT others(10): Show |
intron_variant | MODIFIER | HG00438.hp1 HG01099.hp1 HG01516.hp2 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0005a0001c0001t0019a0001c0004t0005 | a0001c0001t0005g0283 a0001c0001t0019g0280 a0001c0004t0005g0274 others(3): Show |
6 | 292 | 0.0206 | 17 | c.659 others(34): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NBEA_chr13_34937270_35677736 | 35539915 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | NA18979.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0036 | 1 | 122 | 0.0082 | 17 | c.658 others(38): Show |
NBEA | ENSG00000172915.20 | transcript | ENST00000379939.7 | protein_coding | 41/58 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
NBEA_chr13_34937270_35677736 | 35585131 | T | TAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
a0001a0003a0009 | a0001c0001a0003c0007a0009c0018 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(2): Show | a0001c0001t0001g0065 a0001c0001t0001g0095 a0001c0001t0001g0098 others(5): Show |
8 | 122 | 0.0656 | 17 | c.717 others(36): Show |
NBEA | ENSG00000172915.20 | transcript | ENST00000379939.7 | protein_coding | 46/58 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
NBEA_chr13_34937270_35677736 | 35631638 | T | TAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0029 | 1 | 122 | 0.0082 | 17 | c.761 others(36): Show |
NBEA | ENSG00000172915.20 | transcript | ENST00000379939.7 | protein_coding | 49/58 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
NBL1_chr1_19639311_19663452 | 19645002 | G | GCCTCTGG others(10): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0007 | a0007c0004 | a0007c0004t0009 | a0007c0004t0009g0122 | 1 | 412 | 0.0024 | 17 | c.-20 others(32): Show |
NBL1 | ENSG00000158747.15 | transcript | ENST00000375136.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBL1_chr1_19639311_19663452 | 19659561 | C | CAAAAAAA others(10): Show |
downstream_gene_variant | MODIFIER | HG03139.hp1 HG03471.hp1 |
a0001 | a0001c0001 | a0001c0001t0020 | a0001c0001t0020g0099 a0001c0001t0020g0228 |
2 | 412 | 0.0049 | 17 | c.*24 others(28): Show |
NBL1 | ENSG00000158747.15 | transcript | ENST00000375136.8 | protein_coding | 1110 | chr1 | TogoVar | |||||||
NBPF11_chr1_148097151_148157281 | 148126789 | A | AGAGAGAA others(10): Show |
intron_variant | MODIFIER | NA20752.hp1 | a0038 | a0038c0049 | a0038c0049t0033 | a0038c0049t0033g0054 | 1 | 388 | 0.0026 | 17 | c.175 others(30): Show |
NBPF11 | ENSG00000263956.8 | transcript | ENST00000682118.1 | protein_coding | 5/23 | chr1 | TogoVar | |||||||
NBPF11_chr1_148097151_148157281 | 148132723 | C | CTTTTTTT others(10): Show |
intron_variant | MODIFIER | NA18959.hp2 | a0013 | a0013c0011 | a0013c0011t0001 | a0013c0011t0001g0061 | 1 | 388 | 0.0026 | 17 | c.-36 others(34): Show |
NBPF11 | ENSG00000263956.8 | transcript | ENST00000682118.1 | protein_coding | 4/23 | chr1 | TogoVar | |||||||
NBPF12_chr1_146933324_147001198 | 146981282 | A | ATATATAT others(10): Show |
intron_variant | MODIFIER | HG02896.hp1 NA19070.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0008 | a0001c0001t0002g0110 a0001c0001t0008g0113 |
2 | 122 | 0.0164 | 17 | c.245 others(36): Show |
NBPF12 | ENSG00000268043.9 | transcript | ENST00000698835.1 | protein_coding | 22/36 | chr1 | TogoVar | |||||||
NCALD_chr8_101681542_101795969 | 101715003 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG02074.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(1): Show | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0150 others(8): Show |
11 | 300 | 0.0367 | 17 | c.378 others(34): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | TogoVar | |||||||
NCALD_chr8_101681542_101795969 | 101782111 | T | TATATATT others(10): Show |
intron_variant | MODIFIER | HG01346.hp1 HG01433.hp1 HG02083.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0234 a0001c0001t0001g0280 a0001c0001t0001g0289 others(6): Show |
9 | 300 | 0.0300 | 17 | c.-20 others(34): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 1/3 | chr8 | TogoVar | |||||||
NCAM1_chr11_112956420_113283436 | 113199829 | T | TGAAAAAA others(10): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0005 | a0001c0005t0029 | a0001c0005t0029g0202 | 1 | 242 | 0.0041 | 17 | c.53- others(32): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | chr11 | TogoVar | |||||||
NCAM2_chr21_20993409_21548329 | 21009918 | T | TGTGTGTG others(10): Show |
intron_variant | MODIFIER | NA19090.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0019 | 1 | 132 | 0.0076 | 17 | c.55+ others(34): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | chr21 | TogoVar | |||||||
NCAM2_chr21_20993409_21548329 | 21106314 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02258.hp2 HG02630.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0003a0001c0004t0002a0001c0004t0018 | a0001c0001t0003g0117 a0001c0004t0002g0003 a0001c0004t0018g0124 |
3 | 132 | 0.0227 | 17 | c.55+ others(36): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21394469 | C | CTTTTTTT others(10): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0004 | a0001c0004t0036 | a0001c0004t0036g0071 | 1 | 132 | 0.0076 | 17 | c.119 others(38): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21479583 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG00280.hp1 | a0002 | a0002c0002 | a0002c0002t0037 | a0002c0002t0037g0063 | 1 | 132 | 0.0076 | 17 | c.207 others(36): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21480366 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0002 | a0002c0003 | a0002c0003t0017 | a0002c0003t0017g0038 | 1 | 132 | 0.0076 | 17 | c.207 others(36): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21486303 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG00639.hp1 | a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0062 | 1 | 132 | 0.0076 | 17 | c.207 others(36): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAPD2_chr12_6489102_6536955 | 6513715 | C | CTTTTTTT others(10): Show |
intron_variant | MODIFIER | HG01099.hp2 HG01192.hp2 HG01255.hp2 others(4): Show |
a0001a0014a0015 | a0001c0001a0001c0007a0014c0028others(1): Show | a0001c0001t0002a0001c0007t0005a0014c0028t0005others(1): Show | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0007t0005g0275 others(4): Show |
7 | 432 | 0.0162 | 17 | c.588 others(32): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTGT others(10): Show |
intron_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0375 | 1 | 432 | 0.0023 | 17 | c.158 others(34): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTTT others(10): Show |
intron_variant | MODIFIER | HG03490.hp2 HG03669.hp2 HG03710.hp2 |
a0001 | a0001c0001a0001c0027 | a0001c0001t0006a0001c0027t0006 | a0001c0001t0006g0264 a0001c0001t0006g0266 a0001c0027t0006g0268 |
3 | 432 | 0.0069 | 17 | c.158 others(34): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTTT others(10): Show |
intron_variant | MODIFIER | HG02818.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0262 | 1 | 432 | 0.0023 | 17 | c.158 others(34): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTTT others(10): Show |
intron_variant | MODIFIER | HG00408.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
a0003 | a0003c0003a0003c0010 | a0003c0003t0003a0003c0010t0001 | a0003c0003t0003g0001 a0003c0003t0003g0026 a0003c0003t0003g0043 others(8): Show |
13 | 432 | 0.0301 | 17 | c.158 others(34): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCAPD2_chr12_6489102_6536955 | 6518517 | T | TTTTTTTT others(10): Show |
intron_variant | MODIFIER | HG03942.hp1 | a0003 | a0003c0010 | a0003c0010t0003 | a0003c0010t0003g0217 | 1 | 432 | 0.0023 | 17 | c.158 others(34): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCAPD3_chr11_134145113_134228967 | 134212375 | T | TGTGTGTG others(10): Show |
intron_variant | MODIFIER | HG01255.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0093 | 1 | 370 | 0.0027 | 17 | c.383 others(34): Show |
NCAPD3 | ENSG00000151503.14 | transcript | ENST00000534548.7 | protein_coding | 3/34 | chr11 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158669768 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0337 | 1 | 378 | 0.0027 | 17 | c.147 others(36): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCBP1_chr9_97628821_97678748 | 97677082 | T | TCACGTAA others(10): Show |
downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(233): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(17): Show | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(195): Show |
236 | 364 | 0.6484 | 17 | c.*58 others(28): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 3335 | chr9 | TogoVar | |||||||
NCEH1_chr3_172625249_172716067 | 172701449 | C | CTTTTTTT others(10): Show |
intron_variant | MODIFIER | HG02486.hp1 HG02572.hp1 HG02630.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(4): Show | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0073 others(7): Show |
10 | 332 | 0.0301 | 17 | c.138 others(34): Show |
NCEH1 | ENSG00000144959.11 | transcript | ENST00000475381.7 | protein_coding | 1/4 | chr3 | TogoVar | |||||||
NCF2_chr1_183550562_183595459 | 183571964 | A | ATGGATAT others(10): Show |
intron_variant | MODIFIER | NA19006.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0298 | 1 | 406 | 0.0025 | 17 | c.610 others(34): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 5/14 | chr1 | TogoVar | |||||||
NCF2_chr1_183550562_183595459 | 183585624 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG01074.hp1 HG01099.hp2 HG01192.hp1 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0003a0002c0002t0001 | a0001c0001t0001g0308 a0001c0001t0001g0310 a0001c0001t0001g0311 others(11): Show |
14 | 406 | 0.0345 | 17 | c.257 others(34): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | TogoVar | |||||||
NCK2_chr2_105739912_105899272 | 105807746 | C | CCTCCCTC others(10): Show |
intron_variant | MODIFIER | HG00140.hp1 NA18982.hp2 NA19066.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 |
3 | 334 | 0.0090 | 17 | c.-20 others(36): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 1/4 | chr2 | TogoVar | |||||||
NCK2_chr2_105739912_105899272 | 105807842 | C | CCTCCCTC others(10): Show |
intron_variant | MODIFIER | HG01175.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0017others(2): Show | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0192 others(13): Show |
16 | 334 | 0.0479 | 17 | c.-20 others(36): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCK2_chr2_105739912_105899272 | 105807846 | C | CCTCCCTC others(10): Show |
intron_variant | MODIFIER | HG02486.hp2 HG02723.hp2 NA18906.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0297 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | 334 | 0.0120 | 17 | c.-20 others(36): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCKAP1L_chr12_54492752_54553243 | 54506792 | A | ATATATAT others(10): Show |
intron_variant | MODIFIER | HG04228.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0026 | 1 | 350 | 0.0029 | 17 | c.307 others(34): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | TogoVar | |||||||
NCKAP1L_chr12_54492752_54553243 | 54506794 | A | ATATATAT others(10): Show |
intron_variant | MODIFIER | HG01884.hp2 HG03492.hp1 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0236 a0002c0003t0001g0175 |
2 | 350 | 0.0057 | 17 | c.307 others(34): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | TogoVar | |||||||
NCKAP1L_chr12_54492752_54553243 | 54506796 | A | AAAAAAAA others(10): Show |
intron_variant | MODIFIER | NA18993.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0179 | 1 | 350 | 0.0029 | 17 | c.307 others(34): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCKAP1L_chr12_54492752_54553243 | 54506796 | A | AAAAAAAT others(10): Show |
intron_variant | MODIFIER | HG02630.hp1 NA18957.hp1 NA19066.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0007a0001c0002t0005 | a0001c0001t0007g0181 a0001c0001t0007g0182 a0001c0002t0005g0319 |
3 | 350 | 0.0086 | 17 | c.307 others(34): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCKAP1L_chr12_54492752_54553243 | 54506796 | A | AAAAATAT others(10): Show |
intron_variant | MODIFIER | HG02074.hp1 HG02083.hp2 HG03017.hp1 others(8): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(5): Show | a0001c0001t0001g0009 a0001c0001t0001g0194 a0001c0001t0002g0189 others(8): Show |
11 | 350 | 0.0314 | 17 | c.307 others(34): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCKAP1L_chr12_54492752_54553243 | 54506796 | A | AAATATAT others(10): Show |
intron_variant | MODIFIER | HG00642.hp2 HG01978.hp2 HG03669.hp2 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(3): Show | a0001c0001t0001g0117 a0001c0001t0008g0211 a0001c0001t0009g0210 others(3): Show |
6 | 350 | 0.0171 | 17 | c.307 others(34): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCKAP1L_chr12_54492752_54553243 | 54506796 | A | ATATATAT others(10): Show |
intron_variant | MODIFIER | HG01346.hp1 HG01978.hp1 NA19058.hp1 others(1): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0005a0001c0001t0014others(1): Show | a0001c0001t0001g0227 a0001c0001t0005g0225 a0001c0001t0014g0224 others(1): Show |
4 | 350 | 0.0114 | 17 | c.307 others(34): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | chr12 | TogoVar | |||||||
NCMAP_chr1_24551087_24614328 | 24597555 | A | AGGGAAGG others(10): Show |
intron_variant | MODIFIER | HG00558.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0006a0001c0001t0026a0003c0004t0027 | a0001c0001t0006g0141 a0001c0001t0006g0151 a0001c0001t0006g0152 others(13): Show |
16 | 402 | 0.0398 | 17 | c.82+ others(32): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NCMAP_chr1_24551087_24614328 | 24614248 | T | TTATTATT others(10): Show |
downstream_gene_variant | MODIFIER | HG03471.hp2 HG03669.hp2 HG03704.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0002c0002t0004 | a0001c0001t0003g0077 a0001c0001t0003g0243 a0002c0002t0004g0025 |
3 | 402 | 0.0075 | 17 | c.*85 others(28): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 4921 | chr1 | TogoVar | |||||||
NCOA1_chr2_24486254_24775702 | 24523605 | C | CAAAAAAA others(10): Show |
intron_variant | MODIFIER | HG00408.hp2 HG00558.hp2 HG00735.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(1): Show | a0001c0001t0001g0220 a0001c0001t0001g0229 a0001c0001t0001g0230 others(8): Show |
11 | 314 | 0.0350 | 17 | c.-39 others(38): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |