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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NEK11_chr3_131021877_131355465 | 131203767 | GTATATAT others(23): Show |
G | intron_variant | MODIFIER | HG01123.hp2 HG02486.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0185 a0002c0002t0001g0085 |
2 | 136 | 0.0147 | -30 | c.140 others(51): Show |
NEK11 | ENSG00000114670.14 | transcript | ENST00000383366.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
NEK5_chr13_52028611_52134073 | 52084756 | AGAGAGAG others(23): Show |
A | intron_variant | MODIFIER | HG02055.hp1 HG03516.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0048 a0001c0001t0008g0044 |
2 | 306 | 0.0065 | -30 | c.148 others(49): Show |
NEK5 | ENSG00000197168.14 | transcript | ENST00000684899.1 | protein_coding | 16/23 | chr13 | TogoVar | |||||||
NELL1_chr11_20664586_21580686 | 20835320 | AAGTGCTT others(23): Show |
A | intron_variant | MODIFIER | HG02257.hp1 HG02717.hp2 HG02965.hp1 |
a0001a0002 | a0001c0001a0002c0002a0002c0007 | a0001c0001t0002a0002c0002t0001a0002c0007t0001 | a0001c0001t0002g0001 a0002c0002t0001g0067 a0002c0007t0001g0028 |
3 | 86 | 0.0349 | -30 | c.336 others(49): Show |
NELL1 | ENSG00000165973.19 | transcript | ENST00000357134.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NELL1_chr11_20664586_21580686 | 21027282 | CTAGTTTA others(23): Show |
C | intron_variant | MODIFIER | HG02109.hp2 HG02886.hp2 HG02976.hp2 others(2): Show |
a0001a0002a0006 | a0001c0001a0001c0006a0001c0008others(2): Show | a0001c0001t0001a0001c0006t0003a0001c0008t0001others(2): Show | a0001c0001t0001g0022 a0001c0006t0003g0020 a0001c0008t0001g0041 others(2): Show |
5 | 31 | 0.1613 | -30 | c.130 others(51): Show |
NELL1 | ENSG00000165973.19 | transcript | ENST00000357134.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NELL2_chr12_44503278_44881315 | 44791079 | ATACATAT others(23): Show |
A | intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0120 | 1 | 156 | 0.0064 | -30 | c.336 others(49): Show |
NELL2 | ENSG00000184613.11 | transcript | ENST00000429094.7 | protein_coding | 3/19 | chr12 | TogoVar | |||||||
NES_chr1_156663763_156682407 | 156673781 | TCCCACAC others(23): Show |
T | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp2 HG01256.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 9 | 436 | 0.0206 | -30 | c.909 others(45): Show |
NES | ENSG00000132688.11 | transcript | ENST00000368223.4 | protein_coding | 2/3 | chr1 | TogoVar | |||||||
NEU4_chr2_241804193_241822413 | 241806993 | CCCCCCTC others(23): Show |
C | upstream_gene_variant | MODIFIER | HG02148.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 294 | 0.0034 | -30 | c.-22 others(41): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 2199 | chr2 | TogoVar | |||||||
NEXN_chr1_77883624_77948895 | 77887912 | TTTCTTCT others(23): Show |
T | upstream_gene_variant | MODIFIER | HG02818.hp2 NA18612.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0003a0001c0003t0009 | a0001c0001t0003g0140 a0001c0003t0009g0160 |
2 | 177 | 0.0113 | -30 | c.-89 others(39): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 711 | chr1 | TogoVar | |||||||
NF2_chr22_29598633_29703598 | 29692935 | AAGTGACC others(23): Show |
A | intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0097 | 1 | 342 | 0.0029 | -30 | c.173 others(49): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
NFAT5_chr16_69560966_69709654 | 69627323 | CATATATA others(23): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
a0001a0004a0005 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0023a0001c0001t0024others(9): Show | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0041 others(63): Show |
69 | 78 | 0.8846 | -30 | c.253 others(45): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79467290 | TGCTGCCG others(23): Show |
T | intron_variant | MODIFIER | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(8): Show |
a0001a0002 | a0001c0004a0001c0014a0001c0015others(1): Show | a0001c0004t0004a0001c0014t0004a0001c0014t0007others(4): Show | a0001c0004t0004g0078 a0001c0004t0004g0282 a0001c0014t0004g0308 others(7): Show |
11 | 320 | 0.0344 | -30 | c.196 others(47): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79467293 | TGCCGTGG others(23): Show |
T | intron_variant | MODIFIER | HG01891.hp2 HG01928.hp1 HG01934.hp2 others(23): Show |
a0001a0002 | a0001c0001a0001c0005a0001c0006others(4): Show | a0001c0001t0002a0001c0001t0006a0001c0005t0004others(13): Show | a0001c0001t0002g0298 a0001c0001t0006g0005 a0001c0005t0004g0058 others(23): Show |
26 | 270 | 0.0963 | -30 | c.196 others(45): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79483081 | GTACTGGG others(23): Show |
G | intron_variant | MODIFIER | HG02109.hp1 | a0002 | a0002c0002 | a0002c0002t0039 | a0002c0002t0039g0122 | 1 | 317 | 0.0032 | -30 | c.209 others(49): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79483083 | ACTGGGGT others(23): Show |
A | intron_variant | MODIFIER | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(164): Show |
a0001a0002a0006others(3): Show | a0001c0001a0001c0004a0001c0005others(28): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(84): Show | a0001c0001t0001g0195 a0001c0001t0003g0146 a0001c0001t0004g0091 others(163): Show |
167 | 316 | 0.5285 | -30 | c.209 others(49): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79483437 | GTCCTGGG others(23): Show |
G | intron_variant | MODIFIER | HG00741.hp1 | a0003 | a0003c0007 | a0003c0007t0001 | a0003c0007t0001g0206 | 1 | 315 | 0.0032 | -30 | c.209 others(49): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79483455 | AGCGTGAC others(23): Show |
A | intron_variant | MODIFIER | HG00323.hp2 HG01891.hp2 HG01952.hp2 others(22): Show |
a0001a0003 | a0001c0005a0001c0013a0001c0028others(3): Show | a0001c0005t0004a0001c0005t0005a0001c0005t0009others(12): Show | a0001c0005t0004g0058 a0001c0005t0005g0055 a0001c0005t0005g0056 others(22): Show |
25 | 317 | 0.0789 | -30 | c.209 others(49): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79483564 | TGTCACTC others(23): Show |
T | intron_variant | MODIFIER | HG03130.hp2 | a0009 | a0009c0033 | a0009c0033t0026 | a0009c0033t0026g0101 | 1 | 318 | 0.0031 | -30 | c.209 others(49): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79510813 | CTCCTCTG others(23): Show |
C | intron_variant | MODIFIER | HG03225.hp2 HG03453.hp1 HG03704.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0018a0002c0003 | a0001c0001t0006a0001c0018t0009a0002c0003t0001 | a0001c0001t0006g0041 a0001c0018t0009g0128 a0001c0018t0009g0179 others(1): Show |
4 | 111 | 0.0360 | -30 | c.278 others(51): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79510849 | TGCCGGGG others(23): Show |
T | intron_variant | MODIFIER | HG03098.hp1 | a0008 | a0008c0031 | a0008c0031t0004 | a0008c0031t0004g0011 | 1 | 320 | 0.0031 | -30 | c.278 others(51): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC2_chr20_51381963_51547719 | 51396034 | GTATGTAT others(23): Show |
G | intron_variant | MODIFIER | HG00140.hp1 HG00642.hp1 HG00738.hp2 others(10): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(6): Show | a0001c0001t0003g0124 a0001c0001t0003g0287 a0001c0001t0004g0041 others(10): Show |
13 | 113 | 0.1150 | -30 | c.*44 others(47): Show |
NFATC2 | ENSG00000101096.20 | transcript | ENST00000371564.8 | protein_coding | 10/10 | chr20 | TogoVar | |||||||
NFATC2_chr20_51381963_51547719 | 51477535 | CTATATAT others(23): Show |
C | intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0253 | 1 | 106 | 0.0094 | -30 | c.133 others(49): Show |
NFATC2 | ENSG00000101096.20 | transcript | ENST00000371564.8 | protein_coding | 3/10 | chr20 | TogoVar | |||||||
NFIA_chr1_61077561_61467788 | 61200038 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | NA18522.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0045 | 1 | 150 | 0.0067 | -30 | c.560 others(49): Show |
NFIA | ENSG00000162599.18 | transcript | ENST00000403491.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NFIA_chr1_61077561_61467788 | 61334555 | GTATATAT others(23): Show |
G | intron_variant | MODIFIER | HG02895.hp2 HG02897.hp2 |
a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0095 a0001c0001t0015g0096 |
2 | 36 | 0.0556 | -30 | c.700 others(47): Show |
NFIA | ENSG00000162599.18 | transcript | ENST00000403491.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NFIB_chr9_14076848_14319141 | 14216513 | TCTCTCTC others(23): Show |
T | intron_variant | MODIFIER | HG00609.hp2 HG00639.hp2 HG00642.hp1 others(9): Show |
a0001a0004 | a0001c0001a0004c0006 | a0001c0001t0004a0001c0001t0012a0001c0001t0032others(8): Show | a0001c0001t0004g0120 a0001c0001t0004g0286 a0001c0001t0012g0240 others(9): Show |
12 | 302 | 0.0397 | -30 | c.563 others(49): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIB_chr9_14076848_14319141 | 14216524 | CTCTCTCT others(23): Show |
C | intron_variant | MODIFIER | HG00642.hp2 HG01099.hp2 HG02145.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(5): Show | a0001c0001t0002g0266 a0001c0001t0004g0137 a0001c0001t0005g0237 others(5): Show |
8 | 247 | 0.0324 | -30 | c.563 others(49): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIB_chr9_14076848_14319141 | 14216526 | CTCTCTCT others(23): Show |
C | intron_variant | MODIFIER | HG02486.hp2 HG02602.hp2 HG03017.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(2): Show | a0001c0001t0001g0101 a0001c0001t0001g0126 a0001c0001t0002g0292 others(3): Show |
6 | 298 | 0.0201 | -30 | c.563 others(49): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIB_chr9_14076848_14319141 | 14216528 | CTCTCTCT others(23): Show |
C | intron_variant | MODIFIER | HG01099.hp1 HG01257.hp1 HG01361.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0098 a0001c0001t0001g0259 a0001c0001t0001g0268 others(1): Show |
4 | 261 | 0.0153 | -30 | c.563 others(49): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIB_chr9_14076848_14319141 | 14216530 | CTCTCTCT others(23): Show |
C | intron_variant | MODIFIER | HG02080.hp2 NA19063.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0260 a0001c0001t0005g0189 |
2 | 281 | 0.0071 | -30 | c.563 others(49): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIB_chr9_14076848_14319141 | 14216532 | CTCTCTCT others(23): Show |
C | intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0047 | a0001c0001t0047g0040 | 1 | 290 | 0.0034 | -30 | c.563 others(49): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIC_chr19_3361583_3474217 | 3414592 | CTAAAATA others(23): Show |
C | intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0001 | a0001c0001t0201 | a0001c0001t0201g0152 | 1 | 10 | 0.1000 | -30 | c.563 others(49): Show |
NFIC | ENSG00000141905.19 | transcript | ENST00000443272.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NFU1_chr2_69391126_69442435 | 69438845 | TAGTGATC others(23): Show |
T | upstream_gene_variant | MODIFIER | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(87): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0004 | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(1): Show | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0020 others(86): Show |
90 | 366 | 0.2459 | -30 | c.-14 others(41): Show |
NFU1 | ENSG00000169599.13 | transcript | ENST00000410022.7 | protein_coding | 1411 | chr2 | TogoVar | |||||||
NGLY1_chr3_25713944_25788443 | 25760860 | CAAAAAAA others(23): Show |
C | intron_variant | MODIFIER | HG00735.hp1 HG01243.hp2 HG02257.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0067 a0001c0001t0001g0236 a0001c0001t0001g0237 others(7): Show |
10 | 11 | 0.9091 | -30 | c.492 others(47): Show |
NGLY1 | ENSG00000151092.18 | transcript | ENST00000280700.10 | protein_coding | 3/11 | chr3 | TogoVar | |||||||
NHLRC2_chr10_113849661_113922194 | 113874442 | TTGTGTGT others(23): Show |
T | intron_variant | MODIFIER | NA19081.hp2 NA19090.hp1 |
a0004 | a0004c0004a0004c0011 | a0004c0004t0001a0004c0011t0042 | a0004c0004t0001g0135 a0004c0011t0042g0134 |
2 | 29 | 0.0690 | -30 | c.332 others(47): Show |
NHLRC2 | ENSG00000196865.4 | transcript | ENST00000369301.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
NHLRC4_chr16_562005_574495 | 571150 | TAGCCTGG others(23): Show |
T | downstream_gene_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 422 | 0.0024 | -30 | c.*27 others(41): Show |
NHLRC4 | ENSG00000257108.2 | transcript | ENST00000424439.3 | protein_coding | 1656 | chr16 | TogoVar | |||||||
NHSL1_chr6_138417043_138504494 | 138437325 | CACACATA others(23): Show |
C | intron_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0025 | 1 | 329 | 0.0030 | -30 | c.665 others(47): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | TogoVar | |||||||
NHSL1_chr6_138417043_138504494 | 138437373 | CACATATA others(23): Show |
C | intron_variant | MODIFIER | HG02818.hp1 HG03704.hp2 NA21309.hp1 |
a0001 | a0001c0030a0001c0031a0001c0042 | a0001c0030t0025a0001c0031t0041a0001c0042t0011 | a0001c0030t0025g0006 a0001c0031t0041g0149 a0001c0042t0011g0116 |
3 | 330 | 0.0091 | -30 | c.665 others(47): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | TogoVar | |||||||
NHSL1_chr6_138417043_138504494 | 138489825 | GGAGAGAG others(23): Show |
G | intron_variant | MODIFIER | HG01069.hp1 | a0001 | a0001c0001 | a0001c0001t0033 | a0001c0001t0033g0188 | 1 | 323 | 0.0031 | -30 | c.211 others(47): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | TogoVar | |||||||
NHSL2_chrX_71905845_72158286 | 72039067 | TTTTCCTT others(23): Show |
T | intron_variant | MODIFIER | HG02109.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
a0001a0002a0010 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0015a0001c0001t0019others(3): Show | a0001c0001t0001g0052 a0001c0001t0015g0049 a0001c0001t0019g0058 others(5): Show |
8 | 31 | 0.2581 | -30 | c.281 others(49): Show |
NHSL2 | ENSG00000204131.11 | transcript | ENST00000633930.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
NIBAN2_chr9_127500343_127574073 | 127523192 | AATATATA others(23): Show |
A | intron_variant | MODIFIER | HG02486.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0007 | a0001c0001t0002g0159 a0001c0001t0003g0002 a0001c0001t0003g0150 others(1): Show |
5 | 181 | 0.0276 | -30 | c.589 others(45): Show |
NIBAN2 | ENSG00000136830.12 | transcript | ENST00000373312.4 | protein_coding | 5/13 | chr9 | TogoVar | |||||||
NIM1K_chr5_43187225_43285850 | 43213284 | CCTTTCCT others(23): Show |
C | intron_variant | MODIFIER | NA20905.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0202 | 1 | 72 | 0.0139 | -30 | c.-69 others(51): Show |
NIM1K | ENSG00000177453.7 | transcript | ENST00000326035.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
NINJ2_chr12_559296_668445 | 609228 | GCGCACGC others(23): Show |
G | intron_variant | MODIFIER | HG00639.hp1 HG00733.hp2 HG02717.hp1 others(3): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0007t0002 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0002g0074 others(3): Show |
6 | 402 | 0.0149 | -30 | c.34- others(47): Show |
NINJ2 | ENSG00000171840.13 | transcript | ENST00000305108.10 | protein_coding | 1/3 | chr12 | TogoVar | |||||||
NINJ2_chr12_559296_668445 | 658646 | TTATGCTA others(23): Show |
T | intron_variant | MODIFIER | HG00738.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0292 | 1 | 8 | 0.1250 | -30 | c.33+ others(45): Show |
NINJ2 | ENSG00000171840.13 | transcript | ENST00000305108.10 | protein_coding | 1/3 | chr12 | TogoVar | |||||||
NINL_chr20_25447697_25590531 | 25542697 | TAAAAAAA others(23): Show |
T | intron_variant | MODIFIER | HG02809.hp2 | a0004 | a0004c0005 | a0004c0005t0001 | a0004c0005t0001g0210 | 1 | 10 | 0.1000 | -30 | c.-11 others(49): Show |
NINL | ENSG00000101004.16 | transcript | ENST00000278886.11 | protein_coding | 1/23 | chr20 | TogoVar | |||||||
NINL_chr20_25447697_25590531 | 25555970 | CGGCTTAT others(23): Show |
C | intron_variant | MODIFIER | HG02723.hp2 HG03540.hp2 |
a0010 | a0010c0018 | a0010c0018t0005 | a0010c0018t0005g0024 a0010c0018t0005g0025 |
2 | 308 | 0.0065 | -30 | c.-11 others(49): Show |
NINL | ENSG00000101004.16 | transcript | ENST00000278886.11 | protein_coding | 1/23 | chr20 | TogoVar | |||||||
NIPA1_chr15_22781644_22834789 | 22787038 | CCAGGAAT others(23): Show |
C | intron_variant | MODIFIER | HG00642.hp2 HG01175.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0327 a0001c0001t0004g0328 |
2 | 398 | 0.0050 | -30 | c.178 others(45): Show |
NIPA1 | ENSG00000170113.16 | transcript | ENST00000337435.9 | protein_coding | 1/4 | chr15 | TogoVar | |||||||
NIPAL1_chr4_48011772_48045173 | 48012648 | TTGATCAA others(23): Show |
T | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(43): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(3): Show | a0001c0001t0001g0019 a0001c0001t0003g0004 a0001c0001t0003g0080 others(12): Show |
46 | 412 | 0.1117 | -30 | c.-41 others(41): Show |
NIPAL1 | ENSG00000163293.12 | transcript | ENST00000295461.10 | protein_coding | 4123 | chr4 | TogoVar | |||||||
NKAIN2_chr6_123798865_124830640 | 124616437 | CTTTTTTT others(23): Show |
C | intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0052 | 1 | 18 | 0.0556 | -30 | c.274 others(49): Show |
NKAIN2 | ENSG00000188580.16 | transcript | ENST00000368417.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
NKAIN4_chr20_63235784_63259463 | 63257828 | AGGACAGT others(23): Show |
A | upstream_gene_variant | MODIFIER | HG02630.hp1 HG02723.hp2 |
a0001 | a0001c0004 | a0001c0004t0001a0001c0004t0002 | a0001c0004t0001g0017 a0001c0004t0002g0083 |
2 | 352 | 0.0057 | -30 | c.-34 others(41): Show |
NKAIN4 | ENSG00000101198.15 | transcript | ENST00000370316.8 | protein_coding | 3366 | chr20 | TogoVar | |||||||
NKAP_chrX_119915672_119948751 | 119941426 | CTAGTACT others(23): Show |
C | intron_variant | MODIFIER | HG02109.hp1 HG02109.hp2 HG02257.hp2 others(15): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0006a0001c0001t0007a0001c0003t0006others(1): Show | a0001c0001t0006g0089 a0001c0001t0006g0090 a0001c0001t0007g0091 others(14): Show |
18 | 318 | 0.0566 | -30 | c.386 others(47): Show |
NKAP | ENSG00000101882.10 | transcript | ENST00000371410.5 | protein_coding | 1/8 | chrX | TogoVar | |||||||
NKD1_chr16_50543396_50654249 | 50589694 | TTTCTCTT others(23): Show |
T | intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0002 | a0001c0002t0054 | a0001c0002t0054g0027 | 1 | 58 | 0.0172 | -30 | c.193 others(49): Show |
NKD1 | ENSG00000140807.7 | transcript | ENST00000268459.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar |