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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NEK11_chr3_131021877_131355465 | 131203765 | GTGTATAT others(23): Show |
G | intron_variant | MODIFIER | HG01074.hp1 HG01099.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | 292 | 0.0069 | -30 | c.140 others(51): Show |
NEK11 | ENSG00000114670.14 | transcript | ENST00000383366.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
NEK11_chr3_131021877_131355465 | 131203767 | GTATATAT others(23): Show |
G | intron_variant | MODIFIER | HG01123.hp2 HG02486.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0185a0002c0002t0001g0085 | 2 | 292 | 0.0069 | -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 | a0001c0001t0001g0047a0001c0001t0008g0043 | 2 | 334 | 0.0060 | -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 | a0001c0001t0002g0001a0002c0002t0001g0067a0002c0007t0001g0028 | 3 | 88 | 0.0341 | -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 |
a0001a0002a0010 | a0001c0001a0001c0006a0001c0008others(2): Show | a0001c0001t0001a0001c0006t0003a0001c0008t0001others(2): Show | a0001c0001t0001g0022a0001c0006t0003g0020a0001c0008t0001g0041others(2): Show | 5 | 88 | 0.0568 | -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 | 158 | 0.0063 | -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 | 438 | 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 | 319 | 0.0031 | -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 | a0001c0001t0003g0142a0001c0003t0009g0162 | 2 | 268 | 0.0075 | -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 | a0001c0001t0003g0096 | 1 | 344 | 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(67): Show |
a0001a0004a0005 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0024a0001c0001t0025others(9): Show | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(64): Show | 70 | 380 | 0.1842 | -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 | a0001c0004t0004g0078a0001c0004t0004g0282a0001c0014t0004g0308others(7): Show | 11 | 322 | 0.0342 | -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 | a0001c0001t0002g0298a0001c0001t0006g0005a0001c0005t0004g0058others(23): Show | 26 | 322 | 0.0808 | -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 | a0002c0002t0038 | a0002c0002t0038g0122 | 1 | 322 | 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 | 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 | a0001c0001t0001g0195a0001c0001t0003g0143a0001c0001t0004g0092others(163): Show | 167 | 322 | 0.5186 | -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 | 322 | 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 | 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 | a0001c0005t0004g0058a0001c0005t0005g0055a0001c0005t0005g0056others(22): Show | 25 | 322 | 0.0776 | -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 | a0007 | a0007c0033 | a0007c0033t0026 | a0007c0033t0026g0101 | 1 | 322 | 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 | a0001c0001t0006g0041a0001c0018t0009g0128a0001c0018t0009g0176others(1): Show | 4 | 322 | 0.0124 | -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 | a0005 | a0005c0031 | a0005c0031t0004 | a0005c0031t0004g0011 | 1 | 322 | 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 |
a0001a0009 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(6): Show | a0001c0001t0003g0124a0001c0001t0003g0287a0001c0001t0004g0041others(10): Show | 13 | 316 | 0.0411 | -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 | 316 | 0.0032 | -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 | a0001c0001t0022 | a0001c0001t0022g0045 | 1 | 156 | 0.0064 | -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 | a0001c0001t0015g0095a0001c0001t0015g0096 | 2 | 156 | 0.0128 | -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 |
a0001a0003 | a0001c0001a0003c0006 | a0001c0001t0004a0001c0001t0012a0001c0001t0032others(8): Show | a0001c0001t0004g0118a0001c0001t0004g0286a0001c0001t0012g0240others(9): Show | 12 | 304 | 0.0395 | -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 | a0001c0001t0002g0266a0001c0001t0004g0188a0001c0001t0005g0180others(5): Show | 8 | 304 | 0.0263 | -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 | a0001c0001t0001g0100a0001c0001t0001g0124a0001c0001t0002g0292others(3): Show | 6 | 304 | 0.0197 | -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 | a0001c0001t0001g0097a0001c0001t0001g0259a0001c0001t0001g0268others(1): Show | 4 | 304 | 0.0132 | -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 | a0001c0001t0001g0260a0001c0001t0005g0146 | 2 | 304 | 0.0066 | -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 | 304 | 0.0033 | -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 | a0001c0001t0202 | a0001c0001t0202g0152 | 1 | 300 | 0.0033 | -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 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | 368 | 0.2446 | -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 | a0001c0001t0001g0067a0001c0001t0001g0236a0001c0001t0001g0237others(7): Show | 10 | 264 | 0.0379 | -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 | a0004c0004t0001a0004c0011t0043 | a0004c0004t0001g0152a0004c0011t0043g0151 | 2 | 358 | 0.0056 | -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 | 424 | 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 | a0001c0002t0001g0101 | 1 | 332 | 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 | a0001c0030t0025g0006a0001c0031t0041g0149a0001c0042t0011g0116 | 3 | 332 | 0.0090 | -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 | 332 | 0.0030 | -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 |
a0001a0002a0009 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0015a0001c0001t0022others(4): Show | a0001c0001t0001g0053a0001c0001t0015g0049a0001c0001t0022g0052others(5): Show | 8 | 187 | 0.0428 | -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 | a0001c0001t0002g0152a0001c0001t0003g0001a0001c0001t0003g0144others(1): Show | 5 | 332 | 0.0151 | -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 | a0001c0001t0001g0209 | 1 | 292 | 0.0034 | -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 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0002g0074others(3): Show | 6 | 404 | 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 | 404 | 0.0025 | -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 | 310 | 0.0032 | -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 |
a0012 | a0012c0018 | a0012c0018t0005 | a0012c0018t0005g0060a0012c0018t0005g0061 | 2 | 310 | 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 | a0001c0001t0004g0327a0001c0001t0004g0328 | 2 | 400 | 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 | a0001c0001t0001g0018a0001c0001t0003g0004a0001c0001t0003g0082others(12): Show | 46 | 414 | 0.1111 | -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 | 66 | 0.0152 | -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 | a0001c0004t0001g0017a0001c0004t0002g0089 | 2 | 354 | 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 | a0001c0001t0006g0104a0001c0001t0006g0105a0001c0001t0007g0106others(14): Show | 18 | 320 | 0.0563 | -30 | c.386 others(47): Show |
NKAP | ENSG00000101882.10 | transcript | ENST00000371410.5 | protein_coding | 1/8 | chrX | TogoVar |