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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NENF_chr1_212427920_212451379 | 212444551 | GTGTGTGT others(11): Show |
G | intron_variant | MODIFIER | HG03710.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0196 | 1 | 416 | 0.0024 | -18 | c.342 others(33): Show |
NENF | ENSG00000117691.10 | transcript | ENST00000366988.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NEO1_chr15_73047463_73310205 | 73271977 | TACAATTT others(11): Show |
T | intron_variant | MODIFIER | HG01255.hp1 | a0001 | a0001c0019 | a0001c0019t0016 | a0001c0019t0016g0047 | 1 | 324 | 0.0031 | -18 | c.285 others(35): Show |
NEO1 | ENSG00000067141.17 | transcript | ENST00000261908.11 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
NETO1_chr18_72738756_72872987 | 72741875 | AAGAGAAA others(11): Show |
A | downstream_gene_variant | MODIFIER | HG03453.hp1 NA21309.hp1 |
a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0034 a0001c0001t0015g0207 |
2 | 348 | 0.0058 | -18 | c.*62 others(29): Show |
NETO1 | ENSG00000166342.19 | transcript | ENST00000327305.11 | protein_coding | 1880 | chr18 | TogoVar | |||||||
NETO1_chr18_72738756_72872987 | 72772815 | CTCTCTCT others(11): Show |
C | intron_variant | MODIFIER | HG03654.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0310 | 1 | 348 | 0.0029 | -18 | c.868 others(37): Show |
NETO1 | ENSG00000166342.19 | transcript | ENST00000327305.11 | protein_coding | 7/10 | chr18 | TogoVar | |||||||
NETO1_chr18_72738756_72872987 | 72772817 | CTCTCTCT others(11): Show |
C | intron_variant | MODIFIER | HG00323.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015 | 1 | 348 | 0.0029 | -18 | c.868 others(37): Show |
NETO1 | ENSG00000166342.19 | transcript | ENST00000327305.11 | protein_coding | 7/10 | chr18 | TogoVar | |||||||
NETO1_chr18_72738756_72872987 | 72772825 | CTATATAT others(11): Show |
C | intron_variant | MODIFIER | HG02630.hp1 HG02976.hp1 HG03486.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0003c0003t0006 | a0001c0001t0001g0209 a0001c0001t0001g0282 a0003c0003t0006g0294 |
3 | 348 | 0.0086 | -18 | c.868 others(37): Show |
NETO1 | ENSG00000166342.19 | transcript | ENST00000327305.11 | protein_coding | 7/10 | chr18 | TogoVar | |||||||
NEU4_chr2_241804193_241822413 | 241806012 | CTCAGCCC others(11): Show |
C | upstream_gene_variant | MODIFIER | HG02165.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0047 | 1 | 319 | 0.0031 | -18 | c.-32 others(29): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 3180 | chr2 | TogoVar | |||||||
NEURL1B_chr5_172636263_172696540 | 172649345 | CTTTTTTT others(11): Show |
C | intron_variant | MODIFIER | HG01256.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034 | 1 | 392 | 0.0026 | -18 | c.31+ others(33): Show |
NEURL1B | ENSG00000214357.9 | transcript | ENST00000369800.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
NEURL1B_chr5_172636263_172696540 | 172692489 | AAAAAAAA others(11): Show |
A | downstream_gene_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0039 | a0001c0001t0039g0260 | 1 | 392 | 0.0026 | -18 | c.*55 others(29): Show |
NEURL1B | ENSG00000214357.9 | transcript | ENST00000369800.6 | protein_coding | 950 | chr5 | TogoVar | |||||||
NEURL1_chr10_103488705_103597546 | 103515227 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0010others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(17): Show | a0001c0001t0001g0126 a0001c0001t0001g0134 a0001c0001t0001g0136 others(91): Show |
95 | 312 | 0.3045 | -18 | c.85+ others(35): Show |
NEURL1 | ENSG00000107954.11 | transcript | ENST00000369780.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
NEUROD6_chr7_31332465_31345726 | 31334282 | CTTTCTTT others(11): Show |
C | downstream_gene_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 414 | 0.0024 | -18 | c.*39 others(29): Show |
NEUROD6 | ENSG00000164600.7 | transcript | ENST00000297142.4 | protein_coding | 3182 | chr7 | TogoVar | |||||||
NEUROD6_chr7_31332465_31345726 | 31334288 | TTCTTTCT others(11): Show |
T | downstream_gene_variant | MODIFIER | HG01255.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 414 | 0.0024 | -18 | c.*39 others(29): Show |
NEUROD6 | ENSG00000164600.7 | transcript | ENST00000297142.4 | protein_coding | 3176 | chr7 | TogoVar | |||||||
NEXMIF_chrX_74727856_74930452 | 74730276 | TCAACAAC others(11): Show |
T | downstream_gene_variant | MODIFIER | HG02717.hp1 HG02886.hp2 |
a0001a0005 | a0001c0001a0005c0006 | a0001c0001t0001a0005c0006t0034 | a0001c0001t0001g0215 a0005c0006t0034g0118 |
2 | 224 | 0.0089 | -18 | c.*91 others(29): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 2579 | chrX | TogoVar | |||||||
NEXN_chr1_77883624_77948895 | 77887912 | TTTCTTCT others(11): Show |
T | upstream_gene_variant | MODIFIER | NA18960.hp2 NA18975.hp1 NA19011.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0008 | a0001c0001t0003g0109 a0001c0001t0003g0110 a0001c0001t0003g0111 others(1): Show |
4 | 268 | 0.0149 | -18 | c.-89 others(27): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 711 | chr1 | TogoVar | |||||||
NEXN_chr1_77883624_77948895 | 77895029 | ATTTTTTT others(11): Show |
A | intron_variant | MODIFIER | HG02818.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(1): Show |
4 | 268 | 0.0149 | -18 | c.-53 others(35): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NEXN_chr1_77883624_77948895 | 77931231 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(12): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0028 a0001c0001t0001g0054 a0001c0001t0001g0060 others(12): Show |
15 | 268 | 0.0560 | -18 | c.105 others(37): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NF1_chr17_31089977_31382675 | 31278493 | CTTTTTTT others(11): Show |
C | intron_variant | MODIFIER | HG02109.hp2 HG03209.hp1 NA18522.hp2 |
a0001 | a0001c0001a0001c0021 | a0001c0001t0003a0001c0021t0003 | a0001c0001t0003g0123 a0001c0001t0003g0125 a0001c0021t0003g0124 |
3 | 252 | 0.0119 | -18 | c.483 others(39): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 36/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
NF1_chr17_31089977_31382675 | 31293178 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG00597.hp1 HG02015.hp1 |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0031 | a0001c0002t0002g0232 a0001c0002t0031g0154 |
2 | 252 | 0.0079 | -18 | c.483 others(39): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 36/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
NF1_chr17_31089977_31382675 | 31322501 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | NA19012.hp2 | a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0113 | 1 | 252 | 0.0040 | -18 | c.483 others(37): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 36/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
NF2_chr22_29598633_29703598 | 29624798 | CCTCTTTC others(11): Show |
C | intron_variant | MODIFIER | HG02055.hp1 HG02280.hp1 HG02647.hp2 |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0247 a0001c0001t0006g0249 a0001c0001t0006g0296 |
3 | 344 | 0.0087 | -18 | c.115 others(37): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
NFASC_chr1_204823652_205027822 | 204830578 | TTGTGTGT others(11): Show |
T | intron_variant | MODIFIER | HG02015.hp1 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0129 | 1 | 226 | 0.0044 | -18 | c.-20 others(37): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NFASC_chr1_204823652_205027822 | 204839368 | AACACACA others(11): Show |
A | intron_variant | MODIFIER | HG02965.hp1 HG02965.hp2 HG03516.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0033a0001c0001t0051others(6): Show | a0001c0001t0001g0039 a0001c0001t0033g0038 a0001c0001t0051g0036 others(6): Show |
9 | 226 | 0.0398 | -18 | c.-20 others(39): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NFASC_chr1_204865862_205027822 | 204995315 | AGTGTGTG others(11): Show |
A | intron_variant | MODIFIER | HG01433.hp2 | a0005 | a0005c0024 | a0005c0024t0001 | a0005c0024t0001g0052 | 1 | 264 | 0.0038 | -18 | c.313 others(37): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NFAT5_chr16_69560966_69709654 | 69561005 | TAAAAAAA others(11): Show |
T | upstream_gene_variant | MODIFIER | HG00099.hp1 HG01256.hp1 HG03688.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0053 | a0001c0001t0002g0105 a0001c0001t0002g0275 a0001c0001t0002g0289 others(3): Show |
6 | 380 | 0.0158 | -18 | c.-52 others(29): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4960 | chr16 | TogoVar | |||||||
NFAT5_chr16_69560966_69709654 | 69627323 | CATATATA others(11): Show |
C | intron_variant | MODIFIER | NA18940.hp1 NA18992.hp1 NA19081.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0007a0001c0001t0064 | a0001c0001t0006g0097 a0001c0001t0007g0091 a0001c0001t0064g0092 |
3 | 380 | 0.0079 | -18 | c.253 others(33): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79395663 | GCCCCCCC others(11): Show |
G | upstream_gene_variant | MODIFIER | HG00733.hp2 HG01069.hp1 HG01071.hp2 others(18): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0009a0001c0027others(5): Show | a0001c0001t0002a0001c0001t0012a0001c0001t0030others(10): Show | a0001c0001t0002g0015 a0001c0001t0002g0035 a0001c0001t0002g0072 others(18): Show |
21 | 322 | 0.0652 | -18 | c.-56 others(27): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 266 | chr18 | TogoVar | |||||||
NFATC1_chr18_79390930_79534323 | 79512162 | ACCCCAGG others(11): Show |
A | intron_variant | MODIFIER | NA18966.hp2 | a0011 | a0011c0042 | a0011c0042t0003 | a0011c0042t0003g0149 | 1 | 322 | 0.0031 | -18 | c.278 others(39): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC2_chr20_51381963_51547719 | 51393959 | GGATGGAA others(11): Show |
G | intron_variant | MODIFIER | HG01071.hp1 HG01106.hp1 HG01167.hp1 others(22): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(12): Show | a0001c0001t0002g0008 a0001c0001t0002g0015 a0001c0001t0002g0178 others(22): Show |
25 | 316 | 0.0791 | -18 | c.*45 others(35): Show |
NFATC2 | ENSG00000101096.20 | transcript | ENST00000371564.8 | protein_coding | 10/10 | chr20 | TogoVar | |||||||
NFATC2_chr20_51381963_51547719 | 51396038 | GTATATAT others(11): Show |
G | intron_variant | MODIFIER | HG02735.hp1 NA18966.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0003 a0001c0004t0001g0004 |
2 | 316 | 0.0063 | -18 | c.*44 others(35): Show |
NFATC2 | ENSG00000101096.20 | transcript | ENST00000371564.8 | protein_coding | 10/10 | chr20 | TogoVar | |||||||
NFATC2_chr20_51381963_51547719 | 51396984 | CTCATCTC others(11): Show |
C | intron_variant | MODIFIER | HG02723.hp1 HG02896.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0024a0001c0002t0024 | a0001c0001t0024g0197 a0001c0002t0024g0228 |
2 | 316 | 0.0063 | -18 | c.*44 others(35): Show |
NFATC2 | ENSG00000101096.20 | transcript | ENST00000371564.8 | protein_coding | 10/10 | chr20 | TogoVar | |||||||
NFATC2_chr20_51381963_51547719 | 51477564 | TATATATA others(11): Show |
T | intron_variant | MODIFIER | HG00438.hp2 HG00544.hp2 HG00738.hp1 others(19): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0003 a0001c0001t0001g0081 a0001c0001t0001g0082 others(19): Show |
22 | 316 | 0.0696 | -18 | c.133 others(37): Show |
NFATC2 | ENSG00000101096.20 | transcript | ENST00000371564.8 | protein_coding | 3/10 | chr20 | TogoVar | |||||||
NFATC2_chr20_51381963_51547719 | 51504999 | CTTTTTTT others(11): Show |
C | intron_variant | MODIFIER | HG01975.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0101 | 1 | 316 | 0.0032 | -18 | c.133 others(39): Show |
NFATC2 | ENSG00000101096.20 | transcript | ENST00000371564.8 | protein_coding | 3/10 | chr20 | TogoVar | |||||||
NFATC3_chr16_68080370_68234259 | 68222289 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0123 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
6 | 188 | 0.0319 | -18 | c.310 others(37): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
NFATC3_chr16_68080370_68234259 | 68226897 | CAAAAAAA others(11): Show |
C | 3_prime_UTR_variant | MODIFIER | NA18975.hp1 | a0001 | a0001c0001 | a0001c0001t0026 | a0001c0001t0026g0159 | 1 | 188 | 0.0053 | -18 | c.*43 others(27): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 10/10 | 435 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
NFIA_chr1_61077561_61467788 | 61118659 | AGTGTGTG others(11): Show |
A | intron_variant | MODIFIER | HG00735.hp1 HG03098.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0046 | a0001c0001t0001g0033 a0001c0001t0046g0137 |
2 | 156 | 0.0128 | -18 | c.559 others(37): Show |
NFIA | ENSG00000162599.18 | transcript | ENST00000403491.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NFIA_chr1_61077561_61467788 | 61196898 | AGTGTGTG others(11): Show |
A | intron_variant | MODIFIER | HG01943.hp1 HG02698.hp1 HG02717.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(1): Show | a0001c0001t0001g0068 a0001c0001t0003g0066 a0001c0001t0010g0071 others(1): Show |
4 | 156 | 0.0256 | -18 | c.560 others(37): Show |
NFIA | ENSG00000162599.18 | transcript | ENST00000403491.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NFIA_chr1_61077561_61467788 | 61200010 | GTATATAT others(11): Show |
G | intron_variant | MODIFIER | HG02698.hp2 | a0001 | a0001c0002 | a0001c0002t0014 | a0001c0002t0014g0020 | 1 | 156 | 0.0064 | -18 | c.560 others(37): Show |
NFIA | ENSG00000162599.18 | transcript | ENST00000403491.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NFIA_chr1_61077561_61467788 | 61334555 | GTATATAT others(11): Show |
G | intron_variant | MODIFIER | HG01167.hp1 HG02155.hp1 HG02897.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0059 a0001c0001t0002g0060 a0001c0001t0003g0070 others(9): Show |
12 | 156 | 0.0769 | -18 | c.700 others(35): Show |
NFIA | ENSG00000162599.18 | transcript | ENST00000403491.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NFIA_chr1_61077561_61467788 | 61391435 | AACACACA others(11): Show |
A | intron_variant | MODIFIER | HG02615.hp2 NA19043.hp2 |
a0001 | a0001c0001 | a0001c0001t0032a0001c0001t0042 | a0001c0001t0032g0138 a0001c0001t0042g0115 |
2 | 156 | 0.0128 | -18 | c.107 others(37): Show |
NFIA | ENSG00000162599.18 | transcript | ENST00000403491.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NFIB_chr9_14076848_14319141 | 14080447 | CTTTTTTT others(11): Show |
C | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(27): Show | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0199 others(67): Show |
70 | 304 | 0.2303 | -18 | c.*78 others(29): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 1400 | chr9 | TogoVar | |||||||
NFIB_chr9_14076848_14319141 | 14187009 | GTGTGTGT others(11): Show |
G | intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0072 | 1 | 304 | 0.0033 | -18 | c.563 others(35): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIB_chr9_14076848_14319141 | 14216525 | TCTCTCTC others(11): Show |
T | intron_variant | MODIFIER | HG03130.hp2 | a0001 | a0001c0001 | a0001c0001t0023 | a0001c0001t0023g0044 | 1 | 304 | 0.0033 | -18 | c.563 others(37): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIB_chr9_14076848_14319141 | 14216532 | CTCTCTCT others(11): Show |
C | intron_variant | MODIFIER | HG02055.hp2 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0042 | 1 | 304 | 0.0033 | -18 | c.563 others(37): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIB_chr9_14076848_14319141 | 14216534 | CTCTCTCT others(11): Show |
C | intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0071 | a0001c0001t0071g0164 | 1 | 304 | 0.0033 | -18 | c.563 others(37): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIB_chr9_14076848_14319141 | 14216536 | CTCTCTCC others(11): Show |
C | intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0016 | 1 | 304 | 0.0033 | -18 | c.563 others(37): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIB_chr9_14076848_14319141 | 14216542 | CCCTCTGT others(11): Show |
C | intron_variant | MODIFIER | HG02109.hp1 HG02572.hp2 |
a0001 | a0001c0001 | a0001c0001t0017a0001c0001t0062 | a0001c0001t0017g0009 a0001c0001t0062g0027 |
2 | 304 | 0.0066 | -18 | c.563 others(37): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIB_chr9_14076848_14319141 | 14237763 | AGTGTGTG others(11): Show |
A | intron_variant | MODIFIER | HG01099.hp2 HG02083.hp2 HG02922.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(6): Show | a0001c0001t0001g0251 a0001c0001t0002g0132 a0001c0001t0008g0143 others(7): Show |
10 | 304 | 0.0329 | -18 | c.563 others(37): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar | |||||||
NFIC_chr19_3361583_3474217 | 3408153 | CGGCCGAT others(11): Show |
C | intron_variant | MODIFIER | HG01069.hp1 | a0001 | a0001c0001 | a0001c0001t0139 | a0001c0001t0139g0259 | 1 | 300 | 0.0033 | -18 | c.563 others(37): Show |
NFIC | ENSG00000141905.19 | transcript | ENST00000443272.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NFIC_chr19_3361583_3474217 | 3424152 | TGAGTAGC others(11): Show |
T | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0127 | 1 | 300 | 0.0033 | -18 | c.563 others(33): Show |
NFIC | ENSG00000141905.19 | transcript | ENST00000443272.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NFIC_chr19_3361583_3474217 | 3439333 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0252 | 1 | 300 | 0.0033 | -18 | c.958 others(35): Show |
NFIC | ENSG00000141905.19 | transcript | ENST00000443272.3 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |