| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| NEGR1_chr1_71390943_72287539 | 71898949 | AATATATA others(10): Show |
A | intron_variant | MODIFIER | HG02055.hp1 NA20300.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0025a0001c0004t0001 | a0001c0001t0025g0052a0001c0004t0001g0003 | 2 | 64 | 0.0313 | -17 | c.409 others(36): Show |
NEGR1 | ENSG00000172260.15 | transcript | ENST00000357731.10 | protein_coding | 2/6 | chr1 | TogoVar | ||||||
| NEIL3_chr4_177304874_177367936 | 177320466 | CTTTTTTT others(10): Show |
C | intron_variant | MODIFIER | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(44): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0002c0002others(7): Show | a0001c0001t0001a0001c0003t0003a0002c0002t0001others(11): Show | a0001c0001t0001g0344a0001c0001t0001g0356a0001c0001t0001g0366others(44): Show | 47 | 408 | 0.1152 | -17 | c.157 others(34): Show |
NEIL3 | ENSG00000109674.4 | transcript | ENST00000264596.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
| NEK11_chr3_131021877_131355465 | 131309987 | TAAAAAAA others(10): Show |
T | intron_variant | MODIFIER | HG04228.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0177 | 1 | 292 | 0.0034 | -17 | c.171 others(38): Show |
NEK11 | ENSG00000114670.14 | transcript | ENST00000383366.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
| NEK7_chr1_198151998_198327420 | 198239346 | GCCATTTG others(10): Show |
G | intron_variant | MODIFIER | NA18984.hp2 NA19086.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | 346 | 0.0058 | -17 | c.57+ others(32): Show |
NEK7 | ENSG00000151414.15 | transcript | ENST00000367385.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
| NEK9_chr14_75074353_75132048 | 75100128 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG03492.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0158 | 1 | 278 | 0.0036 | -17 | c.200 others(34): Show |
NEK9 | ENSG00000119638.14 | transcript | ENST00000238616.10 | protein_coding | 16/21 | chr14 | TogoVar | ||||||
| NELFCD_chr20_58976256_59000113 | 58982140 | ATTTTTTT others(10): Show |
A | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG01081.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016a0001c0001t0001g0043a0001c0001t0001g0066others(1): Show | 8 | 438 | 0.0183 | -17 | c.60+ others(30): Show |
NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
| NELL1_chr11_20664586_21580686 | 20721200 | GTATATAT others(10): Show |
G | intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0011 | a0001c0011t0001 | a0001c0011t0001g0070 | 1 | 88 | 0.0114 | -17 | c.184 others(36): Show |
NELL1 | ENSG00000165973.19 | transcript | ENST00000357134.10 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| NELL1_chr11_20664586_21580686 | 20755539 | TGTTTTTT others(10): Show |
T | intron_variant | MODIFIER | NA18906.hp1 | a0011 | a0011c0017 | a0011c0017t0005 | a0011c0017t0005g0027 | 1 | 88 | 0.0114 | -17 | c.185 others(36): Show |
NELL1 | ENSG00000165973.19 | transcript | ENST00000357134.10 | protein_coding | 2/19 | chr11 | TogoVar | ||||||
| NELL1_chr11_20664586_21580686 | 20813006 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG02055.hp1 HG02257.hp2 HG02965.hp2 others(2): Show |
a0001a0002a0003others(1): Show | a0001c0005a0002c0002a0003c0020others(1): Show | a0001c0005t0001a0001c0005t0004a0002c0002t0001others(2): Show | a0001c0005t0001g0025a0001c0005t0004g0055a0002c0002t0001g0006others(2): Show | 5 | 88 | 0.0568 | -17 | c.335 others(36): Show |
NELL1 | ENSG00000165973.19 | transcript | ENST00000357134.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| NELL1_chr11_20664586_21580686 | 21337820 | CTTTCTTT others(10): Show |
C | intron_variant | MODIFIER | HG01891.hp1 NA19043.hp2 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0002 | a0001c0001t0001g0078a0001c0006t0002g0082 | 2 | 88 | 0.0227 | -17 | c.155 others(38): Show |
NELL1 | ENSG00000165973.19 | transcript | ENST00000357134.10 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| NELL1_chr11_20664586_21580686 | 21566694 | AGGATTAC others(10): Show |
A | intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0005 | a0001c0005t0004 | a0001c0005t0004g0055 | 1 | 88 | 0.0114 | -17 | c.198 others(36): Show |
NELL1 | ENSG00000165973.19 | transcript | ENST00000357134.10 | protein_coding | 17/19 | chr11 | TogoVar | ||||||
| NELL2_chr12_44503278_44881315 | 44528097 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0150 | 1 | 158 | 0.0063 | -17 | c.180 others(36): Show |
NELL2 | ENSG00000184613.11 | transcript | ENST00000429094.7 | protein_coding | 16/19 | chr12 | TogoVar | ||||||
| NELL2_chr12_44503278_44881315 | 44588075 | CGGGAGGT others(10): Show |
C | intron_variant | MODIFIER | HG02258.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0153a0001c0001t0005g0026 | 2 | 158 | 0.0127 | -17 | c.166 others(38): Show |
NELL2 | ENSG00000184613.11 | transcript | ENST00000429094.7 | protein_coding | 15/19 | chr12 | TogoVar | ||||||
| NET1_chr10_5407557_5464056 | 5436169 | GTGTGTGT others(10): Show |
G | intron_variant | MODIFIER | NA18982.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0339 | 1 | 380 | 0.0026 | -17 | c.255 others(34): Show |
NET1 | ENSG00000173848.19 | transcript | ENST00000355029.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
| NETO1_chr18_72738756_72872987 | 72846504 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0139 | 1 | 348 | 0.0029 | -17 | c.469 others(36): Show |
NETO1 | ENSG00000166342.19 | transcript | ENST00000327305.11 | protein_coding | 4/10 | chr18 | TogoVar | ||||||
| NEURL1B_chr5_172636263_172696540 | 172649345 | CTTTTTTT others(10): Show |
C | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(43): Show |
a0001a0002a0004 | a0001c0001a0002c0003a0004c0013 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0033others(41): Show | 46 | 392 | 0.1174 | -17 | c.31+ others(32): Show |
NEURL1B | ENSG00000214357.9 | transcript | ENST00000369800.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
| NEURL1_chr10_103488705_103597546 | 103515227 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | NA19066.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0129 | 1 | 312 | 0.0032 | -17 | c.85+ others(34): Show |
NEURL1 | ENSG00000107954.11 | transcript | ENST00000369780.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
| NEURL3_chr2_96492646_96510357 | 96494237 | AATATGGG others(10): Show |
A | downstream_gene_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(154): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0003a0003c0004others(3): Show | a0001c0001t0001a0001c0001t0005a0002c0003t0001others(4): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(43): Show | 157 | 394 | 0.3985 | -17 | c.*39 others(28): Show |
NEURL3 | ENSG00000163121.10 | transcript | ENST00000451794.6 | protein_coding | 3408 | chr2 | TogoVar | ||||||
| NEURL4_chr17_7310628_7334335 | 7334314 | GGGGAGGC others(10): Show |
G | upstream_gene_variant | MODIFIER | NA18993.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0103 | 1 | 408 | 0.0025 | -17 | c.-50 others(28): Show |
NEURL4 | ENSG00000215041.10 | transcript | ENST00000399464.7 | protein_coding | 4980 | chr17 | TogoVar | ||||||
| NEUROG3_chr10_69566698_69578422 | 69578168 | ATATGTTG others(10): Show |
A | upstream_gene_variant | MODIFIER | NA20752.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0002 | 1 | 444 | 0.0023 | -17 | c.-49 others(28): Show |
NEUROG3 | ENSG00000122859.5 | transcript | ENST00000242462.5 | protein_coding | 4747 | chr10 | TogoVar | ||||||
| NEXN_chr1_77883624_77948895 | 77887988 | TTCTTCTT others(10): Show |
T | upstream_gene_variant | MODIFIER | HG00639.hp2 HG01071.hp1 HG01433.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0065a0001c0001t0001g0080a0001c0001t0001g0085others(8): Show | 11 | 268 | 0.0410 | -17 | c.-82 others(26): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 635 | chr1 | TogoVar | ||||||
| NEXN_chr1_77883624_77948895 | 77895029 | ATTTTTTT others(10): Show |
A | intron_variant | MODIFIER | HG02258.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0012 | 1 | 268 | 0.0037 | -17 | c.-53 others(34): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
| NF1_chr17_31089977_31382675 | 31109379 | CTTTTTTT others(10): Show |
C | intron_variant | MODIFIER | HG03239.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0078 | 1 | 252 | 0.0040 | -17 | c.60+ others(34): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 1/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
| NF1_chr17_31089977_31382675 | 31117672 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG02145.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0031a0001c0001t0005g0119a0001c0001t0005g0120others(1): Show | 4 | 252 | 0.0159 | -17 | c.60+ others(34): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 1/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
| NF1_chr17_31089977_31382675 | 31242305 | CTTTTTTT others(10): Show |
C | intron_variant | MODIFIER | NA18974.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0171 | 1 | 252 | 0.0040 | -17 | c.397 others(36): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 29/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
| NF1_chr17_31089977_31382675 | 31278493 | CTTTTTTT others(10): Show |
C | intron_variant | MODIFIER | HG03139.hp1 HG03209.hp2 NA19240.hp1 |
a0001 | a0001c0004 | a0001c0004t0009a0001c0004t0021 | a0001c0004t0009g0129a0001c0004t0009g0130a0001c0004t0021g0128 | 3 | 252 | 0.0119 | -17 | c.483 others(38): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 36/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
| NF1_chr17_31089977_31382675 | 31293178 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG03139.hp1 HG03209.hp2 NA19240.hp1 |
a0001 | a0001c0004 | a0001c0004t0009a0001c0004t0021 | a0001c0004t0009g0129a0001c0004t0009g0130a0001c0004t0021g0128 | 3 | 252 | 0.0119 | -17 | c.483 others(38): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 36/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
| NF1_chr17_31089977_31382675 | 31322501 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG02109.hp2 HG03209.hp1 NA18522.hp2 |
a0001 | a0001c0001a0001c0021 | a0001c0001t0003a0001c0021t0003 | a0001c0001t0003g0123a0001c0001t0003g0125a0001c0021t0003g0124 | 3 | 252 | 0.0119 | -17 | c.483 others(36): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 36/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
| NF2_chr22_29598633_29703598 | 29644918 | AGGGAGAG others(10): Show |
A | intron_variant | MODIFIER | NA18984.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0042 | 1 | 344 | 0.0029 | -17 | c.447 others(34): Show |
NF2 | ENSG00000186575.19 | transcript | ENST00000338641.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
| NFAM1_chr22_42375407_42437403 | 42378251 | CAAAAAAA others(10): Show |
C | downstream_gene_variant | MODIFIER | HG01928.hp2 HG02155.hp2 HG03017.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0010a0001c0001t0015a0001c0003t0007 | a0001c0001t0010g0218a0001c0001t0015g0127a0001c0003t0007g0174 | 3 | 384 | 0.0078 | -17 | c.*68 others(28): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2155 | chr22 | TogoVar | ||||||
| NFAM1_chr22_42375407_42437403 | 42419989 | GGTTTTTT others(10): Show |
G | intron_variant | MODIFIER | HG03471.hp1 NA21309.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0031a0001c0001t0004g0033 | 2 | 384 | 0.0052 | -17 | c.122 others(34): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | TogoVar | ||||||
| NFASC_chr1_204823652_205027822 | 204877020 | ATATATAT others(10): Show |
A | intron_variant | MODIFIER | HG03139.hp1 | a0002 | a0002c0006 | a0002c0006t0003 | a0002c0006t0003g0128 | 1 | 226 | 0.0044 | -17 | c.-19 others(38): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000339876.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
| NFASC_chr1_204865862_205027822 | 204877020 | ATATATAT others(10): Show |
A | intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0133 | 1 | 264 | 0.0038 | -17 | c.-91 others(34): Show |
NFASC | ENSG00000163531.17 | transcript | ENST00000539706.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
| NFAT5_chr16_69560966_69709654 | 69561005 | TAAAAAAA others(10): Show |
T | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
a0001a0004a0005 | a0001c0001a0001c0003a0004c0010others(1): Show | a0001c0001t0002a0001c0001t0009a0001c0001t0015others(8): Show | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0108others(61): Show | 64 | 380 | 0.1684 | -17 | c.-52 others(28): Show |
NFAT5 | ENSG00000102908.23 | transcript | ENST00000349945.7 | protein_coding | 4960 | chr16 | TogoVar | ||||||
| NFATC1_chr18_79390930_79534323 | 79395581 | GCCCCCCT others(10): Show |
G | upstream_gene_variant | MODIFIER | HG02258.hp1 NA19043.hp2 |
a0001a0002 | a0001c0013a0002c0002 | a0001c0013t0056a0002c0002t0031 | a0001c0013t0056g0110a0002c0002t0031g0115 | 2 | 322 | 0.0062 | -17 | c.-64 others(26): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 348 | chr18 | TogoVar | ||||||
| NFATC1_chr18_79390930_79534323 | 79395627 | TGCGCCCC others(10): Show |
T | upstream_gene_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0018 | a0001c0018t0009 | a0001c0018t0009g0128 | 1 | 322 | 0.0031 | -17 | c.-59 others(26): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 302 | chr18 | TogoVar | ||||||
| NFATC1_chr18_79390930_79534323 | 79395660 | GGCGCCCC others(10): Show |
G | upstream_gene_variant | MODIFIER | HG01891.hp1 HG02257.hp1 |
a0002 | a0002c0023 | a0002c0023t0019 | a0002c0023t0019g0317a0002c0023t0019g0318 | 2 | 322 | 0.0062 | -17 | c.-56 others(26): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 269 | chr18 | TogoVar | ||||||
| NFATC1_chr18_79390930_79534323 | 79395681 | CCCCCCCC others(10): Show |
C | upstream_gene_variant | MODIFIER | NA20752.hp2 | a0003 | a0003c0007 | a0003c0007t0008 | a0003c0007t0008g0029 | 1 | 322 | 0.0031 | -17 | c.-54 others(26): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 248 | chr18 | TogoVar | ||||||
| NFATC1_chr18_79390930_79534323 | 79417119 | TGGGAGAT others(10): Show |
T | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(95): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0001c0005others(26): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(62): Show | a0001c0001t0001g0242a0001c0001t0001g0257a0001c0001t0003g0143others(94): Show | 98 | 322 | 0.3044 | -17 | c.122 others(36): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
| NFATC1_chr18_79390930_79534323 | 79417540 | ATGGGAGA others(10): Show |
A | intron_variant | MODIFIER | HG01081.hp1 HG02615.hp1 HG03139.hp1 others(1): Show |
a0001 | a0001c0010a0001c0025 | a0001c0010t0004a0001c0025t0002a0001c0025t0025 | a0001c0010t0004g0289a0001c0010t0004g0290a0001c0025t0002g0304others(1): Show | 4 | 322 | 0.0124 | -17 | c.122 others(36): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
| NFATC1_chr18_79390930_79534323 | 79417581 | ATGGGAGA others(10): Show |
A | intron_variant | MODIFIER | HG01255.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
a0001a0002 | a0001c0004a0001c0005a0001c0006others(8): Show | a0001c0004t0002a0001c0005t0005a0001c0006t0002others(11): Show | a0001c0004t0002g0315a0001c0005t0005g0083a0001c0006t0002g0307others(15): Show | 18 | 322 | 0.0559 | -17 | c.122 others(36): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
| NFATC1_chr18_79390930_79534323 | 79417930 | GGGAGATG others(10): Show |
G | intron_variant | MODIFIER | HG01433.hp2 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0216 | 1 | 322 | 0.0031 | -17 | c.122 others(36): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
| NFATC1_chr18_79390930_79534323 | 79487054 | GCAGGGTG others(10): Show |
G | intron_variant | MODIFIER | NA18939.hp1 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0244 | 1 | 322 | 0.0031 | -17 | c.278 others(34): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
| NFATC2_chr20_51381963_51547719 | 51411516 | CTTTTTTT others(10): Show |
C | intron_variant | MODIFIER | HG03654.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0040 | 1 | 316 | 0.0032 | -17 | c.272 others(38): Show |
NFATC2 | ENSG00000101096.20 | transcript | ENST00000371564.8 | protein_coding | 9/10 | chr20 | TogoVar | ||||||
| NFATC3_chr16_68080370_68234259 | 68167810 | CTTTTTTT others(10): Show |
C | intron_variant | MODIFIER | HG02486.hp2 HG02723.hp2 |
a0001 | a0001c0001 | a0001c0001t0012a0001c0001t0028 | a0001c0001t0012g0185a0001c0001t0028g0040 | 2 | 188 | 0.0106 | -17 | c.177 others(34): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
| NFATC3_chr16_68080370_68234259 | 68222289 | CAAAAAAA others(10): Show |
C | intron_variant | MODIFIER | HG01256.hp1 HG01258.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | 188 | 0.0106 | -17 | c.310 others(36): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
| NFE2L3_chr7_26147198_26192137 | 26161348 | TTTTTTTT others(10): Show |
T | intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0002 | a0001c0002t0015 | a0001c0002t0015g0269 | 1 | 400 | 0.0025 | -17 | c.570 others(34): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | TogoVar | ||||||
| NFIA_chr1_61077561_61467788 | 61306261 | ATTTTGTT others(10): Show |
A | intron_variant | MODIFIER | HG02145.hp1 HG02145.hp2 HG02647.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(10): Show | a0001c0001t0001g0068a0001c0001t0004g0146a0001c0001t0008g0123others(10): Show | 13 | 156 | 0.0833 | -17 | c.626 others(36): Show |
NFIA | ENSG00000162599.18 | transcript | ENST00000403491.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
| NFIB_chr9_14076848_14319141 | 14080447 | CTTTTTTT others(10): Show |
C | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0015others(6): Show | a0001c0001t0002g0139a0001c0001t0002g0225a0001c0001t0002g0227others(19): Show | 22 | 304 | 0.0724 | -17 | c.*78 others(28): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 1400 | chr9 | TogoVar | ||||||
| NFIB_chr9_14076848_14319141 | 14231132 | AAAAATAT others(10): Show |
A | intron_variant | MODIFIER | HG02647.hp2 | a0001 | a0001c0001 | a0001c0001t0078 | a0001c0001t0078g0155 | 1 | 304 | 0.0033 | -17 | c.563 others(36): Show |
NFIB | ENSG00000147862.18 | transcript | ENST00000380953.6 | protein_coding | 2/10 | chr9 | TogoVar |