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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
MYT1_chr20_64159452_64247253 | 64174630 | C | CCTGCAGC others(90): Show |
intron_variant | MODIFIER | HG01256.hp1 | a0003 | a0003c0009 | a0003c0009t0001 | a0003c0009t0001g0046 | 1 | 152 | 0.0066 | 97 | c.-99 others(114): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64174968 | C | CTGGCTTC others(90): Show |
intron_variant | MODIFIER | HG01256.hp1 | a0003 | a0003c0009 | a0003c0009t0001 | a0003c0009t0001g0046 | 1 | 222 | 0.0045 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175031 | T | TAGCATCT others(90): Show |
intron_variant | MODIFIER | HG00099.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0089 | 1 | 118 | 0.0085 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175045 | G | GTAGTTGT others(90): Show |
intron_variant | MODIFIER | HG02922.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0002t0002others(1): Show | a0001c0001t0002g0085 a0001c0001t0003g0095 a0001c0002t0002g0003 others(2): Show |
6 | 187 | 0.0321 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175095 | G | GTAGTTGT others(90): Show |
intron_variant | MODIFIER | HG02602.hp1 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0039 | 1 | 219 | 0.0046 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175177 | C | CCTGTAGC others(90): Show |
intron_variant | MODIFIER | HG01256.hp1 | a0003 | a0003c0009 | a0003c0009t0001 | a0003c0009t0001g0046 | 1 | 117 | 0.0085 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175180 | C | CCTGCAGC others(90): Show |
intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0113 | 1 | 221 | 0.0045 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175184 | C | CAGCATCT others(90): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0108 | 1 | 163 | 0.0061 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175198 | G | GTAGTTGT others(90): Show |
intron_variant | MODIFIER | HG01258.hp1 | a0003 | a0003c0009 | a0003c0009t0001 | a0003c0009t0001g0045 | 1 | 214 | 0.0047 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175198 | G | GTAGTTGT others(90): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0002 | a0001c0002t0006 | a0001c0002t0006g0127 | 1 | 214 | 0.0047 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175395 | G | GTAGTTGT others(90): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0153 | 1 | 222 | 0.0045 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175530 | C | CCTGCAGC others(90): Show |
intron_variant | MODIFIER | HG02129.hp2 HG03669.hp2 HG03704.hp1 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0002a0001c0004t0004 | a0001c0002t0002g0036 a0001c0004t0004g0037 a0001c0004t0004g0038 |
3 | 115 | 0.0261 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175651 | G | GTAGTTGT others(90): Show |
intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0218 | 1 | 208 | 0.0048 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175845 | G | GTAGTTGT others(90): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0010 | 1 | 222 | 0.0045 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64175942 | C | CCTGTAGT others(90): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0085 | 1 | 114 | 0.0088 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | chr20 | TogoVar | |||||||
MYT1_chr20_64159452_64247253 | 64176074 | C | CCTGCAGC others(90): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0091 | 1 | 101 | 0.0099 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64176131 | C | CAGCATCT others(90): Show |
intron_variant | MODIFIER | HG00558.hp1 HG00597.hp2 HG01934.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0002t0002a0001c0004t0004 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0002t0002g0123 others(1): Show |
4 | 184 | 0.0217 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64176227 | C | CCTCCTGC others(90): Show |
intron_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0015 | 1 | 49 | 0.0204 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64176227 | C | CCTGCAGC others(90): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00733.hp1 HG01070.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0006a0001c0003t0007others(1): Show | a0001c0001t0001g0162 a0001c0001t0001g0185 a0001c0001t0001g0187 others(7): Show |
10 | 58 | 0.1724 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64176227 | C | CCTGTAGC others(90): Show |
intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0013 | 1 | 49 | 0.0204 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64176280 | C | CCTGCAGC others(90): Show |
intron_variant | MODIFIER | HG01516.hp2 | a0001 | a0001c0003 | a0001c0003t0007 | a0001c0003t0007g0213 | 1 | 206 | 0.0049 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
MYT1_chr20_64159452_64247253 | 64176390 | C | CAGCATCT others(90): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0053 | 1 | 220 | 0.0045 | 97 | c.-99 others(116): Show |
MYT1 | ENSG00000196132.14 | transcript | ENST00000328439.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
NAA15_chr4_139296505_139396384 | 139385283 | A | AATATATA others(90): Show |
intron_variant | MODIFIER | NA19005.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0076 | 1 | 218 | 0.0046 | 97 | c.230 others(114): Show |
NAA15 | ENSG00000164134.14 | transcript | ENST00000296543.10 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21331558 | A | ATATATAT others(90): Show |
intron_variant | MODIFIER | HG02622.hp2 HG02970.hp1 |
a0002 | a0002c0002a0002c0003 | a0002c0002t0004a0002c0003t0017 | a0002c0002t0004g0049 a0002c0003t0017g0038 |
2 | 121 | 0.0165 | 97 | c.738 others(114): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 6/17 | chr21 | TogoVar | |||||||
NCAPH2_chr22_50503224_50529780 | 50504145 | A | ACCCCCCG others(90): Show |
upstream_gene_variant | MODIFIER | HG01109.hp1 | a0003 | a0003c0018 | a0003c0018t0002 | a0003c0018t0002g0058 | 1 | 36 | 0.0278 | 97 | c.-41 others(108): Show |
NCAPH2 | ENSG00000025770.19 | transcript | ENST00000420993.7 | protein_coding | 4078 | chr22 | TogoVar | |||||||
NCEH1_chr3_172625249_172716067 | 172712515 | C | CGGAGGAG others(90): Show |
upstream_gene_variant | MODIFIER | HG03704.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0219 | 1 | 330 | 0.0030 | 97 | c.-15 others(108): Show |
NCEH1 | ENSG00000144959.11 | transcript | ENST00000475381.7 | protein_coding | 1449 | chr3 | TogoVar | |||||||
NCS1_chr9_130167404_130242303 | 130221938 | A | ATATAAAT others(90): Show |
intron_variant | MODIFIER | HG01167.hp1 HG01169.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0095 a0001c0001t0004g0096 |
2 | 330 | 0.0061 | 97 | c.308 others(112): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
NDC80_chr18_2566557_2621635 | 2614649 | G | GAAAGAAA others(90): Show |
intron_variant | MODIFIER | NA18991.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0162 | 1 | 400 | 0.0025 | 97 | c.179 others(116): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NDUFV3_chr21_42888309_42918299 | 42894351 | A | AATATATA others(90): Show |
intron_variant | MODIFIER | HG02280.hp1 HG02896.hp1 NA18906.hp2 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0010 a0002c0002t0002g0163 |
3 | 279 | 0.0108 | 97 | c.48+ others(110): Show |
NDUFV3 | ENSG00000160194.18 | transcript | ENST00000354250.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NDUFV3_chr21_42888309_42918299 | 42894351 | A | AATATATA others(90): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0008 | 1 | 277 | 0.0036 | 97 | c.48+ others(110): Show |
NDUFV3 | ENSG00000160194.18 | transcript | ENST00000354250.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NDUFV3_chr21_42888309_42918299 | 42894351 | A | AATATATA others(90): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0095 | 1 | 277 | 0.0036 | 97 | c.48+ others(110): Show |
NDUFV3 | ENSG00000160194.18 | transcript | ENST00000354250.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NDUFV3_chr21_42888309_42918299 | 42894401 | T | TATTATAT others(90): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0002 | a0002c0002 | a0002c0002t0013 | a0002c0002t0013g0060 | 1 | 202 | 0.0050 | 97 | c.48+ others(112): Show |
NDUFV3 | ENSG00000160194.18 | transcript | ENST00000354250.7 | protein_coding | 1/3 | chr21 | TogoVar | |||||||
NEDD4L_chr18_58039226_58406539 | 58130177 | C | CGGAACTG others(90): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00738.hp2 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0034 a0001c0001t0001g0056 a0001c0001t0001g0083 others(24): Show |
27 | 116 | 0.2328 | 97 | c.49- others(114): Show |
NEDD4L | ENSG00000049759.20 | transcript | ENST00000400345.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NEK11_chr3_131021877_131355465 | 131350127 | A | ACAGAGCT others(90): Show |
3_prime_UTR_variant | MODIFIER | HG02723.hp1 | a0010 | a0010c0012 | a0010c0012t0003 | a0010c0012t0003g0272 | 1 | 290 | 0.0034 | 97 | c.*35 others(106): Show |
NEK11 | ENSG00000114670.14 | transcript | ENST00000383366.9 | protein_coding | 18/18 | 450 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
NEXMIF_chrX_74727856_74930452 | 74796181 | A | ATTTATAT others(90): Show |
intron_variant | MODIFIER | HG02615.hp2 HG02809.hp1 HG03041.hp2 |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0098 a0001c0001t0006g0218 a0001c0001t0006g0219 |
3 | 219 | 0.0137 | 97 | c.-47 others(116): Show |
NEXMIF | ENSG00000050030.16 | transcript | ENST00000055682.12 | protein_coding | 1/3 | chrX | TogoVar | |||||||
NEXN_chr1_77883624_77948895 | 77887930 | C | CTTCTTCT others(90): Show |
upstream_gene_variant | MODIFIER | NA18982.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0074 | 1 | 266 | 0.0038 | 97 | c.-88 others(106): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 693 | chr1 | TogoVar | |||||||
NF1_chr17_31089977_31382675 | 31335275 | T | TATATATA others(90): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00673.hp1 HG00735.hp2 others(14): Show |
a0001a0006 | a0001c0001a0001c0003a0006c0022 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(4): Show | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0033 others(14): Show |
17 | 244 | 0.0697 | 97 | c.600 others(114): Show |
NF1 | ENSG00000196712.20 | transcript | ENST00000358273.9 | protein_coding | 40/57 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400833 | C | CCCCTCCC others(90): Show |
intron_variant | MODIFIER | HG03130.hp2 | a0009 | a0009c0033 | a0009c0033t0026 | a0009c0033t0026g0101 | 1 | 312 | 0.0032 | 97 | c.127 others(114): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400833 | C | CCCCTCCC others(90): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0010 | a0001c0010t0004 | a0001c0010t0004g0289 | 1 | 312 | 0.0032 | 97 | c.127 others(114): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400834 | C | CCCTCCCC others(90): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0018 | a0001c0018t0009 | a0001c0018t0009g0128 | 1 | 297 | 0.0034 | 97 | c.127 others(114): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400834 | C | CCCTCCCC others(90): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0002 | a0002c0036 | a0002c0036t0012 | a0002c0036t0012g0010 | 1 | 297 | 0.0034 | 97 | c.127 others(114): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400834 | C | CCCTCCCC others(90): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0013 | a0001c0013t0056 | a0001c0013t0056g0110 | 1 | 297 | 0.0034 | 97 | c.127 others(114): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79400835 | C | CCTCCCCC others(90): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0004 | a0001c0004t0004 | a0001c0004t0004g0078 | 1 | 290 | 0.0034 | 97 | c.127 others(114): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
NGB_chr14_77260483_77276206 | 77269727 | T | TCTCTCTC others(90): Show |
intron_variant | MODIFIER | HG01433.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0098 | 1 | 285 | 0.0035 | 97 | c.90- others(110): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | TogoVar | |||||||
NGEF_chr2_232873701_233018256 | 232995422 | C | CTGTATAT others(90): Show |
intron_variant | MODIFIER | NA18944.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0350 | 1 | 145 | 0.0069 | 97 | c.-75 others(116): Show |
NGEF | ENSG00000066248.15 | transcript | ENST00000264051.8 | protein_coding | 1/14 | chr2 | TogoVar | |||||||
NLRP4_chr19_55831540_55886855 | 55850788 | C | CCCGAGGC others(90): Show |
intron_variant | MODIFIER | HG03654.hp2 NA20905.hp1 |
a0001a0012 | a0001c0001a0012c0031 | a0001c0001t0018a0012c0031t0001 | a0001c0001t0018g0367 a0012c0031t0001g0027 |
2 | 349 | 0.0057 | 97 | c.-65 others(114): Show |
NLRP4 | ENSG00000160505.16 | transcript | ENST00000301295.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NOC2L_chr1_939203_964256 | 939398 | G | GCCTCCCC others(90): Show |
downstream_gene_variant | MODIFIER | HG02615.hp1 | a0004 | a0004c0005 | a0004c0005t0003 | a0004c0005t0003g0082 | 1 | 376 | 0.0027 | 97 | c.*51 others(108): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4804 | chr1 | TogoVar | |||||||
NOC4L_chr12_132139457_132157468 | 132150015 | T | TCACACAC others(90): Show |
intron_variant | MODIFIER | NA18998.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0049 | 1 | 110 | 0.0091 | 97 | c.902 others(112): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NOTCH3_chr19_15154038_15205995 | 15173744 | A | AGAAGAAG others(90): Show |
intron_variant | MODIFIER | HG02717.hp2 | a0007 | a0007c0036 | a0007c0036t0017 | a0007c0036t0017g0091 | 1 | 331 | 0.0030 | 97 | c.473 others(114): Show |
NOTCH3 | ENSG00000074181.9 | transcript | ENST00000263388.7 | protein_coding | 25/32 | chr19 | TogoVar | |||||||
NPAS3_chr14_32933879_33809173 | 33477059 | A | ACACCCTT others(90): Show |
intron_variant | MODIFIER | HG01261.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0060 | 1 | 90 | 0.0111 | 97 | c.469 others(116): Show |
NPAS3 | ENSG00000151322.20 | transcript | ENST00000356141.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | TogoVar |