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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NFATC1_chr18_79390930_79534323 | 79484495 | TACTCAGT others(34): Show |
T | intron_variant | MODIFIER | HG01256.hp1 HG01258.hp1 |
a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0300a0001c0004t0002g0301 | 2 | 322 | 0.0062 | -41 | c.209 others(60): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
NFIC_chr19_3361583_3474217 | 3381536 | TTGCGTGC others(34): Show |
T | intron_variant | MODIFIER | HG01109.hp2 HG03471.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0194 | a0001c0001t0006g0228a0001c0001t0194g0227 | 2 | 300 | 0.0067 | -41 | c.31- others(54): Show |
NFIC | ENSG00000141905.19 | transcript | ENST00000443272.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
NGB_chr14_77260483_77276206 | 77269686 | CTCTCTCT others(34): Show |
C | intron_variant | MODIFIER | HG00323.hp2 HG01346.hp1 HG02135.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0181others(3): Show | 9 | 366 | 0.0246 | -41 | c.90- others(54): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | TogoVar | ||||||
NGB_chr14_77260483_77276206 | 77269762 | TCTCTCTC others(34): Show |
T | intron_variant | MODIFIER | HG02056.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0205 | 1 | 366 | 0.0027 | -41 | c.90- others(54): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | TogoVar | ||||||
NGLY1_chr3_25713944_25788443 | 25760860 | CAAAAAAA others(34): Show |
C | intron_variant | MODIFIER | HG01169.hp1 HG03688.hp1 HG03704.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0007 | a0001c0001t0001g0198a0001c0001t0004g0090a0001c0001t0007g0167 | 3 | 264 | 0.0114 | -41 | c.492 others(58): Show |
NGLY1 | ENSG00000151092.18 | transcript | ENST00000280700.10 | protein_coding | 3/11 | chr3 | TogoVar | ||||||
NKD2_chr5_1003802_1043943 | 1022149 | CTGTCCCT others(34): Show |
C | intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0109 | 1 | 319 | 0.0031 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1022346 | TCAGCCCA others(34): Show |
T | intron_variant | MODIFIER | NA20752.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0261 | 1 | 319 | 0.0031 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1022353 | ATTGTCCC others(34): Show |
A | intron_variant | MODIFIER | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
a0001a0005a0007 | a0001c0001a0001c0016a0001c0017others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0016t0002others(3): Show | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(63): Show | 75 | 319 | 0.2351 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1022873 | AGTGGGTG others(34): Show |
A | intron_variant | MODIFIER | HG02809.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0003a0001c0005t0011 | a0001c0001t0003g0002a0001c0005t0011g0002 | 4 | 319 | 0.0125 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1022911 | CTCTGTGG others(34): Show |
C | intron_variant | MODIFIER | HG02071.hp1 | a0009 | a0009c0013 | a0009c0013t0017 | a0009c0013t0017g0098 | 1 | 319 | 0.0031 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | TogoVar | ||||||
NKD2_chr5_1003802_1043943 | 1023158 | GCTGTGGG others(34): Show |
G | intron_variant | MODIFIER | HG01358.hp1 HG03225.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0002a0001c0005t0011 | a0001c0001t0002g0029a0001c0005t0011g0114 | 2 | 319 | 0.0063 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1023470 | CCTGCTCT others(34): Show |
C | intron_variant | MODIFIER | HG00639.hp1 HG00741.hp1 HG01496.hp2 others(7): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0003 | a0001c0002t0001g0185a0001c0002t0001g0194a0001c0002t0003g0006others(5): Show | 10 | 319 | 0.0314 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1023486 | GCTGTGGG others(34): Show |
G | intron_variant | MODIFIER | HG00408.hp1 HG01168.hp2 HG02132.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0012a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0012t0001others(1): Show | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0044others(5): Show | 8 | 319 | 0.0251 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1023673 | TCCCTGCT others(34): Show |
T | intron_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0029 | 1 | 319 | 0.0031 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1023855 | GCTGTGGG others(34): Show |
G | intron_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0029 | 1 | 319 | 0.0031 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024019 | GCTGTGGG others(34): Show |
G | intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0086 | 1 | 319 | 0.0031 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024060 | TCTGTGGG others(34): Show |
T | intron_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0029 | 1 | 319 | 0.0031 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024113 | CCAGCCCA others(34): Show |
C | intron_variant | MODIFIER | HG02055.hp2 HG02965.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | 319 | 0.0063 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024154 | TCAGCCCA others(34): Show |
T | intron_variant | MODIFIER | HG00408.hp1 HG01168.hp2 HG01515.hp1 others(13): Show |
a0001 | a0001c0001a0001c0010a0001c0012 | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0036others(13): Show | 16 | 319 | 0.0502 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024306 | GCTGTGGG others(34): Show |
G | intron_variant | MODIFIER | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(88): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0016a0001c0017others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0016t0002others(5): Show | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(78): Show | 91 | 319 | 0.2853 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024325 | GTTGTCCC others(34): Show |
G | intron_variant | MODIFIER | NA18997.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0225 | 1 | 319 | 0.0031 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024550 | CCGCTGTG others(34): Show |
C | intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0054 | 1 | 319 | 0.0031 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024561 | GTCTCAGC others(34): Show |
G | intron_variant | MODIFIER | HG01074.hp2 HG01261.hp2 HG01978.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0049others(4): Show | 7 | 319 | 0.0219 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024564 | TCAGCCCA others(34): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
a0001a0002a0009 | a0001c0001a0001c0006a0001c0008others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(72): Show | 86 | 319 | 0.2696 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024653 | TTTGTCCC others(34): Show |
T | intron_variant | MODIFIER | HG02809.hp2 HG03453.hp1 NA20129.hp1 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0003a0001c0005t0011 | a0001c0001t0003g0002a0001c0005t0011g0002 | 3 | 319 | 0.0094 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024769 | TCAGCCCG others(34): Show |
T | intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0117 | 1 | 319 | 0.0031 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024796 | CCGCTGTG others(34): Show |
C | intron_variant | MODIFIER | HG01106.hp2 HG01358.hp1 HG02040.hp2 others(18): Show |
a0001a0002a0003 | a0001c0001a0002c0003a0003c0004 | a0001c0001t0002a0002c0003t0002a0003c0004t0001others(1): Show | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0029others(17): Show | 21 | 319 | 0.0658 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024810 | CCAGCCCT others(34): Show |
C | intron_variant | MODIFIER | HG00558.hp1 HG02738.hp2 NA19007.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023a0001c0001t0001g0207a0001c0001t0001g0236 | 4 | 319 | 0.0125 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024880 | GCTGTGGG others(34): Show |
G | intron_variant | MODIFIER | HG00558.hp1 HG02055.hp2 HG02738.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0007 | a0001c0001t0001g0023a0001c0001t0001g0207a0001c0001t0001g0236others(3): Show | 7 | 319 | 0.0219 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1024892 | CCAGCCCT others(34): Show |
C | intron_variant | MODIFIER | HG01074.hp2 HG02015.hp1 HG03239.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0012 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0051others(3): Show | 6 | 319 | 0.0188 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1025126 | GCTGTGGG others(34): Show |
G | intron_variant | MODIFIER | HG00558.hp1 HG02738.hp2 NA19064.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0023a0001c0001t0001g0207a0001c0001t0001g0236others(1): Show | 4 | 319 | 0.0125 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1025145 | TTTGTCCC others(34): Show |
T | intron_variant | MODIFIER | NA18939.hp1 NA18981.hp1 |
a0001 | a0001c0006 | a0001c0006t0009 | a0001c0006t0009g0072a0001c0006t0009g0097 | 2 | 319 | 0.0063 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1025493 | CCGCTGTG others(34): Show |
C | intron_variant | MODIFIER | HG02071.hp1 | a0009 | a0009c0013 | a0009c0013t0017 | a0009c0013t0017g0098 | 1 | 319 | 0.0031 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1026001 | TCAGCCCA others(34): Show |
T | intron_variant | MODIFIER | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(102): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0016a0001c0017others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(7): Show | a0001c0001t0001g0047a0001c0001t0001g0168a0001c0001t0001g0177others(89): Show | 105 | 319 | 0.3292 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NKD2_chr5_1003802_1043943 | 1026248 | TCAGCCCA others(34): Show |
T | intron_variant | MODIFIER | NA18948.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0186 | 1 | 319 | 0.0031 | -41 | c.142 others(58): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NLRP4_chr19_55831540_55886855 | 55851492 | TGGCTGCG others(34): Show |
T | intron_variant | MODIFIER | HG02258.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
a0002 | a0002c0002a0002c0003a0002c0017others(1): Show | a0002c0002t0005a0002c0003t0015a0002c0017t0020others(1): Show | a0002c0002t0005g0362a0002c0003t0015g0224a0002c0017t0020g0284others(1): Show | 4 | 424 | 0.0094 | -41 | c.-65 others(56): Show |
NLRP4 | ENSG00000160505.16 | transcript | ENST00000301295.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
NLRP5_chr19_55994726_56066810 | 56000017 | CCCACTCT others(34): Show |
C | intron_variant | MODIFIER | HG02572.hp2 HG02647.hp1 HG02818.hp1 others(5): Show |
a0004a0005a0012others(1): Show | a0004c0020a0004c0035a0005c0113others(2): Show | a0004c0020t0001a0004c0020t0003a0004c0035t0001others(3): Show | a0004c0020t0001g0096a0004c0020t0003g0098a0004c0035t0001g0094others(5): Show | 8 | 396 | 0.0202 | -41 | c.62+ others(54): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
NLRP5_chr19_55994726_56066810 | 56000130 | CGGCCACC others(34): Show |
C | intron_variant | MODIFIER | HG03195.hp2 | a0007 | a0007c0010 | a0007c0010t0001 | a0007c0010t0001g0391 | 1 | 396 | 0.0025 | -41 | c.62+ others(54): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
NME8_chr7_37843597_37905397 | 37848214 | AGAAGAAG others(34): Show |
A | upstream_gene_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0027 | 1 | 388 | 0.0026 | -41 | c.-75 others(50): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 382 | chr7 | TogoVar | ||||||
NME8_chr7_37843597_37905397 | 37848217 | AGAAGAAG others(34): Show |
A | upstream_gene_variant | MODIFIER | NA18975.hp1 NA19058.hp1 NA19078.hp1 others(1): Show |
a0001a0004 | a0001c0001a0004c0012 | a0001c0001t0001a0001c0001t0003a0004c0012t0001 | a0001c0001t0001g0116a0001c0001t0003g0005a0004c0012t0001g0004others(1): Show | 4 | 388 | 0.0103 | -41 | c.-75 others(50): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 379 | chr7 | TogoVar | ||||||
NME8_chr7_37843597_37905397 | 37848220 | AGAAGAAG others(34): Show |
A | upstream_gene_variant | MODIFIER | NA19087.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0046 | 1 | 388 | 0.0026 | -41 | c.-74 others(50): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 376 | chr7 | TogoVar | ||||||
NOL6_chr9_33456353_33478924 | 33475144 | ATATATAT others(34): Show |
A | upstream_gene_variant | MODIFIER | HG02257.hp2 HG03516.hp1 |
a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0080a0001c0002t0005g0081 | 2 | 438 | 0.0046 | -41 | c.-13 others(52): Show |
NOL6 | ENSG00000165271.17 | transcript | ENST00000297990.9 | protein_coding | 1221 | chr9 | TogoVar | ||||||
NOP14_chr4_2932936_2968406 | 2960888 | ATTATTAT others(34): Show |
A | intron_variant | MODIFIER | NA19011.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0213 | 1 | 422 | 0.0024 | -41 | c.195 others(58): Show |
NOP14 | ENSG00000087269.16 | transcript | ENST00000416614.7 | protein_coding | 1/17 | chr4 | TogoVar | ||||||
NOTCH3_chr19_15154038_15205995 | 15173727 | AAAAAAAA others(34): Show |
A | intron_variant | MODIFIER | NA18999.hp1 NA18999.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0001 | a0001c0001t0001g0279a0001c0005t0001g0134 | 2 | 340 | 0.0059 | -41 | c.473 others(58): Show |
NOTCH3 | ENSG00000074181.9 | transcript | ENST00000263388.7 | protein_coding | 25/32 | chr19 | TogoVar | ||||||
NPY4R_chr10_46456099_46470958 | 46466249 | TTCTTTCT others(34): Show |
T | upstream_gene_variant | MODIFIER | HG02622.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0019 | 1 | 290 | 0.0035 | -41 | c.-82 others(50): Show |
NPY4R | ENSG00000204174.8 | transcript | ENST00000374312.5 | protein_coding | 292 | chr10 | TogoVar | ||||||
NRDC_chr1_51784210_51883727 | 51846992 | TGATTGGT others(34): Show |
T | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp1 |
a0002 | a0002c0007 | a0002c0007t0001 | a0002c0007t0001g0160a0002c0007t0001g0182 | 2 | 244 | 0.0082 | -41 | c.342 others(58): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | TogoVar | ||||||
NRDC_chr1_51784210_51883727 | 51847093 | CAGCTAGA others(34): Show |
C | intron_variant | MODIFIER | NA18991.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0009 | 1 | 244 | 0.0041 | -41 | c.342 others(58): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | TogoVar | ||||||
NRXN1_chr2_49913503_51037132 | 50399789 | TAAAAAAA others(34): Show |
T | intron_variant | MODIFIER | HG01884.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0006a0001c0001t0014a0001c0002t0005 | a0001c0001t0006g0023a0001c0001t0006g0027a0001c0001t0014g0022others(2): Show | 5 | 116 | 0.0431 | -41 | c.336 others(62): Show |
NRXN1 | ENSG00000179915.25 | transcript | ENST00000401669.7 | protein_coding | 17/22 | chr2 | TogoVar | ||||||
NTAN1_chr16_15032857_15061074 | 15050888 | AAACTAAA others(34): Show |
A | intron_variant | MODIFIER | HG03017.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0199 | 1 | 453 | 0.0022 | -41 | c.82- others(56): Show |
NTAN1 | ENSG00000157045.9 | transcript | ENST00000287706.8 | protein_coding | 1/9 | chr16 | TogoVar | ||||||
NTM_chr11_131365615_132341822 | 131465801 | GTGGCAGG others(34): Show |
G | intron_variant | MODIFIER | HG01074.hp1 HG02145.hp1 HG02145.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0086others(5): Show | 8 | 86 | 0.0930 | -41 | c.82+ others(58): Show |
NTM | ENSG00000182667.15 | transcript | ENST00000683400.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |