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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NEDD4L_chr18_58039226_58406539 | 58170835 | A | ACCCCAGC others(34): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0001 | a0001c0001t0034 | a0001c0001t0034g0023 | 1 | 118 | 0.0085 | 41 | c.122 others(58): Show |
NEDD4L | ENSG00000049759.20 | transcript | ENST00000400345.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
NEDD4L_chr18_58039226_58406539 | 58171347 | A | AACACTGC others(34): Show |
intron_variant | MODIFIER | HG01884.hp2 HG03130.hp2 NA19030.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007a0001c0001t0047 | a0001c0001t0002g0109a0001c0001t0007g0057a0001c0001t0047g0005 | 3 | 118 | 0.0254 | 41 | c.122 others(58): Show |
NEDD4L | ENSG00000049759.20 | transcript | ENST00000400345.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
NEMF_chr14_49777083_49857788 | 49806257 | T | TATATATA others(34): Show |
intron_variant | MODIFIER | HG03942.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037 | 1 | 222 | 0.0045 | 41 | c.174 others(58): Show |
NEMF | ENSG00000165525.18 | transcript | ENST00000298310.10 | protein_coding | 18/32 | chr14 | TogoVar | ||||||
NEO1_chr15_73047463_73310205 | 73257132 | C | CAAAAAAA others(34): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0244 | 1 | 324 | 0.0031 | 41 | c.209 others(60): Show |
NEO1 | ENSG00000067141.17 | transcript | ENST00000261908.11 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
NEU4_chr2_241804193_241822413 | 241805561 | C | CCCTCCCC others(34): Show |
upstream_gene_variant | MODIFIER | HG02071.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0127 | 1 | 319 | 0.0031 | 41 | c.-37 others(52): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 3631 | chr2 | TogoVar | ||||||
NEU4_chr2_241804193_241822413 | 241805674 | C | CCCTCCCC others(34): Show |
upstream_gene_variant | MODIFIER | HG03927.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0084 | 1 | 319 | 0.0031 | 41 | c.-36 others(52): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 3518 | chr2 | TogoVar | ||||||
NEU4_chr2_241804193_241822413 | 241806195 | C | CCTCCCCC others(34): Show |
upstream_gene_variant | MODIFIER | HG00280.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0004 | 1 | 319 | 0.0031 | 41 | c.-30 others(52): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 2997 | chr2 | TogoVar | ||||||
NEU4_chr2_241804193_241822413 | 241806229 | C | CCCTCCCC others(34): Show |
upstream_gene_variant | MODIFIER | HG00609.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 319 | 0.0031 | 41 | c.-30 others(52): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 2963 | chr2 | TogoVar | ||||||
NEU4_chr2_241804193_241822413 | 241806347 | C | CCCTCCCC others(34): Show |
upstream_gene_variant | MODIFIER | HG04199.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0082 | 1 | 319 | 0.0031 | 41 | c.-29 others(52): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 2845 | chr2 | TogoVar | ||||||
NEU4_chr2_241804193_241822413 | 241806650 | C | CCCTCCCC others(34): Show |
upstream_gene_variant | MODIFIER | NA18966.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0171 | 1 | 319 | 0.0031 | 41 | c.-26 others(52): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 2542 | chr2 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79420266 | A | ACGTTTCC others(34): Show |
intron_variant | MODIFIER | HG01516.hp2 HG01517.hp1 |
a0002 | a0002c0011 | a0002c0011t0002 | a0002c0011t0002g0293a0002c0011t0002g0294 | 2 | 322 | 0.0062 | 41 | c.122 others(60): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
NFATC1_chr18_79390930_79534323 | 79420537 | G | GAGGAAGA others(34): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0015 | a0001c0015t0007 | a0001c0015t0007g0285 | 1 | 322 | 0.0031 | 41 | c.122 others(60): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
NFATC1_chr18_79390930_79534323 | 79420854 | A | ATTGCTGC others(34): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0017 | a0001c0017t0003 | a0001c0017t0003g0138 | 1 | 322 | 0.0031 | 41 | c.122 others(60): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
NFATC1_chr18_79390930_79534323 | 79532216 | G | GCCCCCCG others(34): Show |
downstream_gene_variant | MODIFIER | NA19000.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0268 | 1 | 322 | 0.0031 | 41 | c.*46 others(52): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 2894 | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79532217 | C | CCCCCCGC others(34): Show |
downstream_gene_variant | MODIFIER | HG02738.hp1 | a0001 | a0001c0024 | a0001c0024t0001 | a0001c0024t0001g0266 | 1 | 322 | 0.0031 | 41 | c.*46 others(52): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 2895 | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79532263 | G | GCCCCCCC others(34): Show |
downstream_gene_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0010 | a0001c0010t0004 | a0001c0010t0004g0289 | 1 | 322 | 0.0031 | 41 | c.*46 others(52): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 2941 | chr18 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79532263 | G | GCCCCCCG others(34): Show |
downstream_gene_variant | MODIFIER | NA18947.hp2 | a0002 | a0002c0002 | a0002c0002t0009 | a0002c0002t0009g0169 | 1 | 322 | 0.0031 | 41 | c.*46 others(52): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 2941 | chr18 | TogoVar | ||||||
NFILZ_chr19_8625633_8686151 | 8661104 | T | TTCCTTCC others(34): Show |
intron_variant | MODIFIER | HG02080.hp2 NA18978.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0009a0002c0002t0008 | a0001c0001t0009g0329a0002c0002t0008g0323 | 2 | 366 | 0.0055 | 41 | c.-16 others(62): Show |
NFILZ | ENSG00000268480.4 | transcript | ENST00000691075.1 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
NGEF_chr2_232873701_233018256 | 232993155 | A | ATATATAT others(34): Show |
intron_variant | MODIFIER | HG02723.hp1 HG03225.hp2 HG03540.hp1 |
a0001a0002 | a0001c0012a0002c0006a0002c0018 | a0001c0012t0001a0002c0006t0005a0002c0018t0002 | a0001c0012t0001g0058a0002c0006t0005g0288a0002c0018t0002g0359 | 3 | 362 | 0.0083 | 41 | c.-74 others(60): Show |
NGEF | ENSG00000066248.15 | transcript | ENST00000264051.8 | protein_coding | 1/14 | chr2 | TogoVar | ||||||
NGEF_chr2_232873701_233018256 | 232995422 | C | CTGTATAT others(34): Show |
intron_variant | MODIFIER | HG02257.hp2 HG03492.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0008a0001c0005t0018 | a0001c0001t0008g0176a0001c0005t0018g0007 | 2 | 362 | 0.0055 | 41 | c.-75 others(60): Show |
NGEF | ENSG00000066248.15 | transcript | ENST00000264051.8 | protein_coding | 1/14 | chr2 | TogoVar | ||||||
NHS_chrX_17370200_17740994 | 17521366 | C | CTTTTTTT others(34): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0006 | a0006c0008 | a0006c0008t0008 | a0006c0008t0008g0113 | 1 | 164 | 0.0061 | 41 | c.565 others(62): Show |
NHS | ENSG00000188158.17 | transcript | ENST00000676302.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
NINJ2_chr12_559296_668445 | 629896 | A | AAAAAAAA others(34): Show |
intron_variant | MODIFIER | NA18984.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0226 | 1 | 404 | 0.0025 | 41 | c.33+ others(58): Show |
NINJ2 | ENSG00000171840.13 | transcript | ENST00000305108.10 | protein_coding | 1/3 | chr12 | TogoVar | ||||||
NKAIN3_chr8_62243854_62989904 | 62667345 | C | CATATATA others(34): Show |
intron_variant | MODIFIER | HG01109.hp1 HG02145.hp2 HG02451.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0014a0001c0001t0020a0001c0001t0027others(5): Show | a0001c0001t0014g0013a0001c0001t0020g0070a0001c0001t0020g0142others(6): Show | 9 | 144 | 0.0625 | 41 | c.273 others(60): Show |
NKAIN3 | ENSG00000185942.13 | transcript | ENST00000623646.3 | protein_coding | 3/6 | chr8 | TogoVar | ||||||
NKAIN3_chr8_62243854_62989904 | 62667345 | C | CATATATA others(34): Show |
intron_variant | MODIFIER | HG02258.hp2 | a0001 | a0001c0001 | a0001c0001t0102 | a0001c0001t0102g0141 | 1 | 144 | 0.0069 | 41 | c.273 others(60): Show |
NKAIN3 | ENSG00000185942.13 | transcript | ENST00000623646.3 | protein_coding | 3/6 | chr8 | TogoVar | ||||||
NKD2_chr5_1003802_1043943 | 1022312 | T | TTTGTCCC others(34): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0077 | 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 | 1022593 | C | CCAGCCCA others(34): Show |
intron_variant | MODIFIER | HG04199.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0045 | 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 | 1022953 | G | GCTGTGGG others(34): Show |
intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0071 | 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 | 1023896 | T | TCTGTGGG others(34): Show |
intron_variant | MODIFIER | HG04199.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0045 | 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 | 1023997 | T | TTTGTCCC others(34): Show |
intron_variant | MODIFIER | NA18747.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0136 | 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 | 1024781 | C | CCCTGCTC others(34): Show |
intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0002 | 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 | 1025003 | G | GCTGTGGG others(34): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0005 | a0005c0009 | a0005c0009t0010 | a0005c0009t0010g0111 | 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 | 1025097 | T | TCAGCCCA others(34): Show |
intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0005 | a0001c0005t0011 | a0001c0005t0011g0002 | 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 | 1025249 | G | GCTGTGGG others(34): Show |
intron_variant | MODIFIER | HG01243.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
a0001a0005a0008 | a0001c0001a0005c0009a0008c0011 | a0001c0001t0003a0001c0001t0010a0005c0009t0010others(1): Show | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(3): 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 | 1025249 | G | GCTGTGGG others(34): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0077 | 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 | 1025343 | T | TCAGCCCA others(34): Show |
intron_variant | MODIFIER | HG04199.hp2 NA18747.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0045a0001c0001t0002g0136 | 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 | 1025671 | T | TCAGCCCG others(34): Show |
intron_variant | MODIFIER | HG01261.hp1 HG02818.hp2 HG03209.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0062a0001c0001t0004g0060a0001c0001t0004g0061 | 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 | 1026318 | G | GCTGTGGG others(34): Show |
intron_variant | MODIFIER | HG01243.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
a0001a0005a0008 | a0001c0001a0005c0009a0008c0011 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(3): Show | a0001c0001t0003g0004a0001c0001t0003g0112a0001c0001t0003g0113others(6): Show | 11 | 319 | 0.0345 | 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 | 1026334 | T | TCCATTGT others(34): Show |
intron_variant | MODIFIER | HG01261.hp1 HG02818.hp2 HG03209.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0062a0001c0001t0004g0060a0001c0001t0004g0061 | 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 | 1026576 | C | CCAGCCCG others(34): Show |
intron_variant | MODIFIER | HG03516.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0115 | 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 | |||||
NLRC3_chr16_3534033_3582403 | 3569394 | A | ATATATAT others(34): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0007 | a0007c0012 | a0007c0012t0014 | a0007c0012t0014g0345 | 1 | 396 | 0.0025 | 41 | c.-16 others(60): Show |
NLRC3 | ENSG00000167984.18 | transcript | ENST00000359128.10 | protein_coding | 1/19 | chr16 | TogoVar | ||||||
NLRP5_chr19_55994726_56066810 | 55999988 | C | CATGACAG others(34): Show |
intron_variant | MODIFIER | HG02015.hp1 HG03017.hp2 NA18948.hp2 others(1): Show |
a0001a0011 | a0001c0001a0001c0002a0011c0039 | a0001c0001t0001a0001c0002t0001a0011c0039t0001 | a0001c0001t0001g0091a0001c0002t0001g0032a0011c0039t0001g0092others(1): Show | 4 | 396 | 0.0101 | 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 | 56000058 | T | TCCACTCT others(34): Show |
intron_variant | MODIFIER | HG04199.hp2 NA19043.hp2 NA19082.hp2 |
a0001a0005a0008 | a0001c0003a0005c0006a0008c0017 | a0001c0003t0001a0005c0006t0001a0008c0017t0001 | a0001c0003t0001g0001a0005c0006t0001g0104a0008c0017t0001g0103 | 3 | 396 | 0.0076 | 41 | c.62+ others(54): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
NME2_chr17_51161411_51176744 | 51176422 | A | AAAAAAAA others(34): Show |
downstream_gene_variant | MODIFIER | HG00438.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 | 1 | 413 | 0.0024 | 41 | c.*48 others(52): Show |
NME2 | ENSG00000243678.12 | transcript | ENST00000512737.6 | protein_coding | 4679 | chr17 | TogoVar | ||||||
NME2_chr17_51161411_51176744 | 51176422 | A | AAAAAAAA others(34): Show |
downstream_gene_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 | 1 | 413 | 0.0024 | 41 | c.*48 others(52): Show |
NME2 | ENSG00000243678.12 | transcript | ENST00000512737.6 | protein_coding | 4679 | chr17 | TogoVar | ||||||
NOC2L_chr1_939203_964256 | 948711 | C | CACCCTGG others(34): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
a0001a0003a0005others(7): Show | a0001c0001a0001c0002a0001c0006others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(26): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 376 | 422 | 0.8910 | 41 | c.144 others(58): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132148960 | C | CACACCAC others(34): Show |
intron_variant | MODIFIER | NA18995.hp2 NA19079.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | 294 | 0.0068 | 41 | c.901 others(54): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149004 | C | CACACCAC others(34): Show |
intron_variant | MODIFIER | HG01167.hp2 NA19005.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119a0001c0001t0001g0207 | 2 | 294 | 0.0068 | 41 | c.901 others(56): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149036 | C | CGCCGCCT others(34): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 | 1 | 294 | 0.0034 | 41 | c.901 others(56): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NOC4L_chr12_132139457_132157468 | 132149212 | C | CGCCGCCT others(34): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0076 | 1 | 294 | 0.0034 | 41 | c.901 others(56): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NOC4L_chr12_132139457_132157468 | 132149617 | G | GCTCACAC others(34): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0054 | 1 | 294 | 0.0034 | 41 | c.901 others(56): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |