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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTCTGTGT others(11): Show |
intron_variant | MODIFIER | HG01081.hp2 HG01361.hp1 HG01928.hp1 others(30): Show |
a0003a0005a0026 | a0003c0003a0005c0005a0026c0025 | a0003c0003t0003a0005c0005t0004a0026c0025t0003 | a0003c0003t0003g0014a0003c0003t0003g0017a0003c0003t0003g0051others(21): Show | 33 | 394 | 0.0838 | 18 | c.120 others(35): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG02074.hp1 | a0003 | a0003c0003 | a0003c0003t0023 | a0003c0003t0023g0131 | 1 | 394 | 0.0025 | 18 | c.120 others(35): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF3_chr1_21435137_21489900 | 21479848 | G | GTGTGTGT others(11): Show |
intron_variant | MODIFIER | NA19010.hp2 NA19088.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0194a0001c0001t0001g0253 | 2 | 394 | 0.0051 | 18 | c.120 others(35): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF4_chr1_108217464_108249076 | 108244901 | G | GATATATA others(11): Show |
upstream_gene_variant | MODIFIER | NA19089.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 134 | 0.0075 | 18 | c.-10 others(29): Show |
NBPF4 | ENSG00000196427.14 | transcript | ENST00000415641.8 | protein_coding | 826 | chr1 | TogoVar | ||||||
NBPF6_chr1_108445343_108476920 | 108449416 | C | CTCTATAT others(11): Show |
upstream_gene_variant | MODIFIER | HG02818.hp1 | a0003 | a0003c0002 | a0003c0002t0016 | a0003c0002t0016g0012 | 1 | 68 | 0.0147 | 18 | c.-10 others(29): Show |
NBPF6 | ENSG00000186086.19 | transcript | ENST00000495380.7 | protein_coding | 926 | chr1 | TogoVar | ||||||
NBPF6_chr1_108445343_108476920 | 108456038 | G | GGAAAGAA others(11): Show |
intron_variant | MODIFIER | HG01169.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0048 | 1 | 68 | 0.0147 | 18 | c.784 others(33): Show |
NBPF6 | ENSG00000186086.19 | transcript | ENST00000495380.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF9_chr1_149047186_149108551 | 149060924 | C | CACACACA others(11): Show |
intron_variant | MODIFIER | HG02615.hp2 HG04199.hp1 NA18953.hp2 others(1): Show |
a0002a0007 | a0002c0002a0002c0011a0007c0007 | a0002c0002t0001a0002c0011t0001a0007c0007t0031 | a0002c0002t0001g0171a0002c0011t0001g0176a0002c0011t0001g0209others(1): Show | 4 | 344 | 0.0116 | 18 | c.230 others(35): Show |
NBPF9 | ENSG00000269713.9 | transcript | ENST00000698832.1 | protein_coding | 23/29 | chr1 | TogoVar | ||||||
NBR1_chr17_43166214_43216688 | 43177572 | A | AACACACA others(11): Show |
intron_variant | MODIFIER | HG02280.hp1 HG03041.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0003a0003c0003t0003 | a0001c0001t0003g0140a0003c0003t0003g0150 | 2 | 314 | 0.0064 | 18 | c.103 others(33): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
NBR1_chr17_43166214_43216688 | 43179902 | T | TCTTGAGT others(11): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0004c0004others(2): Show | a0001c0001t0001a0002c0002t0002a0002c0002t0013others(3): Show | a0001c0001t0001g0084a0002c0002t0002g0001a0002c0002t0002g0004others(100): Show | 122 | 314 | 0.3885 | 18 | c.184 others(33): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
NCALD_chr8_101681542_101795969 | 101715003 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG01109.hp2 HG02055.hp2 HG02622.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007a0001c0001t0018 | a0001c0001t0001g0032a0001c0001t0001g0264a0001c0001t0007g0286others(1): Show | 4 | 300 | 0.0133 | 18 | c.378 others(35): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113000817 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0015 | a0001c0015t0006 | a0001c0015t0006g0072 | 1 | 242 | 0.0041 | 18 | c.52+ others(35): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113017635 | T | TTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG02055.hp2 HG02647.hp1 HG03209.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0003a0001c0001t0041a0001c0002t0005others(2): Show | a0001c0001t0003g0197a0001c0001t0003g0198a0001c0001t0041g0219others(3): Show | 6 | 242 | 0.0248 | 18 | c.52+ others(35): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113095315 | C | CGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG01516.hp1 HG01517.hp1 |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | 242 | 0.0083 | 18 | c.53- others(37): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113157136 | G | GACACACA others(11): Show |
intron_variant | MODIFIER | HG01516.hp1 HG01517.hp1 |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0011a0001c0001t0007g0012 | 2 | 242 | 0.0083 | 18 | c.53- others(35): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113173591 | G | GATATATA others(11): Show |
intron_variant | MODIFIER | HG01255.hp2 HG01346.hp1 HG02080.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0001a0001c0002t0002 | a0001c0001t0002g0001a0001c0001t0002g0027a0001c0002t0001g0061others(1): Show | 5 | 242 | 0.0207 | 18 | c.53- others(35): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113185079 | T | TATATATA others(11): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0001 | a0001c0001 | a0001c0001t0046 | a0001c0001t0046g0087 | 1 | 242 | 0.0041 | 18 | c.53- others(35): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113185084 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0129 | 1 | 242 | 0.0041 | 18 | c.53- others(35): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | chr11 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113210775 | A | AACACACA others(11): Show |
intron_variant | MODIFIER | NA18986.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0092 | 1 | 242 | 0.0041 | 18 | c.916 others(35): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21009883 | C | CTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG00741.hp1 HG00741.hp2 HG01346.hp2 others(6): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0011a0001c0001t0016others(4): Show | a0001c0001t0001g0037a0001c0001t0001g0079a0001c0001t0011g0035others(6): Show | 9 | 132 | 0.0682 | 18 | c.55+ others(35): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21116015 | T | TTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0002 | a0002c0003 | a0002c0003t0012 | a0002c0003t0012g0027 | 1 | 132 | 0.0076 | 18 | c.55+ others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21146546 | G | GATATATA others(11): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0002 | a0002c0003 | a0002c0003t0017 | a0002c0003t0017g0038 | 1 | 132 | 0.0076 | 18 | c.56- others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21210967 | A | AACACACA others(11): Show |
intron_variant | MODIFIER | HG02258.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0003 | 1 | 132 | 0.0076 | 18 | c.56- others(35): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21214746 | T | TATATATA others(11): Show |
intron_variant | MODIFIER | HG00558.hp1 HG00673.hp1 HG00733.hp2 others(12): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0014others(8): Show | a0001c0001t0001g0043a0001c0001t0004g0048a0001c0001t0014g0033others(12): Show | 15 | 132 | 0.1136 | 18 | c.56- others(35): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21272934 | T | TCACACAC others(11): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(5): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0013 | a0001c0001t0001a0001c0001t0030a0001c0001t0038others(4): Show | a0001c0001t0001g0079a0001c0001t0030g0112a0001c0001t0038g0053others(5): Show | 8 | 132 | 0.0606 | 18 | c.56- others(33): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21331509 | C | CTATATAT others(11): Show |
intron_variant | MODIFIER | HG01243.hp2 HG01346.hp1 HG01361.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(2): Show | a0001c0001t0001g0043a0001c0001t0002g0109a0001c0001t0010g0056others(2): Show | 5 | 132 | 0.0379 | 18 | c.738 others(35): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21394469 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG06807.hp1 NA18522.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0116a0001c0001t0004g0028 | 2 | 132 | 0.0152 | 18 | c.119 others(39): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21431123 | T | TTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG00733.hp1 HG02970.hp2 |
a0002 | a0002c0002a0002c0003 | a0002c0002t0001a0002c0003t0004 | a0002c0002t0001g0018a0002c0003t0004g0130 | 2 | 132 | 0.0152 | 18 | c.148 others(35): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21437474 | C | CTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG01243.hp2 HG01891.hp1 HG02027.hp2 others(15): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0017a0001c0001t0001g0083a0001c0001t0001g0097others(15): Show | 18 | 132 | 0.1364 | 18 | c.165 others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21450793 | T | TGTATGTA others(11): Show |
intron_variant | MODIFIER | HG02293.hp2 | a0002 | a0002c0002 | a0002c0002t0035 | a0002c0002t0035g0052 | 1 | 132 | 0.0076 | 18 | c.165 others(39): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 12/17 | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21452971 | T | TTATATAT others(11): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0002 | a0002c0003 | a0002c0003t0005 | a0002c0003t0005g0008 | 1 | 132 | 0.0076 | 18 | c.165 others(39): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21467412 | G | GTATATAT others(11): Show |
intron_variant | MODIFIER | HG02293.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002others(2): Show | a0001c0001t0004a0001c0004t0002a0002c0002t0008others(4): Show | a0001c0001t0004g0012a0001c0004t0002g0026a0002c0002t0008g0098others(4): Show | 7 | 132 | 0.0530 | 18 | c.177 others(35): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21479583 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0117 | 1 | 132 | 0.0076 | 18 | c.207 others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21486303 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02258.hp1 |
a0002 | a0002c0003 | a0002c0003t0002a0002c0003t0003 | a0002c0003t0002g0128a0002c0003t0003g0107 | 2 | 132 | 0.0152 | 18 | c.207 others(37): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAPD2_chr12_6489102_6536955 | 6513715 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG01069.hp2 HG01081.hp2 HG01515.hp1 others(20): Show |
a0001 | a0001c0001a0001c0007a0001c0030 | a0001c0001t0002a0001c0001t0007a0001c0007t0005others(1): Show | a0001c0001t0002g0019a0001c0001t0002g0305a0001c0001t0002g0306others(19): Show | 23 | 432 | 0.0532 | 18 | c.588 others(33): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTGT others(11): Show |
intron_variant | MODIFIER | HG01884.hp1 HG01891.hp2 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0353a0001c0001t0002g0354a0001c0001t0002g0388 | 3 | 432 | 0.0069 | 18 | c.158 others(35): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0265 | 1 | 432 | 0.0023 | 18 | c.158 others(35): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(14): Show |
a0001a0003a0005 | a0001c0001a0003c0003a0003c0010others(1): Show | a0001c0001t0002a0003c0003t0003a0003c0010t0001others(1): Show | a0001c0001t0002g0387a0003c0003t0003g0008a0003c0003t0003g0027others(13): Show | 17 | 432 | 0.0394 | 18 | c.158 others(35): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NCAPD3_chr11_134145113_134228967 | 134212375 | T | TTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG00597.hp2 HG01978.hp2 HG02647.hp2 others(6): Show |
a0001a0006a0014 | a0001c0001a0006c0009a0014c0018 | a0001c0001t0002a0001c0001t0033a0001c0001t0046others(3): Show | a0001c0001t0002g0125a0001c0001t0002g0182a0001c0001t0002g0183others(6): Show | 9 | 370 | 0.0243 | 18 | c.383 others(35): Show |
NCAPD3 | ENSG00000151503.14 | transcript | ENST00000534548.7 | protein_coding | 3/34 | chr11 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158660401 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG01346.hp1 HG01891.hp1 |
a0001a0008 | a0001c0001a0008c0014 | a0001c0001t0001a0008c0014t0001 | a0001c0001t0001g0323a0008c0014t0001g0313 | 2 | 378 | 0.0053 | 18 | c.198 others(37): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 16/27 | chr7 | TogoVar | ||||||
NCBP1_chr9_97628821_97678748 | 97632943 | A | AGACATCA others(11): Show |
upstream_gene_variant | MODIFIER | NA18991.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034 | 1 | 364 | 0.0028 | 18 | c.-93 others(27): Show |
NCBP1 | ENSG00000136937.13 | transcript | ENST00000375147.8 | protein_coding | 877 | chr9 | TogoVar | ||||||
NCBP2L_chrX_107772733_107800829 | 107781676 | A | ATCTATCT others(11): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0066 | 1 | 303 | 0.0033 | 18 | c.-73 others(35): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
NCBP2L_chrX_107772733_107800829 | 107781676 | A | ATCTATCT others(11): Show |
intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0068 | 1 | 303 | 0.0033 | 18 | c.-73 others(35): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
NCBP2L_chrX_107772733_107800829 | 107781676 | A | ATCTCTCT others(11): Show |
intron_variant | MODIFIER | HG03490.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0044 | 1 | 303 | 0.0033 | 18 | c.-73 others(35): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
NCBP2L_chrX_107772733_107800829 | 107781692 | C | CTCTCTCT others(11): Show |
intron_variant | MODIFIER | HG00741.hp2 HG01515.hp1 HG01517.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0011a0001c0002t0002g0091 | 3 | 303 | 0.0099 | 18 | c.-73 others(35): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
NCBP2L_chrX_107772733_107800829 | 107781692 | C | CTCTCTCT others(11): Show |
intron_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0092 | 1 | 303 | 0.0033 | 18 | c.-73 others(35): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
NCBP2L_chrX_107772733_107800829 | 107783858 | A | ATGTGTGT others(11): Show |
intron_variant | MODIFIER | HG01071.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0083 | 1 | 303 | 0.0033 | 18 | c.-73 others(35): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
NCBP3_chr17_3797158_3851246 | 3850117 | G | GCTGGTGA others(11): Show |
upstream_gene_variant | MODIFIER | NA18972.hp1 | a0002 | a0002c0002 | a0002c0002t0010 | a0002c0002t0010g0033 | 1 | 370 | 0.0027 | 18 | c.-38 others(29): Show |
NCBP3 | ENSG00000074356.17 | transcript | ENST00000389005.6 | protein_coding | 3872 | chr17 | TogoVar | ||||||
NCCRP1_chr19_39191964_39206884 | 39192703 | A | AAATAATA others(11): Show |
upstream_gene_variant | MODIFIER | HG03209.hp2 HG03516.hp1 HG03654.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0006a0001c0001t0011 | a0001c0001t0004g0007a0001c0001t0006g0023a0001c0001t0011g0047 | 3 | 380 | 0.0079 | 18 | c.-42 others(29): Show |
NCCRP1 | ENSG00000188505.5 | transcript | ENST00000339852.5 | protein_coding | 4260 | chr19 | TogoVar | ||||||
NCEH1_chr3_172625249_172716067 | 172712727 | C | CCTGCCTC others(11): Show |
upstream_gene_variant | MODIFIER | HG03130.hp1 HG03540.hp1 |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0052a0001c0001t0009g0057 | 2 | 332 | 0.0060 | 18 | c.-17 others(29): Show |
NCEH1 | ENSG00000144959.11 | transcript | ENST00000475381.7 | protein_coding | 1661 | chr3 | TogoVar | ||||||
NCF2_chr1_183550562_183595459 | 183585624 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG01433.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0026a0001c0001t0001g0257a0001c0001t0001g0258others(6): Show | 10 | 406 | 0.0246 | 18 | c.257 others(35): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | TogoVar |