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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NAV2_chr11_19707837_20126601 | 20106175 | A | ATATATAT others(19): Show |
intron_variant | MODIFIER | HG00140.hp1 HG01256.hp2 |
a0002a0005 | a0002c0093a0005c0035 | a0002c0093t0001a0005c0035t0001 | a0002c0093t0001g0110a0005c0035t0001g0038 | 2 | 166 | 0.0121 | 26 | c.684 others(43): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NAV2_chr11_19707837_20126601 | 20106175 | A | ATATATAT others(19): Show |
intron_variant | MODIFIER | HG00642.hp2 | a0006 | a0006c0037 | a0006c0037t0034 | a0006c0037t0034g0023 | 1 | 166 | 0.0060 | 26 | c.684 others(43): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NAV2_chr11_19707837_20126601 | 20106175 | A | ATATATAT others(19): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0002 | a0002c0138 | a0002c0138t0001 | a0002c0138t0001g0035 | 1 | 166 | 0.0060 | 26 | c.684 others(43): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NAV3_chr12_77825894_78218010 | 77873744 | G | GTGTATGT others(19): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0001 | a0001c0049 | a0001c0049t0054 | a0001c0049t0054g0150 | 1 | 186 | 0.0054 | 26 | c.243 others(45): Show |
NAV3 | ENSG00000067798.16 | transcript | ENST00000397909.7 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NAV3_chr12_77825894_78218010 | 77873744 | G | GTGTGTAT others(19): Show |
intron_variant | MODIFIER | NA19012.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0182 | 1 | 186 | 0.0054 | 26 | c.243 others(45): Show |
NAV3 | ENSG00000067798.16 | transcript | ENST00000397909.7 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NBDY_chrX_56724243_56824179 | 56726082 | A | ATGTTATA others(19): Show |
upstream_gene_variant | MODIFIER | HG02109.hp1 HG02258.hp1 HG02559.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(2): Show | a0001c0001t0003g0046a0001c0001t0005g0007a0001c0001t0005g0008others(8): Show | 11 | 160 | 0.0688 | 26 | c.-32 others(37): Show |
NBDY | ENSG00000204272.13 | transcript | ENST00000374922.9 | protein_coding | 3160 | chrX | TogoVar | ||||||
NBEA_chr13_34937270_35677736 | 35308454 | A | ATATATAT others(19): Show |
intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0006 | a0001c0006t0019 | a0001c0006t0019g0038 | 1 | 122 | 0.0082 | 26 | c.583 others(45): Show |
NBEA | ENSG00000172915.20 | transcript | ENST00000379939.7 | protein_coding | 35/58 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
NBPF14_chr1_148526385_148601011 | 148557087 | C | CACACACA others(19): Show |
intron_variant | MODIFIER | HG02040.hp2 | a0096 | a0096c0053 | a0096c0053t0001 | a0096c0053t0001g0094 | 1 | 222 | 0.0045 | 26 | c.500 others(43): Show |
NBPF14 | ENSG00000270629.7 | transcript | ENST00000619423.4 | protein_coding | 40/70 | chr1 | TogoVar | ||||||
NBPF15_chr1_144416390_144466669 | 144463598 | C | CAAAAAAA others(19): Show |
upstream_gene_variant | MODIFIER | HG00323.hp2 HG01175.hp2 HG03490.hp1 others(2): Show |
a0001 | a0001c0002a0001c0034 | a0001c0002t0001a0001c0034t0001 | a0001c0002t0001g0057a0001c0002t0001g0082a0001c0002t0001g0167others(2): Show | 5 | 394 | 0.0127 | 26 | c.-31 others(37): Show |
NBPF15 | ENSG00000266338.7 | transcript | ENST00000581897.7 | protein_coding | 1930 | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149528945 | C | CTCTCTCT others(19): Show |
intron_variant | MODIFIER | HG02165.hp1 | a0043 | a0043c0209 | a0043c0209t0004 | a0043c0209t0004g0207 | 1 | 276 | 0.0036 | 26 | c.734 others(43): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF19_chr1_149470045_149561361 | 149528945 | C | CTCTCTCT others(19): Show |
intron_variant | MODIFIER | HG01975.hp1 HG02148.hp1 HG02258.hp1 others(10): Show |
a0002a0014a0052others(8): Show | a0002c0002a0014c0008a0052c0079others(8): Show | a0002c0002t0007a0014c0008t0003a0014c0008t0020others(9): Show | a0002c0002t0007g0190a0002c0002t0007g0193a0014c0008t0003g0181others(10): Show | 13 | 276 | 0.0471 | 26 | c.734 others(43): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF19_chr1_149470045_149561361 | 149528945 | C | CTCTCTGT others(19): Show |
intron_variant | MODIFIER | HG00438.hp1 NA18983.hp2 NA19065.hp1 others(1): Show |
a0011a0012a0118 | a0011c0010a0012c0009a0118c0151 | a0011c0010t0001a0012c0009t0001a0118c0151t0001 | a0011c0010t0001g0010a0012c0009t0001g0050a0012c0009t0001g0172others(1): Show | 4 | 276 | 0.0145 | 26 | c.734 others(43): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF19_chr1_149470045_149561361 | 149528945 | C | CTCTGTGT others(19): Show |
intron_variant | MODIFIER | NA18947.hp2 NA18980.hp1 NA19074.hp1 others(1): Show |
a0012a0033a0140others(1): Show | a0012c0009a0033c0011a0140c0175others(1): Show | a0012c0009t0001a0033c0011t0002a0140c0175t0001others(1): Show | a0012c0009t0001g0195a0033c0011t0002g0254a0140c0175t0001g0051others(1): Show | 4 | 276 | 0.0145 | 26 | c.734 others(43): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF19_chr1_149470045_149561361 | 149543186 | C | CTCTCTGT others(19): Show |
intron_variant | MODIFIER | HG01168.hp2 HG01975.hp1 HG02602.hp1 others(4): Show |
a0006a0014a0142others(3): Show | a0006c0211a0006c0214a0014c0008others(4): Show | a0006c0211t0019a0006c0214t0002a0014c0008t0020others(4): Show | a0006c0211t0019g0211a0006c0214t0002g0265a0014c0008t0020g0184others(4): Show | 7 | 276 | 0.0254 | 26 | c.954 others(43): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF19_chr1_149470045_149561361 | 149543186 | C | CTCTGTGT others(19): Show |
intron_variant | MODIFIER | NA19074.hp2 | a0110 | a0110c0133 | a0110c0133t0001 | a0110c0133t0001g0058 | 1 | 276 | 0.0036 | 26 | c.954 others(43): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF19_chr1_149470045_149561361 | 149547923 | C | CTCTCTCT others(19): Show |
intron_variant | MODIFIER | HG02080.hp2 | a0208 | a0208c0048 | a0208c0048t0002 | a0208c0048t0002g0251 | 1 | 276 | 0.0036 | 26 | c.102 others(45): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF19_chr1_149470045_149561361 | 149547923 | C | CTCTCTGT others(19): Show |
intron_variant | MODIFIER | HG01069.hp2 HG02602.hp2 NA18983.hp1 others(1): Show |
a0037a0186a0202others(1): Show | a0037c0016a0186c0044a0202c0064others(1): Show | a0037c0016t0002a0186c0044t0017a0202c0064t0002others(1): Show | a0037c0016t0002g0257a0186c0044t0017g0239a0202c0064t0002g0262others(1): Show | 4 | 276 | 0.0145 | 26 | c.102 others(45): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF19_chr1_149470045_149561361 | 149547923 | C | CTGTGTGT others(19): Show |
intron_variant | MODIFIER | HG01358.hp2 | a0189 | a0189c0052 | a0189c0052t0027 | a0189c0052t0027g0231 | 1 | 276 | 0.0036 | 26 | c.102 others(45): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTCTCTCT others(19): Show |
intron_variant | MODIFIER | HG01978.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0258 | 1 | 394 | 0.0025 | 26 | c.120 others(43): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTCTCTCT others(19): Show |
intron_variant | MODIFIER | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(46): Show |
a0001a0012a0013 | a0001c0001a0012c0012a0013c0011 | a0001c0001t0001a0001c0001t0007a0001c0001t0018others(2): Show | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(33): Show | 49 | 394 | 0.1244 | 26 | c.120 others(43): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTCTCTGT others(19): Show |
intron_variant | MODIFIER | HG00280.hp1 NA20805.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0211a0001c0001t0001g0217 | 2 | 394 | 0.0051 | 26 | c.120 others(43): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTCTGTGT others(19): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0139 | 1 | 394 | 0.0025 | 26 | c.120 others(43): 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(19): Show |
intron_variant | MODIFIER | HG02602.hp1 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0231 | 1 | 394 | 0.0025 | 26 | c.120 others(43): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF8_chr1_120410035_120474676 | 120457730 | A | AATATATA others(19): Show |
intron_variant | MODIFIER | HG02572.hp2 | a0001 | a0001c0010 | a0001c0010t0032 | a0001c0010t0032g0078 | 1 | 292 | 0.0034 | 26 | c.163 others(45): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113017635 | T | TTGTGTGT others(19): Show |
intron_variant | MODIFIER | HG01123.hp1 HG01928.hp2 HG01993.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(3): Show | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0168others(11): Show | 14 | 242 | 0.0579 | 26 | c.52+ others(43): 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(19): Show |
intron_variant | MODIFIER | HG01070.hp1 HG01934.hp2 HG03130.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006a0001c0001t0008 | a0001c0001t0002g0025a0001c0001t0006g0206a0001c0001t0008g0084 | 3 | 242 | 0.0124 | 26 | c.53- others(43): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113185068 | T | TTTTATAT others(19): Show |
intron_variant | MODIFIER | NA18979.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0195 | 1 | 242 | 0.0041 | 26 | c.53- others(43): 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(19): Show |
intron_variant | MODIFIER | NA18995.hp1 NA20300.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0047a0001c0002t0001 | a0001c0001t0047g0141a0001c0002t0001g0218 | 2 | 242 | 0.0083 | 26 | c.53- others(43): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21106314 | C | CAAAAAAA others(19): Show |
intron_variant | MODIFIER | HG03239.hp1 NA18992.hp1 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0003a0002c0003t0006 | a0001c0001t0003g0055a0002c0003t0006g0031 | 2 | 132 | 0.0152 | 26 | c.55+ others(45): 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(19): Show |
intron_variant | MODIFIER | HG02523.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0036 | 1 | 132 | 0.0076 | 26 | c.56- others(43): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21431123 | T | TTGTGTGT others(19): Show |
intron_variant | MODIFIER | HG01934.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0003others(1): Show | a0001c0001t0032a0002c0002t0001a0002c0003t0006others(1): Show | a0001c0001t0032g0125a0002c0002t0001g0114a0002c0003t0006g0031others(1): Show | 4 | 132 | 0.0303 | 26 | c.148 others(43): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21473373 | A | AATATATA others(19): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0075 | 1 | 132 | 0.0076 | 26 | c.189 others(45): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21479583 | C | CAAAAAAA others(19): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0090 | 1 | 132 | 0.0076 | 26 | c.207 others(45): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21480366 | C | CAAAAAAA others(19): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0012 | 1 | 132 | 0.0076 | 26 | c.207 others(45): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTGT others(19): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02976.hp2 |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0335a0001c0001t0007g0374 | 2 | 432 | 0.0046 | 26 | c.158 others(43): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NCAPG2_chr7_158626169_158709804 | 158660401 | C | CTTTTTTT others(19): Show |
intron_variant | MODIFIER | HG00438.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0245 | 1 | 378 | 0.0027 | 26 | c.198 others(45): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 16/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667374 | C | CCGCCTTA others(19): Show |
intron_variant | MODIFIER | HG02735.hp1 HG03041.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0041a0001c0001t0002g0078 | 2 | 378 | 0.0053 | 26 | c.148 others(45): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667374 | C | CCTCCTTA others(19): Show |
intron_variant | MODIFIER | HG02015.hp2 NA18969.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0008a0001c0001t0002g0068 | 2 | 378 | 0.0053 | 26 | c.148 others(45): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667580 | C | CTTACCTA others(19): Show |
intron_variant | MODIFIER | HG00738.hp1 HG03669.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0029a0001c0001t0002g0135 | 2 | 378 | 0.0053 | 26 | c.148 others(45): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667841 | C | CTTACCTA others(19): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(27): Show |
a0001a0017 | a0001c0001a0001c0018a0017c0011 | a0001c0001t0001a0001c0001t0002a0001c0018t0002others(1): Show | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0354others(27): Show | 30 | 378 | 0.0794 | 26 | c.148 others(45): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667934 | C | CCACTACT others(19): Show |
intron_variant | MODIFIER | NA18950.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0270 | 1 | 378 | 0.0027 | 26 | c.148 others(45): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668211 | C | CCTCCTTA others(19): Show |
intron_variant | MODIFIER | HG02004.hp1 NA18970.hp1 NA18980.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0268a0001c0001t0001g0311a0001c0001t0001g0312 | 3 | 378 | 0.0079 | 26 | c.147 others(45): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668332 | C | CTTACCTA others(19): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0003 | a0003c0006 | a0003c0006t0001 | a0003c0006t0001g0331 | 1 | 378 | 0.0027 | 26 | c.147 others(45): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPH_chr2_96330766_96382091 | 96361778 | A | ATATATAC others(19): Show |
intron_variant | MODIFIER | NA18946.hp2 | a0002 | a0002c0003 | a0002c0003t0004 | a0002c0003t0004g0058 | 1 | 356 | 0.0028 | 26 | c.158 others(45): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCBP3_chr17_3797158_3851246 | 3826723 | G | GGAAGGAA others(19): Show |
intron_variant | MODIFIER | HG02145.hp1 HG02280.hp1 HG03130.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0026a0001c0001t0129 | a0001c0001t0026g0008a0001c0001t0026g0051a0001c0001t0129g0052 | 4 | 370 | 0.0108 | 26 | c.482 others(41): Show |
NCBP3 | ENSG00000074356.17 | transcript | ENST00000389005.6 | protein_coding | 4/12 | chr17 | TogoVar | ||||||
NCK2_chr2_105739912_105899272 | 105750037 | A | AACACACA others(19): Show |
intron_variant | MODIFIER | HG01346.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0174 | 1 | 334 | 0.0030 | 26 | c.-20 others(45): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCK2_chr2_105739912_105899272 | 105835393 | A | ATATATAT others(19): Show |
intron_variant | MODIFIER | HG00408.hp1 HG02129.hp1 NA18939.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0038a0001c0001t0039 | a0001c0001t0004g0040a0001c0001t0004g0041a0001c0001t0004g0044others(4): Show | 7 | 334 | 0.0210 | 26 | c.-17 others(45): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCKAP1L_chr12_54492752_54553243 | 54506794 | A | AATATATA others(19): Show |
intron_variant | MODIFIER | HG00408.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0124 | 1 | 350 | 0.0029 | 26 | c.307 others(43): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NCKAP1L_chr12_54492752_54553243 | 54506796 | A | AAAAAAAA others(19): Show |
intron_variant | MODIFIER | NA19082.hp2 | a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0281 | 1 | 350 | 0.0029 | 26 | c.307 others(43): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NCKAP5_chr2_132666788_133573463 | 132920771 | G | GTATGTAT others(19): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0003 | a0003c0025 | a0003c0025t0003 | a0003c0025t0003g0021 | 1 | 70 | 0.0143 | 26 | c.580 others(45): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 8/19 | chr2 | TogoVar |