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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NBEA_chr13_34937270_35677736 | 35308542 | A | ATATATAT others(27): Show |
intron_variant | MODIFIER | HG02602.hp2 HG02735.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0020a0001c0003t0008 | a0001c0001t0020g0090 a0001c0003t0008g0007 |
2 | 117 | 0.0171 | 34 | c.583 others(51): Show |
NBEA | ENSG00000172915.20 | transcript | ENST00000379939.7 | protein_coding | 35/58 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
NBL1_chr1_19639311_19663452 | 19642035 | C | CTCTCGTC others(27): Show |
upstream_gene_variant | MODIFIER | NA19067.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 410 | 0.0024 | 34 | c.-24 others(45): Show |
NBL1 | ENSG00000158747.15 | transcript | ENST00000375136.8 | protein_coding | 2275 | chr1 | TogoVar | |||||||
NBPF15_chr1_144416390_144466669 | 144463598 | C | CAAAAAAA others(27): Show |
upstream_gene_variant | MODIFIER | HG02165.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0318 | 1 | 168 | 0.0060 | 34 | c.-31 others(45): Show |
NBPF15 | ENSG00000266338.7 | transcript | ENST00000581897.7 | protein_coding | 1930 | chr1 | TogoVar | |||||||
NBPF19_chr1_149470045_149561361 | 149528945 | C | CTCTCTCT others(27): Show |
intron_variant | MODIFIER | HG02895.hp1 | a0008 | a0008c0052 | a0008c0052t0019 | a0008c0052t0019g0190 | 1 | 145 | 0.0069 | 34 | c.734 others(51): 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(27): Show |
intron_variant | MODIFIER | HG02083.hp1 | a0030 | a0030c0029 | a0030c0029t0002 | a0030c0029t0002g0213 | 1 | 75 | 0.0133 | 34 | c.954 others(51): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTCTCTCT others(27): Show |
intron_variant | MODIFIER | HG01109.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0216 | 1 | 162 | 0.0062 | 34 | c.120 others(51): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF6_chr1_108445343_108476920 | 108452962 | G | GTTTGTAT others(27): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0037 | 1 | 21 | 0.0476 | 34 | c.279 others(49): Show |
NBPF6 | ENSG00000186086.19 | transcript | ENST00000495380.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113017635 | T | TTGTGTGT others(27): Show |
intron_variant | MODIFIER | NA18979.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0195 | 1 | 62 | 0.0161 | 34 | c.52+ others(51): 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(27): Show |
intron_variant | MODIFIER | HG00408.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
a0001 | a0001c0001a0001c0014 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(1): Show | a0001c0001t0001g0233 a0001c0001t0002g0019 a0001c0001t0007g0011 others(2): Show |
5 | 14 | 0.3571 | 34 | c.53- others(51): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113185068 | T | TTATATAT others(27): Show |
intron_variant | MODIFIER | HG02148.hp2 NA19088.hp1 |
a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0101 a0001c0001t0011g0107 |
2 | 98 | 0.0204 | 34 | c.53- others(51): 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(27): Show |
intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0001 | a0001c0001t0048 | a0001c0001t0048g0236 | 1 | 180 | 0.0056 | 34 | c.53- others(51): 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(27): Show |
intron_variant | MODIFIER | NA18971.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0184 | 1 | 180 | 0.0056 | 34 | c.53- others(51): 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(27): Show |
intron_variant | MODIFIER | HG01516.hp1 HG01517.hp1 |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0011 a0001c0001t0007g0012 |
2 | 181 | 0.0110 | 34 | c.53- others(51): 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(27): Show |
intron_variant | MODIFIER | NA18939.hp1 NA18940.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0011 | a0001c0001t0003g0182 a0001c0001t0011g0183 |
2 | 181 | 0.0110 | 34 | c.53- others(51): 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(27): Show |
intron_variant | MODIFIER | HG02273.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0098 | 1 | 180 | 0.0056 | 34 | c.53- others(51): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113237905 | G | GATATATA others(27): Show |
intron_variant | MODIFIER | HG01109.hp2 HG01123.hp2 HG02622.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0092 a0001c0001t0002g0152 a0001c0001t0004g0069 others(5): Show |
8 | 235 | 0.0340 | 34 | c.182 others(53): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21265411 | T | TATATATA others(27): Show |
intron_variant | MODIFIER | HG00639.hp1 HG01891.hp2 HG06807.hp2 |
a0002 | a0002c0002a0002c0003 | a0002c0002t0008a0002c0003t0002a0002c0003t0003 | a0002c0002t0008g0098 a0002c0003t0002g0128 a0002c0003t0003g0062 |
3 | 126 | 0.0238 | 34 | c.56- others(51): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21430394 | T | TTATATAT others(27): Show |
intron_variant | MODIFIER | HG03486.hp1 | a0003 | a0003c0006 | a0003c0006t0005 | a0003c0006t0005g0065 | 1 | 96 | 0.0104 | 34 | c.148 others(53): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAPD2_chr12_6489102_6536955 | 6504228 | T | TATATATA others(27): Show |
intron_variant | MODIFIER | HG01168.hp2 HG04199.hp1 |
a0001 | a0001c0004 | a0001c0004t0011 | a0001c0004t0011g0387 a0001c0004t0011g0388 |
2 | 426 | 0.0047 | 34 | c.128 others(51): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCAPD2_chr12_6489102_6536955 | 6513715 | C | CTTTTTTT others(27): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0007 | a0001c0007t0012 | a0001c0007t0012g0269 | 1 | 112 | 0.0089 | 34 | c.588 others(49): 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(27): Show |
intron_variant | MODIFIER | HG02280.hp1 HG02559.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0292 a0001c0001t0002g0332 |
2 | 92 | 0.0217 | 34 | c.158 others(51): 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(27): Show |
intron_variant | MODIFIER | NA18983.hp1 NA18990.hp1 NA19074.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0285 |
3 | 233 | 0.0129 | 34 | c.198 others(53): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 16/27 | chr7 | TogoVar | |||||||
NCBP2L_chrX_107772733_107800829 | 107781692 | C | CTCTCTCT others(27): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0059 | 1 | 174 | 0.0057 | 34 | c.-73 others(51): 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(27): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0060 | 1 | 174 | 0.0057 | 34 | c.-73 others(51): 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(27): Show |
intron_variant | MODIFIER | HG02145.hp1 HG02970.hp2 NA19240.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0057 a0001c0002t0002g0062 a0001c0002t0002g0069 |
3 | 176 | 0.0170 | 34 | c.-73 others(51): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
NCBP3_chr17_3797158_3851246 | 3826723 | G | GGAAGGAA others(27): Show |
intron_variant | MODIFIER | HG02280.hp2 HG03098.hp2 |
a0001 | a0001c0001 | a0001c0001t0046 | a0001c0001t0046g0059 a0001c0001t0046g0213 |
2 | 364 | 0.0055 | 34 | c.482 others(49): Show |
NCBP3 | ENSG00000074356.17 | transcript | ENST00000389005.6 | protein_coding | 4/12 | chr17 | TogoVar | |||||||
NCK2_chr2_105739912_105899272 | 105835393 | A | ATATATAT others(27): Show |
intron_variant | MODIFIER | HG04184.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0079 | 1 | 243 | 0.0041 | 34 | c.-17 others(53): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCK2_chr2_105739912_105899272 | 105835393 | A | ATATATAT others(27): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00673.hp1 HG00733.hp1 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(1): Show | a0001c0001t0003g0119 a0001c0001t0003g0127 a0001c0001t0003g0133 others(16): Show |
20 | 262 | 0.0763 | 34 | c.-17 others(53): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCK2_chr2_105739912_105899272 | 105835393 | A | ATATATAT others(27): Show |
intron_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0062 | 1 | 243 | 0.0041 | 34 | c.-17 others(53): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCK2_chr2_105739912_105899272 | 105844747 | G | GATATATA others(27): Show |
intron_variant | MODIFIER | NA18977.hp1 NA18977.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004 | a0001c0001t0003g0140 a0001c0001t0004g0050 |
2 | 53 | 0.0377 | 34 | c.-16 others(53): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCKAP1L_chr12_54492752_54553243 | 54506796 | A | AAAAAAAA others(27): Show |
intron_variant | MODIFIER | HG02300.hp1 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0275 | 1 | 25 | 0.0400 | 34 | c.307 others(51): 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(27): Show |
intron_variant | MODIFIER | HG01975.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0270 | 1 | 25 | 0.0400 | 34 | c.307 others(51): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCLN_chr19_3180930_3214575 | 3193148 | C | CTGGGCCC others(27): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(75): Show |
a0001a0002a0004others(3): Show | a0001c0002a0002c0003a0002c0005others(7): Show | a0001c0002t0001a0002c0003t0002a0002c0003t0021others(15): Show | a0001c0002t0001g0236 a0002c0003t0002g0003 a0002c0003t0002g0020 others(65): Show |
78 | 228 | 0.3421 | 34 | c.376 others(49): Show |
NCLN | ENSG00000125912.11 | transcript | ENST00000246117.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
NCMAP_chr1_24551087_24614328 | 24597678 | A | AAGAAAGG others(27): Show |
intron_variant | MODIFIER | HG01168.hp2 HG01169.hp2 HG01255.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0142 a0001c0001t0006g0143 a0001c0001t0006g0152 others(4): Show |
7 | 379 | 0.0185 | 34 | c.82+ others(49): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NCMAP_chr1_24551087_24614328 | 24604630 | A | ATGTGTGT others(27): Show |
intron_variant | MODIFIER | HG02723.hp2 | a0002 | a0002c0002 | a0002c0002t0012 | a0002c0002t0012g0147 | 1 | 398 | 0.0025 | 34 | c.168 others(49): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NCMAP_chr1_24551087_24614328 | 24604632 | A | ATGTGTGT others(27): Show |
intron_variant | MODIFIER | HG03209.hp2 HG03486.hp2 |
a0002 | a0002c0002 | a0002c0002t0012 | a0002c0002t0012g0002 | 2 | 398 | 0.0050 | 34 | c.168 others(49): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NCOA2_chr8_70104782_70408808 | 70159222 | T | TTATATAT others(27): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0003 | a0003c0006 | a0003c0006t0006 | a0003c0006t0006g0052 | 1 | 302 | 0.0033 | 34 | c.112 others(51): Show |
NCOA2 | ENSG00000140396.13 | transcript | ENST00000452400.7 | protein_coding | 10/22 | chr8 | TogoVar | |||||||
NCOA2_chr8_70104782_70408808 | 70159236 | A | ATATATAT others(27): Show |
intron_variant | MODIFIER | HG00609.hp2 HG00621.hp1 HG01074.hp1 others(24): Show |
a0001a0010 | a0001c0001a0010c0008 | a0001c0001t0001a0001c0001t0002a0010c0008t0018 | a0001c0001t0001g0091 a0001c0001t0001g0144 a0001c0001t0001g0182 others(24): Show |
27 | 211 | 0.1280 | 34 | c.112 others(51): Show |
NCOA2 | ENSG00000140396.13 | transcript | ENST00000452400.7 | protein_coding | 10/22 | chr8 | TogoVar | |||||||
NCOA2_chr8_70104782_70408808 | 70341590 | G | GAAAAAGA others(27): Show |
intron_variant | MODIFIER | NA19087.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0121 | 1 | 320 | 0.0031 | 34 | c.-76 others(53): Show |
NCOA2 | ENSG00000140396.13 | transcript | ENST00000452400.7 | protein_coding | 1/22 | chr8 | TogoVar | |||||||
NCOA5_chr20_46055991_46094962 | 46078568 | G | GATATGAA others(27): Show |
intron_variant | MODIFIER | HG02280.hp1 HG02970.hp2 HG03098.hp1 others(2): Show |
a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0018 a0001c0005t0001g0149 a0001c0005t0001g0150 |
5 | 380 | 0.0132 | 34 | c.38+ others(47): Show |
NCOA5 | ENSG00000124160.12 | transcript | ENST00000290231.11 | protein_coding | 2/7 | chr20 | TogoVar | |||||||
NCOA6_chr20_34709774_34830651 | 34751376 | C | CAAAAAAA others(27): Show |
intron_variant | MODIFIER | HG01975.hp1 HG02080.hp1 HG03669.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0028 a0001c0001t0002g0042 a0001c0001t0002g0051 others(1): Show |
4 | 66 | 0.0606 | 34 | c.167 others(51): Show |
NCOA6 | ENSG00000198646.14 | transcript | ENST00000359003.7 | protein_coding | 8/14 | chr20 | TogoVar | |||||||
NCOR1_chr17_16024157_16220534 | 16127111 | A | ATATATAT others(27): Show |
intron_variant | MODIFIER | HG01243.hp2 HG02015.hp1 HG02145.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0002a0001c0002t0005a0001c0004t0002others(1): Show | a0001c0001t0002g0196 a0001c0002t0005g0167 a0001c0002t0005g0168 others(7): Show |
10 | 251 | 0.0398 | 34 | c.151 others(51): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 14/45 | chr17 | TogoVar | |||||||
NCOR1_chr17_16024157_16220534 | 16127709 | G | GTATGTGT others(27): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0011 | a0001c0011t0014 | a0001c0011t0014g0280 | 1 | 275 | 0.0036 | 34 | c.151 others(53): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 14/45 | chr17 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124428044 | A | AGTGTGTG others(27): Show |
intron_variant | MODIFIER | HG00621.hp2 HG02300.hp1 NA19240.hp2 |
a0001a0002a0006 | a0001c0091a0002c0016a0006c0007 | a0001c0091t0001a0002c0016t0016a0006c0007t0034 | a0001c0091t0001g0144 a0002c0016t0016g0074 a0006c0007t0034g0109 |
3 | 23 | 0.1304 | 34 | c.115 others(53): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 12/48 | chr12 | TogoVar | |||||||
NCS1_chr9_130167404_130242303 | 130189879 | A | AAAAAAAA others(27): Show |
intron_variant | MODIFIER | HG01123.hp1 | a0001 | a0001c0002 | a0001c0002t0088 | a0001c0002t0088g0259 | 1 | 260 | 0.0038 | 34 | c.65- others(51): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
NDC1_chr1_53760478_53843296 | 53825460 | A | AAAAAAAA others(27): Show |
intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0068 | 1 | 157 | 0.0064 | 34 | c.594 others(49): Show |
NDC1 | ENSG00000058804.12 | transcript | ENST00000371429.4 | protein_coding | 5/17 | chr1 | TogoVar | |||||||
NDC80_chr18_2566557_2621635 | 2614563 | G | GAAAGAAA others(27): Show |
intron_variant | MODIFIER | HG01255.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0157 | 1 | 389 | 0.0026 | 34 | c.179 others(53): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | TogoVar | |||||||
NDE1_chr16_15645245_15731353 | 15712882 | G | GTTTTTTT others(27): Show |
intron_variant | MODIFIER | HG00738.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0339 | 1 | 123 | 0.0081 | 34 | c.948 others(53): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
NDST4_chr4_114822763_115118620 | 115022234 | G | GTTCCACG others(27): Show |
intron_variant | MODIFIER | HG01109.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0065 a0001c0001t0001g0131 a0001c0001t0001g0188 others(4): Show |
7 | 183 | 0.0383 | 34 | c.979 others(53): Show |
NDST4 | ENSG00000138653.10 | transcript | ENST00000264363.7 | protein_coding | 2/13 | chr4 | TogoVar | |||||||
NDUFA10_chr2_239952372_240030342 | 240004577 | C | CCTCCTAG others(27): Show |
intron_variant | MODIFIER | HG03209.hp1 HG03225.hp2 |
a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0148 a0001c0001t0017g0163 |
2 | 409 | 0.0049 | 34 | c.890 others(49): Show |
NDUFA10 | ENSG00000130414.13 | transcript | ENST00000252711.7 | protein_coding | 8/9 | chr2 | TogoVar |