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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NCAPG2_chr7_158626169_158709804 | 158660401 | C | CTTTTTTT others(20): Show |
intron_variant | MODIFIER | NA18945.hp2 NA18999.hp1 NA19054.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0232 a0001c0001t0001g0266 a0001c0001t0001g0307 |
3 | 233 | 0.0129 | 27 | c.198 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 16/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667407 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | HG01175.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0342 a0001c0001t0001g0343 a0001c0001t0002g0021 others(4): Show |
7 | 375 | 0.0187 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667436 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | HG00099.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0069 | 1 | 375 | 0.0027 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667465 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | HG01257.hp1 | a0009 | a0009c0022 | a0009c0022t0002 | a0009c0022t0002g0098 | 1 | 373 | 0.0027 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667494 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | HG03486.hp1 | a0004 | a0004c0007 | a0004c0007t0002 | a0004c0007t0002g0210 | 1 | 349 | 0.0029 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667579 | C | CCTTACCG others(20): Show |
intron_variant | MODIFIER | HG03041.hp1 NA19074.hp2 NA19085.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0001 | a0001c0001t0002g0002 a0001c0001t0002g0085 a0002c0002t0001g0148 |
3 | 254 | 0.0118 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667694 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | HG02523.hp1 HG02717.hp2 HG03486.hp1 others(1): Show |
a0001a0004 | a0001c0001a0004c0007 | a0001c0001t0002a0004c0007t0002 | a0001c0001t0002g0084 a0004c0007t0002g0210 a0004c0007t0002g0214 others(1): Show |
4 | 375 | 0.0107 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667781 | C | CCTTACCG others(20): Show |
intron_variant | MODIFIER | HG02055.hp2 HG03209.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0342 a0001c0001t0001g0343 |
2 | 300 | 0.0067 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667781 | C | CCTTACCG others(20): Show |
intron_variant | MODIFIER | HG02071.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0091 | 1 | 299 | 0.0033 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667870 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | HG02280.hp2 HG03471.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | 372 | 0.0054 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667870 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | NA19090.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0263 | 1 | 371 | 0.0027 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667899 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | HG01255.hp1 HG01975.hp2 HG02004.hp2 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0365 a0001c0001t0002g0026 a0001c0001t0002g0081 others(8): Show |
11 | 374 | 0.0294 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667984 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | HG01516.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0323 | 1 | 376 | 0.0027 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668072 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | NA19082.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0221 | 1 | 373 | 0.0027 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668072 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | NA18940.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0262 | 1 | 373 | 0.0027 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668101 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | HG00099.hp1 HG02698.hp2 HG03239.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0356 a0001c0001t0001g0360 a0001c0001t0001g0362 others(1): Show |
4 | 336 | 0.0119 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668101 | C | CTTACCCA others(20): Show |
intron_variant | MODIFIER | HG02976.hp2 HG03579.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0127 a0001c0001t0002g0129 |
2 | 334 | 0.0060 | 27 | c.148 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668244 | C | CCTTACCT others(20): Show |
intron_variant | MODIFIER | HG02109.hp1 HG02257.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0201 a0001c0003t0001g0204 |
2 | 355 | 0.0056 | 27 | c.147 others(46): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCK2_chr2_105739912_105899272 | 105865902 | A | ATATTATT others(20): Show |
intron_variant | MODIFIER | HG02809.hp1 HG03139.hp1 |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0122 a0001c0001t0007g0276 |
2 | 212 | 0.0094 | 27 | c.226 others(46): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCMAP_chr1_24551087_24614328 | 24573952 | C | CAAAAAAA others(20): Show |
intron_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0304 | 1 | 98 | 0.0102 | 27 | c.-8+ others(44): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NCOA1_chr2_24486254_24775702 | 24690651 | C | CAAAAAAA others(20): Show |
intron_variant | MODIFIER | HG00099.hp2 | a0001 | a0001c0001 | a0001c0001t0022 | a0001c0001t0022g0180 | 1 | 75 | 0.0133 | 27 | c.533 others(42): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCOA2_chr8_70104782_70408808 | 70133200 | C | CTTTTTTT others(20): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0003 | a0001c0003t0009 | a0001c0003t0009g0071 | 1 | 148 | 0.0068 | 27 | c.315 others(46): Show |
NCOA2 | ENSG00000140396.13 | transcript | ENST00000452400.7 | protein_coding | 15/22 | chr8 | TogoVar | |||||||
NCOA2_chr8_70104782_70408808 | 70159243 | T | TATATATA others(20): Show |
intron_variant | MODIFIER | HG02135.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0133 | 1 | 296 | 0.0034 | 27 | c.112 others(44): Show |
NCOA2 | ENSG00000140396.13 | transcript | ENST00000452400.7 | protein_coding | 10/22 | chr8 | TogoVar | |||||||
NCOA2_chr8_70104782_70408808 | 70321793 | C | CTTTTTTT others(20): Show |
intron_variant | MODIFIER | HG03669.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0320 | 1 | 133 | 0.0075 | 27 | c.-76 others(46): Show |
NCOA2 | ENSG00000140396.13 | transcript | ENST00000452400.7 | protein_coding | 1/22 | chr8 | TogoVar | |||||||
NCOA3_chr20_47496887_47661872 | 47511556 | T | TATATACA others(20): Show |
intron_variant | MODIFIER | HG00733.hp1 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0210 | 1 | 81 | 0.0123 | 27 | c.-99 others(44): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | chr20 | TogoVar | |||||||
NCOA3_chr20_47496887_47661872 | 47511556 | T | TATATATA others(20): Show |
intron_variant | MODIFIER | HG00280.hp2 HG01071.hp2 HG01192.hp2 others(5): Show |
a0001a0005 | a0001c0001a0005c0007 | a0001c0001t0001a0001c0001t0003a0001c0001t0033others(1): Show | a0001c0001t0001g0287 a0001c0001t0001g0295 a0001c0001t0003g0111 others(5): Show |
8 | 88 | 0.0909 | 27 | c.-99 others(44): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | chr20 | TogoVar | |||||||
NCOA3_chr20_47496887_47661872 | 47511556 | T | TATATATA others(20): Show |
intron_variant | MODIFIER | HG02109.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0097 | 1 | 81 | 0.0123 | 27 | c.-99 others(44): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | chr20 | TogoVar | |||||||
NCOA3_chr20_47496887_47661872 | 47511556 | T | TATATATA others(20): Show |
intron_variant | MODIFIER | NA19010.hp2 | a0004 | a0004c0006 | a0004c0006t0006 | a0004c0006t0006g0085 | 1 | 81 | 0.0123 | 27 | c.-99 others(44): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | chr20 | TogoVar | |||||||
NCOA3_chr20_47496887_47661872 | 47511556 | T | TATATATA others(20): Show |
intron_variant | MODIFIER | NA19086.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0280 | 1 | 81 | 0.0123 | 27 | c.-99 others(44): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | chr20 | TogoVar | |||||||
NCOA3_chr20_47496887_47661872 | 47511556 | T | TATATATA others(20): Show |
intron_variant | MODIFIER | HG01256.hp2 | a0004 | a0004c0006 | a0004c0006t0006 | a0004c0006t0006g0098 | 1 | 81 | 0.0123 | 27 | c.-99 others(44): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | chr20 | TogoVar | |||||||
NCOA3_chr20_47496887_47661872 | 47511556 | T | TATATATA others(20): Show |
intron_variant | MODIFIER | HG02080.hp2 | a0012 | a0012c0020 | a0012c0020t0002 | a0012c0020t0002g0184 | 1 | 81 | 0.0123 | 27 | c.-99 others(44): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | chr20 | TogoVar | |||||||
NCOA3_chr20_47496887_47661872 | 47542009 | G | GTTTTTTT others(20): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0002 | a0002c0002 | a0002c0002t0008 | a0002c0002t0008g0093 | 1 | 241 | 0.0041 | 27 | c.-99 others(46): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
NCOA3_chr20_47496887_47661872 | 47619668 | T | TATTACTC others(20): Show |
intron_variant | MODIFIER | HG03239.hp1 HG03669.hp2 |
a0001 | a0001c0005 | a0001c0005t0004 | a0001c0005t0004g0010 a0001c0005t0004g0011 |
2 | 314 | 0.0064 | 27 | c.-19 others(44): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
NCOA6_chr20_34709774_34830651 | 34751376 | C | CAAAAAAA others(20): Show |
intron_variant | MODIFIER | HG00621.hp2 HG00673.hp2 HG01192.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0003 a0001c0001t0002g0017 a0001c0001t0002g0035 others(9): Show |
12 | 74 | 0.1622 | 27 | c.167 others(44): Show |
NCOA6 | ENSG00000198646.14 | transcript | ENST00000359003.7 | protein_coding | 8/14 | chr20 | TogoVar | |||||||
NCOR1_chr17_16024157_16220534 | 16219915 | T | TATAAGCA others(20): Show |
upstream_gene_variant | MODIFIER | HG01099.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0145 | 1 | 280 | 0.0036 | 27 | c.-46 others(38): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 4382 | chr17 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124324138 | A | ATGTGAAT others(20): Show |
downstream_gene_variant | MODIFIER | HG01071.hp1 HG01243.hp1 HG01891.hp1 others(38): Show |
a0001a0002a0003others(11): Show | a0001c0021a0001c0027a0001c0082others(33): Show | a0001c0021t0023a0001c0021t0033a0001c0027t0021others(37): Show | a0001c0021t0023g0170 a0001c0021t0033g0187 a0001c0027t0021g0104 others(38): Show |
41 | 232 | 0.1767 | 27 | c.*12 others(38): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 276 | chr12 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124417059 | C | CTCACTCC others(20): Show |
intron_variant | MODIFIER | HG00558.hp1 HG01891.hp1 HG03579.hp1 |
a0002 | a0002c0001a0002c0109a0002c0154 | a0002c0001t0080a0002c0109t0001a0002c0154t0011 | a0002c0001t0080g0231 a0002c0109t0001g0205 a0002c0154t0011g0063 |
3 | 215 | 0.0140 | 27 | c.148 others(46): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 15/48 | chr12 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124417068 | C | CGGAGAGC others(20): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
a0001a0002a0003others(11): Show | a0001c0003a0001c0005a0001c0009others(69): Show | a0001c0003t0004a0001c0003t0012a0001c0003t0016others(93): Show | a0001c0003t0004g0053 a0001c0003t0004g0072 a0001c0003t0012g0046 others(101): Show |
104 | 226 | 0.4602 | 27 | c.148 others(46): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 15/48 | chr12 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124417072 | G | GAGCAGGC others(20): Show |
intron_variant | MODIFIER | HG02004.hp2 | a0002 | a0002c0120 | a0002c0120t0003 | a0002c0120t0003g0200 | 1 | 232 | 0.0043 | 27 | c.148 others(46): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 15/48 | chr12 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124417086 | G | GTCACTCC others(20): Show |
intron_variant | MODIFIER | HG01243.hp2 HG01255.hp2 HG01433.hp1 others(22): Show |
a0001a0002a0003others(4): Show | a0001c0013a0001c0021a0001c0026others(18): Show | a0001c0013t0003a0001c0021t0023a0001c0026t0027others(21): Show | a0001c0013t0003g0142 a0001c0021t0023g0170 a0001c0026t0027g0119 others(22): Show |
25 | 231 | 0.1082 | 27 | c.148 others(46): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 15/48 | chr12 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124417095 | C | CGGAGAGC others(20): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(106): Show |
a0001a0002a0003others(12): Show | a0001c0003a0001c0005a0001c0009others(73): Show | a0001c0003t0004a0001c0003t0012a0001c0003t0016others(98): Show | a0001c0003t0004g0053 a0001c0003t0004g0072 a0001c0003t0012g0046 others(106): Show |
109 | 223 | 0.4888 | 27 | c.148 others(46): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 15/48 | chr12 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124417162 | G | GGACAGTC others(20): Show |
intron_variant | MODIFIER | HG02135.hp1 | a0001 | a0001c0009 | a0001c0009t0003 | a0001c0009t0003g0228 | 1 | 232 | 0.0043 | 27 | c.148 others(46): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 15/48 | chr12 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124417180 | G | GAGCAGGC others(20): Show |
intron_variant | MODIFIER | HG00673.hp1 HG01243.hp1 HG01255.hp2 others(7): Show |
a0001a0002a0003others(2): Show | a0001c0013a0002c0001a0002c0040others(7): Show | a0001c0013t0003a0002c0001t0080a0002c0040t0036others(7): Show | a0001c0013t0003g0142 a0002c0001t0080g0231 a0002c0040t0036g0151 others(7): Show |
10 | 187 | 0.0535 | 27 | c.148 others(46): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 15/48 | chr12 | TogoVar | |||||||
NCR1_chr19_54901148_54918073 | 54916317 | C | CTTTTTTT others(20): Show |
downstream_gene_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 | 1 | 146 | 0.0068 | 27 | c.*34 others(38): Show |
NCR1 | ENSG00000189430.13 | transcript | ENST00000291890.9 | protein_coding | 3245 | chr19 | TogoVar | |||||||
NCS1_chr9_130167404_130242303 | 130176195 | T | TTTCTTTC others(20): Show |
intron_variant | MODIFIER | HG01099.hp1 | a0001 | a0001c0002 | a0001c0002t0086 | a0001c0002t0086g0213 | 1 | 334 | 0.0030 | 27 | c.64+ others(42): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
NCS1_chr9_130167404_130242303 | 130189879 | A | AAAAAAAA others(20): Show |
intron_variant | MODIFIER | HG03491.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0022 | 1 | 260 | 0.0038 | 27 | c.65- others(44): Show |
NCS1 | ENSG00000107130.10 | transcript | ENST00000372398.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
NCSTN_chr1_160338383_160363949 | 160359170 | A | ATTTTTTT others(20): Show |
downstream_gene_variant | MODIFIER | HG00597.hp2 HG01192.hp1 HG01261.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0008g0018 |
3 | 133 | 0.0226 | 27 | c.*89 others(36): Show |
NCSTN | ENSG00000162736.18 | transcript | ENST00000294785.10 | protein_coding | 222 | chr1 | TogoVar | |||||||
NDE1_chr16_15645245_15731353 | 15712882 | G | GTTTTTTT others(20): Show |
intron_variant | MODIFIER | HG02280.hp2 NA18969.hp2 NA18975.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0106 a0001c0001t0002g0342 a0001c0001t0004g0172 |
3 | 125 | 0.0240 | 27 | c.948 others(46): Show |
NDE1 | ENSG00000072864.16 | transcript | ENST00000396354.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
NDST3_chr4_118029486_118263634 | 118066340 | T | TTATATAT others(20): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0133 | 1 | 214 | 0.0047 | 27 | c.981 others(46): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
NDST3_chr4_118029486_118263634 | 118066439 | C | CATATGTT others(20): Show |
intron_variant | MODIFIER | HG02074.hp2 HG02647.hp1 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0001 | a0001c0001t0001g0104 a0001c0006t0001g0056 |
2 | 75 | 0.0267 | 27 | c.981 others(46): Show |
NDST3 | ENSG00000164100.9 | transcript | ENST00000296499.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar |