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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NBPF8_chr1_120410035_120474676 | 120461016 | CTGTGTGT others(17): Show |
C | intron_variant | MODIFIER | HG02071.hp1 NA18941.hp2 NA18961.hp2 others(3): Show |
a0006 | a0006c0006 | a0006c0006t0005 | a0006c0006t0005g0004a0006c0006t0005g0099a0006c0006t0005g0100others(2): Show | 6 | 292 | 0.0206 | -24 | c.185 others(41): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF8_chr1_120410035_120474676 | 120464121 | CTCTCTCT others(17): Show |
C | intron_variant | MODIFIER | HG01175.hp2 | a0001 | a0001c0002 | a0001c0002t0008 | a0001c0002t0008g0054 | 1 | 292 | 0.0034 | -24 | c.230 others(41): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NBPF9_chr1_149047186_149108551 | 149102808 | GCATCCTG others(17): Show |
G | 5_prime_UTR_variant | MODIFIER | HG01496.hp1 | a0003 | a0003c0003 | a0003c0003t0040 | a0003c0003t0040g0016 | 1 | 344 | 0.0029 | -24 | c.-82 others(33): Show |
NBPF9 | ENSG00000269713.9 | transcript | ENST00000698832.1 | protein_coding | 2/30 | 20670 | chr1 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 112962435 | GGTGTGTG others(17): Show |
G | intron_variant | MODIFIER | HG03453.hp2 NA20752.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0031 | a0001c0001t0004g0009a0001c0001t0031g0060 | 2 | 242 | 0.0083 | -24 | c.52+ others(37): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113055978 | GATATATA others(17): Show |
G | intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0048 | 1 | 242 | 0.0041 | -24 | c.52+ others(41): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113237867 | TATATAGA others(17): Show |
T | intron_variant | MODIFIER | HG02615.hp1 HG02647.hp1 HG02886.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0015a0001c0002t0004 | a0001c0001t0003g0198a0001c0001t0015g0128a0001c0002t0004g0204 | 3 | 242 | 0.0124 | -24 | c.182 others(43): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113237883 | GATATATA others(17): Show |
G | intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0010 | a0001c0010t0021 | a0001c0010t0021g0065 | 1 | 242 | 0.0041 | -24 | c.182 others(43): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113237913 | TAGATATA others(17): Show |
T | intron_variant | MODIFIER | NA19011.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0102 | 1 | 242 | 0.0041 | -24 | c.182 others(43): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21259919 | AACACACA others(17): Show |
A | intron_variant | MODIFIER | HG02280.hp1 HG02572.hp1 HG03209.hp1 others(6): Show |
a0001a0002a0003others(1): Show | a0001c0004a0002c0002a0003c0006others(1): Show | a0001c0004t0002a0002c0002t0004a0002c0002t0014others(6): Show | a0001c0004t0002g0058a0002c0002t0004g0073a0002c0002t0014g0119others(6): Show | 9 | 132 | 0.0682 | -24 | c.56- others(41): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21452768 | TTAAAATA others(17): Show |
T | intron_variant | MODIFIER | HG00639.hp2 HG02027.hp2 HG02293.hp1 others(13): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0001c0014others(5): Show | a0001c0001t0001a0001c0001t0029a0001c0004t0036others(10): Show | a0001c0001t0001g0017a0001c0001t0001g0083a0001c0001t0001g0085others(13): Show | 16 | 132 | 0.1212 | -24 | c.165 others(45): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21530207 | AATTTAAT others(17): Show |
A | intron_variant | MODIFIER | HG02895.hp2 NA20905.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0024a0002c0002t0031 | a0001c0001t0024g0132a0002c0002t0031g0039 | 2 | 132 | 0.0152 | -24 | c.228 others(43): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAPD3_chr11_134145113_134228967 | 134154531 | CGGGTGGT others(17): Show |
C | intron_variant | MODIFIER | HG02257.hp2 HG03139.hp2 HG03471.hp2 |
a0007 | a0007c0007 | a0007c0007t0019 | a0007c0007t0019g0206a0007c0007t0019g0207a0007c0007t0019g0208 | 3 | 370 | 0.0081 | -24 | c.425 others(43): Show |
NCAPD3 | ENSG00000151503.14 | transcript | ENST00000534548.7 | protein_coding | 32/34 | chr11 | TogoVar | ||||||
NCAPD3_chr11_134145113_134228967 | 134154547 | ACCCCTCC others(17): Show |
A | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(212): Show |
a0001a0005a0008others(3): Show | a0001c0001a0001c0002a0001c0008others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(38): Show | a0001c0001t0001g0005a0001c0001t0001g0320a0001c0001t0001g0321others(208): Show | 215 | 370 | 0.5811 | -24 | c.425 others(43): Show |
NCAPD3 | ENSG00000151503.14 | transcript | ENST00000534548.7 | protein_coding | 32/34 | chr11 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158672280 | GTGTGTGT others(17): Show |
G | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(40): Show |
a0001a0002a0005others(2): Show | a0001c0001a0002c0002a0005c0009others(2): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(3): Show | a0001c0001t0001g0010a0001c0001t0001g0221a0001c0001t0001g0222others(40): Show | 43 | 378 | 0.1138 | -24 | c.132 others(41): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 12/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158672284 | GTGTGTGT others(17): Show |
G | intron_variant | MODIFIER | HG00408.hp2 HG01175.hp2 HG01257.hp1 others(7): Show |
a0001a0007a0009others(2): Show | a0001c0001a0007c0022a0009c0015others(2): Show | a0001c0001t0001a0001c0001t0002a0007c0022t0002others(3): Show | a0001c0001t0001g0341a0001c0001t0001g0349a0001c0001t0002g0017others(7): Show | 10 | 378 | 0.0265 | -24 | c.132 others(41): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 12/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158672286 | GTGTGTGT others(17): Show |
G | intron_variant | MODIFIER | NA18993.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0044 | 1 | 378 | 0.0027 | -24 | c.132 others(41): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 12/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158672318 | ATATATAT others(17): Show |
A | intron_variant | MODIFIER | HG02083.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0301 | 1 | 378 | 0.0027 | -24 | c.132 others(41): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 12/27 | chr7 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36872671 | ATGGAGGT others(17): Show |
A | intron_variant | MODIFIER | HG01884.hp2 HG02622.hp1 HG03486.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0141a0001c0001t0001g0224a0001c0003t0001g0208 | 3 | 434 | 0.0069 | -24 | c.627 others(39): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
NCK1_chr3_136857208_136956606 | 136867096 | CTTTCTTT others(17): Show |
C | intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0141 | 1 | 232 | 0.0043 | -24 | c.-19 others(41): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
NCK1_chr3_136857208_136956606 | 136867109 | TTTCTTTC others(17): Show |
T | intron_variant | MODIFIER | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(1): Show | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(7): Show | 10 | 232 | 0.0431 | -24 | c.-19 others(41): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
NCK1_chr3_136857208_136956606 | 136867113 | TTTCTTTG others(17): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG01496.hp1 others(3): Show |
a0001a0005 | a0001c0001a0005c0006 | a0001c0001t0001a0001c0001t0003a0001c0001t0014others(2): Show | a0001c0001t0001g0106a0001c0001t0003g0220a0001c0001t0003g0221others(3): Show | 6 | 232 | 0.0259 | -24 | c.-19 others(41): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
NCK1_chr3_136857208_136956606 | 136867117 | TTTGTTTC others(17): Show |
T | intron_variant | MODIFIER | HG00423.hp1 HG00738.hp1 HG02055.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0110a0001c0001t0002g0169a0001c0001t0002g0170others(2): Show | 5 | 232 | 0.0216 | -24 | c.-19 others(41): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
NCKAP1_chr2_182904115_183043457 | 182940298 | CAAAAGAA others(17): Show |
C | intron_variant | MODIFIER | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0037a0001c0002t0041a0001c0002t0042 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | 218 | 0.0184 | -24 | c.269 others(43): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | TogoVar | ||||||
NCKAP1_chr2_182904115_183043457 | 183009469 | AGGAAGGA others(17): Show |
A | intron_variant | MODIFIER | NA20805.hp1 | a0001 | a0001c0002 | a0001c0002t0110 | a0001c0002t0110g0214 | 1 | 218 | 0.0046 | -24 | c.220 others(41): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | TogoVar | ||||||
NCKAP5_chr2_132666788_133573463 | 132794223 | CATATATA others(17): Show |
C | intron_variant | MODIFIER | HG02886.hp1 | a0003 | a0003c0025 | a0003c0025t0003 | a0003c0025t0003g0021 | 1 | 70 | 0.0143 | -24 | c.909 others(41): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 12/19 | chr2 | TogoVar | ||||||
NCKAP5_chr2_132666788_133573463 | 132794253 | TATATATA others(17): Show |
T | intron_variant | MODIFIER | HG03098.hp2 | a0004 | a0004c0003 | a0004c0003t0001 | a0004c0003t0001g0007 | 1 | 70 | 0.0143 | -24 | c.909 others(41): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 12/19 | chr2 | TogoVar | ||||||
NCKAP5_chr2_132666788_133573463 | 132794257 | TATATATA others(17): Show |
T | intron_variant | MODIFIER | HG02630.hp1 | a0018 | a0018c0012 | a0018c0012t0001 | a0018c0012t0001g0031 | 1 | 70 | 0.0143 | -24 | c.909 others(41): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 12/19 | chr2 | TogoVar | ||||||
NCKAP5_chr2_132666788_133573463 | 132920771 | GTATATAT others(17): Show |
G | intron_variant | MODIFIER | HG03098.hp2 | a0004 | a0004c0003 | a0004c0003t0001 | a0004c0003t0001g0007 | 1 | 70 | 0.0143 | -24 | c.580 others(43): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 8/19 | chr2 | TogoVar | ||||||
NCKAP5_chr2_132666788_133573463 | 133115775 | GTATATAT others(17): Show |
G | intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0002 | 1 | 70 | 0.0143 | -24 | c.341 others(43): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 6/19 | chr2 | TogoVar | ||||||
NCKAP5_chr2_132666788_133573463 | 133120524 | CTTAGAGA others(17): Show |
C | intron_variant | MODIFIER | HG02280.hp1 HG02886.hp2 |
a0001a0015 | a0001c0001a0015c0026 | a0001c0001t0002a0015c0026t0001 | a0001c0001t0002g0034a0015c0026t0001g0027 | 2 | 70 | 0.0286 | -24 | c.341 others(41): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 6/19 | chr2 | TogoVar | ||||||
NCKAP5_chr2_132666788_133573463 | 133450124 | CGCACACA others(17): Show |
C | intron_variant | MODIFIER | HG01175.hp1 HG02630.hp2 HG02922.hp1 others(6): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0009a0002c0002others(2): Show | a0001c0001t0001a0001c0009t0001a0002c0002t0004others(4): Show | a0001c0001t0001g0015a0001c0009t0001g0042a0002c0002t0004g0001others(6): Show | 9 | 70 | 0.1286 | -24 | c.69+ others(41): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 3/19 | chr2 | TogoVar | ||||||
NCKAP5_chr2_132666788_133573463 | 133526225 | AAGAAAGG others(17): Show |
A | intron_variant | MODIFIER | NA19004.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0040 | 1 | 70 | 0.0143 | -24 | c.-61 others(41): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 2/19 | chr2 | TogoVar | ||||||
NCMAP_chr1_24551087_24614328 | 24593857 | ATTATTTA others(17): Show |
A | intron_variant | MODIFIER | HG00558.hp1 HG01109.hp2 HG01168.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0006a0001c0001t0026 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0006g0141others(9): Show | 12 | 402 | 0.0299 | -24 | c.-7- others(39): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCMAP_chr1_24551087_24614328 | 24597613 | GAAAGAGA others(17): Show |
G | intron_variant | MODIFIER | NA20905.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0156 | 1 | 402 | 0.0025 | -24 | c.82+ others(39): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCMAP_chr1_24551087_24614328 | 24597617 | GAGAAAGA others(17): Show |
G | intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0379 | 1 | 402 | 0.0025 | -24 | c.82+ others(39): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCMAP_chr1_24551087_24614328 | 24604589 | AAAAAAAA others(17): Show |
A | intron_variant | MODIFIER | HG01516.hp1 HG01517.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0026 | a0001c0001t0006g0141a0001c0001t0026g0142 | 2 | 402 | 0.0050 | -24 | c.168 others(40): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCMAP_chr1_24551087_24614328 | 24604603 | AAAATATA others(17): Show |
A | intron_variant | MODIFIER | HG00558.hp2 HG02040.hp2 HG02056.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0121a0001c0001t0001g0206a0001c0001t0003g0325others(1): Show | 4 | 402 | 0.0100 | -24 | c.168 others(40): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCMAP_chr1_24551087_24614328 | 24604605 | AATATATA others(17): Show |
A | intron_variant | MODIFIER | NA18522.hp1 NA19043.hp2 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0011a0001c0001t0003g0372 | 2 | 402 | 0.0050 | -24 | c.168 others(39): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24576149 | GTTTTTTT others(17): Show |
G | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(104): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(11): Show | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(104): Show | 107 | 314 | 0.3408 | -24 | c.-25 others(43): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24639912 | GTGTGTAT others(17): Show |
G | intron_variant | MODIFIER | HG02735.hp2 HG02965.hp1 HG02970.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0014a0001c0002t0003 | a0001c0001t0014g0216a0001c0001t0014g0217a0001c0002t0003g0048 | 3 | 314 | 0.0096 | -24 | c.-17 others(43): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA2_chr8_70104782_70408808 | 70258186 | GGATTACA others(17): Show |
G | intron_variant | MODIFIER | NA19068.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0259 | 1 | 322 | 0.0031 | -24 | c.-20 others(43): Show |
NCOA2 | ENSG00000140396.13 | transcript | ENST00000452400.7 | protein_coding | 2/22 | chr8 | TogoVar | ||||||
NCOA6_chr20_34709774_34830651 | 34811201 | GTATATAT others(17): Show |
G | intron_variant | MODIFIER | HG02976.hp1 HG03041.hp1 HG03098.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0169a0001c0001t0001g0196a0001c0001t0004g0289 | 3 | 290 | 0.0103 | -24 | c.-16 others(45): Show |
NCOA6 | ENSG00000198646.14 | transcript | ENST00000359003.7 | protein_coding | 1/14 | chr20 | TogoVar | ||||||
NCOA6_chr20_34709774_34830651 | 34817170 | AATGGGTA others(17): Show |
A | intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0159 | 1 | 290 | 0.0035 | -24 | c.-16 others(43): Show |
NCOA6 | ENSG00000198646.14 | transcript | ENST00000359003.7 | protein_coding | 1/14 | chr20 | TogoVar | ||||||
NCOR1_chr17_16024157_16220534 | 16092647 | TTATATAT others(17): Show |
T | intron_variant | MODIFIER | HG02572.hp2 NA19004.hp2 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0002a0001c0008t0011 | a0001c0001t0002g0252a0001c0008t0011g0006 | 2 | 282 | 0.0071 | -24 | c.282 others(41): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 21/45 | chr17 | TogoVar | ||||||
NCOR1_chr17_16024157_16220534 | 16127396 | TGTGTATA others(17): Show |
T | intron_variant | MODIFIER | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0133a0001c0001t0008g0018a0001c0001t0008g0044others(3): Show | 6 | 282 | 0.0213 | -24 | c.151 others(43): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 14/45 | chr17 | TogoVar | ||||||
NCOR2_chr12_124319415_124572612 | 124433876 | ACACACAC others(17): Show |
A | intron_variant | MODIFIER | HG02559.hp1 | a0049 | a0049c0064 | a0049c0064t0028 | a0049c0064t0028g0161 | 1 | 234 | 0.0043 | -24 | c.883 others(41): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 10/48 | chr12 | TogoVar | ||||||
NCOR2_chr12_124319415_124572612 | 124438822 | GAGAGGGA others(17): Show |
G | intron_variant | MODIFIER | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(3): Show |
a0002a0003 | a0002c0107a0003c0002 | a0002c0107t0037a0003c0002t0022a0003c0002t0052others(1): Show | a0002c0107t0037g0169a0003c0002t0022g0015a0003c0002t0022g0018others(3): Show | 6 | 234 | 0.0256 | -24 | c.816 others(39): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 9/48 | chr12 | TogoVar | ||||||
NCOR2_chr12_124319415_124572612 | 124467774 | TCATCATC others(17): Show |
T | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(37): Show |
a0001a0002a0003others(11): Show | a0001c0003a0001c0009a0001c0022others(25): Show | a0001c0003t0012a0001c0003t0016a0001c0009t0002others(35): Show | a0001c0003t0012g0069a0001c0003t0016g0021a0001c0009t0002g0081others(37): Show | 40 | 234 | 0.1709 | -24 | c.592 others(41): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 6/48 | chr12 | TogoVar | ||||||
NCR3LG1_chr11_17346800_17382341 | 17362675 | CCTTCCTT others(17): Show |
C | intron_variant | MODIFIER | HG02572.hp1 HG02723.hp1 NA18948.hp2 others(3): Show |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0025 | a0002c0002t0003g0176a0002c0002t0003g0188a0002c0002t0003g0189others(3): Show | 6 | 380 | 0.0158 | -24 | c.422 others(41): Show |
NCR3LG1 | ENSG00000188211.9 | transcript | ENST00000338965.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCR3LG1_chr11_17346800_17382341 | 17362679 | CCTTCCTT others(17): Show |
C | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00639.hp2 others(17): Show |
a0001a0003a0006 | a0001c0001a0003c0004a0006c0005 | a0001c0001t0001a0001c0001t0004a0001c0001t0047others(4): Show | a0001c0001t0001g0027a0001c0001t0001g0054a0001c0001t0001g0064others(15): Show | 20 | 380 | 0.0526 | -24 | c.422 others(41): Show |
NCR3LG1 | ENSG00000188211.9 | transcript | ENST00000338965.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |