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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NAALADL2_chr3_174854334_175815548 | 175232237 | G | GAAGAAGA others(22): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02451.hp2 |
a0009a0012 | a0009c0023a0012c0017 | a0009c0023t0001a0012c0017t0007 | a0009c0023t0001g0037a0012c0017t0007g0025 | 2 | 64 | 0.0313 | 29 | c.546 others(46): Show |
NAALADL2 | ENSG00000177694.16 | transcript | ENST00000454872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
NACC1_chr19_13113264_13146147 | 13127400 | T | TTTTTTTT others(22): Show |
intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0088 | 1 | 326 | 0.0031 | 29 | c.-8- others(44): Show |
NACC1 | ENSG00000160877.7 | transcript | ENST00000292431.5 | protein_coding | 1/5 | chr19 | TogoVar | ||||||
NACC2_chr9_136001537_136100289 | 136056085 | C | CCCTAGGG others(22): Show |
intron_variant | MODIFIER | NA18612.hp1 | a0001 | a0001c0004 | a0001c0004t0085 | a0001c0004t0085g0134 | 1 | 348 | 0.0029 | 29 | c.-59 others(46): Show |
NACC2 | ENSG00000148411.8 | transcript | ENST00000277554.4 | protein_coding | 1/5 | chr9 | TogoVar | ||||||
NAIP_chr5_70963166_71030339 | 70995975 | T | TTCAAGGA others(22): Show |
intron_variant | MODIFIER | HG01515.hp1 NA18979.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0020 | a0001c0001t0001g0064a0001c0003t0020g0101 | 2 | 141 | 0.0142 | 29 | c.102 others(48): Show |
NAIP | ENSG00000249437.8 | transcript | ENST00000517649.6 | protein_coding | 9/16 | chr5 | TogoVar | ||||||
NALF1_chr13_107158510_107872496 | 107254062 | A | AAAAAAAA others(22): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0059 | a0001c0001t0059g0036 | 1 | 128 | 0.0078 | 29 | c.916 others(48): Show |
NALF1 | ENSG00000204442.4 | transcript | ENST00000375915.4 | protein_coding | 1/2 | chr13 | TogoVar | ||||||
NALF1_chr13_107158510_107872496 | 107254062 | A | AAAAAAAA others(22): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0002 | a0001c0002t0072 | a0001c0002t0072g0083 | 1 | 128 | 0.0078 | 29 | c.916 others(48): Show |
NALF1 | ENSG00000204442.4 | transcript | ENST00000375915.4 | protein_coding | 1/2 | chr13 | TogoVar | ||||||
NAPEPLD_chr7_103094776_103154099 | 103099593 | T | TGTGTGTG others(22): Show |
downstream_gene_variant | MODIFIER | NA19006.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0175 | 1 | 381 | 0.0026 | 29 | c.*38 others(40): Show |
NAPEPLD | ENSG00000161048.12 | transcript | ENST00000465647.6 | protein_coding | 182 | chr7 | TogoVar | ||||||
NASP_chr1_45579041_45623893 | 45587687 | T | TATATATA others(22): Show |
intron_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0197 | 1 | 300 | 0.0033 | 29 | c.59+ others(44): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NAV1_chr1_201534127_201831969 | 201642525 | T | TTTTTCTT others(22): Show |
intron_variant | MODIFIER | HG01433.hp1 HG03704.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0020 | a0001c0001t0002g0027a0001c0001t0020g0083 | 2 | 210 | 0.0095 | 29 | c.827 others(46): Show |
NAV1 | ENSG00000134369.16 | transcript | ENST00000685211.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NAV1_chr1_201534127_201831969 | 201779598 | C | CAAAAAAA others(22): Show |
intron_variant | MODIFIER | HG03130.hp2 HG04228.hp2 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0016 | a0001c0001t0001g0124a0001c0001t0004g0159a0001c0001t0016g0082 | 3 | 210 | 0.0143 | 29 | c.208 others(46): Show |
NAV1 | ENSG00000134369.16 | transcript | ENST00000685211.1 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NAV1_chr1_201534127_201831969 | 201802136 | C | CAAAAAAA others(22): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0006 | a0006c0008 | a0006c0008t0088 | a0006c0008t0088g0089 | 1 | 210 | 0.0048 | 29 | c.437 others(48): Show |
NAV1 | ENSG00000134369.16 | transcript | ENST00000685211.1 | protein_coding | 19/33 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NAV2_chr11_19707837_20126601 | 19776577 | G | GTGTGTGT others(22): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0019 | a0001c0019t0049 | a0001c0019t0049g0142 | 1 | 166 | 0.0060 | 29 | c.268 others(48): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 1/37 | chr11 | TogoVar | ||||||
NBEAL1_chr2_203009875_203230194 | 203119424 | C | CTTTTTTT others(22): Show |
intron_variant | MODIFIER | HG00544.hp2 | a0001 | a0001c0001 | a0001c0001t0038 | a0001c0001t0038g0002 | 1 | 292 | 0.0034 | 29 | c.259 others(48): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NBPF15_chr1_144416390_144466669 | 144442095 | C | CACACGTG others(22): Show |
intron_variant | MODIFIER | HG00741.hp2 | a0001 | a0001c0029 | a0001c0029t0001 | a0001c0029t0001g0053 | 1 | 394 | 0.0025 | 29 | c.-19 others(48): Show |
NBPF15 | ENSG00000266338.7 | transcript | ENST00000581897.7 | protein_coding | 6/21 | chr1 | TogoVar | ||||||
NBPF3_chr1_21435137_21489900 | 21437463 | C | CCATGCAG others(22): Show |
upstream_gene_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0218 | 1 | 394 | 0.0025 | 29 | c.-30 others(40): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 2673 | chr1 | TogoVar | ||||||
NBPF8_chr1_120410035_120474676 | 120457732 | A | ATATATAT others(22): Show |
intron_variant | MODIFIER | HG02280.hp2 HG02451.hp1 HG03195.hp2 |
a0001 | a0001c0010 | a0001c0010t0032a0001c0010t0061a0001c0010t0063 | a0001c0010t0032g0075a0001c0010t0061g0073a0001c0010t0063g0077 | 3 | 292 | 0.0103 | 29 | c.163 others(48): Show |
NBPF8 | ENSG00000270231.5 | transcript | ENST00000698216.1 | protein_coding | 14/22 | chr1 | TogoVar | ||||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTGT others(22): Show |
intron_variant | MODIFIER | HG02965.hp1 HG03540.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0347a0001c0001t0002g0349 | 2 | 432 | 0.0046 | 29 | c.158 others(46): 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(22): Show |
intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG01943.hp2 |
a0006 | a0006c0008 | a0006c0008t0003 | a0006c0008t0003g0002 | 3 | 432 | 0.0069 | 29 | c.158 others(46): 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(22): Show |
intron_variant | MODIFIER | NA18994.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 | 1 | 378 | 0.0027 | 29 | c.198 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 16/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667377 | C | CCCTTACC others(22): Show |
intron_variant | MODIFIER | HG01257.hp2 HG01258.hp1 HG02155.hp2 |
a0001 | a0001c0004 | a0001c0004t0001a0001c0004t0002 | a0001c0004t0001g0003a0001c0004t0002g0187 | 3 | 378 | 0.0079 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667464 | G | GCCTTACC others(22): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0054 | 1 | 378 | 0.0027 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667608 | T | TCCTTACC others(22): Show |
intron_variant | MODIFIER | HG00738.hp2 HG00741.hp2 HG01891.hp2 others(7): Show |
a0001a0016 | a0001c0001a0016c0012 | a0001c0001t0002a0001c0001t0007a0016c0012t0002 | a0001c0001t0002g0044a0001c0001t0002g0065a0001c0001t0002g0071others(7): Show | 10 | 378 | 0.0265 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667636 | T | TCTTACCC others(22): Show |
intron_variant | MODIFIER | HG01952.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
a0001a0014 | a0001c0001a0014c0020 | a0001c0001t0001a0014c0020t0001 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0001g0349others(1): Show | 4 | 378 | 0.0106 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667751 | C | CCCTTACC others(22): Show |
intron_variant | MODIFIER | HG02683.hp2 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0180a0001c0001t0001g0285 | 2 | 378 | 0.0053 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667828 | T | TCCCTCCG others(22): Show |
intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01257.hp1 |
a0001a0007 | a0001c0001a0007c0022 | a0001c0001t0002a0007c0022t0002 | a0001c0001t0002g0029a0001c0001t0002g0107a0007c0022t0002g0099 | 3 | 378 | 0.0079 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667840 | C | CCCTTACC others(22): Show |
intron_variant | MODIFIER | NA18979.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0189 | 1 | 378 | 0.0027 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667840 | C | CCCTTACC others(22): Show |
intron_variant | MODIFIER | NA19066.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0246 | 1 | 378 | 0.0027 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667865 | G | GCCTTCCT others(22): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02572.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0020a0001c0001t0002g0141 | 2 | 378 | 0.0053 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667983 | T | TCCTTACC others(22): Show |
intron_variant | MODIFIER | HG02148.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0291 | 1 | 378 | 0.0027 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667985 | C | CTTACCGA others(22): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0163 | 1 | 378 | 0.0027 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668042 | C | CCCTTACC others(22): Show |
intron_variant | MODIFIER | NA19054.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0309 | 1 | 378 | 0.0027 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668042 | C | CCCTTACC others(22): Show |
intron_variant | MODIFIER | HG01943.hp1 HG02300.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0264a0001c0001t0001g0283 | 2 | 378 | 0.0053 | 29 | c.148 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668214 | C | CCCTTACC others(22): Show |
intron_variant | MODIFIER | HG00733.hp2 HG00735.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0014a0001c0001t0002g0036 | 2 | 378 | 0.0053 | 29 | c.147 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668214 | C | CCGTTACC others(22): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0163 | 1 | 378 | 0.0027 | 29 | c.147 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668237 | C | CCGCCCTC others(22): Show |
intron_variant | MODIFIER | HG02015.hp1 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0188 | 1 | 378 | 0.0027 | 29 | c.147 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668239 | G | GCCTTCCT others(22): Show |
intron_variant | MODIFIER | HG00438.hp1 HG02040.hp2 HG02818.hp1 others(5): Show |
a0001a0004 | a0001c0001a0004c0007 | a0001c0001t0001a0001c0001t0002a0004c0007t0002 | a0001c0001t0001g0223a0001c0001t0001g0245a0001c0001t0001g0280others(5): Show | 8 | 378 | 0.0212 | 29 | c.147 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668243 | T | TCCTTACC others(22): Show |
intron_variant | MODIFIER | HG02015.hp2 NA19002.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | 378 | 0.0053 | 29 | c.147 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668243 | T | TCCTTACC others(22): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0009 | a0009c0015 | a0009c0015t0002 | a0009c0015t0002g0130 | 1 | 378 | 0.0027 | 29 | c.147 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668243 | T | TCCTTACC others(22): Show |
intron_variant | MODIFIER | HG02622.hp1 HG03041.hp2 HG03471.hp2 others(2): Show |
a0001a0003 | a0001c0003a0003c0006 | a0001c0003t0002a0003c0006t0001 | a0001c0003t0002g0202a0001c0003t0002g0208a0001c0003t0002g0209others(2): Show | 5 | 378 | 0.0132 | 29 | c.147 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668245 | C | CTTACCGA others(22): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
a0001a0003a0008 | a0001c0001a0001c0005a0003c0006others(1): Show | a0001c0001t0001a0001c0005t0001a0003c0006t0001others(1): Show | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0005t0001g0225others(2): Show | 5 | 378 | 0.0132 | 29 | c.147 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668324 | C | CTGCCCTC others(22): Show |
intron_variant | MODIFIER | HG01256.hp2 HG01433.hp1 HG01943.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0262a0001c0001t0001g0281a0001c0001t0001g0283 | 3 | 378 | 0.0079 | 29 | c.147 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668342 | A | AACTGGGT others(22): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(6): Show |
a0001a0006 | a0001c0001a0006c0008 | a0001c0001t0001a0006c0008t0001 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(6): Show | 9 | 378 | 0.0238 | 29 | c.147 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158668342 | A | AACTGGGT others(22): Show |
intron_variant | MODIFIER | HG00639.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0236a0001c0001t0001g0321a0001c0001t0001g0325others(2): Show | 5 | 378 | 0.0132 | 29 | c.147 others(48): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCF2_chr1_183550562_183595459 | 183585624 | C | CAAAAAAA others(22): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0005 | a0005c0005 | a0005c0005t0004 | a0005c0005t0004g0034 | 1 | 406 | 0.0025 | 29 | c.257 others(46): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | TogoVar | ||||||
NCK2_chr2_105739912_105899272 | 105807788 | T | TCTCCCTC others(22): Show |
intron_variant | MODIFIER | NA19056.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0296 | 1 | 334 | 0.0030 | 29 | c.-20 others(48): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCMAP_chr1_24551087_24614328 | 24573952 | C | CAAAAAAA others(22): Show |
intron_variant | MODIFIER | NA18955.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0221 | 1 | 402 | 0.0025 | 29 | c.-8+ others(46): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24576149 | G | GTTTTTTT others(22): Show |
intron_variant | MODIFIER | HG00597.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0211 | 1 | 314 | 0.0032 | 29 | c.-25 others(48): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24690651 | C | CAAAAAAA others(22): Show |
intron_variant | MODIFIER | HG02040.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0188 | 1 | 314 | 0.0032 | 29 | c.533 others(44): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA2_chr8_70104782_70408808 | 70159243 | T | TATATATA others(22): Show |
intron_variant | MODIFIER | HG00621.hp2 HG02129.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0133a0001c0001t0002g0137 | 2 | 322 | 0.0062 | 29 | c.112 others(46): Show |
NCOA2 | ENSG00000140396.13 | transcript | ENST00000452400.7 | protein_coding | 10/22 | chr8 | TogoVar | ||||||
NCOA3_chr20_47496887_47661872 | 47511556 | T | TATATATA others(22): Show |
intron_variant | MODIFIER | NA18972.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0272 | 1 | 316 | 0.0032 | 29 | c.-99 others(46): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | chr20 | TogoVar |