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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NCAM1_chr11_112956420_113283436 | 113056012 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | NA18990.hp1 NA18990.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0107a0001c0001t0002g0238 | 2 | 242 | 0.0083 | -13 | c.52+ others(30): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113145850 | GGAGGCAG others(6): Show |
G | intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0089 | 1 | 242 | 0.0041 | -13 | c.53- others(30): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113210774 | AAACACAC others(6): Show |
A | intron_variant | MODIFIER | NA18963.hp2 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0105 | 1 | 242 | 0.0041 | -13 | c.916 others(30): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NCAM1_chr11_112956420_113283436 | 113281898 | GATCACCA others(6): Show |
G | downstream_gene_variant | MODIFIER | HG01070.hp1 NA20129.hp1 |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0084a0001c0001t0008g0232 | 2 | 242 | 0.0083 | -13 | c.*65 others(24): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 3463 | chr11 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21032949 | TTTTTTTT others(6): Show |
T | intron_variant | MODIFIER | HG00280.hp1 HG00733.hp2 HG01361.hp2 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0006a0001c0001t0030others(5): Show | a0001c0001t0003g0113a0001c0001t0003g0120a0001c0001t0006g0067others(7): Show | 10 | 132 | 0.0758 | -13 | c.55+ others(30): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21063210 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG00639.hp2 HG03139.hp1 HG03471.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0002a0001c0001t0020a0001c0001t0029others(2): Show | a0001c0001t0002g0072a0001c0001t0020g0131a0001c0001t0029g0061others(2): Show | 5 | 132 | 0.0379 | -13 | c.55+ others(30): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21248776 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02572.hp1 |
a0002a0003 | a0002c0003a0003c0006 | a0002c0003t0002a0003c0006t0018 | a0002c0003t0002g0128a0003c0006t0018g0016 | 2 | 132 | 0.0152 | -13 | c.56- others(30): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21394469 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG00639.hp1 HG00741.hp1 HG01891.hp2 others(11): Show |
a0002a0003 | a0002c0002a0002c0003a0002c0008others(3): Show | a0002c0002t0002a0002c0002t0008a0002c0002t0033others(8): Show | a0002c0002t0002g0047a0002c0002t0008g0098a0002c0002t0033g0074others(11): Show | 14 | 132 | 0.1061 | -13 | c.119 others(34): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAM2_chr21_20993409_21548329 | 21415330 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | NA18992.hp1 | a0002 | a0002c0003 | a0002c0003t0006 | a0002c0003t0006g0031 | 1 | 132 | 0.0076 | -13 | c.138 others(32): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
NCAN_chr19_19206958_19257233 | 19210613 | CTTTTTTT others(6): Show |
C | upstream_gene_variant | MODIFIER | HG02109.hp2 | a0003 | a0003c0016 | a0003c0016t0005 | a0003c0016t0005g0128 | 1 | 318 | 0.0031 | -13 | c.-14 others(24): Show |
NCAN | ENSG00000130287.14 | transcript | ENST00000252575.11 | protein_coding | 1344 | chr19 | TogoVar | ||||||
NCAPD3_chr11_134145113_134228967 | 134153710 | CAGATTCC others(6): Show |
C | intron_variant | MODIFIER | HG03669.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0179 | 1 | 370 | 0.0027 | -13 | c.425 others(30): Show |
NCAPD3 | ENSG00000151503.14 | transcript | ENST00000534548.7 | protein_coding | 32/34 | chr11 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158628505 | GGGAGGCT others(6): Show |
G | downstream_gene_variant | MODIFIER | HG02717.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
a0001a0004 | a0001c0001a0004c0007 | a0001c0001t0005a0004c0007t0002 | a0001c0001t0005g0168a0001c0001t0005g0214a0004c0007t0002g0212others(2): Show | 5 | 378 | 0.0132 | -13 | c.*31 others(24): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 2663 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158660417 | TTTTTTTT others(6): Show |
T | intron_variant | MODIFIER | HG01243.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
a0001a0011 | a0001c0001a0011c0016 | a0001c0001t0001a0011c0016t0001 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 4 | 378 | 0.0106 | -13 | c.198 others(32): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 16/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667329 | GCTACTGT others(6): Show |
G | intron_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0272 | 1 | 378 | 0.0027 | -13 | c.148 others(32): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158709333 | ATAGGAAG others(6): Show |
A | upstream_gene_variant | MODIFIER | HG02040.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0083 | 1 | 378 | 0.0027 | -13 | c.-46 others(24): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 4530 | chr7 | TogoVar | ||||||
NCAPH_chr2_96330766_96382091 | 96335021 | CTATATTT others(6): Show |
C | upstream_gene_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 356 | 0.0028 | -13 | c.-80 others(22): Show |
NCAPH | ENSG00000121152.10 | transcript | ENST00000240423.9 | protein_coding | 744 | chr2 | TogoVar | ||||||
NCBP2_chr3_196930406_196947528 | 196932728 | ATTTTTTT others(6): Show |
A | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00738.hp1 HG01074.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007 | 3 | 420 | 0.0071 | -13 | c.*42 others(24): Show |
NCBP2 | ENSG00000114503.11 | transcript | ENST00000321256.10 | protein_coding | 2677 | chr3 | TogoVar | ||||||
NCCRP1_chr19_39191964_39206884 | 39199498 | CTTTTTTC others(6): Show |
C | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0002a0001c0001t0002g0002a0001c0001t0002g0011others(8): Show | 104 | 380 | 0.2737 | -13 | c.548 others(28): Show |
NCCRP1 | ENSG00000188505.5 | transcript | ENST00000339852.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
NCEH1_chr3_172625249_172716067 | 172677807 | AGTCCCAG others(6): Show |
A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(30): Show | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0172others(191): Show | 194 | 332 | 0.5843 | -13 | c.139 others(32): Show |
NCEH1 | ENSG00000144959.11 | transcript | ENST00000475381.7 | protein_coding | 1/4 | chr3 | TogoVar | ||||||
NCK1_chr3_136857208_136956606 | 136874402 | AGTCCTGA others(6): Show |
A | intron_variant | MODIFIER | HG04115.hp1 HG04199.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0046a0001c0001t0001g0053 | 2 | 232 | 0.0086 | -13 | c.-19 others(32): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
NCK1_chr3_136857208_136956606 | 136889044 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0012 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 18 | 232 | 0.0776 | -13 | c.-19 others(32): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
NCK2_chr2_105739912_105899272 | 105798403 | TATAAAAT others(6): Show |
T | intron_variant | MODIFIER | NA20905.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0266 | 1 | 334 | 0.0030 | -13 | c.-20 others(34): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCK2_chr2_105739912_105899272 | 105880936 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(119): Show |
a0001a0005 | a0001c0001a0005c0007 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(17): Show | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0183others(118): Show | 122 | 334 | 0.3653 | -13 | c.227 others(28): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCKAP5_chr2_132666788_133573463 | 132761037 | TCCTCTTT others(6): Show |
T | intron_variant | MODIFIER | HG00408.hp1 HG02074.hp1 HG02083.hp1 others(14): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0003c0004others(6): Show | a0001c0001t0002a0002c0002t0001a0002c0002t0004others(9): Show | a0001c0001t0002g0034a0002c0002t0001g0060a0002c0002t0004g0001others(14): Show | 17 | 70 | 0.2429 | -13 | c.512 others(34): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 16/19 | chr2 | TogoVar | ||||||
NCKAP5_chr2_132666788_133573463 | 132771839 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | HG02896.hp2 HG03195.hp1 |
a0001a0012 | a0001c0024a0012c0028 | a0001c0024t0001a0012c0028t0001 | a0001c0024t0001g0013a0012c0028t0001g0006 | 2 | 70 | 0.0286 | -13 | c.512 others(32): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 16/19 | chr2 | TogoVar | ||||||
NCKAP5_chr2_132666788_133573463 | 133242246 | TTTCTTTT others(6): Show |
T | intron_variant | MODIFIER | HG02257.hp1 HG02723.hp1 HG03195.hp1 |
a0001a0002a0012 | a0001c0009a0002c0002a0012c0028 | a0001c0009t0003a0002c0002t0005a0012c0028t0001 | a0001c0009t0003g0056a0002c0002t0005g0069a0012c0028t0001g0006 | 3 | 70 | 0.0429 | -13 | c.144 others(32): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 4/19 | chr2 | TogoVar | ||||||
NCKIPSD_chr3_48668844_48690915 | 48690802 | AAGAAAAA others(6): Show |
A | upstream_gene_variant | MODIFIER | HG01884.hp2 NA19030.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0001 | a0001c0001t0002g0050a0001c0002t0001g0097 | 2 | 310 | 0.0065 | -13 | c.-50 others(24): Show |
NCKIPSD | ENSG00000213672.8 | transcript | ENST00000294129.7 | protein_coding | 4888 | chr3 | TogoVar | ||||||
NCMAP_chr1_24551087_24614328 | 24589290 | CGTTTGAT others(6): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(1): Show | a0001c0001t0003g0392a0001c0001t0003g0394a0001c0001t0008g0150others(4): Show | 7 | 402 | 0.0174 | -13 | c.-7- others(28): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCMAP_chr1_24551087_24614328 | 24604600 | AAAAAAAT others(6): Show |
A | intron_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061 | 1 | 402 | 0.0025 | -13 | c.168 others(29): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCMAP_chr1_24551087_24614328 | 24604602 | AAAAATAT others(6): Show |
A | intron_variant | MODIFIER | HG02897.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0064 | 1 | 402 | 0.0025 | -13 | c.168 others(29): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24523924 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG01884.hp1 HG03453.hp2 HG03579.hp1 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0006a0001c0005t0012 | a0001c0002t0006g0118a0001c0005t0012g0081a0001c0005t0012g0082 | 3 | 314 | 0.0096 | -13 | c.-39 others(34): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24552341 | ATATATAT others(6): Show |
A | intron_variant | MODIFIER | NA18950.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0268 | 1 | 314 | 0.0032 | -13 | c.-39 others(34): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24552347 | ATATATAT others(6): Show |
A | intron_variant | MODIFIER | HG02735.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0048 | 1 | 314 | 0.0032 | -13 | c.-39 others(34): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24552349 | ATATATTT others(6): Show |
A | intron_variant | MODIFIER | HG02451.hp2 HG03098.hp2 HG03453.hp1 |
a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0042a0001c0002t0003g0043a0001c0002t0003g0063 | 3 | 314 | 0.0096 | -13 | c.-39 others(34): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24552351 | ATATTTTT others(6): Show |
A | intron_variant | MODIFIER | HG03486.hp1 NA19063.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0164a0001c0002t0003g0053 | 2 | 314 | 0.0064 | -13 | c.-39 others(34): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24552353 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | HG00621.hp1 HG02027.hp2 HG02074.hp2 others(9): Show |
a0001 | a0001c0001a0001c0014 | a0001c0001t0001a0001c0001t0005a0001c0014t0001 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0133others(9): Show | 12 | 314 | 0.0382 | -13 | c.-39 others(34): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24576157 | TTTTTTGT others(6): Show |
T | intron_variant | MODIFIER | HG00408.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0001a0001c0002t0003 | a0001c0001t0004g0177a0001c0001t0004g0197a0001c0001t0004g0201others(19): Show | 22 | 314 | 0.0701 | -13 | c.-25 others(32): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24614199 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG03239.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0303 | 1 | 314 | 0.0032 | -13 | c.-17 others(34): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24638180 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02647.hp1 HG02886.hp1 |
a0001 | a0001c0002 | a0001c0002t0010 | a0001c0002t0010g0213a0001c0002t0010g0214a0001c0002t0010g0215 | 3 | 314 | 0.0096 | -13 | c.-17 others(32): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24639902 | AAGTATGT others(6): Show |
A | intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0002 | a0001c0002t0010 | a0001c0002t0010g0213 | 1 | 314 | 0.0032 | -13 | c.-17 others(32): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 3/22 | chr2 | TogoVar | ||||||
NCOA1_chr2_24486254_24775702 | 24671245 | TTGAGTGG others(6): Show |
T | intron_variant | MODIFIER | HG02622.hp2 HG02723.hp2 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0001 | a0001c0001t0001g0275a0001c0006t0001g0262 | 2 | 314 | 0.0064 | -13 | c.257 others(30): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24719028 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0262 | 1 | 314 | 0.0032 | -13 | c.260 others(32): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24727138 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0163 | 1 | 314 | 0.0032 | -13 | c.271 others(30): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA1_chr2_24486254_24775702 | 24757671 | GTTACCTA others(6): Show |
G | intron_variant | MODIFIER | HG02965.hp1 HG02970.hp1 |
a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0216a0001c0001t0014g0217 | 2 | 314 | 0.0064 | -13 | c.388 others(30): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
NCOA2_chr8_70104782_70408808 | 70250392 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02055.hp1 HG03098.hp2 others(1): Show |
a0001 | a0001c0005 | a0001c0005t0012 | a0001c0005t0012g0048a0001c0005t0012g0049a0001c0005t0012g0050others(1): Show | 4 | 322 | 0.0124 | -13 | c.-19 others(32): Show |
NCOA2 | ENSG00000140396.13 | transcript | ENST00000452400.7 | protein_coding | 2/22 | chr8 | TogoVar | ||||||
NCOA3_chr20_47496887_47661872 | 47517445 | CTTTTTCT others(6): Show |
C | intron_variant | MODIFIER | HG01106.hp2 HG02572.hp2 HG02922.hp2 others(2): Show |
a0007 | a0007c0010 | a0007c0010t0014 | a0007c0010t0014g0032a0007c0010t0014g0033a0007c0010t0014g0035others(2): Show | 5 | 316 | 0.0158 | -13 | c.-99 others(32): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
NCOA3_chr20_47496887_47661872 | 47550423 | AACAAGAG others(6): Show |
A | intron_variant | MODIFIER | HG01169.hp1 | a0004 | a0004c0006 | a0004c0006t0006 | a0004c0006t0006g0082 | 1 | 316 | 0.0032 | -13 | c.-98 others(32): Show |
NCOA3 | ENSG00000124151.19 | transcript | ENST00000371998.8 | protein_coding | 1/22 | chr20 | TogoVar | ||||||
NCOA6_chr20_34709774_34830651 | 34778958 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0205 | 1 | 290 | 0.0035 | -13 | c.236 others(30): Show |
NCOA6 | ENSG00000198646.14 | transcript | ENST00000359003.7 | protein_coding | 3/14 | chr20 | TogoVar | ||||||
NCOA7_chr6_125785960_125937034 | 125827188 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(6): Show | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0109others(67): Show | 70 | 270 | 0.2593 | -13 | c.50+ others(30): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
NCOA7_chr6_125785960_125937034 | 125840868 | GTTTTTTT others(6): Show |
G | intron_variant | MODIFIER | HG03831.hp1 NA18939.hp2 NA18950.hp1 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0003c0003t0003 | a0001c0001t0001g0043a0003c0003t0003g0111a0003c0003t0003g0115 | 3 | 270 | 0.0111 | -13 | c.51- others(30): Show |
NCOA7 | ENSG00000111912.20 | transcript | ENST00000392477.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr6 | TogoVar |