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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NCAM2_chr21_20993409_21548329 | 21052150 | A | ATTTTTTT others(21): Show |
intron_variant | MODIFIER | HG00741.hp1 HG03579.hp2 |
a0001a0003 | a0001c0007a0003c0005 | a0001c0007t0004a0003c0005t0005 | a0001c0007t0004g0106 a0003c0005t0005g0105 |
2 | 132 | 0.0152 | 28 | c.55+ others(45): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21147054 | C | CTGCCTTC others(21): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(55): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0004a0001c0007others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0079 others(55): Show |
58 | 132 | 0.4394 | 28 | c.56- others(47): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21265498 | T | TATATGTG others(21): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0073 | 1 | 132 | 0.0076 | 28 | c.56- others(45): 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(21): Show |
intron_variant | MODIFIER | HG02293.hp2 HG03209.hp1 HG03516.hp2 |
a0002 | a0002c0002 | a0002c0002t0014a0002c0002t0034a0002c0002t0035 | a0002c0002t0014g0119 a0002c0002t0034g0059 a0002c0002t0035g0052 |
3 | 132 | 0.0227 | 28 | c.148 others(47): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21486303 | C | CAAAAAAA others(21): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0002 | a0002c0003 | a0002c0003t0017 | a0002c0003t0017g0038 | 1 | 132 | 0.0076 | 28 | c.207 others(47): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTGT others(21): Show |
intron_variant | MODIFIER | HG03209.hp1 HG03516.hp1 |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0015 | a0001c0001t0007g0380 a0001c0001t0015g0382 |
2 | 432 | 0.0046 | 28 | c.158 others(45): 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(21): Show |
intron_variant | MODIFIER | HG00323.hp2 NA19081.hp1 |
a0003 | a0003c0003 | a0003c0003t0003a0003c0003t0013 | a0003c0003t0003g0094 a0003c0003t0013g0097 |
2 | 432 | 0.0046 | 28 | c.158 others(45): 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(21): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0302 | 1 | 378 | 0.0027 | 28 | c.198 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 16/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667431 | G | GCTCCTTA others(21): Show |
intron_variant | MODIFIER | HG03491.hp2 HG04228.hp1 |
a0001 | a0001c0004 | a0001c0004t0001a0001c0004t0002 | a0001c0004t0001g0191 a0001c0004t0002g0190 |
2 | 378 | 0.0053 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667533 | C | CGGGTCCC others(21): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0163 | 1 | 378 | 0.0027 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667561 | A | ACTGGGTC others(21): Show |
intron_variant | MODIFIER | HG04199.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0019 | 1 | 378 | 0.0027 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667579 | C | CCTTACCC others(21): Show |
intron_variant | MODIFIER | HG01168.hp1 HG01169.hp1 HG01358.hp1 others(5): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0003t0001 | a0001c0001t0001g0193 a0001c0001t0001g0240 a0001c0001t0002g0026 others(5): Show |
8 | 378 | 0.0212 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667663 | T | TTCCTTAC others(21): Show |
intron_variant | MODIFIER | HG01167.hp2 NA18993.hp2 NA19006.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007 | a0001c0001t0002g0044 a0001c0001t0002g0117 a0001c0001t0002g0138 others(1): Show |
4 | 378 | 0.0106 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667763 | A | ACTGGGTC others(21): Show |
intron_variant | MODIFIER | HG02965.hp1 HG03098.hp2 NA18522.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0349 |
3 | 378 | 0.0079 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667828 | T | TCCCTCCG others(21): Show |
intron_variant | MODIFIER | HG03710.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0055 | 1 | 378 | 0.0027 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667899 | C | CCTTACCC others(21): Show |
intron_variant | MODIFIER | HG01109.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0101 | 1 | 378 | 0.0027 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667982 | T | TTCCTTAC others(21): Show |
intron_variant | MODIFIER | HG01109.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0101 | 1 | 378 | 0.0027 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668030 | T | TCCCTCCG others(21): Show |
intron_variant | MODIFIER | NA19082.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0223 | 1 | 378 | 0.0027 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668035 | C | CTGCCCTC others(21): Show |
intron_variant | MODIFIER | HG01346.hp2 HG01516.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0324 a0001c0001t0001g0326 |
2 | 378 | 0.0053 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668039 | C | CCTCCTTA others(21): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0352 | 1 | 378 | 0.0027 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668042 | C | CCCTTACC others(21): Show |
intron_variant | MODIFIER | HG01943.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0066 | 1 | 378 | 0.0027 | 28 | c.148 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668210 | C | CCCGCCTT others(21): Show |
intron_variant | MODIFIER | HG01346.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0324 | 1 | 378 | 0.0027 | 28 | c.147 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668210 | C | CCCTCCTT others(21): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(68): Show |
a0001a0016a0019 | a0001c0001a0001c0018a0016c0010others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(3): Show | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0034 others(68): Show |
71 | 378 | 0.1878 | 28 | c.147 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668313 | A | ACTGGGTC others(21): Show |
intron_variant | MODIFIER | HG02559.hp1 HG03516.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0237 a0001c0001t0001g0315 |
2 | 378 | 0.0053 | 28 | c.147 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668325 | C | CGCCCTCC others(21): Show |
intron_variant | MODIFIER | HG03491.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0190 | 1 | 378 | 0.0027 | 28 | c.147 others(47): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCBP2L_chrX_107772733_107800829 | 107781676 | A | ATCTATCT others(21): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0071 | 1 | 303 | 0.0033 | 28 | c.-73 others(45): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
NCBP2L_chrX_107772733_107800829 | 107781784 | A | ATAGATAT others(21): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0012a0001c0002t0002others(2): Show | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(80): Show |
97 | 303 | 0.3201 | 28 | c.-73 others(45): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
NCBP2L_chrX_107772733_107800829 | 107781803 | T | TATAGATA others(21): Show |
intron_variant | MODIFIER | NA18963.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0132 | 1 | 303 | 0.0033 | 28 | c.-73 others(45): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
NCBP3_chr17_3797158_3851246 | 3826695 | A | AGAAGGAA others(21): Show |
intron_variant | MODIFIER | HG03654.hp2 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0195 | 1 | 370 | 0.0027 | 28 | c.482 others(43): Show |
NCBP3 | ENSG00000074356.17 | transcript | ENST00000389005.6 | protein_coding | 4/12 | chr17 | TogoVar | |||||||
NCF2_chr1_183550562_183595459 | 183585624 | C | CAAAAAAA others(21): Show |
intron_variant | MODIFIER | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
a0005 | a0005c0005 | a0005c0005t0004 | a0005c0005t0004g0029 a0005c0005t0004g0030 a0005c0005t0004g0031 others(2): Show |
5 | 406 | 0.0123 | 28 | c.257 others(45): Show |
NCF2 | ENSG00000116701.16 | transcript | ENST00000367535.8 | protein_coding | 2/14 | chr1 | TogoVar | |||||||
NCK2_chr2_105739912_105899272 | 105750037 | A | AACACACA others(21): Show |
intron_variant | MODIFIER | HG01261.hp2 HG01981.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0008 | a0001c0001t0003g0176 a0001c0001t0008g0175 |
2 | 334 | 0.0060 | 28 | c.-20 others(47): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCK2_chr2_105739912_105899272 | 105835393 | A | ATATATAT others(21): Show |
intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02027.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0018a0001c0001t0021 | a0001c0001t0004g0038 a0001c0001t0004g0064 a0001c0001t0004g0068 others(3): Show |
6 | 334 | 0.0180 | 28 | c.-17 others(47): 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(21): Show |
intron_variant | MODIFIER | HG03927.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0283 | 1 | 350 | 0.0029 | 28 | c.307 others(45): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCKAP1_chr2_182904115_183043457 | 182912849 | A | AAAGGAAG others(21): Show |
3_prime_UTR_variant | MODIFIER | HG00609.hp1 HG01071.hp2 HG01243.hp1 others(24): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0007a0001c0001t0010a0001c0001t0014others(11): Show | a0001c0001t0007g0060 a0001c0001t0007g0065 a0001c0001t0007g0100 others(24): Show |
27 | 218 | 0.1239 | 28 | c.*12 others(41): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12852 | chr2 | TogoVar | ||||||
NCKAP5_chr2_132666788_133573463 | 133492144 | A | AGTGTGTG others(21): Show |
intron_variant | MODIFIER | HG00738.hp2 HG02630.hp2 HG02922.hp1 others(4): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0009a0002c0002others(3): Show | a0001c0001t0004a0001c0009t0001a0002c0002t0004others(3): Show | a0001c0001t0004g0002 a0001c0009t0001g0042 a0002c0002t0004g0004 others(4): Show |
7 | 70 | 0.1000 | 28 | c.69+ others(45): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 3/19 | chr2 | TogoVar | |||||||
NCMAP_chr1_24551087_24614328 | 24573952 | C | CAAAAAAA others(21): Show |
intron_variant | MODIFIER | NA18966.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0298 | 1 | 402 | 0.0025 | 28 | c.-8+ others(45): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NCOA1_chr2_24486254_24775702 | 24523605 | C | CAAAAAAA others(21): Show |
intron_variant | MODIFIER | NA20300.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0299 | 1 | 314 | 0.0032 | 28 | c.-39 others(49): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCOA1_chr2_24486254_24775702 | 24629809 | C | CATATATA others(21): Show |
intron_variant | MODIFIER | NA20752.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0047 | 1 | 314 | 0.0032 | 28 | c.-17 others(49): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCOA1_chr2_24486254_24775702 | 24642007 | C | CGTGTGTG others(21): Show |
intron_variant | MODIFIER | HG02818.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0001 | 1 | 314 | 0.0032 | 28 | c.-17 others(47): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCOA1_chr2_24486254_24775702 | 24642037 | T | TGTGTGTG others(21): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0002 | a0001c0002t0006 | a0001c0002t0006g0115 | 1 | 314 | 0.0032 | 28 | c.-17 others(47): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCOA1_chr2_24486254_24775702 | 24690651 | C | CAAAAAAA others(21): Show |
intron_variant | MODIFIER | HG00735.hp2 NA19077.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0199 a0001c0001t0004g0206 |
2 | 314 | 0.0064 | 28 | c.533 others(43): 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(21): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0001 | a0001c0003 | a0001c0003t0030 | a0001c0003t0030g0086 | 1 | 322 | 0.0031 | 28 | c.315 others(47): Show |
NCOA2 | ENSG00000140396.13 | transcript | ENST00000452400.7 | protein_coding | 15/22 | chr8 | TogoVar | |||||||
NCOA2_chr8_70104782_70408808 | 70159236 | A | ATATATAT others(21): Show |
intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(14): Show |
a0001a0005 | a0001c0001a0005c0018 | a0001c0001t0001a0001c0001t0002a0005c0018t0002 | a0001c0001t0001g0093 a0001c0001t0001g0156 a0001c0001t0001g0161 others(14): Show |
17 | 322 | 0.0528 | 28 | c.112 others(45): Show |
NCOA2 | ENSG00000140396.13 | transcript | ENST00000452400.7 | protein_coding | 10/22 | chr8 | TogoVar | |||||||
NCOA2_chr8_70104782_70408808 | 70232870 | T | TACACACA others(21): Show |
intron_variant | MODIFIER | HG01981.hp1 HG02257.hp1 NA19043.hp1 |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0009a0002c0002t0003 | a0001c0003t0009g0073 a0001c0003t0009g0081 a0002c0002t0003g0012 |
3 | 322 | 0.0093 | 28 | c.-19 others(47): Show |
NCOA2 | ENSG00000140396.13 | transcript | ENST00000452400.7 | protein_coding | 2/22 | chr8 | TogoVar | |||||||
NCOA6_chr20_34709774_34830651 | 34751376 | C | CAAAAAAA others(21): Show |
intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0047 | 1 | 290 | 0.0035 | 28 | c.167 others(45): Show |
NCOA6 | ENSG00000198646.14 | transcript | ENST00000359003.7 | protein_coding | 8/14 | chr20 | TogoVar | |||||||
NCOA6_chr20_34709774_34830651 | 34811201 | G | GTATATAT others(21): Show |
intron_variant | MODIFIER | HG02056.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0167 | 1 | 290 | 0.0035 | 28 | c.-16 others(49): Show |
NCOA6 | ENSG00000198646.14 | transcript | ENST00000359003.7 | protein_coding | 1/14 | chr20 | TogoVar | |||||||
NCOA6_chr20_34709774_34830651 | 34811201 | G | GTATGTAT others(21): Show |
intron_variant | MODIFIER | NA18941.hp1 NA18955.hp1 NA18979.hp1 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0240 a0001c0002t0001g0241 a0001c0002t0001g0242 others(1): Show |
4 | 290 | 0.0138 | 28 | c.-16 others(49): Show |
NCOA6 | ENSG00000198646.14 | transcript | ENST00000359003.7 | protein_coding | 1/14 | chr20 | TogoVar | |||||||
NCOR1_chr17_16024157_16220534 | 16092695 | A | ATATATAT others(21): Show |
intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0272 | 1 | 282 | 0.0036 | 28 | c.282 others(45): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 21/45 | chr17 | TogoVar | |||||||
NCOR1_chr17_16024157_16220534 | 16106883 | A | ATATATAT others(21): Show |
intron_variant | MODIFIER | HG03453.hp1 NA18987.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0012 | a0001c0001t0002g0152 a0001c0001t0012g0029 |
2 | 282 | 0.0071 | 28 | c.218 others(47): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 19/45 | chr17 | TogoVar | |||||||
NCOR1_chr17_16024157_16220534 | 16127293 | G | GTATGTAT others(21): Show |
intron_variant | MODIFIER | HG00280.hp2 HG01069.hp1 HG01106.hp1 others(7): Show |
a0001a0003 | a0001c0001a0001c0005a0003c0012 | a0001c0001t0001a0001c0005t0001a0003c0012t0001 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0081 others(7): Show |
10 | 282 | 0.0355 | 28 | c.151 others(47): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 14/45 | chr17 | TogoVar |