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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
MYT1L_chr2_1784113_2336275 | 2262915 | A | AATATATA others(35): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0009 | a0001c0009t0008 | a0001c0009t0008g0007 | 1 | 83 | 0.0120 | 42 | c.-42 others(63): Show |
MYT1L | ENSG00000186487.21 | transcript | ENST00000647738.2 | protein_coding | 2/24 | chr2 | TogoVar | |||||||
MYZAP_chr15_57586904_57690364 | 57593188 | G | GCATGCGC others(35): Show |
intron_variant | MODIFIER | NA18952.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0157 | 1 | 31 | 0.0323 | 42 | c.75+ others(57): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MYZAP_chr15_57586904_57690364 | 57593188 | G | GCATGCGC others(35): Show |
intron_variant | MODIFIER | HG02080.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0160 | 1 | 31 | 0.0323 | 42 | c.75+ others(57): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MYZAP_chr15_57586904_57690364 | 57593188 | G | GCATGCGC others(35): Show |
intron_variant | MODIFIER | HG02071.hp1 HG02451.hp2 HG03041.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0013 a0001c0001t0001g0184 a0001c0001t0001g0188 others(2): Show |
5 | 35 | 0.1429 | 42 | c.75+ others(57): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MYZAP_chr15_57586904_57690364 | 57593188 | G | GCATGCGC others(35): Show |
intron_variant | MODIFIER | NA18947.hp1 NA18983.hp2 NA19003.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0261 |
3 | 33 | 0.0909 | 42 | c.75+ others(57): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MYZAP_chr15_57586904_57690364 | 57593188 | G | GCATGCGC others(35): Show |
intron_variant | MODIFIER | HG02135.hp2 HG02897.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0003 | a0001c0001t0001g0287 a0001c0003t0003g0339 |
2 | 32 | 0.0625 | 42 | c.75+ others(57): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MYZAP_chr15_57586904_57690364 | 57593188 | G | GCATGCGC others(35): Show |
intron_variant | MODIFIER | HG03490.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0300 | 1 | 31 | 0.0323 | 42 | c.75+ others(57): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MYZAP_chr15_57586904_57690364 | 57593188 | G | GCATGCGC others(35): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0001 | a0001c0001t0020 | a0001c0001t0020g0309 | 1 | 31 | 0.0323 | 42 | c.75+ others(57): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MYZAP_chr15_57586904_57690364 | 57593188 | G | GCATGCGC others(35): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0328 | 1 | 31 | 0.0323 | 42 | c.75+ others(57): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MYZAP_chr15_57586904_57690364 | 57689151 | C | CATATATG others(35): Show |
downstream_gene_variant | MODIFIER | HG02896.hp2 HG02897.hp2 HG03471.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0003 | a0001c0001t0001g0168 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | 330 | 0.0182 | 42 | c.*46 others(53): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3788 | chr15 | TogoVar | |||||||
MYZAP_chr15_57586904_57690364 | 57689163 | A | ATATACAC others(35): Show |
downstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0003a0001c0007others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0013 a0001c0001t0001g0160 a0001c0001t0001g0161 others(160): Show |
168 | 333 | 0.5045 | 42 | c.*46 others(53): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3800 | chr15 | TogoVar | |||||||
MYZAP_chr15_57586904_57690364 | 57689184 | A | ATATACAC others(35): Show |
downstream_gene_variant | MODIFIER | NA19079.hp2 | a0002 | a0002c0004 | a0002c0004t0001 | a0002c0004t0001g0163 | 1 | 349 | 0.0029 | 42 | c.*46 others(53): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3821 | chr15 | TogoVar | |||||||
NAALAD2_chr11_90129663_90197894 | 90155364 | T | TATGTAAT others(35): Show |
intron_variant | MODIFIER | HG03704.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0152 | 1 | 332 | 0.0030 | 42 | c.797 others(59): Show |
NAALAD2 | ENSG00000077616.11 | transcript | ENST00000534061.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NAALADL2_chr3_174854334_175815548 | 175181717 | G | GTGTGTGT others(35): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02895.hp2 HG03579.hp2 others(1): Show |
a0001a0002a0004 | a0001c0001a0002c0003a0004c0002others(1): Show | a0001c0001t0007a0002c0003t0004a0004c0002t0008others(1): Show | a0001c0001t0007g0031 a0002c0003t0004g0046 a0004c0002t0008g0039 others(1): Show |
4 | 46 | 0.0870 | 42 | c.546 others(61): Show |
NAALADL2 | ENSG00000177694.16 | transcript | ENST00000454872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
NAALADL2_chr3_174854334_175815548 | 175463701 | G | GGAGAGAG others(35): Show |
intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0031 | 1 | 33 | 0.0303 | 42 | c.132 others(59): Show |
NAALADL2 | ENSG00000177694.16 | transcript | ENST00000454872.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
NACAD_chr7_45075437_45093969 | 45079388 | C | CGGTGAGG others(35): Show |
downstream_gene_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
a0002a0003a0007others(12): Show | a0002c0041a0003c0003a0007c0007others(12): Show | a0002c0041t0001a0003c0003t0001a0003c0003t0003others(13): Show | a0002c0041t0001g0033 a0003c0003t0001g0002 a0003c0003t0001g0028 others(16): Show |
71 | 357 | 0.1989 | 42 | c.*11 others(53): Show |
NACAD | ENSG00000136274.9 | transcript | ENST00000490531.3 | protein_coding | 1048 | chr7 | TogoVar | |||||||
NACAD_chr7_45075437_45093969 | 45079632 | G | GGAGAGTA others(35): Show |
downstream_gene_variant | MODIFIER | HG01884.hp2 HG02970.hp1 HG03130.hp1 others(4): Show |
a0004a0034a0036 | a0004c0005a0004c0033a0004c0074others(2): Show | a0004c0005t0001a0004c0033t0001a0004c0074t0001others(2): Show | a0004c0005t0001g0004 a0004c0033t0001g0089 a0004c0074t0001g0093 others(2): Show |
7 | 405 | 0.0173 | 42 | c.*87 others(51): Show |
NACAD | ENSG00000136274.9 | transcript | ENST00000490531.3 | protein_coding | 804 | chr7 | TogoVar | |||||||
NALF1_chr13_107158510_107872496 | 107254062 | A | AAAAAAAA others(35): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0065 | a0001c0001t0065g0025 | 1 | 105 | 0.0095 | 42 | c.916 others(61): Show |
NALF1 | ENSG00000204442.4 | transcript | ENST00000375915.4 | protein_coding | 1/2 | chr13 | TogoVar | |||||||
NALF1_chr13_107158510_107872496 | 107638201 | A | ATATATAT others(35): Show |
intron_variant | MODIFIER | HG00609.hp1 NA19002.hp1 NA19002.hp2 |
a0001 | a0001c0001 | a0001c0001t0039a0001c0001t0042a0001c0001t0048 | a0001c0001t0039g0052 a0001c0001t0042g0044 a0001c0001t0048g0056 |
3 | 52 | 0.0577 | 42 | c.915 others(63): Show |
NALF1 | ENSG00000204442.4 | transcript | ENST00000375915.4 | protein_coding | 1/2 | chr13 | TogoVar | |||||||
NAP1L1_chr12_76031585_76089685 | 76058191 | C | CTTCATAT others(35): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0162 | 1 | 334 | 0.0030 | 42 | c.429 others(59): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | TogoVar | |||||||
NAPEPLD_chr7_103094776_103154099 | 103099575 | C | CGTGTGTG others(35): Show |
downstream_gene_variant | MODIFIER | HG00438.hp2 HG00558.hp2 HG01070.hp1 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0005a0002c0002t0001 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0014 others(8): Show |
11 | 68 | 0.1618 | 42 | c.*38 others(53): Show |
NAPEPLD | ENSG00000161048.12 | transcript | ENST00000465647.6 | protein_coding | 200 | chr7 | TogoVar | |||||||
NASP_chr1_45579041_45623893 | 45587687 | T | TATATATA others(35): Show |
intron_variant | MODIFIER | HG02071.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0075 | 1 | 8 | 0.1250 | 42 | c.59+ others(57): Show |
NASP | ENSG00000132780.17 | transcript | ENST00000350030.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NAT8_chr2_73635723_73647422 | 73643813 | G | GGTGTGTG others(35): Show |
upstream_gene_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 301 | 0.0033 | 42 | c.-15 others(53): Show |
NAT8 | ENSG00000144035.4 | transcript | ENST00000272425.4 | protein_coding | 1392 | chr2 | TogoVar | |||||||
NAV1_chr1_201534127_201831969 | 201642551 | T | TTCTTTCT others(35): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0008 | a0008c0017 | a0008c0017t0029 | a0008c0017t0029g0133 | 1 | 181 | 0.0055 | 42 | c.827 others(59): Show |
NAV1 | ENSG00000134369.16 | transcript | ENST00000685211.1 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NAV1_chr1_201534127_201831969 | 201734493 | G | GAGAAGAA others(35): Show |
intron_variant | MODIFIER | HG00140.hp1 HG01257.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0007a0002c0002t0004 | a0001c0001t0007g0084 a0002c0002t0004g0023 |
2 | 179 | 0.0112 | 42 | c.208 others(63): Show |
NAV1 | ENSG00000134369.16 | transcript | ENST00000685211.1 | protein_coding | 7/33 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NAV2_chr11_19707837_20126601 | 19897883 | G | GATCTATA others(35): Show |
intron_variant | MODIFIER | HG00558.hp1 | a0005 | a0005c0026 | a0005c0026t0002 | a0005c0026t0002g0120 | 1 | 159 | 0.0063 | 42 | c.931 others(59): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 6/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NAV2_chr11_19707837_20126601 | 19897886 | T | TTATATAT others(35): Show |
intron_variant | MODIFIER | HG01255.hp2 HG02723.hp1 HG03139.hp2 others(3): Show |
a0004a0007a0008 | a0004c0005a0004c0041a0004c0043others(3): Show | a0004c0005t0005a0004c0041t0028a0004c0043t0009others(3): Show | a0004c0005t0005g0131 a0004c0041t0028g0138 a0004c0043t0009g0147 others(3): Show |
6 | 94 | 0.0638 | 42 | c.931 others(59): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 6/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NAV2_chr11_19707837_20126601 | 19897886 | T | TTTTATAT others(35): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0001 | a0001c0050 | a0001c0050t0035 | a0001c0050t0035g0150 | 1 | 89 | 0.0112 | 42 | c.931 others(59): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 6/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NAV2_chr11_19707837_20126601 | 20106155 | G | GTGTATAT others(35): Show |
intron_variant | MODIFIER | HG02451.hp2 HG02559.hp2 HG02922.hp2 others(5): Show |
a0001a0002a0004 | a0001c0007a0001c0018a0002c0012others(5): Show | a0001c0007t0007a0001c0018t0048a0002c0012t0003others(5): Show | a0001c0007t0007g0088 a0001c0018t0048g0141 a0002c0012t0003g0012 others(5): Show |
8 | 136 | 0.0588 | 42 | c.684 others(59): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NBDY_chrX_56724243_56824179 | 56771475 | T | TCCTCCGC others(35): Show |
intron_variant | MODIFIER | HG00544.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0055 | 1 | 123 | 0.0081 | 42 | c.*16 others(63): Show |
NBDY | ENSG00000204272.13 | transcript | ENST00000374922.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
NBDY_chrX_56724243_56824179 | 56771502 | T | TCCTCCTC others(35): Show |
intron_variant | MODIFIER | HG01167.hp1 HG03041.hp2 HG03453.hp2 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0040 |
3 | 152 | 0.0197 | 42 | c.*16 others(63): Show |
NBDY | ENSG00000204272.13 | transcript | ENST00000374922.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
NBDY_chrX_56724243_56824179 | 56776904 | T | TCCTCCTC others(35): Show |
intron_variant | MODIFIER | HG03041.hp2 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0031 a0001c0001t0003g0033 |
2 | 157 | 0.0127 | 42 | c.*16 others(63): Show |
NBDY | ENSG00000204272.13 | transcript | ENST00000374922.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113173591 | G | GATATATA others(35): Show |
intron_variant | MODIFIER | HG01993.hp1 | a0001 | a0001c0002 | a0001c0002t0017 | a0001c0002t0017g0235 | 1 | 10 | 0.1000 | 42 | c.53- others(59): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21214722 | C | CATATATA others(35): Show |
intron_variant | MODIFIER | HG04228.hp1 | a0001 | a0001c0001 | a0001c0001t0038 | a0001c0001t0038g0053 | 1 | 104 | 0.0096 | 42 | c.56- others(59): 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(35): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00733.hp1 HG02622.hp2 others(1): Show |
a0001a0002 | a0001c0004a0002c0002 | a0001c0004t0001a0002c0002t0001a0002c0002t0004others(1): Show | a0001c0004t0001g0101 a0002c0002t0001g0018 a0002c0002t0004g0049 others(1): Show |
4 | 99 | 0.0404 | 42 | c.148 others(61): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTGT others(35): Show |
intron_variant | MODIFIER | HG02145.hp1 HG02976.hp1 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0270 a0001c0001t0002g0275 a0001c0001t0002g0276 |
3 | 93 | 0.0323 | 42 | c.158 others(59): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCAPG2_chr7_158626169_158709804 | 158667329 | G | GCCCGCCT others(35): Show |
intron_variant | MODIFIER | HG02615.hp1 HG02622.hp1 HG03453.hp2 others(6): Show |
a0001a0016a0018 | a0001c0001a0001c0003a0016c0010others(1): Show | a0001c0001t0002a0001c0001t0007a0001c0003t0001others(3): Show | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0128 others(6): Show |
9 | 130 | 0.0692 | 42 | c.148 others(61): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667329 | G | GCCCTCCT others(35): Show |
intron_variant | MODIFIER | HG00621.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0247 | 1 | 122 | 0.0082 | 42 | c.148 others(61): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCK2_chr2_105739912_105899272 | 105807747 | T | TTCCCTCC others(35): Show |
intron_variant | MODIFIER | HG03491.hp1 HG03492.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0001 | 2 | 243 | 0.0082 | 42 | c.-20 others(61): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCK2_chr2_105739912_105899272 | 105807835 | A | ATCCCTCC others(35): Show |
intron_variant | MODIFIER | HG00099.hp1 HG03942.hp2 NA18951.hp1 others(5): Show |
a0001a0004 | a0001c0001a0004c0003 | a0001c0001t0012a0001c0001t0014a0001c0001t0024others(1): Show | a0001c0001t0012g0322 a0001c0001t0012g0323 a0001c0001t0012g0325 others(5): Show |
8 | 274 | 0.0292 | 42 | c.-20 others(61): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCK2_chr2_105739912_105899272 | 105807842 | C | CCTCCCTC others(35): Show |
intron_variant | MODIFIER | HG03704.hp1 HG03927.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0063 a0001c0001t0004g0064 |
2 | 257 | 0.0078 | 42 | c.-20 others(61): 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(35): Show |
intron_variant | MODIFIER | HG00140.hp2 HG02647.hp1 NA18966.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0011 | a0001c0001t0003g0188 a0001c0001t0004g0093 a0001c0001t0011g0096 |
3 | 245 | 0.0122 | 42 | c.-17 others(61): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCMAP_chr1_24551087_24614328 | 24597593 | A | AGAAGAAA others(35): Show |
intron_variant | MODIFIER | HG00558.hp1 NA18999.hp2 NA19066.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0190 a0001c0001t0006g0281 a0001c0001t0006g0283 others(1): Show |
4 | 400 | 0.0100 | 42 | c.82+ others(57): Show |
NCMAP | ENSG00000184454.7 | transcript | ENST00000374392.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NCOA1_chr2_24486254_24775702 | 24758059 | G | GGAAAAGA others(35): Show |
stop_gained others(1): Show |
HIGH | NA19006.hp1 | a0004 | a0004c0009 | a0004c0009t0001 | a0004c0009t0001g0150 | 1 | 312 | 0.0032 | 42 | c.396 others(51): Show |
p.Gly others(57): Show |
NCOA1 | ENSG00000084676.16 | transcript | ENST00000348332.8 | protein_coding | 21/23 | 4713/7381 | 3969/4326 | 1323/1441 | chr2 | TogoVar | |||
NCOR1_chr17_16024157_16220534 | 16077501 | A | AGGGGAGG others(35): Show |
intron_variant | MODIFIER | NA18995.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0267 | 1 | 280 | 0.0036 | 42 | c.350 others(61): Show |
NCOR1 | ENSG00000141027.23 | transcript | ENST00000268712.8 | protein_coding | 26/45 | chr17 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124373365 | A | ACGAGGCC others(35): Show |
intron_variant | MODIFIER | HG01099.hp1 HG01106.hp2 HG01168.hp2 others(7): Show |
a0001a0002a0003others(1): Show | a0001c0028a0001c0048a0001c0049others(5): Show | a0001c0028t0033a0001c0048t0064a0001c0049t0042others(7): Show | a0001c0028t0033g0137 a0001c0048t0064g0182 a0001c0049t0042g0089 others(7): Show |
10 | 223 | 0.0448 | 42 | c.221 others(59): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 21/48 | chr12 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124373410 | A | ATGAGGCC others(35): Show |
intron_variant | MODIFIER | HG02109.hp1 | a0002 | a0002c0014 | a0002c0014t0001 | a0002c0014t0001g0120 | 1 | 225 | 0.0044 | 42 | c.221 others(59): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 21/48 | chr12 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124373665 | A | ATGAGGCC others(35): Show |
intron_variant | MODIFIER | HG00558.hp1 NA18940.hp1 NA19000.hp2 others(4): Show |
a0002a0005a0011 | a0002c0033a0002c0152a0002c0154others(2): Show | a0002c0033t0047a0002c0033t0056a0002c0152t0040others(4): Show | a0002c0033t0047g0054 a0002c0033t0056g0043 a0002c0152t0040g0217 others(4): Show |
7 | 149 | 0.0470 | 42 | c.221 others(59): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 21/48 | chr12 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124373681 | C | CGCAGGGG others(35): Show |
intron_variant | MODIFIER | HG00280.hp1 HG01099.hp2 HG01256.hp1 others(9): Show |
a0001a0003a0004others(2): Show | a0001c0132a0003c0042a0003c0070others(6): Show | a0001c0132t0035a0003c0042t0017a0003c0070t0049others(7): Show | a0001c0132t0035g0129 a0003c0042t0017g0095 a0003c0070t0049g0094 others(9): Show |
12 | 222 | 0.0541 | 42 | c.221 others(59): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 21/48 | chr12 | TogoVar | |||||||
NCOR2_chr12_124319415_124572612 | 124373846 | T | TGAGGCCA others(35): Show |
intron_variant | MODIFIER | HG01099.hp1 HG01106.hp2 HG01168.hp2 others(9): Show |
a0001a0002a0003others(1): Show | a0001c0027a0001c0028a0001c0048others(6): Show | a0001c0027t0021a0001c0027t0025a0001c0028t0033others(9): Show | a0001c0027t0021g0104 a0001c0027t0025g0168 a0001c0028t0033g0137 others(9): Show |
12 | 96 | 0.1250 | 42 | c.221 others(59): Show |
NCOR2 | ENSG00000196498.15 | transcript | ENST00000405201.6 | protein_coding | 21/48 | chr12 | TogoVar |