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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNN2_chr19_1021608_1044065 | 1028969 | G | GTCAGGGG others(33): Show |
intron_variant | MODIFIER | HG04115.hp2 | a0001 | a0001c0013 | a0001c0013t0001 | a0001c0013t0001g0056 | 1 | 388 | 0.0026 | 40 | c.64- others(55): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
CNN2_chr19_1021608_1044065 | 1029364 | T | TAGCTCAG others(33): Show |
intron_variant | MODIFIER | HG01934.hp2 | a0001 | a0001c0005 | a0001c0005t0008 | a0001c0005t0008g0200 | 1 | 388 | 0.0026 | 40 | c.64- others(55): Show |
CNN2 | ENSG00000064666.15 | transcript | ENST00000263097.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
CNOT10_chr3_32680188_32778875 | 32754489 | A | AAAAAAAA others(33): Show |
intron_variant | MODIFIER | HG02155.hp1 NA18960.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0102 a0001c0001t0001g0132 |
2 | 74 | 0.0270 | 40 | c.159 others(59): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNOT10_chr3_32680188_32778875 | 32754489 | A | AAAAAATA others(33): Show |
intron_variant | MODIFIER | HG00323.hp2 NA18973.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 a0001c0001t0001g0165 |
2 | 74 | 0.0270 | 40 | c.159 others(59): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNOT1_chr16_58514951_58634826 | 58516124 | T | TGGGGCGG others(33): Show |
downstream_gene_variant | MODIFIER | NA18951.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148 | 1 | 167 | 0.0060 | 40 | c.*48 others(51): Show |
CNOT1 | ENSG00000125107.19 | transcript | ENST00000317147.10 | protein_coding | 3826 | chr16 | TogoVar | |||||||
CNOT2_chr12_70238433_70359993 | 70265273 | T | TTCTTCTC others(33): Show |
intron_variant | MODIFIER | HG01257.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0206 | 1 | 84 | 0.0119 | 40 | c.-95 others(59): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNOT3_chr19_54132762_54160681 | 54133831 | C | CCCTCTCT others(33): Show |
upstream_gene_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0005 | 1 | 213 | 0.0047 | 40 | c.-42 others(51): Show |
CNOT3 | ENSG00000088038.20 | transcript | ENST00000221232.11 | protein_coding | 3930 | chr19 | TogoVar | |||||||
CNOT3_chr19_54132762_54160681 | 54133923 | C | CCCCTCTC others(33): Show |
upstream_gene_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0141 | 1 | 205 | 0.0049 | 40 | c.-41 others(51): Show |
CNOT3 | ENSG00000088038.20 | transcript | ENST00000221232.11 | protein_coding | 3838 | chr19 | TogoVar | |||||||
CNOT3_chr19_54132762_54160681 | 54134031 | T | TCCCCTCT others(33): Show |
upstream_gene_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015 | 1 | 221 | 0.0045 | 40 | c.-40 others(51): Show |
CNOT3 | ENSG00000088038.20 | transcript | ENST00000221232.11 | protein_coding | 3730 | chr19 | TogoVar | |||||||
CNOT3_chr19_54132762_54160681 | 54142433 | T | TACACACA others(33): Show |
intron_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0056 | 1 | 59 | 0.0169 | 40 | c.-50 others(55): Show |
CNOT3 | ENSG00000088038.20 | transcript | ENST00000221232.11 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
CNOT6L_chr4_77708387_77824368 | 77819049 | G | GACACACA others(33): Show |
intron_variant | MODIFIER | HG04184.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0299 | 1 | 75 | 0.0133 | 40 | c.5+2 others(51): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | TogoVar | |||||||
CNOT6_chr5_180489379_180583358 | 180531190 | G | GGGCGGCT others(33): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0013 | a0001c0001t0001g0106 a0001c0001t0013g0104 a0001c0001t0013g0105 others(2): Show |
5 | 332 | 0.0151 | 40 | c.112 others(57): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
CNOT6_chr5_180489379_180583358 | 180533312 | C | CTATATAT others(33): Show |
intron_variant | MODIFIER | NA18967.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0070 | 1 | 76 | 0.0132 | 40 | c.112 others(57): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
CNOT9_chr2_218563839_218602080 | 218575424 | A | AGCTCAGG others(33): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00639.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005 | a0001c0001t0002g0087 a0001c0001t0005g0053 |
2 | 320 | 0.0063 | 40 | c.25- others(55): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNPY1_chr7_155496129_155551559 | 155527030 | T | TTTTCTTT others(33): Show |
intron_variant | MODIFIER | HG00597.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0159 | 1 | 315 | 0.0032 | 40 | c.100 others(59): Show |
CNPY1 | ENSG00000146910.14 | transcript | ENST00000636446.2 | protein_coding | 2/4 | chr7 | TogoVar | |||||||
CNST_chr1_246561456_246673595 | 246605789 | G | GGTGTCTT others(33): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
a0001a0005a0006 | a0001c0001a0001c0009a0001c0012others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0024 a0001c0001t0001g0154 a0001c0001t0001g0158 others(100): Show |
103 | 290 | 0.3552 | 40 | c.379 others(59): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
CNST_chr1_246561456_246673595 | 246605789 | G | GGTGTCTT others(33): Show |
intron_variant | MODIFIER | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0016 | a0001c0001t0001g0132 a0001c0001t0004g0018 a0001c0001t0004g0044 others(6): Show |
9 | 196 | 0.0459 | 40 | c.379 others(59): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40813058 | T | TCTTTCTT others(33): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0103 | 1 | 196 | 0.0051 | 40 | c.-76 others(59): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40924881 | C | CATATATA others(33): Show |
intron_variant | MODIFIER | NA18984.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0138 | 1 | 96 | 0.0104 | 40 | c.496 others(55): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74366780 | G | GTGTGTAT others(33): Show |
intron_variant | MODIFIER | HG04199.hp1 | a0002 | a0002c0005 | a0002c0005t0003 | a0002c0005t0003g0056 | 1 | 8 | 0.1250 | 40 | c.947 others(57): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 8/22 | chr3 | TogoVar | |||||||
CNTN4_chr3_2093866_3062959 | 2400404 | A | AATATATA others(33): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0036 | 1 | 114 | 0.0088 | 40 | c.-89 others(59): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2400420 | T | TATATATA others(33): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0054 | 1 | 115 | 0.0087 | 40 | c.-89 others(59): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2481033 | T | TTTTCTTT others(33): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0110 | 1 | 55 | 0.0182 | 40 | c.-88 others(59): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2481055 | T | TTCTTTCT others(33): Show |
intron_variant | MODIFIER | HG01175.hp2 HG01257.hp1 HG03041.hp2 |
a0001 | a0001c0003a0001c0004a0001c0005 | a0001c0003t0006a0001c0004t0001a0001c0005t0010 | a0001c0003t0006g0040 a0001c0004t0001g0106 a0001c0005t0010g0001 |
3 | 101 | 0.0297 | 40 | c.-88 others(59): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2687248 | T | TGCCTTCT others(33): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(22): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | a0001c0001t0001g0036 a0001c0001t0001g0050 a0001c0001t0001g0059 others(90): Show |
93 | 116 | 0.8017 | 40 | c.56- others(57): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99941571 | A | AACACACA others(33): Show |
intron_variant | MODIFIER | NA19000.hp1 | a0004 | a0004c0006 | a0004c0006t0014 | a0004c0006t0014g0058 | 1 | 43 | 0.0233 | 40 | c.674 others(59): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100090505 | C | CCCTCCCT others(33): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(8): Show |
a0001a0002a0004others(3): Show | a0001c0001a0002c0002a0004c0006others(3): Show | a0001c0001t0004a0001c0001t0010a0002c0002t0003others(5): Show | a0001c0001t0004g0011 a0001c0001t0004g0044 a0001c0001t0010g0047 others(8): Show |
11 | 46 | 0.2391 | 40 | c.158 others(61): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100090525 | C | CCCTCCCT others(33): Show |
intron_variant | MODIFIER | NA18522.hp1 | a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0007 | 1 | 51 | 0.0196 | 40 | c.158 others(61): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1158824 | A | ATATATAT others(33): Show |
intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(47): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0003others(15): Show | a0001c0001t0001g0037 a0001c0001t0001g0056 a0001c0001t0001g0106 others(47): Show |
50 | 173 | 0.2890 | 40 | c.55+ others(57): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1384412 | A | AAAGGCAG others(33): Show |
intron_variant | MODIFIER | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
a0001 | a0001c0005a0001c0006a0001c0023 | a0001c0005t0001a0001c0005t0004a0001c0006t0001others(2): Show | a0001c0005t0001g0005 a0001c0005t0001g0163 a0001c0005t0001g0180 others(11): Show |
14 | 230 | 0.0609 | 40 | c.251 others(59): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1384772 | C | CATATATA others(33): Show |
intron_variant | MODIFIER | HG02074.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0057 | 1 | 190 | 0.0053 | 40 | c.251 others(57): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146451851 | T | TGTATATA others(33): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01891.hp2 HG02486.hp1 others(13): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(12): Show | a0001c0001t0001g0003 a0001c0001t0006g0009 a0001c0001t0007g0018 others(13): Show |
16 | 33 | 0.4848 | 40 | c.98- others(59): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 146502227 | A | ATATATGT others(33): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0003 | a0001c0003t0023 | a0001c0003t0023g0030 | 1 | 40 | 0.0250 | 40 | c.98- others(59): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147802025 | G | GGCTGCCG others(33): Show |
intron_variant | MODIFIER | HG02451.hp1 HG03139.hp2 |
a0001 | a0001c0002a0001c0011 | a0001c0002t0001a0001c0011t0016 | a0001c0002t0001g0007 a0001c0011t0016g0019 |
2 | 40 | 0.0500 | 40 | c.209 others(63): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147802233 | A | ACGCTCCT others(33): Show |
intron_variant | MODIFIER | HG02486.hp1 HG02630.hp2 HG02886.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0007a0001c0002t0002a0001c0005t0022others(2): Show | a0001c0001t0007g0020 a0001c0002t0002g0013 a0001c0005t0022g0032 others(2): Show |
5 | 37 | 0.1351 | 40 | c.209 others(63): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147802233 | A | ATGCTCCT others(33): Show |
intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 NA18522.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0007a0001c0004t0003 | a0001c0001t0007g0018 a0001c0004t0003g0035 a0001c0004t0003g0036 |
3 | 35 | 0.0857 | 40 | c.209 others(63): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | chr7 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 148297187 | A | AGGAAGGA others(33): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 39 | 0.0256 | 40 | c.347 others(61): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148301306 | A | AAAATATA others(33): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0003 | a0001c0003t0011 | a0001c0003t0011g0023 | 1 | 5 | 0.2000 | 40 | c.347 others(61): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41934112 | T | TATATATA others(33): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG01255.hp2 others(3): Show |
a0002a0014 | a0002c0002a0002c0020a0014c0022 | a0002c0002t0001a0002c0002t0012a0002c0002t0022others(2): Show | a0002c0002t0001g0049 a0002c0002t0001g0059 a0002c0002t0012g0050 others(3): Show |
6 | 88 | 0.0682 | 40 | c.223 others(59): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | TogoVar | |||||||
CNTNAP3B_chr9_41885536_42134426 | 42090783 | C | CATATGTG others(33): Show |
intron_variant | MODIFIER | HG01255.hp1 HG02040.hp1 HG02273.hp2 others(3): Show |
a0001a0006a0017 | a0001c0001a0001c0042a0006c0007others(1): Show | a0001c0001t0003a0001c0042t0013a0006c0007t0002others(1): Show | a0001c0001t0003g0095 a0001c0001t0003g0101 a0001c0001t0003g0102 others(3): Show |
6 | 62 | 0.0968 | 40 | c.197 others(59): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | TogoVar | |||||||
CNTNAP3B_chr9_41885536_42134426 | 42090783 | C | CATATGTG others(33): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0021 | a0021c0039 | a0021c0039t0014 | a0021c0039t0014g0025 | 1 | 57 | 0.0175 | 40 | c.197 others(59): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | TogoVar | |||||||
CNTNAP4_chr16_76272401_76565757 | 76460773 | A | AAAAAAAA others(33): Show |
intron_variant | MODIFIER | NA18943.hp2 | a0006 | a0006c0009 | a0006c0009t0001 | a0006c0009t0001g0023 | 1 | 104 | 0.0096 | 40 | c.133 others(59): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76460773 | A | AAAAAAAA others(33): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0051 | 1 | 104 | 0.0096 | 40 | c.133 others(59): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76460773 | A | AAAAAAAA others(33): Show |
intron_variant | MODIFIER | NA19007.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 | 1 | 104 | 0.0096 | 40 | c.133 others(59): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76470482 | A | AATATATA others(33): Show |
intron_variant | MODIFIER | HG03098.hp1 NA18994.hp2 |
a0002a0003 | a0002c0005a0003c0003 | a0002c0005t0004a0003c0003t0007 | a0002c0005t0004g0132 a0003c0003t0007g0260 |
2 | 99 | 0.0202 | 40 | c.165 others(59): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76470495 | A | ATATATAT others(33): Show |
intron_variant | MODIFIER | HG00673.hp1 | a0008 | a0008c0017 | a0008c0017t0002 | a0008c0017t0002g0214 | 1 | 184 | 0.0054 | 40 | c.165 others(59): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76522687 | C | CTTTCTTT others(33): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0003 | a0003c0006 | a0003c0006t0001 | a0003c0006t0001g0067 | 1 | 164 | 0.0061 | 40 | c.275 others(57): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124571527 | C | CTTTTTCT others(33): Show |
intron_variant | MODIFIER | HG02897.hp1 NA19043.hp2 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0006a0002c0004t0001 | a0001c0001t0006g0040 a0002c0004t0001g0001 |
2 | 8 | 0.2500 | 40 | c.175 others(59): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
COA1_chr7_43634257_43734523 | 43644787 | C | CAGAGAGA others(33): Show |
intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0273 | 1 | 195 | 0.0051 | 40 | c.264 others(55): Show |
COA1 | ENSG00000106603.20 | transcript | ENST00000223336.11 | protein_coding | 4/5 | chr7 | TogoVar | |||||||
COA1_chr7_43634257_43734523 | 43664103 | A | AAGAGAGA others(33): Show |
intron_variant | MODIFIER | HG02074.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0143 | 1 | 91 | 0.0110 | 40 | c.-38 others(59): Show |
COA1 | ENSG00000106603.20 | transcript | ENST00000223336.11 | protein_coding | 1/5 | chr7 | TogoVar |