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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNOT3_chr19_54132762_54160681 | 54134207 | T | TCCCTCCC others(4): Show |
upstream_gene_variant | MODIFIER | HG02080.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0126 | 1 | 223 | 0.0045 | 11 | c.-38 others(22): Show |
CNOT3 | ENSG00000088038.20 | transcript | ENST00000221232.11 | protein_coding | 3554 | chr19 | TogoVar | ||||||
CNOT4_chr7_135356795_135515102 | 135453847 | T | TATATATA others(4): Show |
intron_variant | MODIFIER | NA18989.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0041 | 1 | 362 | 0.0028 | 11 | c.-92 others(30): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | TogoVar | ||||||
CNOT4_chr7_135356795_135515102 | 135472510 | A | ATATATAT others(4): Show |
intron_variant | MODIFIER | HG01074.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0166 | 1 | 362 | 0.0028 | 11 | c.-92 others(30): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | TogoVar | ||||||
CNOT4_chr7_135356795_135515102 | 135472514 | A | AAAAAAAT others(4): Show |
intron_variant | MODIFIER | NA19002.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0169 | 1 | 362 | 0.0028 | 11 | c.-92 others(30): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | TogoVar | ||||||
CNOT4_chr7_135356795_135515102 | 135472514 | A | ATATATAT others(4): Show |
intron_variant | MODIFIER | NA18940.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0156 | 1 | 362 | 0.0028 | 11 | c.-92 others(30): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | TogoVar | ||||||
CNOT6L_chr4_77708387_77824368 | 77754888 | T | TAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(22): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0109others(22): Show | 25 | 328 | 0.0762 | 11 | c.490 others(28): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 5/11 | chr4 | TogoVar | ||||||
CNOT6L_chr4_77708387_77824368 | 77760860 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00280.hp1 HG01069.hp1 HG01081.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0001t0003g0006others(9): Show | 12 | 328 | 0.0366 | 11 | c.401 others(28): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | TogoVar | ||||||
CNOT6L_chr4_77708387_77824368 | 77779046 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0183 | 1 | 328 | 0.0031 | 11 | c.6-2 others(24): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | TogoVar | ||||||
CNOT6L_chr4_77708387_77824368 | 77789290 | A | AGCTCCCC others(4): Show |
intron_variant | MODIFIER | HG00323.hp1 HG02257.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0161a0001c0001t0001g0163 | 2 | 328 | 0.0061 | 11 | c.6-1 others(26): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | TogoVar | ||||||
CNOT6L_chr4_77708387_77824368 | 77807276 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0037 | a0001c0001t0037g0269 | 1 | 328 | 0.0031 | 11 | c.5+1 others(26): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 1/11 | chr4 | TogoVar | ||||||
CNOT6_chr5_180489379_180583358 | 180510134 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00609.hp1 HG02723.hp2 NA18980.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0008a0001c0001t0058 | a0001c0001t0002g0077a0001c0001t0008g0285a0001c0001t0058g0095 | 3 | 334 | 0.0090 | 11 | c.-3+ others(28): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CNOT6_chr5_180489379_180583358 | 180577163 | A | ATTGTGTG others(4): Show |
3_prime_UTR_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0001 | a0001c0001t0044 | a0001c0001t0044g0169 | 1 | 334 | 0.0030 | 11 | c.*29 others(22): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2965 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||
CNOT7_chr8_17219966_17251857 | 17226029 | C | CTTTTTTT others(4): Show |
3_prime_UTR_variant | MODIFIER | NA21309.hp1 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0105a0001c0001t0106 | a0001c0001t0105g0210a0001c0001t0106g0205 | 2 | 408 | 0.0049 | 11 | c.*46 others(22): Show |
CNOT7 | ENSG00000198791.12 | transcript | ENST00000361272.9 | protein_coding | 7/7 | 4690 | chr8 | TogoVar | |||||
CNOT9_chr2_218563839_218602080 | 218588588 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02083.hp1 HG02897.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0013 | a0001c0001t0004g0199a0001c0001t0013g0154 | 2 | 322 | 0.0062 | 11 | c.540 others(26): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNOT9_chr2_218563839_218602080 | 218595404 | C | CTTTTTTT others(4): Show |
3_prime_UTR_variant | MODIFIER | HG01884.hp2 HG02055.hp1 |
a0001 | a0001c0001 | a0001c0001t0040a0001c0001t0041 | a0001c0001t0040g0018a0001c0001t0041g0181 | 2 | 322 | 0.0062 | 11 | c.*11 others(22): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||
CNPY1_chr7_155496129_155551559 | 155500534 | C | CTTTTTTT others(4): Show |
downstream_gene_variant | MODIFIER | HG01891.hp2 HG03139.hp2 HG03492.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0007a0001c0001t0042a0001c0002t0015others(1): Show | a0001c0001t0007g0095a0001c0001t0007g0192a0001c0001t0042g0085others(2): Show | 5 | 426 | 0.0117 | 11 | c.*25 others(22): Show |
CNPY1 | ENSG00000146910.14 | transcript | ENST00000636446.2 | protein_coding | 594 | chr7 | TogoVar | ||||||
CNPY1_chr7_155496129_155551559 | 155507471 | T | TAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG03209.hp1 HG03209.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0010a0001c0003t0022 | a0001c0001t0010g0103a0001c0003t0022g0080 | 2 | 426 | 0.0047 | 11 | c.304 others(26): Show |
CNPY1 | ENSG00000146910.14 | transcript | ENST00000636446.2 | protein_coding | 3/4 | chr7 | TogoVar | ||||||
CNPY1_chr7_155496129_155551559 | 155527030 | T | TTTTCTTC others(4): Show |
intron_variant | MODIFIER | NA18992.hp2 | a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0296 | 1 | 426 | 0.0024 | 11 | c.100 others(30): Show |
CNPY1 | ENSG00000146910.14 | transcript | ENST00000636446.2 | protein_coding | 2/4 | chr7 | TogoVar | ||||||
CNPY1_chr7_155496129_155551559 | 155527055 | T | TTTCTTTC others(4): Show |
intron_variant | MODIFIER | HG01255.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0015 | a0001c0001t0007g0078a0001c0001t0007g0079a0001c0001t0007g0264others(3): Show | 6 | 426 | 0.0141 | 11 | c.100 others(30): Show |
CNPY1 | ENSG00000146910.14 | transcript | ENST00000636446.2 | protein_coding | 2/4 | chr7 | TogoVar | ||||||
CNPY2_chr12_56304844_56320988 | 56312222 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02083.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0051 | 1 | 372 | 0.0027 | 11 | c.205 others(26): Show |
CNPY2 | ENSG00000257727.6 | transcript | ENST00000273308.9 | protein_coding | 3/5 | chr12 | TogoVar | ||||||
CNPY4_chr7_100114634_100130508 | 100121116 | A | ATATACAT others(4): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0074 | 1 | 416 | 0.0024 | 11 | c.119 others(28): Show |
CNPY4 | ENSG00000166997.8 | transcript | ENST00000262932.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNPY4_chr7_100114634_100130508 | 100121116 | A | ATATATTT others(4): Show |
intron_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 416 | 0.0024 | 11 | c.119 others(28): Show |
CNPY4 | ENSG00000166997.8 | transcript | ENST00000262932.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNPY4_chr7_100114634_100130508 | 100121117 | T | TATATATA others(4): Show |
intron_variant | MODIFIER | NA18971.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0090 | 1 | 416 | 0.0024 | 11 | c.119 others(28): Show |
CNPY4 | ENSG00000166997.8 | transcript | ENST00000262932.5 | protein_coding | 1/5 | chr7 | TogoVar | ||||||
CNR2_chr1_23865515_23918362 | 23869244 | A | AAGGAAGG others(4): Show |
downstream_gene_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(115): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(21): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | 268 | 0.4403 | 11 | c.*52 others(22): Show |
CNR2 | ENSG00000188822.8 | transcript | ENST00000374472.5 | protein_coding | 1270 | chr1 | TogoVar | ||||||
CNR2_chr1_23865515_23918362 | 23891275 | T | TGTGTGTG others(4): Show |
intron_variant | MODIFIER | HG04115.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0154 | 1 | 268 | 0.0037 | 11 | c.-45 others(30): Show |
CNR2 | ENSG00000188822.8 | transcript | ENST00000374472.5 | protein_coding | 1/1 | chr1 | TogoVar | ||||||
CNR2_chr1_23865515_23918362 | 23904668 | G | GTGGGAGG others(4): Show |
intron_variant | MODIFIER | NA19077.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0021 | 1 | 268 | 0.0037 | 11 | c.-46 others(28): Show |
CNR2 | ENSG00000188822.8 | transcript | ENST00000374472.5 | protein_coding | 1/1 | chr1 | TogoVar | ||||||
CNRIP1_chr2_68288010_68324949 | 68306124 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG01243.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0054a0001c0001t0001g0122a0001c0001t0001g0197others(1): Show | 4 | 424 | 0.0094 | 11 | c.330 others(30): Show |
CNRIP1 | ENSG00000119865.9 | transcript | ENST00000263655.4 | protein_coding | 2/2 | chr2 | TogoVar | ||||||
CNST_chr1_246561456_246673595 | 246577995 | T | TGCCTTTG others(4): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0044 | 1 | 320 | 0.0031 | 11 | c.-52 others(30): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | chr1 | TogoVar | ||||||
CNST_chr1_246561456_246673595 | 246642132 | G | GTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG01981.hp1 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0008 | 1 | 320 | 0.0031 | 11 | c.937 others(24): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | TogoVar | ||||||
CNST_chr1_246561456_246673595 | 246646279 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(59): Show |
a0001a0002 | a0001c0001a0001c0009a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0160others(59): Show | 62 | 320 | 0.1938 | 11 | c.938 others(26): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CNTD1_chr17_42793861_42816587 | 42801510 | A | AAATATAT others(4): Show |
intron_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0194 | 1 | 306 | 0.0033 | 11 | c.170 others(28): Show |
CNTD1 | ENSG00000176563.10 | transcript | ENST00000588408.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
CNTFR_chr9_34546433_34594724 | 34582297 | A | AAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | 402 | 0.0100 | 11 | c.-11 others(30): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | TogoVar | ||||||
CNTLN_chr9_17130040_17508923 | 17202646 | G | GTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG03209.hp1 NA18943.hp2 NA18954.hp1 |
a0001a0020 | a0001c0004a0020c0041 | a0001c0004t0001a0020c0041t0001 | a0001c0004t0001g0005a0001c0004t0001g0007a0020c0041t0001g0106 | 3 | 218 | 0.0138 | 11 | c.450 others(30): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17338337 | G | GTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG01109.hp1 | a0013 | a0013c0019 | a0013c0019t0002 | a0013c0019t0002g0120 | 1 | 218 | 0.0046 | 11 | c.164 others(30): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17359717 | T | TAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02622.hp1 HG02735.hp1 HG03453.hp1 others(2): Show |
a0004a0008 | a0004c0003a0008c0009 | a0004c0003t0001a0004c0003t0002a0004c0003t0004others(2): Show | a0004c0003t0001g0146a0004c0003t0002g0181a0004c0003t0004g0180others(2): Show | 5 | 218 | 0.0229 | 11 | c.188 others(30): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17359728 | A | AAACAAAC others(4): Show |
intron_variant | MODIFIER | HG01109.hp1 HG02109.hp1 HG02895.hp1 others(2): Show |
a0011a0013 | a0011c0015a0013c0019 | a0011c0015t0002a0013c0019t0002 | a0011c0015t0002g0213a0011c0015t0002g0214a0011c0015t0002g0215others(2): Show | 5 | 218 | 0.0229 | 11 | c.188 others(30): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17359732 | A | AAACAAAC others(4): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0021 | a0021c0054 | a0021c0054t0002 | a0021c0054t0002g0016 | 1 | 218 | 0.0046 | 11 | c.188 others(30): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40698228 | A | ATTTTTTT others(4): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0004 | a0001c0004t0007 | a0001c0004t0007g0057 | 1 | 230 | 0.0044 | 11 | c.-77 others(28): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40809850 | A | ACACACAC others(4): Show |
intron_variant | MODIFIER | HG01258.hp1 HG01433.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0038a0001c0001t0002g0019 | 2 | 230 | 0.0087 | 11 | c.-76 others(30): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40813038 | C | CTTTCTTT others(4): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0009 | a0001c0009t0004 | a0001c0009t0004g0046 | 1 | 230 | 0.0044 | 11 | c.-76 others(30): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40924881 | C | CATACTAT others(4): Show |
intron_variant | MODIFIER | HG02004.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0218 | 1 | 230 | 0.0044 | 11 | c.496 others(26): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 41053428 | A | ATATATAT others(4): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0061 | 1 | 230 | 0.0044 | 11 | c.298 others(32): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 23/23 | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 41075673 | A | AAGAGAAG others(4): Show |
downstream_gene_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0005 | a0001c0005t0002 | a0001c0005t0002g0053 | 1 | 230 | 0.0044 | 11 | c.*56 others(22): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 3259 | chr12 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2198028 | G | GAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02257.hp1 HG03041.hp1 HG03516.hp2 |
a0001 | a0001c0001a0001c0022 | a0001c0001t0001a0001c0001t0004a0001c0022t0003 | a0001c0001t0001g0033a0001c0001t0004g0042a0001c0022t0003g0083 | 3 | 116 | 0.0259 | 11 | c.-14 others(32): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2294288 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG01243.hp2 HG02559.hp2 NA18906.hp2 |
a0001a0005 | a0001c0002a0001c0006a0005c0012 | a0001c0002t0002a0001c0006t0002a0005c0012t0009 | a0001c0002t0002g0102a0001c0006t0002g0051a0005c0012t0009g0093 | 3 | 116 | 0.0259 | 11 | c.-14 others(32): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2600005 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02165.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0020 | 1 | 116 | 0.0086 | 11 | c.55+ others(28): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2611297 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02647.hp2 HG03139.hp2 HG03486.hp1 others(1): Show |
a0001 | a0001c0002a0001c0005a0001c0010others(1): Show | a0001c0002t0001a0001c0005t0001a0001c0010t0003others(1): Show | a0001c0002t0001g0088a0001c0005t0001g0090a0001c0010t0003g0011others(1): Show | 4 | 116 | 0.0345 | 11 | c.55+ others(28): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2820961 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02572.hp1 HG03516.hp1 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0001a0001c0005t0001 | a0001c0002t0001g0110a0001c0005t0001g0090 | 2 | 116 | 0.0172 | 11 | c.454 others(28): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 3050763 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(2): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0009a0001c0002t0003a0001c0002t0004others(2): Show | a0001c0001t0009g0052a0001c0002t0003g0024a0001c0002t0004g0017others(2): Show | 5 | 116 | 0.0431 | 11 | c.281 others(30): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99131249 | G | GAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01099.hp2 HG01243.hp1 others(3): Show |
a0001a0002a0009 | a0001c0001a0002c0002a0009c0012 | a0001c0001t0003a0001c0001t0006a0002c0002t0003others(2): Show | a0001c0001t0003g0021a0001c0001t0006g0040a0002c0002t0003g0036others(3): Show | 6 | 66 | 0.0909 | 11 | c.-21 others(34): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |