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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNPY1_chr7_155496129_155551559 | 155527054 | C | CTTTCTTT others(6): Show |
intron_variant | MODIFIER | HG01516.hp1 NA18986.hp2 NA18994.hp2 others(1): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0015a0001c0002t0029a0001c0003t0006 | a0001c0002t0015g0365 a0001c0002t0029g0309 a0001c0003t0006g0047 others(1): Show |
4 | 183 | 0.0219 | 13 | c.100 others(32): Show |
CNPY1 | ENSG00000146910.14 | transcript | ENST00000636446.2 | protein_coding | 2/4 | chr7 | TogoVar | |||||||
CNPY4_chr7_100114634_100130508 | 100121117 | T | TATATATA others(6): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0040 | 1 | 363 | 0.0028 | 13 | c.119 others(30): Show |
CNPY4 | ENSG00000166997.8 | transcript | ENST00000262932.5 | protein_coding | 1/5 | chr7 | TogoVar | |||||||
CNR1_chr6_88134864_88171347 | 88164947 | T | TACACAAC others(6): Show |
intron_variant | MODIFIER | NA19001.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0238 | 1 | 396 | 0.0025 | 13 | c.-64 others(28): Show |
CNR1 | ENSG00000118432.13 | transcript | ENST00000369501.3 | protein_coding | 1/1 | chr6 | TogoVar | |||||||
CNR2_chr1_23865515_23918362 | 23895996 | T | TTGCTACC others(6): Show |
intron_variant | MODIFIER | NA18956.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0041 | 1 | 266 | 0.0038 | 13 | c.-46 others(32): Show |
CNR2 | ENSG00000188822.8 | transcript | ENST00000374472.5 | protein_coding | 1/1 | chr1 | TogoVar | |||||||
CNRIP1_chr2_68288010_68324949 | 68306124 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG00738.hp2 HG03017.hp2 HG03453.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0003t0001 | a0001c0001t0002g0323 a0001c0003t0001g0238 a0001c0003t0001g0239 others(1): Show |
4 | 63 | 0.0635 | 13 | c.330 others(32): Show |
CNRIP1 | ENSG00000119865.9 | transcript | ENST00000263655.4 | protein_coding | 2/2 | chr2 | TogoVar | |||||||
CNST_chr1_246561456_246673595 | 246642132 | G | GTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG00735.hp1 HG02647.hp2 HG02922.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0008 | a0001c0001t0001g0175 a0001c0001t0001g0180 a0001c0001t0004g0016 others(3): Show |
6 | 254 | 0.0236 | 13 | c.937 others(26): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | chr1 | TogoVar | |||||||
CNST_chr1_246561456_246673595 | 246646279 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG00733.hp1 HG01243.hp2 HG01891.hp2 others(23): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(6): Show | a0001c0001t0001g0013 a0001c0001t0001g0132 a0001c0001t0001g0165 others(23): Show |
26 | 168 | 0.1548 | 13 | c.938 others(28): 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(6): Show |
intron_variant | MODIFIER | HG01952.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0133 | 1 | 259 | 0.0039 | 13 | c.170 others(30): Show |
CNTD1 | ENSG00000176563.10 | transcript | ENST00000588408.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
CNTD1_chr17_42793861_42816587 | 42801547 | A | ATATATAT others(6): Show |
intron_variant | MODIFIER | HG01346.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 284 | 0.0035 | 13 | c.170 others(30): Show |
CNTD1 | ENSG00000176563.10 | transcript | ENST00000588408.6 | protein_coding | 1/6 | chr17 | TogoVar | |||||||
CNTFR_chr9_34546433_34594724 | 34548545 | G | GAAGAGAC others(6): Show |
downstream_gene_variant | MODIFIER | NA19089.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0135 | 1 | 400 | 0.0025 | 13 | c.*35 others(24): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2887 | chr9 | TogoVar | |||||||
CNTLN_chr9_17130040_17508923 | 17179261 | A | AAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0030 | a0001c0030t0002 | a0001c0030t0002g0048 | 1 | 135 | 0.0074 | 13 | c.449 others(32): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
CNTLN_chr9_17130040_17508923 | 17202646 | G | GTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0019 | a0019c0045 | a0019c0045t0002 | a0019c0045t0002g0046 | 1 | 77 | 0.0130 | 13 | c.450 others(32): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
CNTLN_chr9_17130040_17508923 | 17359732 | A | AAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02895.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0126 | 1 | 210 | 0.0048 | 13 | c.188 others(32): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40690834 | T | TTTATTTT others(6): Show |
upstream_gene_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0055 | 1 | 229 | 0.0044 | 13 | c.-18 others(24): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1604 | chr12 | TogoVar | |||||||
CNTN1_chr12_40687439_41077415 | 40698228 | A | ATTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0059 | 1 | 24 | 0.0417 | 13 | c.-77 others(30): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40813026 | T | TTTTCTTT others(6): Show |
intron_variant | MODIFIER | HG00621.hp1 HG00735.hp1 HG00738.hp2 others(26): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(6): Show | a0001c0001t0001g0037 a0001c0001t0001g0076 a0001c0001t0001g0077 others(26): Show |
29 | 191 | 0.1518 | 13 | c.-76 others(32): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40974436 | C | CATAAAAA others(6): Show |
intron_variant | MODIFIER | HG02083.hp2 NA18952.hp2 NA19065.hp2 |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0135 a0001c0001t0006g0139 a0001c0001t0006g0140 |
3 | 230 | 0.0130 | 13 | c.180 others(32): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 41075740 | A | AGGAAGGA others(6): Show |
downstream_gene_variant | MODIFIER | NA18952.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0093 | 1 | 212 | 0.0047 | 13 | c.*57 others(24): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 3326 | chr12 | TogoVar | |||||||
CNTN4_chr3_2093866_3062959 | 2237652 | G | GTATTTTA others(6): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02683.hp1 HG02818.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0025others(2): Show | a0001c0001t0003a0001c0002t0002a0001c0002t0007others(3): Show | a0001c0001t0003g0095 a0001c0002t0002g0063 a0001c0002t0007g0080 others(3): Show |
6 | 116 | 0.0517 | 13 | c.-14 others(36): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2400943 | T | TCTTATAG others(6): Show |
intron_variant | MODIFIER | HG03927.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0038 | 1 | 116 | 0.0086 | 13 | c.-89 others(32): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | chr3 | TogoVar | |||||||
CNTN4_chr3_2093866_3062959 | 2611297 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02257.hp1 HG02809.hp2 HG02897.hp2 others(1): Show |
a0001a0003 | a0001c0001a0001c0006a0001c0022others(1): Show | a0001c0001t0003a0001c0006t0002a0001c0022t0003others(1): Show | a0001c0001t0003g0006 a0001c0006t0002g0060 a0001c0022t0003g0083 others(1): Show |
4 | 45 | 0.0889 | 13 | c.55+ others(30): 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(6): Show |
intron_variant | MODIFIER | HG02257.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
a0001 | a0001c0002a0001c0006a0001c0022 | a0001c0002t0001a0001c0002t0003a0001c0006t0004others(1): Show | a0001c0002t0001g0088 a0001c0002t0003g0024 a0001c0006t0004g0004 others(1): Show |
4 | 25 | 0.1600 | 13 | c.454 others(30): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99121138 | T | TCTTTCTT others(6): Show |
intron_variant | MODIFIER | HG02258.hp2 | a0006 | a0006c0005 | a0006c0005t0003 | a0006c0005t0003g0045 | 1 | 47 | 0.0213 | 13 | c.-21 others(34): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | chr11 | TogoVar | |||||||
CNTN5_chr11_99015949_100363885 | 99131115 | A | AGCTGGGC others(6): Show |
intron_variant | MODIFIER | HG03471.hp1 | a0009 | a0009c0008 | a0009c0008t0007 | a0009c0008t0007g0038 | 1 | 66 | 0.0152 | 13 | c.-21 others(36): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | chr11 | TogoVar | |||||||
CNTN5_chr11_99015949_100363885 | 99342571 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG00733.hp1 NA19043.hp1 |
a0001a0011 | a0001c0001a0011c0009 | a0001c0001t0009a0011c0009t0005 | a0001c0001t0009g0063 a0011c0009t0005g0056 |
2 | 13 | 0.1538 | 13 | c.-71 others(32): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99382845 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02004.hp2 HG02132.hp2 HG03041.hp1 |
a0001a0005a0008 | a0001c0001a0005c0004a0008c0012 | a0001c0001t0001a0005c0004t0002a0008c0012t0008 | a0001c0001t0001g0004 a0005c0004t0002g0051 a0008c0012t0008g0026 |
3 | 10 | 0.3000 | 13 | c.-71 others(32): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99508686 | C | CTTTCTTT others(6): Show |
intron_variant | MODIFIER | HG02723.hp2 HG02976.hp1 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0004a0003c0003t0007 | a0001c0001t0004g0044 a0003c0003t0007g0034 |
2 | 60 | 0.0333 | 13 | c.-70 others(32): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99637010 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02004.hp1 HG03041.hp2 NA19000.hp2 |
a0001a0005 | a0001c0001a0005c0004 | a0001c0001t0001a0001c0001t0010a0005c0004t0002 | a0001c0001t0001g0054 a0001c0001t0010g0023 a0005c0004t0002g0001 |
3 | 4 | 0.7500 | 13 | c.55+ others(30): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100072990 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02976.hp2 HG03130.hp1 |
a0006 | a0006c0005 | a0006c0005t0001 | a0006c0005t0001g0017 a0006c0005t0001g0035 |
2 | 12 | 0.1667 | 13 | c.143 others(32): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100161870 | C | CACACACA others(6): Show |
intron_variant | MODIFIER | HG00733.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0063 | 1 | 66 | 0.0152 | 13 | c.158 others(34): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1233734 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02109.hp1 | a0005 | a0005c0027 | a0005c0027t0001 | a0005c0027t0001g0191 | 1 | 87 | 0.0115 | 13 | c.358 others(30): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245303 | T | TATATATA others(6): Show |
intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0003a0001c0004t0001 | a0001c0002t0003g0109 a0001c0004t0001g0151 |
2 | 229 | 0.0087 | 13 | c.358 others(32): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1280459 | A | ATTTTTTT others(6): Show |
intron_variant | MODIFIER | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0003others(4): Show | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0096 others(9): Show |
12 | 52 | 0.2308 | 13 | c.454 others(30): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1348157 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0010 | a0001c0010t0001 | a0001c0010t0001g0207 | 1 | 112 | 0.0089 | 13 | c.136 others(32): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTNAP1_chr17_42677531_42704993 | 42686469 | G | GTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0184 | 1 | 181 | 0.0055 | 13 | c.900 others(28): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146322634 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0003 | a0003c0014 | a0003c0014t0021 | a0003c0014t0021g0022 | 1 | 15 | 0.0667 | 13 | c.97+ others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146352750 | G | GTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0006 | 1 | 10 | 0.1000 | 13 | c.97+ others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146404124 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02897.hp1 NA20129.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0023 | a0001c0002t0001g0008 a0001c0003t0023g0030 |
2 | 14 | 0.1429 | 13 | c.97+ others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146451853 | T | TATATATA others(6): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
a0001a0003 | a0001c0002a0001c0004a0001c0012others(1): Show | a0001c0002t0001a0001c0004t0003a0001c0004t0005others(2): Show | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0004t0003g0035 others(4): Show |
7 | 39 | 0.1795 | 13 | c.98- others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 146486046 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 4 | 0.2500 | 13 | c.98- others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146633832 | G | GAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG03139.hp2 NA18522.hp1 |
a0001 | a0001c0011a0001c0013 | a0001c0011t0016a0001c0013t0003 | a0001c0011t0016g0019 a0001c0013t0003g0039 |
2 | 6 | 0.3333 | 13 | c.98- others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146665783 | T | TAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0040 | 1 | 15 | 0.0667 | 13 | c.98- others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146708588 | A | ATTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0005 | a0001c0005t0022 | a0001c0005t0022g0032 | 1 | 3 | 0.3333 | 13 | c.98- others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146760409 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 4 | 0.2500 | 13 | c.98- others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146871537 | A | ATAAATAA others(6): Show |
intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0006 | 1 | 39 | 0.0256 | 13 | c.402 others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147237049 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0020 | 1 | 3 | 0.3333 | 13 | c.134 others(34): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147469506 | A | ATTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02486.hp1 NA20129.hp1 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0007a0001c0006t0009 | a0001c0001t0007g0020 a0001c0006t0009g0028 |
2 | 23 | 0.0870 | 13 | c.167 others(34): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147527015 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0003 | a0001c0003t0013 | a0001c0003t0013g0010 | 1 | 10 | 0.1000 | 13 | c.177 others(34): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147560168 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0008 | a0001c0008t0001 | a0001c0008t0001g0025 | 1 | 8 | 0.1250 | 13 | c.177 others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147860589 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0004 | 1 | 37 | 0.0270 | 13 | c.209 others(34): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |