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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNST_chr1_246561456_246673595 | 246646279 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(4): Show | a0001c0001t0001g0025 a0001c0001t0001g0290 a0001c0001t0002g0172 others(10): Show |
13 | 320 | 0.0406 | 14 | c.938 others(29): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
CNTLN_chr9_17130040_17508923 | 17179261 | A | AAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02647.hp1 | a0008 | a0008c0010 | a0008c0010t0002 | a0008c0010t0002g0049 | 1 | 218 | 0.0046 | 14 | c.449 others(33): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
CNTLN_chr9_17130040_17508923 | 17185771 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00544.hp1 HG01070.hp1 others(18): Show |
a0001a0002a0005others(4): Show | a0001c0001a0001c0004a0002c0006others(7): Show | a0001c0001t0001a0001c0004t0001a0002c0006t0001others(9): Show | a0001c0001t0001g0124 a0001c0004t0001g0009 a0001c0004t0001g0012 others(18): Show |
21 | 218 | 0.0963 | 14 | c.450 others(33): 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(7): Show |
intron_variant | MODIFIER | HG02895.hp1 HG02896.hp2 HG03225.hp2 others(1): Show |
a0001a0002a0011 | a0001c0004a0002c0048a0011c0015 | a0001c0004t0001a0002c0048t0007a0011c0015t0002 | a0001c0004t0001g0013 a0002c0048t0007g0216 a0011c0015t0002g0213 others(1): Show |
4 | 218 | 0.0184 | 14 | c.450 others(33): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
CNTLN_chr9_17130040_17508923 | 17302089 | T | TACACACA others(7): Show |
intron_variant | MODIFIER | NA19060.hp1 | a0004 | a0004c0003 | a0004c0003t0001 | a0004c0003t0001g0062 | 1 | 218 | 0.0046 | 14 | c.114 others(33): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
CNTLN_chr9_17130040_17508923 | 17440588 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG00673.hp2 HG02056.hp1 HG02155.hp1 others(13): Show |
a0001a0004a0015others(4): Show | a0001c0001a0004c0003a0015c0035others(4): Show | a0001c0001t0001a0004c0003t0001a0004c0003t0002others(5): Show | a0001c0001t0001g0169 a0004c0003t0001g0052 a0004c0003t0001g0054 others(13): Show |
16 | 218 | 0.0734 | 14 | c.311 others(35): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40737357 | G | GTATATAT others(7): Show |
intron_variant | MODIFIER | NA18747.hp1 NA18943.hp2 NA18957.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0002g0175 others(3): Show |
6 | 230 | 0.0261 | 14 | c.-77 others(33): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40747305 | A | ATGTGTGT others(7): Show |
intron_variant | MODIFIER | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(20): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(7): Show | a0001c0001t0001g0206 a0001c0001t0002g0091 a0001c0002t0001g0001 others(20): Show |
23 | 230 | 0.1000 | 14 | c.-77 others(33): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40813051 | C | CTTTCTTT others(7): Show |
intron_variant | MODIFIER | HG01109.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0160 | 1 | 230 | 0.0044 | 14 | c.-76 others(33): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40822148 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG03654.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0024 | 1 | 230 | 0.0044 | 14 | c.-76 others(33): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40862208 | T | TACACACA others(7): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02717.hp1 NA21309.hp1 |
a0001 | a0001c0003a0001c0006 | a0001c0003t0003a0001c0003t0019a0001c0006t0006 | a0001c0003t0003g0061 a0001c0003t0019g0056 a0001c0006t0006g0119 |
3 | 230 | 0.0130 | 14 | c.-76 others(33): 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(7): Show |
intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01070.hp2 others(8): Show |
a0001a0002a0005 | a0001c0001a0001c0005a0002c0007others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0024others(3): Show | a0001c0001t0001g0177 a0001c0001t0001g0229 a0001c0001t0005g0020 others(8): Show |
11 | 230 | 0.0478 | 14 | c.496 others(29): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 41053428 | A | AATATATA others(7): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG01515.hp1 others(22): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(9): Show | a0001c0001t0002g0016 a0001c0001t0002g0067 a0001c0001t0002g0069 others(22): Show |
25 | 230 | 0.1087 | 14 | c.298 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 41057019 | T | TATTATAA others(7): Show |
intron_variant | MODIFIER | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(25): Show |
a0001a0002 | a0001c0001a0001c0009a0002c0007 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(2): Show | a0001c0001t0001g0037 a0001c0001t0001g0076 a0001c0001t0001g0077 others(25): Show |
28 | 230 | 0.1217 | 14 | c.298 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 23/23 | chr12 | TogoVar | |||||||
CNTN2_chr1_205038212_205083289 | 205080525 | T | TACACACA others(7): Show |
downstream_gene_variant | MODIFIER | HG03139.hp2 HG03453.hp2 |
a0005a0012 | a0005c0007a0012c0020 | a0005c0007t0009a0012c0020t0014 | a0005c0007t0009g0267 a0012c0020t0014g0109 |
2 | 380 | 0.0053 | 14 | c.*67 others(25): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2237 | chr1 | TogoVar | |||||||
CNTN3_chr3_74257568_74619659 | 74366780 | G | GTATATAT others(7): Show |
intron_variant | MODIFIER | HG00323.hp1 HG02129.hp1 HG02258.hp1 others(2): Show |
a0001 | a0001c0001a0001c0006a0001c0009 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(2): Show | a0001c0001t0001g0106 a0001c0001t0002g0038 a0001c0001t0005g0154 others(2): Show |
5 | 174 | 0.0287 | 14 | c.947 others(31): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 8/22 | chr3 | TogoVar | |||||||
CNTN3_chr3_74257568_74619659 | 74366780 | G | GTGTATAT others(7): Show |
intron_variant | MODIFIER | NA18961.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0114 | 1 | 174 | 0.0058 | 14 | c.947 others(31): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 8/22 | chr3 | TogoVar | |||||||
CNTN3_chr3_74257568_74619659 | 74366780 | G | GTGTGTAT others(7): Show |
intron_variant | MODIFIER | HG03041.hp1 HG06807.hp2 |
a0003a0009 | a0003c0003a0009c0025 | a0003c0003t0002a0009c0025t0029 | a0003c0003t0002g0052 a0009c0025t0029g0125 |
2 | 174 | 0.0115 | 14 | c.947 others(31): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 8/22 | chr3 | TogoVar | |||||||
CNTN3_chr3_74257568_74619659 | 74424474 | C | CAGAGAGA others(7): Show |
intron_variant | MODIFIER | HG02895.hp2 HG02896.hp1 HG03098.hp2 others(1): Show |
a0001a0002a0003 | a0001c0008a0002c0005a0003c0003 | a0001c0008t0002a0002c0005t0002a0002c0005t0023others(1): Show | a0001c0008t0002g0068 a0002c0005t0002g0037 a0002c0005t0023g0032 others(1): Show |
4 | 174 | 0.0230 | 14 | c.454 others(29): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 5/22 | chr3 | TogoVar | |||||||
CNTN3_chr3_74257568_74619659 | 74575606 | A | AACACACA others(7): Show |
intron_variant | MODIFIER | HG01934.hp2 HG01943.hp2 HG01978.hp1 others(16): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0006others(5): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(10): Show | a0001c0001t0002g0038 a0001c0001t0004g0098 a0001c0001t0004g0102 others(16): Show |
19 | 174 | 0.1092 | 14 | c.-81 others(33): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 1/22 | chr3 | TogoVar | |||||||
CNTN3_chr3_74257568_74619659 | 74582783 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG02451.hp2 HG02622.hp2 |
a0003a0006 | a0003c0003a0006c0012 | a0003c0003t0007a0006c0012t0003 | a0003c0003t0007g0074 a0006c0012t0003g0050 |
2 | 174 | 0.0115 | 14 | c.-81 others(33): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 1/22 | chr3 | TogoVar | |||||||
CNTN4_chr3_2093866_3062959 | 2120384 | T | TATATATA others(7): Show |
intron_variant | MODIFIER | HG04184.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0070 | 1 | 116 | 0.0086 | 14 | c.-14 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2124433 | A | AACACACA others(7): Show |
intron_variant | MODIFIER | HG01261.hp2 | a0004 | a0004c0011 | a0004c0011t0003 | a0004c0011t0003g0111 | 1 | 116 | 0.0086 | 14 | c.-14 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2125330 | C | CTCTCTGT others(7): Show |
intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0022 | a0001c0022t0003 | a0001c0022t0003g0083 | 1 | 116 | 0.0086 | 14 | c.-14 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2125330 | C | CTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG01257.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0098 | 1 | 116 | 0.0086 | 14 | c.-14 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2270463 | T | TATATATA others(7): Show |
intron_variant | MODIFIER | HG01243.hp2 HG02257.hp1 HG02897.hp2 |
a0001 | a0001c0001a0001c0002a0001c0022 | a0001c0001t0003a0001c0002t0002a0001c0022t0003 | a0001c0001t0003g0006 a0001c0002t0002g0102 a0001c0022t0003g0083 |
3 | 116 | 0.0259 | 14 | c.-14 others(35): 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(7): Show |
intron_variant | MODIFIER | HG02897.hp1 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0002 | 1 | 116 | 0.0086 | 14 | c.-14 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2340710 | T | TATAGAGA others(7): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0086 | 1 | 116 | 0.0086 | 14 | c.-89 others(31): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2340710 | T | TATATATA others(7): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0115 | 1 | 116 | 0.0086 | 14 | c.-89 others(31): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2390215 | A | AGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG02257.hp2 HG02451.hp1 HG02559.hp2 others(1): Show |
a0001a0006 | a0001c0001a0001c0006a0006c0027 | a0001c0001t0002a0001c0001t0008a0001c0006t0002others(1): Show | a0001c0001t0002g0030 a0001c0001t0008g0089 a0001c0006t0002g0051 others(1): Show |
4 | 116 | 0.0345 | 14 | c.-89 others(33): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2400418 | T | TATATATA others(7): Show |
intron_variant | MODIFIER | HG03927.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0035 | 1 | 116 | 0.0086 | 14 | c.-89 others(33): 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(7): Show |
intron_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0007 | a0001c0007t0016 | a0001c0007t0016g0105 | 1 | 116 | 0.0086 | 14 | c.-89 others(33): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2801103 | A | AAGTTCCA others(7): Show |
intron_variant | MODIFIER | HG01257.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0005a0001c0004t0001others(1): Show | a0001c0001t0001g0050 a0001c0001t0005g0098 a0001c0004t0001g0097 others(2): Show |
5 | 116 | 0.0431 | 14 | c.359 others(33): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2820961 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02897.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0006 | 1 | 116 | 0.0086 | 14 | c.454 others(31): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2864740 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG01884.hp2 HG01891.hp1 HG03516.hp1 |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0009a0001c0002t0001a0001c0005t0001 | a0001c0001t0009g0052 a0001c0002t0001g0029 a0001c0005t0001g0090 |
3 | 116 | 0.0259 | 14 | c.455 others(31): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2878553 | C | CTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0002t0002others(4): Show | a0001c0001t0001g0012 a0001c0001t0008g0053 a0001c0002t0002g0078 others(4): Show |
7 | 116 | 0.0603 | 14 | c.653 others(31): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2961231 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(13): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0099 others(13): Show |
16 | 116 | 0.1379 | 14 | c.135 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2994594 | C | CATATATA others(7): Show |
intron_variant | MODIFIER | HG01261.hp2 HG01361.hp1 |
a0004 | a0004c0011 | a0004c0011t0003 | a0004c0011t0003g0065 a0004c0011t0003g0111 |
2 | 116 | 0.0172 | 14 | c.148 others(33): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2994613 | A | ATATATAT others(7): Show |
intron_variant | MODIFIER | HG01256.hp1 HG01258.hp2 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0018 a0001c0001t0005g0019 |
2 | 116 | 0.0172 | 14 | c.148 others(33): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99131115 | A | AGCTGGGC others(7): Show |
intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(62): Show |
a0001a0002a0003others(12): Show | a0001c0001a0002c0002a0003c0003others(12): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(38): Show | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(62): Show |
65 | 66 | 0.9849 | 14 | c.-21 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | chr11 | TogoVar | |||||||
CNTN5_chr11_99015949_100363885 | 99338919 | G | GATATATA others(7): Show |
intron_variant | MODIFIER | HG02004.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 1 | 66 | 0.0152 | 14 | c.-71 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99382844 | A | ATTTTTTT others(7): Show |
intron_variant | MODIFIER | HG01099.hp2 HG02965.hp2 NA18522.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0002c0002t0003a0002c0002t0004 | a0001c0001t0003g0022 a0002c0002t0003g0037 a0002c0002t0004g0007 |
3 | 66 | 0.0455 | 14 | c.-71 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | chr11 | TogoVar | |||||||
CNTN5_chr11_99015949_100363885 | 99382845 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01169.hp2 NA19000.hp1 |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0011a0006c0006t0001a0006c0006t0014 | a0001c0001t0011g0062 a0006c0006t0001g0005 a0006c0006t0014g0058 |
3 | 66 | 0.0455 | 14 | c.-71 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99408448 | G | GAAAGAAA others(7): Show |
intron_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0030 | 1 | 66 | 0.0152 | 14 | c.-71 others(33): 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(7): Show |
intron_variant | MODIFIER | HG01169.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0043 | 1 | 66 | 0.0152 | 14 | c.-70 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99553977 | C | CACACACA others(7): Show |
intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0044 | 1 | 66 | 0.0152 | 14 | c.-70 others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99553979 | C | CACACACA others(7): Show |
intron_variant | MODIFIER | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(22): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0003c0003others(5): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(15): Show | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0052 others(22): Show |
25 | 66 | 0.3788 | 14 | c.-70 others(31): 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(7): Show |
intron_variant | MODIFIER | HG02602.hp1 HG02723.hp1 HG02965.hp1 others(2): Show |
a0001a0006a0016 | a0001c0001a0006c0006a0016c0015 | a0001c0001t0001a0001c0001t0006a0006c0006t0011others(1): Show | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0006g0066 others(2): Show |
5 | 66 | 0.0758 | 14 | c.55+ others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99738615 | A | AAGTGTGT others(7): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0039 | 1 | 66 | 0.0152 | 14 | c.56- others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | chr11 | TogoVar | |||||||
CNTN5_chr11_99015949_100363885 | 99738616 | C | CGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01169.hp1 HG02004.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(1): Show | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0003g0021 others(3): Show |
6 | 66 | 0.0909 | 14 | c.56- others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |