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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN4_chr3_2093866_3062959 | 2340710 | T | TATATAGA others(11): Show |
intron_variant | MODIFIER | HG01257.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0106 | 1 | 116 | 0.0086 | 18 | c.-89 others(35): 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(11): Show |
intron_variant | MODIFIER | HG02738.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0038 | 1 | 116 | 0.0086 | 18 | c.-89 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2340711 | A | AGAGAGAG others(11): Show |
intron_variant | MODIFIER | HG02809.hp2 | a0003 | a0003c0019 | a0003c0019t0002 | a0003c0019t0002g0031 | 1 | 116 | 0.0086 | 18 | c.-89 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2400424 | T | TATATATA others(11): Show |
intron_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0094 | 1 | 116 | 0.0086 | 18 | c.-89 others(37): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2527409 | A | ATGCTGCT others(11): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0007 | a0007c0018 | a0007c0018t0003 | a0007c0018t0003g0062 | 1 | 116 | 0.0086 | 18 | c.-88 others(37): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2607610 | C | CCACACAC others(11): Show |
intron_variant | MODIFIER | HG02647.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
a0001a0009 | a0001c0001a0001c0013a0009c0012 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(2): Show | a0001c0001t0001g0059 a0001c0001t0004g0042 a0001c0001t0008g0043 others(2): Show |
5 | 116 | 0.0431 | 18 | c.55+ others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2834898 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG02257.hp2 HG02622.hp1 HG02622.hp2 others(3): Show |
a0001a0002a0003 | a0001c0001a0001c0006a0002c0014others(1): Show | a0001c0001t0001a0001c0001t0008a0001c0006t0002others(3): Show | a0001c0001t0001g0033 a0001c0001t0008g0089 a0001c0006t0002g0060 others(3): Show |
6 | 116 | 0.0517 | 18 | c.454 others(37): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2834898 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG01175.hp1 HG01261.hp2 HG02165.hp1 others(8): Show |
a0001a0004 | a0001c0002a0001c0003a0001c0004others(3): Show | a0001c0002t0002a0001c0002t0003a0001c0002t0005others(6): Show | a0001c0002t0002g0078 a0001c0002t0003g0024 a0001c0002t0005g0002 others(8): Show |
11 | 116 | 0.0948 | 18 | c.454 others(37): 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(11): Show |
intron_variant | MODIFIER | HG02132.hp1 HG03453.hp2 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0002 | a0001c0001t0001g0012 a0001c0006t0002g0060 |
2 | 116 | 0.0172 | 18 | c.455 others(35): 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(11): Show |
intron_variant | MODIFIER | HG03927.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050 | 1 | 116 | 0.0086 | 18 | c.653 others(35): 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(11): Show |
intron_variant | MODIFIER | HG01175.hp2 HG02738.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0006 | a0001c0002t0001g0038 a0001c0003t0006g0040 |
2 | 116 | 0.0172 | 18 | c.135 others(39): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2969515 | G | GGATTATT others(11): Show |
intron_variant | MODIFIER | HG03041.hp2 | a0001 | a0001c0005 | a0001c0005t0010 | a0001c0005t0010g0001 | 1 | 116 | 0.0086 | 18 | c.135 others(39): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2969516 | G | GATTATTA others(11): Show |
intron_variant | MODIFIER | HG02074.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
a0001a0003 | a0001c0002a0001c0005a0001c0009others(1): Show | a0001c0002t0001a0001c0002t0012a0001c0005t0001others(2): Show | a0001c0002t0001g0088 a0001c0002t0012g0013 a0001c0005t0001g0104 others(2): Show |
5 | 116 | 0.0431 | 18 | c.135 others(39): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99253897 | T | TTATATAT others(11): Show |
intron_variant | MODIFIER | NA19070.hp2 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0016 | 1 | 66 | 0.0152 | 18 | c.-20 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99338919 | G | GATATATA others(11): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0005 | a0005c0005 | a0005c0005t0002 | a0005c0005t0002g0041 | 1 | 66 | 0.0152 | 18 | c.-71 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99727312 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG01099.hp2 HG02965.hp2 NA19070.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0014a0002c0002t0003 | a0001c0001t0003g0022 a0001c0001t0014g0016 a0002c0002t0003g0037 |
3 | 66 | 0.0455 | 18 | c.56- others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99738616 | C | CGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01123.hp2 HG01496.hp2 others(3): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0006a0001c0001t0012a0001c0001t0015others(3): Show | a0001c0001t0006g0032 a0001c0001t0012g0018 a0001c0001t0015g0064 others(3): Show |
6 | 66 | 0.0909 | 18 | c.56- others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99792573 | G | GTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02723.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0004a0002c0002t0004 | a0001c0001t0004g0044 a0002c0002t0004g0039 |
2 | 66 | 0.0303 | 18 | c.56- others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99930796 | A | AACACACA others(11): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0012 | a0012c0014 | a0012c0014t0008 | a0012c0014t0008g0026 | 1 | 66 | 0.0152 | 18 | c.673 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99981077 | G | GATATATA others(11): Show |
intron_variant | MODIFIER | HG00733.hp2 HG01169.hp1 HG02004.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0009a0002c0002t0022 | a0001c0001t0001g0054 a0001c0001t0009g0043 a0002c0002t0022g0013 |
3 | 66 | 0.0455 | 18 | c.878 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100072990 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG03041.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0023 | 1 | 66 | 0.0152 | 18 | c.143 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100204297 | A | AATATATA others(11): Show |
intron_variant | MODIFIER | NA19000.hp2 NA19070.hp2 |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0014a0005c0005t0002 | a0001c0001t0014g0016 a0005c0005t0002g0001 |
2 | 66 | 0.0303 | 18 | c.188 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100342152 | G | GACACACA others(11): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02965.hp1 |
a0006a0010 | a0006c0006a0010c0013 | a0006c0006t0011a0010c0013t0011 | a0006c0006t0011g0033 a0010c0013t0011g0009 |
2 | 66 | 0.0303 | 18 | c.303 others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1098785 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG00639.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0013 | 1 | 232 | 0.0043 | 18 | c.-83 others(35): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1098787 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG01099.hp2 HG01175.hp2 HG02602.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0002t0002g0020 |
3 | 232 | 0.0129 | 18 | c.-83 others(35): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1098789 | C | CACATATA others(11): Show |
intron_variant | MODIFIER | NA19065.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035 | 1 | 232 | 0.0043 | 18 | c.-83 others(35): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1098789 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG03654.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0093 | 1 | 232 | 0.0043 | 18 | c.-83 others(35): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1119322 | C | CGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(41): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0003others(13): Show | a0001c0001t0001g0024 a0001c0001t0001g0035 a0001c0001t0001g0086 others(41): Show |
44 | 232 | 0.1897 | 18 | c.-83 others(37): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1160344 | G | GTATATAT others(11): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00609.hp1 HG00735.hp2 others(13): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(5): Show | a0001c0001t0001g0067 a0001c0001t0001g0097 a0001c0001t0001g0141 others(13): Show |
16 | 232 | 0.0690 | 18 | c.55+ others(35): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245217 | T | TATAACAT others(11): Show |
intron_variant | MODIFIER | HG03516.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0164 | 1 | 232 | 0.0043 | 18 | c.358 others(37): 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(11): Show |
intron_variant | MODIFIER | HG03710.hp1 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0002a0001c0007 | a0001c0002t0001a0001c0007t0001 | a0001c0002t0001g0122 a0001c0007t0001g0102 |
2 | 232 | 0.0086 | 18 | c.454 others(35): 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(11): Show |
intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG02055.hp1 others(2): Show |
a0001a0003 | a0001c0004a0001c0005a0003c0015 | a0001c0004t0002a0001c0005t0001a0001c0005t0002others(1): Show | a0001c0004t0002g0039 a0001c0005t0001g0164 a0001c0005t0002g0019 others(2): Show |
5 | 232 | 0.0216 | 18 | c.136 others(37): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1406642 | G | GGTGTGTG others(11): Show |
downstream_gene_variant | MODIFIER | HG00423.hp2 HG00733.hp1 HG01099.hp2 others(2): Show |
a0001 | a0001c0001a0001c0004a0001c0018 | a0001c0001t0001a0001c0001t0002a0001c0004t0002others(1): Show | a0001c0001t0001g0046 a0001c0001t0001g0152 a0001c0001t0002g0124 others(2): Show |
5 | 232 | 0.0216 | 18 | c.*32 others(29): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2426 | chr3 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 146422359 | G | GTATATAT others(11): Show |
intron_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0018 | 1 | 40 | 0.0250 | 18 | c.97+ others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146426185 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 40 | 0.0250 | 18 | c.97+ others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146622131 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02486.hp1 others(11): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0018others(11): Show | a0001c0001t0001g0038 a0001c0001t0007g0020 a0001c0001t0018g0001 others(11): Show |
14 | 40 | 0.3500 | 18 | c.98- others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146639465 | T | TATTCCCA others(11): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02486.hp1 others(11): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0018others(11): Show | a0001c0001t0001g0038 a0001c0001t0007g0020 a0001c0001t0018g0001 others(11): Show |
14 | 40 | 0.3500 | 18 | c.98- others(37): 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(11): Show |
intron_variant | MODIFIER | HG02486.hp2 NA19030.hp2 |
a0001a0002 | a0001c0003a0002c0016 | a0001c0003t0011a0002c0016t0004 | a0001c0003t0011g0023 a0002c0016t0004g0024 |
2 | 40 | 0.0500 | 18 | c.98- others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146671429 | T | TCACACAC others(11): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0002 | a0002c0017 | a0002c0017t0015 | a0002c0017t0015g0037 | 1 | 40 | 0.0250 | 18 | c.98- others(37): 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(11): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0002 | a0002c0016 | a0002c0016t0004 | a0002c0016t0004g0024 | 1 | 40 | 0.0250 | 18 | c.98- others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146964893 | T | TGGCCAGA others(11): Show |
intron_variant | MODIFIER | HG00735.hp1 HG02451.hp1 HG02896.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(4): Show | a0001c0001t0001g0038 a0001c0002t0001g0007 a0001c0002t0002g0040 others(5): Show |
8 | 40 | 0.2000 | 18 | c.403 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147317796 | G | GTGTGTAT others(11): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 40 | 0.0250 | 18 | c.149 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147317804 | G | GTGTATAT others(11): Show |
intron_variant | MODIFIER | HG02886.hp1 NA20129.hp2 |
a0001 | a0001c0003 | a0001c0003t0013a0001c0003t0023 | a0001c0003t0013g0010 a0001c0003t0023g0030 |
2 | 40 | 0.0500 | 18 | c.149 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147421585 | C | CTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG01891.hp2 HG03139.hp1 HG03540.hp2 |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0006a0001c0003t0004a0001c0008t0001 | a0001c0001t0006g0009 a0001c0003t0004g0029 a0001c0008t0001g0025 |
3 | 40 | 0.0750 | 18 | c.167 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147448484 | G | GTATATAT others(11): Show |
intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0009 | 1 | 40 | 0.0250 | 18 | c.167 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147486889 | C | CTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
a0001a0003 | a0001c0006a0001c0012a0001c0018others(1): Show | a0001c0006t0009a0001c0012t0004a0001c0018t0002others(1): Show | a0001c0006t0009g0028 a0001c0012t0004g0026 a0001c0018t0002g0012 others(1): Show |
4 | 40 | 0.1000 | 18 | c.177 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147510850 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG02897.hp1 HG03239.hp1 NA19030.hp2 |
a0001a0002a0005 | a0001c0002a0002c0016a0005c0007 | a0001c0002t0001a0002c0016t0004a0005c0007t0017 | a0001c0002t0001g0008 a0002c0016t0004g0024 a0005c0007t0017g0031 |
3 | 40 | 0.0750 | 18 | c.177 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147635198 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG02896.hp1 NA21309.hp2 |
a0001a0004 | a0001c0001a0004c0020 | a0001c0001t0018a0004c0020t0005 | a0001c0001t0018g0001 a0004c0020t0005g0016 |
2 | 40 | 0.0500 | 18 | c.189 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147802794 | G | GGGGAGAG others(11): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0009 | a0001c0009t0019 | a0001c0009t0019g0027 | 1 | 40 | 0.0250 | 18 | c.209 others(41): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147839939 | T | TACACACA others(11): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0015 | a0001c0015t0001 | a0001c0015t0001g0011 | 1 | 40 | 0.0250 | 18 | c.209 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |