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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN4_chr3_2093866_3062959 | 2798397 | C | CTATCTAT others(17): Show |
intron_variant | MODIFIER | HG00738.hp1 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0112 | 1 | 116 | 0.0086 | 24 | c.359 others(43): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2815873 | C | CATATATA others(17): Show |
intron_variant | MODIFIER | HG02886.hp2 HG03041.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0002a0001c0005t0010 | a0001c0001t0002g0030a0001c0005t0010g0001 | 2 | 116 | 0.0172 | 24 | c.359 others(41): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2864740 | C | CAAAAAAA others(17): Show |
intron_variant | MODIFIER | HG02818.hp1 | a0002 | a0002c0017 | a0002c0017t0008 | a0002c0017t0008g0067 | 1 | 116 | 0.0086 | 24 | c.455 others(41): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2917332 | G | GGGAGAGG others(17): Show |
intron_variant | MODIFIER | HG02257.hp1 HG02258.hp1 HG03471.hp1 others(1): Show |
a0001 | a0001c0005a0001c0006a0001c0021others(1): Show | a0001c0005t0010a0001c0006t0002a0001c0021t0002others(1): Show | a0001c0005t0010g0085a0001c0006t0002g0026a0001c0021t0002g0025others(1): Show | 4 | 116 | 0.0345 | 24 | c.120 others(43): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2994613 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0002 | a0002c0014 | a0002c0014t0001 | a0002c0014t0001g0016 | 1 | 116 | 0.0086 | 24 | c.148 others(43): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99201351 | T | TTTCCTTC others(17): Show |
intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0044 | 1 | 66 | 0.0152 | 24 | c.-20 others(47): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99408428 | A | AAAAGAAA others(17): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0029 | 1 | 66 | 0.0152 | 24 | c.-71 others(43): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99620027 | A | AAAAAAAA others(17): Show |
intron_variant | MODIFIER | HG00733.hp1 HG01081.hp1 HG01081.hp2 others(5): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(5): Show | a0001c0001t0004g0044a0001c0001t0005g0048a0001c0001t0009g0063others(5): Show | 8 | 66 | 0.1212 | 24 | c.55+ others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99727312 | C | CAAAAAAA others(17): Show |
intron_variant | MODIFIER | HG00738.hp2 HG01099.hp1 HG02723.hp1 others(2): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0004others(1): Show | a0001c0001t0001a0001c0001t0004a0002c0002t0001others(2): Show | a0001c0001t0001g0008a0001c0001t0004g0010a0002c0002t0001g0003others(2): Show | 5 | 66 | 0.0758 | 24 | c.56- others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99941571 | A | AACACACA others(17): Show |
intron_variant | MODIFIER | HG01081.hp2 HG02735.hp2 NA18939.hp2 |
a0001a0003a0007 | a0001c0001a0003c0003a0007c0007 | a0001c0001t0010a0003c0003t0002a0007c0007t0023 | a0001c0001t0010g0047a0003c0003t0002g0061a0007c0007t0023g0046 | 3 | 66 | 0.0455 | 24 | c.674 others(43): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100161830 | T | TACACATA others(17): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0002 | a0002c0002 | a0002c0002t0008 | a0002c0002t0008g0019 | 1 | 66 | 0.0152 | 24 | c.158 others(45): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1098789 | C | CACATATA others(17): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0036 | 1 | 232 | 0.0043 | 24 | c.-83 others(41): 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(17): Show |
intron_variant | MODIFIER | HG01109.hp1 HG01123.hp1 HG01361.hp2 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(6): Show | a0001c0001t0001g0057a0001c0001t0001g0198a0001c0002t0001g0094others(13): Show | 16 | 232 | 0.0690 | 24 | c.-83 others(43): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1132658 | A | AAAATAAA others(17): Show |
intron_variant | MODIFIER | HG00609.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0083 | 1 | 232 | 0.0043 | 24 | c.-82 others(43): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1142968 | G | GTGTATAT others(17): Show |
intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0010 | a0001c0010t0001 | a0001c0010t0001g0206 | 1 | 232 | 0.0043 | 24 | c.-82 others(41): 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(17): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(13): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(5): Show | a0001c0001t0001g0024a0001c0001t0001g0047a0001c0001t0001g0126others(13): Show | 16 | 232 | 0.0690 | 24 | c.55+ others(41): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1160365 | T | TATATATA others(17): Show |
intron_variant | MODIFIER | HG02109.hp1 HG02717.hp2 HG02965.hp1 others(1): Show |
a0001a0006 | a0001c0006a0001c0007a0006c0027 | a0001c0006t0001a0001c0007t0001a0006c0027t0001 | a0001c0006t0001g0223a0001c0007t0001g0134a0001c0007t0001g0135others(1): Show | 4 | 232 | 0.0172 | 24 | c.55+ others(41): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1160367 | T | TATATATA others(17): Show |
intron_variant | MODIFIER | HG02647.hp2 HG03516.hp1 |
a0001 | a0001c0005a0001c0006 | a0001c0005t0001a0001c0006t0001 | a0001c0005t0001g0164a0001c0006t0001g0037 | 2 | 232 | 0.0086 | 24 | c.55+ others(41): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245225 | T | TAACATAT others(17): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0182 | 1 | 232 | 0.0043 | 24 | c.358 others(43): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245242 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | HG02896.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0210 | 1 | 232 | 0.0043 | 24 | c.358 others(43): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1332495 | A | AAAGGAAG others(17): Show |
intron_variant | MODIFIER | HG02559.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0228 | 1 | 232 | 0.0043 | 24 | c.136 others(43): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146231015 | A | AAAATAAA others(17): Show |
intron_variant | MODIFIER | HG02486.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
a0001 | a0001c0002a0001c0003a0001c0004 | a0001c0002t0001a0001c0002t0010a0001c0003t0011others(1): Show | a0001c0002t0001g0008a0001c0002t0001g0021a0001c0002t0010g0002others(2): Show | 5 | 40 | 0.1250 | 24 | c.97+ others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146486046 | C | CTTTTTTT others(17): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0034 | 1 | 40 | 0.0250 | 24 | c.98- others(43): 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(17): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0012 | a0001c0012t0004 | a0001c0012t0004g0026 | 1 | 40 | 0.0250 | 24 | c.98- others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146721060 | T | TATATTAT others(17): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0029 | 1 | 40 | 0.0250 | 24 | c.98- others(41): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146721339 | C | CATTCTAT others(17): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0029 | 1 | 40 | 0.0250 | 24 | c.98- others(41): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146721391 | C | CTATATAT others(17): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02486.hp1 others(3): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0009others(3): Show | a0001c0001t0007a0001c0003t0020a0001c0009t0019others(3): Show | a0001c0001t0007g0020a0001c0003t0020g0017a0001c0009t0019g0027others(3): Show | 6 | 40 | 0.1500 | 24 | c.98- others(41): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146721529 | C | CTATATAC others(17): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02896.hp1 HG02922.hp1 |
a0001a0005 | a0001c0001a0005c0020 | a0001c0001t0006a0001c0001t0012a0005c0020t0005 | a0001c0001t0006g0009a0001c0001t0012g0034a0005c0020t0005g0016 | 3 | 40 | 0.0750 | 24 | c.98- others(41): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146721889 | A | ATATTTTT others(17): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0002 | a0002c0016 | a0002c0016t0004 | a0002c0016t0004g0024 | 1 | 40 | 0.0250 | 24 | c.98- others(41): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146948314 | G | GAAAAATT others(17): Show |
intron_variant | MODIFIER | HG02451.hp2 HG02630.hp1 HG02896.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(6): Show | a0001c0001t0001g0038a0001c0001t0002g0006a0001c0001t0007g0018others(7): Show | 10 | 40 | 0.2500 | 24 | c.403 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147249604 | T | TAAAAAAA others(17): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0003 | a0001c0003t0011 | a0001c0003t0011g0023 | 1 | 40 | 0.0250 | 24 | c.134 others(45): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147510850 | C | CATATATA others(17): Show |
intron_variant | MODIFIER | HG02922.hp1 HG02922.hp2 NA20129.hp1 |
a0001 | a0001c0001a0001c0004a0001c0006 | a0001c0001t0012a0001c0004t0005a0001c0006t0009 | a0001c0001t0012g0034a0001c0004t0005g0004a0001c0006t0009g0028 | 3 | 40 | 0.0750 | 24 | c.177 others(45): 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(17): Show |
intron_variant | MODIFIER | HG02486.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
a0001 | a0001c0003a0001c0004a0001c0011 | a0001c0003t0011a0001c0004t0003a0001c0004t0005others(1): Show | a0001c0003t0011g0023a0001c0004t0003g0035a0001c0004t0003g0036others(2): Show | 5 | 40 | 0.1250 | 24 | c.177 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147586529 | G | GGAAGGAA others(17): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0002 | a0002c0017 | a0002c0017t0015 | a0002c0017t0015g0037 | 1 | 40 | 0.0250 | 24 | c.189 others(45): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147919459 | C | CTTTCTTT others(17): Show |
intron_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0006 | a0001c0006t0014 | a0001c0006t0014g0033 | 1 | 40 | 0.0250 | 24 | c.225 others(45): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147975006 | T | TATACAAT others(17): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0003 | a0001c0003t0023 | a0001c0003t0023g0030 | 1 | 40 | 0.0250 | 24 | c.225 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147975026 | A | ATATAATA others(17): Show |
intron_variant | MODIFIER | HG03239.hp1 NA20129.hp1 |
a0001a0003 | a0001c0006a0003c0007 | a0001c0006t0009a0003c0007t0017 | a0001c0006t0009g0028a0003c0007t0017g0031 | 2 | 40 | 0.0500 | 24 | c.225 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147975049 | C | CATATAAT others(17): Show |
intron_variant | MODIFIER | HG02630.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
a0001 | a0001c0002a0001c0005 | a0001c0002t0002a0001c0002t0010a0001c0005t0008others(1): Show | a0001c0002t0002g0013a0001c0002t0010g0002a0001c0005t0008g0005others(1): Show | 4 | 40 | 0.1000 | 24 | c.225 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147981786 | G | GGTGTGTG others(17): Show |
intron_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0018 | 1 | 40 | 0.0250 | 24 | c.238 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148136017 | A | AAGGAAGG others(17): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0001 | 1 | 40 | 0.0250 | 24 | c.255 others(45): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148136017 | A | AAGGAAGG others(17): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02486.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0006a0001c0003t0011 | a0001c0001t0006g0009a0001c0003t0011g0023 | 2 | 40 | 0.0500 | 24 | c.255 others(45): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148137675 | A | AGGAAGGA others(17): Show |
intron_variant | MODIFIER | HG02976.hp2 HG03540.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0010a0001c0003t0020 | a0001c0002t0010g0002a0001c0003t0020g0017 | 2 | 40 | 0.0500 | 24 | c.255 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148222495 | T | TATGAATG others(17): Show |
intron_variant | MODIFIER | HG00735.hp2 NA21309.hp1 NA21309.hp2 |
a0001 | a0001c0001a0001c0010a0001c0019 | a0001c0001t0018a0001c0010t0002a0001c0019t0006 | a0001c0001t0018g0001a0001c0010t0002g0014a0001c0019t0006g0015 | 3 | 40 | 0.0750 | 24 | c.324 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148222543 | G | GATGAATG others(17): Show |
intron_variant | MODIFIER | HG00735.hp1 HG02451.hp1 HG02451.hp2 others(21): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0002a0001c0001t0007a0001c0002t0001others(18): Show | a0001c0001t0002g0006a0001c0001t0007g0018a0001c0001t0007g0020others(21): Show | 24 | 40 | 0.6000 | 24 | c.324 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148253055 | T | TAGATAGA others(17): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0008 | a0001c0008t0001 | a0001c0008t0001g0025 | 1 | 40 | 0.0250 | 24 | c.338 others(45): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 20/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148297187 | A | AGGAAGGA others(17): Show |
intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0013 | 1 | 40 | 0.0250 | 24 | c.347 others(45): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP3B_chr9_41885536_42134426 | 41934100 | C | CATATATA others(17): Show |
intron_variant | MODIFIER | HG00642.hp2 HG01175.hp1 HG01175.hp2 others(1): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0002a0001c0001t0017a0004c0004t0005 | a0001c0001t0002g0022a0001c0001t0017g0012a0004c0004t0005g0032others(1): Show | 4 | 108 | 0.0370 | 24 | c.223 others(43): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41934122 | T | TATATATA others(17): Show |
intron_variant | MODIFIER | HG03486.hp1 | a0007 | a0007c0009 | a0007c0009t0025 | a0007c0009t0025g0037 | 1 | 108 | 0.0093 | 24 | c.223 others(43): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41956387 | A | AAATAATA others(17): Show |
intron_variant | MODIFIER | HG01175.hp1 HG02717.hp1 NA18968.hp1 |
a0001 | a0001c0001a0001c0012a0001c0042 | a0001c0001t0002a0001c0012t0002a0001c0042t0013 | a0001c0001t0002g0022a0001c0012t0002g0007a0001c0042t0013g0001 | 3 | 108 | 0.0278 | 24 | c.187 others(43): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42030750 | C | CAGAGAGA others(17): Show |
intron_variant | MODIFIER | HG01981.hp2 HG02083.hp2 HG02273.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0041a0002c0002t0001g0045a0002c0002t0001g0052others(1): Show | 4 | 108 | 0.0370 | 24 | c.391 others(43): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | TogoVar |