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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN5_chr11_99015949_100363885 | 99253897 | T | TTATATAT others(13): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0008 | a0008c0010 | a0008c0010t0005 | a0008c0010t0005g0014 | 1 | 66 | 0.0152 | 20 | c.-20 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99382845 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0005 | a0005c0005 | a0005c0005t0002 | a0005c0005t0002g0041 | 1 | 66 | 0.0152 | 20 | c.-71 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99388982 | C | CTTATTTT others(13): Show |
intron_variant | MODIFIER | HG00735.hp2 HG02602.hp2 HG03041.hp1 others(1): Show |
a0001a0006a0012 | a0001c0001a0006c0006a0012c0014 | a0001c0001t0001a0001c0001t0011a0006c0006t0014others(1): Show | a0001c0001t0001g0053 a0001c0001t0011g0062 a0006c0006t0014g0058 others(1): Show |
4 | 66 | 0.0606 | 20 | c.-71 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99408428 | A | AAAAGAAA others(13): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0039 | 1 | 66 | 0.0152 | 20 | c.-71 others(39): 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(13): Show |
intron_variant | MODIFIER | NA19070.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0003 | 1 | 66 | 0.0152 | 20 | c.-71 others(39): 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(13): Show |
intron_variant | MODIFIER | HG02976.hp2 NA18522.hp2 |
a0003a0004 | a0003c0003a0004c0004 | a0003c0003t0007a0004c0004t0001 | a0003c0003t0007g0057 a0004c0004t0001g0017 |
2 | 66 | 0.0303 | 20 | c.-71 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99432464 | C | CCTTTTCT others(13): Show |
intron_variant | MODIFIER | HG00735.hp2 HG00738.hp2 HG01123.hp2 others(2): Show |
a0001a0003a0005others(1): Show | a0001c0001a0003c0003a0005c0005others(1): Show | a0001c0001t0001a0001c0001t0011a0003c0003t0002others(2): Show | a0001c0001t0001g0053 a0001c0001t0011g0062 a0003c0003t0002g0012 others(2): Show |
5 | 66 | 0.0758 | 20 | c.-71 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99448730 | T | TTTTTATT others(13): Show |
intron_variant | MODIFIER | HG02109.hp1 NA19070.hp1 |
a0002a0004 | a0002c0002a0004c0004 | a0002c0002t0001a0004c0004t0010 | a0002c0002t0001g0003 a0004c0004t0010g0006 |
2 | 66 | 0.0303 | 20 | c.-70 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99463108 | A | AAAATAAA others(13): Show |
intron_variant | MODIFIER | HG00738.hp2 HG02723.hp1 HG02735.hp2 others(1): Show |
a0001a0003a0005others(1): Show | a0001c0001a0003c0003a0005c0005others(1): Show | a0001c0001t0001a0003c0003t0002a0005c0005t0002others(1): Show | a0001c0001t0001g0008 a0003c0003t0002g0061 a0005c0005t0002g0041 others(1): Show |
4 | 66 | 0.0606 | 20 | c.-70 others(39): 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(13): Show |
intron_variant | MODIFIER | HG02109.hp1 HG02109.hp2 HG02257.hp2 others(2): Show |
a0001a0004a0014 | a0001c0001a0004c0004a0014c0009 | a0001c0001t0003a0001c0001t0006a0001c0001t0015others(2): Show | a0001c0001t0003g0021 a0001c0001t0006g0032 a0001c0001t0015g0064 others(2): Show |
5 | 66 | 0.0758 | 20 | c.56- others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99732418 | A | AACTCAGT others(13): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01099.hp2 HG02109.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0006a0001c0001t0015others(2): Show | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0006g0032 others(4): Show |
7 | 66 | 0.1061 | 20 | c.56- others(37): 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(13): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0004 | a0004c0004 | a0004c0004t0001 | a0004c0004t0001g0035 | 1 | 66 | 0.0152 | 20 | c.56- others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99827072 | T | TTTTGTTT others(13): Show |
intron_variant | MODIFIER | HG02004.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 1 | 66 | 0.0152 | 20 | c.277 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99923757 | G | GTCTGTCT others(13): Show |
intron_variant | MODIFIER | HG01081.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0047 | 1 | 66 | 0.0152 | 20 | 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 | 99947036 | T | TTCATCAT others(13): Show |
intron_variant | MODIFIER | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0002a0003c0003others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(18): Show | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0053 others(30): Show |
33 | 66 | 0.5000 | 20 | c.674 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | chr11 | TogoVar | |||||||
CNTN5_chr11_99015949_100363885 | 99947036 | T | TTCATCAT others(13): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0010 | a0010c0013 | a0010c0013t0011 | a0010c0013t0011g0009 | 1 | 66 | 0.0152 | 20 | c.674 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | chr11 | TogoVar | |||||||
CNTN5_chr11_99015949_100363885 | 99981098 | A | ATATATAT others(13): Show |
intron_variant | MODIFIER | HG01496.hp1 | a0002 | a0002c0002 | a0002c0002t0021 | a0002c0002t0021g0055 | 1 | 66 | 0.0152 | 20 | c.878 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99981103 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | HG02132.hp1 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0049 | 1 | 66 | 0.0152 | 20 | c.878 others(39): 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(13): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0005 | a0005c0005 | a0005c0005t0020 | a0005c0005t0020g0024 | 1 | 66 | 0.0152 | 20 | c.143 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100090505 | C | CCCTCCCT others(13): Show |
intron_variant | MODIFIER | HG02965.hp1 NA20300.hp1 |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0005a0006c0006t0011 | a0001c0001t0005g0048 a0006c0006t0011g0033 |
2 | 66 | 0.0303 | 20 | c.158 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100161830 | T | TACACACA others(13): Show |
intron_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0030 | 1 | 66 | 0.0152 | 20 | c.158 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100161830 | T | TACACATA others(13): Show |
intron_variant | MODIFIER | HG01081.hp1 | a0004 | a0004c0004 | a0004c0004t0018 | a0004c0004t0018g0028 | 1 | 66 | 0.0152 | 20 | c.158 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1098787 | C | CATATATA others(13): Show |
intron_variant | MODIFIER | HG01106.hp1 HG01175.hp1 HG01993.hp1 |
a0001 | a0001c0001a0001c0003a0001c0007 | a0001c0001t0001a0001c0003t0001a0001c0007t0001 | a0001c0001t0001g0156 a0001c0003t0001g0154 a0001c0007t0001g0155 |
3 | 232 | 0.0129 | 20 | 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 | 1119322 | C | CGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(60): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0005others(12): Show | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0044 others(60): Show |
63 | 232 | 0.2716 | 20 | c.-83 others(39): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1119327 | G | GTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0177 | 1 | 232 | 0.0043 | 20 | c.-83 others(39): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1122397 | A | AGAAGGAA others(13): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0207 | 1 | 232 | 0.0043 | 20 | c.-82 others(39): 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(13): Show |
intron_variant | MODIFIER | HG02630.hp2 HG02647.hp2 HG02809.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(3): Show | a0001c0001t0001g0082 a0001c0002t0001g0160 a0001c0002t0001g0209 others(4): Show |
7 | 232 | 0.0302 | 20 | c.-82 others(39): 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(13): Show |
intron_variant | MODIFIER | HG00423.hp2 HG01261.hp2 HG01515.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0003t0001a0001c0004t0001others(1): Show | a0001c0001t0001g0046 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | 232 | 0.0302 | 20 | c.55+ others(37): 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(13): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0002 | a0001c0002t0009 | a0001c0002t0009g0205 | 1 | 232 | 0.0043 | 20 | c.55+ others(37): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1220006 | A | ATAAAAAA others(13): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(55): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0004others(13): Show | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0029 others(55): Show |
58 | 232 | 0.2500 | 20 | c.56- others(33): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | chr3 | TogoVar | |||||||
CNTN6_chr3_1088024_1409217 | 1220023 | A | AAAGAAAG others(13): Show |
intron_variant | MODIFIER | HG02738.hp1 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0052 | 1 | 232 | 0.0043 | 20 | c.56- others(33): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1300449 | C | CAGGAAGG others(13): Show |
intron_variant | MODIFIER | HG02809.hp1 | a0001 | a0001c0010 | a0001c0010t0001 | a0001c0010t0001g0009 | 1 | 232 | 0.0043 | 20 | c.761 others(37): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1319833 | G | GAAAATAA others(13): Show |
intron_variant | MODIFIER | HG01361.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0005others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(7): Show | a0001c0001t0001g0024 a0001c0002t0001g0018 a0001c0002t0001g0117 others(15): Show |
18 | 232 | 0.0776 | 20 | c.762 others(37): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1332495 | A | AAAGGAAG others(13): Show |
intron_variant | MODIFIER | HG02717.hp2 HG03139.hp1 |
a0001 | a0001c0005a0001c0006 | a0001c0005t0001a0001c0006t0001 | a0001c0005t0001g0182 a0001c0006t0001g0223 |
2 | 232 | 0.0086 | 20 | c.136 others(39): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1384780 | T | TACATATA others(13): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
a0001a0003a0005 | a0001c0013a0001c0025a0003c0015others(1): Show | a0001c0013t0001a0001c0025t0001a0003c0015t0001others(1): Show | a0001c0013t0001g0199 a0001c0013t0001g0208 a0001c0025t0001g0192 others(3): Show |
6 | 232 | 0.0259 | 20 | c.251 others(37): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1406642 | G | GGGGTGTG others(13): Show |
downstream_gene_variant | MODIFIER | NA19002.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0077 | 1 | 232 | 0.0043 | 20 | c.*32 others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2426 | chr3 | TogoVar | |||||||
CNTN6_chr3_1088024_1409217 | 1406642 | G | GGTGTGTG others(13): Show |
downstream_gene_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG03130.hp2 others(1): Show |
a0001 | a0001c0004a0001c0005a0001c0025 | a0001c0004t0001a0001c0004t0002a0001c0005t0002others(1): Show | a0001c0004t0001g0058 a0001c0004t0002g0039 a0001c0005t0002g0019 others(1): Show |
4 | 232 | 0.0172 | 20 | c.*32 others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2426 | chr3 | TogoVar | |||||||
CNTN6_chr3_1088024_1409217 | 1406667 | G | GTGTGTGT others(13): Show |
downstream_gene_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0006 | a0001c0006t0002 | a0001c0006t0002g0178 | 1 | 232 | 0.0043 | 20 | c.*32 others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2451 | chr3 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 146231015 | A | AAAATAAA others(13): Show |
intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02630.hp1 others(3): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0012others(1): Show | a0001c0001t0001a0001c0001t0006a0001c0003t0004others(3): Show | a0001c0001t0001g0003 a0001c0001t0006g0009 a0001c0003t0004g0029 others(3): Show |
6 | 40 | 0.1500 | 20 | c.97+ others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146422359 | G | GTATATAT others(13): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0009 | a0001c0009t0019 | a0001c0009t0019g0027 | 1 | 40 | 0.0250 | 20 | c.97+ others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146450935 | A | ATATTTAT others(13): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02630.hp1 |
a0001a0003 | a0001c0012a0003c0014 | a0001c0012t0004a0003c0014t0021 | a0001c0012t0004g0026 a0003c0014t0021g0022 |
2 | 40 | 0.0500 | 20 | c.98- others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146599743 | G | GAGATAGA others(13): Show |
intron_variant | MODIFIER | HG02451.hp2 HG02976.hp1 |
a0001 | a0001c0001a0001c0015 | a0001c0001t0002a0001c0015t0001 | a0001c0001t0002g0006 a0001c0015t0001g0011 |
2 | 40 | 0.0500 | 20 | c.98- others(39): 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(13): Show |
intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG03098.hp1 others(1): Show |
a0001 | a0001c0001a0001c0013a0001c0019 | a0001c0001t0001a0001c0001t0007a0001c0013t0003others(1): Show | a0001c0001t0001g0003 a0001c0001t0007g0020 a0001c0013t0003g0039 others(1): Show |
4 | 40 | 0.1000 | 20 | 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 | 146721586 | A | ATATATAT others(13): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0005 | a0001c0005t0022 | a0001c0005t0022g0032 | 1 | 40 | 0.0250 | 20 | 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 | 146721875 | G | GTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0035 a0001c0004t0003g0036 |
2 | 40 | 0.0500 | 20 | 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 | 147025440 | A | AGGGGAGG others(13): Show |
intron_variant | MODIFIER | HG03239.hp1 | a0005 | a0005c0007 | a0005c0007t0017 | a0005c0007t0017g0031 | 1 | 40 | 0.0250 | 20 | c.403 others(39): 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(13): Show |
intron_variant | MODIFIER | HG02886.hp2 NA21309.hp1 |
a0001 | a0001c0005a0001c0010 | a0001c0005t0022a0001c0010t0002 | a0001c0005t0022g0032 a0001c0010t0002g0014 |
2 | 40 | 0.0500 | 20 | c.134 others(41): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147273748 | T | TATGTAAT others(13): Show |
intron_variant | MODIFIER | HG02630.hp2 NA18522.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0007a0001c0002t0002 | a0001c0001t0007g0018 a0001c0002t0002g0013 |
2 | 40 | 0.0500 | 20 | c.134 others(41): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147421585 | C | CTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0013 | 1 | 40 | 0.0250 | 20 | c.167 others(41): 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(13): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0029 | 1 | 40 | 0.0250 | 20 | c.177 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |