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 | 99792538 | G | GGGGGGTG others(7): Show |
intron_variant | MODIFIER | HG03041.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0023 | 1 | 66 | 0.0152 | 14 | c.56- others(31): 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(7): Show |
intron_variant | MODIFIER | HG02723.hp1 HG02965.hp1 |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0001a0006c0006t0011 | a0001c0001t0001g0008 a0006c0006t0011g0033 |
2 | 66 | 0.0303 | 14 | c.56- others(31): 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(7): Show |
intron_variant | MODIFIER | HG02257.hp1 NA19000.hp2 |
a0005a0009 | a0005c0005a0009c0016 | a0005c0005t0002a0009c0016t0019 | a0005c0005t0002g0001 a0009c0016t0019g0059 |
2 | 66 | 0.0303 | 14 | c.56- others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99846129 | G | GACACACA others(7): Show |
intron_variant | MODIFIER | HG01496.hp1 | a0002 | a0002c0002 | a0002c0002t0021 | a0002c0002t0021g0055 | 1 | 66 | 0.0152 | 14 | c.577 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99930796 | A | AACACACA others(7): Show |
intron_variant | MODIFIER | HG00735.hp1 HG01243.hp1 HG02602.hp1 |
a0001a0002a0007 | a0001c0001a0002c0002a0007c0011 | a0001c0001t0006a0002c0002t0004a0007c0011t0009 | a0001c0001t0006g0066 a0002c0002t0004g0039 a0007c0011t0009g0042 |
3 | 66 | 0.0455 | 14 | c.673 others(33): 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(7): Show |
intron_variant | MODIFIER | HG00738.hp2 HG01081.hp2 HG02258.hp1 others(2): Show |
a0001a0003a0005others(2): Show | a0001c0001a0003c0003a0005c0005others(2): Show | a0001c0001t0010a0003c0003t0002a0005c0005t0002others(2): Show | a0001c0001t0010g0047 a0003c0003t0002g0002 a0005c0005t0002g0041 others(2): Show |
5 | 66 | 0.0758 | 14 | c.878 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99990447 | T | TACACACA others(7): Show |
intron_variant | MODIFIER | HG02976.hp2 HG03130.hp1 |
a0004 | a0004c0004 | a0004c0004t0001 | a0004c0004t0001g0017 a0004c0004t0001g0035 |
2 | 66 | 0.0303 | 14 | c.878 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99990453 | T | TACACACA others(7): Show |
intron_variant | MODIFIER | HG02886.hp1 HG02965.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0003a0003c0003t0002 | a0001c0001t0003g0022 a0003c0003t0002g0027 |
2 | 66 | 0.0303 | 14 | c.878 others(33): 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(7): Show |
intron_variant | MODIFIER | HG03471.hp1 | a0013 | a0013c0008 | a0013c0008t0007 | a0013c0008t0007g0038 | 1 | 66 | 0.0152 | 14 | c.143 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100161830 | T | TACACACA others(7): Show |
intron_variant | MODIFIER | HG01496.hp2 HG02735.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0012a0003c0003t0002 | a0001c0001t0012g0018 a0003c0003t0002g0061 |
2 | 66 | 0.0303 | 14 | c.158 others(35): 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(7): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 | 1 | 66 | 0.0152 | 14 | c.158 others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100203799 | T | TACACACA others(7): Show |
intron_variant | MODIFIER | HG02004.hp1 HG02132.hp1 HG02132.hp2 others(5): Show |
a0001a0004a0005others(1): Show | a0001c0001a0004c0004a0005c0005others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(4): Show | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0004g0044 others(5): Show |
8 | 66 | 0.1212 | 14 | c.188 others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100204297 | A | AATATATA others(7): Show |
intron_variant | MODIFIER | HG02132.hp2 NA18957.hp2 |
a0003a0005 | a0003c0003a0005c0005 | a0003c0003t0002a0005c0005t0002 | a0003c0003t0002g0002 a0005c0005t0002g0051 |
2 | 66 | 0.0303 | 14 | c.188 others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100267253 | C | CCACACAC others(7): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01099.hp2 HG03471.hp1 others(1): Show |
a0002a0013 | a0002c0002a0013c0008 | a0002c0002t0003a0002c0002t0008a0013c0008t0007 | a0002c0002t0003g0036 a0002c0002t0003g0037 a0002c0002t0008g0019 others(1): Show |
4 | 66 | 0.0606 | 14 | c.216 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100267280 | C | CACACACA others(7): Show |
intron_variant | MODIFIER | HG01123.hp2 HG01934.hp2 NA18939.hp2 others(2): Show |
a0001a0003a0005others(1): Show | a0001c0001a0003c0003a0005c0005others(1): Show | a0001c0001t0001a0003c0003t0002a0005c0005t0002others(1): Show | a0001c0001t0001g0052 a0003c0003t0002g0011 a0003c0003t0002g0012 others(2): Show |
5 | 66 | 0.0758 | 14 | c.216 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100342152 | G | GACACACA others(7): Show |
intron_variant | MODIFIER | HG02723.hp2 NA19043.hp1 |
a0001a0015 | a0001c0001a0015c0012 | a0001c0001t0004a0015c0012t0005 | a0001c0001t0004g0044 a0015c0012t0005g0056 |
2 | 66 | 0.0303 | 14 | c.303 others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1098787 | C | CATATATA others(7): Show |
intron_variant | MODIFIER | HG00741.hp1 HG01978.hp1 HG03239.hp1 others(3): Show |
a0001a0007 | a0001c0002a0001c0003a0001c0007others(1): Show | a0001c0002t0001a0001c0003t0001a0001c0007t0001others(1): Show | a0001c0002t0001g0145 a0001c0002t0001g0147 a0001c0002t0001g0176 others(3): Show |
6 | 232 | 0.0259 | 14 | c.-83 others(31): 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(7): Show |
intron_variant | MODIFIER | HG02074.hp2 HG03209.hp2 HG03834.hp1 others(2): Show |
a0001a0006 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0003t0001a0001c0004t0001others(1): Show | a0001c0001t0001g0088 a0001c0003t0001g0092 a0001c0004t0001g0089 others(2): Show |
5 | 232 | 0.0216 | 14 | c.-83 others(31): 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(7): Show |
intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(14): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0007others(9): Show | a0001c0001t0001g0029 a0001c0001t0001g0204 a0001c0002t0001g0108 others(14): Show |
17 | 232 | 0.0733 | 14 | c.-83 others(33): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1201097 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG03516.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0164 | 1 | 232 | 0.0043 | 14 | c.56- others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1201099 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG00609.hp1 HG04115.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 a0001c0001t0001g0171 |
2 | 232 | 0.0086 | 14 | c.56- others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245223 | T | TAACATAT others(7): Show |
intron_variant | MODIFIER | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(3): Show |
a0001a0002 | a0001c0005a0001c0007a0001c0008others(2): Show | a0001c0005t0001a0001c0007t0001a0001c0008t0001others(2): Show | a0001c0005t0001g0207 a0001c0007t0001g0012 a0001c0008t0001g0143 others(3): Show |
6 | 232 | 0.0259 | 14 | c.358 others(33): 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(7): Show |
intron_variant | MODIFIER | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(7): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(1): Show | a0001c0001t0001a0001c0005t0001a0001c0005t0002others(3): Show | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0153 others(7): Show |
10 | 232 | 0.0431 | 14 | c.454 others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1308287 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | NA18747.hp2 NA18972.hp1 |
a0001 | a0001c0007a0001c0008 | a0001c0007t0006a0001c0008t0001 | a0001c0007t0006g0170 a0001c0008t0001g0075 |
2 | 232 | 0.0086 | 14 | c.761 others(33): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1348157 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(12): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0005t0001others(3): Show | a0001c0001t0001g0198 a0001c0003t0001g0042 a0001c0003t0001g0177 others(12): Show |
15 | 232 | 0.0647 | 14 | c.136 others(33): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1406642 | G | GGGGTGTG others(7): Show |
downstream_gene_variant | MODIFIER | HG02738.hp2 HG03834.hp2 |
a0001 | a0001c0004a0001c0007 | a0001c0004t0001a0001c0007t0001 | a0001c0004t0001g0066 a0001c0007t0001g0048 |
2 | 232 | 0.0086 | 14 | c.*32 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2426 | chr3 | TogoVar | |||||||
CNTN6_chr3_1088024_1409217 | 1406642 | G | GGTGTGTG others(7): Show |
downstream_gene_variant | MODIFIER | HG01175.hp2 HG01517.hp2 HG03225.hp1 others(1): Show |
a0001 | a0001c0002a0001c0005a0001c0007others(1): Show | a0001c0002t0002a0001c0005t0001a0001c0007t0002others(1): Show | a0001c0002t0002g0020 a0001c0005t0001g0193 a0001c0007t0002g0032 others(1): Show |
4 | 232 | 0.0172 | 14 | c.*32 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2426 | chr3 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 146404124 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0011 | a0001c0011t0016 | a0001c0011t0016g0019 | 1 | 40 | 0.0250 | 14 | c.97+ others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146404141 | A | AAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02886.hp1 HG03225.hp2 |
a0001 | a0001c0003a0001c0018 | a0001c0003t0013a0001c0018t0002 | a0001c0003t0013g0010 a0001c0018t0002g0012 |
2 | 40 | 0.0500 | 14 | c.97+ others(33): 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(7): Show |
intron_variant | MODIFIER | HG01891.hp2 NA21309.hp1 |
a0001 | a0001c0001a0001c0010 | a0001c0001t0006a0001c0010t0002 | a0001c0001t0006g0009 a0001c0010t0002g0014 |
2 | 40 | 0.0500 | 14 | c.97+ others(33): 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(7): Show |
intron_variant | MODIFIER | HG02717.hp2 HG02976.hp2 |
a0001 | a0001c0003a0001c0005 | a0001c0003t0020a0001c0005t0008 | a0001c0003t0020g0017 a0001c0005t0008g0005 |
2 | 40 | 0.0500 | 14 | c.97+ others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146446392 | G | GAAACCCC others(7): Show |
intron_variant | MODIFIER | HG01891.hp2 HG03098.hp2 HG03225.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0009others(1): Show | a0001c0001t0006a0001c0001t0007a0001c0002t0001others(2): Show | a0001c0001t0006g0009 a0001c0001t0007g0018 a0001c0002t0001g0021 others(2): Show |
5 | 40 | 0.1250 | 14 | c.98- others(33): 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(7): Show |
intron_variant | MODIFIER | HG00735.hp1 NA18522.hp1 NA20129.hp1 others(1): Show |
a0001 | a0001c0001a0001c0006a0001c0013 | a0001c0001t0018a0001c0006t0009a0001c0006t0014others(1): Show | a0001c0001t0018g0001 a0001c0006t0009g0028 a0001c0006t0014g0033 others(1): Show |
4 | 40 | 0.1000 | 14 | c.98- others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146721875 | G | GTGTGTAT others(7): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0004 | 1 | 40 | 0.0250 | 14 | c.98- others(31): 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(7): Show |
intron_variant | MODIFIER | HG00735.hp2 NA18522.hp1 |
a0001 | a0001c0013a0001c0019 | a0001c0013t0003a0001c0019t0006 | a0001c0013t0003g0039 a0001c0019t0006g0015 |
2 | 40 | 0.0500 | 14 | c.98- others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146721889 | A | ATTTTTTT others(7): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0020 | 1 | 40 | 0.0250 | 14 | c.98- others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147090322 | C | CGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG02717.hp2 HG03225.hp1 |
a0001 | a0001c0005a0001c0009 | a0001c0005t0008a0001c0009t0019 | a0001c0005t0008g0005 a0001c0009t0019g0027 |
2 | 40 | 0.0500 | 14 | c.551 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147341070 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG03239.hp1 | a0005 | a0005c0007 | a0005c0007t0017 | a0005c0007t0017g0031 | 1 | 40 | 0.0250 | 14 | c.149 others(35): 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(7): Show |
intron_variant | MODIFIER | HG03239.hp1 NA20129.hp1 |
a0001a0005 | a0001c0006a0005c0007 | a0001c0006t0009a0005c0007t0017 | a0001c0006t0009g0028 a0005c0007t0017g0031 |
2 | 40 | 0.0500 | 14 | c.167 others(35): 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(7): Show |
intron_variant | MODIFIER | HG00735.hp2 HG02922.hp2 |
a0001 | a0001c0004a0001c0019 | a0001c0004t0005a0001c0019t0006 | a0001c0004t0005g0004 a0001c0019t0006g0015 |
2 | 40 | 0.0500 | 14 | c.177 others(31): 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(7): Show |
intron_variant | MODIFIER | HG02630.hp1 HG03225.hp2 |
a0001 | a0001c0012a0001c0018 | a0001c0012t0004a0001c0018t0002 | a0001c0012t0004g0026 a0001c0018t0002g0012 |
2 | 40 | 0.0500 | 14 | 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 | 147527015 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02486.hp2 HG03225.hp2 |
a0001 | a0001c0001a0001c0003a0001c0018 | a0001c0001t0006a0001c0003t0011a0001c0018t0002 | a0001c0001t0006g0009 a0001c0003t0011g0023 a0001c0018t0002g0012 |
3 | 40 | 0.0750 | 14 | 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 | 147560168 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02717.hp2 HG02886.hp2 |
a0001 | a0001c0005 | a0001c0005t0008a0001c0005t0022 | a0001c0005t0008g0005 a0001c0005t0022g0032 |
2 | 40 | 0.0500 | 14 | c.177 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147583531 | T | TATATATA others(7): Show |
intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0006 | 1 | 40 | 0.0250 | 14 | c.189 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147586519 | A | AGAGAGAA others(7): Show |
intron_variant | MODIFIER | HG02976.hp2 | a0001 | a0001c0003 | a0001c0003t0020 | a0001c0003t0020g0017 | 1 | 40 | 0.0250 | 14 | c.189 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147839939 | T | TACACACA others(7): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0020 | 1 | 40 | 0.0250 | 14 | c.209 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147860589 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02486.hp2 HG02630.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0002a0001c0003t0011 | a0001c0002t0002g0013 a0001c0003t0011g0023 |
2 | 40 | 0.0500 | 14 | c.209 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147925154 | A | AGAGAAGG others(7): Show |
intron_variant | MODIFIER | HG03239.hp1 HG03239.hp2 NA21309.hp1 |
a0001a0005 | a0001c0002a0001c0010a0005c0007 | a0001c0002t0002a0001c0010t0002a0005c0007t0017 | a0001c0002t0002g0040 a0001c0010t0002g0014 a0005c0007t0017g0031 |
3 | 40 | 0.0750 | 14 | c.225 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147949440 | G | GTGTATAT others(7): Show |
intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 NA18522.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0007a0001c0004t0003 | a0001c0001t0007g0018 a0001c0004t0003g0035 a0001c0004t0003g0036 |
3 | 40 | 0.0750 | 14 | c.225 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147973160 | T | TAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0035 a0001c0004t0003g0036 |
2 | 40 | 0.0500 | 14 | c.225 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |