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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTNAP2_chr7_146111801_148425998 | 148283264 | AAAG | A | intron_variant | MODIFIER | HG02976.hp1 HG03098.hp2 |
a0001 | a0001c0002a0001c0015 | a0001c0002t0001a0001c0015t0001 | a0001c0002t0001g0021a0001c0015t0001g0011 | 2 | 40 | 0.0500 | -3 | c.347 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148288944 | CAAA | C | intron_variant | MODIFIER | HG01891.hp2 HG02486.hp1 HG02717.hp1 others(5): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0012others(5): Show | a0001c0001t0006g0009a0001c0001t0007g0020a0001c0001t0012g0034others(5): Show | 8 | 40 | 0.2000 | -3 | c.347 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148294039 | CAAA | C | intron_variant | MODIFIER | HG00735.hp1 HG01891.hp2 HG02486.hp2 others(12): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0006a0001c0001t0012a0001c0001t0018others(12): Show | a0001c0001t0006g0009a0001c0001t0012g0034a0001c0001t0018g0001others(12): Show | 15 | 40 | 0.3750 | -3 | c.347 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148305222 | CAAA | C | intron_variant | MODIFIER | HG00735.hp1 HG02976.hp2 HG03239.hp1 others(2): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0006others(2): Show | a0001c0001t0007a0001c0003t0020a0001c0006t0014others(2): Show | a0001c0001t0007g0018a0001c0003t0020g0017a0001c0006t0014g0033others(2): Show | 5 | 40 | 0.1250 | -3 | c.347 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148323294 | CTTT | C | intron_variant | MODIFIER | HG02896.hp2 HG02976.hp2 HG03098.hp1 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0018a0001c0003t0020others(5): Show | a0001c0001t0001g0003a0001c0001t0018g0001a0001c0003t0020g0017others(5): Show | 8 | 40 | 0.2000 | -3 | c.347 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148324794 | CAAA | C | intron_variant | MODIFIER | HG02451.hp1 HG02717.hp1 HG02922.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0012a0001c0002t0001a0001c0008t0001others(2): Show | a0001c0001t0012g0034a0001c0002t0001g0007a0001c0002t0001g0021others(3): Show | 6 | 40 | 0.1500 | -3 | c.347 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148360813 | TTTC | T | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp2 HG03098.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0006a0001c0002t0001 | a0001c0001t0002g0006a0001c0001t0006g0009a0001c0002t0001g0021 | 3 | 40 | 0.0750 | -3 | c.347 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148369181 | CTTT | C | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0007a0001c0002t0001others(7): Show | a0001c0001t0001g0038a0001c0001t0007g0018a0001c0001t0007g0020others(9): Show | 12 | 40 | 0.3000 | -3 | c.347 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148369643 | CATT | C | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 NA20129.hp2 |
a0001 | a0001c0003a0001c0004 | a0001c0003t0023a0001c0004t0003 | a0001c0003t0023g0030a0001c0004t0003g0035a0001c0004t0003g0036 | 3 | 40 | 0.0750 | -3 | c.347 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148402027 | AAGT | A | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp2 HG02922.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0019 | a0001c0001t0006a0001c0001t0012a0001c0002t0010others(1): Show | a0001c0001t0006g0009a0001c0001t0012g0034a0001c0002t0010g0002others(1): Show | 4 | 40 | 0.1000 | -3 | c.371 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148405603 | ATTT | A | intron_variant | MODIFIER | HG02451.hp2 HG02896.hp2 HG02922.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0013others(2): Show | a0001c0001t0002a0001c0004t0003a0001c0004t0005others(3): Show | a0001c0001t0002g0006a0001c0004t0003g0035a0001c0004t0005g0004others(3): Show | 6 | 40 | 0.1500 | -3 | c.371 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148413402 | ATAT | A | intron_variant | MODIFIER | HG02486.hp2 HG02630.hp1 |
a0001 | a0001c0003a0001c0012 | a0001c0003t0011a0001c0012t0004 | a0001c0003t0011g0023a0001c0012t0004g0026 | 2 | 40 | 0.0500 | -3 | c.379 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 23/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148414099 | TCCC | T | intron_variant | MODIFIER | HG00735.hp1 HG02886.hp2 HG02896.hp1 others(9): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0004others(8): Show | a0001c0001t0001g0003a0001c0002t0001g0021a0001c0003t0004g0029others(9): Show | 12 | 40 | 0.3000 | -3 | c.379 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP3B_chr9_41885536_42134426 | 41902027 | TAAA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
a0001a0002a0003others(30): Show | a0001c0001a0001c0012a0001c0042others(41): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(54): Show | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(103): Show | 106 | 108 | 0.9815 | -3 | c.344 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41950747 | CTTT | C | intron_variant | MODIFIER | HG00280.hp2 HG01175.hp2 HG02083.hp1 others(6): Show |
a0004a0011a0028others(1): Show | a0004c0004a0011c0037a0011c0040others(2): Show | a0004c0004t0005a0011c0037t0007a0011c0040t0007others(2): Show | a0004c0004t0005g0029a0004c0004t0005g0030a0004c0004t0005g0031others(6): Show | 9 | 108 | 0.0833 | -3 | c.208 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41953801 | CGAT | C | intron_variant | MODIFIER | HG01516.hp2 HG03831.hp2 |
a0010 | a0010c0013 | a0010c0013t0003 | a0010c0013t0003g0103a0010c0013t0003g0108 | 2 | 108 | 0.0185 | -3 | c.187 others(20): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 12/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41977786 | ATTT | A | intron_variant | MODIFIER | HG00280.hp1 HG00735.hp1 HG01106.hp1 others(24): Show |
a0001a0006a0008others(4): Show | a0001c0001a0001c0042a0001c0046others(7): Show | a0001c0001t0002a0001c0001t0003a0001c0042t0013others(9): Show | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0003g0093others(24): Show | 27 | 108 | 0.2500 | -3 | c.147 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41979944 | CTTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(29): Show |
a0001a0002a0004others(6): Show | a0001c0001a0001c0012a0001c0043others(10): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(13): Show | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(29): Show | 32 | 108 | 0.2963 | -3 | c.147 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41981892 | CAAT | C | intron_variant | MODIFIER | HG02109.hp2 HG02486.hp2 HG02622.hp2 |
a0001a0026a0027 | a0001c0046a0026c0025a0027c0026 | a0001c0046t0016a0026c0025t0019a0027c0026t0020 | a0001c0046t0016g0015a0026c0025t0019g0028a0027c0026t0020g0027 | 3 | 108 | 0.0278 | -3 | c.147 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41985629 | TATG | T | intron_variant | MODIFIER | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
a0008 | a0008c0006 | a0008c0006t0010 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | 108 | 0.0278 | -3 | c.147 others(20): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 9/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42026595 | GAAA | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
a0001a0006a0009others(7): Show | a0001c0001a0001c0012a0001c0042others(13): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(18): Show | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | 108 | 0.3704 | -3 | c.391 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42042986 | AATC | A | intron_variant | MODIFIER | HG01081.hp1 HG02109.hp2 |
a0016a0027 | a0016c0017a0027c0026 | a0016c0017t0001a0027c0026t0020 | a0016c0017t0001g0042a0027c0026t0020g0027 | 2 | 108 | 0.0185 | -3 | c.391 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42056326 | TTTA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(41): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0012a0001c0042others(19): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(24): Show | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0011others(41): Show | 44 | 108 | 0.4074 | -3 | c.390 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42058332 | CAGT | C | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(25): Show |
a0002a0012a0014others(2): Show | a0002c0002a0002c0010a0002c0015others(6): Show | a0002c0002t0001a0002c0002t0012a0002c0002t0022others(9): Show | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0044others(25): Show | 28 | 108 | 0.2593 | -3 | c.390 others(22): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42069187 | CAAT | C | intron_variant | MODIFIER | HG02559.hp2 HG02886.hp2 HG03453.hp1 |
a0008 | a0008c0006 | a0008c0006t0010 | a0008c0006t0010g0069a0008c0006t0010g0070a0008c0006t0010g0071 | 3 | 108 | 0.0278 | -3 | c.390 others(20): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42075836 | CTTA | C | intron_variant | MODIFIER | HG02486.hp1 HG02886.hp2 HG02922.hp2 others(1): Show |
a0008a0019a0032 | a0008c0006a0019c0031a0032c0039 | a0008c0006t0010a0019c0031t0028a0032c0039t0014 | a0008c0006t0010g0070a0008c0006t0010g0071a0019c0031t0028g0088others(1): Show | 4 | 108 | 0.0370 | -3 | c.390 others(20): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42134353 | AAAG | A | upstream_gene_variant | MODIFIER | HG01175.hp1 HG02135.hp1 HG02145.hp2 others(1): Show |
a0001a0006 | a0001c0001a0006c0007 | a0001c0001t0002a0001c0001t0003a0006c0007t0011 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0003g0093others(1): Show | 4 | 108 | 0.0370 | -3 | c.-52 others(14): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 4928 | chr9 | TogoVar | ||||||
CNTNAP3_chr9_39059710_39293167 | 39085085 | GTTT | G | intron_variant | MODIFIER | HG02109.hp1 HG02109.hp2 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0003a0002c0003t0004 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | 4 | 0.5000 | -3 | c.344 others(20): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | TogoVar | ||||||
CNTNAP3_chr9_39059710_39293167 | 39212017 | CACT | C | intron_variant | MODIFIER | HG02109.hp1 homoSapiens_chm13v2.hp1 |
a0002a0004 | a0002c0003a0004c0002 | a0002c0003t0004a0004c0002t0001 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | 4 | 0.5000 | -3 | c.391 others(22): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | TogoVar | ||||||
CNTNAP3_chr9_39059710_39293167 | 39260749 | AAAC | A | intron_variant | MODIFIER | HG02109.hp1 homoSapiens_chm13v2.hp1 |
a0002a0004 | a0002c0003a0004c0002 | a0002c0003t0004a0004c0002t0001 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | 4 | 0.5000 | -3 | c.196 others(20): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76299061 | GTAC | G | intron_variant | MODIFIER | HG00738.hp2 HG01433.hp1 HG02615.hp2 others(8): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0015a0002c0002others(8): Show | a0001c0001t0004a0001c0015t0006a0002c0002t0002others(8): Show | a0001c0001t0004g0172a0001c0015t0006g0166a0002c0002t0002g0167others(8): Show | 11 | 274 | 0.0402 | -3 | c.86- others(20): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76317289 | AAAC | A | intron_variant | MODIFIER | HG00280.hp1 HG00738.hp2 HG01074.hp2 others(25): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0002c0002others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0185others(25): Show | 28 | 274 | 0.1022 | -3 | c.196 others(18): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 2/23 | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76318748 | CATA | C | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0014others(2): Show | a0001c0001t0004a0001c0001t0006a0002c0002t0002others(7): Show | a0001c0001t0004g0051a0001c0001t0004g0053a0001c0001t0006g0052others(10): Show | 13 | 274 | 0.0475 | -3 | c.196 others(20): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76334176 | TATA | T | intron_variant | MODIFIER | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(9): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0012a0003c0003others(5): Show | a0001c0001t0006a0002c0012t0002a0003c0003t0005others(8): Show | a0001c0001t0006g0052a0002c0012t0002g0048a0003c0003t0005g0047others(9): Show | 12 | 274 | 0.0438 | -3 | c.196 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76342465 | CTTT | C | intron_variant | MODIFIER | HG02109.hp2 HG02280.hp1 HG03098.hp1 others(3): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0004a0002c0002t0010a0003c0003t0005others(3): Show | a0001c0001t0004g0053a0002c0002t0010g0204a0003c0003t0005g0047others(3): Show | 6 | 274 | 0.0219 | -3 | c.197 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76370995 | AAAG | A | intron_variant | MODIFIER | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
a0001a0002a0004 | a0001c0001a0002c0014a0004c0007 | a0001c0001t0004a0002c0014t0013a0004c0007t0014 | a0001c0001t0004g0051a0001c0001t0004g0053a0001c0001t0004g0191others(3): Show | 6 | 274 | 0.0219 | -3 | c.390 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76374742 | CTAT | C | intron_variant | MODIFIER | HG01433.hp1 HG01884.hp1 HG02630.hp1 others(3): Show |
a0001a0002a0003others(1): Show | a0001c0015a0002c0014a0003c0003others(2): Show | a0001c0015t0006a0002c0014t0013a0003c0003t0027others(3): Show | a0001c0015t0006g0166a0002c0014t0013g0263a0003c0003t0027g0237others(3): Show | 6 | 274 | 0.0219 | -3 | c.390 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76382060 | CAAA | C | intron_variant | MODIFIER | HG00673.hp1 HG02015.hp2 HG02723.hp1 others(10): Show |
a0001a0002a0003others(4): Show | a0001c0004a0002c0005a0002c0012others(7): Show | a0001c0004t0001a0002c0005t0004a0002c0012t0008others(7): Show | a0001c0004t0001g0155a0002c0005t0004g0132a0002c0012t0008g0242others(10): Show | 13 | 274 | 0.0475 | -3 | c.390 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76400504 | TTGA | T | intron_variant | MODIFIER | NA19030.hp1 NA19030.hp2 |
a0001a0003 | a0001c0015a0003c0028 | a0001c0015t0006a0003c0028t0005 | a0001c0015t0006g0166a0003c0028t0005g0274 | 2 | 274 | 0.0073 | -3 | c.391 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76408049 | TATG | T | intron_variant | MODIFIER | HG02451.hp2 HG02895.hp1 HG02897.hp2 |
a0001a0006 | a0001c0001a0006c0009 | a0001c0001t0015a0006c0009t0001 | a0001c0001t0015g0099a0001c0001t0015g0272a0006c0009t0001g0251 | 3 | 274 | 0.0110 | -3 | c.391 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76408263 | TATG | T | intron_variant | MODIFIER | HG00280.hp1 HG00558.hp2 HG00621.hp1 others(68): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0015others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0024others(68): Show | 71 | 274 | 0.2591 | -3 | c.391 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76439331 | GTGT | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(76): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0018others(11): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(27): Show | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0040others(76): Show | 79 | 274 | 0.2883 | -3 | c.539 others(20): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76456622 | CAGA | C | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(102): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0018a0002c0002others(15): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(32): Show | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0026others(102): Show | 105 | 274 | 0.3832 | -3 | c.133 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76460774 | ATAT | A | intron_variant | MODIFIER | HG00741.hp1 HG01074.hp2 HG01168.hp1 others(13): Show |
a0001a0002a0021others(1): Show | a0001c0001a0002c0002a0021c0037others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0038a0001c0001t0001g0062a0001c0001t0001g0083others(13): Show | 16 | 274 | 0.0584 | -3 | c.133 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 8/23 | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76471853 | TGTG | T | intron_variant | MODIFIER | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
a0001a0027 | a0001c0001a0027c0040 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(1): Show | a0001c0001t0004g0051a0001c0001t0005g0046a0001c0001t0005g0202others(2): Show | 5 | 274 | 0.0183 | -3 | c.165 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76473848 | TTTG | T | intron_variant | MODIFIER | HG02055.hp1 HG02723.hp2 HG03209.hp2 others(6): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0014others(2): Show | a0001c0001t0001a0001c0001t0009a0002c0002t0002others(5): Show | a0001c0001t0001g0151a0001c0001t0009g0231a0002c0002t0002g0212others(6): Show | 9 | 274 | 0.0329 | -3 | c.165 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76473868 | TTTG | T | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(74): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0018a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(17): Show | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0026others(74): Show | 77 | 274 | 0.2810 | -3 | c.165 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76496086 | TGTG | T | intron_variant | MODIFIER | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
a0003a0021 | a0003c0003a0003c0006a0021c0037 | a0003c0003t0006a0003c0003t0011a0003c0003t0030others(2): Show | a0003c0003t0006g0045a0003c0003t0006g0264a0003c0003t0006g0268others(6): Show | 9 | 274 | 0.0329 | -3 | c.223 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 14/23 | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76499065 | ATTT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0004a0001c0015others(24): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(53): Show | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0037others(144): Show | 147 | 274 | 0.5365 | -3 | c.236 others(20): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76507791 | CAAG | C | intron_variant | MODIFIER | HG00738.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0015a0002c0002others(3): Show | a0001c0001t0005a0001c0001t0010a0001c0015t0004others(6): Show | a0001c0001t0005g0046a0001c0001t0005g0202a0001c0001t0010g0250others(8): Show | 11 | 274 | 0.0402 | -3 | c.236 others(22): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar |