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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN6_chr3_1088024_1409217 | 1245223 | TATATATA others(7): Show |
T | intron_variant | MODIFIER | HG00738.hp2 HG02723.hp1 NA18948.hp1 others(1): Show |
a0001 | a0001c0002a0001c0022a0001c0023 | a0001c0002t0001a0001c0022t0001a0001c0023t0001 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0022t0001g0137others(1): Show | 4 | 232 | 0.0172 | -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 | 1245268 | TATATATA others(7): Show |
T | intron_variant | MODIFIER | NA19084.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0161 | 1 | 232 | 0.0043 | -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 | 1300591 | AAGAAAGA others(7): Show |
A | intron_variant | MODIFIER | HG02109.hp1 HG02630.hp2 NA19043.hp1 others(1): Show |
a0001a0002a0006 | a0001c0002a0001c0013a0002c0011others(1): Show | a0001c0002t0001a0001c0013t0001a0002c0011t0001others(1): Show | a0001c0002t0001g0209a0001c0013t0001g0199a0002c0011t0001g0217others(1): Show | 4 | 232 | 0.0172 | -14 | c.761 others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146151668 | ATATATAT others(7): Show |
A | intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0029 | 1 | 40 | 0.0250 | -14 | c.97+ others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146285765 | CCCCTCCC others(7): Show |
C | intron_variant | MODIFIER | HG02486.hp2 HG03540.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0010a0001c0003t0011 | a0001c0002t0010g0002a0001c0003t0011g0023 | 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 | 146356052 | TACACACA others(7): Show |
T | intron_variant | MODIFIER | HG02630.hp1 HG02886.hp1 NA19030.hp1 |
a0001 | a0001c0001a0001c0003a0001c0012 | a0001c0001t0001a0001c0003t0013a0001c0012t0004 | a0001c0001t0001g0038a0001c0003t0013g0010a0001c0012t0004g0026 | 3 | 40 | 0.0750 | -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 | 146457481 | AATATATA others(7): Show |
A | intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0008 | a0001c0008t0001 | a0001c0008t0001g0025 | 1 | 40 | 0.0250 | -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 | 146477624 | AACACACA others(7): Show |
A | intron_variant | MODIFIER | HG02897.hp1 HG02922.hp1 HG02922.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0012a0001c0002t0001a0001c0003t0023others(1): Show | a0001c0001t0012g0034a0001c0002t0001g0008a0001c0003t0023g0030others(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 | 146622265 | ATCTATCT others(7): Show |
A | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0005others(6): Show | a0001c0001t0007a0001c0001t0018a0001c0003t0011others(7): Show | a0001c0001t0007g0020a0001c0001t0018g0001a0001c0003t0011g0023others(7): Show | 10 | 40 | 0.2500 | -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 | 146885928 | GGTGTGTG others(7): Show |
G | intron_variant | MODIFIER | NA19030.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0010 | a0001c0001t0001a0001c0010t0002 | a0001c0001t0001g0038a0001c0010t0002g0014 | 2 | 40 | 0.0500 | -14 | c.402 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146985308 | ATTTTTTT others(7): Show |
A | intron_variant | MODIFIER | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(18): Show | a0001c0001t0001g0003a0001c0001t0006g0009a0001c0001t0007g0020others(18): Show | 21 | 40 | 0.5250 | -14 | c.403 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146991216 | GATATAGT others(7): Show |
G | intron_variant | MODIFIER | HG03239.hp2 NA18522.hp1 |
a0001 | a0001c0002a0001c0013 | a0001c0002t0002a0001c0013t0003 | a0001c0002t0002g0040a0001c0013t0003g0039 | 2 | 40 | 0.0500 | -14 | c.403 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147033160 | GTATATAT others(7): Show |
G | intron_variant | MODIFIER | HG02717.hp1 | a0002 | a0002c0017 | a0002c0017t0015 | a0002c0017t0015g0037 | 1 | 40 | 0.0250 | -14 | c.403 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147104873 | CATATATA others(7): Show |
C | intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0013 | 1 | 40 | 0.0250 | -14 | c.551 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147131068 | GTGTATAT others(7): Show |
G | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02886.hp2 others(2): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0012a0001c0002t0001a0001c0005t0022others(2): Show | a0001c0001t0012g0034a0001c0002t0001g0007a0001c0005t0022g0032others(2): Show | 5 | 40 | 0.1250 | -14 | c.108 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147237049 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02630.hp2 HG02886.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0012others(9): Show | a0001c0001t0006g0009a0001c0001t0007g0018a0001c0001t0012g0034others(10): Show | 13 | 40 | 0.3250 | -14 | c.134 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147301590 | CTCTGTGT others(7): Show |
C | intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0005 | a0001c0005t0008 | a0001c0005t0008g0005 | 1 | 40 | 0.0250 | -14 | c.149 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147301592 | CTGTGTGT others(7): Show |
C | intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0012 | a0001c0012t0004 | a0001c0012t0004g0026 | 1 | 40 | 0.0250 | -14 | c.149 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147407467 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG03239.hp1 | a0003 | a0003c0007 | a0003c0007t0017 | a0003c0007t0017g0031 | 1 | 40 | 0.0250 | -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 | 147636136 | AAGGCAGT others(7): Show |
A | intron_variant | MODIFIER | HG02451.hp1 HG02896.hp1 HG02922.hp2 others(6): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0018a0001c0002t0001a0001c0002t0010others(6): Show | a0001c0001t0018g0001a0001c0002t0001g0007a0001c0002t0010g0002others(6): Show | 9 | 40 | 0.2250 | -14 | c.189 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147775281 | ATAAATAT others(7): Show |
A | intron_variant | MODIFIER | HG03139.hp1 HG03225.hp2 |
a0001 | a0001c0008a0001c0018 | a0001c0008t0001a0001c0018t0002 | a0001c0008t0001g0025a0001c0018t0002g0012 | 2 | 40 | 0.0500 | -14 | c.209 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147784494 | AATATATA others(7): Show |
A | intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0006 | 1 | 40 | 0.0250 | -14 | c.209 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147902800 | GTGTGTGT others(7): Show |
G | intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0009 | 1 | 40 | 0.0250 | -14 | c.209 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148308424 | AACGAATG others(7): Show |
A | intron_variant | MODIFIER | HG02451.hp1 HG02717.hp1 HG02896.hp1 others(10): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0012a0001c0002t0001others(8): Show | a0001c0001t0001g0038a0001c0001t0012g0034a0001c0002t0001g0007others(10): Show | 13 | 40 | 0.3250 | -14 | c.347 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148323294 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0040 | 1 | 40 | 0.0250 | -14 | c.347 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP3B_chr9_41885536_42134426 | 41924645 | GCACACAC others(7): Show |
G | intron_variant | MODIFIER | HG01943.hp2 HG02622.hp2 |
a0001a0026 | a0001c0012a0026c0025 | a0001c0012t0002a0026c0025t0019 | a0001c0012t0002g0009a0026c0025t0019g0028 | 2 | 108 | 0.0185 | -14 | c.236 others(31): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41996618 | GTTAAATT others(7): Show |
G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(37): Show |
a0001a0006a0009others(7): Show | a0001c0001a0001c0012a0001c0042others(12): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(17): Show | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(37): Show | 40 | 108 | 0.3704 | -14 | c.928 others(29): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 6/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42030750 | CAGAGAGA others(7): Show |
C | intron_variant | MODIFIER | HG02622.hp2 | a0026 | a0026c0025 | a0026c0025t0019 | a0026c0025t0019g0028 | 1 | 108 | 0.0093 | -14 | c.391 others(33): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42130111 | CGGAGGCG others(7): Show |
C | upstream_gene_variant | MODIFIER | HG01081.hp1 | a0016 | a0016c0017 | a0016c0017t0001 | a0016c0017t0001g0042 | 1 | 108 | 0.0093 | -14 | c.-10 others(25): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 686 | chr9 | TogoVar | ||||||
CNTNAP3_chr9_39059710_39293167 | 39159633 | TAGATAGA others(7): Show |
T | intron_variant | MODIFIER | HG02109.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0002 | 1 | 4 | 0.2500 | -14 | c.147 others(33): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76286174 | AGTGTGTG others(7): Show |
A | intron_variant | MODIFIER | HG03491.hp1 HG03492.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0065a0001c0001t0003g0066 | 2 | 274 | 0.0073 | -14 | c.85+ others(29): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76307503 | CATATATA others(7): Show |
C | intron_variant | MODIFIER | HG02486.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
a0002a0003 | a0002c0002a0002c0014a0003c0003 | a0002c0002t0002a0002c0002t0023a0002c0014t0013others(2): Show | a0002c0002t0002g0212a0002c0002t0023g0265a0002c0014t0013g0263others(3): Show | 6 | 274 | 0.0219 | -14 | c.86- others(29): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76338327 | GCTCCATT others(7): Show |
G | intron_variant | MODIFIER | HG01884.hp1 HG02109.hp2 HG03209.hp1 others(1): Show |
a0003a0013 | a0003c0003a0003c0006a0013c0033 | a0003c0003t0005a0003c0003t0027a0003c0006t0006others(1): Show | a0003c0003t0005g0047a0003c0003t0027g0237a0003c0006t0006g0205others(1): Show | 4 | 274 | 0.0146 | -14 | c.197 others(33): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76372665 | TGCCATGA others(7): Show |
T | intron_variant | MODIFIER | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(5): Show |
a0002a0003 | a0002c0002a0003c0003 | a0002c0002t0028a0003c0003t0006a0003c0003t0007others(2): Show | a0002c0002t0028g0239a0003c0003t0006g0264a0003c0003t0006g0268others(5): Show | 8 | 274 | 0.0292 | -14 | c.390 others(33): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76376907 | TTGTGTGT others(7): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0004a0001c0015others(24): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0062others(101): Show | 104 | 274 | 0.3796 | -14 | c.390 others(33): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76397938 | TTATATAC others(7): Show |
T | intron_variant | MODIFIER | HG00408.hp2 HG00738.hp1 HG01243.hp1 others(12): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0015a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(7): Show | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0185others(12): Show | 15 | 274 | 0.0547 | -14 | c.391 others(33): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76483231 | AACACACA others(7): Show |
A | intron_variant | MODIFIER | HG03453.hp1 | a0006 | a0006c0009 | a0006c0009t0004 | a0006c0009t0004g0273 | 1 | 274 | 0.0037 | -14 | c.188 others(33): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76518603 | GCATGCAT others(7): Show |
G | intron_variant | MODIFIER | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(161): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0004a0001c0015others(29): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(65): Show | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0062others(161): Show | 164 | 274 | 0.5985 | -14 | c.236 others(33): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76522686 | CCTTTCTT others(7): Show |
C | intron_variant | MODIFIER | HG02055.hp2 HG02109.hp2 HG02258.hp2 others(1): Show |
a0001a0002a0013 | a0001c0001a0002c0002a0013c0033 | a0001c0001t0010a0002c0002t0002a0002c0002t0023others(1): Show | a0001c0001t0010g0250a0002c0002t0002g0043a0002c0002t0023g0265others(1): Show | 4 | 274 | 0.0146 | -14 | c.275 others(31): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124255573 | ATAAAATA others(7): Show |
A | intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0040 | 1 | 64 | 0.0156 | -14 | c.381 others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 3/23 | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124264389 | TACACACA others(7): Show |
T | intron_variant | MODIFIER | HG02886.hp1 HG02897.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007 | a0001c0001t0003g0006a0001c0001t0007g0039 | 2 | 64 | 0.0313 | -14 | c.381 others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124306719 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0002 | a0001c0002t0008 | a0001c0002t0008g0058 | 1 | 64 | 0.0156 | -14 | c.381 others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124316804 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0002 | a0001c0002t0008 | a0001c0002t0008g0058 | 1 | 64 | 0.0156 | -14 | c.381 others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124510477 | GTATATAT others(7): Show |
G | intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0011 | 1 | 64 | 0.0156 | -14 | c.132 others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124565574 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG00423.hp1 HG01069.hp1 HG01891.hp1 others(8): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0024others(8): Show | 11 | 64 | 0.1719 | -14 | c.175 others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124619842 | CATATATA others(7): Show |
C | intron_variant | MODIFIER | HG00423.hp1 HG01069.hp2 HG01070.hp1 others(9): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(4): Show | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0043others(9): Show | 12 | 64 | 0.1875 | -14 | c.187 others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124620745 | GCACACAC others(7): Show |
G | intron_variant | MODIFIER | HG02257.hp1 HG02886.hp1 HG02886.hp2 others(6): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0007 | a0001c0001t0002a0001c0001t0003a0001c0002t0001others(4): Show | a0001c0001t0002g0024a0001c0001t0003g0006a0001c0002t0001g0007others(6): Show | 9 | 64 | 0.1406 | -14 | c.187 others(35): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124655939 | GAGAGAGA others(7): Show |
G | intron_variant | MODIFIER | HG01069.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0003 | 1 | 64 | 0.0156 | -14 | c.207 others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124713229 | TTCTTTCT others(7): Show |
T | intron_variant | MODIFIER | HG02145.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0008 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(1): Show | a0001c0001t0002g0022a0001c0001t0003g0006a0001c0001t0009g0061others(1): Show | 4 | 64 | 0.0625 | -14 | c.207 others(35): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124728911 | GATGTGAA others(7): Show |
G | intron_variant | MODIFIER | HG00423.hp2 HG01070.hp2 HG02698.hp2 others(2): Show |
a0001a0004a0005 | a0001c0001a0001c0002a0004c0006others(1): Show | a0001c0001t0001a0001c0002t0008a0004c0006t0001others(1): Show | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0002t0008g0058others(2): Show | 5 | 64 | 0.0781 | -14 | c.207 others(35): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |