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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTNAP2_chr7_146111801_148425998 | 147784381 | CATATATA others(3): Show |
C | intron_variant | MODIFIER | HG02486.hp1 HG02486.hp2 HG02717.hp2 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0007a0001c0002t0010a0001c0003t0011others(7): Show | a0001c0001t0007g0020 a0001c0002t0010g0002 a0001c0003t0011g0023 others(7): Show |
10 | 40 | 0.2500 | -10 | c.209 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147894955 | TTCTTTCT others(3): Show |
T | intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0009 | 1 | 40 | 0.0250 | -10 | c.209 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147894957 | CTTTCTTT others(3): Show |
C | intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0004 | 1 | 40 | 0.0250 | -10 | c.209 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147902804 | GTGTGTGT others(3): Show |
G | intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 40 | 0.0250 | -10 | c.209 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147925152 | AGAGAAGG others(3): Show |
A | intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0034 | 1 | 40 | 0.0250 | -10 | c.225 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147929092 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0001 | 1 | 40 | 0.0250 | -10 | c.225 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148062028 | AGTGTGTG others(3): Show |
A | intron_variant | MODIFIER | HG03098.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
a0001 | a0001c0002a0001c0008a0001c0009others(1): Show | a0001c0002t0001a0001c0008t0001a0001c0009t0019others(1): Show | a0001c0002t0001g0021 a0001c0008t0001g0025 a0001c0009t0019g0027 others(1): Show |
4 | 40 | 0.1000 | -10 | c.238 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148099421 | TTGTGTGT others(3): Show |
T | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(3): Show |
a0001a0004a0005 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0002a0001c0001t0006a0001c0002t0001others(3): Show | a0001c0001t0002g0006 a0001c0001t0006g0009 a0001c0002t0001g0008 others(3): Show |
6 | 40 | 0.1500 | -10 | c.238 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148101350 | AGTGTGTG others(3): Show |
A | intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0015 | a0001c0015t0001 | a0001c0015t0001g0011 | 1 | 40 | 0.0250 | -10 | c.238 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148227884 | CGTGTGTG others(3): Show |
C | intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0019 | a0001c0019t0006 | a0001c0019t0006g0015 | 1 | 40 | 0.0250 | -10 | c.324 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148296545 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG03540.hp2 NA18522.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0007a0001c0003t0004 | a0001c0001t0007g0018 a0001c0003t0004g0029 |
2 | 40 | 0.0500 | -10 | c.347 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148305222 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG02886.hp2 HG02976.hp1 |
a0001 | a0001c0005a0001c0015 | a0001c0005t0022a0001c0015t0001 | a0001c0005t0022g0032 a0001c0015t0001g0011 |
2 | 40 | 0.0500 | -10 | c.347 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148365698 | GTATACTT others(3): Show |
G | intron_variant | MODIFIER | HG03139.hp2 HG03239.hp1 HG03239.hp2 |
a0001a0003 | a0001c0002a0001c0011a0003c0007 | a0001c0002t0002a0001c0011t0016a0003c0007t0017 | a0001c0002t0002g0040 a0001c0011t0016g0019 a0003c0007t0017g0031 |
3 | 40 | 0.0750 | -10 | c.347 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148365956 | GCATGTAT others(3): Show |
G | intron_variant | MODIFIER | HG02717.hp1 | a0002 | a0002c0017 | a0002c0017t0015 | a0002c0017t0015g0037 | 1 | 40 | 0.0250 | -10 | c.347 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | chr7 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 148366170 | GCATGTAT others(3): Show |
G | intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0002 | a0001c0002t0010 | a0001c0002t0010g0002 | 1 | 40 | 0.0250 | -10 | c.347 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | chr7 | TogoVar | |||||||
CNTNAP3B_chr9_41885536_42134426 | 41888506 | CTAAAATA others(3): Show |
C | downstream_gene_variant | MODIFIER | HG01106.hp2 | a0009 | a0009c0008 | a0009c0008t0009 | a0009c0008t0009g0107 | 1 | 108 | 0.0093 | -10 | c.*54 others(21): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2029 | chr9 | TogoVar | |||||||
CNTNAP3B_chr9_41885536_42134426 | 41904311 | GTTTTTTT others(3): Show |
G | intron_variant | MODIFIER | HG02922.hp2 | a0019 | a0019c0031 | a0019c0031t0028 | a0019c0031t0028g0088 | 1 | 108 | 0.0093 | -10 | c.344 others(29): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | TogoVar | |||||||
CNTNAP3B_chr9_41885536_42134426 | 41924645 | GCACACAC others(3): Show |
G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(32): Show |
a0001a0004a0005others(7): Show | a0001c0001a0001c0012a0001c0043others(10): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(15): Show | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(32): Show |
35 | 108 | 0.3241 | -10 | c.236 others(27): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | TogoVar | |||||||
CNTNAP3B_chr9_41885536_42134426 | 41950747 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | HG01943.hp2 NA18970.hp2 |
a0001 | a0001c0001a0001c0012 | a0001c0001t0002a0001c0012t0002 | a0001c0001t0002g0024 a0001c0012t0002g0009 |
2 | 108 | 0.0185 | -10 | c.208 others(29): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 13/23 | chr9 | TogoVar | |||||||
CNTNAP3_chr9_39059710_39293167 | 39072240 | GAATTTCC others(3): Show |
G | 3_prime_UTR_variant | MODIFIER | HG02109.hp1 HG02109.hp2 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0003a0002c0003t0004 | a0001c0001t0003g0002 a0002c0003t0004g0001 |
2 | 4 | 0.5000 | -10 | c.*16 others(21): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 1640 | chr9 | TogoVar | ||||||
CNTNAP3_chr9_39059710_39293167 | 39213191 | GAGAGAAG others(3): Show |
G | intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0004 | a0004c0002 | a0004c0002t0001 | a0004c0002t0001g0003 | 1 | 4 | 0.2500 | -10 | c.391 others(29): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | TogoVar | |||||||
CNTNAP4_chr16_76272401_76565757 | 76274704 | TTTTTGTT others(3): Show |
T | upstream_gene_variant | MODIFIER | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(1): Show |
a0003a0015 | a0003c0003a0015c0034 | a0003c0003t0011a0003c0003t0030a0015c0034t0006 | a0003c0003t0011g0243 a0003c0003t0011g0244 a0003c0003t0030g0245 others(1): Show |
4 | 274 | 0.0146 | -10 | c.-29 others(21): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 2696 | chr16 | TogoVar | |||||||
CNTNAP4_chr16_76272401_76565757 | 76286174 | AGTGTGTG others(3): Show |
A | intron_variant | MODIFIER | HG01884.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0014others(1): Show | a0001c0001t0015a0002c0002t0002a0002c0014t0006others(2): Show | a0001c0001t0015g0272 a0002c0002t0002g0212 a0002c0014t0006g0269 others(2): Show |
5 | 274 | 0.0183 | -10 | c.85+ others(25): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76298486 | ATGTGTGT others(3): Show |
A | intron_variant | MODIFIER | HG01433.hp1 HG03130.hp2 NA18522.hp2 |
a0003a0004a0021 | a0003c0003a0004c0007a0021c0037 | a0003c0003t0018a0004c0007t0004a0021c0037t0006 | a0003c0003t0018g0164 a0004c0007t0004g0055 a0021c0037t0006g0171 |
3 | 274 | 0.0110 | -10 | c.86- others(27): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76298521 | TGTGTGTG others(3): Show |
T | intron_variant | MODIFIER | NA18970.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0256 | 1 | 274 | 0.0037 | -10 | c.86- others(27): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76307503 | CATATATA others(3): Show |
C | intron_variant | MODIFIER | HG00408.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(7): Show | a0001c0001t0001g0158 a0001c0001t0003g0127 a0001c0001t0003g0169 others(9): Show |
12 | 274 | 0.0438 | -10 | c.86- others(25): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76343663 | GTTACATT others(3): Show |
G | intron_variant | MODIFIER | HG02970.hp2 | a0002 | a0002c0002 | a0002c0002t0024 | a0002c0002t0024g0049 | 1 | 274 | 0.0037 | -10 | c.197 others(29): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76364233 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG04204.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0064 | 1 | 274 | 0.0037 | -10 | c.390 others(27): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76376907 | TTGTGTGT others(3): Show |
T | intron_variant | MODIFIER | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
a0003 | a0003c0003a0003c0006 | a0003c0003t0006a0003c0003t0011a0003c0003t0027others(2): Show | a0003c0003t0006g0264 a0003c0003t0006g0268 a0003c0003t0011g0243 others(5): Show |
8 | 274 | 0.0292 | -10 | c.390 others(29): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76385547 | AGTGTGTG others(3): Show |
A | intron_variant | MODIFIER | HG02809.hp1 HG03209.hp2 |
a0003a0027 | a0003c0003a0027c0040 | a0003c0003t0006a0027c0040t0001 | a0003c0003t0006g0262 a0027c0040t0001g0267 |
2 | 274 | 0.0073 | -10 | c.390 others(29): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76392558 | TGAGGAAA others(3): Show |
T | intron_variant | MODIFIER | HG02055.hp2 NA21309.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0010a0003c0003t0007 | a0001c0001t0010g0250 a0003c0003t0007g0259 |
2 | 274 | 0.0073 | -10 | c.391 others(29): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | chr16 | TogoVar | |||||||
CNTNAP4_chr16_76272401_76565757 | 76397938 | TTATATAC others(3): Show |
T | intron_variant | MODIFIER | HG02647.hp1 HG04184.hp2 NA19003.hp1 others(3): Show |
a0001a0002a0010 | a0001c0001a0001c0015a0001c0018others(2): Show | a0001c0001t0001a0001c0001t0016a0001c0015t0006others(3): Show | a0001c0001t0001g0158 a0001c0001t0016g0088 a0001c0015t0006g0166 others(3): Show |
6 | 274 | 0.0219 | -10 | c.391 others(29): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76483231 | AACACACA others(3): Show |
A | intron_variant | MODIFIER | HG01168.hp2 HG02056.hp1 HG02698.hp2 others(6): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0002c0002others(4): Show | a0001c0001t0003a0001c0001t0005a0001c0004t0003others(5): Show | a0001c0001t0003g0124 a0001c0001t0005g0163 a0001c0004t0003g0156 others(6): Show |
9 | 274 | 0.0329 | -10 | c.188 others(29): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76491767 | ATTCTGTT others(3): Show |
A | intron_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0016 | 1 | 274 | 0.0037 | -10 | c.208 others(29): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76522687 | CTTTCTTT others(3): Show |
C | intron_variant | MODIFIER | HG00408.hp1 HG00558.hp2 HG02809.hp1 others(6): Show |
a0001a0003a0020others(2): Show | a0001c0001a0003c0003a0003c0006others(3): Show | a0001c0001t0001a0001c0001t0009a0003c0003t0001others(5): Show | a0001c0001t0001g0158 a0001c0001t0009g0189 a0003c0003t0001g0098 others(6): Show |
9 | 274 | 0.0329 | -10 | c.275 others(27): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124035910 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0037 | 1 | 64 | 0.0156 | -10 | c.82+ others(27): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124044889 | AACACACA others(3): Show |
A | intron_variant | MODIFIER | HG02897.hp2 HG03225.hp1 HG03704.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0001a0001c0002t0019 | a0001c0001t0002g0024 a0001c0001t0002g0048 a0001c0002t0001g0054 others(1): Show |
4 | 64 | 0.0625 | -10 | c.82+ others(27): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124105031 | TGCTCTAC others(3): Show |
T | intron_variant | MODIFIER | HG02897.hp2 NA21309.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0001 | a0001c0001t0002g0024 a0001c0002t0001g0054 |
2 | 64 | 0.0313 | -10 | c.82+ others(27): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 1/23 | chr2 | TogoVar | |||||||
CNTNAP5_chr2_124020287_124926219 | 124194402 | TATATATA others(3): Show |
T | intron_variant | MODIFIER | HG01261.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0002 a0001c0001t0002g0049 a0001c0002t0001g0062 others(1): Show |
4 | 64 | 0.0625 | -10 | c.83- others(27): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124227640 | ATGTGTGT others(3): Show |
A | intron_variant | MODIFIER | HG03130.hp1 | a0006 | a0006c0003 | a0006c0003t0008 | a0006c0003t0008g0035 | 1 | 64 | 0.0156 | -10 | c.187 others(27): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124255524 | AAAAATAA others(3): Show |
A | intron_variant | MODIFIER | HG01070.hp2 HG01261.hp2 HG02293.hp1 others(14): Show |
a0001a0005 | a0001c0001a0001c0002a0005c0005 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(9): Show | a0001c0001t0002g0027 a0001c0001t0002g0050 a0001c0001t0003g0006 others(14): Show |
17 | 64 | 0.2656 | -10 | c.381 others(29): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124264379 | CACACACA others(3): Show |
C | intron_variant | MODIFIER | HG01070.hp1 HG01261.hp1 HG02922.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0042 others(1): Show |
4 | 64 | 0.0625 | -10 | c.381 others(29): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124264389 | TACACACA others(3): Show |
T | intron_variant | MODIFIER | HG00423.hp1 HG02293.hp2 HG02698.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0013others(1): Show | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0004g0053 others(2): Show |
5 | 64 | 0.0781 | -10 | c.381 others(29): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124320336 | CTACTTTT others(3): Show |
C | intron_variant | MODIFIER | HG01069.hp1 HG02886.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0001 | a0001c0001t0003g0006 a0001c0002t0001g0003 |
2 | 64 | 0.0313 | -10 | c.381 others(29): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124322161 | TAATAAAA others(3): Show |
T | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(26): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0008others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0002g0022 others(26): Show |
29 | 64 | 0.4531 | -10 | c.381 others(29): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124349874 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | HG01070.hp1 HG01261.hp2 HG02145.hp2 others(13): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0002g0022 others(13): Show |
16 | 64 | 0.2500 | -10 | c.382 others(29): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124493965 | TACACACA others(3): Show |
T | intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0057 | 1 | 64 | 0.0156 | -10 | c.106 others(31): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124510348 | AACACACA others(3): Show |
A | intron_variant | MODIFIER | HG02451.hp1 HG03453.hp2 NA19240.hp1 |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0004 | a0001c0002t0001g0046 a0001c0002t0004g0044 a0001c0002t0004g0047 |
3 | 64 | 0.0469 | -10 | c.132 others(29): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124510477 | GTATATAT others(3): Show |
G | intron_variant | MODIFIER | HG02897.hp2 HG03704.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0024 a0001c0001t0002g0048 |
2 | 64 | 0.0313 | -10 | c.132 others(29): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124567856 | GATAGATA others(3): Show |
G | intron_variant | MODIFIER | HG00423.hp1 NA21309.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0019 a0001c0001t0003g0057 |
2 | 64 | 0.0313 | -10 | c.175 others(29): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |