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 | 146352750 | G | GTTTTTTT others(9): Show |
intron_variant | MODIFIER | HG03139.hp2 NA20129.hp1 |
a0001 | a0001c0006a0001c0011 | a0001c0006t0009a0001c0011t0016 | a0001c0006t0009g0028a0001c0011t0016g0019 | 2 | 40 | 0.0500 | 16 | c.97+ others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146395779 | T | TAGATGAT others(9): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0002 | a0002c0017 | a0002c0017t0015 | a0002c0017t0015g0037 | 1 | 40 | 0.0250 | 16 | c.97+ others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146422359 | G | GTGTATAT others(9): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0021 | 1 | 40 | 0.0250 | 16 | c.97+ others(35): 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(9): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0011 | a0001c0011t0016 | a0001c0011t0016g0019 | 1 | 40 | 0.0250 | 16 | c.97+ others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146443230 | T | TAATAAAT others(9): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0002 | a0002c0016 | a0002c0016t0004 | a0002c0016t0004g0024 | 1 | 40 | 0.0250 | 16 | c.97+ others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146450935 | A | ATATTTAT others(9): Show |
intron_variant | MODIFIER | HG02451.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0004t0003a0001c0004t0005 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0004t0003g0035others(2): Show | 5 | 40 | 0.1250 | 16 | c.98- others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146464187 | G | GTTTTTTT others(9): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0004 | a0004c0014 | a0004c0014t0021 | a0004c0014t0021g0022 | 1 | 40 | 0.0250 | 16 | c.98- others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146535154 | A | AATATATA others(9): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02630.hp2 others(3): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0006a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0006g0009a0001c0002t0001g0007a0001c0002t0002g0013others(3): Show | 6 | 40 | 0.1500 | 16 | c.98- others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146599743 | G | GAGATAGA others(9): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0005t0008others(1): Show | a0001c0001t0001g0003a0001c0002t0002g0013a0001c0005t0008g0005others(1): Show | 4 | 40 | 0.1000 | 16 | c.98- others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146721875 | G | GTGTGTGT others(9): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0012 | a0001c0012t0004 | a0001c0012t0004g0026 | 1 | 40 | 0.0250 | 16 | 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 | 146760409 | C | CTTTTTTT others(9): Show |
intron_variant | MODIFIER | HG02897.hp1 HG03239.hp1 |
a0001a0003 | a0001c0002a0003c0007 | a0001c0002t0001a0003c0007t0017 | a0001c0002t0001g0008a0003c0007t0017g0031 | 2 | 40 | 0.0500 | 16 | 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 | 147317800 | A | ATATGTGT others(9): Show |
intron_variant | MODIFIER | HG02717.hp2 HG02896.hp1 HG02976.hp1 others(3): Show |
a0001a0003a0005 | a0001c0005a0001c0006a0001c0008others(3): Show | a0001c0005t0008a0001c0006t0009a0001c0008t0001others(3): Show | a0001c0005t0008g0005a0001c0006t0009g0028a0001c0008t0001g0025others(3): Show | 6 | 40 | 0.1500 | 16 | c.149 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147347461 | T | TATATATA others(9): Show |
intron_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0018 | 1 | 40 | 0.0250 | 16 | c.149 others(37): 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(9): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0034 | 1 | 40 | 0.0250 | 16 | c.167 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147469506 | A | ATTTTTTT others(9): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0003 | a0001c0003t0011 | a0001c0003t0011g0023 | 1 | 40 | 0.0250 | 16 | c.167 others(37): 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(9): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(2): Show | a0001c0001t0001g0038a0001c0001t0006g0009a0001c0001t0007g0020others(3): Show | 6 | 40 | 0.1500 | 16 | 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 | 147510850 | C | CATATATA others(9): Show |
intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG02486.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0007a0001c0002t0002others(2): Show | a0001c0001t0001g0038a0001c0001t0007g0020a0001c0002t0002g0013others(3): Show | 6 | 40 | 0.1500 | 16 | c.177 others(37): 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(9): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0015 | a0001c0015t0001 | a0001c0015t0001g0011 | 1 | 40 | 0.0250 | 16 | c.177 others(37): 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(9): Show |
intron_variant | MODIFIER | HG03098.hp2 HG03239.hp2 |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002 | a0001c0002t0001g0021a0001c0002t0002g0040 | 2 | 40 | 0.0500 | 16 | 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 | 147583531 | T | TATATATA others(9): Show |
intron_variant | MODIFIER | HG03098.hp1 NA18522.hp1 |
a0001 | a0001c0001a0001c0013 | a0001c0001t0001a0001c0013t0003 | a0001c0001t0001g0003a0001c0013t0003g0039 | 2 | 40 | 0.0500 | 16 | c.189 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147784381 | C | CATATATA others(9): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0004 | a0004c0014 | a0004c0014t0021 | a0004c0014t0021g0022 | 1 | 40 | 0.0250 | 16 | c.209 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147886475 | C | CAAAAAAA others(9): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0003 | a0001c0003t0011 | a0001c0003t0011g0023 | 1 | 40 | 0.0250 | 16 | 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 | 147919459 | C | CTTTCTTT others(9): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0008 | a0001c0008t0001 | a0001c0008t0001g0025 | 1 | 40 | 0.0250 | 16 | c.225 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147949440 | G | GTATATAT others(9): Show |
intron_variant | MODIFIER | HG02897.hp1 HG03098.hp2 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0008a0001c0002t0001g0021 | 2 | 40 | 0.0500 | 16 | c.225 others(37): 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(9): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0012 | a0001c0012t0004 | a0001c0012t0004g0026 | 1 | 40 | 0.0250 | 16 | 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 | 147981786 | G | GGTGTGTG others(9): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0012 | a0001c0012t0004 | a0001c0012t0004g0026 | 1 | 40 | 0.0250 | 16 | c.238 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148106493 | G | GAGAGAGA others(9): Show |
intron_variant | MODIFIER | HG02630.hp1 HG02717.hp2 |
a0001 | a0001c0005a0001c0012 | a0001c0005t0008a0001c0012t0004 | a0001c0005t0008g0005a0001c0012t0004g0026 | 2 | 40 | 0.0500 | 16 | c.238 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148106493 | G | GATATATA others(9): Show |
intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0035a0001c0004t0003g0036 | 2 | 40 | 0.0500 | 16 | c.238 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148136017 | A | AAGGAAGG others(9): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0010 | a0001c0010t0002 | a0001c0010t0002g0014 | 1 | 40 | 0.0250 | 16 | c.255 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148136017 | A | AAGGAAGG others(9): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0040 | 1 | 40 | 0.0250 | 16 | c.255 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148136017 | A | AAGGGAGG others(9): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0034 | 1 | 40 | 0.0250 | 16 | c.255 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148137669 | A | AAAGGAAG others(9): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0001 | 1 | 40 | 0.0250 | 16 | c.255 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148187147 | C | CACACACA others(9): Show |
intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0035a0001c0004t0003g0036 | 2 | 40 | 0.0500 | 16 | c.301 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148283255 | A | AAAAGAAA others(9): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0034 | 1 | 40 | 0.0250 | 16 | c.347 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148297165 | A | AAAGGAAG others(9): Show |
intron_variant | MODIFIER | HG02451.hp1 HG02451.hp2 HG02897.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0001 | a0001c0001t0002g0006a0001c0002t0001g0007a0001c0002t0001g0008 | 3 | 40 | 0.0750 | 16 | c.347 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148297197 | G | GAAGGAAG others(9): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0009 | a0001c0009t0019 | a0001c0009t0019g0027 | 1 | 40 | 0.0250 | 16 | c.347 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148405420 | A | ATTTTTTT others(9): Show |
intron_variant | MODIFIER | HG00735.hp2 HG03139.hp1 |
a0001 | a0001c0008a0001c0019 | a0001c0008t0001a0001c0019t0006 | a0001c0008t0001g0025a0001c0019t0006g0015 | 2 | 40 | 0.0500 | 16 | c.371 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP3B_chr9_41885536_42134426 | 41934100 | C | CATATATA others(9): Show |
intron_variant | MODIFIER | HG00280.hp1 HG01516.hp2 HG01943.hp2 others(6): Show |
a0001a0002a0010others(1): Show | a0001c0001a0001c0012a0001c0042others(3): Show | a0001c0001t0003a0001c0012t0002a0001c0042t0013others(3): Show | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0099others(6): Show | 9 | 108 | 0.0833 | 16 | c.223 others(35): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 14/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41996187 | C | CCGATTAG others(9): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0007 | a0007c0016 | a0007c0016t0001 | a0007c0016t0001g0036 | 1 | 108 | 0.0093 | 16 | c.107 others(31): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 7/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42030750 | C | CAGAGAGA others(9): Show |
intron_variant | MODIFIER | HG03453.hp1 HG03669.hp1 |
a0002a0008 | a0002c0002a0008c0006 | a0002c0002t0001a0008c0006t0010 | a0002c0002t0001g0040a0008c0006t0010g0071 | 2 | 108 | 0.0185 | 16 | c.391 others(35): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42030813 | G | GGAGAGAG others(9): Show |
intron_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0012 | 1 | 108 | 0.0093 | 16 | c.391 others(35): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42034174 | G | GTATCTAT others(9): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0042 | a0001c0042t0013 | a0001c0042t0013g0001 | 1 | 108 | 0.0093 | 16 | c.391 others(35): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42034186 | G | GTATCTAT others(9): Show |
intron_variant | MODIFIER | HG00642.hp2 HG01071.hp2 HG01943.hp2 others(3): Show |
a0001a0027 | a0001c0001a0001c0012a0027c0026 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(2): Show | a0001c0001t0002g0004a0001c0001t0002g0018a0001c0001t0003g0093others(3): Show | 6 | 108 | 0.0556 | 16 | c.391 others(35): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 3/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 42089145 | G | GAAAGGGA others(9): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(39): Show |
a0001a0006a0009others(8): Show | a0001c0001a0001c0012a0001c0042others(14): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(19): Show | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(39): Show | 42 | 108 | 0.3889 | 16 | c.197 others(35): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2/23 | chr9 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76376907 | T | TTGTGTGT others(9): Show |
intron_variant | MODIFIER | NA18960.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0222 | 1 | 274 | 0.0037 | 16 | c.390 others(35): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76397938 | T | TTATGTAT others(9): Show |
intron_variant | MODIFIER | HG02074.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0126 | 1 | 274 | 0.0037 | 16 | c.391 others(35): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76436961 | A | ATATCTAT others(9): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(23): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0018others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(12): Show | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0056others(23): Show | 26 | 274 | 0.0949 | 16 | c.538 others(33): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76436989 | C | CTATCTAT others(9): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(32): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(16): Show | a0001c0001t0001g0076a0001c0001t0001g0119a0001c0001t0001g0151others(32): Show | 35 | 274 | 0.1277 | 16 | c.538 others(33): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76451599 | A | ATGTGTGT others(9): Show |
intron_variant | MODIFIER | HG00738.hp2 HG03195.hp2 NA18962.hp1 others(2): Show |
a0001a0002a0023 | a0001c0001a0002c0002a0002c0011others(1): Show | a0001c0001t0005a0002c0002t0002a0002c0011t0005others(1): Show | a0001c0001t0005g0163a0002c0002t0002g0039a0002c0002t0002g0167others(2): Show | 5 | 274 | 0.0183 | 16 | c.107 others(33): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76460773 | A | AAAAAAAA others(9): Show |
intron_variant | MODIFIER | HG02155.hp1 | a0005 | a0005c0008 | a0005c0008t0001 | a0005c0008t0001g0108 | 1 | 274 | 0.0037 | 16 | c.133 others(35): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar |