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 | 146171659 | ATTTTC | A | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0006a0001c0002t0001others(1): Show | a0001c0001t0002g0006a0001c0001t0006g0009a0001c0002t0001g0007others(2): Show | 5 | 40 | 0.1250 | -5 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146172032 | ATTTTT | A | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0006a0001c0002t0001others(4): Show | a0001c0001t0002g0006a0001c0001t0006g0009a0001c0002t0001g0007others(4): Show | 7 | 40 | 0.1750 | -5 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146182095 | ATACTT | A | intron_variant | MODIFIER | HG02922.hp2 HG03098.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0004a0001c0010 | a0001c0001t0001a0001c0004t0005a0001c0010t0002 | a0001c0001t0001g0003a0001c0004t0005g0004a0001c0010t0002g0014 | 3 | 40 | 0.0750 | -5 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146238748 | AGCATG | A | intron_variant | MODIFIER | HG03225.hp1 NA18522.hp2 |
a0001 | a0001c0001a0001c0009 | a0001c0001t0007a0001c0009t0019 | a0001c0001t0007g0018a0001c0009t0019g0027 | 2 | 40 | 0.0500 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146252731 | TAAAAA | T | intron_variant | MODIFIER | NA18522.hp1 NA20129.hp2 |
a0001 | a0001c0003a0001c0013 | a0001c0003t0023a0001c0013t0003 | a0001c0003t0023g0030a0001c0013t0003g0039 | 2 | 40 | 0.0500 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146268619 | TGAGTA | T | intron_variant | MODIFIER | HG03225.hp2 NA18522.hp1 |
a0001 | a0001c0013a0001c0018 | a0001c0013t0003a0001c0018t0002 | a0001c0013t0003g0039a0001c0018t0002g0012 | 2 | 40 | 0.0500 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146285691 | TTCCCC | T | intron_variant | MODIFIER | HG02451.hp2 HG02486.hp2 HG02630.hp1 others(12): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(11): Show | a0001c0001t0001g0038a0001c0001t0002g0006a0001c0001t0012g0034others(12): Show | 15 | 40 | 0.3750 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146285805 | CTCCCT | C | intron_variant | MODIFIER | HG01891.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0006a0001c0003t0013a0001c0004t0003others(1): Show | a0001c0001t0006g0009a0001c0003t0013g0010a0001c0004t0003g0035others(2): Show | 5 | 40 | 0.1250 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146288793 | ATTTTT | A | intron_variant | MODIFIER | HG01891.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0006a0001c0003t0013a0001c0004t0003others(1): Show | a0001c0001t0006g0009a0001c0003t0013g0010a0001c0004t0003g0035others(2): Show | 5 | 40 | 0.1250 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146321067 | TGTAAA | T | intron_variant | MODIFIER | HG02451.hp2 HG02717.hp1 HG02897.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0002a0001c0001t0012a0001c0002t0001others(4): Show | a0001c0001t0002g0006a0001c0001t0012g0034a0001c0002t0001g0008others(5): Show | 8 | 40 | 0.2000 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146332941 | ATTTTT | A | intron_variant | MODIFIER | HG01891.hp2 HG02886.hp1 HG02896.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0006a0001c0001t0012a0001c0003t0013others(5): Show | a0001c0001t0006g0009a0001c0001t0012g0034a0001c0003t0013g0010others(6): Show | 9 | 40 | 0.2250 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146340283 | GTTGTT | G | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0019a0002c0017 | a0001c0001t0001a0001c0001t0007a0001c0001t0018others(2): Show | a0001c0001t0001g0003a0001c0001t0007g0018a0001c0001t0007g0020others(3): Show | 6 | 40 | 0.1500 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146351239 | GAAAAT | G | intron_variant | MODIFIER | HG02717.hp2 HG02896.hp1 HG02976.hp2 |
a0001a0005 | a0001c0003a0001c0005a0005c0020 | a0001c0003t0020a0001c0005t0008a0005c0020t0005 | a0001c0003t0020g0017a0001c0005t0008g0005a0005c0020t0005g0016 | 3 | 40 | 0.0750 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146360515 | TTAGAA | T | intron_variant | MODIFIER | HG02717.hp2 HG02896.hp1 HG02976.hp2 |
a0001a0005 | a0001c0003a0001c0005a0005c0020 | a0001c0003t0020a0001c0005t0008a0005c0020t0005 | a0001c0003t0020g0017a0001c0005t0008g0005a0005c0020t0005g0016 | 3 | 40 | 0.0750 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146370260 | TAAAAA | T | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(2): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0009others(1): Show | a0001c0001t0002a0001c0001t0006a0001c0002t0001others(2): Show | a0001c0001t0002g0006a0001c0001t0006g0009a0001c0002t0001g0021others(2): Show | 5 | 40 | 0.1250 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146411798 | TTTTTA | T | intron_variant | MODIFIER | HG01891.hp2 HG03098.hp2 NA18522.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0010 | a0001c0001t0006a0001c0001t0007a0001c0002t0001others(1): Show | a0001c0001t0006g0009a0001c0001t0007g0018a0001c0002t0001g0021others(1): Show | 4 | 40 | 0.1000 | -5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146513539 | CAAAGA | C | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02486.hp1 others(3): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0012others(3): Show | a0001c0001t0007a0001c0003t0023a0001c0012t0004others(3): Show | a0001c0001t0007g0020a0001c0003t0023g0030a0001c0012t0004g0026others(3): Show | 6 | 40 | 0.1500 | -5 | c.98- others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146533107 | CAAAAA | C | intron_variant | MODIFIER | HG02897.hp1 HG02976.hp1 HG03139.hp2 others(2): Show |
a0001 | a0001c0002a0001c0003a0001c0011others(2): Show | a0001c0002t0001a0001c0003t0023a0001c0011t0016others(2): Show | a0001c0002t0001g0008a0001c0003t0023g0030a0001c0011t0016g0019others(2): Show | 5 | 40 | 0.1250 | -5 | c.98- others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146574198 | TAAAAC | T | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp1 others(33): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(27): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(33): Show | 36 | 40 | 0.9000 | -5 | c.98- others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146597748 | ATATAC | A | intron_variant | MODIFIER | HG03098.hp2 HG03139.hp1 |
a0001 | a0001c0002a0001c0008 | a0001c0002t0001a0001c0008t0001 | a0001c0002t0001g0021a0001c0008t0001g0025 | 2 | 40 | 0.0500 | -5 | c.98- others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146602875 | AGGGTC | A | intron_variant | MODIFIER | HG02451.hp2 HG02922.hp2 HG03540.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0002t0010a0001c0003t0004others(1): Show | a0001c0001t0002g0006a0001c0002t0010g0002a0001c0003t0004g0029others(1): Show | 4 | 40 | 0.1000 | -5 | c.98- others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146681659 | TAACTA | T | intron_variant | MODIFIER | HG00735.hp1 HG01891.hp2 HG02451.hp2 others(15): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(14): Show | a0001c0001t0002g0006a0001c0001t0006g0009a0001c0001t0012g0034others(15): Show | 18 | 40 | 0.4500 | -5 | c.98- others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146701397 | TCTGGG | T | intron_variant | MODIFIER | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
a0001 | a0001c0001a0001c0004a0001c0012 | a0001c0001t0001a0001c0004t0003a0001c0004t0005others(1): Show | a0001c0001t0001g0038a0001c0004t0003g0035a0001c0004t0003g0036others(2): Show | 5 | 40 | 0.1250 | -5 | c.98- others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146843744 | GTACTC | G | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 |
a0001 | a0001c0001a0001c0019 | a0001c0001t0007a0001c0019t0006 | a0001c0001t0007g0020a0001c0019t0006g0015 | 2 | 40 | 0.0500 | -5 | c.402 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146864834 | AAACAG | A | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(29): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(25): Show | a0001c0001t0001g0003a0001c0001t0002g0006a0001c0001t0006g0009others(29): Show | 32 | 40 | 0.8000 | -5 | c.402 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146875934 | CAAAAA | C | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(9): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0012a0001c0002t0001a0001c0002t0010others(7): Show | a0001c0001t0012g0034a0001c0002t0001g0007a0001c0002t0001g0008others(9): Show | 12 | 40 | 0.3000 | -5 | c.402 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147019995 | AGTATG | A | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG02717.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0007a0001c0001t0018a0001c0002t0001others(10): Show | a0001c0001t0007g0018a0001c0001t0018g0001a0001c0002t0001g0008others(10): Show | 13 | 40 | 0.3250 | -5 | c.403 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147072848 | CTTTTT | C | intron_variant | MODIFIER | HG02486.hp1 HG02976.hp1 HG02976.hp2 |
a0001 | a0001c0001a0001c0003a0001c0015 | a0001c0001t0007a0001c0003t0020a0001c0015t0001 | a0001c0001t0007g0020a0001c0003t0020g0017a0001c0015t0001g0011 | 3 | 40 | 0.0750 | -5 | c.550 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147249604 | TAAAAA | T | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(1): Show |
a0001 | a0001c0004a0001c0008a0001c0015 | a0001c0004t0003a0001c0008t0001a0001c0015t0001 | a0001c0004t0003g0035a0001c0004t0003g0036a0001c0008t0001g0025others(1): Show | 4 | 40 | 0.1000 | -5 | c.134 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147292754 | ATGAAG | A | intron_variant | MODIFIER | HG02976.hp1 HG03139.hp1 |
a0001 | a0001c0008a0001c0015 | a0001c0008t0001a0001c0015t0001 | a0001c0008t0001g0025a0001c0015t0001g0011 | 2 | 40 | 0.0500 | -5 | c.134 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147323892 | CTTTAA | C | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(26): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(21): Show | a0001c0001t0001g0003a0001c0001t0002g0006a0001c0001t0006g0009others(26): Show | 29 | 40 | 0.7250 | -5 | c.149 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147335876 | AAAAAT | A | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(11): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(10): Show | a0001c0001t0001g0038a0001c0001t0002g0006a0001c0001t0006g0009others(11): Show | 14 | 40 | 0.3500 | -5 | c.149 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147406194 | AAAAGG | A | intron_variant | MODIFIER | HG00735.hp2 HG02451.hp2 HG02717.hp1 others(12): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(12): Show | a0001c0001t0001g0003a0001c0001t0002g0006a0001c0001t0007g0018others(12): Show | 15 | 40 | 0.3750 | -5 | c.167 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147407467 | CAAAAA | C | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(25): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(21): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(25): Show | 28 | 40 | 0.7000 | -5 | c.167 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147454011 | AAAAAT | A | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(35): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(29): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(35): Show | 38 | 40 | 0.9500 | -5 | c.167 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147507550 | CTTTTT | C | intron_variant | MODIFIER | HG00735.hp1 HG02486.hp1 HG02630.hp1 others(12): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0007a0001c0002t0001others(12): Show | a0001c0001t0001g0003a0001c0001t0007g0020a0001c0002t0001g0021others(12): Show | 15 | 40 | 0.3750 | -5 | c.177 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147588206 | AAAAAC | A | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp1 others(20): Show |
a0001a0004a0005 | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(19): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(20): Show | 23 | 40 | 0.5750 | -5 | c.189 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147615277 | CAAAAA | C | intron_variant | MODIFIER | HG02451.hp1 HG02897.hp1 HG03239.hp1 others(3): Show |
a0001a0002a0003 | a0001c0002a0001c0013a0002c0016others(1): Show | a0001c0002t0001a0001c0002t0002a0001c0013t0003others(2): Show | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0002t0002g0040others(3): Show | 6 | 40 | 0.1500 | -5 | c.189 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147832668 | ATATAT | A | intron_variant | MODIFIER | HG02630.hp1 HG02717.hp2 HG03540.hp1 |
a0001 | a0001c0002a0001c0005a0001c0012 | a0001c0002t0010a0001c0005t0008a0001c0012t0004 | a0001c0002t0010g0002a0001c0005t0008g0005a0001c0012t0004g0026 | 3 | 40 | 0.0750 | -5 | c.209 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147859436 | AAAAAC | A | intron_variant | MODIFIER | HG02896.hp2 HG02922.hp1 HG03540.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0012a0001c0003t0004a0001c0004t0003others(1): Show | a0001c0001t0012g0034a0001c0003t0004g0029a0001c0004t0003g0035others(1): Show | 4 | 40 | 0.1000 | -5 | c.209 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147861999 | CAAAAA | C | intron_variant | MODIFIER | HG02486.hp1 HG02886.hp2 HG02896.hp2 others(7): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0007a0001c0001t0012a0001c0001t0018others(5): Show | a0001c0001t0007g0018a0001c0001t0007g0020a0001c0001t0012g0034others(7): Show | 10 | 40 | 0.2500 | -5 | c.209 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147894960 | TCTTTC | T | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0011 | a0001c0002t0001g0007a0001c0003t0011g0023 | 2 | 40 | 0.0500 | -5 | c.209 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147920355 | CAAAAA | C | intron_variant | MODIFIER | HG01891.hp1 HG02630.hp1 HG02886.hp1 others(3): Show |
a0001a0002a0004 | a0001c0003a0001c0004a0001c0005others(3): Show | a0001c0003t0013a0001c0004t0005a0001c0005t0022others(3): Show | a0001c0003t0013g0010a0001c0004t0005g0004a0001c0005t0022g0032others(3): Show | 6 | 40 | 0.1500 | -5 | c.225 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147943766 | CAAAAA | C | intron_variant | MODIFIER | HG02630.hp1 HG02630.hp2 HG02717.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0010others(4): Show | a0001c0001t0001g0003a0001c0002t0002g0013a0001c0002t0010g0002others(4): Show | 7 | 40 | 0.1750 | -5 | c.225 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147973160 | TAAAAA | T | intron_variant | MODIFIER | HG00735.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
a0001 | a0001c0002a0001c0006 | a0001c0002t0001a0001c0002t0002a0001c0006t0014 | a0001c0002t0001g0008a0001c0002t0001g0021a0001c0002t0002g0040others(1): Show | 4 | 40 | 0.1000 | -5 | c.225 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147975443 | ATTCAT | A | intron_variant | MODIFIER | HG02486.hp2 HG02717.hp1 HG02886.hp1 others(6): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(3): Show | a0001c0001t0012a0001c0001t0018a0001c0003t0004others(6): Show | a0001c0001t0012g0034a0001c0001t0018g0001a0001c0003t0004g0029others(6): Show | 9 | 40 | 0.2250 | -5 | c.225 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148022480 | AAAAAG | A | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02896.hp1 others(7): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0009others(6): Show | a0001c0001t0018a0001c0002t0001a0001c0002t0002others(7): Show | a0001c0001t0018g0001a0001c0002t0001g0007a0001c0002t0002g0040others(7): Show | 10 | 40 | 0.2500 | -5 | c.238 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148077985 | TAATAG | T | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp2 HG02451.hp1 others(6): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0002a0001c0001t0006a0001c0002t0001others(6): Show | a0001c0001t0002g0006a0001c0001t0006g0009a0001c0002t0001g0007others(6): Show | 9 | 40 | 0.2250 | -5 | c.238 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148109351 | GTGTTT | G | intron_variant | MODIFIER | HG02630.hp1 HG02717.hp2 |
a0001 | a0001c0005a0001c0012 | a0001c0005t0008a0001c0012t0004 | a0001c0005t0008g0005a0001c0012t0004g0026 | 2 | 40 | 0.0500 | -5 | c.238 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148293073 | ATAAAT | A | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp2 HG02486.hp1 others(14): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0012others(13): Show | a0001c0001t0006g0009a0001c0001t0007g0020a0001c0001t0012g0034others(14): Show | 17 | 40 | 0.4250 | -5 | c.347 others(26): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | chr7 | TogoVar |