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 | 146347138 | TAAA | T | intron_variant | MODIFIER | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0006a0001c0001t0012a0001c0002t0001others(5): Show | a0001c0001t0006g0009a0001c0001t0012g0034a0001c0002t0001g0008others(7): Show | 10 | 40 | 0.2500 | -3 | 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 | 146380784 | CTTT | C | intron_variant | MODIFIER | HG02717.hp1 HG02896.hp1 NA18522.hp1 others(2): Show |
a0001a0002a0005 | a0001c0001a0001c0013a0002c0016others(2): Show | a0001c0001t0018a0001c0013t0003a0002c0016t0004others(2): Show | a0001c0001t0018g0001a0001c0013t0003g0039a0002c0016t0004g0024others(2): Show | 5 | 40 | 0.1250 | -3 | 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 | 146391750 | TTTG | T | intron_variant | MODIFIER | HG00735.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(8): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(10): Show | 13 | 40 | 0.3250 | -3 | 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 | 146395776 | AGAT | A | intron_variant | MODIFIER | HG02630.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
a0001 | a0001c0002a0001c0008a0001c0011others(1): Show | a0001c0002t0002a0001c0008t0001a0001c0011t0016others(1): Show | a0001c0002t0002g0013a0001c0008t0001g0025a0001c0011t0016g0019others(1): Show | 4 | 40 | 0.1000 | -3 | 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 | 146395823 | AGAG | A | intron_variant | MODIFIER | HG02451.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
a0001 | a0001c0001a0001c0005a0001c0010 | a0001c0001t0001a0001c0001t0002a0001c0005t0008others(1): Show | a0001c0001t0001g0003a0001c0001t0002g0006a0001c0005t0008g0005others(1): Show | 4 | 40 | 0.1000 | -3 | 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 | 146426877 | CAAT | C | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02451.hp2 others(25): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(23): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(25): Show | 28 | 40 | 0.7000 | -3 | 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 | 146442431 | TTGG | T | intron_variant | MODIFIER | HG02886.hp1 HG03225.hp2 NA19030.hp2 |
a0001a0002 | a0001c0003a0001c0018a0002c0016 | a0001c0003t0013a0001c0018t0002a0002c0016t0004 | a0001c0003t0013g0010a0001c0018t0002g0012a0002c0016t0004g0024 | 3 | 40 | 0.0750 | -3 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146464185 | CTGT | C | intron_variant | MODIFIER | HG02486.hp2 HG02630.hp2 HG02976.hp1 others(4): Show |
a0001 | a0001c0002a0001c0003a0001c0006others(2): Show | a0001c0002t0002a0001c0002t0010a0001c0003t0011others(4): Show | a0001c0002t0002g0013a0001c0002t0010g0002a0001c0003t0011g0023others(4): Show | 7 | 40 | 0.1750 | -3 | 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 | 146464187 | GTTT | G | intron_variant | MODIFIER | HG02717.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
a0001a0002a0005 | a0001c0002a0001c0004a0001c0013others(3): Show | a0001c0002t0001a0001c0004t0005a0001c0013t0003others(3): Show | a0001c0002t0001g0008a0001c0004t0005g0004a0001c0013t0003g0039others(3): Show | 6 | 40 | 0.1500 | -3 | 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 | 146484995 | TATA | T | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0035a0001c0004t0003g0036 | 2 | 40 | 0.0500 | -3 | 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 | 146529965 | AAAC | A | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0008others(3): Show | a0001c0001t0002a0001c0001t0006a0001c0002t0001others(5): Show | a0001c0001t0002g0006a0001c0001t0006g0009a0001c0002t0001g0007others(5): Show | 8 | 40 | 0.2000 | -3 | 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 | 146533107 | CAAA | C | intron_variant | MODIFIER | HG02717.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0018a0001c0003t0013a0001c0003t0020others(3): Show | a0001c0001t0018g0001a0001c0003t0013g0010a0001c0003t0020g0017others(3): Show | 6 | 40 | 0.1500 | -3 | 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 | 146535138 | ATAT | A | intron_variant | MODIFIER | HG01891.hp1 HG02630.hp1 |
a0001a0004 | a0001c0012a0004c0014 | a0001c0012t0004a0004c0014t0021 | a0001c0012t0004g0026a0004c0014t0021g0022 | 2 | 40 | 0.0500 | -3 | 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 | 146535194 | TATC | T | intron_variant | MODIFIER | HG01891.hp1 HG02630.hp1 |
a0001a0004 | a0001c0012a0004c0014 | a0001c0012t0004a0004c0014t0021 | a0001c0012t0004g0026a0004c0014t0021g0022 | 2 | 40 | 0.0500 | -3 | 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 | 146535275 | ATAT | A | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG02886.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0013others(1): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(4): Show | a0001c0001t0001g0038a0001c0001t0007g0020a0001c0001t0012g0034others(4): Show | 7 | 40 | 0.1750 | -3 | 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 | 146535302 | TATG | T | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG02922.hp1 others(5): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0013others(2): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(4): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0007g0020others(5): Show | 8 | 40 | 0.2000 | -3 | 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 | 146535427 | ATAT | A | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp2 others(20): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(17): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0006g0009others(20): Show | 23 | 40 | 0.5750 | -3 | 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 | 146538794 | TTGA | T | intron_variant | MODIFIER | NA18522.hp1 NA20129.hp2 |
a0001 | a0001c0003a0001c0013 | a0001c0003t0023a0001c0013t0003 | a0001c0003t0023g0030a0001c0013t0003g0039 | 2 | 40 | 0.0500 | -3 | 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 | 146564556 | ATAT | A | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
a0001a0002 | a0001c0004a0002c0016 | a0001c0004t0003a0002c0016t0004 | a0001c0004t0003g0035a0001c0004t0003g0036a0002c0016t0004g0024 | 3 | 40 | 0.0750 | -3 | 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 | 146599603 | TCTC | T | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02486.hp1 others(12): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0018others(12): Show | a0001c0001t0001g0038a0001c0001t0007g0020a0001c0001t0018g0001others(12): Show | 15 | 40 | 0.3750 | -3 | 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 | 146664157 | CTTT | C | intron_variant | MODIFIER | HG00735.hp1 HG02717.hp1 HG02886.hp1 others(5): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0018a0001c0002t0002a0001c0003t0013others(5): Show | a0001c0001t0018g0001a0001c0002t0002g0040a0001c0003t0013g0010others(5): Show | 8 | 40 | 0.2000 | -3 | 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 | 146666748 | AGTG | A | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0035a0001c0004t0003g0036 | 2 | 40 | 0.0500 | -3 | 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 | 146724561 | CTTT | C | intron_variant | MODIFIER | HG02886.hp2 HG02896.hp1 HG02922.hp1 |
a0001a0005 | a0001c0001a0001c0005a0005c0020 | a0001c0001t0012a0001c0005t0022a0005c0020t0005 | a0001c0001t0012g0034a0001c0005t0022g0032a0005c0020t0005g0016 | 3 | 40 | 0.0750 | -3 | c.98- others(20): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146733429 | CAAG | C | intron_variant | MODIFIER | HG02896.hp1 HG03239.hp1 HG03540.hp1 others(1): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0003c0007others(1): Show | a0001c0001t0001a0001c0002t0010a0003c0007t0017others(1): Show | a0001c0001t0001g0038a0001c0002t0010g0002a0003c0007t0017g0031others(1): Show | 4 | 40 | 0.1000 | -3 | c.98- others(20): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146756040 | TATG | T | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp1 HG02897.hp2 others(2): Show |
a0001 | a0001c0002a0001c0003a0001c0004others(1): Show | a0001c0002t0001a0001c0003t0023a0001c0004t0003others(1): Show | a0001c0002t0001g0008a0001c0003t0023g0030a0001c0004t0003g0035others(2): Show | 5 | 40 | 0.1250 | -3 | c.98- others(20): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146767385 | ATGT | A | intron_variant | MODIFIER | HG01891.hp2 HG02486.hp2 HG02976.hp2 others(1): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0016 | a0001c0001t0006a0001c0003t0011a0001c0003t0020others(1): Show | a0001c0001t0006g0009a0001c0003t0011g0023a0001c0003t0020g0017others(1): Show | 4 | 40 | 0.1000 | -3 | c.98- others(18): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146857198 | AAGG | A | intron_variant | MODIFIER | HG03239.hp2 NA20129.hp1 |
a0001 | a0001c0002a0001c0006 | a0001c0002t0002a0001c0006t0009 | a0001c0002t0002g0040a0001c0006t0009g0028 | 2 | 40 | 0.0500 | -3 | 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 | 146873894 | ATAT | A | intron_variant | MODIFIER | HG02897.hp1 HG03540.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0004 | a0001c0002t0001g0008a0001c0003t0004g0029 | 2 | 40 | 0.0500 | -3 | 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 | 146901030 | GTAA | G | intron_variant | MODIFIER | HG02451.hp2 HG02896.hp2 HG02897.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(5): Show | a0001c0001t0001g0038a0001c0001t0002g0006a0001c0001t0007g0018others(6): Show | 9 | 40 | 0.2250 | -3 | 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 | 146906822 | GAGA | G | intron_variant | MODIFIER | HG00735.hp1 HG02451.hp1 |
a0001 | a0001c0002a0001c0006 | a0001c0002t0001a0001c0006t0014 | a0001c0002t0001g0007a0001c0006t0014g0033 | 2 | 40 | 0.0500 | -3 | 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 | 146938388 | AAGT | A | intron_variant | MODIFIER | HG00735.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(8): Show | a0001c0001t0001g0038a0001c0001t0002g0006a0001c0001t0007g0018others(10): Show | 13 | 40 | 0.3250 | -3 | 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 | 147017288 | TATA | T | intron_variant | MODIFIER | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(9): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0023others(7): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0002t0001g0021others(9): Show | 12 | 40 | 0.3000 | -3 | c.403 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147021262 | ATTC | 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 | -3 | c.403 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147025863 | TTTA | T | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02486.hp2 others(11): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0012others(9): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0006g0009others(11): Show | 14 | 40 | 0.3500 | -3 | c.403 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147032673 | TAAA | T | intron_variant | MODIFIER | HG01891.hp2 HG02922.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0012 | a0001c0001t0006g0009a0001c0001t0012g0034 | 2 | 40 | 0.0500 | -3 | c.403 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147040451 | ATTT | A | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02630.hp2 others(8): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(7): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0002t0001g0007others(8): Show | 11 | 40 | 0.2750 | -3 | c.403 others(20): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147062127 | CAAA | C | intron_variant | MODIFIER | HG02897.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0012a0001c0002t0001a0001c0004t0003others(1): Show | a0001c0001t0012g0034a0001c0002t0001g0008a0001c0004t0003g0036others(1): Show | 4 | 40 | 0.1000 | -3 | c.550 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147067289 | CAAA | C | intron_variant | MODIFIER | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(7): Show |
a0001a0003a0004 | a0001c0001a0001c0003a0001c0005others(4): Show | a0001c0001t0006a0001c0001t0007a0001c0003t0004others(7): Show | a0001c0001t0006g0009a0001c0001t0007g0020a0001c0003t0004g0029others(7): Show | 10 | 40 | 0.2500 | -3 | c.550 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147073122 | CTTT | C | intron_variant | MODIFIER | HG00735.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(13): Show | a0001c0001t0001g0003a0001c0001t0007g0020a0001c0001t0012g0034others(13): Show | 16 | 40 | 0.4000 | -3 | c.550 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147083674 | ATAT | A | intron_variant | MODIFIER | HG02630.hp1 HG02922.hp1 HG03098.hp1 |
a0001 | a0001c0001a0001c0012 | a0001c0001t0001a0001c0001t0012a0001c0012t0004 | a0001c0001t0001g0003a0001c0001t0012g0034a0001c0012t0004g0026 | 3 | 40 | 0.0750 | -3 | c.551 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147192335 | TCTC | T | intron_variant | MODIFIER | HG00735.hp1 HG02451.hp2 HG02486.hp1 others(19): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(16): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(19): Show | 22 | 40 | 0.5500 | -3 | 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 | 147198232 | CTTT | C | intron_variant | MODIFIER | HG02717.hp1 HG02976.hp2 HG03098.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0016others(1): Show | a0001c0001t0001a0001c0003t0020a0002c0016t0004others(1): Show | a0001c0001t0001g0003a0001c0003t0020g0017a0002c0016t0004g0024others(1): Show | 4 | 40 | 0.1000 | -3 | 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 | 147210473 | ATCT | A | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp1 HG03098.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0016 | a0001c0001t0001a0001c0001t0007a0001c0002t0001others(1): Show | a0001c0001t0001g0003a0001c0001t0007g0020a0001c0002t0001g0007others(1): Show | 4 | 40 | 0.1000 | -3 | 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 | 147253383 | GTTT | G | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(1): Show |
a0001 | a0001c0004a0001c0008a0001c0015 | a0001c0004t0003a0001c0008t0001a0001c0015t0001 | a0001c0004t0003g0035a0001c0004t0003g0036a0001c0008t0001g0025others(1): Show | 4 | 40 | 0.1000 | -3 | 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 | 147273993 | ATAT | A | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(1): Show |
a0001 | a0001c0002a0001c0003a0001c0004others(1): Show | a0001c0002t0001a0001c0003t0011a0001c0004t0005others(1): Show | a0001c0002t0001g0007a0001c0003t0011g0023a0001c0004t0005g0004others(1): Show | 4 | 40 | 0.1000 | -3 | 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 | 147314631 | CAAA | 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 | -3 | c.149 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147315478 | CTTT | C | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(17): Show | a0001c0001t0001g0003a0001c0001t0002g0006a0001c0001t0006g0009others(21): Show | 24 | 40 | 0.6000 | -3 | c.149 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147326057 | GGAC | G | intron_variant | MODIFIER | HG02976.hp1 HG03139.hp1 |
a0001 | a0001c0008a0001c0015 | a0001c0008t0001a0001c0015t0001 | a0001c0008t0001g0025a0001c0015t0001g0011 | 2 | 40 | 0.0500 | -3 | c.149 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147329770 | GTTC | G | intron_variant | MODIFIER | HG01891.hp1 HG02486.hp1 HG02922.hp2 others(3): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0007a0001c0003t0004a0001c0004t0005others(3): Show | a0001c0001t0007g0020a0001c0003t0004g0029a0001c0004t0005g0004others(3): Show | 6 | 40 | 0.1500 | -3 | c.149 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147339138 | TTTG | T | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp2 HG02630.hp1 others(2): Show |
a0001 | a0001c0002a0001c0003a0001c0012others(1): Show | a0001c0002t0001a0001c0003t0011a0001c0003t0020others(2): Show | a0001c0002t0001g0007a0001c0003t0011g0023a0001c0003t0020g0017others(2): Show | 5 | 40 | 0.1250 | -3 | c.149 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |