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 | 147346150 | TTTA | T | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(11): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(10): Show | a0001c0001t0001g0038a0001c0001t0002g0006a0001c0001t0006g0009others(11): Show | 14 | 40 | 0.3500 | -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 | 147365383 | GAAA | G | intron_variant | MODIFIER | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0006a0001c0002t0002a0001c0004t0003others(2): Show | a0001c0001t0006g0009a0001c0002t0002g0013a0001c0004t0003g0035others(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 | 147390288 | TAGC | T | intron_variant | MODIFIER | HG02630.hp1 HG03098.hp1 |
a0001 | a0001c0001a0001c0012 | a0001c0001t0001a0001c0012t0004 | a0001c0001t0001g0003a0001c0012t0004g0026 | 2 | 40 | 0.0500 | -3 | c.149 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147440443 | TGTA | T | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0035a0001c0004t0003g0036 | 2 | 40 | 0.0500 | -3 | c.167 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147458141 | CATA | C | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(17): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(15): Show | a0001c0001t0001g0038a0001c0001t0006g0009a0001c0001t0007g0020others(17): Show | 20 | 40 | 0.5000 | -3 | c.167 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147476928 | TTAA | T | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp2 HG02451.hp1 others(32): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(27): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(32): Show | 35 | 40 | 0.8750 | -3 | c.167 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147486186 | CAAA | C | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(22): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(27): Show | 30 | 40 | 0.7500 | -3 | c.177 others(20): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147504699 | AAAC | A | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp1 others(9): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0007a0001c0002t0002others(6): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0007g0018others(9): Show | 12 | 40 | 0.3000 | -3 | c.177 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147517820 | TAGC | T | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG02486.hp1 others(10): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0012others(9): Show | a0001c0001t0001g0038a0001c0001t0007g0020a0001c0001t0012g0034others(10): Show | 13 | 40 | 0.3250 | -3 | c.177 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147527127 | ATTC | A | intron_variant | MODIFIER | HG03139.hp1 NA18522.hp2 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0007a0001c0008t0001 | a0001c0001t0007g0018a0001c0008t0001g0025 | 2 | 40 | 0.0500 | -3 | c.177 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147554548 | AACT | A | intron_variant | MODIFIER | HG02486.hp1 HG02630.hp2 HG02922.hp1 others(2): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0016others(1): Show | a0001c0001t0007a0001c0001t0012a0001c0002t0002others(2): Show | a0001c0001t0007g0020a0001c0001t0012g0034a0001c0002t0002g0013others(2): Show | 5 | 40 | 0.1250 | -3 | c.177 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147556263 | ATTC | A | intron_variant | MODIFIER | HG02897.hp1 HG03239.hp2 NA20129.hp1 |
a0001 | a0001c0002a0001c0006 | a0001c0002t0001a0001c0002t0002a0001c0006t0009 | a0001c0002t0001g0008a0001c0002t0002g0040a0001c0006t0009g0028 | 3 | 40 | 0.0750 | -3 | c.177 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147580144 | TCTC | T | intron_variant | MODIFIER | HG02886.hp1 HG02922.hp1 HG03225.hp2 |
a0001 | a0001c0001a0001c0003a0001c0018 | a0001c0001t0012a0001c0003t0013a0001c0018t0002 | a0001c0001t0012g0034a0001c0003t0013g0010a0001c0018t0002g0012 | 3 | 40 | 0.0750 | -3 | c.189 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147586347 | GAAA | G | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0007a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0007g0020a0001c0002t0001g0007a0001c0002t0002g0013others(4): Show | 7 | 40 | 0.1750 | -3 | c.189 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147586349 | AAGG | A | intron_variant | MODIFIER | HG02886.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0012a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0012g0034a0001c0002t0001g0008a0001c0002t0002g0040others(2): Show | 5 | 40 | 0.1250 | -3 | c.189 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147591844 | TACA | T | intron_variant | MODIFIER | HG02630.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005a0001c0008others(1): Show | a0001c0001t0001a0001c0005t0008a0001c0005t0022others(2): Show | a0001c0001t0001g0038a0001c0005t0008g0005a0001c0005t0022g0032others(2): Show | 5 | 40 | 0.1250 | -3 | c.189 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147599481 | CAAA | C | intron_variant | MODIFIER | HG02630.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005a0001c0008others(1): Show | a0001c0001t0001a0001c0005t0008a0001c0005t0022others(2): Show | a0001c0001t0001g0038a0001c0005t0008g0005a0001c0005t0022g0032others(2): Show | 5 | 40 | 0.1250 | -3 | c.189 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147601645 | ATAT | A | intron_variant | MODIFIER | HG02630.hp2 HG02717.hp1 |
a0001a0002 | a0001c0002a0002c0017 | a0001c0002t0002a0002c0017t0015 | a0001c0002t0002g0013a0002c0017t0015g0037 | 2 | 40 | 0.0500 | -3 | c.189 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147621485 | CAGA | C | intron_variant | MODIFIER | HG02451.hp1 NA21309.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0018a0001c0002t0001 | a0001c0001t0018g0001a0001c0002t0001g0007 | 2 | 40 | 0.0500 | -3 | c.189 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147629406 | AAAT | A | intron_variant | MODIFIER | HG02451.hp2 HG02486.hp1 HG03540.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0002a0001c0001t0007a0001c0002t0010others(2): Show | a0001c0001t0002g0006a0001c0001t0007g0020a0001c0002t0010g0002others(2): Show | 5 | 40 | 0.1250 | -3 | c.189 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147633667 | CTTG | C | intron_variant | MODIFIER | HG02717.hp2 HG02886.hp2 NA19030.hp1 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0008a0001c0005t0022 | a0001c0001t0001g0038a0001c0005t0008g0005a0001c0005t0022g0032 | 3 | 40 | 0.0750 | -3 | c.189 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147659863 | TAAC | T | intron_variant | MODIFIER | HG01891.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0012a0001c0003t0004a0001c0003t0023others(4): Show | a0001c0001t0012g0034a0001c0003t0004g0029a0001c0003t0023g0030others(4): Show | 7 | 40 | 0.1750 | -3 | c.209 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147661555 | CTTT | C | intron_variant | MODIFIER | HG01891.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0012a0001c0003t0004a0001c0003t0023others(4): Show | a0001c0001t0012g0034a0001c0003t0004g0029a0001c0003t0023g0030others(4): Show | 7 | 40 | 0.1750 | -3 | c.209 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147688743 | AGAG | A | intron_variant | MODIFIER | HG00735.hp1 HG02897.hp1 |
a0001 | a0001c0002a0001c0006 | a0001c0002t0001a0001c0006t0014 | a0001c0002t0001g0008a0001c0006t0014g0033 | 2 | 40 | 0.0500 | -3 | c.209 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147721189 | ATGT | A | intron_variant | MODIFIER | HG01891.hp1 HG02630.hp1 HG02922.hp1 others(1): Show |
a0001a0002a0004 | a0001c0001a0001c0012a0002c0016others(1): Show | a0001c0001t0012a0001c0012t0004a0002c0016t0004others(1): Show | a0001c0001t0012g0034a0001c0012t0004g0026a0002c0016t0004g0024others(1): Show | 4 | 40 | 0.1000 | -3 | c.209 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147816151 | CAGG | C | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp2 HG03139.hp2 |
a0001 | a0001c0002a0001c0003a0001c0011 | a0001c0002t0001a0001c0003t0011a0001c0011t0016 | a0001c0002t0001g0007a0001c0003t0011g0023a0001c0011t0016g0019 | 3 | 40 | 0.0750 | -3 | c.209 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147842587 | CTTT | C | intron_variant | MODIFIER | HG02451.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
a0001 | a0001c0002a0001c0004a0001c0011others(1): Show | a0001c0002t0001a0001c0004t0005a0001c0011t0016others(1): Show | a0001c0002t0001g0007a0001c0004t0005g0004a0001c0011t0016g0019others(1): Show | 4 | 40 | 0.1000 | -3 | c.209 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147856629 | CTTT | C | intron_variant | MODIFIER | HG02717.hp1 HG02896.hp1 HG03139.hp1 others(1): Show |
a0001a0002a0005 | a0001c0008a0001c0018a0002c0017others(1): Show | a0001c0008t0001a0001c0018t0002a0002c0017t0015others(1): Show | a0001c0008t0001g0025a0001c0018t0002g0012a0002c0017t0015g0037others(1): Show | 4 | 40 | 0.1000 | -3 | c.209 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147859422 | CAAA | C | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp1 HG02976.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0011others(1): Show | a0001c0001t0007a0001c0002t0001a0001c0011t0016others(1): Show | a0001c0001t0007g0020a0001c0002t0001g0007a0001c0011t0016g0019others(1): Show | 4 | 40 | 0.1000 | -3 | c.209 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147862399 | TATA | T | intron_variant | MODIFIER | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(26): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(21): Show | a0001c0001t0001g0003a0001c0001t0002g0006a0001c0001t0006g0009others(26): Show | 29 | 40 | 0.7250 | -3 | c.209 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147886475 | CAAA | C | intron_variant | MODIFIER | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(6): Show | a0001c0001t0001g0003a0001c0001t0006g0009a0001c0001t0007g0018others(8): Show | 11 | 40 | 0.2750 | -3 | c.209 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147888811 | AAAT | A | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(12): Show | a0001c0001t0001g0003a0001c0001t0006g0009a0001c0001t0007g0018others(16): Show | 19 | 40 | 0.4750 | -3 | c.209 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147916591 | GAAA | G | intron_variant | MODIFIER | HG01891.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0018a0001c0002t0010a0001c0005t0008others(3): Show | a0001c0001t0018g0001a0001c0002t0010g0002a0001c0005t0008g0005others(3): Show | 6 | 40 | 0.1500 | -3 | 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 | 147947454 | CAAA | C | intron_variant | MODIFIER | HG00735.hp2 HG02451.hp2 HG02976.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0006others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0020others(3): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(4): Show | 7 | 40 | 0.1750 | -3 | 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 | 147980933 | CAAA | C | intron_variant | MODIFIER | HG00735.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
a0001 | a0001c0002a0001c0005a0001c0006 | a0001c0002t0001a0001c0002t0002a0001c0002t0010others(3): Show | a0001c0002t0001g0008a0001c0002t0001g0021a0001c0002t0002g0013others(5): Show | 8 | 40 | 0.2000 | -3 | c.238 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147998103 | CTTT | C | intron_variant | MODIFIER | HG01891.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0012others(4): Show | a0001c0001t0006g0009a0001c0001t0007g0018a0001c0001t0012g0034others(5): Show | 8 | 40 | 0.2000 | -3 | 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 | 148010661 | GTTT | G | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp2 HG02717.hp1 others(6): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(4): Show | a0001c0001t0012a0001c0003t0004a0001c0003t0011others(6): Show | a0001c0001t0012g0034a0001c0003t0004g0029a0001c0003t0011g0023others(6): Show | 9 | 40 | 0.2250 | -3 | 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 | 148026956 | TTTG | T | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp2 HG02717.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(3): Show | a0001c0001t0012a0001c0003t0004a0001c0003t0011others(4): Show | a0001c0001t0012g0034a0001c0003t0004g0029a0001c0003t0011g0023others(4): Show | 7 | 40 | 0.1750 | -3 | 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 | 148030669 | CTTT | C | intron_variant | MODIFIER | HG03239.hp1 NA19030.hp1 NA20129.hp1 others(1): Show |
a0001a0003 | a0001c0001a0001c0006a0003c0007 | a0001c0001t0001a0001c0001t0018a0001c0006t0009others(1): Show | a0001c0001t0001g0038a0001c0001t0018g0001a0001c0006t0009g0028others(1): Show | 4 | 40 | 0.1000 | -3 | 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 | 148044205 | ATTT | A | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp2 HG02630.hp2 others(9): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0012a0001c0002t0002a0001c0003t0004others(8): Show | a0001c0001t0012g0034a0001c0002t0002g0013a0001c0003t0004g0029others(9): Show | 12 | 40 | 0.3000 | -3 | 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 | 148057950 | CTTA | C | intron_variant | MODIFIER | HG02717.hp2 HG02886.hp1 HG02922.hp2 others(3): Show |
a0001 | a0001c0002a0001c0003a0001c0004others(2): Show | a0001c0002t0010a0001c0003t0013a0001c0003t0020others(3): Show | a0001c0002t0010g0002a0001c0003t0013g0010a0001c0003t0020g0017others(3): Show | 6 | 40 | 0.1500 | -3 | 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 | 148099868 | GTTT | G | intron_variant | MODIFIER | HG03225.hp1 HG03225.hp2 NA18522.hp1 others(1): Show |
a0001 | a0001c0009a0001c0010a0001c0013others(1): Show | a0001c0009t0019a0001c0010t0002a0001c0013t0003others(1): Show | a0001c0009t0019g0027a0001c0010t0002g0014a0001c0013t0003g0039others(1): Show | 4 | 40 | 0.1000 | -3 | 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 | 148108364 | TAAA | T | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02630.hp1 others(17): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0018others(15): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0007g0018others(17): Show | 20 | 40 | 0.5000 | -3 | c.238 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148112415 | GTAT | G | intron_variant | MODIFIER | HG00735.hp1 HG03098.hp2 HG03225.hp1 others(4): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0006others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0006t0014others(4): Show | a0001c0001t0001g0038a0001c0002t0001g0021a0001c0006t0014g0033others(4): Show | 7 | 40 | 0.1750 | -3 | c.238 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148164611 | CTTT | C | intron_variant | MODIFIER | HG02486.hp1 HG02896.hp1 HG03098.hp2 |
a0001a0005 | a0001c0001a0001c0002a0005c0020 | a0001c0001t0007a0001c0002t0001a0005c0020t0005 | a0001c0001t0007g0020a0001c0002t0001g0021a0005c0020t0005g0016 | 3 | 40 | 0.0750 | -3 | c.277 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148174417 | ACCG | A | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 HG02976.hp1 |
a0001 | a0001c0004a0001c0015 | a0001c0004t0003a0001c0015t0001 | a0001c0004t0003g0035a0001c0004t0003g0036a0001c0015t0001g0011 | 3 | 40 | 0.0750 | -3 | c.301 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148181741 | CTTT | C | intron_variant | MODIFIER | HG02630.hp2 HG02976.hp1 NA21309.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0010others(1): Show | a0001c0001t0018a0001c0002t0002a0001c0010t0002others(1): Show | a0001c0001t0018g0001a0001c0002t0002g0013a0001c0010t0002g0014others(1): Show | 4 | 40 | 0.1000 | -3 | c.301 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148208088 | CAAA | C | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp1 others(17): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(16): Show | a0001c0001t0001g0003a0001c0001t0006g0009a0001c0001t0007g0020others(17): Show | 20 | 40 | 0.5000 | -3 | c.301 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148254775 | CAAA | C | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp2 others(23): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(18): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(23): Show | 26 | 40 | 0.6500 | -3 | c.338 others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148268653 | TTAA | T | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp2 others(35): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(16): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(29): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0006g0009others(35): Show | 38 | 40 | 0.9500 | -3 | c.347 others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |