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 | 146263288 | AGGAAGGA others(5): Show |
A | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp2 HG02486.hp1 others(13): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0018others(11): Show | a0001c0001t0006g0009a0001c0001t0007g0018a0001c0001t0007g0020others(13): Show | 16 | 40 | 0.4000 | -12 | c.97+ others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146279429 | AACACACA others(5): Show |
A | intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0012 | a0001c0012t0004 | a0001c0012t0004g0026 | 1 | 40 | 0.0250 | -12 | c.97+ others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146285978 | CTGTGTGT others(5): Show |
C | intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 40 | 0.0250 | -12 | c.97+ others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146301749 | CACAGTGG others(5): Show |
C | intron_variant | MODIFIER | HG02451.hp2 NA19030.hp2 |
a0001a0002 | a0001c0001a0002c0016 | a0001c0001t0002a0002c0016t0004 | a0001c0001t0002g0006a0002c0016t0004g0024 | 2 | 40 | 0.0500 | -12 | c.97+ others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146303072 | ATGTGTGT others(5): Show |
A | intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 40 | 0.0250 | -12 | c.97+ others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146319835 | GGCTGTGT others(5): Show |
G | 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 | -12 | c.97+ others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146356052 | TACACACA others(5): Show |
T | intron_variant | MODIFIER | HG00735.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(5): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0018others(7): Show | a0001c0001t0001g0003a0001c0001t0007g0020a0001c0001t0018g0001others(7): Show | 10 | 40 | 0.2500 | -12 | c.97+ others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146380784 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0021 | 1 | 40 | 0.0250 | -12 | c.97+ others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146395826 | GGAGAGAG others(5): Show |
G | intron_variant | MODIFIER | HG02630.hp2 HG02976.hp1 HG03139.hp1 |
a0001 | a0001c0002a0001c0008a0001c0015 | a0001c0002t0002a0001c0008t0001a0001c0015t0001 | a0001c0002t0002g0013a0001c0008t0001g0025a0001c0015t0001g0011 | 3 | 40 | 0.0750 | -12 | c.97+ others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146457481 | AATATATA others(5): Show |
A | intron_variant | MODIFIER | HG02630.hp2 HG02976.hp1 |
a0001 | a0001c0002a0001c0015 | a0001c0002t0002a0001c0015t0001 | a0001c0002t0002g0013a0001c0015t0001g0011 | 2 | 40 | 0.0500 | -12 | c.98- others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146469518 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0003 | a0001c0003t0023 | a0001c0003t0023g0030 | 1 | 40 | 0.0250 | -12 | c.98- others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146502224 | AATATATA others(5): Show |
A | intron_variant | MODIFIER | HG00735.hp1 HG02886.hp2 |
a0001 | a0001c0005a0001c0006 | a0001c0005t0022a0001c0006t0014 | a0001c0005t0022g0032a0001c0006t0014g0033 | 2 | 40 | 0.0500 | -12 | c.98- others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146525532 | TTATCTAT others(5): Show |
T | intron_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0006 | a0001c0006t0014 | a0001c0006t0014g0033 | 1 | 40 | 0.0250 | -12 | c.98- others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146525566 | ATCTATCT others(5): Show |
A | intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0034 | 1 | 40 | 0.0250 | -12 | c.98- others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146555492 | GTCTGTCT others(5): Show |
G | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 HG03540.hp1 others(1): Show |
a0001a0002 | a0001c0002a0001c0004a0002c0016 | a0001c0002t0010a0001c0004t0003a0002c0016t0004 | a0001c0002t0010g0002a0001c0004t0003g0035a0001c0004t0003g0036others(1): Show | 4 | 40 | 0.1000 | -12 | c.98- others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146596595 | CAGAGAGA others(5): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
a0001a0004 | a0001c0003a0001c0005a0001c0012others(1): Show | a0001c0003t0011a0001c0005t0008a0001c0012t0004others(1): Show | a0001c0003t0011g0023a0001c0005t0008g0005a0001c0012t0004g0026others(1): Show | 4 | 40 | 0.1000 | -12 | c.98- others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146613824 | GTTCTTTC others(5): Show |
G | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02486.hp1 others(13): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0018others(13): Show | a0001c0001t0001g0038a0001c0001t0007g0020a0001c0001t0018g0001others(13): Show | 16 | 40 | 0.4000 | -12 | c.98- others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146622243 | ATATCTAT others(5): Show |
A | intron_variant | MODIFIER | HG02451.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0002a0001c0001t0007a0001c0002t0002others(4): Show | a0001c0001t0002g0006a0001c0001t0007g0018a0001c0002t0002g0040others(5): Show | 8 | 40 | 0.2000 | -12 | c.98- others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146622271 | CTATCTAT others(5): Show |
C | intron_variant | MODIFIER | HG02896.hp1 | a0005 | a0005c0020 | a0005c0020t0005 | a0005c0020t0005g0016 | 1 | 40 | 0.0250 | -12 | c.98- others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146712106 | TTATGTAT others(5): Show |
T | intron_variant | MODIFIER | HG02451.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
a0001 | a0001c0002a0001c0008a0001c0010others(1): Show | a0001c0002t0001a0001c0002t0002a0001c0008t0001others(2): Show | a0001c0002t0001g0007a0001c0002t0002g0013a0001c0008t0001g0025others(2): Show | 5 | 40 | 0.1250 | -12 | c.98- others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146761284 | TGGAAGGA others(5): Show |
T | intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0003 | a0001c0003t0023 | a0001c0003t0023g0030 | 1 | 40 | 0.0250 | -12 | c.98- others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146855807 | GTATATAT others(5): Show |
G | intron_variant | MODIFIER | HG02630.hp2 HG02922.hp2 NA20129.hp2 |
a0001 | a0001c0002a0001c0003a0001c0004 | a0001c0002t0002a0001c0003t0023a0001c0004t0005 | a0001c0002t0002g0013a0001c0003t0023g0030a0001c0004t0005g0004 | 3 | 40 | 0.0750 | -12 | c.402 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146856261 | TATAGATA others(5): Show |
T | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG02486.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0007a0001c0001t0012a0001c0001t0018others(4): Show | a0001c0001t0007g0020a0001c0001t0012g0034a0001c0001t0018g0001others(4): Show | 7 | 40 | 0.1750 | -12 | c.402 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146856297 | GATACATA others(5): Show |
G | intron_variant | MODIFIER | HG02897.hp1 HG03540.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0004 | a0001c0002t0001g0008a0001c0003t0004g0029 | 2 | 40 | 0.0500 | -12 | c.402 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146885928 | GGTGTGTG others(5): Show |
G | intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0007 | 1 | 40 | 0.0250 | -12 | c.402 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147062127 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0040 | 1 | 40 | 0.0250 | -12 | c.550 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147081583 | TTGTGTGT others(5): Show |
T | intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0012 | a0001c0012t0004 | a0001c0012t0004g0026 | 1 | 40 | 0.0250 | -12 | c.551 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147083940 | TTATATAG others(5): Show |
T | intron_variant | MODIFIER | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(3): Show |
a0001a0003a0004 | a0001c0001a0001c0006a0001c0011others(3): Show | a0001c0001t0006a0001c0006t0014a0001c0011t0016others(3): Show | a0001c0001t0006g0009a0001c0006t0014g0033a0001c0011t0016g0019others(3): Show | 6 | 40 | 0.1500 | -12 | c.551 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147104873 | CATATATA others(5): Show |
C | intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0019 | a0001c0019t0006 | a0001c0019t0006g0015 | 1 | 40 | 0.0250 | -12 | c.551 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147137905 | ATAGATAG others(5): Show |
A | intron_variant | MODIFIER | HG02976.hp2 | a0001 | a0001c0003 | a0001c0003t0020 | a0001c0003t0020g0017 | 1 | 40 | 0.0250 | -12 | c.134 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147225742 | AGAAGGAA others(5): Show |
A | intron_variant | MODIFIER | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(12): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(11): Show | a0001c0001t0001g0038a0001c0001t0006g0009a0001c0001t0007g0018others(12): Show | 15 | 40 | 0.3750 | -12 | c.134 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147237049 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0018 | a0001c0018t0002 | a0001c0018t0002g0012 | 1 | 40 | 0.0250 | -12 | c.134 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147301588 | CTCTCTGT others(5): Show |
C | intron_variant | MODIFIER | HG02886.hp1 HG03239.hp1 |
a0001a0003 | a0001c0003a0003c0007 | a0001c0003t0013a0003c0007t0017 | a0001c0003t0013g0010a0003c0007t0017g0031 | 2 | 40 | 0.0500 | -12 | c.149 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147301592 | CTGTGTGT others(5): Show |
C | intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0003 | a0001c0003t0023 | a0001c0003t0023g0030 | 1 | 40 | 0.0250 | -12 | c.149 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147482720 | CAATAAAT others(5): Show |
C | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp1 HG02922.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0009others(1): Show | a0001c0001t0002a0001c0001t0012a0001c0002t0001others(3): Show | a0001c0001t0002g0006a0001c0001t0012g0034a0001c0002t0001g0008others(3): Show | 6 | 40 | 0.1500 | -12 | c.167 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147558697 | TTTCCTTC others(5): Show |
T | intron_variant | MODIFIER | HG02486.hp1 HG02717.hp1 NA19030.hp2 |
a0001a0002 | a0001c0001a0002c0016a0002c0017 | a0001c0001t0007a0002c0016t0004a0002c0017t0015 | a0001c0001t0007g0020a0002c0016t0004g0024a0002c0017t0015g0037 | 3 | 40 | 0.0750 | -12 | c.177 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147572701 | AACACACA others(5): Show |
A | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(19): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(15): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(19): Show | 22 | 40 | 0.5500 | -12 | c.189 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147575371 | GGTGTGTG others(5): Show |
G | intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0009 | a0001c0009t0019 | a0001c0009t0019g0027 | 1 | 40 | 0.0250 | -12 | c.189 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147615277 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02896.hp1 HG03098.hp2 |
a0001a0004a0005 | a0001c0002a0004c0014a0005c0020 | a0001c0002t0001a0004c0014t0021a0005c0020t0005 | a0001c0002t0001g0021a0004c0014t0021g0022a0005c0020t0005g0016 | 3 | 40 | 0.0750 | -12 | c.189 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147772446 | CTATATAT others(5): Show |
C | intron_variant | MODIFIER | HG02451.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
a0001a0003 | a0001c0001a0001c0009a0001c0012others(1): Show | a0001c0001t0002a0001c0009t0019a0001c0012t0004others(1): Show | a0001c0001t0002g0006a0001c0009t0019g0027a0001c0012t0004g0026others(1): Show | 4 | 40 | 0.1000 | -12 | c.209 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147775392 | AATATATA others(5): Show |
A | intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0019 | a0001c0019t0006 | a0001c0019t0006g0015 | 1 | 40 | 0.0250 | -12 | c.209 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147784381 | CATATATA others(5): Show |
C | intron_variant | MODIFIER | HG03239.hp1 | a0003 | a0003c0007 | a0003c0007t0017 | a0003c0007t0017g0031 | 1 | 40 | 0.0250 | -12 | c.209 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147894957 | CTTTCTTT others(5): Show |
C | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 NA18522.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0007a0001c0004t0003 | a0001c0001t0007g0018a0001c0004t0003g0035a0001c0004t0003g0036 | 3 | 40 | 0.0750 | -12 | c.209 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147902802 | GTGTGTGT others(5): Show |
G | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0001 | 1 | 40 | 0.0250 | -12 | c.209 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147925154 | AGAAGGAA others(5): Show |
A | intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0020 | 1 | 40 | 0.0250 | -12 | c.225 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147933494 | GAGATAGA others(5): Show |
G | intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0006 | a0001c0006t0009 | a0001c0006t0009g0028 | 1 | 40 | 0.0250 | -12 | c.225 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147957877 | CCAGTCTG others(5): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0006a0001c0001t0007a0001c0004t0003 | a0001c0001t0006g0009a0001c0001t0007g0018a0001c0004t0003g0035others(1): Show | 4 | 40 | 0.1000 | -12 | c.225 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148061878 | TATAGATA others(5): Show |
T | intron_variant | MODIFIER | HG02630.hp2 HG02717.hp2 HG03098.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0007a0001c0001t0018a0001c0002t0001others(4): Show | a0001c0001t0007g0018a0001c0001t0018g0001a0001c0002t0001g0021others(4): Show | 7 | 40 | 0.1750 | -12 | c.238 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148061954 | TATAGATA others(5): Show |
T | intron_variant | MODIFIER | HG00735.hp1 HG03540.hp1 NA21309.hp2 |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0018a0001c0002t0010a0001c0006t0014 | a0001c0001t0018g0001a0001c0002t0010g0002a0001c0006t0014g0033 | 3 | 40 | 0.0750 | -12 | c.238 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148099421 | TTGTGTGT others(5): Show |
T | intron_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0006 | a0001c0006t0014 | a0001c0006t0014g0033 | 1 | 40 | 0.0250 | -12 | c.238 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |