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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN5_chr11_99015949_100363885 | 100204297 | AATATATA others(9): Show |
A | intron_variant | MODIFIER | HG02258.hp1 | a0010 | a0010c0010 | a0010c0010t0011 | a0010c0010t0011g0009 | 1 | 66 | 0.0152 | -16 | c.188 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100291774 | TAAATAAA others(9): Show |
T | intron_variant | MODIFIER | HG01099.hp1 HG01169.hp2 HG03471.hp1 others(2): Show |
a0001a0002a0006others(1): Show | a0001c0001a0002c0002a0006c0006others(1): Show | a0001c0001t0004a0001c0001t0005a0002c0002t0004others(2): Show | a0001c0001t0004g0010a0001c0001t0005g0048a0002c0002t0004g0007others(2): Show | 5 | 66 | 0.0758 | -16 | c.231 others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1158801 | TACACACA others(9): Show |
T | intron_variant | MODIFIER | NA18953.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0058 | 1 | 232 | 0.0043 | -16 | c.55+ others(33): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1201099 | TTGTGTGT others(9): Show |
T | intron_variant | MODIFIER | HG01952.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0183 | 1 | 232 | 0.0043 | -16 | c.56- others(33): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1202543 | AAAATAAA others(9): Show |
A | intron_variant | MODIFIER | HG02055.hp2 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0222 | 1 | 232 | 0.0043 | -16 | c.56- others(33): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1209730 | GGTAAAAC others(9): Show |
G | intron_variant | MODIFIER | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(30): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(10): Show | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0067others(30): Show | 33 | 232 | 0.1422 | -16 | c.56- others(33): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245221 | TATATATA others(9): Show |
T | intron_variant | MODIFIER | NA18747.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0145 | 1 | 232 | 0.0043 | -16 | c.358 others(35): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1300449 | CAGGAAGG others(9): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(39): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(7): Show | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0033others(39): Show | 42 | 232 | 0.1810 | -16 | c.761 others(33): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1300557 | AAAAGAAA others(9): Show |
A | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01258.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(5): Show | a0001c0001t0001g0035a0001c0001t0001g0044a0001c0002t0001g0018others(16): Show | 19 | 232 | 0.0819 | -16 | c.761 others(33): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1357848 | ATAAATGC others(9): Show |
A | intron_variant | MODIFIER | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(6): Show |
a0001a0002a0006 | a0001c0002a0001c0005a0001c0006others(6): Show | a0001c0002t0009a0001c0005t0001a0001c0006t0001others(6): Show | a0001c0002t0009g0205a0001c0005t0001g0159a0001c0006t0001g0185others(6): Show | 9 | 232 | 0.0388 | -16 | c.149 others(35): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146151666 | ATATATAT others(9): Show |
A | intron_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0006 | a0001c0006t0014 | a0001c0006t0014g0033 | 1 | 40 | 0.0250 | -16 | c.97+ others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146285864 | CCCCCCTC others(9): Show |
C | intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0012 | a0001c0012t0004 | a0001c0012t0004g0026 | 1 | 40 | 0.0250 | -16 | c.97+ others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146477624 | AACACACA others(9): Show |
A | intron_variant | MODIFIER | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0004t0003 | a0001c0002t0001g0007a0001c0004t0003g0035a0001c0004t0003g0036 | 3 | 40 | 0.0750 | -16 | c.98- others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146555492 | GTCTGTCT others(9): Show |
G | intron_variant | MODIFIER | HG02451.hp2 HG02922.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0002a0001c0004t0005 | a0001c0001t0002g0006a0001c0004t0005g0004 | 2 | 40 | 0.0500 | -16 | c.98- others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146622243 | ATATCTAT others(9): Show |
A | intron_variant | MODIFIER | HG03098.hp1 HG03098.hp2 HG03540.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0010others(1): Show | a0001c0001t0001g0003a0001c0002t0001g0021a0001c0002t0010g0002others(1): Show | 4 | 40 | 0.1000 | -16 | c.98- others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146622267 | CTATCTAT others(9): Show |
C | intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0008 | a0001c0008t0001 | a0001c0008t0001g0025 | 1 | 40 | 0.0250 | -16 | c.98- others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146761284 | TGGAAGGA others(9): Show |
T | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp1 HG02897.hp2 others(1): Show |
a0001 | a0001c0002a0001c0004a0001c0010 | a0001c0002t0001a0001c0004t0003a0001c0010t0002 | a0001c0002t0001g0008a0001c0004t0003g0035a0001c0004t0003g0036others(1): Show | 4 | 40 | 0.1000 | -16 | c.98- others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146855807 | GTATATAT others(9): Show |
G | intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0005 | a0001c0005t0008 | a0001c0005t0008g0005 | 1 | 40 | 0.0250 | -16 | c.402 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146856261 | TATAGATA others(9): Show |
T | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02717.hp1 others(5): Show |
a0001a0002a0004 | a0001c0002a0001c0003a0001c0004others(5): Show | a0001c0002t0001a0001c0003t0013a0001c0004t0005others(5): Show | a0001c0002t0001g0007a0001c0003t0013g0010a0001c0004t0005g0004others(5): Show | 8 | 40 | 0.2000 | -16 | c.402 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146856297 | GATACATA others(9): Show |
G | intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0006 | 1 | 40 | 0.0250 | -16 | c.402 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146947553 | GTGTGTAT others(9): Show |
G | intron_variant | MODIFIER | NA19030.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0010 | a0001c0001t0001a0001c0010t0002 | a0001c0001t0001g0038a0001c0010t0002g0014 | 2 | 40 | 0.0500 | -16 | c.403 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146947560 | TATATATA others(9): Show |
T | intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0021 | 1 | 40 | 0.0250 | -16 | c.403 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147104873 | CATATATA others(9): Show |
C | intron_variant | MODIFIER | HG02717.hp2 HG02976.hp1 |
a0001 | a0001c0005a0001c0015 | a0001c0005t0008a0001c0015t0001 | a0001c0005t0008g0005a0001c0015t0001g0011 | 2 | 40 | 0.0500 | -16 | c.551 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147149035 | CGCTGCTG others(9): Show |
C | intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0029 | 1 | 40 | 0.0250 | -16 | c.134 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147225742 | AGAAGGAA others(9): Show |
A | intron_variant | MODIFIER | HG02886.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0012a0001c0003t0013a0001c0005t0022others(1): Show | a0001c0001t0012g0034a0001c0003t0013g0010a0001c0005t0022g0032others(1): Show | 4 | 40 | 0.1000 | -16 | c.134 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147225830 | GGAAGGAA others(9): Show |
G | intron_variant | MODIFIER | HG02451.hp2 HG03225.hp2 HG03540.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0002t0010a0001c0003t0023others(2): Show | a0001c0001t0002g0006a0001c0002t0010g0002a0001c0003t0023g0030others(2): Show | 5 | 40 | 0.1250 | -16 | c.134 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147237049 | CTTTTTTT others(9): Show |
C | intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0019 | a0001c0019t0006 | a0001c0019t0006g0015 | 1 | 40 | 0.0250 | -16 | c.134 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147301592 | CTGTGTGT others(9): Show |
C | intron_variant | MODIFIER | HG02897.hp1 HG03225.hp1 |
a0001 | a0001c0002a0001c0009 | a0001c0002t0001a0001c0009t0019 | a0001c0002t0001g0008a0001c0009t0019g0027 | 2 | 40 | 0.0500 | -16 | c.149 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147368096 | TCACACAC others(9): Show |
T | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp1 HG03225.hp1 |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0002a0001c0002t0001a0001c0009t0019 | a0001c0001t0002g0006a0001c0002t0001g0008a0001c0009t0019g0027 | 3 | 40 | 0.0750 | -16 | c.149 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147902798 | GTGTGTGT others(9): Show |
G | intron_variant | MODIFIER | HG00735.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
a0001 | a0001c0002a0001c0006 | a0001c0002t0001a0001c0002t0002a0001c0006t0014 | a0001c0002t0001g0008a0001c0002t0001g0021a0001c0002t0002g0040others(1): Show | 4 | 40 | 0.1000 | -16 | c.209 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148061954 | TATAGATA others(9): Show |
T | intron_variant | MODIFIER | HG01891.hp2 HG02717.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0006a0001c0005t0008 | a0001c0001t0006g0009a0001c0005t0008g0005 | 2 | 40 | 0.0500 | -16 | c.238 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148137669 | AAAGGAAG others(9): Show |
A | intron_variant | MODIFIER | HG02486.hp1 HG02976.hp1 HG03139.hp2 others(1): Show |
a0001 | a0001c0001a0001c0010a0001c0011others(1): Show | a0001c0001t0007a0001c0010t0002a0001c0011t0016others(1): Show | a0001c0001t0007g0020a0001c0010t0002g0014a0001c0011t0016g0019others(1): Show | 4 | 40 | 0.1000 | -16 | c.255 others(35): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148283304 | AAAGGAAG others(9): Show |
A | intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0004 | 1 | 40 | 0.0250 | -16 | c.347 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148297165 | AAAGGAAG others(9): Show |
A | intron_variant | MODIFIER | HG02717.hp2 NA20129.hp2 |
a0001 | a0001c0003a0001c0005 | a0001c0003t0023a0001c0005t0008 | a0001c0003t0023g0030a0001c0005t0008g0005 | 2 | 40 | 0.0500 | -16 | c.347 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148305222 | CAAAAAAA others(9): Show |
C | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 HG03540.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0003t0004a0001c0004t0003others(1): Show | a0001c0001t0001g0038a0001c0003t0004g0029a0001c0004t0003g0035others(2): Show | 5 | 40 | 0.1250 | -16 | c.347 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP3_chr9_39059710_39293167 | 39077559 | AAAACAAA others(9): Show |
A | intron_variant | MODIFIER | HG02109.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0002 | 1 | 4 | 0.2500 | -16 | c.374 others(33): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | TogoVar | ||||||
CNTNAP3_chr9_39059710_39293167 | 39096985 | GTATTTTC others(9): Show |
G | intron_variant | MODIFIER | HG02109.hp1 HG02109.hp2 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0003a0002c0003t0004 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | 4 | 0.5000 | -16 | c.299 others(35): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | TogoVar | ||||||
CNTNAP4_chr16_76272401_76565757 | 76298486 | ATGTGTGT others(9): Show |
A | intron_variant | MODIFIER | HG02615.hp2 HG02717.hp2 HG03041.hp1 |
a0003a0007a0017 | a0003c0006a0007c0013a0017c0036 | a0003c0006t0005a0007c0013t0002a0017c0036t0004 | a0003c0006t0005g0131a0007c0013t0002g0210a0017c0036t0004g0248 | 3 | 274 | 0.0110 | -16 | c.86- others(33): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76355840 | TTTTATTT others(9): Show |
T | intron_variant | MODIFIER | NA18968.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0006 | 1 | 274 | 0.0037 | -16 | c.390 others(31): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76355876 | ATTTATTT others(9): Show |
A | intron_variant | MODIFIER | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0014 | a0001c0001t0004a0002c0002t0002a0002c0002t0010others(1): Show | a0001c0001t0004g0051a0001c0001t0004g0053a0002c0002t0002g0206others(3): Show | 6 | 274 | 0.0219 | -16 | c.390 others(31): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76376907 | TTGTGTGT others(9): Show |
T | intron_variant | MODIFIER | HG00673.hp1 HG02015.hp2 HG02155.hp1 others(7): Show |
a0001a0002a0003others(3): Show | a0001c0004a0002c0005a0003c0003others(3): Show | a0001c0004t0001a0002c0005t0004a0003c0003t0005others(3): Show | a0001c0004t0001g0155a0002c0005t0004g0132a0003c0003t0005g0047others(7): Show | 10 | 274 | 0.0365 | -16 | c.390 others(35): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP4_chr16_76272401_76565757 | 76397938 | TTATATAC others(9): Show |
T | intron_variant | MODIFIER | HG00423.hp2 HG01934.hp1 HG03491.hp2 others(6): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0002c0002t0002others(4): Show | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0123others(6): Show | 9 | 274 | 0.0329 | -16 | c.391 others(35): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124042783 | CATCTATC others(9): Show |
C | intron_variant | MODIFIER | HG02897.hp2 NA21309.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0001 | a0001c0001t0002g0024a0001c0002t0001g0054 | 2 | 64 | 0.0313 | -16 | c.82+ others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124148774 | CATATGTG others(9): Show |
C | intron_variant | MODIFIER | HG00423.hp2 HG01069.hp2 HG01070.hp1 others(24): Show |
a0001a0004a0005others(1): Show | a0001c0001a0001c0002a0004c0006others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0026others(24): Show | 27 | 64 | 0.4219 | -16 | c.83- others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124178907 | GTTATTTA others(9): Show |
G | intron_variant | MODIFIER | HG02145.hp1 HG02717.hp1 HG02922.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0010 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0002t0002g0031others(1): Show | 4 | 64 | 0.0625 | -16 | c.83- others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124194396 | TATATATA others(9): Show |
T | intron_variant | MODIFIER | HG01070.hp2 | a0005 | a0005c0005 | a0005c0005t0001 | a0005c0005t0001g0008 | 1 | 64 | 0.0156 | -16 | c.83- others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124226505 | CCTTATGA others(9): Show |
C | intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0021 | 1 | 64 | 0.0156 | -16 | c.187 others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124274129 | CTGTTTTT others(9): Show |
C | intron_variant | MODIFIER | NA19043.hp2 | a0002 | a0002c0004 | a0002c0004t0001 | a0002c0004t0001g0001 | 1 | 64 | 0.0156 | -16 | c.381 others(35): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124290874 | CTTTATTT others(9): Show |
C | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG01261.hp2 others(20): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0002g0019others(20): Show | 23 | 64 | 0.3594 | -16 | c.381 others(35): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNTNAP5_chr2_124020287_124926219 | 124419896 | TTTTCTTT others(9): Show |
T | intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0009 | 1 | 64 | 0.0156 | -16 | c.529 others(33): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |