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 | 99201351 | T | TTCCTTCC others(4): Show |
intron_variant | MODIFIER | HG00735.hp1 HG02258.hp2 NA19000.hp1 |
a0005a0006 | a0005c0005a0006c0006 | a0005c0005t0003a0006c0006t0009a0006c0006t0014 | a0005c0005t0003g0045a0006c0006t0009g0042a0006c0006t0014g0058 | 3 | 66 | 0.0455 | 11 | c.-20 others(34): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99358255 | A | ATTTTTTT others(4): Show |
intron_variant | MODIFIER | HG01496.hp2 HG02004.hp2 NA19043.hp1 |
a0001a0011 | a0001c0001a0011c0009 | a0001c0001t0001a0001c0001t0012a0011c0009t0005 | a0001c0001t0001g0004a0001c0001t0012g0018a0011c0009t0005g0056 | 3 | 66 | 0.0455 | 11 | c.-71 others(30): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99382845 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00733.hp2 HG01081.hp1 HG01496.hp1 others(4): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0014a0002c0002t0021a0002c0002t0022others(4): Show | a0001c0001t0014g0016a0002c0002t0021g0055a0002c0002t0022g0013others(4): Show | 7 | 66 | 0.1061 | 11 | c.-71 others(30): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99432495 | C | CTTTTCTT others(4): Show |
intron_variant | MODIFIER | HG01081.hp1 | a0005 | a0005c0005 | a0005c0005t0018 | a0005c0005t0018g0028 | 1 | 66 | 0.0152 | 11 | c.-71 others(32): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99508686 | C | CTTTCTTT others(4): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 | 1 | 66 | 0.0152 | 11 | c.-70 others(30): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99637010 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | NA18957.hp2 | a0003 | a0003c0003 | a0003c0003t0002 | a0003c0003t0002g0002 | 1 | 66 | 0.0152 | 11 | c.55+ others(28): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99727312 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG01243.hp2 HG03130.hp1 |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0005a0005c0005t0001 | a0001c0001t0005g0014a0005c0005t0001g0035 | 2 | 66 | 0.0303 | 11 | c.56- others(28): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99819306 | T | TCCCCTCT others(4): Show |
intron_variant | MODIFIER | HG02257.hp1 | a0003 | a0003c0011 | a0003c0011t0019 | a0003c0011t0019g0059 | 1 | 66 | 0.0152 | 11 | c.56- others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99819321 | T | TCTCCTCC others(4): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0039 | 1 | 66 | 0.0152 | 11 | c.56- others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99819331 | T | TCCCCTCC others(4): Show |
intron_variant | MODIFIER | HG01099.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0010 | 1 | 66 | 0.0152 | 11 | c.56- others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100072990 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00738.hp2 HG02258.hp2 HG02895.hp2 |
a0004a0005 | a0004c0004a0005c0005 | a0004c0004t0002a0004c0004t0013a0005c0005t0003 | a0004c0004t0002g0041a0004c0004t0013g0050a0005c0005t0003g0045 | 3 | 66 | 0.0455 | 11 | c.143 others(30): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100161872 | C | CACACACA others(4): Show |
intron_variant | MODIFIER | HG00733.hp2 | a0002 | a0002c0002 | a0002c0002t0022 | a0002c0002t0022g0013 | 1 | 66 | 0.0152 | 11 | c.158 others(32): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100161873 | A | ACACACAC others(4): Show |
intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0032 | 1 | 66 | 0.0152 | 11 | c.158 others(32): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100205691 | T | TACAAATA others(4): Show |
intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
a0001a0002a0003others(9): Show | a0001c0001a0002c0002a0003c0003others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0052others(55): Show | 58 | 66 | 0.8788 | 11 | c.188 others(32): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1154444 | C | CTTTTCTT others(4): Show |
intron_variant | MODIFIER | HG02615.hp1 | a0002 | a0002c0014 | a0002c0014t0001 | a0002c0014t0001g0232 | 1 | 232 | 0.0043 | 11 | c.55+ others(26): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1154444 | C | CTTTTCTT others(4): Show |
intron_variant | MODIFIER | HG02148.hp1 NA18948.hp1 NA18954.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0029a0001c0002t0001g0062a0001c0002t0001g0063others(1): Show | 4 | 232 | 0.0172 | 11 | c.55+ others(26): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1154452 | T | TTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02622.hp2 HG03130.hp2 |
a0001 | a0001c0006a0001c0025 | a0001c0006t0002a0001c0025t0001 | a0001c0006t0002g0178a0001c0025t0001g0192 | 2 | 232 | 0.0086 | 11 | c.55+ others(26): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1210425 | G | GGAAAAAG others(4): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(24): Show | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0029others(104): Show | 107 | 232 | 0.4612 | 11 | c.56- others(28): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1233734 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02572.hp2 HG02922.hp2 HG02976.hp2 |
a0001 | a0001c0005a0001c0006a0001c0008 | a0001c0005t0001a0001c0006t0001a0001c0008t0001 | a0001c0005t0001g0196a0001c0006t0001g0195a0001c0008t0001g0143 | 3 | 232 | 0.0129 | 11 | c.358 others(28): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245217 | T | TATATATA others(4): Show |
intron_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0005 | a0001c0005t0002 | a0001c0005t0002g0019 | 1 | 232 | 0.0043 | 11 | c.358 others(30): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1265044 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0190 | 1 | 232 | 0.0043 | 11 | c.359 others(30): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1280459 | A | ATTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02165.hp1 HG02280.hp2 HG02622.hp2 others(1): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0005t0001a0001c0006t0001others(1): Show | a0001c0001t0001g0054a0001c0005t0001g0164a0001c0006t0001g0036others(1): Show | 4 | 232 | 0.0172 | 11 | c.454 others(28): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1332519 | G | GAAGGGGC others(4): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
a0001a0003a0006 | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(21): Show | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0001g0057others(107): Show | 110 | 232 | 0.4741 | 11 | c.136 others(30): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1348157 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02109.hp1 HG02486.hp2 |
a0002a0006 | a0002c0011a0006c0027 | a0002c0011t0001a0006c0027t0001 | a0002c0011t0001g0006a0006c0027t0001g0191 | 2 | 232 | 0.0086 | 11 | c.136 others(30): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTNAP1_chr17_42677531_42704993 | 42686469 | G | GTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02258.hp1 HG03579.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0182a0001c0001t0002g0183 | 2 | 364 | 0.0055 | 11 | c.900 others(26): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146192476 | A | AAGGCAAA others(4): Show |
intron_variant | MODIFIER | HG02630.hp1 NA19030.hp2 |
a0001a0002 | a0001c0012a0002c0016 | a0001c0012t0004a0002c0016t0004 | a0001c0012t0004g0026a0002c0016t0004g0024 | 2 | 40 | 0.0500 | 11 | c.97+ others(28): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146322634 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00735.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0013others(2): Show | a0001c0001t0001a0001c0001t0007a0001c0002t0001others(3): Show | a0001c0001t0001g0003a0001c0001t0007g0020a0001c0002t0001g0007others(3): Show | 6 | 40 | 0.1500 | 11 | c.97+ others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146352750 | G | GTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG01891.hp2 HG03139.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0008a0001c0010 | a0001c0001t0006a0001c0008t0001a0001c0010t0002 | a0001c0001t0006g0009a0001c0008t0001g0025a0001c0010t0002g0014 | 3 | 40 | 0.0750 | 11 | c.97+ others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146398184 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG03098.hp2 HG03225.hp1 |
a0001 | a0001c0002a0001c0009 | a0001c0002t0001a0001c0009t0019 | a0001c0002t0001g0021a0001c0009t0019g0027 | 2 | 40 | 0.0500 | 11 | c.97+ others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146404124 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02717.hp2 HG02896.hp1 HG02896.hp2 others(3): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0003t0020a0001c0004t0003others(2): Show | a0001c0001t0001g0003a0001c0003t0020g0017a0001c0004t0003g0035others(3): Show | 6 | 40 | 0.1500 | 11 | c.97+ others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146404141 | A | AAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0004 | a0004c0014 | a0004c0014t0021 | a0004c0014t0021g0022 | 1 | 40 | 0.0250 | 11 | c.97+ others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146426185 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02922.hp2 HG02976.hp1 HG03139.hp1 |
a0001 | a0001c0004a0001c0008a0001c0015 | a0001c0004t0005a0001c0008t0001a0001c0015t0001 | a0001c0004t0005g0004a0001c0008t0001g0025a0001c0015t0001g0011 | 3 | 40 | 0.0750 | 11 | c.97+ others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146464187 | G | GTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0035a0001c0004t0003g0036 | 2 | 40 | 0.0500 | 11 | c.98- others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146535217 | T | TAATATAT others(4): Show |
intron_variant | MODIFIER | HG00735.hp1 HG02451.hp2 HG02886.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0002t0002a0001c0003t0020others(4): Show | a0001c0001t0002g0006a0001c0002t0002g0040a0001c0003t0020g0017others(4): Show | 7 | 40 | 0.1750 | 11 | c.98- others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146535217 | T | TAATATAT others(4): Show |
intron_variant | MODIFIER | HG02886.hp1 NA21309.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0018a0001c0003t0013 | a0001c0001t0018g0001a0001c0003t0013g0010 | 2 | 40 | 0.0500 | 11 | c.98- others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146535241 | T | TATATAAT others(4): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0011 | a0001c0011t0016 | a0001c0011t0016g0019 | 1 | 40 | 0.0250 | 11 | c.98- others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146535278 | T | TATAATAT others(4): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0010 | a0001c0010t0002 | a0001c0010t0002g0014 | 1 | 40 | 0.0250 | 11 | c.98- others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146535351 | T | TATAATAT others(4): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02630.hp1 |
a0001a0004 | a0001c0012a0004c0014 | a0001c0012t0004a0004c0014t0021 | a0001c0012t0004g0026a0004c0014t0021g0022 | 2 | 40 | 0.0500 | 11 | c.98- others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146535397 | A | AATTATTA others(4): Show |
intron_variant | MODIFIER | HG02976.hp2 | a0001 | a0001c0003 | a0001c0003t0020 | a0001c0003t0020g0017 | 1 | 40 | 0.0250 | 11 | c.98- others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146665783 | T | TAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02976.hp2 | a0001 | a0001c0003 | a0001c0003t0020 | a0001c0003t0020g0017 | 1 | 40 | 0.0250 | 11 | c.98- others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146721264 | C | CTATATAT others(4): Show |
intron_variant | MODIFIER | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(1): Show |
a0001 | a0001c0002a0001c0008a0001c0010others(1): Show | a0001c0002t0001a0001c0008t0001a0001c0010t0002others(1): Show | a0001c0002t0001g0007a0001c0008t0001g0025a0001c0010t0002g0014others(1): Show | 4 | 40 | 0.1000 | 11 | c.98- others(28): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146985308 | A | ATTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0003 | a0001c0003t0011 | a0001c0003t0011g0023 | 1 | 40 | 0.0250 | 11 | c.403 others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147102282 | G | GAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0007 | 1 | 40 | 0.0250 | 11 | c.551 others(28): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147242987 | A | ATTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02451.hp1 NA21309.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0018a0001c0002t0001 | a0001c0001t0018g0001a0001c0002t0001g0007 | 2 | 40 | 0.0500 | 11 | c.134 others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147469506 | A | ATTTTTTT others(4): Show |
intron_variant | MODIFIER | HG03098.hp2 HG03540.hp2 NA19030.hp1 |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0004 | a0001c0001t0001g0038a0001c0002t0001g0021a0001c0003t0004g0029 | 3 | 40 | 0.0750 | 11 | c.167 others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147614778 | C | CCTGATTT others(4): Show |
intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp1 others(30): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(25): Show | a0001c0001t0001g0038a0001c0001t0006g0009a0001c0001t0007g0018others(30): Show | 33 | 40 | 0.8250 | 11 | c.189 others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147886475 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02451.hp1 HG03139.hp2 |
a0001 | a0001c0002a0001c0011 | a0001c0002t0001a0001c0011t0016 | a0001c0002t0001g0007a0001c0011t0016g0019 | 2 | 40 | 0.0500 | 11 | c.209 others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147940303 | T | TAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0005 | a0001c0005t0022 | a0001c0005t0022g0032 | 1 | 40 | 0.0250 | 11 | c.225 others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147980768 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02717.hp1 HG02886.hp1 HG02922.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(3): Show | a0001c0001t0012a0001c0003t0004a0001c0003t0013others(4): Show | a0001c0001t0012g0034a0001c0003t0004g0029a0001c0003t0013g0010others(4): Show | 7 | 40 | 0.1750 | 11 | c.238 others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147984699 | C | CTACAGGG others(4): Show |
intron_variant | MODIFIER | HG02486.hp2 HG02717.hp1 HG02886.hp1 others(6): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(3): Show | a0001c0001t0012a0001c0001t0018a0001c0003t0004others(6): Show | a0001c0001t0012g0034a0001c0001t0018g0001a0001c0003t0004g0029others(6): Show | 9 | 40 | 0.2250 | 11 | c.238 others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |