view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 | 99508686 | C | CTTTCTTT others(4): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 | 1 | 59 | 0.0169 | 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 | 2 | 0.5000 | 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 |
a0001a0006 | a0001c0001a0006c0005 | a0001c0001t0005a0006c0005t0001 | a0001c0001t0005g0012 a0006c0005t0001g0035 |
2 | 19 | 0.1053 | 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 | a0001c0001t0004g0011 | 1 | 65 | 0.0154 | 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 |
a0005a0006 | a0005c0004a0006c0005 | a0005c0004t0002a0005c0004t0013a0006c0005t0003 | a0005c0004t0002g0041 a0005c0004t0013g0050 a0006c0005t0003g0045 |
3 | 13 | 0.2308 | 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 | a0002c0002t0022g0010 | 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 | 63 | 0.0159 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0052 others(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 | 168 | 0.0060 | 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 | a0001c0001t0001g0079 a0001c0002t0001g0148 a0001c0002t0001g0149 others(1): Show |
4 | 171 | 0.0234 | 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 | a0001c0006t0002g0178 a0001c0025t0001g0192 |
2 | 230 | 0.0087 | 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(103): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(24): Show | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0045 others(103): Show |
106 | 228 | 0.4649 | 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 | a0001c0005t0001g0196 a0001c0006t0001g0195 a0001c0008t0001g0118 |
3 | 89 | 0.0337 | 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 | a0001c0005t0002g0016 | 1 | 227 | 0.0044 | 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 | 54 | 0.0185 | 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 | a0001c0001t0001g0138 a0001c0005t0001g0163 a0001c0006t0001g0154 others(1): Show |
4 | 44 | 0.0909 | 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(106): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(21): Show | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0049 others(106): Show |
109 | 230 | 0.4739 | 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 |
a0002a0005 | a0002c0011a0005c0027 | a0002c0011t0001a0005c0027t0001 | a0002c0011t0001g0007 a0005c0027t0001g0191 |
2 | 113 | 0.0177 | 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 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | 182 | 0.0110 | 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 | a0001c0012t0004g0026 a0002c0016t0004g0024 |
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 | a0001c0001t0001g0003 a0001c0001t0007g0020 a0001c0002t0001g0007 others(3): Show |
6 | 20 | 0.3000 | 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 | a0001c0001t0006g0009 a0001c0008t0001g0025 a0001c0010t0002g0014 |
3 | 12 | 0.2500 | 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 | a0001c0002t0001g0021 a0001c0009t0019g0027 |
2 | 12 | 0.1667 | 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 |
a0001a0004 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0003t0020a0001c0004t0003others(2): Show | a0001c0001t0001g0003 a0001c0003t0020g0017 a0001c0004t0003g0035 others(3): Show |
6 | 18 | 0.3333 | 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 | a0003 | a0003c0014 | a0003c0014t0021 | a0003c0014t0021g0022 | 1 | 36 | 0.0278 | 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 | a0001c0004t0005g0004 a0001c0008t0001g0025 a0001c0015t0001g0011 |
3 | 10 | 0.3000 | 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 | a0001c0004t0003g0035 a0001c0004t0003g0036 |
2 | 12 | 0.1667 | 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 | a0001c0001t0002g0006 a0001c0002t0002g0040 a0001c0003t0020g0017 others(4): Show |
7 | 34 | 0.2059 | 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 | a0001c0001t0018g0001 a0001c0003t0013g0010 |
2 | 29 | 0.0690 | 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 | 35 | 0.0286 | 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 | 30 | 0.0333 | 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 |
a0001a0003 | a0001c0012a0003c0014 | a0001c0012t0004a0003c0014t0021 | a0001c0012t0004g0026 a0003c0014t0021g0022 |
2 | 24 | 0.0833 | 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 | 17 | 0.0588 | 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 | 15 | 0.0667 | 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 | a0001c0002t0001g0007 a0001c0008t0001g0025 a0001c0010t0002g0014 others(1): Show |
4 | 32 | 0.1250 | 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 | 7 | 0.1429 | 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 | 10 | 0.1000 | 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 | a0001c0001t0018g0001 a0001c0002t0001g0007 |
2 | 3 | 0.6667 | 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 | a0001c0001t0001g0038 a0001c0002t0001g0021 a0001c0003t0004g0029 |
3 | 24 | 0.1250 | 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 | a0001c0001t0001g0038 a0001c0001t0006g0009 a0001c0001t0007g0018 others(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 | a0001c0002t0001g0007 a0001c0011t0016g0019 |
2 | 12 | 0.1667 | 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 | 4 | 0.2500 | 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 | a0001c0001t0012g0034 a0001c0003t0004g0029 a0001c0003t0013g0010 others(4): Show |
7 | 30 | 0.2333 | 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 | a0001c0001t0012g0034 a0001c0001t0018g0001 a0001c0003t0004g0029 others(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 | ||||||
CNTNAP2_chr7_146111801_148425998 | 148122867 | A | AAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02451.hp2 HG02976.hp1 HG03139.hp1 |
a0001 | a0001c0001a0001c0008a0001c0015 | a0001c0001t0002a0001c0008t0001a0001c0015t0001 | a0001c0001t0002g0006 a0001c0008t0001g0025 a0001c0015t0001g0011 |
3 | 40 | 0.0750 | 11 | c.255 others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148157571 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00735.hp1 HG01891.hp2 HG02451.hp1 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(15): Show | a0001c0001t0001g0003 a0001c0001t0002g0006 a0001c0001t0006g0009 others(16): Show |
19 | 35 | 0.5429 | 11 | c.277 others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148157586 | A | AAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0003 | a0003c0014 | a0003c0014t0021 | a0003c0014t0021g0022 | 1 | 39 | 0.0256 | 11 | c.277 others(30): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 17/23 | chr7 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 148158222 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02451.hp1 HG02451.hp2 HG02896.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0002a0001c0001t0012a0001c0002t0001others(14): Show | a0001c0001t0002g0006 a0001c0001t0012g0034 a0001c0002t0001g0007 others(16): Show |
19 | 21 | 0.9048 | 11 | c.277 others(32): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |