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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN6_chr3_1088024_1409217 | 1247037 | GTCTTTT | G | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(19): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(5): Show | a0001c0001t0001g0046 a0001c0001t0001g0105 a0001c0001t0001g0141 others(19): Show |
22 | 232 | 0.0948 | -6 | c.358 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1259860 | TACACAC | T | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(4): Show |
a0001a0003 | a0001c0006a0001c0019a0001c0021others(1): Show | a0001c0006t0001a0001c0019t0001a0001c0021t0001others(1): Show | a0001c0006t0001g0195 a0001c0006t0001g0200 a0001c0006t0001g0201 others(4): Show |
7 | 232 | 0.0302 | -6 | c.359 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1277346 | CTTTTTT | C | intron_variant | MODIFIER | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(52): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(15): Show | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0054 others(52): Show |
55 | 232 | 0.2371 | -6 | c.359 others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1281983 | TACACAC | T | intron_variant | MODIFIER | HG00609.hp1 HG00741.hp1 HG01261.hp1 others(17): Show |
a0001a0005a0006 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(6): Show | a0001c0001t0001g0035 a0001c0001t0001g0082 a0001c0001t0001g0130 others(17): Show |
20 | 232 | 0.0862 | -6 | c.454 others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1297781 | CCTAACT | C | intron_variant | MODIFIER | HG02015.hp1 HG02055.hp2 HG02280.hp2 others(14): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0003others(9): Show | a0001c0001t0001g0093 a0001c0002t0001g0018 a0001c0002t0001g0227 others(14): Show |
17 | 232 | 0.0733 | -6 | c.659 others(21): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1297996 | GGTTTTT | G | intron_variant | MODIFIER | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(107): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(21): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0003others(28): Show | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0071 others(107): Show |
110 | 232 | 0.4741 | -6 | c.761 others(19): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1300599 | AAGAAAG | A | intron_variant | MODIFIER | HG02965.hp1 HG03130.hp2 HG03195.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0005t0001others(3): Show | a0001c0001t0001g0190 a0001c0003t0001g0177 a0001c0005t0001g0164 others(4): Show |
7 | 232 | 0.0302 | -6 | c.761 others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1308287 | TTGTGTG | T | intron_variant | MODIFIER | HG02109.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
a0001a0006 | a0001c0005a0001c0006a0001c0008others(2): Show | a0001c0005t0001a0001c0006t0001a0001c0008t0001others(2): Show | a0001c0005t0001g0189 a0001c0005t0001g0193 a0001c0005t0001g0207 others(5): Show |
8 | 232 | 0.0345 | -6 | c.761 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1316164 | GTACTAT | G | intron_variant | MODIFIER | HG01255.hp1 HG01256.hp2 HG01258.hp1 |
a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0014 a0001c0007t0001g0015 a0001c0007t0001g0100 |
3 | 232 | 0.0129 | -6 | c.762 others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1316727 | GTTATTA | G | intron_variant | MODIFIER | HG00140.hp2 HG01106.hp1 HG01167.hp1 others(14): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0004t0005others(4): Show | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0071 others(14): Show |
17 | 232 | 0.0733 | -6 | c.762 others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1383640 | AAAAAAC | A | intron_variant | MODIFIER | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(15): Show |
a0001 | a0001c0007a0001c0008 | a0001c0007t0001a0001c0007t0002a0001c0007t0006others(1): Show | a0001c0007t0001g0001 a0001c0007t0001g0014 a0001c0007t0001g0015 others(15): Show |
18 | 232 | 0.0776 | -6 | c.251 others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1384740 | CATATAT | C | intron_variant | MODIFIER | NA18948.hp2 NA18951.hp1 NA18953.hp2 others(2): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0044 a0001c0001t0001g0129 a0001c0004t0001g0080 others(2): Show |
5 | 232 | 0.0216 | -6 | c.251 others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTNAP1_chr17_42677531_42704993 | 42698445 | ATGTGTG | A | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02109.hp1 others(24): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0034 others(11): Show |
27 | 364 | 0.0742 | -6 | c.386 others(23): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146151676 | ATATATG | A | intron_variant | MODIFIER | HG02896.hp2 NA19030.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0003 | a0001c0001t0001g0038 a0001c0004t0003g0035 |
2 | 40 | 0.0500 | -6 | c.97+ others(23): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146163579 | ATCTATC | A | intron_variant | MODIFIER | HG01891.hp1 HG02486.hp2 HG02630.hp1 others(3): Show |
a0001a0002a0004 | a0001c0002a0001c0003a0001c0008others(3): Show | a0001c0002t0001a0001c0003t0011a0001c0008t0001others(3): Show | a0001c0002t0001g0021 a0001c0003t0011g0023 a0001c0008t0001g0025 others(3): Show |
6 | 40 | 0.1500 | -6 | c.97+ others(23): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146180401 | GTTAAAC | G | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(15): Show | a0001c0001t0002g0006 a0001c0001t0006g0009 a0001c0001t0007g0018 others(18): Show |
21 | 40 | 0.5250 | -6 | c.97+ others(23): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146201639 | AGTGTGT | A | intron_variant | MODIFIER | HG02486.hp2 HG02630.hp1 HG03139.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(3): Show | a0001c0001t0007a0001c0003t0011a0001c0008t0001others(3): Show | a0001c0001t0007g0018 a0001c0003t0011g0023 a0001c0008t0001g0025 others(3): Show |
6 | 40 | 0.1500 | -6 | c.97+ others(23): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146222541 | AGTGTGT | A | intron_variant | MODIFIER | NA20129.hp1 NA20129.hp2 |
a0001 | a0001c0003a0001c0006 | a0001c0003t0023a0001c0006t0009 | a0001c0003t0023g0030 a0001c0006t0009g0028 |
2 | 40 | 0.0500 | -6 | c.97+ others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146254129 | GCACACA | G | intron_variant | MODIFIER | NA18522.hp2 NA20129.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0007a0001c0003t0023 | a0001c0001t0007g0018 a0001c0003t0023g0030 |
2 | 40 | 0.0500 | -6 | c.97+ others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146254159 | ACACAAG | A | intron_variant | MODIFIER | HG02897.hp1 HG03540.hp1 NA21309.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0018a0001c0002t0001a0001c0002t0010 | a0001c0001t0018g0001 a0001c0002t0001g0008 a0001c0002t0010g0002 |
3 | 40 | 0.0750 | -6 | c.97+ others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146303072 | ATGTGTG | A | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG02486.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0007a0001c0002t0002a0001c0002t0010others(4): Show | a0001c0001t0007g0020 a0001c0002t0002g0013 a0001c0002t0010g0002 others(4): Show |
7 | 40 | 0.1750 | -6 | c.97+ others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146332941 | ATTTTTT | A | intron_variant | MODIFIER | HG02897.hp1 HG03098.hp2 HG03225.hp1 |
a0001 | a0001c0002a0001c0009 | a0001c0002t0001a0001c0009t0019 | a0001c0002t0001g0008 a0001c0002t0001g0021 a0001c0009t0019g0027 |
3 | 40 | 0.0750 | -6 | c.97+ others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146356052 | TACACAC | T | intron_variant | MODIFIER | HG02717.hp2 HG02896.hp1 HG02976.hp2 |
a0001a0005 | a0001c0003a0001c0005a0005c0020 | a0001c0003t0020a0001c0005t0008a0005c0020t0005 | a0001c0003t0020g0017 a0001c0005t0008g0005 a0005c0020t0005g0016 |
3 | 40 | 0.0750 | -6 | c.97+ others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146391750 | TTTGTTG | T | intron_variant | MODIFIER | HG02451.hp1 HG02922.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0012a0001c0002t0001 | a0001c0001t0012g0034 a0001c0002t0001g0007 |
2 | 40 | 0.0500 | -6 | c.97+ others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146477570 | GTTGAAC | G | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp2 HG02630.hp1 others(6): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0009others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(6): Show | a0001c0001t0001g0038 a0001c0001t0002g0006 a0001c0001t0012g0034 others(6): Show |
9 | 40 | 0.2250 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146477624 | AACACAC | A | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG02630.hp2 others(7): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0008others(4): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0018others(7): Show | a0001c0001t0001g0003 a0001c0001t0007g0020 a0001c0001t0018g0001 others(7): Show |
10 | 40 | 0.2500 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146486046 | CTTTTTT | C | intron_variant | MODIFIER | HG01891.hp2 HG02486.hp2 HG03139.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0006a0001c0001t0007a0001c0002t0010others(4): Show | a0001c0001t0006g0009 a0001c0001t0007g0018 a0001c0002t0010g0002 others(4): Show |
7 | 40 | 0.1750 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146495552 | ATTTTTT | A | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0005others(5): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(7): Show | a0001c0001t0001g0003 a0001c0001t0006g0009 a0001c0001t0007g0018 others(8): Show |
11 | 40 | 0.2750 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146502224 | AATATAT | A | intron_variant | MODIFIER | HG02451.hp2 HG02976.hp2 HG03098.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0003t0020 | a0001c0001t0001g0003 a0001c0001t0002g0006 a0001c0003t0020g0017 |
3 | 40 | 0.0750 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146512823 | TTAACTC | T | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02630.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0006a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0006g0009 a0001c0002t0001g0007 a0001c0002t0002g0013 others(3): Show |
6 | 40 | 0.1500 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 146520313 | CATATAT | C | intron_variant | MODIFIER | HG00735.hp1 HG02886.hp2 HG03239.hp2 |
a0001 | a0001c0002a0001c0005a0001c0006 | a0001c0002t0002a0001c0005t0022a0001c0006t0014 | a0001c0002t0002g0040 a0001c0005t0022g0032 a0001c0006t0014g0033 |
3 | 40 | 0.0750 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146533107 | CAAAAAA | C | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02630.hp2 others(4): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0006a0001c0002t0001others(4): Show | a0001c0001t0001g0038 a0001c0001t0006g0009 a0001c0002t0001g0007 others(4): Show |
7 | 40 | 0.1750 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146566696 | CAAAAAT | C | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp1 others(9): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0005others(6): Show | a0001c0001t0007a0001c0001t0018a0001c0003t0011others(9): Show | a0001c0001t0007g0020 a0001c0001t0018g0001 a0001c0003t0011g0023 others(9): Show |
12 | 40 | 0.3000 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146596595 | CAGAGAG | C | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(1): Show |
a0001a0005 | a0001c0001a0001c0019a0005c0020 | a0001c0001t0007a0001c0001t0018a0001c0019t0006others(1): Show | a0001c0001t0007g0020 a0001c0001t0018g0001 a0001c0019t0006g0015 others(1): Show |
4 | 40 | 0.1000 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146633832 | GAAAAAA | G | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02630.hp2 others(6): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0006others(4): Show | a0001c0001t0006a0001c0002t0001a0001c0002t0002others(5): Show | a0001c0001t0006g0009 a0001c0002t0001g0007 a0001c0002t0001g0021 others(6): Show |
9 | 40 | 0.2250 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146663293 | AAAAAAG | A | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0004others(4): Show | a0001c0001t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0021 others(5): Show |
8 | 40 | 0.2000 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146668428 | CTGTGTG | C | intron_variant | MODIFIER | HG01891.hp1 HG02896.hp2 HG02897.hp2 |
a0001a0004 | a0001c0004a0004c0014 | a0001c0004t0003a0004c0014t0021 | a0001c0004t0003g0035 a0001c0004t0003g0036 a0004c0014t0021g0022 |
3 | 40 | 0.0750 | -6 | c.98- others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146754794 | ATCTGTT | A | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
a0001a0004a0005 | a0001c0002a0004c0014a0005c0020 | a0001c0002t0001a0001c0002t0002a0001c0002t0010others(2): Show | a0001c0002t0001g0007 a0001c0002t0002g0013 a0001c0002t0010g0002 others(2): Show |
5 | 40 | 0.1250 | -6 | c.98- others(23): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146760409 | CTTTTTT | C | intron_variant | MODIFIER | HG02717.hp2 HG02976.hp1 HG03139.hp1 others(2): Show |
a0001 | a0001c0005a0001c0008a0001c0009others(2): Show | a0001c0005t0008a0001c0008t0001a0001c0009t0019others(2): Show | a0001c0005t0008g0005 a0001c0008t0001g0025 a0001c0009t0019g0027 others(2): Show |
5 | 40 | 0.1250 | -6 | c.98- others(23): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146841288 | TGAAGAG | T | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(17): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(16): Show | a0001c0001t0001g0038 a0001c0001t0002g0006 a0001c0001t0006g0009 others(17): Show |
20 | 40 | 0.5000 | -6 | c.402 others(23): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146851650 | CTGTGTG | C | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
a0001a0002 | a0001c0004a0002c0016 | a0001c0004t0003a0001c0004t0005a0002c0016t0004 | a0001c0004t0003g0035 a0001c0004t0003g0036 a0001c0004t0005g0004 others(1): Show |
4 | 40 | 0.1000 | -6 | c.402 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146855807 | GTATATA | G | intron_variant | MODIFIER | HG02717.hp1 HG02896.hp1 HG03225.hp2 others(2): Show |
a0001a0002a0003others(1): Show | a0001c0006a0001c0018a0002c0017others(2): Show | a0001c0006t0009a0001c0018t0002a0002c0017t0015others(2): Show | a0001c0006t0009g0028 a0001c0018t0002g0012 a0002c0017t0015g0037 others(2): Show |
5 | 40 | 0.1250 | -6 | c.402 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146862432 | TAAAAAA | T | intron_variant | MODIFIER | HG02451.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0009others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0020others(2): Show | a0001c0001t0001g0003 a0001c0001t0002g0006 a0001c0003t0020g0017 others(2): Show |
5 | 40 | 0.1250 | -6 | c.402 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146875934 | CAAAAAA | C | intron_variant | MODIFIER | HG02717.hp1 HG03139.hp2 HG03225.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0010a0001c0011others(3): Show | a0001c0001t0018a0001c0010t0002a0001c0011t0016others(3): Show | a0001c0001t0018g0001 a0001c0010t0002g0014 a0001c0011t0016g0019 others(3): Show |
6 | 40 | 0.1500 | -6 | c.402 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146885928 | GGTGTGT | G | intron_variant | MODIFIER | HG02486.hp2 HG02922.hp2 |
a0001 | a0001c0003a0001c0004 | a0001c0003t0011a0001c0004t0005 | a0001c0003t0011g0023 a0001c0004t0005g0004 |
2 | 40 | 0.0500 | -6 | c.402 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146927960 | GTATATA | G | intron_variant | MODIFIER | HG03098.hp2 NA18522.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0007a0001c0002t0001 | a0001c0001t0007g0018 a0001c0002t0001g0021 |
2 | 40 | 0.0500 | -6 | c.402 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147033160 | GTATATA | G | intron_variant | MODIFIER | HG02486.hp2 HG02976.hp2 |
a0001 | a0001c0003 | a0001c0003t0011a0001c0003t0020 | a0001c0003t0011g0023 a0001c0003t0020g0017 |
2 | 40 | 0.0500 | -6 | c.403 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147060193 | ATGTATC | A | intron_variant | MODIFIER | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(14): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0002a0001c0001t0007a0001c0001t0018others(13): Show | a0001c0001t0002g0006 a0001c0001t0007g0018 a0001c0001t0018g0001 others(14): Show |
17 | 40 | 0.4250 | -6 | c.550 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147072848 | CTTTTTT | C | intron_variant | MODIFIER | HG00735.hp1 HG01891.hp1 HG02886.hp2 others(4): Show |
a0001a0003a0004 | a0001c0005a0001c0006a0001c0011others(3): Show | a0001c0005t0022a0001c0006t0009a0001c0006t0014others(4): Show | a0001c0005t0022g0032 a0001c0006t0009g0028 a0001c0006t0014g0033 others(4): Show |
7 | 40 | 0.1750 | -6 | c.550 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147081583 | TTGTGTG | T | intron_variant | MODIFIER | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
a0001 | a0001c0004a0001c0005a0001c0009 | a0001c0004t0003a0001c0005t0008a0001c0009t0019 | a0001c0004t0003g0035 a0001c0004t0003g0036 a0001c0005t0008g0005 others(1): Show |
4 | 40 | 0.1000 | -6 | c.551 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |