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 | 1160344 | GTATATAT others(3): Show |
G | intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0219 | 1 | 232 | 0.0043 | -10 | c.55+ others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1161769 | TACACACA others(3): Show |
T | intron_variant | MODIFIER | HG02896.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0210 | 1 | 232 | 0.0043 | -10 | c.55+ others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1170236 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00733.hp2 HG00735.hp1 others(19): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0005others(10): Show | a0001c0001t0001g0047 a0001c0001t0001g0156 a0001c0002t0001g0098 others(19): Show |
22 | 232 | 0.0948 | -10 | c.55+ others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1172620 | CTGTGTGT others(3): Show |
C | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
a0001a0002a0004others(1): Show | a0001c0002a0001c0005a0001c0006others(6): Show | a0001c0002t0009a0001c0005t0001a0001c0006t0001others(7): Show | a0001c0002t0009g0205 a0001c0005t0001g0188 a0001c0006t0001g0111 others(13): Show |
16 | 232 | 0.0690 | -10 | c.55+ others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1189042 | AAAAACAA others(3): Show |
A | intron_variant | MODIFIER | HG00741.hp1 HG01099.hp2 HG01106.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0007others(1): Show | a0001c0001t0001a0001c0003t0001a0001c0007t0001others(1): Show | a0001c0001t0001g0152 a0001c0003t0001g0074 a0001c0003t0001g0142 others(4): Show |
7 | 232 | 0.0302 | -10 | c.56- others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1201097 | TTTTGTGT others(3): Show |
T | intron_variant | MODIFIER | HG02074.hp2 HG02738.hp1 NA18961.hp2 |
a0001 | a0001c0003a0001c0007 | a0001c0003t0001a0001c0007t0001 | a0001c0003t0001g0011 a0001c0003t0001g0092 a0001c0007t0001g0052 |
3 | 232 | 0.0129 | -10 | c.56- others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1201099 | TTGTGTGT others(3): Show |
T | intron_variant | MODIFIER | HG00140.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(15): Show | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0002t0001g0053 others(47): Show |
50 | 232 | 0.2155 | -10 | c.56- others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1219977 | GTGCAACA others(3): Show |
G | intron_variant | MODIFIER | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(57): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0004others(13): Show | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0029 others(57): Show |
60 | 232 | 0.2586 | -10 | c.56- others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245197 | GATATATA others(3): Show |
G | intron_variant | MODIFIER | HG00639.hp2 HG01099.hp1 HG01109.hp1 others(7): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0005others(5): Show | a0001c0001t0001a0001c0003t0001a0001c0005t0001others(6): Show | a0001c0001t0001g0126 a0001c0001t0001g0204 a0001c0003t0001g0101 others(7): Show |
10 | 232 | 0.0431 | -10 | c.358 others(29): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245227 | TATATATA others(3): Show |
T | intron_variant | MODIFIER | HG02615.hp1 | a0002 | a0002c0014 | a0002c0014t0001 | a0002c0014t0001g0232 | 1 | 232 | 0.0043 | -10 | c.358 others(29): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1277346 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | HG01169.hp2 HG01884.hp2 |
a0001 | a0001c0005a0001c0006 | a0001c0005t0001a0001c0006t0001 | a0001c0005t0001g0188 a0001c0006t0001g0200 |
2 | 232 | 0.0086 | -10 | c.359 others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1300595 | AAGAAAGA others(3): Show |
A | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(5): Show |
a0001a0003 | a0001c0002a0001c0006a0001c0007others(2): Show | a0001c0002t0008a0001c0006t0001a0001c0007t0001others(2): Show | a0001c0002t0008g0221 a0001c0006t0001g0200 a0001c0006t0001g0201 others(5): Show |
8 | 232 | 0.0345 | -10 | c.761 others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1301024 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | HG01071.hp1 HG01258.hp2 HG01993.hp1 others(22): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(5): Show | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0105 others(22): Show |
25 | 232 | 0.1078 | -10 | c.761 others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1319833 | GAAAATAA others(3): Show |
G | intron_variant | MODIFIER | HG01978.hp2 HG02809.hp1 HG03195.hp1 others(2): Show |
a0001 | a0001c0002a0001c0003a0001c0006others(1): Show | a0001c0002t0003a0001c0002t0008a0001c0003t0001others(2): Show | a0001c0002t0003g0069 a0001c0002t0008g0221 a0001c0003t0001g0177 others(2): Show |
5 | 232 | 0.0216 | -10 | c.762 others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1336172 | TAAATAAA others(3): Show |
T | intron_variant | MODIFIER | HG01169.hp1 HG02148.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0029 a0001c0004t0001g0158 |
2 | 232 | 0.0086 | -10 | c.136 others(29): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTNAP1_chr17_42677531_42704993 | 42678361 | GGGGCGGG others(3): Show |
G | upstream_gene_variant | MODIFIER | HG03453.hp1 | a0002 | a0002c0014 | a0002c0014t0010 | a0002c0014t0010g0150 | 1 | 364 | 0.0028 | -10 | c.-44 others(21): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 4169 | chr17 | TogoVar | |||||||
CNTNAP1_chr17_42677531_42704993 | 42698534 | CGTGTGTG others(3): Show |
C | intron_variant | MODIFIER | NA18995.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0162 | 1 | 364 | 0.0028 | -10 | c.386 others(25): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146163499 | CTATATAT others(3): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0006a0001c0002t0001others(1): Show | a0001c0001t0002g0006 a0001c0001t0006g0009 a0001c0002t0001g0007 others(2): Show |
5 | 40 | 0.1250 | -10 | c.97+ others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146254129 | GCACACAC others(3): Show |
G | intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0013 | 1 | 40 | 0.0250 | -10 | c.97+ others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146254155 | ACACACAC others(3): Show |
A | intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 40 | 0.0250 | -10 | c.97+ others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146303071 | CATGTGTG others(3): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG03139.hp2 |
a0001a0004 | a0001c0002a0001c0011a0004c0014 | a0001c0002t0001a0001c0011t0016a0004c0014t0021 | a0001c0002t0001g0007 a0001c0011t0016g0019 a0004c0014t0021g0022 |
3 | 40 | 0.0750 | -10 | c.97+ others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 146303072 | ATGTGTGT others(3): Show |
A | intron_variant | MODIFIER | HG02630.hp1 HG03225.hp2 |
a0001 | a0001c0012a0001c0018 | a0001c0012t0004a0001c0018t0002 | a0001c0012t0004g0026 a0001c0018t0002g0012 |
2 | 40 | 0.0500 | -10 | c.97+ others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146356052 | TACACACA others(3): Show |
T | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(6): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0002t0001a0001c0003t0023others(4): Show | a0001c0001t0002g0006 a0001c0002t0001g0008 a0001c0002t0001g0021 others(6): Show |
9 | 40 | 0.2250 | -10 | c.97+ others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146380784 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | HG02897.hp1 HG02922.hp2 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0004t0005 | a0001c0002t0001g0008 a0001c0004t0005g0004 |
2 | 40 | 0.0500 | -10 | c.97+ others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146395821 | ATAGAGGA others(3): Show |
A | intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0021 | 1 | 40 | 0.0250 | -10 | c.97+ others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 146457481 | AATATATA others(3): Show |
A | intron_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0018 | 1 | 40 | 0.0250 | -10 | c.98- others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146477624 | AACACACA others(3): Show |
A | intron_variant | MODIFIER | HG01891.hp1 HG02630.hp1 HG02976.hp2 |
a0001a0004 | a0001c0003a0001c0012a0004c0014 | a0001c0003t0020a0001c0012t0004a0004c0014t0021 | a0001c0003t0020g0017 a0001c0012t0004g0026 a0004c0014t0021g0022 |
3 | 40 | 0.0750 | -10 | c.98- others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146502224 | AATATATA others(3): Show |
A | intron_variant | MODIFIER | HG02922.hp2 HG03239.hp1 HG03239.hp2 others(1): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0018a0001c0002t0002a0001c0004t0005others(1): Show | a0001c0001t0018g0001 a0001c0002t0002g0040 a0001c0004t0005g0004 others(1): Show |
4 | 40 | 0.1000 | -10 | c.98- others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146585101 | GTGTTTTG others(3): Show |
G | intron_variant | MODIFIER | HG02451.hp2 HG02922.hp2 HG03540.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0002t0010a0001c0003t0004others(1): Show | a0001c0001t0002g0006 a0001c0002t0010g0002 a0001c0003t0004g0029 others(1): Show |
4 | 40 | 0.1000 | -10 | c.98- others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146633832 | GAAAAAAA others(3): Show |
G | intron_variant | MODIFIER | HG02451.hp2 HG02922.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0002a0001c0004t0005 | a0001c0001t0002g0006 a0001c0004t0005g0004 |
2 | 40 | 0.0500 | -10 | c.98- others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146664157 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | NA18522.hp1 | a0001 | a0001c0013 | a0001c0013t0003 | a0001c0013t0003g0039 | 1 | 40 | 0.0250 | -10 | c.98- others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146708588 | ATTTTTTT others(3): Show |
A | intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0021 | 1 | 40 | 0.0250 | -10 | c.98- others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146851650 | CTGTGTGT others(3): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp2 HG02630.hp1 others(1): Show |
a0001a0004 | a0001c0001a0001c0012a0004c0014 | a0001c0001t0002a0001c0001t0007a0001c0012t0004others(1): Show | a0001c0001t0002g0006 a0001c0001t0007g0018 a0001c0012t0004g0026 others(1): Show |
4 | 40 | 0.1000 | -10 | c.402 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146855807 | GTATATAT others(3): Show |
G | intron_variant | MODIFIER | HG02486.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0008others(2): Show | a0001c0001t0001a0001c0003t0011a0001c0008t0001others(2): Show | a0001c0001t0001g0003 a0001c0003t0011g0023 a0001c0008t0001g0025 others(2): Show |
5 | 40 | 0.1250 | -10 | c.402 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146885928 | GGTGTGTG others(3): Show |
G | intron_variant | MODIFIER | HG00735.hp1 HG01891.hp1 HG02896.hp2 others(5): Show |
a0001a0003a0004 | a0001c0002a0001c0004a0001c0006others(3): Show | a0001c0002t0010a0001c0004t0003a0001c0006t0009others(4): Show | a0001c0002t0010g0002 a0001c0004t0003g0035 a0001c0004t0003g0036 others(5): Show |
8 | 40 | 0.2000 | -10 | c.402 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146885965 | GTGTGTGT others(3): Show |
G | intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0006 | 1 | 40 | 0.0250 | -10 | c.402 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146947406 | CTCTCTAT others(3): Show |
C | intron_variant | MODIFIER | HG02976.hp2 | a0001 | a0001c0003 | a0001c0003t0020 | a0001c0003t0020g0017 | 1 | 40 | 0.0250 | -10 | c.403 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146985308 | ATTTTTTT others(3): Show |
A | intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0003 | a0001c0003t0023 | a0001c0003t0023g0030 | 1 | 40 | 0.0250 | -10 | c.403 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147081583 | TTGTGTGT others(3): Show |
T | intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0029 | 1 | 40 | 0.0250 | -10 | c.551 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147237049 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 40 | 0.0250 | -10 | c.134 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147301590 | CTCTGTGT others(3): Show |
C | intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0040 | 1 | 40 | 0.0250 | -10 | c.149 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147301592 | CTGTGTGT others(3): Show |
C | intron_variant | MODIFIER | HG00735.hp2 HG02451.hp1 HG02486.hp2 others(9): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0007a0001c0002t0001a0001c0002t0002others(8): Show | a0001c0001t0007g0018 a0001c0002t0001g0007 a0001c0002t0001g0021 others(9): Show |
12 | 40 | 0.3000 | -10 | c.149 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147347431 | TATATATA others(3): Show |
T | intron_variant | MODIFIER | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(4): Show |
a0001a0005 | a0001c0001a0001c0005a0001c0010others(3): Show | a0001c0001t0001a0001c0005t0008a0001c0005t0022others(4): Show | a0001c0001t0001g0003 a0001c0005t0008g0005 a0001c0005t0022g0032 others(4): Show |
7 | 40 | 0.1750 | -10 | c.149 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147394807 | TTGTGTGT others(3): Show |
T | intron_variant | MODIFIER | HG02922.hp1 HG03540.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0012a0001c0002t0010 | a0001c0001t0012g0034 a0001c0002t0010g0002 |
2 | 40 | 0.0500 | -10 | c.149 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147441813 | TTCTCTCT others(3): Show |
T | intron_variant | MODIFIER | HG01891.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
a0001a0003a0004 | a0001c0002a0001c0008a0003c0007others(1): Show | a0001c0002t0001a0001c0008t0001a0003c0007t0017others(1): Show | a0001c0002t0001g0021 a0001c0008t0001g0025 a0003c0007t0017g0031 others(1): Show |
4 | 40 | 0.1000 | -10 | c.167 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147500153 | GGATAAAA others(3): Show |
G | intron_variant | MODIFIER | HG00735.hp1 HG02451.hp2 HG02717.hp2 others(11): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0005others(7): Show | a0001c0001t0002a0001c0001t0012a0001c0002t0001others(10): Show | a0001c0001t0002g0006 a0001c0001t0012g0034 a0001c0002t0001g0008 others(11): Show |
14 | 40 | 0.3500 | -10 | c.177 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147502733 | GTGTGTGT others(3): Show |
G | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp2 HG02976.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0011a0001c0003t0020 | a0001c0002t0001g0007 a0001c0003t0011g0023 a0001c0003t0020g0017 |
3 | 40 | 0.0750 | -10 | c.177 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147615277 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0002 | a0001c0002t0010 | a0001c0002t0010g0002 | 1 | 40 | 0.0250 | -10 | c.189 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147729428 | GCACACAC others(3): Show |
G | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02451.hp2 others(21): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(19): Show | a0001c0001t0001g0038 a0001c0001t0002g0006 a0001c0001t0007g0018 others(21): Show |
24 | 40 | 0.6000 | -10 | c.209 others(31): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147772446 | CTATATAT others(3): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02886.hp1 NA19030.hp1 others(2): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0010others(1): Show | a0001c0001t0001a0001c0003t0013a0001c0003t0023others(2): Show | a0001c0001t0001g0038 a0001c0003t0013g0010 a0001c0003t0023g0030 others(2): Show |
5 | 40 | 0.1250 | -10 | c.209 others(33): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |