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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN1_chr12_40687439_41077415 | 40690769 | ATTATTTT others(13): Show |
A | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00673.hp1 HG00733.hp2 others(25): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(11): Show | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(25): Show | 28 | 230 | 0.1217 | -20 | c.-18 others(31): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1669 | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40707221 | CTTTTTCT others(13): Show |
C | intron_variant | MODIFIER | NA18980.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0076 | 1 | 230 | 0.0044 | -20 | c.-77 others(39): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40707227 | CTTTTTTT others(13): Show |
C | intron_variant | MODIFIER | HG01981.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0005 | 1 | 230 | 0.0044 | -20 | c.-77 others(39): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40795301 | ACACACAC others(13): Show |
A | intron_variant | MODIFIER | HG01255.hp2 NA18984.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0118a0001c0002t0001g0035 | 2 | 230 | 0.0087 | -20 | c.-77 others(41): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40872208 | TTGTTTGT others(13): Show |
T | intron_variant | MODIFIER | HG02109.hp2 HG03130.hp1 HG03471.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007 | a0001c0001t0003g0222a0001c0001t0003g0224a0001c0001t0007g0055 | 3 | 230 | 0.0130 | -20 | c.-76 others(39): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40961650 | TAAGATTT others(13): Show |
T | intron_variant | MODIFIER | HG01070.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0012 | 1 | 230 | 0.0044 | -20 | c.180 others(39): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 15/23 | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40975178 | TTATATAT others(13): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(34): Show |
a0001 | a0001c0001a0001c0004a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0037a0001c0001t0001g0076a0001c0001t0001g0077others(34): Show | 37 | 230 | 0.1609 | -20 | c.180 others(39): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40982708 | AAAACCTG others(13): Show |
A | intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0012 | a0001c0012t0021 | a0001c0012t0021g0204 | 1 | 230 | 0.0044 | -20 | c.196 others(39): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 16/23 | chr12 | TogoVar | ||||||
CNTN2_chr1_205038212_205083289 | 205080525 | TACACACA others(13): Show |
T | downstream_gene_variant | MODIFIER | NA19009.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0059 | 1 | 380 | 0.0026 | -20 | c.*67 others(31): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2237 | chr1 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74285790 | GATATATA others(13): Show |
G | intron_variant | MODIFIER | HG01884.hp1 HG01952.hp1 HG02129.hp2 others(4): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0003 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(2): Show | a0001c0001t0001g0099a0001c0001t0001g0112a0001c0001t0001g0118others(4): Show | 7 | 174 | 0.0402 | -20 | c.251 others(37): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 19/22 | chr3 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74344397 | GTTTTTTT others(13): Show |
G | intron_variant | MODIFIER | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
a0001a0002a0003 | a0001c0002a0002c0004a0002c0005others(2): Show | a0001c0002t0019a0002c0004t0028a0002c0005t0002others(3): Show | a0001c0002t0019g0002a0002c0004t0028g0137a0002c0005t0002g0037others(4): Show | 7 | 174 | 0.0402 | -20 | c.136 others(39): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 11/22 | chr3 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74460772 | CATATATA others(13): Show |
C | intron_variant | MODIFIER | HG02257.hp1 HG03225.hp2 HG03486.hp1 others(1): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0003c0023others(1): Show | a0001c0001t0008a0001c0002t0002a0003c0023t0016others(1): Show | a0001c0001t0008g0001a0001c0002t0002g0044a0003c0023t0016g0096others(1): Show | 4 | 174 | 0.0230 | -20 | c.358 others(39): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 4/22 | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2269902 | GTTTGTTT others(13): Show |
G | intron_variant | MODIFIER | HG00140.hp1 HG00639.hp2 HG00738.hp1 others(8): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(7): Show | a0001c0001t0001g0099a0001c0001t0002g0055a0001c0001t0005g0098others(8): Show | 11 | 116 | 0.0948 | -20 | c.-14 others(41): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2269910 | GTTTGTTT others(13): Show |
G | intron_variant | MODIFIER | HG01175.hp2 | a0001 | a0001c0003 | a0001c0003t0006 | a0001c0003t0006g0040 | 1 | 116 | 0.0086 | -20 | c.-14 others(41): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2708727 | TCACACAC others(13): Show |
T | intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0006 | a0001c0006t0004 | a0001c0006t0004g0004 | 1 | 116 | 0.0086 | -20 | c.56- others(37): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99063507 | CATAAATA others(13): Show |
C | intron_variant | MODIFIER | HG01496.hp1 HG02004.hp1 HG02258.hp1 others(6): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(4): Show | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0004g0029others(6): Show | 9 | 66 | 0.1364 | -20 | c.-21 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99284600 | GGTGTGTG others(13): Show |
G | intron_variant | MODIFIER | HG03130.hp2 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0006 | a0001c0001t0005g0048a0001c0001t0006g0040 | 2 | 66 | 0.0303 | -20 | c.-20 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99383069 | CTGGTCTT others(13): Show |
C | intron_variant | MODIFIER | HG01169.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
a0001a0003a0010 | a0001c0001a0003c0003a0010c0010 | a0001c0001t0009a0003c0003t0002a0003c0003t0007others(1): Show | a0001c0001t0009g0043a0003c0003t0002g0027a0003c0003t0007g0034others(1): Show | 4 | 66 | 0.0606 | -20 | c.-71 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99523644 | TAGAATAG others(13): Show |
T | intron_variant | MODIFIER | HG02257.hp1 HG02723.hp1 |
a0001a0003 | a0001c0001a0003c0011 | a0001c0001t0001a0003c0011t0019 | a0001c0001t0001g0008a0003c0011t0019g0059 | 2 | 66 | 0.0303 | -20 | c.-70 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99523649 | TAGAACAG others(13): Show |
T | intron_variant | MODIFIER | HG03471.hp1 | a0008 | a0008c0008 | a0008c0008t0007 | a0008c0008t0007g0038 | 1 | 66 | 0.0152 | -20 | c.-70 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99523694 | CAGAATAG others(13): Show |
C | intron_variant | MODIFIER | HG02735.hp1 HG02895.hp2 NA18939.hp1 |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0004 | a0001c0001t0006a0003c0003t0017a0004c0004t0013 | a0001c0001t0006g0032a0003c0003t0017g0065a0004c0004t0013g0050 | 3 | 66 | 0.0455 | -20 | c.-70 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99556554 | AATATATA others(13): Show |
A | intron_variant | MODIFIER | HG02109.hp1 | a0005 | a0005c0005 | a0005c0005t0010 | a0005c0005t0010g0006 | 1 | 66 | 0.0152 | -20 | c.55+ others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99732418 | AACTCAGT others(13): Show |
A | intron_variant | MODIFIER | HG00733.hp1 HG01123.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0009 | a0001c0001t0003g0060a0001c0001t0009g0063 | 2 | 66 | 0.0303 | -20 | c.56- others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99934898 | GTATATAT others(13): Show |
G | intron_variant | MODIFIER | HG01099.hp1 HG01123.hp2 HG01169.hp2 others(2): Show |
a0001a0003a0006 | a0001c0001a0003c0003a0006c0006 | a0001c0001t0001a0001c0001t0004a0003c0003t0002others(1): Show | a0001c0001t0001g0054a0001c0001t0004g0010a0003c0003t0002g0012others(2): Show | 5 | 66 | 0.0758 | -20 | c.673 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99934929 | TATATATA others(13): Show |
T | intron_variant | MODIFIER | HG02976.hp1 HG03041.hp1 |
a0003a0009 | a0003c0003a0009c0012 | a0003c0003t0007a0009c0012t0008 | a0003c0003t0007g0034a0009c0012t0008g0026 | 2 | 66 | 0.0303 | -20 | c.673 others(39): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100094765 | AAAGGAAG others(13): Show |
A | intron_variant | MODIFIER | HG00735.hp1 | a0006 | a0006c0006 | a0006c0006t0009 | a0006c0006t0009g0042 | 1 | 66 | 0.0152 | -20 | c.158 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100161830 | TACACACA others(13): Show |
T | intron_variant | MODIFIER | HG01243.hp1 | a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0039 | 1 | 66 | 0.0152 | -20 | c.158 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100204295 | CTAATATA others(13): Show |
C | intron_variant | MODIFIER | HG01123.hp2 | a0003 | a0003c0003 | a0003c0003t0002 | a0003c0003t0002g0012 | 1 | 66 | 0.0152 | -20 | c.188 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 15/24 | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100204297 | AATATATA others(13): Show |
A | intron_variant | MODIFIER | NA19043.hp1 | a0011 | a0011c0009 | a0011c0009t0005 | a0011c0009t0005g0056 | 1 | 66 | 0.0152 | -20 | c.188 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1202543 | AAAATAAA others(13): Show |
A | intron_variant | MODIFIER | HG00140.hp1 HG00733.hp2 HG00735.hp1 others(10): Show |
a0001 | a0001c0002a0001c0004a0001c0005others(2): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0005others(4): Show | a0001c0002t0001g0098a0001c0002t0001g0116a0001c0002t0001g0122others(10): Show | 13 | 232 | 0.0560 | -20 | c.56- others(37): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245262 | TATATATA others(13): Show |
T | intron_variant | MODIFIER | HG03209.hp2 | a0005 | a0005c0026 | a0005c0026t0001 | a0005c0026t0001g0091 | 1 | 232 | 0.0043 | -20 | c.358 others(39): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1300449 | CAGGAAGG others(13): Show |
C | intron_variant | MODIFIER | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(20): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0008others(8): Show | a0001c0001t0001g0190a0001c0002t0001g0209a0001c0002t0008g0221others(20): Show | 23 | 232 | 0.0991 | -20 | c.761 others(37): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1300557 | AAAAGAAA others(13): Show |
A | intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0020 | a0001c0020t0001 | a0001c0020t0001g0151 | 1 | 232 | 0.0043 | -20 | c.761 others(37): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146151662 | ATATATAT others(13): Show |
A | intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0040 | 1 | 40 | 0.0250 | -20 | c.97+ others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146151678 | ATATGTAT others(13): Show |
A | intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0015 | a0001c0015t0001 | a0001c0015t0001g0011 | 1 | 40 | 0.0250 | -20 | c.97+ others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146285735 | CCTCGCCT others(13): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02886.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0006a0001c0003t0013 | a0001c0001t0006g0009a0001c0003t0013g0010 | 2 | 40 | 0.0500 | -20 | c.97+ others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146285886 | TTCCCTTC others(13): Show |
T | intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0007 | 1 | 40 | 0.0250 | -20 | c.97+ others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146356052 | TACACACA others(13): Show |
T | intron_variant | MODIFIER | HG02630.hp2 HG02922.hp2 HG02976.hp1 others(2): Show |
a0001a0002 | a0001c0002a0001c0004a0001c0010others(2): Show | a0001c0002t0002a0001c0004t0005a0001c0010t0002others(2): Show | a0001c0002t0002g0013a0001c0004t0005g0004a0001c0010t0002g0014others(2): Show | 5 | 40 | 0.1250 | -20 | c.97+ others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146457481 | AATATATA others(13): Show |
A | intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0003 | a0001c0003t0013 | a0001c0003t0013g0010 | 1 | 40 | 0.0250 | -20 | c.98- others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146761284 | TGGAAGGA others(13): Show |
T | intron_variant | MODIFIER | HG02451.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
a0001 | a0001c0001a0001c0005a0001c0008others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0005t0008others(4): Show | a0001c0001t0001g0003a0001c0001t0002g0006a0001c0005t0008g0005others(4): Show | 7 | 40 | 0.1750 | -20 | c.98- others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146851650 | CTGTGTGT others(13): Show |
C | intron_variant | MODIFIER | HG02486.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
a0001a0002 | a0001c0002a0001c0003a0002c0017 | a0001c0002t0001a0001c0002t0002a0001c0003t0011others(1): Show | a0001c0002t0001g0021a0001c0002t0002g0013a0001c0003t0011g0023others(1): Show | 4 | 40 | 0.1000 | -20 | c.402 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146855807 | GTATATAT others(13): Show |
G | intron_variant | MODIFIER | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
a0001 | a0001c0002a0001c0003a0001c0010others(1): Show | a0001c0002t0001a0001c0003t0013a0001c0010t0002others(1): Show | a0001c0002t0001g0007a0001c0002t0001g0021a0001c0003t0013g0010others(2): Show | 5 | 40 | 0.1250 | -20 | c.402 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146856261 | TATAGATA others(13): Show |
T | intron_variant | MODIFIER | HG02976.hp1 HG03139.hp1 NA20129.hp2 |
a0001 | a0001c0003a0001c0008a0001c0015 | a0001c0003t0023a0001c0008t0001a0001c0015t0001 | a0001c0003t0023g0030a0001c0008t0001g0025a0001c0015t0001g0011 | 3 | 40 | 0.0750 | -20 | c.402 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146885928 | GGTGTGTG others(13): Show |
G | intron_variant | MODIFIER | HG02717.hp1 | a0002 | a0002c0017 | a0002c0017t0015 | a0002c0017t0015g0037 | 1 | 40 | 0.0250 | -20 | c.402 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147033160 | GTATATAT others(13): Show |
G | intron_variant | MODIFIER | HG02717.hp2 HG02897.hp1 HG02922.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0007a0001c0002t0001a0001c0002t0002others(4): Show | a0001c0001t0007g0018a0001c0002t0001g0008a0001c0002t0002g0040others(4): Show | 7 | 40 | 0.1750 | -20 | c.403 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147066248 | GTCGTCAG others(13): Show |
G | intron_variant | MODIFIER | HG02717.hp1 HG02922.hp2 HG03139.hp1 |
a0001a0002 | a0001c0004a0001c0008a0002c0017 | a0001c0004t0005a0001c0008t0001a0002c0017t0015 | a0001c0004t0005g0004a0001c0008t0001g0025a0002c0017t0015g0037 | 3 | 40 | 0.0750 | -20 | c.550 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147902794 | GTGTGTGT others(13): Show |
G | intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0015 | a0001c0015t0001 | a0001c0015t0001g0011 | 1 | 40 | 0.0250 | -20 | c.209 others(37): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148061954 | TATAGATA others(13): Show |
T | intron_variant | MODIFIER | HG02451.hp1 HG02896.hp1 NA18522.hp2 others(2): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0002c0016others(1): Show | a0001c0001t0001a0001c0001t0007a0001c0002t0001others(2): Show | a0001c0001t0001g0038a0001c0001t0007g0018a0001c0002t0001g0007others(2): Show | 5 | 40 | 0.1250 | -20 | c.238 others(41): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148123633 | CAGGAAGG others(13): Show |
C | intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0002 | a0001c0002t0010 | a0001c0002t0010g0002 | 1 | 40 | 0.0250 | -20 | c.255 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148137669 | AAAGGAAG others(13): Show |
A | intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 40 | 0.0250 | -20 | c.255 others(39): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |