regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN5_chr11_99015949_100363885 | 99432504 | C | CTTTCT | intron_variant | MODIFIER | HG00733.hp1 HG01081.hp1 HG01934.hp1 others(7): Show |
a0001a0003a0005others(2): Show | a0001c0001a0003c0003a0005c0005others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(7): Show | a0001c0001t0001g0054a0001c0001t0004g0044a0001c0001t0009g0063others(7): Show | 10 | 66 | 0.1515 | 5 | c.-71 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99433371 | A | AATGTG | intron_variant | MODIFIER | HG01169.hp1 HG01169.hp2 HG01934.hp2 others(6): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0005a0001c0001t0009a0002c0002t0004others(5): Show | a0001c0001t0005g0048a0001c0001t0009g0043a0002c0002t0004g0007others(6): Show | 9 | 66 | 0.1364 | 5 | c.-71 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99448730 | T | TTTTTA | intron_variant | MODIFIER | HG00738.hp1 HG01099.hp2 HG01123.hp2 others(14): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0012a0002c0002t0003others(9): Show | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0012g0018others(14): Show | 17 | 66 | 0.2576 | 5 | c.-70 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99452372 | G | GTTTTT | intron_variant | MODIFIER | HG00735.hp2 HG01081.hp2 HG01496.hp1 others(18): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0003c0003others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(16): Show | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0006g0032others(18): Show | 21 | 66 | 0.3182 | 5 | c.-70 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99523597 | G | GATAGA | intron_variant | MODIFIER | HG01169.hp2 HG02735.hp2 |
a0003a0006 | a0003c0003a0006c0006 | a0003c0003t0002a0006c0006t0001 | a0003c0003t0002g0061a0006c0006t0001g0005 | 2 | 66 | 0.0303 | 5 | c.-70 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99523709 | T | TAGAAC | intron_variant | MODIFIER | HG02602.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
a0001a0009a0011 | a0001c0001a0009c0012a0011c0009 | a0001c0001t0006a0009c0012t0008a0011c0009t0005 | a0001c0001t0006g0040a0001c0001t0006g0066a0009c0012t0008g0026others(1): Show | 4 | 66 | 0.0606 | 5 | c.-70 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99525997 | T | TTTTAA | intron_variant | MODIFIER | HG02257.hp1 HG02257.hp2 HG02602.hp2 others(7): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0015others(6): Show | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0006g0032others(7): Show | 10 | 66 | 0.1515 | 5 | c.-70 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99620926 | T | TTTCTC | intron_variant | MODIFIER | HG00733.hp1 HG01081.hp1 HG01081.hp2 others(23): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(16): Show | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0004g0029others(23): Show | 26 | 66 | 0.3939 | 5 | c.55+ others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99643857 | T | TTAAAA | intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(56): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0002a0003c0003others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(34): Show | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0020others(56): Show | 59 | 66 | 0.8939 | 5 | c.55+ others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99645102 | T | TAAAAA | intron_variant | MODIFIER | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(22): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(16): Show | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0004g0010others(22): Show | 25 | 66 | 0.3788 | 5 | c.55+ others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99675011 | C | CTGGTT | intron_variant | MODIFIER | HG02602.hp1 HG02895.hp2 NA19000.hp2 |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0006a0004c0004t0002a0004c0004t0013 | a0001c0001t0006g0066a0004c0004t0002g0001a0004c0004t0013g0050 | 3 | 66 | 0.0455 | 5 | c.55+ others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99675013 | G | GGTTTT | intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(35): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(22): Show | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0020others(35): Show | 38 | 66 | 0.5758 | 5 | c.55+ others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99698281 | A | ATAACT | intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(52): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0002a0003c0003others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(35): Show | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0052others(52): Show | 55 | 66 | 0.8333 | 5 | 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 | 99753119 | C | CTTTTT | intron_variant | MODIFIER | HG00735.hp2 HG01496.hp2 HG01934.hp2 others(6): Show |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0004 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(3): Show | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0011g0062others(6): Show | 9 | 66 | 0.1364 | 5 | c.56- others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99804551 | A | ATTACT | intron_variant | MODIFIER | HG00735.hp2 HG01123.hp2 HG01496.hp2 others(8): Show |
a0001a0003a0006others(1): Show | a0001c0001a0003c0003a0006c0006others(1): Show | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(5): Show | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0011g0062others(8): Show | 11 | 66 | 0.1667 | 5 | c.56- others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99919802 | A | ATTTAT | intron_variant | MODIFIER | HG02132.hp1 HG02735.hp2 HG02976.hp1 others(3): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0006a0001c0001t0016a0002c0002t0008others(3): Show | a0001c0001t0006g0040a0001c0001t0016g0049a0002c0002t0008g0019others(3): Show | 6 | 66 | 0.0909 | 5 | c.673 others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100080302 | T | TTTTTC | intron_variant | MODIFIER | HG00733.hp2 HG02257.hp1 NA18957.hp1 others(1): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0011others(1): Show | a0001c0001t0001a0002c0002t0022a0003c0011t0019others(1): Show | a0001c0001t0001g0052a0002c0002t0022g0013a0003c0011t0019g0059others(1): Show | 4 | 66 | 0.0606 | 5 | c.158 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100090507 | C | CTCCCT | intron_variant | MODIFIER | HG02602.hp1 HG02735.hp1 NA18939.hp2 others(1): Show |
a0001a0003a0007 | a0001c0001a0003c0003a0007c0007 | a0001c0001t0006a0003c0003t0002a0007c0007t0023 | a0001c0001t0006g0032a0001c0001t0006g0066a0003c0003t0002g0002others(1): Show | 4 | 66 | 0.0606 | 5 | c.158 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100149230 | G | GAAAGT | intron_variant | MODIFIER | HG01169.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
a0001a0003a0004others(2): Show | a0001c0001a0003c0011a0004c0004others(2): Show | a0001c0001t0010a0003c0011t0019a0004c0004t0013others(3): Show | a0001c0001t0010g0023a0003c0011t0019g0059a0004c0004t0013g0050others(3): Show | 6 | 66 | 0.0909 | 5 | c.158 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100150525 | T | TTAATC | intron_variant | MODIFIER | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(10): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(6): Show | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(10): Show | 13 | 66 | 0.1970 | 5 | c.158 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100153848 | C | CAGTAA | intron_variant | MODIFIER | HG02965.hp1 NA20300.hp1 |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0005a0006c0006t0011 | a0001c0001t0005g0048a0006c0006t0011g0033 | 2 | 66 | 0.0303 | 5 | c.158 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100159518 | A | AGAGAT | intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0009a0002c0002t0022 | a0001c0001t0009g0063a0002c0002t0022g0013 | 2 | 66 | 0.0303 | 5 | c.158 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1088755 | C | CTTTTT | upstream_gene_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG02280.hp1 others(4): Show |
a0001 | a0001c0002a0001c0005a0001c0006others(3): Show | a0001c0002t0009a0001c0005t0001a0001c0006t0001others(3): Show | a0001c0002t0009g0205a0001c0005t0001g0207a0001c0006t0001g0200others(4): Show | 7 | 232 | 0.0302 | 5 | c.-44 others(16): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4268 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1157229 | A | AATTTT | intron_variant | MODIFIER | HG00609.hp2 HG00738.hp1 HG00738.hp2 others(47): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(12): Show | a0001c0001t0001g0035a0001c0001t0001g0071a0001c0001t0001g0082others(47): Show | 50 | 232 | 0.2155 | 5 | c.55+ others(20): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1182585 | C | CATTCT | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(148): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(28): Show | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0027others(148): Show | 151 | 232 | 0.6509 | 5 | c.55+ others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245223 | T | TATAAC | intron_variant | MODIFIER | HG00738.hp1 HG01106.hp2 HG01361.hp1 others(3): Show |
a0001 | a0001c0002a0001c0004a0001c0008 | a0001c0002t0001a0001c0004t0001a0001c0008t0001 | a0001c0002t0001g0084a0001c0004t0001g0041a0001c0004t0001g0073others(3): Show | 6 | 232 | 0.0259 | 5 | c.358 others(24): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245266 | T | TATAAC | intron_variant | MODIFIER | HG00639.hp1 HG01175.hp1 HG01255.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0012 | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 7 | 232 | 0.0302 | 5 | c.358 others(24): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245268 | T | TATAAC | intron_variant | MODIFIER | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(4): Show | a0001c0001t0001g0067a0001c0001t0001g0095a0001c0001t0001g0096others(11): Show | 14 | 232 | 0.0603 | 5 | c.358 others(24): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245301 | T | TATAAC | intron_variant | MODIFIER | HG02165.hp2 HG03516.hp1 |
a0001 | a0001c0003a0001c0005 | a0001c0003t0001a0001c0005t0001 | a0001c0003t0001g0025a0001c0005t0001g0164 | 2 | 232 | 0.0086 | 5 | c.358 others(24): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245302 | A | ATATAT | intron_variant | MODIFIER | HG01952.hp1 HG03239.hp2 NA20129.hp2 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0001a0001c0002t0007a0001c0005t0001 | a0001c0002t0001g0099a0001c0002t0007g0059a0001c0005t0001g0230 | 3 | 232 | 0.0129 | 5 | c.358 others(24): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1255425 | A | AAAAAG | intron_variant | MODIFIER | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(10): Show |
a0001a0002a0004 | a0001c0002a0001c0003a0001c0005others(7): Show | a0001c0002t0001a0001c0002t0009a0001c0003t0001others(8): Show | a0001c0002t0001g0209a0001c0002t0009g0205a0001c0003t0001g0219others(10): Show | 13 | 232 | 0.0560 | 5 | c.359 others(24): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1265044 | C | CTTTTT | intron_variant | MODIFIER | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
a0001 | a0001c0002a0001c0003a0001c0006others(1): Show | a0001c0002t0001a0001c0002t0003a0001c0002t0004others(3): Show | a0001c0002t0001g0209a0001c0002t0003g0079a0001c0002t0004g0228others(3): Show | 6 | 232 | 0.0259 | 5 | c.359 others(24): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1319833 | G | GAAAAT | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(48): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(12): Show | a0001c0001t0001g0033a0001c0001t0001g0054a0001c0001t0001g0057others(48): Show | 51 | 232 | 0.2198 | 5 | c.762 others(22): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTNAP1_chr17_42677531_42704993 | 42686469 | G | GTTTTT | intron_variant | MODIFIER | HG00597.hp1 HG01175.hp1 HG02015.hp2 others(12): Show |
a0001a0008 | a0001c0001a0001c0005a0008c0013 | a0001c0001t0002a0001c0005t0002a0008c0013t0001 | a0001c0001t0002g0047a0001c0001t0002g0115a0001c0001t0002g0116others(10): Show | 15 | 364 | 0.0412 | 5 | c.900 others(20): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
CNTNAP1_chr17_42677531_42704993 | 42686476 | T | TTTTTG | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
a0001 | a0001c0001a0001c0004a0001c0018 | a0001c0001t0002a0001c0004t0002a0001c0018t0002 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0009others(10): Show | 36 | 364 | 0.0989 | 5 | c.900 others(20): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
CNTNAP1_chr17_42677531_42704993 | 42686479 | T | TTGTTG | intron_variant | MODIFIER | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
a0001 | a0001c0002a0001c0010a0001c0011 | a0001c0002t0001a0001c0010t0001a0001c0011t0001 | a0001c0002t0001g0008a0001c0002t0001g0098a0001c0002t0001g0099others(8): Show | 15 | 364 | 0.0412 | 5 | c.900 others(20): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146135724 | C | CATACA | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(1): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0019others(1): Show | a0001c0001t0007a0001c0003t0020a0001c0019t0006others(1): Show | a0001c0001t0007g0020a0001c0003t0020g0017a0001c0019t0006g0015others(1): Show | 4 | 40 | 0.1000 | 5 | c.97+ others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146243068 | T | TTTAAG | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp1 others(32): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(27): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(32): Show | 35 | 40 | 0.8750 | 5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146285172 | T | TAAGTA | intron_variant | MODIFIER | HG02486.hp2 HG03540.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0010a0001c0003t0011 | a0001c0002t0010g0002a0001c0003t0011g0023 | 2 | 40 | 0.0500 | 5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146285891 | T | TTCCCC | intron_variant | MODIFIER | HG02630.hp2 HG02976.hp1 |
a0001 | a0001c0002a0001c0015 | a0001c0002t0002a0001c0015t0001 | a0001c0002t0002g0013a0001c0015t0001g0011 | 2 | 40 | 0.0500 | 5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146330012 | C | CTTTTT | intron_variant | MODIFIER | HG02630.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0012a0001c0002t0002a0001c0003t0023others(2): Show | a0001c0001t0012g0034a0001c0002t0002g0013a0001c0003t0023g0030others(2): Show | 5 | 40 | 0.1250 | 5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146337624 | T | TTTTTG | intron_variant | MODIFIER | HG01891.hp2 HG02486.hp2 HG02886.hp1 others(11): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0006a0001c0001t0012a0001c0002t0001others(9): Show | a0001c0001t0006g0009a0001c0001t0012g0034a0001c0002t0001g0008others(11): Show | 14 | 40 | 0.3500 | 5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146404124 | C | CAAAAA | intron_variant | MODIFIER | HG02630.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
a0001a0002 | a0001c0002a0001c0005a0001c0008others(3): Show | a0001c0002t0002a0001c0005t0022a0001c0008t0001others(3): Show | a0001c0002t0002g0013a0001c0005t0022g0032a0001c0008t0001g0025others(3): Show | 6 | 40 | 0.1500 | 5 | c.97+ others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146457196 | A | AAATAC | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
a0001a0004 | a0001c0002a0001c0004a0001c0012others(1): Show | a0001c0002t0001a0001c0004t0003a0001c0004t0005others(2): Show | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0004t0003g0035others(4): Show | 7 | 40 | 0.1750 | 5 | c.98- others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146461420 | A | ATATAT | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
a0001a0004 | a0001c0002a0001c0004a0001c0012others(1): Show | a0001c0002t0001a0001c0004t0003a0001c0004t0005others(2): Show | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0004t0003g0035others(4): Show | 7 | 40 | 0.1750 | 5 | c.98- others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146585101 | G | GTGTTT | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(15): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0006a0001c0002t0001others(13): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0006g0009others(15): Show | 18 | 40 | 0.4500 | 5 | c.98- others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146591407 | G | GGAGCT | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp1 others(34): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(28): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(34): Show | 37 | 40 | 0.9250 | 5 | c.98- others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146669849 | A | AGTTCT | intron_variant | MODIFIER | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(28): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(25): Show | a0001c0001t0001g0003a0001c0001t0002g0006a0001c0001t0006g0009others(28): Show | 31 | 40 | 0.7750 | 5 | c.98- others(24): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146684639 | C | CAAAAA | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02451.hp2 others(8): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0012a0001c0002t0001others(7): Show | a0001c0001t0002g0006a0001c0001t0012g0034a0001c0002t0001g0007others(8): Show | 11 | 40 | 0.2750 | 5 | c.98- others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146720995 | A | ATACTC | intron_variant | MODIFIER | HG02451.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
a0001 | a0001c0002a0001c0008a0001c0010others(1): Show | a0001c0002t0001a0001c0002t0002a0001c0008t0001others(2): Show | a0001c0002t0001g0007a0001c0002t0002g0013a0001c0008t0001g0025others(2): Show | 5 | 40 | 0.1250 | 5 | c.98- others(22): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |