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 | 99738635 | GTGTGTGT others(1): Show |
G | intron_variant | MODIFIER | HG02723.hp1 HG02895.hp2 |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0001a0004c0004t0013 | a0001c0001t0001g0008a0004c0004t0013g0050 | 2 | 66 | 0.0303 | -8 | c.56- others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99752039 | ACTTCCAG others(1): Show |
A | intron_variant | MODIFIER | HG00735.hp2 HG01123.hp2 HG01243.hp1 others(17): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0003c0003others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(13): Show | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0006g0040others(17): Show | 20 | 66 | 0.3030 | -8 | c.56- others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99889291 | GGTGTGTG others(1): Show |
G | intron_variant | MODIFIER | HG01243.hp2 HG02602.hp2 NA18957.hp2 others(1): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0005a0002c0002t0001others(1): Show | a0001c0001t0001g0053a0001c0001t0005g0014a0002c0002t0001g0003others(1): Show | 4 | 66 | 0.0606 | -8 | c.578 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99934941 | TATATATA others(1): Show |
T | intron_variant | MODIFIER | HG00735.hp2 HG01081.hp1 HG01169.hp1 others(6): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0009a0001c0001t0011others(5): Show | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0009g0043others(6): Show | 9 | 66 | 0.1364 | -8 | c.673 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100021661 | GATGTATG others(1): Show |
G | intron_variant | MODIFIER | HG02965.hp1 NA20300.hp1 |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0005a0006c0006t0011 | a0001c0001t0005g0048a0006c0006t0011g0033 | 2 | 66 | 0.0303 | -8 | c.980 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100094765 | AAAGGAAG others(1): Show |
A | intron_variant | MODIFIER | HG02257.hp1 HG06807.hp2 NA18522.hp2 others(1): Show |
a0001a0003a0012 | a0001c0001a0003c0003a0003c0011others(1): Show | a0001c0001t0001a0003c0003t0007a0003c0011t0019others(1): Show | a0001c0001t0001g0020a0003c0003t0007g0057a0003c0011t0019g0059others(1): Show | 4 | 66 | 0.0606 | -8 | c.158 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100113417 | CAAAAAAA others(1): Show |
C | intron_variant | MODIFIER | HG02723.hp2 HG02886.hp2 HG02895.hp2 others(6): Show |
a0001a0003a0004others(2): Show | a0001c0001a0003c0003a0004c0004others(2): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(6): Show | a0001c0001t0004g0044a0001c0001t0005g0048a0001c0001t0006g0040others(6): Show | 9 | 66 | 0.1364 | -8 | c.158 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100161830 | TACACACA others(1): Show |
T | intron_variant | MODIFIER | NA19000.hp1 NA19070.hp1 |
a0002a0006 | a0002c0002a0006c0006 | a0002c0002t0001a0006c0006t0014 | a0002c0002t0001g0003a0006c0006t0014g0058 | 2 | 66 | 0.0303 | -8 | c.158 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100176851 | GGTGTGTG others(1): Show |
G | intron_variant | MODIFIER | HG01081.hp2 HG01099.hp1 HG01123.hp2 others(11): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(5): Show | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(11): Show | 14 | 66 | 0.2121 | -8 | c.158 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100204431 | TATCTATA others(1): Show |
T | intron_variant | MODIFIER | HG02132.hp2 NA18957.hp2 |
a0003a0004 | a0003c0003a0004c0004 | a0003c0003t0002a0004c0004t0002 | a0003c0003t0002g0002a0004c0004t0002g0051 | 2 | 66 | 0.0303 | -8 | c.188 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100291751 | TAATAAAT others(1): Show |
T | intron_variant | MODIFIER | HG00738.hp1 HG01099.hp2 NA19043.hp2 |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0008 | a0002c0002t0003g0036a0002c0002t0003g0037a0002c0002t0008g0019 | 3 | 66 | 0.0455 | -8 | c.231 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1142966 | GTGTATAT others(1): Show |
G | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp1 |
a0001a0006 | a0001c0005a0006c0027 | a0001c0005t0001a0006c0027t0001 | a0001c0005t0001g0188a0006c0027t0001g0191 | 2 | 232 | 0.0086 | -8 | c.-82 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1142968 | GTATATAT others(1): Show |
G | intron_variant | MODIFIER | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(29): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(10): Show | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0097others(29): Show | 32 | 232 | 0.1379 | -8 | c.-82 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1152124 | ATATTTGT others(1): Show |
A | intron_variant | MODIFIER | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
a0001a0002a0003 | a0001c0003a0001c0005a0001c0006others(5): Show | a0001c0003t0001a0001c0005t0001a0001c0006t0001others(6): Show | a0001c0003t0001g0219a0001c0005t0001g0005a0001c0006t0001g0037others(10): Show | 13 | 232 | 0.0560 | -8 | c.55+ others(23): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1158891 | CATATATA others(1): Show |
C | intron_variant | MODIFIER | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
a0001a0003 | a0001c0005a0001c0010a0001c0021others(1): Show | a0001c0005t0001a0001c0010t0001a0001c0021t0001others(1): Show | a0001c0005t0001g0005a0001c0010t0001g0009a0001c0010t0001g0206others(3): Show | 6 | 232 | 0.0259 | -8 | c.55+ others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1158953 | TACACACA others(1): Show |
T | intron_variant | MODIFIER | HG00609.hp2 HG02559.hp2 HG02922.hp1 others(2): Show |
a0001 | a0001c0002a0001c0004a0001c0008 | a0001c0002t0001a0001c0004t0001a0001c0008t0001 | a0001c0002t0001g0160a0001c0004t0001g0083a0001c0008t0001g0075others(2): Show | 5 | 232 | 0.0216 | -8 | c.55+ others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1160361 | TATATATA others(1): Show |
T | intron_variant | MODIFIER | HG00639.hp1 HG01175.hp1 HG01255.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003a0001c0012 | a0001c0001t0001a0001c0003t0001a0001c0012t0001 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0153others(3): Show | 6 | 232 | 0.0259 | -8 | c.55+ others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1172620 | CTGTGTGT others(1): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0005others(6): Show | a0001c0001t0001g0126a0001c0002t0001g0098a0001c0002t0001g0116others(13): Show | 16 | 232 | 0.0690 | -8 | c.55+ others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1201099 | TTGTGTGT others(1): Show |
T | intron_variant | MODIFIER | HG01099.hp1 HG01123.hp1 HG02109.hp2 others(13): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(8): Show | a0001c0001t0001g0086a0001c0001t0001g0204a0001c0002t0001g0045others(13): Show | 16 | 232 | 0.0690 | -8 | c.56- others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1202543 | AAAATAAA others(1): Show |
A | intron_variant | MODIFIER | HG01099.hp1 HG01123.hp1 HG01496.hp2 others(37): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0004others(15): Show | a0001c0001t0001g0173a0001c0001t0001g0190a0001c0001t0001g0204others(37): Show | 40 | 232 | 0.1724 | -8 | c.56- others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1215685 | GTTTTACT others(1): Show |
G | 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 | -8 | 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(1): Show |
G | intron_variant | MODIFIER | HG00741.hp1 HG01109.hp2 HG01515.hp1 others(6): Show |
a0001 | a0001c0002a0001c0003a0001c0005others(2): Show | a0001c0002t0001a0001c0002t0004a0001c0003t0001others(3): Show | a0001c0002t0001g0138a0001c0002t0001g0139a0001c0002t0001g0147others(6): Show | 9 | 232 | 0.0388 | -8 | c.358 others(27): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1277346 | CTTTTTTT others(1): Show |
C | intron_variant | MODIFIER | HG00609.hp1 HG01070.hp2 HG01099.hp2 others(73): Show |
a0001a0002a0007 | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0005others(21): Show | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0047others(73): Show | 76 | 232 | 0.3276 | -8 | 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 | 1300449 | CAGGAAGG others(1): Show |
C | intron_variant | MODIFIER | HG00140.hp2 HG00642.hp2 HG01106.hp1 others(14): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(4): Show | a0001c0001t0001a0001c0003t0001a0001c0005t0001others(5): Show | a0001c0001t0001g0071a0001c0003t0001g0026a0001c0003t0001g0118others(14): Show | 17 | 232 | 0.0733 | -8 | 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 | 1300557 | AAAAGAAA others(1): Show |
A | intron_variant | MODIFIER | HG01261.hp2 HG01496.hp1 HG02015.hp1 others(6): Show |
a0001 | a0001c0002a0001c0003a0001c0005others(1): Show | a0001c0002t0001a0001c0002t0003a0001c0003t0001others(3): Show | a0001c0002t0001g0227a0001c0002t0003g0079a0001c0003t0001g0101others(6): Show | 9 | 232 | 0.0388 | -8 | 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 | 1301024 | CTTTTTTT others(1): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp2 HG00639.hp1 others(53): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(12): Show | a0001c0001t0001g0013a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 56 | 232 | 0.2414 | -8 | 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 | 1384666 | CTATATAT others(1): Show |
C | intron_variant | MODIFIER | HG03492.hp2 HG03669.hp1 HG03710.hp2 |
a0001 | a0001c0009a0001c0010 | a0001c0009t0001a0001c0009t0003a0001c0010t0001 | a0001c0009t0001g0114a0001c0009t0003g0051a0001c0010t0001g0056 | 3 | 232 | 0.0129 | -8 | c.251 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1384681 | TATATATA others(1): Show |
T | intron_variant | MODIFIER | HG00609.hp1 HG00642.hp2 HG01099.hp2 others(45): Show |
a0001a0005 | a0001c0001a0001c0004a0001c0005others(4): Show | a0001c0001t0001a0001c0004t0001a0001c0005t0001others(8): Show | a0001c0001t0001g0033a0001c0001t0001g0044a0001c0001t0001g0088others(45): Show | 48 | 232 | 0.2069 | -8 | c.251 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1384732 | TATATATA others(1): Show |
T | intron_variant | MODIFIER | HG02055.hp2 HG02257.hp2 HG03579.hp1 |
a0001 | a0001c0007a0001c0021 | a0001c0007t0001a0001c0021t0001 | a0001c0007t0001g0012a0001c0007t0001g0222a0001c0021t0001g0231 | 3 | 232 | 0.0129 | -8 | c.251 others(25): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146254157 | ACACACAA others(1): Show |
A | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG02486.hp1 |
a0001 | a0001c0001a0001c0006a0001c0019 | a0001c0001t0007a0001c0006t0014a0001c0019t0006 | a0001c0001t0007g0020a0001c0006t0014g0033a0001c0019t0006g0015 | 3 | 40 | 0.0750 | -8 | 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 | 146269339 | AAATCAAT others(1): Show |
A | intron_variant | MODIFIER | HG03225.hp2 NA18522.hp1 |
a0001 | a0001c0013a0001c0018 | a0001c0013t0003a0001c0018t0002 | a0001c0013t0003g0039a0001c0018t0002g0012 | 2 | 40 | 0.0500 | -8 | 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 | 146298531 | TCTGAGAA others(1): Show |
T | intron_variant | MODIFIER | HG02486.hp2 HG03540.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0010a0001c0003t0011 | a0001c0002t0010g0002a0001c0003t0011g0023 | 2 | 40 | 0.0500 | -8 | 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 | 146303072 | ATGTGTGT others(1): Show |
A | intron_variant | MODIFIER | HG02717.hp1 HG02922.hp1 HG02922.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0010others(1): Show | a0001c0001t0007a0001c0001t0012a0001c0001t0018others(3): Show | a0001c0001t0007g0018a0001c0001t0012g0034a0001c0001t0018g0001others(3): Show | 6 | 40 | 0.1500 | -8 | 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 | 146356052 | TACACACA others(1): Show |
T | intron_variant | MODIFIER | HG01891.hp2 HG02922.hp1 HG03225.hp2 |
a0001 | a0001c0001a0001c0018 | a0001c0001t0006a0001c0001t0012a0001c0018t0002 | a0001c0001t0006g0009a0001c0001t0012g0034a0001c0018t0002g0012 | 3 | 40 | 0.0750 | -8 | 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 | 146358022 | TTTTATTT others(1): Show |
T | intron_variant | MODIFIER | HG02630.hp1 HG02886.hp1 NA19030.hp1 |
a0001 | a0001c0001a0001c0003a0001c0012 | a0001c0001t0001a0001c0003t0013a0001c0012t0004 | a0001c0001t0001g0038a0001c0003t0013g0010a0001c0012t0004g0026 | 3 | 40 | 0.0750 | -8 | 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 | 146369029 | GTATATAT others(1): Show |
G | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0002a0001c0001t0006a0001c0002t0001others(1): Show | a0001c0001t0002g0006a0001c0001t0006g0009a0001c0002t0001g0021others(1): Show | 4 | 40 | 0.1000 | -8 | 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 | 146380784 | CTTTTTTT others(1): Show |
C | intron_variant | MODIFIER | HG02630.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
a0001 | a0001c0002a0001c0003a0001c0005others(4): Show | a0001c0002t0002a0001c0003t0023a0001c0005t0008others(4): Show | a0001c0002t0002g0013a0001c0003t0023g0030a0001c0005t0008g0005others(4): Show | 7 | 40 | 0.1750 | -8 | 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 | 146395826 | GGAGAGAG others(1): Show |
G | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG02897.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0007a0001c0001t0018a0001c0002t0001others(3): Show | a0001c0001t0007g0020a0001c0001t0018g0001a0001c0002t0001g0008others(3): Show | 6 | 40 | 0.1500 | -8 | 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 | 146411819 | TTTATTTA others(1): Show |
T | intron_variant | MODIFIER | HG02717.hp2 HG02976.hp2 HG03098.hp1 |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0003t0020a0001c0005t0008 | a0001c0001t0001g0003a0001c0003t0020g0017a0001c0005t0008g0005 | 3 | 40 | 0.0750 | -8 | 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 | 146426402 | TATATATA others(1): Show |
T | intron_variant | MODIFIER | HG01891.hp2 HG03225.hp1 NA18522.hp2 others(1): Show |
a0001 | a0001c0001a0001c0009a0001c0010 | a0001c0001t0006a0001c0001t0007a0001c0009t0019others(1): Show | a0001c0001t0006g0009a0001c0001t0007g0018a0001c0009t0019g0027others(1): Show | 4 | 40 | 0.1000 | -8 | 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 | 146457481 | AATATATA others(1): Show |
A | intron_variant | MODIFIER | HG03139.hp2 NA20129.hp2 |
a0001 | a0001c0003a0001c0011 | a0001c0003t0023a0001c0011t0016 | a0001c0003t0023g0030a0001c0011t0016g0019 | 2 | 40 | 0.0500 | -8 | 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 | 146486046 | CTTTTTTT others(1): Show |
C | intron_variant | MODIFIER | HG02451.hp1 HG02897.hp1 HG02922.hp2 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0004t0005 | a0001c0002t0001g0007a0001c0002t0001g0008a0001c0004t0005g0004 | 3 | 40 | 0.0750 | -8 | 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 | 146525532 | TTATCTAT others(1): Show |
T | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG02922.hp2 |
a0001 | a0001c0001a0001c0004a0001c0019 | a0001c0001t0007a0001c0004t0005a0001c0019t0006 | a0001c0001t0007g0020a0001c0004t0005g0004a0001c0019t0006g0015 | 3 | 40 | 0.0750 | -8 | 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 | 146555492 | GTCTGTCT others(1): Show |
G | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp2 others(10): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0006a0001c0001t0007a0001c0002t0001others(8): Show | a0001c0001t0006g0009a0001c0001t0007g0020a0001c0002t0001g0007others(10): Show | 13 | 40 | 0.3250 | -8 | 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 | 146596595 | CAGAGAGA others(1): Show |
C | intron_variant | MODIFIER | HG03540.hp1 HG03540.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0010a0001c0003t0004 | a0001c0002t0010g0002a0001c0003t0004g0029 | 2 | 40 | 0.0500 | -8 | 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 | 146622275 | CTATCTAT others(1): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0002a0001c0010 | a0001c0001t0006a0001c0002t0001a0001c0010t0002 | a0001c0001t0006g0009a0001c0002t0001g0007a0001c0010t0002g0014 | 3 | 40 | 0.0750 | -8 | 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 | 146668428 | CTGTGTGT others(1): Show |
C | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 HG03139.hp2 others(1): Show |
a0001 | a0001c0001a0001c0011a0001c0019 | a0001c0001t0007a0001c0011t0016a0001c0019t0006 | a0001c0001t0007g0018a0001c0001t0007g0020a0001c0011t0016g0019others(1): Show | 4 | 40 | 0.1000 | -8 | 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 | 146759681 | CAAAAAAA others(1): Show |
C | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0019others(1): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0018others(4): Show | a0001c0001t0006g0009a0001c0001t0007g0020a0001c0001t0018g0001others(4): Show | 7 | 40 | 0.1750 | -8 | 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 | 146761284 | TGGAAGGA others(1): Show |
T | intron_variant | MODIFIER | HG00735.hp1 HG02630.hp1 HG02717.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0006a0001c0012others(1): Show | a0001c0001t0001a0001c0001t0012a0001c0006t0014others(2): Show | a0001c0001t0001g0038a0001c0001t0012g0034a0001c0006t0014g0033others(2): Show | 5 | 40 | 0.1250 | -8 | 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 | 146799973 | GTATGAAA others(1): Show |
G | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(28): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(24): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(28): Show | 31 | 40 | 0.7750 | -8 | c.208 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |