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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNPY4_chr7_100114634_100130508 | 100121116 | ATTTTTTT others(8): Show |
A | intron_variant | MODIFIER | HG00438.hp2 HG01099.hp1 HG01106.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0024 others(4): Show |
16 | 266 | 0.0602 | -15 | c.119 others(32): Show |
CNPY4 | ENSG00000166997.8 | transcript | ENST00000262932.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNR1_chr6_88134864_88171347 | 88140079 | CAGTACTT others(8): Show |
C | 3_prime_UTR_variant | MODIFIER | NA18612.hp2 | a0001 | a0001c0001 | a0001c0001t0036 | a0001c0001t0036g0179 | 1 | 396 | 0.0025 | -15 | c.*37 others(26): Show |
CNR1 | ENSG00000118432.13 | transcript | ENST00000369501.3 | protein_coding | 2/2 | 3762 | chr6 | TogoVar | ||||||
CNRIP1_chr2_68288010_68324949 | 68297567 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | NA19064.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0159 | 1 | 59 | 0.0169 | -15 | c.331 others(32): Show |
CNRIP1 | ENSG00000119865.9 | transcript | ENST00000263655.4 | protein_coding | 2/2 | chr2 | TogoVar | |||||||
CNST_chr1_246561456_246673595 | 246576445 | TTTTGGTT others(8): Show |
T | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0012a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0192 others(133): Show |
136 | 318 | 0.4277 | -15 | c.-52 others(32): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
CNTD1_chr17_42793861_42816587 | 42801507 | AAAAATAT others(8): Show |
A | intron_variant | MODIFIER | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(4): Show |
a0002 | a0002c0002a0002c0003 | a0002c0002t0001a0002c0003t0001 | a0002c0002t0001g0020 a0002c0002t0001g0050 a0002c0003t0001g0019 others(3): Show |
7 | 303 | 0.0231 | -15 | c.170 others(32): Show |
CNTD1 | ENSG00000176563.10 | transcript | ENST00000588408.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
CNTD1_chr17_42793861_42816587 | 42801509 | AAATATAT others(8): Show |
A | intron_variant | MODIFIER | HG02809.hp1 HG03579.hp2 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0049 a0002c0002t0001g0055 |
2 | 295 | 0.0068 | -15 | c.170 others(32): Show |
CNTD1 | ENSG00000176563.10 | transcript | ENST00000588408.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
CNTFR_chr9_34546433_34594724 | 34546544 | TCCAGCTG others(8): Show |
T | downstream_gene_variant | MODIFIER | HG02559.hp2 NA19043.hp2 |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0009t0001 | a0001c0001t0001g0203 a0001c0009t0001g0061 |
2 | 400 | 0.0050 | -15 | c.*55 others(26): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4888 | chr9 | TogoVar | |||||||
CNTLN_chr9_17130040_17508923 | 17312349 | ATATATAT others(8): Show |
A | intron_variant | MODIFIER | HG01109.hp1 HG02109.hp1 |
a0013 | a0013c0019 | a0013c0019t0002 | a0013c0019t0002g0119 a0013c0019t0002g0120 |
2 | 215 | 0.0093 | -15 | c.134 others(34): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40690764 | ATTTTATT others(8): Show |
A | upstream_gene_variant | MODIFIER | NA18980.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0076 | 1 | 230 | 0.0043 | -15 | c.-19 others(26): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1674 | chr12 | TogoVar | |||||||
CNTN1_chr12_40687439_41077415 | 40690769 | ATTATTTT others(8): Show |
A | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00621.hp1 HG00621.hp2 others(31): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0100 others(31): Show |
34 | 51 | 0.6667 | -15 | c.-18 others(26): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1669 | chr12 | TogoVar | |||||||
CNTN1_chr12_40687439_41077415 | 40698228 | ATTTTTTT others(8): Show |
A | intron_variant | MODIFIER | HG01346.hp2 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0082 | 1 | 24 | 0.0417 | -15 | c.-77 others(32): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40755190 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG00280.hp1 HG01070.hp2 HG01496.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0005 | a0001c0001t0001g0095 a0001c0001t0001g0177 a0001c0001t0001g0208 others(1): Show |
4 | 146 | 0.0274 | -15 | c.-77 others(34): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40877988 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(32): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0118 others(32): Show |
35 | 165 | 0.2121 | -15 | c.-76 others(34): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40977764 | CTGTTTTG others(8): Show |
C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0042 others(72): Show |
75 | 95 | 0.7895 | -15 | c.180 others(34): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74344397 | GTTTTTTT others(8): Show |
G | intron_variant | MODIFIER | NA20300.hp2 | a0011 | a0011c0017 | a0011c0017t0001 | a0011c0017t0001g0115 | 1 | 123 | 0.0081 | -15 | c.136 others(34): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 11/22 | chr3 | TogoVar | |||||||
CNTN3_chr3_74257568_74619659 | 74551754 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG01261.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0064 | 1 | 48 | 0.0208 | -15 | c.-80 others(34): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 1/22 | chr3 | TogoVar | |||||||
CNTN3_chr3_74257568_74619659 | 74614433 | TCGCCGCC others(8): Show |
T | 5_prime_UTR_variant | MODIFIER | HG01884.hp2 HG02257.hp1 HG02615.hp1 others(3): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0026 | a0001c0001t0008a0001c0002t0010a0001c0002t0018others(1): Show | a0001c0001t0008g0001 a0001c0001t0008g0003 a0001c0001t0008g0006 others(3): Show |
6 | 63 | 0.0952 | -15 | c.-13 others(24): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 1/23 | 93322 | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2287626 | GAGAAGGA others(8): Show |
G | intron_variant | MODIFIER | HG04184.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0048 | 1 | 115 | 0.0087 | -15 | c.-14 others(36): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2287678 | AGAAGAAG others(8): Show |
A | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp1 HG02451.hp1 others(2): Show |
a0001a0003a0006 | a0001c0001a0001c0002a0001c0025others(2): Show | a0001c0001t0002a0001c0002t0001a0001c0025t0001others(2): Show | a0001c0001t0002g0086 a0001c0002t0001g0033 a0001c0025t0001g0099 others(2): Show |
5 | 107 | 0.0467 | -15 | c.-14 others(36): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2527421 | CTGCTGCT others(8): Show |
C | intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0086 | 1 | 116 | 0.0086 | -15 | c.-88 others(34): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2983213 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02965.hp2 others(1): Show |
a0001a0006 | a0001c0005a0001c0006a0006c0027 | a0001c0005t0001a0001c0006t0003a0006c0027t0001 | a0001c0005t0001g0091 a0001c0005t0001g0092 a0001c0006t0003g0069 others(1): Show |
4 | 5 | 0.8000 | -15 | c.135 others(34): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99355811 | GTTTTTTT others(8): Show |
G | intron_variant | MODIFIER | HG01081.hp1 | a0006 | a0006c0005 | a0006c0005t0018 | a0006c0005t0018g0028 | 1 | 66 | 0.0152 | -15 | c.-71 others(34): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99380094 | TGTGTGTG others(8): Show |
T | intron_variant | MODIFIER | HG06807.hp1 NA18957.hp2 NA20300.hp1 |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0006 | a0001c0001t0005a0003c0003t0002a0004c0006t0013 | a0001c0001t0005g0048 a0003c0003t0002g0002 a0004c0006t0013g0025 |
3 | 66 | 0.0455 | -15 | c.-71 others(34): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99432449 | TCTTTTCT others(8): Show |
T | intron_variant | MODIFIER | HG01169.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0043 | 1 | 66 | 0.0152 | -15 | c.-71 others(36): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99523597 | GATAGAAT others(8): Show |
G | intron_variant | MODIFIER | HG02976.hp1 | a0003 | a0003c0003 | a0003c0003t0007 | a0003c0003t0007g0034 | 1 | 56 | 0.0179 | -15 | c.-70 others(34): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99523639 | TAGAATAG others(8): Show |
T | intron_variant | MODIFIER | HG02004.hp2 HG02723.hp2 HG03041.hp1 others(1): Show |
a0001a0008a0012 | a0001c0001a0008c0012a0012c0013 | a0001c0001t0001a0001c0001t0004a0008c0012t0008others(1): Show | a0001c0001t0001g0004 a0001c0001t0004g0044 a0008c0012t0008g0026 others(1): Show |
4 | 66 | 0.0606 | -15 | c.-70 others(34): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99523648 | ATAGAACA others(8): Show |
A | intron_variant | MODIFIER | HG01123.hp2 HG01496.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0012a0003c0003t0002 | a0001c0001t0012g0018 a0003c0003t0002g0015 |
2 | 66 | 0.0303 | -15 | c.-70 others(34): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | chr11 | TogoVar | |||||||
CNTN5_chr11_99015949_100363885 | 99523649 | TAGAACAG others(8): Show |
T | intron_variant | MODIFIER | HG01243.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0002a0005c0004others(1): Show | a0001c0001t0005a0002c0002t0004a0002c0002t0005others(2): Show | a0001c0001t0005g0012 a0001c0001t0005g0048 a0002c0002t0004g0007 others(3): Show |
6 | 57 | 0.1053 | -15 | c.-70 others(34): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99523694 | CAGAATAG others(8): Show |
C | intron_variant | MODIFIER | HG02257.hp2 HG02602.hp2 NA18957.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0015 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0015g0064 |
3 | 59 | 0.0508 | -15 | c.-70 others(34): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 100291748 | TAATAATA others(8): Show |
T | intron_variant | MODIFIER | HG02976.hp1 | a0003 | a0003c0003 | a0003c0003t0007 | a0003c0003t0007g0034 | 1 | 66 | 0.0152 | -15 | c.231 others(34): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1245265 | ATATATAT others(8): Show |
A | intron_variant | MODIFIER | HG00609.hp1 HG02165.hp1 HG03654.hp2 others(6): Show |
a0001a0002a0007 | a0001c0001a0001c0003a0002c0011others(1): Show | a0001c0001t0001a0001c0003t0001a0002c0011t0001others(1): Show | a0001c0001t0001g0037 a0001c0001t0001g0104 a0001c0001t0001g0106 others(6): Show |
9 | 229 | 0.0393 | -15 | c.358 others(34): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | chr3 | TogoVar | |||||||
CNTN6_chr3_1088024_1409217 | 1245269 | ATATATAC others(8): Show |
A | intron_variant | MODIFIER | HG02109.hp1 | a0005 | a0005c0027 | a0005c0027t0001 | a0005c0027t0001g0191 | 1 | 230 | 0.0043 | -15 | c.358 others(34): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | chr3 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 146370260 | TAAAAAAA others(8): Show |
T | intron_variant | MODIFIER | HG02717.hp1 NA18522.hp1 |
a0001a0002 | a0001c0013a0002c0017 | a0001c0013t0003a0002c0017t0015 | a0001c0013t0003g0039 a0002c0017t0015g0037 |
2 | 16 | 0.1250 | -15 | c.97+ others(34): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146483283 | ATATATAT others(8): Show |
A | intron_variant | MODIFIER | HG02451.hp1 HG02897.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0007 a0001c0002t0001g0008 |
2 | 31 | 0.0645 | -15 | c.98- others(34): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | chr7 | TogoVar | |||||||
CNTNAP2_chr7_146111801_148425998 | 146486046 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02630.hp1 |
a0001a0003 | a0001c0012a0003c0014 | a0001c0012t0004a0003c0014t0021 | a0001c0012t0004g0026 a0003c0014t0021g0022 |
2 | 5 | 0.4000 | -15 | c.98- others(34): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146525573 | TATCTCTC others(8): Show |
T | intron_variant | MODIFIER | HG02630.hp2 HG02976.hp1 |
a0001 | a0001c0002a0001c0015 | a0001c0002t0002a0001c0015t0001 | a0001c0002t0002g0013 a0001c0015t0001g0011 |
2 | 40 | 0.0500 | -15 | c.98- others(34): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146985308 | ATTTTTTT others(8): Show |
A | intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0013 | 1 | 7 | 0.1429 | -15 | c.403 others(34): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147062127 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG03098.hp2 |
a0001a0003 | a0001c0002a0003c0014 | a0001c0002t0001a0003c0014t0021 | a0001c0002t0001g0021 a0003c0014t0021g0022 |
2 | 12 | 0.1667 | -15 | c.550 others(34): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147216548 | AACACTAA others(8): Show |
A | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp1 HG02451.hp2 others(22): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(20): Show | a0001c0001t0001g0003 a0001c0001t0002g0006 a0001c0001t0007g0018 others(22): Show |
25 | 40 | 0.6250 | -15 | c.134 others(36): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147237049 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG02717.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0018a0001c0002t0002a0001c0005t0008others(3): Show | a0001c0001t0018g0001 a0001c0002t0002g0040 a0001c0005t0008g0005 others(3): Show |
6 | 8 | 0.7500 | -15 | c.134 others(36): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147462365 | AACAAGAA others(8): Show |
A | intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0009 | 1 | 40 | 0.0250 | -15 | c.167 others(36): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147741709 | TAAAGCTA others(8): Show |
T | intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 40 | 0.0250 | -15 | c.209 others(38): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147832543 | CAATATAT others(8): Show |
C | intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0020 | 1 | 40 | 0.0250 | -15 | c.209 others(36): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148380081 | ACGTACTG others(8): Show |
A | intron_variant | MODIFIER | NA18522.hp1 | a0001 | a0001c0013 | a0001c0013t0003 | a0001c0013t0003g0039 | 1 | 40 | 0.0250 | -15 | c.347 others(34): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | chr7 | TogoVar | |||||||
CNTNAP3B_chr9_41885536_42134426 | 41888506 | CTAAAATA others(8): Show |
C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
a0002a0003a0005others(17): Show | a0002c0002a0002c0010a0002c0015others(23): Show | a0002c0002t0001a0002c0002t0012a0002c0002t0022others(31): Show | a0002c0002t0001g0040 a0002c0002t0001g0043 a0002c0002t0001g0044 others(56): Show |
59 | 66 | 0.8939 | -15 | c.*54 others(26): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 2029 | chr9 | TogoVar | |||||||
CNTNAP3_chr9_39059710_39293167 | 39204967 | AATCATCA others(8): Show |
A | intron_variant | MODIFIER | HG02109.hp2 | a0003 | a0003c0001 | a0003c0001t0002 | a0003c0001t0002g0004 | 1 | 2 | 0.5000 | -15 | c.391 others(34): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | TogoVar | |||||||
CNTNAP3_chr9_39059710_39293167 | 39213186 | GAGAGGAG others(8): Show |
G | intron_variant | MODIFIER | HG02109.hp2 | a0003 | a0003c0001 | a0003c0001t0002 | a0003c0001t0002g0004 | 1 | 2 | 0.5000 | -15 | c.391 others(34): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | TogoVar | |||||||
CNTNAP4_chr16_76272401_76565757 | 76418148 | TGTCATTA others(8): Show |
T | intron_variant | MODIFIER | HG02486.hp2 HG03516.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0046 a0001c0001t0005g0202 |
2 | 272 | 0.0074 | -15 | c.391 others(32): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 3/23 | chr16 | TogoVar | |||||||
CNTNAP4_chr16_76272401_76565757 | 76522687 | CTTTCTTT others(8): Show |
C | intron_variant | MODIFIER | HG00423.hp2 HG00597.hp1 HG02132.hp2 others(5): Show |
a0001a0006a0023 | a0001c0001a0001c0004a0006c0009others(1): Show | a0001c0001t0001a0001c0001t0009a0001c0004t0001others(2): Show | a0001c0001t0001g0105 a0001c0001t0001g0123 a0001c0001t0009g0231 others(5): Show |
8 | 171 | 0.0468 | -15 | c.275 others(32): Show |
CNTNAP4 | ENSG00000152910.19 | transcript | ENST00000611870.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CNTNAP5_chr2_124020287_124926219 | 124086188 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG02922.hp2 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | 18 | 0.1111 | -15 | c.82+ others(32): Show |
CNTNAP5 | ENSG00000155052.15 | transcript | ENST00000682447.1 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |