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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNOT6L_chr4_77708387_77824368 | 77714437 | TTAAAAAA others(17): Show |
T | 3_prime_UTR_variant | MODIFIER | NA19075.hp2 | a0001 | a0001c0001 | a0001c0001t0046 | a0001c0001t0046g0246 | 1 | 328 | 0.0031 | -24 | c.*59 others(35): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 12/12 | 5970 | chr4 | TogoVar | |||||
CNOT6L_chr4_77708387_77824368 | 77743586 | CTTTTTTT others(17): Show |
C | intron_variant | MODIFIER | HG01993.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0221 | 1 | 328 | 0.0031 | -24 | c.717 others(41): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 7/11 | chr4 | TogoVar | ||||||
CNOT6L_chr4_77708387_77824368 | 77768470 | AATAAATA others(17): Show |
A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(28): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(235): Show | 239 | 328 | 0.7287 | -24 | c.400 others(41): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | TogoVar | ||||||
CNOT6L_chr4_77708387_77824368 | 77768474 | AATATATA others(17): Show |
A | intron_variant | MODIFIER | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0037a0001c0001t0038 | a0001c0001t0001g0140a0001c0001t0037g0269a0001c0001t0038g0223 | 3 | 328 | 0.0092 | -24 | c.400 others(41): Show |
CNOT6L | ENSG00000138767.14 | transcript | ENST00000504123.7 | protein_coding | 4/11 | chr4 | TogoVar | ||||||
CNOT6_chr5_180489379_180583358 | 180539551 | CTTTTTTT others(17): Show |
C | intron_variant | MODIFIER | HG00741.hp2 HG01257.hp2 HG01358.hp2 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(6): Show | a0001c0001t0001g0265a0001c0001t0003g0170a0001c0001t0003g0181others(14): Show | 17 | 334 | 0.0509 | -24 | c.112 others(43): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
CNOT9_chr2_218563839_218602080 | 218583219 | GTGTGTGT others(17): Show |
G | intron_variant | MODIFIER | NA18952.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0213 | 1 | 322 | 0.0031 | -24 | c.320 others(39): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNOT9_chr2_218563839_218602080 | 218583221 | GTGTGTGT others(17): Show |
G | intron_variant | MODIFIER | HG00558.hp2 HG00621.hp1 HG02135.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0010a0001c0001t0048others(1): Show | a0001c0001t0004g0010a0001c0001t0004g0038a0001c0001t0004g0040others(10): Show | 18 | 322 | 0.0559 | -24 | c.320 others(39): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNOT9_chr2_218563839_218602080 | 218583227 | GTGTGTGT others(17): Show |
G | intron_variant | MODIFIER | HG02135.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0076 | 1 | 322 | 0.0031 | -24 | c.320 others(39): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNOT9_chr2_218563839_218602080 | 218583231 | GTGTCTCT others(17): Show |
G | intron_variant | MODIFIER | HG02155.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0029 | a0001c0001t0002g0026a0001c0001t0003g0026a0001c0001t0003g0027others(1): Show | 5 | 322 | 0.0155 | -24 | c.320 others(39): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
CNR1_chr6_88134864_88171347 | 88136582 | GATTCATC others(17): Show |
G | downstream_gene_variant | MODIFIER | HG00735.hp2 NA19043.hp1 |
a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0070a0001c0001t0017g0089 | 2 | 398 | 0.0050 | -24 | c.*72 others(35): Show |
CNR1 | ENSG00000118432.13 | transcript | ENST00000369501.3 | protein_coding | 3281 | chr6 | TogoVar | ||||||
CNRIP1_chr2_68288010_68324949 | 68305272 | ATATGTGT others(17): Show |
A | intron_variant | MODIFIER | HG02129.hp1 HG02735.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0025 | 2 | 424 | 0.0047 | -24 | c.331 others(43): Show |
CNRIP1 | ENSG00000119865.9 | transcript | ENST00000263655.4 | protein_coding | 2/2 | chr2 | TogoVar | ||||||
CNTLN_chr9_17130040_17508923 | 17237354 | TACACACA others(17): Show |
T | intron_variant | MODIFIER | HG03209.hp1 | a0020 | a0020c0041 | a0020c0041t0001 | a0020c0041t0001g0106 | 1 | 218 | 0.0046 | -24 | c.849 others(39): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTLN_chr9_17130040_17508923 | 17295987 | AGAGAGAG others(17): Show |
A | intron_variant | MODIFIER | HG01109.hp2 NA18951.hp1 NA18978.hp2 |
a0002a0005a0014 | a0002c0006a0005c0005a0014c0034 | a0002c0006t0002a0005c0005t0001a0014c0034t0001 | a0002c0006t0002g0144a0005c0005t0001g0093a0014c0034t0001g0088 | 3 | 218 | 0.0138 | -24 | c.984 others(41): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40767993 | CATTTCTA others(17): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0042others(217): Show | 220 | 230 | 0.9565 | -24 | c.-77 others(43): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40830791 | GTATATAT others(17): Show |
G | intron_variant | MODIFIER | HG00408.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0100 | 1 | 230 | 0.0044 | -24 | c.-76 others(43): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40836068 | GTATATAT others(17): Show |
G | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(24): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0002a0001c0001t0007a0001c0003t0005others(7): Show | a0001c0001t0002g0059a0001c0001t0007g0058a0001c0003t0005g0070others(24): Show | 27 | 230 | 0.1174 | -24 | c.-76 others(43): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40975178 | TTATATAT others(17): Show |
T | intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0117 | 1 | 230 | 0.0044 | -24 | c.180 others(43): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN3_chr3_74257568_74619659 | 74285790 | GATATATA others(17): Show |
G | intron_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0132 | 1 | 174 | 0.0058 | -24 | c.251 others(41): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 19/22 | chr3 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74344396 | GGTTTTTT others(17): Show |
G | intron_variant | MODIFIER | HG01346.hp2 HG01884.hp1 HG01978.hp2 others(14): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(10): Show | a0001c0001t0001g0112a0001c0001t0001g0140a0001c0001t0002g0038others(14): Show | 17 | 174 | 0.0977 | -24 | c.136 others(43): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 11/22 | chr3 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74344397 | GTTTTTTT others(17): Show |
G | intron_variant | MODIFIER | HG02293.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
a0001a0003 | a0001c0010a0003c0003a0003c0026 | a0001c0010t0003a0003c0003t0002a0003c0003t0007others(1): Show | a0001c0010t0003g0025a0003c0003t0002g0079a0003c0003t0007g0074others(1): Show | 4 | 174 | 0.0230 | -24 | c.136 others(43): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 11/22 | chr3 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74614433 | TCGCCGCC others(17): Show |
T | 5_prime_UTR_variant | MODIFIER | HG02809.hp1 HG02965.hp2 |
a0001a0003 | a0001c0002a0003c0003 | a0001c0002t0012a0003c0003t0012 | a0001c0002t0012g0011a0003c0003t0012g0012 | 2 | 174 | 0.0115 | -24 | c.-14 others(33): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 1/23 | 93322 | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2287626 | GAGAAGGA others(17): Show |
G | intron_variant | MODIFIER | NA18990.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0075 | 1 | 116 | 0.0086 | -24 | c.-14 others(45): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2287687 | AGAAGAGG others(17): Show |
A | intron_variant | MODIFIER | HG01978.hp2 HG03130.hp1 HG03130.hp2 |
a0001a0002 | a0001c0002a0001c0003a0002c0016 | a0001c0002t0001a0001c0003t0002a0002c0016t0003 | a0001c0002t0001g0108a0001c0003t0002g0073a0002c0016t0003g0079 | 3 | 116 | 0.0259 | -24 | c.-14 others(45): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2287693 | GGAAGAAG others(17): Show |
G | intron_variant | MODIFIER | HG00438.hp1 HG02074.hp1 HG02818.hp2 |
a0001 | a0001c0001a0001c0009a0001c0013 | a0001c0001t0002a0001c0009t0004a0001c0013t0007 | a0001c0001t0002g0074a0001c0009t0004g0005a0001c0013t0007g0056 | 3 | 116 | 0.0259 | -24 | c.-14 others(45): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2374018 | AGGATTAG others(17): Show |
A | intron_variant | MODIFIER | HG02257.hp2 HG02647.hp2 HG02818.hp2 |
a0001 | a0001c0001a0001c0010a0001c0013 | a0001c0001t0008a0001c0010t0003a0001c0013t0007 | a0001c0001t0008g0089a0001c0010t0003g0011a0001c0013t0007g0056 | 3 | 116 | 0.0259 | -24 | c.-89 others(43): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2547230 | ATATTTAT others(17): Show |
A | intron_variant | MODIFIER | HG01257.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0106 | 1 | 116 | 0.0086 | -24 | c.-88 others(43): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2708727 | TCACACAC others(17): Show |
T | intron_variant | MODIFIER | HG01175.hp2 | a0001 | a0001c0003 | a0001c0003t0006 | a0001c0003t0006g0040 | 1 | 116 | 0.0086 | -24 | c.56- others(41): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2742556 | ACAGCGAA others(17): Show |
A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(101): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(23): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(49): Show | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0049others(101): Show | 104 | 116 | 0.8966 | -24 | c.183 others(41): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99284600 | GGTGTGTG others(17): Show |
G | intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0032 | 1 | 66 | 0.0152 | -24 | c.-20 others(45): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99422516 | TTTTATAT others(17): Show |
T | intron_variant | MODIFIER | HG03130.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0040 | 1 | 66 | 0.0152 | -24 | c.-71 others(43): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99889291 | GGTGTGTG others(17): Show |
G | intron_variant | MODIFIER | NA19000.hp1 | a0006 | a0006c0006 | a0006c0006t0014 | a0006c0006t0014g0058 | 1 | 66 | 0.0152 | -24 | c.578 others(43): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99923753 | GTCTGTCT others(17): Show |
G | intron_variant | MODIFIER | NA19000.hp1 | a0006 | a0006c0006 | a0006c0006t0014 | a0006c0006t0014g0058 | 1 | 66 | 0.0152 | -24 | c.673 others(41): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99934925 | TATATATA others(17): Show |
T | intron_variant | MODIFIER | HG00738.hp1 HG01099.hp2 HG03130.hp1 others(1): Show |
a0002a0005a0012 | a0002c0002a0005c0005a0012c0013 | a0002c0002t0003a0005c0005t0001a0012c0013t0008 | a0002c0002t0003g0036a0002c0002t0003g0037a0005c0005t0001g0035others(1): Show | 4 | 66 | 0.0606 | -24 | c.673 others(43): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100094765 | AAAGGAAG others(17): Show |
A | intron_variant | MODIFIER | HG01169.hp1 HG01496.hp2 HG01934.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0009a0001c0001t0012 | a0001c0001t0001g0052a0001c0001t0009g0043a0001c0001t0012g0018others(1): Show | 4 | 66 | 0.0606 | -24 | c.158 others(45): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100155691 | TTCCTTGA others(17): Show |
T | intron_variant | MODIFIER | HG03041.hp1 | a0009 | a0009c0012 | a0009c0012t0008 | a0009c0012t0008g0026 | 1 | 66 | 0.0152 | -24 | c.158 others(45): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1300557 | AAAAGAAA others(17): Show |
A | intron_variant | MODIFIER | HG01123.hp1 HG02896.hp2 HG03516.hp2 |
a0001 | a0001c0002a0001c0003a0001c0006 | a0001c0002t0001a0001c0003t0001a0001c0006t0001 | a0001c0002t0001g0094a0001c0003t0001g0219a0001c0006t0001g0210 | 3 | 232 | 0.0129 | -24 | c.761 others(41): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1406922 | TTCAGGCC others(17): Show |
T | downstream_gene_variant | MODIFIER | NA19000.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0053 | 1 | 232 | 0.0043 | -24 | c.*35 others(35): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2706 | chr3 | TogoVar | ||||||
CNTNAP1_chr17_42677531_42704993 | 42685742 | ATGAAATA others(17): Show |
A | intron_variant | MODIFIER | NA18968.hp2 | a0003 | a0003c0012 | a0003c0012t0001 | a0003c0012t0001g0062 | 1 | 364 | 0.0028 | -24 | c.716 others(39): Show |
CNTNAP1 | ENSG00000108797.12 | transcript | ENST00000264638.9 | protein_coding | 5/23 | chr17 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 146151674 | ATATATAT others(17): Show |
A | intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0002 | a0001c0002t0010 | a0001c0002t0010g0002 | 1 | 40 | 0.0250 | -24 | c.97+ others(41): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146457481 | AATATATA others(17): Show |
A | intron_variant | MODIFIER | HG02451.hp2 HG02896.hp1 |
a0001a0005 | a0001c0001a0005c0020 | a0001c0001t0002a0005c0020t0005 | a0001c0001t0002g0006a0005c0020t0005g0016 | 2 | 40 | 0.0500 | -24 | c.98- others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146477624 | AACACACA others(17): Show |
A | intron_variant | MODIFIER | HG02717.hp1 | a0002 | a0002c0017 | a0002c0017t0015 | a0002c0017t0015g0037 | 1 | 40 | 0.0250 | -24 | c.98- others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146721562 | CTATATAT others(17): Show |
C | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp2 HG02717.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0018a0001c0002t0001others(6): Show | a0001c0001t0001g0038a0001c0001t0018g0001a0001c0002t0001g0007others(7): Show | 10 | 40 | 0.2500 | -24 | c.98- others(41): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146855807 | GTATATAT others(17): Show |
G | intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0002 | a0001c0002t0010 | a0001c0002t0010g0002 | 1 | 40 | 0.0250 | -24 | c.402 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147062127 | CAAAAAAA others(17): Show |
C | intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0019 | a0001c0019t0006 | a0001c0019t0006g0015 | 1 | 40 | 0.0250 | -24 | c.550 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147104873 | CATATATA others(17): Show |
C | intron_variant | MODIFIER | HG02451.hp2 HG02886.hp2 HG02896.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0005others(3): Show | a0001c0001t0002a0001c0004t0003a0001c0005t0022others(3): Show | a0001c0001t0002g0006a0001c0004t0003g0035a0001c0004t0003g0036others(4): Show | 7 | 40 | 0.1750 | -24 | c.551 others(41): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147347433 | TATATATG others(17): Show |
T | intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0008 | a0001c0008t0001 | a0001c0008t0001g0025 | 1 | 40 | 0.0250 | -24 | c.149 others(45): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147557030 | GGGAGGCT others(17): Show |
G | intron_variant | MODIFIER | HG02717.hp1 | a0002 | a0002c0017 | a0002c0017t0015 | a0002c0017t0015g0037 | 1 | 40 | 0.0250 | -24 | c.177 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148061954 | TATAGATA others(17): Show |
T | intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0011 | a0001c0011t0016 | a0001c0011t0016g0019 | 1 | 40 | 0.0250 | -24 | c.238 others(45): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148283288 | AAAGAAAG others(17): Show |
A | intron_variant | MODIFIER | HG02451.hp1 HG02630.hp1 |
a0001 | a0001c0002a0001c0012 | a0001c0002t0001a0001c0012t0004 | a0001c0002t0001g0007a0001c0012t0004g0026 | 2 | 40 | 0.0500 | -24 | c.347 others(45): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148413424 | ATATATAT others(17): Show |
A | intron_variant | MODIFIER | HG02922.hp1 HG03540.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0012a0001c0002t0010 | a0001c0001t0012g0034a0001c0002t0010g0002 | 2 | 40 | 0.0500 | -24 | c.379 others(43): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 23/23 | chr7 | TogoVar |