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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTLN_chr9_17130040_17508923 | 17279830 | G | GGGCCTTT others(21): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
a0001a0002a0005others(8): Show | a0001c0001a0001c0014a0001c0030others(21): Show | a0001c0001t0001a0001c0001t0002a0001c0014t0001others(32): Show | a0001c0001t0001g0205a0001c0001t0002g0204a0001c0014t0001g0038others(60): Show | 63 | 218 | 0.2890 | 28 | c.983 others(45): Show |
CNTLN | ENSG00000044459.15 | transcript | ENST00000380647.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40813038 | C | CCTTTCTT others(21): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00738.hp1 |
a0001 | a0001c0002a0001c0013 | a0001c0002t0001a0001c0013t0001 | a0001c0002t0001g0174a0001c0013t0001g0050 | 2 | 230 | 0.0087 | 28 | c.-76 others(47): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40813058 | T | TCTTTCTT others(21): Show |
intron_variant | MODIFIER | NA18906.hp2 NA18972.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0003a0001c0005t0002 | a0001c0001t0003g0166a0001c0005t0002g0053 | 2 | 230 | 0.0087 | 28 | c.-76 others(47): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40844069 | A | ATTTTTTT others(21): Show |
intron_variant | MODIFIER | HG03704.hp2 NA18952.hp2 NA21309.hp1 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0006a0001c0006t0006 | a0001c0001t0006g0140a0001c0006t0006g0018a0001c0006t0006g0119 | 3 | 230 | 0.0130 | 28 | c.-76 others(47): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40863926 | T | TCCTTCCT others(21): Show |
intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0195a0001c0002t0001g0196 | 2 | 230 | 0.0087 | 28 | c.-76 others(47): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40863926 | T | TCCTTCCT others(21): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02559.hp1 NA19030.hp2 |
a0001 | a0001c0004 | a0001c0004t0001a0001c0004t0002a0001c0004t0007 | a0001c0004t0001g0217a0001c0004t0002g0008a0001c0004t0007g0213 | 3 | 230 | 0.0130 | 28 | c.-76 others(47): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40924881 | C | CATATATA others(21): Show |
intron_variant | MODIFIER | HG01070.hp1 HG01258.hp1 HG01361.hp2 others(11): Show |
a0001a0005 | a0001c0001a0001c0002a0005c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0049a0001c0001t0002g0005a0001c0001t0002g0016others(11): Show | 14 | 230 | 0.0609 | 28 | c.496 others(43): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40925573 | A | ATATATAC others(21): Show |
intron_variant | MODIFIER | HG02572.hp2 | a0001 | a0001c0003 | a0001c0003t0016 | a0001c0003t0016g0226 | 1 | 230 | 0.0044 | 28 | c.496 others(43): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2120364 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0027 | 1 | 116 | 0.0086 | 28 | c.-14 others(49): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2340707 | A | AGAGAGAG others(21): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02647.hp1 HG03139.hp1 |
a0001a0003 | a0001c0001a0001c0002a0003c0008 | a0001c0001t0001a0001c0002t0001a0003c0008t0013 | a0001c0001t0001g0059a0001c0002t0001g0029a0003c0008t0013g0109 | 3 | 116 | 0.0259 | 28 | c.-89 others(45): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2340708 | T | TAGAGAGA others(21): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0006 | a0001c0006t0004 | a0001c0006t0004g0004 | 1 | 116 | 0.0086 | 28 | c.-89 others(45): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2340710 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00438.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0099a0001c0001t0002g0074 | 2 | 116 | 0.0172 | 28 | c.-89 others(45): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2340710 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | HG01256.hp1 HG02074.hp2 |
a0001 | a0001c0001a0001c0007 | a0001c0001t0005a0001c0007t0016 | a0001c0001t0005g0019a0001c0007t0016g0105 | 2 | 116 | 0.0172 | 28 | c.-89 others(45): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2340710 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | HG01258.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0018 | 1 | 116 | 0.0086 | 28 | c.-89 others(45): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2340710 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0081 | 1 | 116 | 0.0086 | 28 | c.-89 others(45): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2340710 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | HG02818.hp1 | a0002 | a0002c0017 | a0002c0017t0008 | a0002c0017t0008g0067 | 1 | 116 | 0.0086 | 28 | c.-89 others(45): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2481033 | T | TTTTCTTT others(21): Show |
intron_variant | MODIFIER | HG01261.hp2 HG01361.hp1 HG02074.hp1 others(3): Show |
a0001a0004a0006 | a0001c0005a0001c0009a0004c0011others(1): Show | a0001c0005t0001a0001c0005t0010a0001c0009t0004others(2): Show | a0001c0005t0001g0090a0001c0005t0010g0085a0001c0009t0004g0005others(3): Show | 6 | 116 | 0.0517 | 28 | c.-88 others(47): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2481055 | T | TTCTTTCT others(21): Show |
intron_variant | MODIFIER | HG03130.hp2 HG03139.hp1 NA19043.hp1 |
a0001a0003 | a0001c0001a0001c0002a0003c0008 | a0001c0001t0003a0001c0002t0001a0003c0008t0013 | a0001c0001t0003g0095a0001c0002t0001g0108a0003c0008t0013g0109 | 3 | 116 | 0.0259 | 28 | c.-88 others(47): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2607610 | C | CCACACAC others(21): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(5): Show | a0001c0001t0001g0050a0001c0001t0001g0099a0001c0001t0002g0028others(7): Show | 10 | 116 | 0.0862 | 28 | c.55+ others(45): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2778304 | A | ATAAGAGA others(21): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(62): Show |
a0001a0004a0005others(3): Show | a0001c0001a0001c0002a0001c0003others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | a0001c0001t0001g0033a0001c0001t0001g0049a0001c0001t0001g0050others(62): Show | 65 | 116 | 0.5603 | 28 | c.358 others(47): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2798365 | A | ATATCTAT others(21): Show |
intron_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0036 | 1 | 116 | 0.0086 | 28 | c.359 others(47): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 6/24 | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2798365 | A | ATATCTAT others(21): Show |
intron_variant | MODIFIER | HG00438.hp1 HG02486.hp2 HG03831.hp2 |
a0001a0007 | a0001c0001a0001c0002a0007c0018 | a0001c0001t0002a0001c0002t0002a0007c0018t0003 | a0001c0001t0002g0074a0001c0002t0002g0078a0007c0018t0003g0062 | 3 | 116 | 0.0259 | 28 | c.359 others(47): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 6/24 | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2815873 | C | CATATATA others(21): Show |
intron_variant | MODIFIER | HG02818.hp2 NA19043.hp2 |
a0001 | a0001c0001a0001c0013 | a0001c0001t0002a0001c0013t0007 | a0001c0001t0002g0086a0001c0013t0007g0056 | 2 | 116 | 0.0172 | 28 | c.359 others(45): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2994613 | A | ATATATAT others(21): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0021 | 1 | 116 | 0.0086 | 28 | c.148 others(47): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2994613 | A | ATATATAT others(21): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0088 | 1 | 116 | 0.0086 | 28 | c.148 others(47): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99201351 | T | TTTCCTTC others(21): Show |
intron_variant | MODIFIER | HG02602.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0053 | 1 | 66 | 0.0152 | 28 | c.-20 others(51): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99213374 | G | GTATATAC others(21): Show |
intron_variant | MODIFIER | NA18939.hp2 NA18957.hp2 |
a0003a0007 | a0003c0003a0007c0007 | a0003c0003t0002a0007c0007t0023 | a0003c0003t0002g0002a0007c0007t0023g0046 | 2 | 66 | 0.0303 | 28 | c.-20 others(51): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99358255 | A | ATTTTTTT others(21): Show |
intron_variant | MODIFIER | HG00733.hp2 NA19000.hp1 |
a0002a0006 | a0002c0002a0006c0006 | a0002c0002t0022a0006c0006t0014 | a0002c0002t0022g0013a0006c0006t0014g0058 | 2 | 66 | 0.0303 | 28 | c.-71 others(47): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99408448 | G | GAAAGAAA others(21): Show |
intron_variant | MODIFIER | HG02735.hp2 HG03041.hp1 NA19000.hp1 others(1): Show |
a0001a0003a0006others(1): Show | a0001c0001a0003c0003a0006c0006others(1): Show | a0001c0001t0014a0003c0003t0002a0006c0006t0014others(1): Show | a0001c0001t0014g0016a0003c0003t0002g0061a0006c0006t0014g0058others(1): Show | 4 | 66 | 0.0606 | 28 | c.-71 others(47): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99408448 | G | GAAAGAAA others(21): Show |
intron_variant | MODIFIER | HG02132.hp1 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0049 | 1 | 66 | 0.0152 | 28 | c.-71 others(47): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99408448 | G | GAAAGAAA others(21): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0004 | a0004c0004 | a0004c0004t0002 | a0004c0004t0002g0041 | 1 | 66 | 0.0152 | 28 | c.-71 others(47): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100090505 | C | CCCTCCCT others(21): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02895.hp1 |
a0002a0010 | a0002c0002a0010c0010 | a0002c0002t0005a0010c0010t0011 | a0002c0002t0005g0015a0010c0010t0011g0009 | 2 | 66 | 0.0303 | 28 | c.158 others(49): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1098787 | C | CATATATA others(21): Show |
intron_variant | MODIFIER | HG01109.hp1 NA18961.hp2 |
a0001 | a0001c0003a0001c0005 | a0001c0003t0001a0001c0005t0001 | a0001c0003t0001g0011a0001c0005t0001g0157 | 2 | 232 | 0.0086 | 28 | c.-83 others(45): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1119322 | C | CGTGTGTG others(21): Show |
intron_variant | MODIFIER | HG01978.hp1 HG02622.hp2 |
a0001 | a0001c0002a0001c0006 | a0001c0002t0001a0001c0006t0002 | a0001c0002t0001g0147a0001c0006t0002g0178 | 2 | 232 | 0.0086 | 28 | c.-83 others(47): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1160344 | G | GTATATAT others(21): Show |
intron_variant | MODIFIER | HG01255.hp1 HG02165.hp2 NA18979.hp1 others(2): Show |
a0001 | a0001c0002a0001c0003a0001c0004others(1): Show | a0001c0002t0001a0001c0003t0001a0001c0004t0001others(1): Show | a0001c0002t0001g0227a0001c0003t0001g0025a0001c0003t0001g0168others(2): Show | 5 | 232 | 0.0216 | 28 | c.55+ others(45): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1160365 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | NA18522.hp1 NA19030.hp2 |
a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0111a0001c0006t0001g0213 | 2 | 232 | 0.0086 | 28 | c.55+ others(45): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1280459 | A | ATTTTTTT others(21): Show |
intron_variant | MODIFIER | HG02738.hp2 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0048 | 1 | 232 | 0.0043 | 28 | c.454 others(45): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146352750 | G | GTTGTTTT others(21): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0021 | 1 | 40 | 0.0250 | 28 | c.97+ others(47): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146451880 | C | CATACGTG others(21): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0003 | a0001c0003t0023 | a0001c0003t0023g0030 | 1 | 40 | 0.0250 | 28 | c.98- others(47): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146638476 | C | CTTTTTTT others(21): Show |
intron_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0006 | a0001c0006t0014 | a0001c0006t0014g0033 | 1 | 40 | 0.0250 | 28 | c.98- others(47): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146721889 | A | ATATATAT others(21): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0003 | a0001c0003t0011 | a0001c0003t0011g0023 | 1 | 40 | 0.0250 | 28 | c.98- others(45): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146735687 | G | GTATGTGC others(21): Show |
intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 NA18522.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003a0001c0013others(1): Show | a0001c0001t0007a0001c0003t0023a0001c0013t0003others(1): Show | a0001c0001t0007g0020a0001c0003t0023g0030a0001c0013t0003g0039others(1): Show | 4 | 40 | 0.1000 | 28 | c.98- others(45): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147347461 | T | TATATATA others(21): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0029 | 1 | 40 | 0.0250 | 28 | c.149 others(49): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147422105 | A | ATATATAT others(21): Show |
intron_variant | MODIFIER | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
a0001a0005 | a0001c0001a0001c0005a0001c0010others(2): Show | a0001c0001t0001a0001c0005t0008a0001c0005t0022others(3): Show | a0001c0001t0001g0038a0001c0005t0008g0005a0001c0005t0022g0032others(3): Show | 6 | 40 | 0.1500 | 28 | c.167 others(49): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147560168 | C | CAAAAAAA others(21): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0012 | a0001c0012t0004 | a0001c0012t0004g0026 | 1 | 40 | 0.0250 | 28 | c.177 others(47): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147784381 | C | CATATATA others(21): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0012 | a0001c0012t0004 | a0001c0012t0004g0026 | 1 | 40 | 0.0250 | 28 | c.209 others(51): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147919459 | C | CTTTCTTT others(21): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0034 | 1 | 40 | 0.0250 | 28 | c.225 others(49): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148106493 | G | GATAGATA others(21): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0011 | a0001c0011t0016 | a0001c0011t0016g0019 | 1 | 40 | 0.0250 | 28 | c.238 others(49): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148136017 | A | AAGGAAGG others(21): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 40 | 0.0250 | 28 | c.255 others(49): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148136017 | A | AAGGAAGG others(21): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0029 | 1 | 40 | 0.0250 | 28 | c.255 others(49): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar |