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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN1_chr12_40687439_41077415 | 40690758 | TATTTTAT others(7): Show |
T | upstream_gene_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0004 | a0001c0004t0007 | a0001c0004t0007g0057 | 1 | 230 | 0.0044 | -14 | c.-19 others(25): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1680 | chr12 | TogoVar | ||||||
CNTN1_chr12_40687439_41077415 | 40707046 | GCACACAC others(7): Show |
G | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(78): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0107others(78): Show | 81 | 230 | 0.3522 | -14 | c.-77 others(33): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40755190 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(139): Show | 142 | 230 | 0.6174 | -14 | c.-77 others(33): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40773644 | TATATATA others(7): Show |
T | intron_variant | MODIFIER | HG02148.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0106 | 1 | 230 | 0.0044 | -14 | c.-77 others(33): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40795274 | TACACACA others(7): Show |
T | intron_variant | MODIFIER | HG03704.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0113 | 1 | 230 | 0.0044 | -14 | c.-77 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40872208 | TTGTTTGT others(7): Show |
T | intron_variant | MODIFIER | HG02572.hp1 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0014a0001c0001t0015 | a0001c0001t0014g0185a0001c0001t0015g0219 | 2 | 230 | 0.0087 | -14 | c.-76 others(33): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40925820 | ATATATAT others(7): Show |
A | intron_variant | MODIFIER | HG03486.hp1 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0006a0001c0001t0007g0058 | 2 | 230 | 0.0087 | -14 | c.496 others(31): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40947774 | TATATATA others(7): Show |
T | intron_variant | MODIFIER | HG02572.hp2 | a0001 | a0001c0003 | a0001c0003t0016 | a0001c0003t0016g0226 | 1 | 230 | 0.0044 | -14 | c.168 others(33): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40950097 | GGTGTGTG others(7): Show |
G | intron_variant | MODIFIER | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(79): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0043others(79): Show | 82 | 230 | 0.3565 | -14 | c.168 others(33): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40975178 | TTATATAT others(7): Show |
T | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(34): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0095a0001c0001t0002g0045a0001c0001t0002g0096others(34): Show | 37 | 230 | 0.1609 | -14 | c.180 others(33): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 40978338 | TCATATCA others(7): Show |
T | intron_variant | MODIFIER | HG01884.hp2 HG02559.hp1 HG02895.hp2 others(6): Show |
a0001 | a0001c0004 | a0001c0004t0001a0001c0004t0002a0001c0004t0003others(1): Show | a0001c0004t0001g0217a0001c0004t0002g0008a0001c0004t0003g0168others(6): Show | 9 | 230 | 0.0391 | -14 | c.180 others(33): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 41051893 | AACACACA others(7): Show |
A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(40): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(7): Show | a0001c0001t0001g0101a0001c0001t0002g0005a0001c0001t0002g0011others(40): Show | 43 | 230 | 0.1870 | -14 | c.298 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN1_chr12_40687439_41077415 | 41053428 | AATATATA others(7): Show |
A | intron_variant | MODIFIER | HG02273.hp1 | a0001 | a0001c0006 | a0001c0006t0006 | a0001c0006t0006g0051 | 1 | 230 | 0.0044 | -14 | c.298 others(35): Show |
CNTN1 | ENSG00000018236.15 | transcript | ENST00000551295.7 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CNTN2_chr1_205038212_205083289 | 205048910 | CGTGTGTG others(7): Show |
C | intron_variant | MODIFIER | HG03492.hp2 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0130 | 1 | 380 | 0.0026 | -14 | c.-86 others(31): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CNTN2_chr1_205038212_205083289 | 205067927 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG01192.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
a0003a0012 | a0003c0013a0012c0020 | a0003c0013t0014a0012c0020t0014 | a0003c0013t0014g0037a0003c0013t0014g0136a0012c0020t0014g0109 | 4 | 380 | 0.0105 | -14 | c.212 others(31): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CNTN3_chr3_74257568_74619659 | 74285790 | GATATATA others(7): Show |
G | intron_variant | MODIFIER | HG02895.hp1 HG02897.hp2 |
a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0016a0001c0002t0003g0055 | 2 | 174 | 0.0115 | -14 | c.251 others(31): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 19/22 | chr3 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74344397 | GTTTTTTT others(7): Show |
G | intron_variant | MODIFIER | NA19074.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0156 | 1 | 174 | 0.0058 | -14 | c.136 others(33): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 11/22 | chr3 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74460772 | CATATATA others(7): Show |
C | intron_variant | MODIFIER | HG01261.hp1 HG01884.hp1 HG02055.hp1 others(4): Show |
a0001a0002a0003 | a0001c0001a0002c0005a0003c0021 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(2): Show | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0003g0067others(4): Show | 7 | 174 | 0.0402 | -14 | c.358 others(33): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 4/22 | chr3 | TogoVar | ||||||
CNTN3_chr3_74257568_74619659 | 74479263 | AATTCGAC others(7): Show |
A | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG01261.hp2 others(31): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0006others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | a0001c0001t0001g0108a0001c0001t0001g0139a0001c0001t0002g0083others(31): Show | 34 | 174 | 0.1954 | -14 | c.358 others(31): Show |
CNTN3 | ENSG00000113805.9 | transcript | ENST00000263665.7 | protein_coding | 4/22 | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2190821 | CACACACA others(7): Show |
C | intron_variant | MODIFIER | HG02523.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0076 | 1 | 116 | 0.0086 | -14 | c.-14 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2192800 | ACCACTAT others(7): Show |
A | intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0086 | 1 | 116 | 0.0086 | -14 | c.-14 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2300560 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG02602.hp2 HG03139.hp2 HG03453.hp2 |
a0001 | a0001c0002a0001c0006a0001c0007 | a0001c0002t0001a0001c0006t0002a0001c0007t0004 | a0001c0002t0001g0088a0001c0006t0002g0060a0001c0007t0004g0066 | 3 | 116 | 0.0259 | -14 | c.-14 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2326485 | TACACACA others(7): Show |
T | intron_variant | MODIFIER | HG01175.hp1 HG02809.hp2 |
a0001a0003 | a0001c0010a0003c0019 | a0001c0010t0003a0003c0019t0002 | a0001c0010t0003g0077a0003c0019t0002g0031 | 2 | 116 | 0.0172 | -14 | c.-14 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2600005 | CTTCTTTT others(7): Show |
C | intron_variant | MODIFIER | HG02886.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0003a0001c0005t0009others(1): Show | a0001c0001t0001g0033a0001c0001t0003g0095a0001c0005t0009g0091others(1): Show | 4 | 116 | 0.0345 | -14 | c.55+ others(31): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2782465 | CTGTGTGT others(7): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02818.hp2 |
a0001 | a0001c0002a0001c0013 | a0001c0002t0001a0001c0013t0007 | a0001c0002t0001g0029a0001c0013t0007g0056 | 2 | 116 | 0.0172 | -14 | c.358 others(33): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2983213 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
a0001a0002 | a0001c0002a0001c0023a0002c0016 | a0001c0002t0001a0001c0002t0007a0001c0023t0004others(1): Show | a0001c0002t0001g0029a0001c0002t0007g0080a0001c0023t0004g0041others(1): Show | 4 | 116 | 0.0345 | -14 | c.135 others(33): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 3003684 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
a0001a0003 | a0001c0002a0001c0005a0003c0008 | a0001c0002t0001a0001c0002t0012a0001c0005t0001others(1): Show | a0001c0002t0001g0029a0001c0002t0012g0013a0001c0005t0001g0104others(1): Show | 4 | 116 | 0.0345 | -14 | c.148 others(35): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 3019765 | AATATATA others(7): Show |
A | intron_variant | MODIFIER | HG00738.hp2 HG01169.hp2 HG01175.hp1 others(23): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0059others(23): Show | 26 | 116 | 0.2241 | -14 | c.148 others(33): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99208567 | GCTGTTTG others(7): Show |
G | intron_variant | MODIFIER | HG00738.hp2 HG01169.hp2 HG02004.hp2 others(4): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0002c0002t0001a0003c0003t0017others(2): Show | a0001c0001t0001g0004a0001c0001t0001g0052a0002c0002t0001g0003others(4): Show | 7 | 66 | 0.1061 | -14 | c.-20 others(37): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99284600 | GGTGTGTG others(7): Show |
G | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG03041.hp1 others(1): Show |
a0002a0004a0009 | a0002c0002a0004c0004a0009c0012 | a0002c0002t0008a0002c0002t0022a0004c0004t0002others(1): Show | a0002c0002t0008g0019a0002c0002t0022g0013a0004c0004t0002g0041others(1): Show | 4 | 66 | 0.0606 | -14 | c.-20 others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99329914 | GACACACA others(7): Show |
G | intron_variant | MODIFIER | HG02109.hp1 HG02886.hp2 HG02895.hp1 others(3): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0004c0004others(2): Show | a0001c0001t0010a0002c0002t0005a0004c0004t0020others(3): Show | a0001c0001t0010g0023a0002c0002t0005g0015a0004c0004t0020g0024others(3): Show | 6 | 66 | 0.0909 | -14 | c.-71 others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99408434 | AAGAAAGA others(7): Show |
A | intron_variant | MODIFIER | HG02257.hp1 HG02602.hp2 HG03130.hp1 others(1): Show |
a0001a0003a0005 | a0001c0001a0003c0011a0005c0005 | a0001c0001t0001a0003c0011t0019a0005c0005t0001 | a0001c0001t0001g0020a0001c0001t0001g0053a0003c0011t0019g0059others(1): Show | 4 | 66 | 0.0606 | -14 | c.-71 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99422516 | TTTTATAT others(7): Show |
T | intron_variant | MODIFIER | HG02132.hp2 | a0004 | a0004c0004 | a0004c0004t0002 | a0004c0004t0002g0051 | 1 | 66 | 0.0152 | -14 | c.-71 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99422518 | TTATATAT others(7): Show |
T | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp2 HG01934.hp1 others(2): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0006a0001c0001t0011a0001c0001t0012others(2): Show | a0001c0001t0006g0066a0001c0001t0011g0062a0001c0001t0012g0030others(2): Show | 5 | 66 | 0.0758 | -14 | c.-71 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99541956 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG01169.hp2 HG01934.hp2 |
a0003a0006 | a0003c0003a0006c0006 | a0003c0003t0002a0006c0006t0001 | a0003c0003t0002g0011a0006c0006t0001g0005 | 2 | 66 | 0.0303 | -14 | c.-70 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99556554 | AATATATA others(7): Show |
A | intron_variant | MODIFIER | HG01934.hp1 HG02886.hp1 HG03471.hp1 others(3): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0012a0001c0001t0014a0002c0002t0001others(3): Show | a0001c0001t0012g0030a0001c0001t0014g0016a0002c0002t0001g0003others(3): Show | 6 | 66 | 0.0909 | -14 | c.55+ others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99598361 | TCTCTCTC others(7): Show |
T | intron_variant | MODIFIER | HG01243.hp1 HG01243.hp2 HG01496.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0005a0002c0002t0004a0002c0002t0021 | a0001c0001t0005g0014a0002c0002t0004g0039a0002c0002t0021g0055 | 3 | 66 | 0.0455 | -14 | c.55+ others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99625915 | TATATATA others(7): Show |
T | intron_variant | MODIFIER | HG00735.hp2 NA18957.hp2 NA19000.hp2 |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0004 | a0001c0001t0011a0003c0003t0002a0004c0004t0002 | a0001c0001t0011g0062a0003c0003t0002g0002a0004c0004t0002g0001 | 3 | 66 | 0.0455 | -14 | c.55+ others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99835648 | AATGGAAA others(7): Show |
A | intron_variant | MODIFIER | HG00733.hp1 HG00735.hp1 HG02257.hp2 others(4): Show |
a0001a0003a0005others(1): Show | a0001c0001a0003c0003a0005c0005others(1): Show | a0001c0001t0004a0001c0001t0009a0001c0001t0015others(3): Show | a0001c0001t0004g0029a0001c0001t0004g0044a0001c0001t0009g0063others(4): Show | 7 | 66 | 0.1061 | -14 | c.278 others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99889291 | GGTGTGTG others(7): Show |
G | intron_variant | MODIFIER | NA18522.hp2 | a0003 | a0003c0003 | a0003c0003t0007 | a0003c0003t0007g0057 | 1 | 66 | 0.0152 | -14 | c.578 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99934935 | TATATATA others(7): Show |
T | intron_variant | MODIFIER | HG02886.hp1 HG02886.hp2 HG03471.hp1 |
a0003a0004a0008 | a0003c0003a0004c0004a0008c0008 | a0003c0003t0002a0004c0004t0020a0008c0008t0007 | a0003c0003t0002g0027a0004c0004t0020g0024a0008c0008t0007g0038 | 3 | 66 | 0.0455 | -14 | c.673 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99968656 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG02723.hp1 HG02886.hp2 HG02976.hp1 |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0004 | a0001c0001t0001a0003c0003t0007a0004c0004t0020 | a0001c0001t0001g0008a0003c0003t0007g0034a0004c0004t0020g0024 | 3 | 66 | 0.0455 | -14 | c.877 others(33): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100204297 | AATATATA others(7): Show |
A | intron_variant | MODIFIER | HG01081.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(1): Show | a0001c0001t0001g0008a0001c0001t0006g0040a0001c0001t0010g0047others(1): Show | 4 | 66 | 0.0606 | -14 | c.188 others(35): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1098783 | CACACACA others(7): Show |
C | intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 | 1 | 232 | 0.0043 | -14 | c.-83 others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1098806 | ATATATAT others(7): Show |
A | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0227 | 1 | 232 | 0.0043 | -14 | c.-83 others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | chr3 | TogoVar | ||||||
CNTN6_chr3_1088024_1409217 | 1142968 | GTATATAT others(7): Show |
G | intron_variant | MODIFIER | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(47): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(8): Show | a0001c0001t0001g0033a0001c0001t0001g0044a0001c0001t0001g0054others(47): Show | 50 | 232 | 0.2155 | -14 | c.-82 others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1161769 | TACACACA others(7): Show |
T | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0108a0001c0002t0001g0109 | 2 | 232 | 0.0086 | -14 | c.55+ others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1201097 | TTTTGTGT others(7): Show |
T | intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0209 | 1 | 232 | 0.0043 | -14 | c.56- others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1202545 | AATAAATA others(7): Show |
A | intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0013 | a0001c0013t0001 | a0001c0013t0001g0199 | 1 | 232 | 0.0043 | -14 | c.56- others(31): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN6_chr3_1088024_1409217 | 1245197 | GATATATA others(7): Show |
G | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp1 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0003a0001c0004t0001 | a0001c0002t0003g0079a0001c0004t0001g0065 | 2 | 232 | 0.0086 | -14 | c.358 others(33): Show |
CNTN6 | ENSG00000134115.13 | transcript | ENST00000446702.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr3 | TogoVar |