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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTN4_chr3_2093866_3062959 | 2440866 | CATATATG others(1): Show |
C | intron_variant | MODIFIER | HG00140.hp2 HG00438.hp2 HG00642.hp1 others(20): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(17): Show | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0002g0028others(20): Show | 23 | 116 | 0.1983 | -8 | c.-89 others(29): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2444731 | TTGGCTGG others(1): Show |
T | intron_variant | MODIFIER | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(2): Show |
a0001a0005 | a0001c0002a0001c0005a0001c0006others(2): Show | a0001c0002t0012a0001c0005t0006a0001c0006t0002others(2): Show | a0001c0002t0012g0013a0001c0005t0006g0032a0001c0006t0002g0026others(2): Show | 5 | 116 | 0.0431 | -8 | c.-89 others(29): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2450367 | AAAATAAA others(1): Show |
A | intron_variant | MODIFIER | HG02523.hp1 HG03453.hp2 |
a0001 | a0001c0003a0001c0006 | a0001c0003t0001a0001c0006t0002 | a0001c0003t0001g0014a0001c0006t0002g0060 | 2 | 116 | 0.0172 | -8 | c.-89 others(29): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2490157 | AAAACAAG others(1): Show |
A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(113): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0003others(25): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(53): Show | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0049others(113): Show | 116 | 116 | 1.0000 | -8 | c.-88 others(27): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2522146 | AGTTTGTG others(1): Show |
A | intron_variant | MODIFIER | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(30): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0059a0001c0001t0002g0030a0001c0001t0002g0055others(30): Show | 33 | 116 | 0.2845 | -8 | c.-88 others(27): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2547230 | ATATTTAT others(1): Show |
A | intron_variant | MODIFIER | HG00140.hp1 HG01884.hp1 HG02451.hp1 others(4): Show |
a0001a0009 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(4): Show | a0001c0001t0001g0099a0001c0001t0003g0095a0001c0001t0004g0081others(4): Show | 7 | 116 | 0.0603 | -8 | c.-88 others(27): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2612107 | TACACACA others(1): Show |
T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(20): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0050a0001c0001t0001g0099a0001c0001t0002g0028others(20): Show | 23 | 116 | 0.1983 | -8 | c.55+ others(25): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2630701 | AGTGTGTG others(1): Show |
A | intron_variant | MODIFIER | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(9): Show |
a0001a0002a0009 | a0001c0001a0001c0002a0001c0005others(5): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(7): Show | a0001c0001t0002g0086a0001c0001t0003g0008a0001c0001t0008g0053others(9): Show | 12 | 116 | 0.1035 | -8 | c.55+ others(25): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2658965 | GACACACA others(1): Show |
G | intron_variant | MODIFIER | HG01884.hp2 HG02897.hp2 HG03041.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0003a0001c0001t0009a0001c0002t0001others(2): Show | a0001c0001t0003g0006a0001c0001t0009g0052a0001c0002t0001g0088others(2): Show | 5 | 116 | 0.0431 | -8 | c.56- others(25): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2664309 | ATTTTCTT others(1): Show |
A | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(9): Show | a0001c0001t0002g0030a0001c0001t0003g0058a0001c0001t0005g0115others(11): Show | 14 | 116 | 0.1207 | -8 | c.56- others(25): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2677482 | ATATCTAT others(1): Show |
A | intron_variant | MODIFIER | HG01261.hp2 NA19043.hp1 |
a0001a0004 | a0001c0001a0004c0011 | a0001c0001t0003a0004c0011t0003 | a0001c0001t0003g0095a0004c0011t0003g0111 | 2 | 116 | 0.0172 | -8 | c.56- others(25): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2683478 | ACACATGT others(1): Show |
A | intron_variant | MODIFIER | HG02257.hp2 HG02451.hp1 HG02897.hp1 others(2): Show |
a0001a0003a0009 | a0001c0001a0001c0002a0003c0008others(1): Show | a0001c0001t0008a0001c0002t0003a0001c0002t0005others(2): Show | a0001c0001t0008g0089a0001c0002t0003g0024a0001c0002t0005g0002others(2): Show | 5 | 116 | 0.0431 | -8 | c.56- others(25): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2705555 | TAATTTAT others(1): Show |
T | intron_variant | MODIFIER | HG02258.hp1 HG03209.hp2 |
a0001 | a0001c0005a0001c0006 | a0001c0005t0006a0001c0006t0002 | a0001c0005t0006g0032a0001c0006t0002g0026 | 2 | 116 | 0.0172 | -8 | c.56- others(25): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2708727 | TCACACAC others(1): Show |
T | intron_variant | MODIFIER | HG02738.hp1 HG02809.hp1 HG02818.hp1 |
a0001a0002 | a0001c0001a0001c0002a0002c0017 | a0001c0001t0003a0001c0002t0001a0002c0017t0008 | a0001c0001t0003g0058a0001c0002t0001g0038a0002c0017t0008g0067 | 3 | 116 | 0.0259 | -8 | c.56- others(25): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2761437 | CCTGTGTG others(1): Show |
C | intron_variant | MODIFIER | HG01978.hp2 HG02074.hp2 |
a0001 | a0001c0003a0001c0007 | a0001c0003t0002a0001c0007t0016 | a0001c0003t0002g0073a0001c0007t0016g0105 | 2 | 116 | 0.0172 | -8 | c.358 others(27): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 6/24 | chr3 | TogoVar | ||||||
CNTN4_chr3_2093866_3062959 | 2778213 | CAAATAAA others(1): Show |
C | intron_variant | MODIFIER | HG00735.hp1 HG01361.hp1 HG01891.hp1 others(17): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(14): Show | a0001c0001t0002g0030a0001c0001t0003g0101a0001c0001t0004g0042others(17): Show | 20 | 116 | 0.1724 | -8 | c.358 others(27): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2782465 | CTGTGTGT others(1): Show |
C | intron_variant | MODIFIER | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(16): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0002a0001c0001t0005a0001c0002t0001others(14): Show | a0001c0001t0002g0086a0001c0001t0005g0018a0001c0001t0005g0019others(16): Show | 19 | 116 | 0.1638 | -8 | c.358 others(27): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2804065 | GCACACAC others(1): Show |
G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(24): Show |
a0001a0003a0006others(1): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0033a0001c0001t0001g0049a0001c0001t0001g0099others(24): Show | 27 | 116 | 0.2328 | -8 | c.359 others(27): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2878551 | CTCTGTGT others(1): Show |
C | intron_variant | MODIFIER | HG01243.hp2 HG01891.hp1 HG02965.hp1 others(3): Show |
a0001a0005 | a0001c0002a0005c0012 | a0001c0002t0001a0001c0002t0002a0001c0002t0007others(2): Show | a0001c0002t0001g0029a0001c0002t0001g0108a0001c0002t0002g0102others(3): Show | 6 | 116 | 0.0517 | -8 | c.653 others(25): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2878553 | CTGTGTGT others(1): Show |
C | intron_variant | MODIFIER | HG02622.hp1 HG02818.hp1 HG03130.hp1 others(2): Show |
a0001a0002 | a0001c0021a0002c0014a0002c0015others(2): Show | a0001c0021t0002a0002c0014t0001a0002c0015t0003others(2): Show | a0001c0021t0002g0025a0002c0014t0001g0016a0002c0015t0003g0103others(2): Show | 5 | 116 | 0.0431 | -8 | c.653 others(25): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2932800 | CTTTATTT others(1): Show |
C | intron_variant | MODIFIER | HG00438.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0002a0001c0002t0001a0001c0002t0007others(8): Show | a0001c0001t0002g0074a0001c0002t0001g0088a0001c0002t0001g0110others(10): Show | 13 | 116 | 0.1121 | -8 | c.135 others(27): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2971350 | GTCTATCT others(1): Show |
G | intron_variant | MODIFIER | HG01169.hp1 HG01243.hp1 HG01243.hp2 others(59): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(20): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | a0001c0001t0001g0059a0001c0001t0002g0030a0001c0001t0003g0006others(59): Show | 62 | 116 | 0.5345 | -8 | c.135 others(29): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 2989627 | AAGAGTTA others(1): Show |
A | intron_variant | MODIFIER | HG02451.hp1 HG02965.hp2 HG03516.hp1 |
a0001a0009 | a0001c0005a0009c0027 | a0001c0005t0001a0009c0027t0001 | a0001c0005t0001g0090a0001c0005t0001g0092a0009c0027t0001g0007 | 3 | 116 | 0.0259 | -8 | c.148 others(27): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 3014047 | TACACACA others(1): Show |
T | intron_variant | MODIFIER | HG03041.hp2 NA19043.hp1 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0003a0001c0005t0010 | a0001c0001t0003g0095a0001c0005t0010g0001 | 2 | 116 | 0.0172 | -8 | c.148 others(29): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN4_chr3_2093866_3062959 | 3019765 | AATATATA others(1): Show |
A | intron_variant | MODIFIER | HG00438.hp2 HG00642.hp1 HG01884.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0005a0001c0020others(2): Show | a0001c0001t0003a0001c0001t0009a0001c0005t0001others(3): Show | a0001c0001t0003g0008a0001c0001t0003g0058a0001c0001t0009g0052others(4): Show | 7 | 116 | 0.0603 | -8 | c.148 others(27): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99099549 | TACACACA others(1): Show |
T | intron_variant | MODIFIER | HG01169.hp2 HG02004.hp2 HG02132.hp2 others(3): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0002c0002t0001a0003c0003t0017others(2): Show | a0001c0001t0001g0004a0001c0001t0001g0052a0002c0002t0001g0003others(3): Show | 6 | 66 | 0.0909 | -8 | c.-21 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99121891 | ATTTCTTT others(1): Show |
A | intron_variant | MODIFIER | HG01243.hp2 HG02602.hp1 HG02976.hp1 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0005a0001c0001t0006a0003c0003t0007 | a0001c0001t0005g0014a0001c0001t0006g0066a0003c0003t0007g0034 | 3 | 66 | 0.0455 | -8 | c.-21 others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99178314 | CCACACAC others(1): Show |
C | intron_variant | MODIFIER | HG01081.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0015a0002c0002t0001a0002c0002t0008others(3): Show | a0001c0001t0015g0064a0002c0002t0001g0003a0002c0002t0008g0019others(3): Show | 6 | 66 | 0.0909 | -8 | c.-20 others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99213356 | GTGTATAT others(1): Show |
G | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01123.hp2 others(17): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(12): Show | a0001c0001t0001g0020a0001c0001t0001g0054a0001c0001t0005g0048others(17): Show | 20 | 66 | 0.3030 | -8 | c.-20 others(31): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99267920 | GCACACAC others(1): Show |
G | intron_variant | MODIFIER | HG02886.hp2 HG02895.hp1 HG02965.hp1 others(1): Show |
a0002a0004a0005others(1): Show | a0002c0002a0004c0004a0005c0005others(1): Show | a0002c0002t0005a0004c0004t0020a0005c0005t0001others(1): Show | a0002c0002t0005g0015a0004c0004t0020g0024a0005c0005t0001g0035others(1): Show | 4 | 66 | 0.0606 | -8 | c.-20 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99284600 | GGTGTGTG others(1): Show |
G | intron_variant | MODIFIER | HG01123.hp1 HG02735.hp2 HG02886.hp2 others(1): Show |
a0001a0003a0004others(1): Show | a0001c0001a0003c0003a0004c0004others(1): Show | a0001c0001t0003a0003c0003t0002a0004c0004t0020others(1): Show | a0001c0001t0003g0060a0003c0003t0002g0061a0004c0004t0020g0024others(1): Show | 4 | 66 | 0.0606 | -8 | c.-20 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99297472 | ATGCTGTA others(1): Show |
A | intron_variant | MODIFIER | HG01081.hp1 HG01123.hp2 HG01496.hp2 others(15): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(10): Show | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0053others(15): Show | 18 | 66 | 0.2727 | -8 | c.-20 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99315052 | AAAGTAAT others(1): Show |
A | intron_variant | MODIFIER | HG00733.hp1 HG01081.hp2 NA19043.hp1 |
a0001a0011 | a0001c0001a0011c0009 | a0001c0001t0009a0001c0001t0010a0011c0009t0005 | a0001c0001t0009g0063a0001c0001t0010g0047a0011c0009t0005g0056 | 3 | 66 | 0.0455 | -8 | c.-20 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99329914 | GACACACA others(1): Show |
G | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01099.hp1 others(13): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(11): Show | a0001c0001t0001g0054a0001c0001t0003g0060a0001c0001t0004g0010others(13): Show | 16 | 66 | 0.2424 | -8 | c.-71 others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99406399 | GTCTCTCT others(1): Show |
G | intron_variant | MODIFIER | HG00738.hp1 HG01099.hp2 HG02109.hp2 others(7): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0011others(2): Show | a0001c0001t0001a0001c0001t0003a0002c0002t0003others(4): Show | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0003g0021others(7): Show | 10 | 66 | 0.1515 | -8 | c.-71 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99409856 | ATGTGATA others(1): Show |
A | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(9): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0014others(9): Show | a0001c0001t0004g0029a0001c0001t0005g0048a0001c0001t0014g0016others(9): Show | 12 | 66 | 0.1818 | -8 | c.-71 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99422516 | TTTTATAT others(1): Show |
T | intron_variant | MODIFIER | HG01099.hp1 HG01169.hp1 HG02723.hp2 others(1): Show |
a0001a0008 | a0001c0001a0008c0008 | a0001c0001t0004a0001c0001t0009a0008c0008t0007 | a0001c0001t0004g0010a0001c0001t0004g0044a0001c0001t0009g0043others(1): Show | 4 | 66 | 0.0606 | -8 | c.-71 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99422518 | TTATATAT others(1): Show |
T | intron_variant | MODIFIER | NA18957.hp2 NA20300.hp2 |
a0003a0012 | a0003c0003a0012c0013 | a0003c0003t0002a0012c0013t0008 | a0003c0003t0002g0002a0012c0013t0008g0031 | 2 | 66 | 0.0303 | -8 | c.-71 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99450257 | AATATATA others(1): Show |
A | intron_variant | MODIFIER | NA18939.hp2 NA19070.hp2 |
a0001a0007 | a0001c0001a0007c0007 | a0001c0001t0014a0007c0007t0023 | a0001c0001t0014g0016a0007c0007t0023g0046 | 2 | 66 | 0.0303 | -8 | c.-70 others(29): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99461662 | TGTATTCT others(1): Show |
T | intron_variant | MODIFIER | HG02886.hp1 HG03471.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0004a0003c0003t0002 | a0001c0001t0004g0029a0003c0003t0002g0027 | 2 | 66 | 0.0303 | -8 | c.-70 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99515959 | AAACAAAA others(1): Show |
A | intron_variant | MODIFIER | HG02723.hp1 HG02723.hp2 HG02976.hp1 others(1): Show |
a0001a0003a0009 | a0001c0001a0003c0003a0009c0012 | a0001c0001t0001a0001c0001t0004a0003c0003t0007others(1): Show | a0001c0001t0001g0008a0001c0001t0004g0044a0003c0003t0007g0034others(1): Show | 4 | 66 | 0.0606 | -8 | c.-70 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99543917 | TCAAAAAA others(1): Show |
T | intron_variant | MODIFIER | HG02976.hp1 HG03041.hp2 NA18957.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0010a0003c0003t0002a0003c0003t0007 | a0001c0001t0010g0023a0003c0003t0002g0002a0003c0003t0007g0034 | 3 | 66 | 0.0455 | -8 | c.-70 others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99591337 | CTTTTTTT others(1): Show |
C | intron_variant | MODIFIER | HG00738.hp1 HG01099.hp2 HG02109.hp2 others(6): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0003a0001c0001t0005a0002c0002t0003others(4): Show | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0005g0048others(6): Show | 9 | 66 | 0.1364 | -8 | c.55+ others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99598367 | TCTCTCTC others(1): Show |
T | intron_variant | MODIFIER | HG02258.hp1 HG02895.hp1 |
a0002a0010 | a0002c0002a0010c0010 | a0002c0002t0005a0010c0010t0011 | a0002c0002t0005g0015a0010c0010t0011g0009 | 2 | 66 | 0.0303 | -8 | c.55+ others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99625917 | TATATATA others(1): Show |
T | intron_variant | MODIFIER | HG01243.hp2 HG01496.hp1 HG02004.hp1 others(9): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(6): Show | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(9): Show | 12 | 66 | 0.1818 | -8 | c.55+ others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99630240 | GTATATAC others(1): Show |
G | intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(27): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(19): Show | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0004g0010others(27): Show | 30 | 66 | 0.4546 | -8 | c.55+ others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99630247 | CATATATA others(1): Show |
C | intron_variant | MODIFIER | HG01243.hp2 HG01496.hp1 HG02004.hp1 others(13): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(9): Show | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(13): Show | 16 | 66 | 0.2424 | -8 | c.55+ others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99637010 | CAAAAAAA others(1): Show |
C | intron_variant | MODIFIER | HG00733.hp1 HG01081.hp2 HG01243.hp1 others(5): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(5): Show | a0001c0001t0001g0004a0001c0001t0004g0044a0001c0001t0009g0063others(5): Show | 8 | 66 | 0.1212 | -8 | c.55+ others(25): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99669468 | GTGTGTAT others(1): Show |
G | intron_variant | MODIFIER | HG01081.hp1 HG02258.hp2 HG02976.hp2 others(1): Show |
a0003a0005 | a0003c0003a0005c0005 | a0003c0003t0017a0005c0005t0001a0005c0005t0003others(1): Show | a0003c0003t0017g0065a0005c0005t0001g0017a0005c0005t0003g0045others(1): Show | 4 | 66 | 0.0606 | -8 | 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 | 99710567 | ATGTGTGT others(1): Show |
A | intron_variant | MODIFIER | HG01243.hp1 HG02257.hp2 HG02735.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0006a0001c0001t0015a0002c0002t0004 | a0001c0001t0006g0032a0001c0001t0006g0040a0001c0001t0015g0064others(1): Show | 4 | 66 | 0.0606 | -8 | c.56- others(27): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |