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 | 3062933 | ATGT | A | downstream_gene_variant | MODIFIER | HG01243.hp1 HG02257.hp2 HG03209.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0003a0001c0001t0008a0001c0002t0012others(2): Show | a0001c0001t0003g0095a0001c0001t0008g0053a0001c0001t0008g0089others(3): Show | 6 | 116 | 0.0517 | -3 | c.*67 others(14): Show |
CNTN4 | ENSG00000144619.15 | transcript | ENST00000418658.6 | protein_coding | 4975 | chr3 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99058385 | ATAG | A | intron_variant | MODIFIER | HG01081.hp1 HG02109.hp1 |
a0005 | a0005c0005 | a0005c0005t0010a0005c0005t0018 | a0005c0005t0010g0006a0005c0005t0018g0028 | 2 | 66 | 0.0303 | -3 | c.-21 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99067186 | TCTC | T | intron_variant | MODIFIER | HG02004.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
a0001a0003a0009 | a0001c0001a0003c0003a0009c0012 | a0001c0001t0001a0001c0001t0006a0003c0003t0007others(1): Show | a0001c0001t0001g0054a0001c0001t0006g0040a0003c0003t0007g0034others(1): Show | 4 | 66 | 0.0606 | -3 | c.-21 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99123654 | GTTT | G | intron_variant | MODIFIER | HG01243.hp2 HG02602.hp1 HG02886.hp1 others(5): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(5): Show | a0001c0001t0004g0029a0001c0001t0005g0014a0001c0001t0006g0066others(5): Show | 8 | 66 | 0.1212 | -3 | c.-21 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99139101 | ACCC | A | intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(61): Show |
a0001a0002a0003others(9): Show | a0001c0001a0002c0002a0003c0003others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0020others(61): Show | 64 | 66 | 0.9697 | -3 | c.-21 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99199967 | ACAT | A | intron_variant | MODIFIER | HG02723.hp1 HG02886.hp1 HG02886.hp2 others(6): Show |
a0001a0003a0004others(4): Show | a0001c0001a0003c0003a0004c0004others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(6): Show | a0001c0001t0001g0008a0001c0001t0004g0029a0001c0001t0006g0040others(6): Show | 9 | 66 | 0.1364 | -3 | c.-20 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99205173 | AAAC | A | intron_variant | MODIFIER | HG00733.hp1 HG00738.hp2 HG01081.hp2 others(9): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(8): Show | a0001c0001t0003g0060a0001c0001t0005g0014a0001c0001t0009g0043others(9): Show | 12 | 66 | 0.1818 | -3 | c.-20 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99206618 | TTAC | T | intron_variant | MODIFIER | HG00733.hp1 HG00738.hp1 HG01081.hp2 others(14): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(9): Show | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0060others(14): Show | 17 | 66 | 0.2576 | -3 | c.-20 others(26): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99243736 | ATTT | A | intron_variant | MODIFIER | HG01169.hp2 NA18939.hp1 NA18957.hp1 others(1): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0002c0002t0001a0003c0003t0017others(1): Show | a0001c0001t0001g0052a0002c0002t0001g0003a0003c0003t0017g0065others(1): Show | 4 | 66 | 0.0606 | -3 | c.-20 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99246296 | CCCA | C | intron_variant | MODIFIER | HG01099.hp1 HG02735.hp1 NA18939.hp2 others(2): Show |
a0001a0003a0004others(1): Show | a0001c0001a0003c0003a0004c0004others(1): Show | a0001c0001t0004a0001c0001t0006a0003c0003t0002others(2): Show | a0001c0001t0004g0010a0001c0001t0006g0032a0003c0003t0002g0002others(2): Show | 5 | 66 | 0.0758 | -3 | c.-20 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99302619 | AAAT | A | intron_variant | MODIFIER | HG01169.hp2 NA18939.hp1 NA19070.hp1 |
a0002a0003a0006 | a0002c0002a0003c0003a0006c0006 | a0002c0002t0001a0003c0003t0017a0006c0006t0001 | a0002c0002t0001g0003a0003c0003t0017g0065a0006c0006t0001g0005 | 3 | 66 | 0.0455 | -3 | c.-20 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99306746 | GATA | G | intron_variant | MODIFIER | HG00733.hp1 HG00738.hp1 HG01081.hp2 others(19): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(13): Show | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0003g0021others(19): Show | 22 | 66 | 0.3333 | -3 | c.-20 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99403008 | CTTT | C | intron_variant | MODIFIER | HG00735.hp2 HG01934.hp1 HG02004.hp1 others(5): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0011others(5): Show | a0001c0001t0001g0054a0001c0001t0006g0066a0001c0001t0011g0062others(5): Show | 8 | 66 | 0.1212 | -3 | c.-71 others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99483174 | CAAA | C | intron_variant | MODIFIER | HG01496.hp1 HG02132.hp1 HG02257.hp2 others(5): Show |
a0001a0002a0012 | a0001c0001a0002c0002a0012c0013 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(4): Show | a0001c0001t0001g0008a0001c0001t0006g0032a0001c0001t0006g0066others(5): Show | 8 | 66 | 0.1212 | -3 | c.-70 others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99535257 | ATAG | A | intron_variant | MODIFIER | NA18522.hp2 NA19070.hp1 |
a0002a0003 | a0002c0002a0003c0003 | a0002c0002t0001a0003c0003t0007 | a0002c0002t0001g0003a0003c0003t0007g0057 | 2 | 66 | 0.0303 | -3 | c.-70 others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99543923 | AAAC | A | intron_variant | MODIFIER | HG00733.hp1 HG00738.hp2 HG01081.hp2 others(15): Show |
a0001a0003a0004others(3): Show | a0001c0001a0003c0003a0004c0004others(3): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(10): Show | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0054others(15): Show | 18 | 66 | 0.2727 | -3 | c.-70 others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99560268 | GTAT | G | intron_variant | MODIFIER | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(14): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(5): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0010others(12): Show | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0005g0048others(14): Show | 17 | 66 | 0.2576 | -3 | c.55+ others(18): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99577823 | TTTA | T | intron_variant | MODIFIER | HG00733.hp2 HG00735.hp1 HG01099.hp1 others(2): Show |
a0001a0002a0005others(2): Show | a0001c0001a0002c0002a0005c0005others(2): Show | a0001c0001t0004a0002c0002t0022a0005c0005t0010others(2): Show | a0001c0001t0004g0010a0002c0002t0022g0013a0005c0005t0010g0006others(2): Show | 5 | 66 | 0.0758 | -3 | c.55+ others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99588343 | CAAA | C | intron_variant | MODIFIER | HG00733.hp1 HG01243.hp2 HG02132.hp1 others(4): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0005a0001c0001t0009a0001c0001t0016others(4): Show | a0001c0001t0005g0014a0001c0001t0009g0063a0001c0001t0016g0049others(4): Show | 7 | 66 | 0.1061 | -3 | c.55+ others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99624251 | AGTT | A | intron_variant | MODIFIER | HG00733.hp1 HG01081.hp2 HG01243.hp1 others(6): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(6): Show | a0001c0001t0004g0044a0001c0001t0005g0048a0001c0001t0009g0063others(6): Show | 9 | 66 | 0.1364 | -3 | c.55+ others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99629620 | CTCA | C | intron_variant | MODIFIER | HG01243.hp2 HG01496.hp1 HG02004.hp1 others(12): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(9): Show | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(12): Show | 15 | 66 | 0.2273 | -3 | c.55+ others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99629676 | TTAC | T | intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(21): Show | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0004g0010others(30): Show | 33 | 66 | 0.5000 | -3 | c.55+ others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99631962 | ATTG | A | intron_variant | MODIFIER | NA19000.hp1 NA19070.hp1 |
a0002a0006 | a0002c0002a0006c0006 | a0002c0002t0001a0006c0006t0014 | a0002c0002t0001g0003a0006c0006t0014g0058 | 2 | 66 | 0.0303 | -3 | c.55+ others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99641409 | ATCC | A | intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(28): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(19): Show | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0004g0010others(28): Show | 31 | 66 | 0.4697 | -3 | c.55+ others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99645258 | TCAA | T | intron_variant | MODIFIER | HG01243.hp1 NA19000.hp1 |
a0002a0006 | a0002c0002a0006c0006 | a0002c0002t0004a0006c0006t0014 | a0002c0002t0004g0039a0006c0006t0014g0058 | 2 | 66 | 0.0303 | -3 | c.55+ others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99690835 | TAAC | T | intron_variant | MODIFIER | HG02602.hp1 NA18957.hp2 NA19000.hp2 |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0004 | a0001c0001t0006a0003c0003t0002a0004c0004t0002 | a0001c0001t0006g0066a0003c0003t0002g0002a0004c0004t0002g0001 | 3 | 66 | 0.0455 | -3 | c.56- others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99695949 | AAAT | A | intron_variant | MODIFIER | HG02258.hp1 HG02895.hp1 |
a0002a0010 | a0002c0002a0010c0010 | a0002c0002t0005a0010c0010t0011 | a0002c0002t0005g0015a0010c0010t0011g0009 | 2 | 66 | 0.0303 | -3 | c.56- others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99709508 | AAAT | A | intron_variant | MODIFIER | HG02258.hp1 HG02895.hp1 NA19000.hp1 others(2): Show |
a0002a0006a0010others(1): Show | a0002c0002a0006c0006a0010c0010others(1): Show | a0002c0002t0001a0002c0002t0005a0006c0006t0014others(2): Show | a0002c0002t0001g0003a0002c0002t0005g0015a0006c0006t0014g0058others(2): Show | 5 | 66 | 0.0758 | -3 | c.56- others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99733397 | CATG | C | intron_variant | MODIFIER | HG02257.hp1 HG03130.hp1 |
a0003a0005 | a0003c0011a0005c0005 | a0003c0011t0019a0005c0005t0001 | a0003c0011t0019g0059a0005c0005t0001g0035 | 2 | 66 | 0.0303 | -3 | c.56- others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99740052 | ATAT | A | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG01081.hp1 others(18): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(12): Show | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0054others(18): Show | 21 | 66 | 0.3182 | -3 | c.56- others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99744543 | TAAA | T | intron_variant | MODIFIER | HG01169.hp1 HG02004.hp2 HG02735.hp1 others(4): Show |
a0001a0003a0004others(1): Show | a0001c0001a0003c0003a0004c0004others(1): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(3): Show | a0001c0001t0001g0004a0001c0001t0006g0032a0001c0001t0006g0040others(4): Show | 7 | 66 | 0.1061 | -3 | c.56- others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99760799 | TAAG | T | intron_variant | MODIFIER | HG01123.hp1 HG02109.hp2 HG02895.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0002c0002t0005a0002c0002t0008 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0060others(2): Show | 5 | 66 | 0.0758 | -3 | c.56- others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99763136 | CAAT | C | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp1 HG00738.hp2 others(24): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0002a0003c0011others(7): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(17): Show | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0054others(24): Show | 27 | 66 | 0.4091 | -3 | c.56- others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | chr11 | TogoVar | ||||||
CNTN5_chr11_99015949_100363885 | 99773671 | ATAG | A | intron_variant | MODIFIER | HG02132.hp2 NA18939.hp2 NA19000.hp2 |
a0004a0007 | a0004c0004a0007c0007 | a0004c0004t0002a0007c0007t0023 | a0004c0004t0002g0001a0004c0004t0002g0051a0007c0007t0023g0046 | 3 | 66 | 0.0455 | -3 | c.56- others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99811459 | TATA | T | intron_variant | MODIFIER | HG01081.hp1 HG01169.hp1 HG01934.hp1 others(3): Show |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(3): Show | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0009g0043others(3): Show | 6 | 66 | 0.0909 | -3 | c.56- others(18): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99811880 | AACT | A | intron_variant | MODIFIER | HG02132.hp2 NA18939.hp2 NA19000.hp2 |
a0004a0007 | a0004c0004a0007c0007 | a0004c0004t0002a0007c0007t0023 | a0004c0004t0002g0001a0004c0004t0002g0051a0007c0007t0023g0046 | 3 | 66 | 0.0455 | -3 | c.56- others(18): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99817596 | GTTT | G | intron_variant | MODIFIER | HG01099.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
a0001a0003a0010others(1): Show | a0001c0001a0003c0003a0003c0011others(2): Show | a0001c0001t0004a0001c0001t0006a0003c0003t0002others(4): Show | a0001c0001t0004g0010a0001c0001t0006g0066a0003c0003t0002g0027others(4): Show | 7 | 66 | 0.1061 | -3 | c.56- others(18): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99837684 | TAAA | T | intron_variant | MODIFIER | HG01081.hp2 HG01169.hp2 HG02004.hp1 others(3): Show |
a0001a0005a0006others(1): Show | a0001c0001a0005c0005a0006c0006others(1): Show | a0001c0001t0001a0001c0001t0010a0005c0005t0001others(3): Show | a0001c0001t0001g0054a0001c0001t0010g0047a0005c0005t0001g0035others(3): Show | 6 | 66 | 0.0909 | -3 | c.278 others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99841800 | TGTG | T | intron_variant | MODIFIER | HG06807.hp1 NA20300.hp2 |
a0006a0012 | a0006c0006a0012c0013 | a0006c0006t0013a0012c0013t0008 | a0006c0006t0013g0025a0012c0013t0008g0031 | 2 | 66 | 0.0303 | -3 | c.278 others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99968656 | CTTT | C | intron_variant | MODIFIER | HG00733.hp2 HG00735.hp2 HG00738.hp2 others(14): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(10): Show | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0054others(14): Show | 17 | 66 | 0.2576 | -3 | c.877 others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 99994313 | TGTC | T | intron_variant | MODIFIER | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(17): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(11): Show | a0001c0001t0001g0020a0001c0001t0001g0053a0001c0001t0003g0021others(17): Show | 20 | 66 | 0.3030 | -3 | c.878 others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100011373 | AAAC | A | intron_variant | MODIFIER | HG00738.hp2 HG01081.hp1 HG02895.hp2 |
a0004a0005 | a0004c0004a0005c0005 | a0004c0004t0002a0004c0004t0013a0005c0005t0018 | a0004c0004t0002g0041a0004c0004t0013g0050a0005c0005t0018g0028 | 3 | 66 | 0.0455 | -3 | c.980 others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100055028 | TAAA | T | intron_variant | MODIFIER | HG00735.hp1 HG00738.hp1 HG01081.hp2 others(23): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0003c0003others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(16): Show | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0003g0021others(23): Show | 26 | 66 | 0.3939 | -3 | c.981 others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100150405 | ATTT | A | intron_variant | MODIFIER | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(10): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(6): Show | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(10): Show | 13 | 66 | 0.1970 | -3 | c.158 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100151434 | TAGG | T | intron_variant | MODIFIER | HG00738.hp1 HG01081.hp1 HG01099.hp2 others(7): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0005 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(4): Show | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0060others(7): Show | 10 | 66 | 0.1515 | -3 | c.158 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100151938 | TTAA | T | intron_variant | MODIFIER | HG01081.hp2 HG01123.hp2 HG01934.hp2 others(5): Show |
a0001a0003a0004 | a0001c0001a0003c0003a0004c0004 | a0001c0001t0001a0001c0001t0010a0001c0001t0016others(2): Show | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0010g0047others(5): Show | 8 | 66 | 0.1212 | -3 | c.158 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100163058 | AAAC | A | intron_variant | MODIFIER | HG06807.hp2 NA18522.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0003c0003t0007 | a0001c0001t0001g0020a0003c0003t0007g0057 | 2 | 66 | 0.0303 | -3 | c.158 others(24): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100190727 | CTGT | C | intron_variant | MODIFIER | HG00735.hp1 HG01123.hp1 HG01169.hp1 others(22): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(5): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(18): Show | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0060others(22): Show | 25 | 66 | 0.3788 | -3 | c.158 others(20): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100196332 | GTAT | G | intron_variant | MODIFIER | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(30): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0002a0003c0003others(7): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(21): Show | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(30): Show | 33 | 66 | 0.5000 | -3 | c.188 others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
CNTN5_chr11_99015949_100363885 | 100199244 | CATT | C | intron_variant | MODIFIER | HG01081.hp2 HG02723.hp1 HG02895.hp2 others(2): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(2): Show | a0001c0001t0001g0008a0001c0001t0006g0040a0001c0001t0010g0047others(2): Show | 5 | 66 | 0.0758 | -3 | c.188 others(22): Show |
CNTN5 | ENSG00000149972.12 | transcript | ENST00000524871.6 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |