view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ANO3_chr11_26327130_26668289 | 26637779 | C | CTTAA | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(133): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(13): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0015others(35): Show | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(133): Show |
136 | 188 | 0.7234 | 4 | c.204 others(23): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26642486 | G | GAAGT | intron_variant | MODIFIER | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(63): Show |
a0001 | a0001c0002a0001c0003a0001c0005others(3): Show | a0001c0002t0002a0001c0002t0007a0001c0002t0011others(11): Show | a0001c0002t0002g0031 a0001c0002t0002g0032 a0001c0002t0002g0033 others(63): Show |
66 | 188 | 0.3511 | 4 | c.227 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 22/26 | chr11 | TogoVar | |||||||
ANO3_chr11_26327130_26668289 | 26642829 | C | CTCTT | intron_variant | MODIFIER | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(63): Show |
a0001 | a0001c0002a0001c0003a0001c0005others(3): Show | a0001c0002t0002a0001c0002t0007a0001c0002t0011others(11): Show | a0001c0002t0002g0031 a0001c0002t0002g0032 a0001c0002t0002g0033 others(63): Show |
66 | 188 | 0.3511 | 4 | c.227 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26644815 | T | TCACA | intron_variant | MODIFIER | HG01255.hp1 HG02451.hp2 HG02486.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0018a0001c0001t0020a0001c0002t0007others(6): Show | a0001c0001t0018g0099 a0001c0001t0020g0080 a0001c0002t0007g0083 others(11): Show |
14 | 49 | 0.2857 | 4 | c.242 others(23): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26659099 | C | CACAT | intron_variant | MODIFIER | HG01109.hp2 HG02922.hp2 HG03486.hp1 others(2): Show |
a0001 | a0001c0008 | a0001c0008t0008 | a0001c0008t0008g0093 a0001c0008t0008g0151 a0001c0008t0008g0152 others(2): Show |
5 | 147 | 0.0340 | 4 | c.276 others(23): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26659184 | A | ATACT | intron_variant | MODIFIER | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(86): Show |
a0001 | a0001c0002a0001c0003a0001c0005others(5): Show | a0001c0002t0002a0001c0002t0007a0001c0002t0011others(20): Show | a0001c0002t0002g0031 a0001c0002t0002g0032 a0001c0002t0002g0033 others(86): Show |
89 | 188 | 0.4734 | 4 | c.276 others(23): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100801093 | G | GTCTC | intron_variant | MODIFIER | HG00738.hp1 HG02257.hp1 HG02486.hp1 others(3): Show |
a0001 | a0001c0001a0001c0003a0001c0013others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0003t0001others(3): Show | a0001c0001t0001g0108 a0001c0001t0004g0038 a0001c0003t0001g0041 others(3): Show |
6 | 62 | 0.0968 | 4 | c.-14 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100806524 | G | GTTTT | intron_variant | MODIFIER | HG00558.hp1 HG02148.hp2 HG02486.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0003t0006a0001c0005t0001 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0035 others(4): Show |
7 | 36 | 0.1944 | 4 | c.-14 others(25): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100812470 | G | GTATA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(1): Show | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0077 others(6): Show |
9 | 234 | 0.0385 | 4 | c.-14 others(25): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100820355 | C | CAAAA | intron_variant | MODIFIER | HG00438.hp1 HG02273.hp2 HG03688.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(3): Show |
6 | 18 | 0.3333 | 4 | c.-14 others(25): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100838229 | C | CAAAA | intron_variant | MODIFIER | HG00621.hp1 HG01361.hp1 HG01928.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0002a0001c0003t0005 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0143 others(4): Show |
7 | 45 | 0.1556 | 4 | c.-14 others(25): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100843987 | C | CTTCA | intron_variant | MODIFIER | HG00738.hp2 HG01167.hp1 HG02280.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0139 others(4): Show |
7 | 232 | 0.0302 | 4 | c.-14 others(25): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100847475 | A | ATTTT | intron_variant | MODIFIER | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(48): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(7): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(48): Show |
51 | 86 | 0.5930 | 4 | c.-14 others(25): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100867612 | T | TCACA | intron_variant | MODIFIER | HG02976.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0003g0052 others(2): Show |
5 | 68 | 0.0735 | 4 | c.-14 others(25): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100876278 | C | CAAAA | intron_variant | MODIFIER | HG01168.hp1 HG01192.hp1 HG01258.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0163 others(8): Show |
11 | 111 | 0.0991 | 4 | c.-14 others(25): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100886379 | G | GTTGC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(16): Show | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0021 others(101): Show |
104 | 234 | 0.4444 | 4 | c.-14 others(25): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100895561 | G | GTTTT | intron_variant | MODIFIER | HG00738.hp1 HG01081.hp2 HG01884.hp1 others(6): Show |
a0001 | a0001c0003a0001c0007a0001c0013 | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(2): Show | a0001c0003t0001g0041 a0001c0003t0001g0044 a0001c0003t0001g0049 others(6): Show |
9 | 186 | 0.0484 | 4 | c.-14 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100900097 | C | CAGAA | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(36): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(3): Show | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(36): Show |
39 | 234 | 0.1667 | 4 | c.-14 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100919670 | C | CTGTG | intron_variant | MODIFIER | HG03834.hp1 NA18612.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0034 a0001c0002t0002g0183 |
2 | 175 | 0.0114 | 4 | c.56- others(19): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100919718 | A | ATGTG | intron_variant | MODIFIER | HG01192.hp2 HG02258.hp2 HG03225.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0162 a0001c0001t0003g0109 a0001c0001t0003g0186 others(1): Show |
4 | 229 | 0.0175 | 4 | c.56- others(19): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100919726 | G | GTGTA | intron_variant | MODIFIER | HG00438.hp1 HG01167.hp2 HG01346.hp1 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(3): Show | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0024 others(17): Show |
20 | 183 | 0.1093 | 4 | c.56- others(19): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100919736 | G | GTATC | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG01123.hp2 others(20): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0002others(3): Show | a0001c0001t0001g0019 a0001c0001t0001g0059 a0001c0001t0001g0071 others(20): Show |
23 | 124 | 0.1855 | 4 | c.56- others(19): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100921107 | C | CTCAT | intron_variant | MODIFIER | HG02258.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0003g0109 others(2): Show |
5 | 234 | 0.0214 | 4 | c.56- others(19): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100925812 | T | TATAC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(20): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(147): Show |
150 | 234 | 0.6410 | 4 | c.160 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100925856 | C | CATAT | intron_variant | MODIFIER | HG01261.hp2 HG02004.hp1 HG02273.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0021 a0001c0001t0001g0090 a0001c0001t0001g0121 |
3 | 187 | 0.0160 | 4 | c.160 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100926602 | T | TTGTG | intron_variant | MODIFIER | HG01261.hp2 HG02004.hp1 HG02273.hp1 others(9): Show |
a0001a0002 | a0001c0001a0002c0008 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0024 others(9): Show |
12 | 205 | 0.0585 | 4 | c.160 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100960260 | G | GCACA | intron_variant | MODIFIER | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(45): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0036 others(45): Show |
48 | 228 | 0.2105 | 4 | c.457 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100966884 | T | TACAC | intron_variant | MODIFIER | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(41): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0013others(6): Show | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0018 others(41): Show |
44 | 183 | 0.2404 | 4 | c.457 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100970663 | C | CGCCT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0002a0001c0003t0001 | a0001c0001t0001g0026 a0001c0001t0001g0079 a0001c0001t0001g0082 others(9): Show |
12 | 35 | 0.3429 | 4 | c.457 others(19): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 5/27 | chr12 | TogoVar | |||||||
ANO4_chr12_100789776_101133629 | 100970663 | C | CTCCT | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01074.hp1 others(20): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(20): Show |
23 | 46 | 0.5000 | 4 | c.457 others(19): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100989551 | G | GTGGA | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(37): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0016 others(37): Show |
40 | 208 | 0.1923 | 4 | c.734 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100989621 | A | AGATG | intron_variant | MODIFIER | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(34): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0002others(6): Show | a0001c0001t0001g0014 a0001c0001t0001g0082 a0001c0001t0001g0084 others(34): Show |
37 | 174 | 0.2126 | 4 | c.734 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100989750 | T | TATGG | intron_variant | MODIFIER | HG01517.hp1 HG01517.hp2 HG02055.hp1 others(8): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(3): Show | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0078 others(8): Show |
11 | 85 | 0.1294 | 4 | c.734 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100989975 | A | AGATG | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(44): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(44): Show |
47 | 152 | 0.3092 | 4 | c.734 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100991513 | T | TAAAA | intron_variant | MODIFIER | HG00099.hp2 HG00621.hp1 HG00673.hp1 others(27): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(3): Show | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0077 others(27): Show |
30 | 66 | 0.4545 | 4 | c.734 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100998379 | T | TTATC | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(11): Show | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0026 others(61): Show |
64 | 111 | 0.5766 | 4 | c.734 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 101063745 | C | CTTTT | intron_variant | MODIFIER | HG00438.hp2 HG00621.hp2 HG01192.hp1 others(16): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0008 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0078 others(16): Show |
19 | 36 | 0.5278 | 4 | c.131 others(25): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 101075636 | A | AATAT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(73): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(13): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(73): Show |
76 | 230 | 0.3304 | 4 | c.131 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 101080883 | T | TATTA | intron_variant | MODIFIER | HG02280.hp2 HG02559.hp2 HG02922.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0005a0001c0003t0001others(1): Show | a0001c0001t0001g0172 a0001c0001t0001g0204 a0001c0001t0005g0062 others(5): Show |
8 | 164 | 0.0488 | 4 | c.139 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 15/27 | chr12 | TogoVar | |||||||
ANO4_chr12_100789776_101133629 | 101080883 | T | TTATA | intron_variant | MODIFIER | HG01884.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0080 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | 160 | 0.0250 | 4 | c.139 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 101081022 | A | AGTGT | intron_variant | MODIFIER | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(83): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(13): Show | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0021 others(83): Show |
86 | 211 | 0.4076 | 4 | c.139 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 101086080 | C | CTGTG | intron_variant | MODIFIER | HG01192.hp2 HG01261.hp1 HG02615.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(3): Show | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0131 others(11): Show |
14 | 30 | 0.4667 | 4 | c.153 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 101103181 | T | TTATA | intron_variant | MODIFIER | HG01346.hp2 HG01496.hp1 HG02897.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0004 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0132 others(4): Show |
7 | 45 | 0.1556 | 4 | c.214 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 101104627 | G | GTGTA | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp1 HG01074.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0154 others(2): Show |
5 | 185 | 0.0270 | 4 | c.214 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 101106573 | G | GTATA | intron_variant | MODIFIER | HG00639.hp1 HG00733.hp1 HG01070.hp1 others(34): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0006others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(8): Show | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0102 others(34): Show |
37 | 140 | 0.2643 | 4 | c.215 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 101107550 | C | CTAAG | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(129): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(24): Show | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0021 others(129): Show |
132 | 234 | 0.5641 | 4 | c.215 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 101127936 | A | ATGAC | 3_prime_UTR_variant | MODIFIER | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0006 | a0001c0001t0004a0001c0003t0004a0001c0006t0004 | a0001c0001t0004g0038 a0001c0001t0004g0046 a0001c0001t0004g0051 others(5): Show |
8 | 234 | 0.0342 | 4 | c.*82 others(11): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 28/28 | 872 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ANO4_chr12_100789776_101133629 | 101129819 | G | GTGAT | downstream_gene_variant | MODIFIER | HG01884.hp1 HG01884.hp2 HG02647.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0054 a0001c0001t0001g0080 a0001c0001t0001g0227 others(4): Show |
7 | 234 | 0.0299 | 4 | c.*19 others(15): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1191 | chr12 | TogoVar | |||||||
ANO4_chr12_100789776_101133629 | 101131783 | C | CGTGT | downstream_gene_variant | MODIFIER | HG00621.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0014others(4): Show | a0001c0001t0001g0006 a0001c0001t0001g0047 a0001c0001t0001g0095 others(7): Show |
10 | 50 | 0.2000 | 4 | c.*39 others(15): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 3155 | chr12 | TogoVar | |||||||
ANO4_chr12_100789776_101133629 | 101131783 | C | CTTGT | downstream_gene_variant | MODIFIER | HG01081.hp1 HG01258.hp1 HG01952.hp1 others(5): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0003t0001 | a0001c0001t0001g0028 a0001c0001t0001g0082 a0001c0001t0001g0125 others(5): Show |
8 | 48 | 0.1667 | 4 | c.*39 others(15): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 3155 | chr12 | TogoVar |