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 | 26577564 | CAA | C | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 HG00639.hp2 others(79): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0002others(22): Show | a0001c0001t0001g0040 a0001c0001t0001g0077 a0001c0001t0001g0080 others(79): Show |
82 | 190 | 0.4316 | -2 | c.144 others(23): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26581688 | CAA | C | intron_variant | MODIFIER | HG00735.hp1 HG01168.hp2 HG01243.hp1 others(30): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(14): Show | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0123 others(30): Show |
33 | 190 | 0.1737 | -2 | c.144 others(23): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26586354 | CTT | C | intron_variant | MODIFIER | HG02280.hp1 HG02559.hp2 HG02896.hp1 others(3): Show |
a0001 | a0001c0005a0001c0006 | a0001c0005t0006a0001c0005t0026a0001c0006t0005others(2): Show | a0001c0005t0006g0085 a0001c0005t0006g0155 a0001c0005t0026g0161 others(3): Show |
6 | 190 | 0.0316 | -2 | c.144 others(23): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26603669 | TAC | T | intron_variant | MODIFIER | HG00140.hp1 HG00597.hp1 HG00639.hp2 others(52): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0007others(12): Show | a0001c0001t0001g0139 a0001c0002t0002g0030 a0001c0002t0002g0031 others(52): Show |
55 | 190 | 0.2895 | -2 | c.183 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26615394 | TTA | T | intron_variant | MODIFIER | HG00140.hp1 HG06807.hp1 NA18942.hp1 others(6): Show |
a0001 | a0001c0002a0001c0006a0001c0008 | a0001c0002t0002a0001c0006t0030a0001c0008t0009 | a0001c0002t0002g0030 a0001c0002t0002g0031 a0001c0002t0002g0056 others(6): Show |
9 | 190 | 0.0474 | -2 | c.183 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26615414 | ATT | A | intron_variant | MODIFIER | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(14): Show | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0040 others(61): Show |
64 | 190 | 0.3368 | -2 | c.183 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26616436 | GTT | G | intron_variant | MODIFIER | HG00140.hp1 HG00597.hp1 HG00639.hp2 others(52): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0007others(12): Show | a0001c0001t0001g0139 a0001c0002t0002g0030 a0001c0002t0002g0031 others(52): Show |
55 | 190 | 0.2895 | -2 | c.183 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26627814 | AGT | A | intron_variant | MODIFIER | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(35): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0007others(7): Show | a0001c0001t0001g0139 a0001c0002t0002g0030 a0001c0002t0002g0031 others(35): Show |
38 | 190 | 0.2000 | -2 | c.187 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26627854 | TGC | T | intron_variant | MODIFIER | HG00140.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
a0001 | a0001c0001a0001c0004a0001c0006others(3): Show | a0001c0001t0003a0001c0004t0003a0001c0006t0025others(3): Show | a0001c0001t0003g0132 a0001c0004t0003g0001 a0001c0004t0003g0002 others(6): Show |
9 | 190 | 0.0474 | -2 | c.187 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26628194 | ATT | A | intron_variant | MODIFIER | HG01168.hp1 HG01169.hp1 |
a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0036 a0001c0003t0002g0037 |
2 | 190 | 0.0105 | -2 | c.187 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 18/26 | chr11 | TogoVar | |||||||
ANO3_chr11_26327130_26668289 | 26632622 | AAC | A | intron_variant | MODIFIER | HG02572.hp2 HG02895.hp2 |
a0001 | a0001c0001 | a0001c0001t0018a0001c0001t0020 | a0001c0001t0018g0099 a0001c0001t0020g0079 |
2 | 190 | 0.0105 | -2 | c.187 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26641210 | TCA | T | intron_variant | MODIFIER | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(64): Show |
a0001 | a0001c0002a0001c0003a0001c0005others(3): Show | a0001c0002t0002a0001c0002t0007a0001c0002t0008others(13): Show | a0001c0002t0002g0030 a0001c0002t0002g0031 a0001c0002t0002g0033 others(64): Show |
67 | 190 | 0.3526 | -2 | c.214 others(19): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26642342 | CTT | C | intron_variant | MODIFIER | HG01361.hp2 HG02071.hp1 HG02257.hp2 others(11): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(5): Show | a0001c0001t0003a0001c0004t0004a0001c0005t0010others(7): Show | a0001c0001t0003g0132 a0001c0004t0004g0116 a0001c0005t0010g0008 others(11): Show |
14 | 190 | 0.0737 | -2 | c.227 others(19): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26644815 | TCA | T | intron_variant | MODIFIER | HG00558.hp2 HG00733.hp1 HG01167.hp1 others(26): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0005t0005others(10): Show | a0001c0001t0001g0082 a0001c0001t0001g0139 a0001c0001t0001g0173 others(26): Show |
29 | 190 | 0.1526 | -2 | c.242 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26659079 | TAC | T | intron_variant | MODIFIER | HG01070.hp1 HG01255.hp1 HG03490.hp2 others(1): Show |
a0001 | a0001c0005a0001c0006 | a0001c0005t0012a0001c0006t0012 | a0001c0005t0012g0062 a0001c0005t0012g0175 a0001c0006t0012g0027 others(1): Show |
4 | 190 | 0.0211 | -2 | c.276 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26659099 | CAT | C | intron_variant | MODIFIER | HG00735.hp1 HG01346.hp1 HG01358.hp2 others(5): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0023a0001c0001t0027others(1): Show | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(5): Show |
8 | 190 | 0.0421 | -2 | c.276 others(21): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ANO3_chr11_26327130_26668289 | 26665110 | AAG | A | downstream_gene_variant | MODIFIER | HG01070.hp1 HG01255.hp1 HG03490.hp2 others(1): Show |
a0001 | a0001c0005a0001c0006 | a0001c0005t0012a0001c0006t0012 | a0001c0005t0012g0062 a0001c0005t0012g0175 a0001c0006t0012g0027 others(1): Show |
4 | 190 | 0.0211 | -2 | c.*46 others(13): Show |
ANO3 | ENSG00000134343.14 | transcript | ENST00000256737.8 | protein_coding | 1822 | chr11 | TogoVar | |||||||
ANO4_chr12_100789776_101133629 | 100796036 | ATT | A | intron_variant | MODIFIER | HG00738.hp1 HG01884.hp1 HG02055.hp2 others(17): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0050 others(17): Show |
20 | 236 | 0.0848 | -2 | c.-14 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100796545 | ACG | A | intron_variant | MODIFIER | HG02257.hp2 HG02976.hp2 HG03130.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | 236 | 0.0254 | -2 | c.-14 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | chr12 | TogoVar | |||||||
ANO4_chr12_100789776_101133629 | 100797145 | TAC | T | intron_variant | MODIFIER | HG03041.hp1 HG03486.hp1 NA20300.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0012a0001c0003t0003 | a0001c0001t0001g0059 a0001c0001t0012g0061 a0001c0003t0003g0060 |
3 | 236 | 0.0127 | -2 | c.-14 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100801093 | GTC | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(17): Show | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0059 others(120): Show |
123 | 236 | 0.5212 | -2 | c.-14 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100801124 | TCA | T | intron_variant | MODIFIER | HG01884.hp2 HG02451.hp2 HG02622.hp2 others(10): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(5): Show | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0229 others(10): Show |
13 | 236 | 0.0551 | -2 | c.-14 others(21): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | chr12 | TogoVar | |||||||
ANO4_chr12_100789776_101133629 | 100812039 | TAC | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(158): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(25): Show | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0050 others(158): Show |
161 | 236 | 0.6822 | -2 | 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 | 100815753 | ATG | A | intron_variant | MODIFIER | HG01081.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
a0001a0002 | a0001c0003a0001c0007a0002c0004 | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(2): Show | a0001c0003t0001g0028 a0001c0003t0001g0044 a0001c0003t0001g0049 others(5): Show |
8 | 236 | 0.0339 | -2 | 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 | 100819035 | GTA | G | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(53): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(14): Show | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0058 others(53): Show |
56 | 236 | 0.2373 | -2 | 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 | 100820355 | CAA | C | intron_variant | MODIFIER | HG00733.hp1 HG02886.hp2 HG02922.hp1 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0003t0003others(1): Show | a0001c0001t0001g0058 a0001c0001t0001g0127 a0001c0001t0001g0132 others(3): Show |
6 | 236 | 0.0254 | -2 | 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 | 100834531 | CAT | C | intron_variant | MODIFIER | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(2): Show | a0001c0001t0001g0080 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
11 | 236 | 0.0466 | -2 | 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 | 100837720 | TAA | T | intron_variant | MODIFIER | HG01884.hp2 HG01928.hp2 HG02145.hp1 others(14): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(4): Show | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0080 others(14): Show |
17 | 236 | 0.0720 | -2 | 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 | 100838229 | CAA | C | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp2 HG01109.hp1 others(32): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(4): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(32): Show |
35 | 236 | 0.1483 | -2 | 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 | 100842061 | ACC | A | intron_variant | MODIFIER | HG00738.hp1 HG00738.hp2 HG00741.hp2 others(23): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0002others(9): Show | a0001c0001t0001g0024 a0001c0001t0001g0113 a0001c0001t0001g0114 others(23): Show |
26 | 236 | 0.1102 | -2 | 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 | 100846945 | ACC | A | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(90): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(18): Show | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0026 others(90): Show |
93 | 236 | 0.3941 | -2 | 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 | 100847495 | GGA | G | intron_variant | MODIFIER | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(39): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0002others(4): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(39): Show |
42 | 236 | 0.1780 | -2 | 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 | 100862726 | CAT | C | intron_variant | MODIFIER | HG01884.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0080 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | 236 | 0.0170 | -2 | c.-14 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | chr12 | TogoVar | |||||||
ANO4_chr12_100789776_101133629 | 100867612 | TCA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(23): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(160): Show |
163 | 236 | 0.6907 | -2 | 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 | 100881413 | CTG | C | intron_variant | MODIFIER | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(31): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(3): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(31): Show |
34 | 236 | 0.1441 | -2 | 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 | 100890291 | CCA | C | intron_variant | MODIFIER | HG01258.hp2 HG02280.hp2 HG02559.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0005g0075 |
3 | 236 | 0.0127 | -2 | c.-14 others(23): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 1/27 | chr12 | TogoVar | |||||||
ANO4_chr12_100789776_101133629 | 100912392 | CAA | C | intron_variant | MODIFIER | HG02258.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0003g0051 others(3): Show |
6 | 236 | 0.0254 | -2 | c.56- others(17): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100916053 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(27): Show | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
181 | 236 | 0.7670 | -2 | c.56- others(17): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100919670 | CTG | C | intron_variant | MODIFIER | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(29): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0009a0001c0002t0002others(3): Show | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(29): Show |
32 | 236 | 0.1356 | -2 | c.56- others(17): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100922079 | TTC | T | intron_variant | MODIFIER | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(4): Show | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0053 others(14): Show |
17 | 236 | 0.0720 | -2 | c.56- others(15): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100925765 | GTA | G | intron_variant | MODIFIER | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(47): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0009a0001c0002t0002others(6): Show | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(47): Show |
50 | 236 | 0.2119 | -2 | c.160 others(19): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100925856 | CAT | C | intron_variant | MODIFIER | HG01123.hp1 HG03834.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0102 a0001c0001t0001g0114 |
2 | 236 | 0.0085 | -2 | c.160 others(19): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100935350 | CAT | C | intron_variant | MODIFIER | HG01123.hp1 HG03834.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0102 a0001c0001t0001g0114 |
2 | 236 | 0.0085 | -2 | c.161 others(19): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 3/27 | chr12 | TogoVar | |||||||
ANO4_chr12_100789776_101133629 | 100941746 | ATG | A | intron_variant | MODIFIER | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(4): Show | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0058 others(12): Show |
15 | 236 | 0.0636 | -2 | c.298 others(17): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100948150 | CAA | C | intron_variant | MODIFIER | HG02622.hp2 HG02809.hp1 HG02818.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(4): Show | a0001c0001t0001g0207 a0001c0001t0003g0228 a0001c0001t0005g0062 others(5): Show |
8 | 236 | 0.0339 | -2 | c.456 others(19): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ANO4_chr12_100789776_101133629 | 100966816 | CAT | C | intron_variant | MODIFIER | HG01261.hp2 HG02004.hp1 HG02273.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0017 others(3): Show |
6 | 236 | 0.0254 | -2 | 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 | 100966838 | TAC | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(24): Show | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0017 others(118): Show |
121 | 236 | 0.5127 | -2 | 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 | 100966861 | GTA | G | intron_variant | MODIFIER | HG00558.hp1 HG00673.hp1 HG01109.hp2 others(40): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | a0001c0001t0001g0036 a0001c0001t0001g0080 a0001c0001t0001g0091 others(40): Show |
43 | 236 | 0.1822 | -2 | 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 | 100967570 | GAC | G | intron_variant | MODIFIER | HG00140.hp2 HG00438.hp2 HG00738.hp1 others(42): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(7): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(42): Show |
45 | 236 | 0.1907 | -2 | 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 | 100975943 | AAG | A | intron_variant | MODIFIER | HG00558.hp1 HG00673.hp1 HG00733.hp1 others(39): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0014others(8): Show | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0036 others(39): Show |
42 | 236 | 0.1780 | -2 | c.602 others(19): Show |
ANO4 | ENSG00000151572.18 | transcript | ENST00000392977.8 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |