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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AFF1_chr4_86930011_87146039 | 87001207 | C | CTT | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(58): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0003a0001c0005others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0090a0001c0001t0002g0018a0001c0001t0002g0024others(58): Show | 61 | 294 | 0.2075 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87002425 | G | GTT | intron_variant | MODIFIER | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(10): Show |
a0001a0006 | a0001c0001a0006c0031 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(5): Show | a0001c0001t0001g0125a0001c0001t0001g0154a0001c0001t0001g0163others(10): Show | 13 | 294 | 0.0442 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87005815 | A | AAT | intron_variant | MODIFIER | HG01167.hp1 HG01175.hp2 HG01243.hp1 others(10): Show |
a0001a0013 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(7): Show | a0001c0001t0002g0189a0001c0001t0002g0191a0001c0001t0002g0248others(10): Show | 13 | 294 | 0.0442 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87012217 | C | CTT | intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
a0001a0010 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0002a0001c0001t0008a0001c0001t0015others(4): Show | a0001c0001t0002g0248a0001c0001t0008g0115a0001c0001t0015g0114others(5): Show | 8 | 294 | 0.0272 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87017940 | T | TAA | intron_variant | MODIFIER | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(16): Show |
a0001a0003 | a0001c0003a0001c0007a0001c0014others(1): Show | a0001c0003t0001a0001c0003t0003a0001c0003t0007others(9): Show | a0001c0003t0001g0179a0001c0003t0001g0180a0001c0003t0003g0108others(16): Show | 19 | 294 | 0.0646 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87019884 | C | CGG | intron_variant | MODIFIER | HG00140.hp1 HG00558.hp1 HG00639.hp2 others(64): Show |
a0001a0009 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0001t0001g0119others(64): Show | 67 | 294 | 0.2279 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87019885 | G | GGT | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(13): Show |
a0001a0002a0007others(1): Show | a0001c0001a0001c0002a0002c0008others(2): Show | a0001c0001t0003a0001c0002t0005a0001c0002t0044others(5): Show | a0001c0001t0003g0192a0001c0002t0005g0185a0001c0002t0005g0193others(13): Show | 16 | 294 | 0.0544 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87022543 | G | GAT | intron_variant | MODIFIER | HG02630.hp2 HG03209.hp2 NA19030.hp1 others(1): Show |
a0001 | a0001c0001a0001c0006a0001c0030 | a0001c0001t0010a0001c0001t0013a0001c0006t0003others(1): Show | a0001c0001t0010g0253a0001c0001t0013g0287a0001c0006t0003g0291others(1): Show | 4 | 294 | 0.0136 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87022584 | C | CTG | intron_variant | MODIFIER | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0014a0001c0001t0017 | a0001c0001t0011g0094a0001c0001t0011g0265a0001c0001t0011g0266others(4): Show | 7 | 294 | 0.0238 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87022592 | A | ATC | intron_variant | MODIFIER | HG00558.hp1 HG02523.hp1 HG03516.hp1 others(2): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0048a0001c0004t0023 | a0001c0001t0001g0140a0001c0001t0001g0161a0001c0001t0001g0168others(2): Show | 5 | 294 | 0.0170 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87022661 | T | TAG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
a0001a0006a0008others(4): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(37): Show | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0077others(112): Show | 115 | 294 | 0.3912 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87026061 | C | CTT | intron_variant | MODIFIER | HG01167.hp1 HG01175.hp2 HG01243.hp1 others(17): Show |
a0001a0013 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(11): Show | a0001c0001t0002g0051a0001c0001t0002g0189a0001c0001t0002g0191others(17): Show | 20 | 294 | 0.0680 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87027784 | G | GTT | intron_variant | MODIFIER | HG00140.hp1 HG00673.hp2 HG00738.hp2 others(18): Show |
a0001a0006a0009others(1): Show | a0001c0001a0001c0004a0001c0011others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0046a0001c0001t0001g0140a0001c0001t0001g0143others(18): Show | 21 | 294 | 0.0714 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87030769 | A | ACT | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(14): Show |
a0001a0002a0007others(1): Show | a0001c0001a0001c0002a0002c0008others(2): Show | a0001c0001t0003a0001c0001t0045a0001c0002t0005others(6): Show | a0001c0001t0003g0192a0001c0001t0045g0093a0001c0002t0005g0185others(14): Show | 17 | 294 | 0.0578 | 2 | c.39- others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87040871 | C | CTT | intron_variant | MODIFIER | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(26): Show |
a0001a0002a0007others(3): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(18): Show | a0001c0001t0003g0079a0001c0001t0003g0192a0001c0001t0007g0269others(26): Show | 29 | 294 | 0.0986 | 2 | c.39- others(17): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87063228 | C | CTT | intron_variant | MODIFIER | HG00323.hp2 HG00621.hp2 HG00738.hp1 others(28): Show |
a0001a0008a0012 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0270a0001c0001t0002g0285a0001c0001t0003g0006others(28): Show | 31 | 294 | 0.1054 | 2 | c.105 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87064878 | G | GAA | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
a0001a0006a0009others(2): Show | a0001c0001a0001c0003a0001c0010others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(88): Show | 91 | 294 | 0.3095 | 2 | c.105 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87065510 | T | TAA | intron_variant | MODIFIER | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(7): Show |
a0001a0005 | a0001c0001a0005c0032 | a0001c0001t0004a0001c0001t0011a0001c0001t0017others(2): Show | a0001c0001t0004g0123a0001c0001t0011g0094a0001c0001t0011g0240others(7): Show | 10 | 294 | 0.0340 | 2 | c.105 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87068257 | G | GCC | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
a0001a0006a0009 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(22): Show | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(69): Show | 72 | 294 | 0.2449 | 2 | c.106 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87069271 | C | CTT | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
a0001a0009a0010others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0125a0001c0001t0001g0138a0001c0001t0001g0143others(34): Show | 37 | 294 | 0.1259 | 2 | c.106 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87069816 | A | ATT | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(30): Show |
a0001a0016 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(17): Show | a0001c0001t0001g0153a0001c0001t0003g0017a0001c0001t0003g0027others(30): Show | 33 | 294 | 0.1122 | 2 | c.106 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87072362 | C | CAA | intron_variant | MODIFIER | HG01884.hp2 HG02015.hp1 HG02056.hp2 others(4): Show |
a0001a0016 | a0001c0001a0016c0023 | a0001c0001t0001a0016c0023t0015 | a0001c0001t0001g0077a0001c0001t0001g0139a0001c0001t0001g0141others(4): Show | 7 | 294 | 0.0238 | 2 | c.106 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87073280 | C | CAA | intron_variant | MODIFIER | HG00280.hp1 HG01175.hp2 HG01517.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0028 | a0001c0001t0002a0001c0003t0020a0001c0028t0002 | a0001c0001t0002g0024a0001c0001t0002g0040a0001c0001t0002g0050others(5): Show | 8 | 294 | 0.0272 | 2 | c.106 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87081152 | A | ATT | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(21): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(9): Show | a0001c0001t0002g0255a0001c0001t0003g0006a0001c0001t0003g0007others(21): Show | 24 | 294 | 0.0816 | 2 | c.106 others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87083662 | A | ATT | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(98): Show |
a0001a0003a0004others(5): Show | a0001c0001a0001c0003a0001c0005others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0270a0001c0001t0002g0029a0001c0001t0002g0246others(98): Show | 101 | 294 | 0.3435 | 2 | c.106 others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87085751 | C | CTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(45): Show |
a0001a0009 | a0001c0001a0009c0024 | a0001c0001t0001a0001c0001t0002a0001c0001t0014others(4): Show | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(45): Show | 48 | 294 | 0.1633 | 2 | c.110 others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87101584 | G | GAA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
a0001a0002a0005others(8): Show | a0001c0001a0001c0002a0001c0003others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(43): Show | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(149): Show | 152 | 294 | 0.5170 | 2 | c.128 others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87116831 | G | GGT | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(1): Show | a0001c0001t0002g0049a0001c0001t0003g0002a0001c0001t0003g0005others(9): Show | 12 | 294 | 0.0408 | 2 | c.246 others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87118309 | C | CAT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
a0001a0002a0005others(8): Show | a0001c0001a0001c0002a0001c0003others(21): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(62): Show | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(186): Show | 189 | 294 | 0.6429 | 2 | c.246 others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 12/20 | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87122881 | T | TAA | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp1 HG00741.hp1 others(54): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(23): Show | a0001c0001t0002g0018a0001c0001t0002g0020a0001c0001t0002g0021others(54): Show | 57 | 294 | 0.1939 | 2 | c.246 others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87127163 | G | GTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(28): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0006a0001c0028others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(6): Show | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0001t0001g0077others(28): Show | 31 | 294 | 0.1054 | 2 | c.290 others(17): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 15/20 | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87138490 | G | GGT | 3_prime_UTR_variant | MODIFIER | HG01516.hp2 HG01981.hp1 HG03669.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0007a0001c0003t0007 | a0001c0001t0007g0004a0001c0001t0007g0081a0001c0001t0007g0145others(6): Show | 9 | 294 | 0.0306 | 2 | c.*28 others(13): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 21/21 | 2822 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||
AFF1_chr4_86930011_87146039 | 87143604 | C | CAA | downstream_gene_variant | MODIFIER | HG00621.hp2 HG01361.hp1 HG01891.hp2 others(15): Show |
a0001 | a0001c0001a0001c0002a0001c0014others(2): Show | a0001c0001t0003a0001c0001t0010a0001c0002t0005others(5): Show | a0001c0001t0003g0027a0001c0001t0010g0272a0001c0002t0005g0116others(15): Show | 18 | 294 | 0.0612 | 2 | c.*79 others(13): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2566 | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87145999 | C | CAA | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(50): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0003a0001c0007others(5): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(17): Show | a0001c0001t0003g0019a0001c0001t0003g0044a0001c0001t0003g0061others(50): Show | 53 | 294 | 0.1803 | 2 | c.*10 others(15): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4961 | chr4 | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148505955 | C | CTG | intron_variant | MODIFIER | HG03492.hp1 HG06807.hp1 NA19083.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0006a0001c0001t0043a0001c0003t0028others(1): Show | a0001c0001t0006g0138a0001c0001t0043g0006a0001c0003t0028g0005others(1): Show | 4 | 169 | 0.0237 | 2 | c.47+ others(17): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148506580 | T | TTA | intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0002 | a0001c0002t0094 | a0001c0002t0094g0106 | 1 | 169 | 0.0059 | 2 | c.47+ others(17): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148517861 | C | CAA | intron_variant | MODIFIER | NA19000.hp1 | a0001 | a0001c0001 | a0001c0001t0059 | a0001c0001t0059g0014 | 1 | 169 | 0.0059 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148521374 | G | GCA | intron_variant | MODIFIER | HG01192.hp1 HG01256.hp1 HG03209.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0008a0001c0001t0013others(3): Show | a0001c0001t0002g0166a0001c0001t0008g0073a0001c0001t0013g0072others(3): Show | 6 | 169 | 0.0355 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148524097 | T | TTC | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(24): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0009others(19): Show | a0001c0001t0006g0138a0001c0001t0006g0144a0001c0001t0006g0163others(24): Show | 27 | 169 | 0.1598 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148524123 | C | CTG | intron_variant | MODIFIER | HG02630.hp1 NA20300.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0077a0001c0002t0034 | a0001c0001t0077g0095a0001c0002t0034g0077 | 2 | 169 | 0.0118 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148526366 | G | GTT | intron_variant | MODIFIER | NA18967.hp1 NA19004.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0042 | a0001c0001t0003g0066a0001c0001t0042g0012 | 2 | 169 | 0.0118 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148529908 | G | GGT | intron_variant | MODIFIER | NA18974.hp1 | a0003 | a0003c0008 | a0003c0008t0045 | a0003c0008t0045g0010 | 1 | 169 | 0.0059 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148530593 | C | CTT | intron_variant | MODIFIER | HG01884.hp2 HG06807.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0031a0001c0003t0028 | a0001c0002t0031g0148a0001c0003t0028g0005 | 2 | 169 | 0.0118 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148532856 | A | ATG | intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0003 | a0001c0003t0079 | a0001c0003t0079g0161 | 1 | 169 | 0.0059 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148540407 | C | CTT | intron_variant | MODIFIER | HG01891.hp1 HG02280.hp1 HG02965.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0038a0001c0002t0019a0001c0002t0020others(2): Show | a0001c0001t0038g0102a0001c0002t0019g0123a0001c0002t0020g0132others(2): Show | 5 | 169 | 0.0296 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148551482 | G | GAA | intron_variant | MODIFIER | HG01891.hp2 HG01928.hp1 HG02895.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0046a0001c0001t0057others(3): Show | a0001c0001t0003g0063a0001c0001t0046g0165a0001c0001t0057g0135others(3): Show | 6 | 169 | 0.0355 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148560836 | T | TGG | intron_variant | MODIFIER | HG01243.hp1 HG02647.hp1 |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0044 | a0001c0001t0011g0128a0001c0001t0044g0127 | 2 | 169 | 0.0118 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148560881 | T | TTC | intron_variant | MODIFIER | NA18974.hp1 | a0003 | a0003c0008 | a0003c0008t0045 | a0003c0008t0045g0010 | 1 | 169 | 0.0059 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148560965 | A | ACT | intron_variant | MODIFIER | NA18974.hp1 | a0003 | a0003c0008 | a0003c0008t0045 | a0003c0008t0045g0010 | 1 | 169 | 0.0059 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148561641 | C | CCT | intron_variant | MODIFIER | NA18974.hp1 | a0003 | a0003c0008 | a0003c0008t0045 | a0003c0008t0045g0010 | 1 | 169 | 0.0059 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar |