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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AFF2_chrX_148495617_149005663 | 148620526 | AAT | A | intron_variant | MODIFIER | HG01109.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0124 | 1 | 169 | 0.0059 | -2 | c.48- others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148629101 | TTG | T | intron_variant | MODIFIER | HG02602.hp1 HG03017.hp1 HG03130.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0002t0022a0001c0002t0108 | a0001c0001t0009g0142 a0001c0001t0009g0143 a0001c0002t0022g0003 others(1): Show |
4 | 169 | 0.0237 | -2 | c.48- others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148646329 | GAA | G | intron_variant | MODIFIER | HG02572.hp1 HG02809.hp2 HG02886.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0066a0001c0002t0040a0001c0002t0082others(1): Show | a0001c0001t0066g0015 a0001c0002t0040g0111 a0001c0002t0082g0016 others(1): Show |
4 | 169 | 0.0237 | -2 | c.48- others(17): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148648561 | CAA | C | intron_variant | MODIFIER | HG02818.hp1 | a0001 | a0001c0002 | a0001c0002t0009 | a0001c0002t0009g0126 | 1 | 169 | 0.0059 | -2 | c.48- others(17): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148653360 | AGT | A | intron_variant | MODIFIER | HG00140.hp1 HG00673.hp1 HG02027.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(5): Show | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0005g0001 others(9): Show |
12 | 169 | 0.0710 | -2 | c.180 others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148656493 | ATT | A | intron_variant | MODIFIER | HG02818.hp1 | a0001 | a0001c0002 | a0001c0002t0009 | a0001c0002t0009g0126 | 1 | 169 | 0.0059 | -2 | c.180 others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148676057 | ATT | A | intron_variant | MODIFIER | HG01109.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0010a0001c0001t0016a0001c0001t0022others(9): Show | a0001c0001t0010g0124 a0001c0001t0016g0154 a0001c0001t0022g0134 others(9): Show |
12 | 169 | 0.0710 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148681536 | ATG | A | intron_variant | MODIFIER | HG01109.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0006a0001c0001t0010a0001c0001t0037others(5): Show | a0001c0001t0006g0138 a0001c0001t0010g0124 a0001c0001t0037g0037 others(5): Show |
8 | 169 | 0.0473 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148681565 | AGT | A | intron_variant | MODIFIER | NA19091.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0020 | 1 | 169 | 0.0059 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148681583 | TGA | T | intron_variant | MODIFIER | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(35): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0001g0082 others(35): Show |
38 | 169 | 0.2249 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148694810 | CTT | C | intron_variant | MODIFIER | HG02451.hp1 HG03041.hp2 HG03540.hp1 others(5): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0008 | a0001c0001t0002a0001c0001t0016a0001c0001t0085others(4): Show | a0001c0001t0002g0020 a0001c0001t0002g0062 a0001c0001t0016g0154 others(5): Show |
8 | 169 | 0.0473 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148698797 | GTT | G | intron_variant | MODIFIER | HG00609.hp1 HG00639.hp2 HG01074.hp1 others(51): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(45): Show | a0001c0001t0002g0029 a0001c0001t0002g0062 a0001c0001t0002g0166 others(51): Show |
54 | 169 | 0.3195 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148700419 | AGT | A | intron_variant | MODIFIER | HG01891.hp2 HG01934.hp1 HG02622.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0010others(7): Show | a0001c0001t0001g0070 a0001c0001t0005g0001 a0001c0001t0010g0115 others(8): Show |
11 | 169 | 0.0651 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148701012 | ATG | A | intron_variant | MODIFIER | HG01952.hp1 HG03041.hp2 HG03471.hp1 |
a0001a0002 | a0001c0001a0001c0002a0002c0009 | a0001c0001t0025a0001c0002t0072a0002c0009t0103 | a0001c0001t0025g0081 a0001c0002t0072g0018 a0002c0009t0103g0050 |
3 | 169 | 0.0178 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148704216 | CTA | C | intron_variant | MODIFIER | HG01891.hp2 HG02896.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0110a0001c0004t0095 | a0001c0001t0110g0118 a0001c0004t0095g0113 |
2 | 169 | 0.0118 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148704288 | GTA | G | intron_variant | MODIFIER | HG01243.hp1 HG02647.hp1 HG02895.hp1 |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0044a0001c0001t0106 | a0001c0001t0011g0128 a0001c0001t0044g0127 a0001c0001t0106g0121 |
3 | 169 | 0.0178 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148704404 | TTA | T | intron_variant | MODIFIER | HG00621.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0042 | 1 | 169 | 0.0059 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148704438 | GTA | G | intron_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0001 | a0001c0001t0119 | a0001c0001t0119g0061 | 1 | 169 | 0.0059 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148731512 | ACT | A | intron_variant | MODIFIER | HG02818.hp1 | a0001 | a0001c0002 | a0001c0002t0009 | a0001c0002t0009g0126 | 1 | 169 | 0.0059 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148761465 | TTG | T | intron_variant | MODIFIER | HG02451.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0066a0001c0001t0098a0001c0001t0106others(4): Show | a0001c0001t0066g0015 a0001c0001t0098g0119 a0001c0001t0106g0121 others(4): Show |
7 | 169 | 0.0414 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148762448 | GAT | G | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0006a0001c0001t0025a0001c0001t0077others(4): Show | a0001c0001t0006g0144 a0001c0001t0006g0163 a0001c0001t0025g0081 others(5): Show |
8 | 169 | 0.0473 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148762480 | ATG | A | intron_variant | MODIFIER | HG02809.hp2 HG03041.hp2 |
a0001 | a0001c0002 | a0001c0002t0040a0001c0002t0072 | a0001c0002t0040g0111 a0001c0002t0072g0018 |
2 | 169 | 0.0118 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148772542 | CTT | C | intron_variant | MODIFIER | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(150): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(114): Show | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0068 others(150): Show |
153 | 169 | 0.9053 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148788747 | GTC | G | intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0002 | a0001c0002t0032 | a0001c0002t0032g0114 | 1 | 169 | 0.0059 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148795800 | CAA | C | intron_variant | MODIFIER | HG01106.hp1 HG01256.hp1 HG01891.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0042others(3): Show | a0001c0001t0001g0076 a0001c0001t0002g0166 a0001c0001t0042g0012 others(3): Show |
6 | 169 | 0.0355 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148795832 | AAT | A | intron_variant | MODIFIER | HG01167.hp1 HG01978.hp1 HG02074.hp1 others(10): Show |
a0001a0003 | a0001c0001a0003c0008 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(8): Show | a0001c0001t0003g0065 a0001c0001t0003g0066 a0001c0001t0003g0086 others(10): Show |
13 | 169 | 0.0769 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148797229 | AAC | A | intron_variant | MODIFIER | HG01884.hp1 HG02280.hp1 HG02622.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0022a0001c0002t0009a0001c0002t0018others(12): Show | a0001c0001t0022g0134 a0001c0002t0009g0126 a0001c0002t0018g0151 others(13): Show |
16 | 169 | 0.0947 | -2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148806788 | ACT | A | intron_variant | MODIFIER | HG02132.hp1 | a0001 | a0001c0001 | a0001c0001t0024 | a0001c0001t0024g0091 | 1 | 169 | 0.0059 | -2 | c.104 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148811983 | CTT | C | intron_variant | MODIFIER | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0020a0001c0001t0038a0001c0001t0089others(3): Show | a0001c0001t0020g0109 a0001c0001t0038g0102 a0001c0001t0089g0110 others(3): Show |
6 | 169 | 0.0355 | -2 | c.108 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148816933 | CAA | C | intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0005 | a0001c0005t0023 | a0001c0005t0023g0129 | 1 | 169 | 0.0059 | -2 | c.108 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148822704 | GGT | G | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(95): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0009others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(69): Show | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0039 others(95): Show |
98 | 169 | 0.5799 | -2 | c.108 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148825052 | CCA | C | intron_variant | MODIFIER | HG02895.hp1 | a0001 | a0001c0001 | a0001c0001t0106 | a0001c0001t0106g0121 | 1 | 169 | 0.0059 | -2 | c.108 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148827619 | CAT | C | intron_variant | MODIFIER | HG01884.hp2 HG02145.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0031a0001c0003t0109 | a0001c0002t0031g0148 a0001c0003t0109g0122 |
2 | 169 | 0.0118 | -2 | c.108 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148833601 | CAA | C | intron_variant | MODIFIER | HG01891.hp2 HG03486.hp1 NA20752.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0046a0001c0001t0110 | a0001c0001t0005g0022 a0001c0001t0046g0165 a0001c0001t0110g0118 |
3 | 169 | 0.0178 | -2 | c.108 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148834505 | ATG | A | intron_variant | MODIFIER | HG01884.hp1 HG02074.hp1 HG02145.hp1 others(29): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0004a0001c0001t0011a0001c0001t0014others(27): Show | a0001c0001t0004g0043 a0001c0001t0011g0112 a0001c0001t0014g0055 others(29): Show |
32 | 169 | 0.1894 | -2 | c.108 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148839894 | GGT | G | intron_variant | MODIFIER | HG00642.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0011a0001c0001t0039a0001c0001t0077others(18): Show | a0001c0001t0011g0112 a0001c0001t0039g0101 a0001c0001t0077g0095 others(18): Show |
21 | 169 | 0.1243 | -2 | c.117 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148845143 | ACG | A | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(95): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(65): Show | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0039 others(95): Show |
98 | 169 | 0.5799 | -2 | c.126 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148849352 | GTC | G | intron_variant | MODIFIER | HG02818.hp1 | a0001 | a0001c0002 | a0001c0002t0009 | a0001c0002t0009g0126 | 1 | 169 | 0.0059 | -2 | c.126 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148852389 | GTT | G | intron_variant | MODIFIER | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0001t0010a0001c0001t0014others(14): Show | a0001c0001t0004g0043 a0001c0001t0010g0115 a0001c0001t0010g0116 others(18): Show |
21 | 169 | 0.1243 | -2 | c.126 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148871938 | CTG | C | intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0002 | a0001c0002t0034 | a0001c0002t0034g0077 | 1 | 169 | 0.0059 | -2 | c.126 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148874434 | GAA | G | intron_variant | MODIFIER | HG01891.hp2 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0046a0001c0001t0110 | a0001c0001t0046g0165 a0001c0001t0110g0118 |
2 | 169 | 0.0118 | -2 | c.126 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148883980 | TAC | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(116): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(83): Show | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0039 others(116): Show |
119 | 169 | 0.7041 | -2 | c.126 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148895570 | AGT | A | intron_variant | MODIFIER | HG01884.hp1 HG02258.hp1 HG02451.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0009a0001c0001t0057a0001c0001t0074others(13): Show | a0001c0001t0009g0142 a0001c0001t0057g0135 a0001c0001t0074g0033 others(14): Show |
17 | 169 | 0.1006 | -2 | c.136 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148897221 | CTA | C | intron_variant | MODIFIER | HG01934.hp1 HG02074.hp1 HG02451.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0010a0001c0001t0016others(2): Show | a0001c0001t0004g0043 a0001c0001t0010g0115 a0001c0001t0010g0116 others(3): Show |
6 | 169 | 0.0355 | -2 | c.136 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148897271 | ATG | A | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(23): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0070 a0001c0001t0001g0076 a0001c0001t0002g0054 others(23): Show |
26 | 169 | 0.1539 | -2 | c.136 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148899949 | AAT | A | intron_variant | MODIFIER | HG02280.hp1 NA21309.hp1 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0054a0001c0005t0023 | a0001c0002t0054g0133 a0001c0005t0023g0129 |
2 | 169 | 0.0118 | -2 | c.136 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148911075 | TTA | T | intron_variant | MODIFIER | HG00280.hp1 HG01106.hp1 HG02055.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0006a0001c0001t0011others(8): Show | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0006g0144 others(10): Show |
13 | 169 | 0.0769 | -2 | c.139 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148916196 | CTT | C | intron_variant | MODIFIER | HG03486.hp2 NA18967.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0042a0001c0002t0105 | a0001c0001t0042g0012 a0001c0002t0105g0117 |
2 | 169 | 0.0118 | -2 | c.139 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148935161 | CAT | C | intron_variant | MODIFIER | HG01261.hp1 HG01928.hp1 HG01978.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0055a0001c0001t0056others(1): Show | a0001c0001t0007g0048 a0001c0001t0055g0025 a0001c0001t0056g0023 others(1): Show |
4 | 169 | 0.0237 | -2 | c.139 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148935396 | TAC | T | intron_variant | MODIFIER | HG01891.hp2 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0046a0001c0001t0110 | a0001c0001t0046g0165 a0001c0001t0110g0118 |
2 | 169 | 0.0118 | -2 | c.139 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar |