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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AFF2_chrX_148495617_149005663 | 148761465 | TTG | T | intron_variant | MODIFIER | HG02451.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0066a0001c0001t0098a0001c0001t0106others(4): Show | a0001c0001t0066g0015a0001c0001t0098g0119a0001c0001t0106g0121others(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 | a0001c0001t0006g0144a0001c0001t0006g0163a0001c0001t0025g0081others(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 | a0001c0002t0040g0111a0001c0002t0072g0018 | 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 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0068others(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 | a0001c0001t0001g0076a0001c0001t0002g0166a0001c0001t0042g0012others(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 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0086others(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 | a0001c0001t0022g0134a0001c0002t0009g0126a0001c0002t0018g0151others(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 | a0001c0001t0020g0109a0001c0001t0038g0102a0001c0001t0089g0110others(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 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(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 | a0001c0002t0031g0148a0001c0003t0109g0122 | 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 | a0001c0001t0005g0022a0001c0001t0046g0165a0001c0001t0110g0118 | 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 | a0001c0001t0004g0043a0001c0001t0011g0112a0001c0001t0014g0055others(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 | a0001c0001t0011g0112a0001c0001t0039g0101a0001c0001t0077g0095others(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 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(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 | a0001c0001t0004g0043a0001c0001t0010g0115a0001c0001t0010g0116others(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 | a0001c0001t0046g0165a0001c0001t0110g0118 | 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 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(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 | a0001c0001t0009g0142a0001c0001t0057g0135a0001c0001t0074g0033others(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 | a0001c0001t0004g0043a0001c0001t0010g0115a0001c0001t0010g0116others(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 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0002g0054others(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 | a0001c0002t0054g0133a0001c0005t0023g0129 | 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 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0006g0144others(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 | a0001c0001t0042g0012a0001c0002t0105g0117 | 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 | a0001c0001t0007g0048a0001c0001t0055g0025a0001c0001t0056g0023others(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 | a0001c0001t0046g0165a0001c0001t0110g0118 | 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 | 148942817 | GAA | G | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(114): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(82): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(114): Show | 117 | 169 | 0.6923 | -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 | 148951181 | GCA | G | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(140): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(103): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(140): Show | 143 | 169 | 0.8462 | -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 | 148953812 | CAG | C | intron_variant | MODIFIER | HG02630.hp2 HG02976.hp1 |
a0001 | a0001c0002 | a0001c0002t0029a0001c0002t0032 | a0001c0002t0029g0149a0001c0002t0032g0114 | 2 | 169 | 0.0118 | -2 | c.155 others(17): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148958995 | GAA | G | intron_variant | MODIFIER | HG02055.hp1 HG02145.hp1 HG02630.hp2 others(4): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0019a0001c0002t0022a0001c0002t0029others(4): Show | a0001c0002t0019g0107a0001c0002t0022g0003a0001c0002t0029g0149others(4): Show | 7 | 169 | 0.0414 | -2 | c.269 others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148966677 | CTT | C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(87): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(63): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0068others(87): Show | 90 | 169 | 0.5325 | -2 | c.291 others(17): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148971747 | CTT | C | intron_variant | MODIFIER | HG02074.hp1 HG02257.hp1 HG02615.hp1 others(6): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0004a0001c0001t0011a0001c0001t0035others(5): Show | a0001c0001t0004g0043a0001c0001t0011g0112a0001c0001t0011g0128others(6): Show | 9 | 169 | 0.0533 | -2 | c.326 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148971771 | ATG | A | intron_variant | MODIFIER | HG02486.hp1 HG02615.hp1 HG02809.hp1 |
a0001 | a0001c0001 | a0001c0001t0035a0001c0001t0092a0001c0001t0093 | a0001c0001t0035g0078a0001c0001t0092g0008a0001c0001t0093g0007 | 3 | 169 | 0.0178 | -2 | c.326 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148977614 | GAC | G | intron_variant | MODIFIER | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0046a0001c0002t0031a0001c0002t0054others(1): Show | a0001c0001t0046g0165a0001c0002t0031g0148a0001c0002t0054g0133others(1): Show | 4 | 169 | 0.0237 | -2 | c.340 others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148985285 | CTT | C | intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0002 | a0001c0002t0105 | a0001c0002t0105g0117 | 1 | 169 | 0.0059 | -2 | c.362 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148991933 | CTA | C | 3_prime_UTR_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0074 | a0001c0001t0074g0033 | 1 | 169 | 0.0059 | -2 | c.*60 others(11): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 21/21 | 603 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||
AFF2_chrX_148495617_149005663 | 148997299 | ACT | A | 3_prime_UTR_variant | MODIFIER | HG02572.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
a0001 | a0001c0004a0001c0005 | a0001c0004t0075a0001c0004t0113a0001c0005t0023 | a0001c0004t0075g0004a0001c0004t0113g0159a0001c0005t0023g0125others(1): Show | 4 | 169 | 0.0237 | -2 | c.*59 others(13): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 21/21 | 5969 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||
AFF2_chrX_148495617_149005663 | 148999579 | AGT | A | 3_prime_UTR_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0001 | a0001c0001t0025 | a0001c0001t0025g0081 | 1 | 169 | 0.0059 | -2 | c.*82 others(13): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 21/21 | 8269 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||
AFF2_chrX_148495617_149005663 | 148999601 | TGC | T | 3_prime_UTR_variant | MODIFIER | HG01192.hp1 HG01258.hp1 HG01433.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0051a0001c0001t0104 | a0001c0001t0008g0051a0001c0001t0008g0059a0001c0001t0008g0073others(2): Show | 5 | 169 | 0.0296 | -2 | c.*82 others(13): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 21/21 | 8274 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||
AFF3_chr2_99540419_100147590 | 99553917 | CCA | C | intron_variant | MODIFIER | HG00099.hp1 HG00639.hp1 HG01071.hp1 others(20): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0005others(5): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0022others(12): Show | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0036others(20): Show | 23 | 100 | 0.2300 | -2 | c.355 others(19): Show |
AFF3 | ENSG00000144218.21 | transcript | ENST00000672756.2 | protein_coding | 24/24 | chr2 | TogoVar | ||||||
AFF3_chr2_99540419_100147590 | 99567134 | ATT | A | intron_variant | MODIFIER | HG01358.hp1 HG02615.hp2 HG03516.hp2 others(3): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0005a0001c0009others(3): Show | a0001c0001t0024a0001c0005t0003a0001c0009t0009others(3): Show | a0001c0001t0024g0058a0001c0005t0003g0071a0001c0009t0009g0017others(3): Show | 6 | 100 | 0.0600 | -2 | c.298 others(21): Show |
AFF3 | ENSG00000144218.21 | transcript | ENST00000672756.2 | protein_coding | 19/24 | chr2 | TogoVar | ||||||
AFF3_chr2_99540419_100147590 | 99579746 | GTA | G | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(49): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0004others(9): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(36): Show | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0062others(49): Show | 52 | 100 | 0.5200 | -2 | c.279 others(21): Show |
AFF3 | ENSG00000144218.21 | transcript | ENST00000672756.2 | protein_coding | 17/24 | chr2 | TogoVar | ||||||
AFF3_chr2_99540419_100147590 | 99581308 | TAA | T | intron_variant | MODIFIER | HG01358.hp2 HG01891.hp2 HG02647.hp1 others(6): Show |
a0001a0003 | a0001c0001a0001c0004a0001c0005others(2): Show | a0001c0001t0004a0001c0001t0016a0001c0001t0030others(4): Show | a0001c0001t0004g0042a0001c0001t0004g0050a0001c0001t0004g0082others(6): Show | 9 | 100 | 0.0900 | -2 | c.279 others(21): Show |
AFF3 | ENSG00000144218.21 | transcript | ENST00000672756.2 | protein_coding | 17/24 | chr2 | TogoVar | ||||||
AFF3_chr2_99540419_100147590 | 99634964 | TAC | T | intron_variant | MODIFIER | HG00099.hp2 HG01167.hp1 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0007a0001c0005t0009 | a0001c0001t0007g0044a0001c0005t0009g0016 | 2 | 100 | 0.0200 | -2 | c.118 others(23): Show |
AFF3 | ENSG00000144218.21 | transcript | ENST00000672756.2 | protein_coding | 13/24 | chr2 | TogoVar | ||||||
AFF3_chr2_99540419_100147590 | 99644348 | CCT | C | intron_variant | MODIFIER | HG00438.hp2 HG01169.hp2 HG02055.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0062a0001c0001t0002g0045a0001c0001t0002g0047others(4): Show | 7 | 100 | 0.0700 | -2 | c.118 others(21): Show |
AFF3 | ENSG00000144218.21 | transcript | ENST00000672756.2 | protein_coding | 13/24 | chr2 | TogoVar |