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 | 148564468 | G | GAA | intron_variant | MODIFIER | HG01928.hp1 | a0001 | a0001c0001 | a0001c0001t0090 | a0001c0001t0090g0099 | 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 | 148565909 | C | CAT | intron_variant | MODIFIER | NA18983.hp1 | a0001 | a0001c0001 | a0001c0001t0122 | a0001c0001t0122g0092 | 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 | 148572047 | C | CAA | intron_variant | MODIFIER | HG02056.hp1 HG02451.hp2 HG02886.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0012a0001c0001t0015others(6): Show | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0012g0168others(7): Show | 10 | 169 | 0.0592 | 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 | 148573676 | C | CAT | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(32): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0006a0001c0001t0010a0001c0001t0011others(27): Show | a0001c0001t0006g0138a0001c0001t0006g0144a0001c0001t0006g0163others(32): Show | 35 | 169 | 0.2071 | 2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148574943 | G | GGT | intron_variant | MODIFIER | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0008a0001c0001t0011a0001c0001t0020others(6): Show | a0001c0001t0008g0051a0001c0001t0011g0112a0001c0001t0020g0109others(6): Show | 9 | 169 | 0.0533 | 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 | 148576793 | A | ATG | intron_variant | MODIFIER | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(119): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(90): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(119): Show | 122 | 169 | 0.7219 | 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 | 148579485 | C | CAT | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(122): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(90): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(122): Show | 125 | 169 | 0.7396 | 2 | c.48- others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148580717 | T | TTA | intron_variant | MODIFIER | HG01884.hp1 HG02622.hp1 HG03139.hp1 |
a0001 | a0001c0002a0001c0003a0001c0004 | a0001c0002t0018a0001c0003t0030a0001c0004t0113 | a0001c0002t0018g0151a0001c0003t0030g0158a0001c0004t0113g0159 | 3 | 169 | 0.0178 | 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 | 148580729 | A | ATG | intron_variant | MODIFIER | NA18971.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0048 | 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 | 148580743 | G | GTA | intron_variant | MODIFIER | HG02451.hp1 HG03540.hp1 |
a0001 | a0001c0002 | a0001c0002t0078a0001c0002t0101 | a0001c0002t0078g0152a0001c0002t0101g0160 | 2 | 169 | 0.0118 | 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 | 148580745 | G | GTA | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(142): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(109): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(142): Show | 145 | 169 | 0.8580 | 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 | 148581057 | G | GTA | intron_variant | MODIFIER | HG00140.hp1 HG00621.hp1 HG00642.hp1 others(101): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(73): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(101): Show | 104 | 169 | 0.6154 | 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 | 148581243 | T | TAC | intron_variant | MODIFIER | HG01891.hp1 HG02965.hp1 |
a0001 | a0001c0002 | a0001c0002t0019a0001c0002t0020 | a0001c0002t0019g0123a0001c0002t0020g0132 | 2 | 169 | 0.0118 | 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 | 148581253 | T | TAC | intron_variant | MODIFIER | HG02572.hp1 HG02886.hp1 HG03098.hp1 |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0066a0001c0002t0082a0001c0004t0075 | a0001c0001t0066g0015a0001c0002t0082g0016a0001c0004t0075g0004 | 3 | 169 | 0.0178 | 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 | 148581297 | T | TAC | intron_variant | MODIFIER | HG01891.hp1 HG02965.hp1 |
a0001 | a0001c0002 | a0001c0002t0019a0001c0002t0020 | a0001c0002t0019g0123a0001c0002t0020g0132 | 2 | 169 | 0.0118 | 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 | 148581307 | T | TAC | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(57): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0009others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0068others(57): Show | 60 | 169 | 0.3550 | 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 | 148581307 | T | TGC | intron_variant | MODIFIER | HG03130.hp1 NA20129.hp2 |
a0001 | a0001c0002 | a0001c0002t0022a0001c0002t0108 | a0001c0002t0022g0003a0001c0002t0108g0002 | 2 | 169 | 0.0118 | 2 | c.48- others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148581334 | G | GTA | intron_variant | MODIFIER | HG00140.hp1 HG01106.hp1 HG01884.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(14): Show | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0004g0043others(16): Show | 19 | 169 | 0.1124 | 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 | 148581337 | T | TAC | intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0074 | a0001c0001t0074g0033 | 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 | 148581411 | C | CAT | intron_variant | MODIFIER | HG01891.hp1 HG02280.hp2 |
a0001 | a0001c0002 | a0001c0002t0019a0001c0002t0091 | a0001c0002t0019g0123a0001c0002t0091g0136 | 2 | 169 | 0.0118 | 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 | 148581415 | T | TAC | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(49): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0070others(49): Show | 52 | 169 | 0.3077 | 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 | 148581418 | G | GTA | intron_variant | MODIFIER | HG01891.hp2 HG02280.hp2 NA19070.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0110a0001c0001t0120a0001c0002t0091 | a0001c0001t0110g0118a0001c0001t0120g0035a0001c0002t0091g0136 | 3 | 169 | 0.0178 | 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 | 148581448 | G | GTA | intron_variant | MODIFIER | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0010a0001c0001t0077a0001c0001t0110others(3): Show | a0001c0001t0010g0124a0001c0001t0077g0095a0001c0001t0110g0118others(3): Show | 6 | 169 | 0.0355 | 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 | 148581622 | G | GTA | intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0004 | a0001c0004t0095 | a0001c0004t0095g0113 | 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 | 148584557 | A | ATT | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(111): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(81): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(111): Show | 114 | 169 | 0.6746 | 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 | 148592487 | T | TAA | intron_variant | MODIFIER | HG02451.hp1 HG03540.hp1 |
a0001 | a0001c0002 | a0001c0002t0078a0001c0002t0101 | a0001c0002t0078g0152a0001c0002t0101g0160 | 2 | 169 | 0.0118 | 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 | 148594514 | A | ATT | intron_variant | MODIFIER | NA18967.hp1 | a0001 | a0001c0001 | a0001c0001t0042 | a0001c0001t0042g0012 | 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 | 148596187 | G | GAT | intron_variant | MODIFIER | HG01243.hp1 HG02647.hp1 |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0044 | a0001c0001t0011g0128a0001c0001t0044g0127 | 2 | 169 | 0.0118 | 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 | 148602823 | G | GTT | intron_variant | MODIFIER | HG01891.hp2 HG02040.hp1 HG02886.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0006a0001c0001t0022a0001c0001t0046others(7): Show | a0001c0001t0006g0120a0001c0001t0022g0134a0001c0001t0046g0165others(7): Show | 10 | 169 | 0.0592 | 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 | 148614709 | C | CTT | intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0001 | a0001c0001t0098 | a0001c0001t0098g0119 | 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 | 148614796 | T | TTC | intron_variant | MODIFIER | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0011a0001c0001t0021a0001c0001t0036others(21): Show | a0001c0001t0011g0128a0001c0001t0021g0150a0001c0001t0036g0139others(21): Show | 24 | 169 | 0.1420 | 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 | 148620526 | A | AAT | intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0002 | a0001c0002t0091 | a0001c0002t0091g0136 | 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 | 148623600 | A | AAT | intron_variant | MODIFIER | HG01243.hp1 HG02071.hp1 HG02280.hp2 others(10): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0003c0008others(1): Show | a0001c0001t0011a0001c0001t0025a0001c0001t0033others(10): Show | a0001c0001t0011g0128a0001c0001t0025g0081a0001c0001t0033g0083others(10): Show | 13 | 169 | 0.0769 | 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 | T | TTG | intron_variant | MODIFIER | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(15): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0011a0001c0001t0020others(15): Show | a0001c0001t0001g0070a0001c0001t0011g0128a0001c0001t0020g0109others(15): Show | 18 | 169 | 0.1065 | 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 | 148655285 | C | CTT | intron_variant | MODIFIER | NA18948.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0062 | 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 | 148656493 | A | ATT | intron_variant | MODIFIER | HG01884.hp1 HG02622.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0089a0001c0003t0030 | a0001c0001t0089g0110a0001c0003t0030g0158 | 2 | 169 | 0.0118 | 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 | 148671772 | C | CTT | intron_variant | MODIFIER | HG01891.hp2 HG02257.hp1 HG02818.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0011a0001c0001t0110a0001c0002t0009others(3): Show | a0001c0001t0011g0112a0001c0001t0110g0118a0001c0002t0009g0126others(3): Show | 6 | 169 | 0.0355 | 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 | 148681536 | A | ATG | intron_variant | MODIFIER | NA18994.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0072 | 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 | 148683667 | G | GTT | intron_variant | MODIFIER | NA18974.hp1 | a0003 | a0003c0008 | a0003c0008t0045 | a0003c0008t0045g0010 | 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 | 148685914 | T | TTC | intron_variant | MODIFIER | NA18974.hp1 | a0003 | a0003c0008 | a0003c0008t0045 | a0003c0008t0045g0010 | 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 | 148688768 | C | CAT | intron_variant | MODIFIER | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0011a0001c0001t0016a0001c0001t0020others(16): Show | a0001c0001t0011g0128a0001c0001t0016g0154a0001c0001t0016g0155others(18): Show | 21 | 169 | 0.1243 | 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 | 148692046 | C | CTT | intron_variant | MODIFIER | HG01243.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0011a0001c0001t0013others(5): Show | a0001c0001t0001g0070a0001c0001t0011g0128a0001c0001t0013g0034others(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 | 148700419 | A | AGT | intron_variant | MODIFIER | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0021a0001c0001t0022a0001c0001t0036others(20): Show | a0001c0001t0021g0103a0001c0001t0021g0150a0001c0001t0022g0134others(21): Show | 24 | 169 | 0.1420 | 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 | 148701009 | A | AAT | intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0002 | a0001c0002t0018 | a0001c0002t0018g0151 | 1 | 169 | 0.0059 | 2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148701012 | A | ATG | intron_variant | MODIFIER | HG00280.hp1 NA18962.hp1 NA20129.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0006a0001c0001t0015a0001c0002t0022 | a0001c0001t0006g0144a0001c0001t0015g0060a0001c0002t0022g0003 | 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 | 148701014 | G | GAA | intron_variant | MODIFIER | HG01109.hp1 HG02280.hp2 HG04115.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0010a0001c0001t0118a0001c0002t0091 | a0001c0001t0010g0124a0001c0001t0118g0088a0001c0002t0091g0136 | 3 | 169 | 0.0178 | 2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148701016 | G | GAA | intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0002 | a0001c0002t0101 | a0001c0002t0101g0160 | 1 | 169 | 0.0059 | 2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148704091 | T | TTA | intron_variant | MODIFIER | HG01099.hp1 HG01978.hp1 |
a0001 | a0001c0001 | a0001c0001t0053a0001c0001t0055 | a0001c0001t0053g0027a0001c0001t0055g0025 | 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 | 148704300 | T | TTA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(123): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(89): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(123): Show | 126 | 169 | 0.7456 | 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 | 148704326 | T | TTA | intron_variant | MODIFIER | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(116): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(89): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(116): Show | 119 | 169 | 0.7041 | 2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar |