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 | 148704380 | T | TTA | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0010a0001c0001t0011a0001c0001t0098others(7): Show | a0001c0001t0010g0115a0001c0001t0010g0116a0001c0001t0011g0112others(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 | 148704388 | A | ATG | intron_variant | MODIFIER | HG00639.hp1 HG02055.hp1 HG02486.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0016a0001c0001t0020a0001c0001t0039others(10): Show | a0001c0001t0016g0154a0001c0001t0016g0155a0001c0001t0020g0109others(11): Show | 14 | 169 | 0.0828 | 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 | 148704460 | G | GTA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(127): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(90): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(127): Show | 130 | 169 | 0.7692 | 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 | 148705563 | T | TTG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(151): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(111): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(151): Show | 154 | 169 | 0.9112 | 2 | c.104 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148718022 | G | GTT | intron_variant | MODIFIER | HG00738.hp1 HG01978.hp2 HG02257.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0017a0001c0001t0020a0001c0001t0021others(10): Show | a0001c0001t0017g0145a0001c0001t0020g0109a0001c0001t0021g0150others(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 | 148723919 | C | CTT | intron_variant | MODIFIER | HG02027.hp1 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0038a0001c0001t0088 | a0001c0001t0038g0102a0001c0001t0088g0104 | 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 | 148762448 | G | GAT | intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0128 | 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 | 148762480 | A | ATG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0006a0001c0001t0025a0001c0001t0037others(8): Show | a0001c0001t0006g0144a0001c0001t0006g0163a0001c0001t0025g0081others(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 | 148762508 | G | GTA | intron_variant | MODIFIER | NA20805.hp1 | a0001 | a0001c0001 | a0001c0001t0058 | a0001c0001t0058g0097 | 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 | 148776014 | C | CCA | intron_variant | MODIFIER | NA19086.hp1 | a0001 | a0001c0001 | a0001c0001t0041 | a0001c0001t0041g0071 | 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 | 148783352 | A | ATT | 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 | 148787312 | C | CTG | intron_variant | MODIFIER | NA19086.hp1 | a0001 | a0001c0001 | a0001c0001t0041 | a0001c0001t0041g0071 | 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 | C | CAA | intron_variant | MODIFIER | HG03688.hp1 | a0001 | a0001c0001 | a0001c0001t0036 | a0001c0001t0036g0139 | 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 | 148795830 | A | AAT | intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0115 | 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 | 148795832 | A | AAT | intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0002 | a0001c0002t0019 | a0001c0002t0019g0123 | 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 | 148795872 | T | TAC | intron_variant | MODIFIER | HG02622.hp1 HG04115.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0118a0001c0002t0018 | a0001c0001t0118g0088a0001c0002t0018g0151 | 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 | 148816933 | C | CAA | intron_variant | MODIFIER | HG01891.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0037a0001c0001t0042a0001c0001t0059others(7): Show | a0001c0001t0037g0037a0001c0001t0042g0012a0001c0001t0059g0014others(7): Show | 10 | 169 | 0.0592 | 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 | G | GGT | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0009a0001c0001t0022a0001c0001t0037others(17): Show | a0001c0001t0009g0143a0001c0001t0022g0134a0001c0001t0037g0037others(17): Show | 20 | 169 | 0.1183 | 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 | 148824060 | C | CCT | intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0002 | a0001c0002t0032 | a0001c0002t0032g0114 | 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 | 148825052 | C | CCA | intron_variant | MODIFIER | NA18971.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0048 | 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 | 148825590 | G | GTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(100): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(70): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(100): Show | 103 | 169 | 0.6095 | 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 | 148834505 | A | ATG | intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0002 | a0001c0002t0022 | a0001c0002t0022g0003 | 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 | 148839894 | G | GGT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(79): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0070others(79): Show | 82 | 169 | 0.4852 | 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 | 148845120 | T | TAC | intron_variant | MODIFIER | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(23): Show | a0001c0001t0004g0043a0001c0001t0010g0115a0001c0001t0010g0124others(26): Show | 29 | 169 | 0.1716 | 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 | 148849366 | T | TCC | intron_variant | MODIFIER | HG01884.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0011a0001c0002t0032a0001c0003t0026others(2): Show | a0001c0001t0011g0128a0001c0002t0032g0114a0001c0003t0026g0157others(2): Show | 5 | 169 | 0.0296 | 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 | G | GTT | intron_variant | MODIFIER | HG02132.hp1 HG02738.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0024 | a0001c0001t0005g0001a0001c0001t0024g0091 | 2 | 169 | 0.0118 | 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 | 148864569 | G | GAT | intron_variant | MODIFIER | NA18974.hp1 | a0003 | a0003c0008 | a0003c0008t0045 | a0003c0008t0045g0010 | 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 | 148879777 | G | GAA | intron_variant | MODIFIER | HG01358.hp1 HG01884.hp1 HG02071.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0033a0001c0001t0117a0001c0003t0026others(4): Show | a0001c0001t0033g0083a0001c0001t0117g0164a0001c0003t0026g0157others(4): Show | 7 | 169 | 0.0414 | 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 | 148883980 | T | TAC | intron_variant | MODIFIER | HG00738.hp1 HG01978.hp2 HG02572.hp1 others(12): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0009a0001c0001t0017a0001c0001t0020others(12): Show | a0001c0001t0009g0142a0001c0001t0017g0145a0001c0001t0020g0109others(12): Show | 15 | 169 | 0.0888 | 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 | 148894888 | G | GAT | intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0002 | a0001c0002t0105 | a0001c0002t0105g0117 | 1 | 169 | 0.0059 | 2 | c.135 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148894892 | G | GAT | intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0002 | a0001c0002t0107 | a0001c0002t0107g0131 | 1 | 169 | 0.0059 | 2 | c.135 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148894896 | G | GAT | intron_variant | MODIFIER | HG04199.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0089 | 1 | 169 | 0.0059 | 2 | c.135 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148895570 | A | AGT | intron_variant | MODIFIER | HG01891.hp1 HG02145.hp1 HG02615.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0020a0001c0001t0037a0001c0001t0038others(10): Show | a0001c0001t0020g0109a0001c0001t0037g0037a0001c0001t0038g0102others(10): Show | 13 | 169 | 0.0769 | 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 | C | CTA | intron_variant | MODIFIER | HG00639.hp1 HG01256.hp1 HG02886.hp2 others(4): Show |
a0001a0003 | a0001c0001a0003c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0036a0001c0001t0002g0166a0001c0001t0003g0063others(4): Show | 7 | 169 | 0.0414 | 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 | T | TTA | intron_variant | MODIFIER | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0005a0001c0001t0020a0001c0001t0037others(18): Show | a0001c0001t0005g0001a0001c0001t0020g0109a0001c0001t0037g0037others(18): Show | 21 | 169 | 0.1243 | 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 | C | CTT | intron_variant | MODIFIER | HG01884.hp2 HG02258.hp1 HG03209.hp1 |
a0001 | a0001c0002a0001c0007 | a0001c0002t0031a0001c0002t0111a0001c0007t0080 | a0001c0002t0031g0148a0001c0002t0111g0096a0001c0007t0080g0162 | 3 | 169 | 0.0178 | 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 | 148920629 | T | TGC | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(19): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0011a0001c0001t0035a0001c0001t0039others(16): Show | a0001c0001t0011g0112a0001c0001t0011g0128a0001c0001t0035g0078others(19): Show | 22 | 169 | 0.1302 | 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 | 148920630 | G | GCA | intron_variant | MODIFIER | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0009a0001c0002t0019a0001c0002t0022others(2): Show | a0001c0002t0009g0126a0001c0002t0019g0107a0001c0002t0022g0003others(2): Show | 5 | 169 | 0.0296 | 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 | 148920633 | C | CGT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(123): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(89): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(123): Show | 126 | 169 | 0.7456 | 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 | 148931253 | C | CAA | intron_variant | MODIFIER | HG01884.hp1 HG01884.hp2 HG02071.hp1 others(22): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(22): Show | a0001c0001t0001g0019a0001c0001t0005g0001a0001c0001t0006g0138others(22): Show | 25 | 169 | 0.1479 | 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 | C | CAT | intron_variant | MODIFIER | HG02622.hp2 HG02717.hp1 NA19043.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0020a0001c0001t0038a0001c0001t0089others(2): Show | a0001c0001t0020g0109a0001c0001t0038g0102a0001c0001t0089g0110others(2): Show | 5 | 169 | 0.0296 | 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 | T | TAC | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(100): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0009a0003c0008others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(66): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(100): Show | 103 | 169 | 0.6095 | 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 | 148935872 | G | GTT | intron_variant | MODIFIER | HG01891.hp2 HG01928.hp1 HG03486.hp1 others(6): Show |
a0001a0004 | a0001c0001a0004c0006 | a0001c0001t0001a0001c0001t0013a0001c0001t0015others(5): Show | a0001c0001t0001g0036a0001c0001t0001g0068a0001c0001t0013g0034others(6): Show | 9 | 169 | 0.0533 | 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 | 148953798 | A | AAC | intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0002 | a0001c0002t0082 | a0001c0002t0082g0016 | 1 | 169 | 0.0059 | 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 | 148953814 | G | GAC | intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0005 | a0001c0005t0023 | a0001c0005t0023g0125 | 1 | 169 | 0.0059 | 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 | 148966677 | C | CTT | intron_variant | MODIFIER | HG02257.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0011a0001c0001t0039a0001c0002t0054others(3): Show | a0001c0001t0011g0112a0001c0001t0011g0128a0001c0001t0039g0101others(4): Show | 7 | 169 | 0.0414 | 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 | 148975943 | C | CAA | intron_variant | MODIFIER | HG02055.hp1 HG02630.hp2 HG03041.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0077a0001c0002t0019a0001c0002t0022others(6): Show | a0001c0001t0077g0095a0001c0002t0019g0107a0001c0002t0022g0003others(6): Show | 9 | 169 | 0.0533 | 2 | c.340 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148977614 | G | GAC | intron_variant | MODIFIER | HG00639.hp1 HG02895.hp1 NA18522.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0016a0001c0001t0076a0001c0001t0106 | a0001c0001t0016g0154a0001c0001t0016g0155a0001c0001t0076g0153others(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 | C | CTT | intron_variant | MODIFIER | HG00280.hp1 HG00673.hp1 HG01069.hp1 others(31): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0076others(31): Show | 34 | 169 | 0.2012 | 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 | 148995488 | G | GGT | 3_prime_UTR_variant | MODIFIER | HG02027.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0073a0001c0001t0088a0001c0001t0123others(5): Show | a0001c0001t0073g0074a0001c0001t0088g0104a0001c0001t0123g0090others(5): Show | 8 | 169 | 0.0473 | 2 | c.*41 others(13): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 21/21 | 4158 | INFO_REALIGN_3_PRIME | chrX | TogoVar |