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 | 148531908 | TAA | T | intron_variant | MODIFIER | HG01256.hp1 NA18974.hp1 |
a0001a0003 | a0001c0001a0003c0008 | a0001c0001t0002a0003c0008t0045 | a0001c0001t0002g0166a0003c0008t0045g0010 | 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 | 148540407 | CTT | C | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0006a0001c0001t0009a0001c0001t0016others(12): Show | a0001c0001t0006g0138a0001c0001t0006g0144a0001c0001t0006g0163others(17): Show | 20 | 169 | 0.1183 | -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 | 148546165 | TAA | T | intron_variant | MODIFIER | NA19062.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0085 | 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 | 148551482 | GAA | G | intron_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0002 | a0001c0002t0019 | a0001c0002t0019g0107 | 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 | 148566428 | TTA | T | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(22): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0006a0001c0001t0016a0001c0001t0017others(18): Show | a0001c0001t0006g0138a0001c0001t0006g0144a0001c0001t0006g0163others(22): Show | 25 | 169 | 0.1479 | -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 | 148574943 | GGT | G | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(77): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(77): Show | 80 | 169 | 0.4734 | -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 | ATG | A | intron_variant | MODIFIER | NA18940.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0070 | 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 | 148577279 | ATG | A | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0006a0001c0001t0016a0001c0001t0017others(7): Show | a0001c0001t0006g0138a0001c0001t0006g0144a0001c0001t0006g0163others(11): Show | 14 | 169 | 0.0828 | -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 | 148581020 | CAT | C | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(110): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(80): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(110): Show | 113 | 169 | 0.6686 | -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 | 148581027 | GTA | G | intron_variant | MODIFIER | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0011a0001c0001t0020a0001c0001t0039others(8): Show | a0001c0001t0011g0112a0001c0001t0020g0109a0001c0001t0039g0101others(8): Show | 11 | 169 | 0.0651 | -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 | 148581070 | TAC | T | 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 | 148581160 | TAC | T | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(114): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(114): Show | 117 | 169 | 0.6923 | -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 | 148581180 | TAC | T | intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0004 | a0001c0004t0075 | a0001c0004t0075g0004 | 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 | 148581186 | CAT | C | intron_variant | MODIFIER | HG01891.hp2 HG02145.hp1 HG02738.hp1 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0005a0001c0001t0006a0001c0001t0022others(5): Show | a0001c0001t0005g0001a0001c0001t0006g0120a0001c0001t0022g0134others(5): Show | 8 | 169 | 0.0473 | -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 | 148581280 | GTA | G | intron_variant | MODIFIER | NA19066.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019 | 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 | 148581325 | CAT | C | intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0002 | a0001c0002t0094 | a0001c0002t0094g0106 | 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 | 148581373 | TAC | T | intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0002 | a0001c0002t0078 | a0001c0002t0078g0152 | 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 | 148581379 | CAT | C | intron_variant | MODIFIER | HG02056.hp1 HG02129.hp1 NA18967.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0027a0001c0001t0042 | a0001c0001t0002g0054a0001c0001t0027g0017a0001c0001t0042g0012 | 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 | 148581388 | GTA | G | intron_variant | MODIFIER | HG00673.hp1 HG01099.hp1 HG01255.hp1 others(24): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0070others(24): Show | 27 | 169 | 0.1598 | -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 | 148581439 | CAT | C | intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0002 | a0001c0002t0105 | a0001c0002t0105g0117 | 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 | 148581469 | CAT | C | intron_variant | MODIFIER | HG02615.hp1 HG02622.hp2 |
a0001 | a0001c0001 | a0001c0001t0089a0001c0001t0092 | a0001c0001t0089g0110a0001c0001t0092g0008 | 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 | 148581475 | TAC | T | intron_variant | MODIFIER | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0011a0001c0001t0020a0001c0001t0039others(6): Show | a0001c0001t0011g0112a0001c0001t0020g0109a0001c0001t0039g0101others(6): Show | 9 | 169 | 0.0533 | -2 | c.48- others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148581499 | CAT | C | intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0005 | a0001c0005t0023 | a0001c0005t0023g0125 | 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 | 148581529 | CAT | C | intron_variant | MODIFIER | HG02818.hp1 | a0001 | a0001c0002 | a0001c0002t0009 | a0001c0002t0009g0126 | 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 | 148581535 | TAC | T | intron_variant | MODIFIER | HG02615.hp1 HG02622.hp2 |
a0001 | a0001c0001 | a0001c0001t0089a0001c0001t0092 | a0001c0001t0089g0110a0001c0001t0092g0008 | 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 | 148585856 | AAG | A | intron_variant | MODIFIER | HG02040.hp1 HG02129.hp1 HG02735.hp1 others(2): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0048others(2): Show | a0001c0001t0001g0076a0001c0001t0002g0054a0001c0001t0048g0013others(2): Show | 5 | 169 | 0.0296 | -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 | 148603455 | GTT | G | intron_variant | MODIFIER | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0011a0001c0001t0020a0001c0001t0039others(9): Show | a0001c0001t0011g0112a0001c0001t0020g0109a0001c0001t0039g0101others(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 | 148614631 | TTC | T | intron_variant | MODIFIER | HG03688.hp1 | a0001 | a0001c0001 | a0001c0001t0036 | a0001c0001t0036g0139 | 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 | 148614792 | TCC | T | intron_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0002 | a0001c0002t0040 | a0001c0002t0040g0111 | 1 | 169 | 0.0059 | -2 | c.48- others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148614796 | TTC | T | intron_variant | MODIFIER | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0020a0001c0001t0039a0001c0001t0089others(6): Show | a0001c0001t0020g0109a0001c0001t0039g0101a0001c0001t0089g0110others(6): Show | 9 | 169 | 0.0533 | -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 | 148615570 | GAT | G | intron_variant | MODIFIER | HG02895.hp1 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0022a0001c0001t0106 | a0001c0001t0022g0134a0001c0001t0106g0121 | 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 | 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 | a0001c0001t0009g0142a0001c0001t0009g0143a0001c0002t0022g0003others(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 | a0001c0001t0066g0015a0001c0002t0040g0111a0001c0002t0082g0016others(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 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0005g0001others(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 | a0001c0001t0010g0124a0001c0001t0016g0154a0001c0001t0022g0134others(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 | a0001c0001t0006g0138a0001c0001t0010g0124a0001c0001t0037g0037others(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 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0082others(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 | a0001c0001t0002g0020a0001c0001t0002g0062a0001c0001t0016g0154others(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 | a0001c0001t0002g0029a0001c0001t0002g0062a0001c0001t0002g0166others(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 | a0001c0001t0001g0070a0001c0001t0005g0001a0001c0001t0010g0115others(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 | a0001c0001t0025g0081a0001c0002t0072g0018a0002c0009t0103g0050 | 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 | a0001c0001t0110g0118a0001c0004t0095g0113 | 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 | a0001c0001t0011g0128a0001c0001t0044g0127a0001c0001t0106g0121 | 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 |