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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AFF1_chr4_86930011_87146039 | 87072362 | CAA | C | intron_variant | MODIFIER | HG01981.hp1 HG02258.hp1 HG02451.hp1 others(16): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0007a0001c0001t0011a0001c0001t0025others(12): Show | a0001c0001t0007g0081 a0001c0001t0011g0265 a0001c0001t0025g0190 others(16): Show |
19 | 294 | 0.0646 | -2 | c.106 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87073280 | CAA | C | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0006a0001c0003t0027 | a0001c0001t0002g0041 a0001c0001t0002g0049 a0001c0001t0006g0106 others(3): Show |
6 | 294 | 0.0204 | -2 | c.106 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87085775 | GTC | G | intron_variant | MODIFIER | HG02572.hp2 HG02809.hp2 HG02976.hp2 others(3): Show |
a0001a0002a0009others(1): Show | a0001c0001a0002c0008a0009c0030others(1): Show | a0001c0001t0045a0002c0008t0021a0002c0008t0042others(2): Show | a0001c0001t0045g0093 a0002c0008t0021g0014 a0002c0008t0021g0016 others(3): Show |
6 | 294 | 0.0204 | -2 | c.110 others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87091021 | CAA | C | intron_variant | MODIFIER | HG01496.hp1 HG01981.hp1 HG02129.hp2 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(3): Show | a0001c0001t0003g0245 a0001c0001t0004g0063 a0001c0001t0004g0203 others(6): Show |
9 | 294 | 0.0306 | -2 | c.119 others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87096298 | CTT | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
a0001a0003a0004others(9): Show | a0001c0001a0001c0002a0001c0003others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(52): Show | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0042 others(177): Show |
180 | 294 | 0.6122 | -2 | c.128 others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87116351 | TTC | T | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003a0001c0016 | a0001c0001t0028a0001c0003t0027a0001c0003t0028others(2): Show | a0001c0001t0028g0257 a0001c0003t0027g0186 a0001c0003t0027g0188 others(3): Show |
6 | 294 | 0.0204 | -2 | c.246 others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87121026 | CAG | C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
a0001a0002a0007others(9): Show | a0001c0001a0001c0002a0001c0003others(22): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(63): Show | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0042 others(186): Show |
189 | 294 | 0.6429 | -2 | c.246 others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87122881 | TAA | T | intron_variant | MODIFIER | HG00558.hp2 HG01167.hp1 HG02129.hp2 others(4): Show |
a0001a0006 | a0001c0001a0001c0005a0006c0021 | a0001c0001t0004a0001c0001t0025a0001c0005t0041others(3): Show | a0001c0001t0004g0063 a0001c0001t0004g0223 a0001c0001t0025g0190 others(4): Show |
7 | 294 | 0.0238 | -2 | c.246 others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87134850 | TTG | T | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG00639.hp1 others(46): Show |
a0001a0008a0015 | a0001c0001a0001c0003a0001c0029others(2): Show | a0001c0001t0002a0001c0001t0018a0001c0001t0019others(6): Show | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0020 others(46): Show |
49 | 294 | 0.1667 | -2 | c.353 others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 20/20 | chr4 | TogoVar | |||||||
AFF1_chr4_86930011_87146039 | 87138490 | GGT | G | 3_prime_UTR_variant | MODIFIER | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0003a0001c0004others(7): Show | a0001c0001t0004a0001c0001t0009a0001c0001t0010others(17): Show | a0001c0001t0004g0028 a0001c0001t0004g0035 a0001c0001t0004g0053 others(54): Show |
57 | 294 | 0.1939 | -2 | c.*28 others(13): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 21/21 | 2820 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87138546 | CTG | C | 3_prime_UTR_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(105): Show |
a0001a0007a0008others(6): Show | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(41): Show | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0020 others(105): Show |
108 | 294 | 0.3674 | -2 | c.*28 others(13): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 21/21 | 2847 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87141428 | CTT | C | downstream_gene_variant | MODIFIER | HG00323.hp1 HG00741.hp1 HG01069.hp1 others(12): Show |
a0001a0011 | a0001c0001a0001c0003a0001c0010others(1): Show | a0001c0001t0006a0001c0001t0024a0001c0001t0058others(4): Show | a0001c0001t0006g0073 a0001c0001t0006g0074 a0001c0001t0006g0075 others(12): Show |
15 | 294 | 0.0510 | -2 | c.*57 others(13): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 390 | chr4 | TogoVar | |||||||
AFF1_chr4_86930011_87146039 | 87142614 | CCA | C | downstream_gene_variant | MODIFIER | HG01891.hp2 HG02132.hp2 HG02258.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002a0001c0014others(2): Show | a0001c0001t0002a0001c0002t0005a0001c0002t0044others(4): Show | a0001c0001t0002g0018 a0001c0001t0002g0020 a0001c0001t0002g0021 others(17): Show |
20 | 294 | 0.0680 | -2 | c.*69 others(13): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 1576 | chr4 | TogoVar | |||||||
AFF1_chr4_86930011_87146039 | 87145999 | CAA | C | downstream_gene_variant | MODIFIER | HG02572.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
a0001a0002 | a0001c0005a0002c0008 | a0001c0005t0043a0001c0005t0052a0001c0005t0053others(2): Show | a0001c0005t0043g0173 a0001c0005t0052g0172 a0001c0005t0053g0174 others(3): Show |
6 | 294 | 0.0204 | -2 | c.*10 others(15): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4961 | chr4 | TogoVar | |||||||
AFF2_chrX_148495617_149005663 | 148505955 | CTG | C | intron_variant | MODIFIER | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(35): Show | a0001c0001t0002g0085 a0001c0001t0002g0166 a0001c0001t0003g0086 others(42): Show |
45 | 169 | 0.2663 | -2 | c.47+ others(17): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148509270 | CTT | C | intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0009 | 1 | 169 | 0.0059 | -2 | c.47+ others(17): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148521410 | ACT | A | intron_variant | MODIFIER | HG02965.hp1 HG03225.hp1 |
a0001 | a0001c0002 | a0001c0002t0020a0001c0002t0107 | a0001c0002t0020g0132 a0001c0002t0107g0131 |
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 | 148524123 | CTG | C | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(84): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0039 others(84): Show |
87 | 169 | 0.5148 | -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 | 148531907 | TTA | T | intron_variant | MODIFIER | NA18948.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0062 | 1 | 169 | 0.0059 | -2 | c.47+ others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | |||||||
AFF2_chrX_148495617_149005663 | 148531908 | TAA | T | intron_variant | MODIFIER | HG01256.hp1 NA18974.hp1 |
a0001a0003 | a0001c0001a0003c0008 | a0001c0001t0002a0003c0008t0045 | a0001c0001t0002g0166 a0003c0008t0045g0010 |
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 | a0001c0001t0006g0138 a0001c0001t0006g0144 a0001c0001t0006g0163 others(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 | a0001c0001t0006g0138 a0001c0001t0006g0144 a0001c0001t0006g0163 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0039 others(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 | a0001c0001t0006g0138 a0001c0001t0006g0144 a0001c0001t0006g0163 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0039 others(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 | a0001c0001t0011g0112 a0001c0001t0020g0109 a0001c0001t0039g0101 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0039 others(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 | a0001c0001t0005g0001 a0001c0001t0006g0120 a0001c0001t0022g0134 others(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 | a0001c0001t0002g0054 a0001c0001t0027g0017 a0001c0001t0042g0012 |
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 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0070 others(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 | a0001c0001t0089g0110 a0001c0001t0092g0008 |
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 | a0001c0001t0011g0112 a0001c0001t0020g0109 a0001c0001t0039g0101 others(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 | a0001c0001t0089g0110 a0001c0001t0092g0008 |
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 | a0001c0001t0001g0076 a0001c0001t0002g0054 a0001c0001t0048g0013 others(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 | a0001c0001t0011g0112 a0001c0001t0020g0109 a0001c0001t0039g0101 others(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 | a0001c0001t0020g0109 a0001c0001t0039g0101 a0001c0001t0089g0110 others(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 | a0001c0001t0022g0134 a0001c0001t0106g0121 |
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 |