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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AFF1_chr4_86930011_87146039 | 86982848 | CAAAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG00639.hp1 others(51): Show |
a0001a0003a0007others(2): Show | a0001c0001a0001c0003a0001c0005others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0090others(51): Show | 54 | 294 | 0.1837 | -4 | c.38+ others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86983536 | TAAAA | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(76): Show |
a0001a0006a0009others(2): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0001t0001g0119others(76): Show | 79 | 294 | 0.2687 | -4 | c.38+ others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86985127 | AATAT | A | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(35): Show |
a0001a0011 | a0001c0001a0001c0028a0011c0018 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0001t0002g0013others(35): Show | 38 | 294 | 0.1293 | -4 | c.38+ others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86985161 | AATAT | A | intron_variant | MODIFIER | HG00558.hp1 HG00639.hp2 HG00673.hp2 others(43): Show |
a0001a0006a0016others(1): Show | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0001t0001g0119others(43): Show | 46 | 294 | 0.1565 | -4 | c.38+ others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86985181 | CTATA | C | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(30): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0010a0003c0012others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0077a0001c0001t0002g0013a0001c0001t0002g0040others(30): Show | 33 | 294 | 0.1122 | -4 | c.38+ others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86985934 | AATTG | A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
a0001a0003a0004others(8): Show | a0001c0001a0001c0003a0001c0005others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0077others(143): Show | 146 | 294 | 0.4966 | -4 | c.38+ others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86991445 | CAAAA | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
a0001a0003a0004others(7): Show | a0001c0001a0001c0003a0001c0005others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(45): Show | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0077others(140): Show | 143 | 294 | 0.4864 | -4 | c.38+ others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86993942 | GAGAC | G | intron_variant | MODIFIER | HG00738.hp1 HG01069.hp2 HG01099.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0025 | a0001c0001t0003g0002a0001c0001t0003g0005a0001c0001t0003g0006others(6): Show | 9 | 294 | 0.0306 | -4 | c.38+ others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86995235 | AAAAC | A | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(12): Show |
a0001a0002a0010 | a0001c0001a0001c0002a0002c0008others(1): Show | a0001c0001t0003a0001c0002t0005a0001c0002t0044others(4): Show | a0001c0001t0003g0192a0001c0002t0005g0185a0001c0002t0005g0193others(12): Show | 15 | 294 | 0.0510 | -4 | c.38+ others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86996723 | AAAAC | A | intron_variant | MODIFIER | HG01074.hp2 HG02145.hp2 HG02280.hp1 others(19): Show |
a0001a0018 | a0001c0001a0001c0003a0001c0007others(4): Show | a0001c0001t0002a0001c0003t0001a0001c0003t0003others(12): Show | a0001c0001t0002g0041a0001c0003t0001g0179a0001c0003t0001g0180others(19): Show | 22 | 294 | 0.0748 | -4 | c.38+ others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87000605 | CTGTG | C | intron_variant | MODIFIER | HG01109.hp1 HG01496.hp1 HG01993.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0001t0010a0001c0002t0005 | a0001c0001t0009g0216a0001c0001t0009g0218a0001c0001t0009g0219others(2): Show | 5 | 294 | 0.0170 | -4 | c.39- others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87004873 | TGTAA | T | intron_variant | MODIFIER | HG02559.hp1 HG02717.hp1 HG02723.hp2 others(2): Show |
a0001a0005 | a0001c0005a0005c0032 | a0001c0005t0041a0001c0005t0043a0001c0005t0052others(2): Show | a0001c0005t0041g0175a0001c0005t0043g0173a0001c0005t0052g0172others(2): Show | 5 | 294 | 0.0170 | -4 | c.39- others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87013032 | CTTTT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(50): Show |
a0001a0003a0004others(1): Show | a0001c0001a0003c0012a0004c0009others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0221a0001c0001t0002g0052a0001c0001t0002g0226others(50): Show | 53 | 294 | 0.1803 | -4 | c.39- others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87022543 | GATAT | G | intron_variant | MODIFIER | HG02717.hp2 HG02970.hp1 HG03195.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010a0001c0001t0032others(2): Show | a0001c0001t0002g0255a0001c0001t0010g0254a0001c0001t0010g0256others(3): Show | 6 | 294 | 0.0204 | -4 | c.39- others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87022676 | ATGTG | A | intron_variant | MODIFIER | HG02559.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
a0001 | a0001c0005 | a0001c0005t0041a0001c0005t0043a0001c0005t0052others(1): Show | a0001c0005t0041g0175a0001c0005t0043g0173a0001c0005t0052g0172others(1): Show | 4 | 294 | 0.0136 | -4 | c.39- others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87022700 | GTATA | G | intron_variant | MODIFIER | HG01167.hp1 HG01175.hp2 HG01243.hp1 others(11): Show |
a0001a0013 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(7): Show | a0001c0001t0002g0189a0001c0001t0002g0191a0001c0001t0002g0248others(11): Show | 14 | 294 | 0.0476 | -4 | c.39- others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87023042 | ACAGG | A | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(14): Show |
a0001a0002a0007others(1): Show | a0001c0001a0001c0002a0002c0008others(2): Show | a0001c0001t0003a0001c0001t0045a0001c0002t0005others(6): Show | a0001c0001t0003g0192a0001c0001t0045g0093a0001c0002t0005g0185others(14): Show | 17 | 294 | 0.0578 | -4 | c.39- others(21): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87068084 | AACTT | A | intron_variant | MODIFIER | HG01981.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003a0001c0014 | a0001c0001t0007a0001c0001t0025a0001c0003t0001others(4): Show | a0001c0001t0007g0081a0001c0001t0025g0190a0001c0003t0001g0179others(6): Show | 9 | 294 | 0.0306 | -4 | c.106 others(25): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87073280 | CAAAA | C | intron_variant | MODIFIER | HG00323.hp1 HG01099.hp2 HG01192.hp2 others(6): Show |
a0001a0015 | a0001c0001a0001c0003a0001c0010others(1): Show | a0001c0001t0006a0001c0001t0024a0001c0001t0028others(4): Show | a0001c0001t0006g0074a0001c0001t0006g0075a0001c0001t0006g0076others(6): Show | 9 | 294 | 0.0306 | -4 | c.106 others(25): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87077625 | ACTTT | A | intron_variant | MODIFIER | HG02280.hp1 HG02622.hp1 HG02630.hp2 others(7): Show |
a0001 | a0001c0001a0001c0003a0001c0006others(2): Show | a0001c0001t0003a0001c0003t0001a0001c0003t0003others(5): Show | a0001c0001t0003g0192a0001c0003t0001g0179a0001c0003t0001g0180others(7): Show | 10 | 294 | 0.0340 | -4 | 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 | 87079137 | GCTCT | G | intron_variant | MODIFIER | HG02451.hp1 HG02559.hp2 HG02970.hp2 |
a0001 | a0001c0003 | a0001c0003t0027a0001c0003t0067 | a0001c0003t0027g0186a0001c0003t0027g0188a0001c0003t0067g0187 | 3 | 294 | 0.0102 | -4 | 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 | 87081152 | ATTTT | A | intron_variant | MODIFIER | HG00558.hp1 HG02055.hp1 HG02083.hp1 others(13): Show |
a0001 | a0001c0001a0001c0003a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0031others(4): Show | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0119others(13): Show | 16 | 294 | 0.0544 | -4 | 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 | 87084550 | CAATA | C | intron_variant | MODIFIER | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(40): Show |
a0001a0018 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(14): Show | a0001c0001t0001g0034a0001c0001t0001g0140a0001c0001t0001g0151others(40): Show | 43 | 294 | 0.1463 | -4 | 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 | 87102388 | GTCTC | G | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG00639.hp1 others(43): Show |
a0001a0011 | a0001c0001a0001c0003a0001c0028others(1): Show | a0001c0001t0002a0001c0001t0018a0001c0001t0019others(5): Show | a0001c0001t0002g0013a0001c0001t0002g0018a0001c0001t0002g0020others(43): Show | 46 | 294 | 0.1565 | -4 | c.128 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148505955 | CTGTG | C | intron_variant | MODIFIER | HG01884.hp1 HG01928.hp1 HG03139.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0090a0001c0002t0101a0001c0003t0030others(1): Show | a0001c0001t0090g0099a0001c0002t0101g0160a0001c0003t0030g0158others(1): Show | 4 | 169 | 0.0237 | -4 | 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 | 148524121 | CTCTG | C | intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0002 | a0001c0002t0094 | a0001c0002t0094g0106 | 1 | 169 | 0.0059 | -4 | c.47+ others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148524123 | CTGTG | C | intron_variant | MODIFIER | HG02818.hp1 HG06807.hp2 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0009a0001c0005t0023 | a0001c0002t0009g0126a0001c0005t0023g0125 | 2 | 169 | 0.0118 | -4 | c.47+ others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148551482 | GAAAA | G | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(21): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0006a0001c0001t0010a0001c0001t0011others(17): Show | a0001c0001t0006g0144a0001c0001t0006g0163a0001c0001t0010g0115others(21): Show | 24 | 169 | 0.1420 | -4 | c.47+ others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148569328 | AAACC | A | intron_variant | MODIFIER | HG02572.hp1 HG02886.hp1 HG03098.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0066a0001c0002t0082a0001c0004t0075others(1): Show | a0001c0001t0066g0015a0001c0002t0082g0016a0001c0004t0075g0004others(1): Show | 4 | 169 | 0.0237 | -4 | c.47+ others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148574943 | GGTGT | G | intron_variant | MODIFIER | HG02258.hp1 HG03654.hp1 NA19063.hp1 others(1): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0005a0001c0001t0074a0001c0001t0077others(1): Show | a0001c0001t0005g0021a0001c0001t0074g0033a0001c0001t0077g0095others(1): Show | 4 | 169 | 0.0237 | -4 | c.47+ others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148577279 | ATGTG | A | intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0002 | a0001c0002t0087 | a0001c0002t0087g0147 | 1 | 169 | 0.0059 | -4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148581293 | CGTGT | C | intron_variant | MODIFIER | NA19066.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019 | 1 | 169 | 0.0059 | -4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148581379 | CATAT | C | intron_variant | MODIFIER | NA19070.hp1 | a0001 | a0001c0001 | a0001c0001t0120 | a0001c0001t0120g0035 | 1 | 169 | 0.0059 | -4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148581417 | CGTAT | C | intron_variant | MODIFIER | NA18962.hp1 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0060 | 1 | 169 | 0.0059 | -4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148581579 | CGTGT | C | intron_variant | MODIFIER | HG02027.hp1 HG02735.hp1 HG02886.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0025others(3): Show | a0001c0001t0001g0076a0001c0001t0006g0120a0001c0001t0025g0081others(3): Show | 6 | 169 | 0.0355 | -4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148614693 | TTTTC | T | intron_variant | MODIFIER | HG00639.hp2 HG01074.hp1 HG01167.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0013a0001c0001t0015others(6): Show | a0001c0001t0002g0029a0001c0001t0002g0062a0001c0001t0013g0034others(7): Show | 10 | 169 | 0.0592 | -4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148614730 | TTTCC | T | intron_variant | MODIFIER | HG03471.hp1 HG03490.hp1 NA18612.hp1 others(2): Show |
a0001a0004 | a0001c0001a0004c0006 | a0001c0001t0004a0001c0001t0021a0001c0001t0025others(2): Show | a0001c0001t0004g0041a0001c0001t0021g0103a0001c0001t0025g0081others(2): Show | 5 | 169 | 0.0296 | -4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148614734 | CTTCT | C | intron_variant | MODIFIER | HG00738.hp1 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0145 | 1 | 169 | 0.0059 | -4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148614738 | TTTTC | T | intron_variant | MODIFIER | HG01255.hp1 HG01256.hp1 HG01258.hp1 others(23): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(22): Show | a0001c0001t0001g0019a0001c0001t0002g0029a0001c0001t0002g0166others(23): Show | 26 | 169 | 0.1539 | -4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148617400 | GCCCA | G | intron_variant | MODIFIER | NA20300.hp1 | a0001 | a0001c0001 | a0001c0001t0077 | a0001c0001t0077g0095 | 1 | 169 | 0.0059 | -4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148628990 | ATATG | A | intron_variant | MODIFIER | HG02895.hp1 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0022a0001c0001t0106 | a0001c0001t0022g0134a0001c0001t0106g0121 | 2 | 169 | 0.0118 | -4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148639955 | TAGAG | T | intron_variant | MODIFIER | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0016a0001c0001t0020a0001c0001t0039others(11): Show | a0001c0001t0016g0154a0001c0001t0016g0155a0001c0001t0020g0109others(13): Show | 16 | 169 | 0.0947 | -4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148654812 | GGTAA | G | intron_variant | MODIFIER | HG01891.hp2 HG02896.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0110a0001c0004t0095 | a0001c0001t0110g0118a0001c0004t0095g0113 | 2 | 169 | 0.0118 | -4 | c.180 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148666585 | AAAAT | A | intron_variant | MODIFIER | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(27): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | a0001c0001t0001g0070a0001c0001t0002g0085a0001c0001t0003g0042others(27): Show | 30 | 169 | 0.1775 | -4 | 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 | ATGTG | A | intron_variant | MODIFIER | HG01106.hp1 HG01243.hp1 HG01884.hp1 others(23): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0010a0001c0001t0011a0001c0001t0021others(22): Show | a0001c0001t0010g0115a0001c0001t0010g0116a0001c0001t0011g0128others(23): Show | 26 | 169 | 0.1539 | -4 | c.104 others(25): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148681561 | TGTCA | T | intron_variant | MODIFIER | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0016a0001c0001t0020a0001c0001t0039others(11): Show | a0001c0001t0016g0154a0001c0001t0016g0155a0001c0001t0020g0109others(13): Show | 16 | 169 | 0.0947 | -4 | c.104 others(25): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148681610 | GAAGA | G | intron_variant | MODIFIER | HG00639.hp1 HG01255.hp1 HG02055.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0016a0001c0001t0020a0001c0001t0039others(13): Show | a0001c0001t0016g0154a0001c0001t0016g0155a0001c0001t0020g0109others(14): Show | 17 | 169 | 0.1006 | -4 | c.104 others(25): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148681712 | CAAAG | C | intron_variant | MODIFIER | NA18990.hp1 NA19000.hp1 |
a0001 | a0001c0001 | a0001c0001t0059a0001c0001t0063 | a0001c0001t0059g0014a0001c0001t0063g0053 | 2 | 169 | 0.0118 | -4 | c.104 others(25): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148682578 | GTGGA | G | intron_variant | MODIFIER | HG00140.hp1 HG00673.hp1 HG01243.hp1 others(34): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(27): Show | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0082others(34): Show | 37 | 169 | 0.2189 | -4 | c.104 others(25): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148700419 | AGTGT | A | intron_variant | MODIFIER | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0002g0085others(18): Show | 21 | 169 | 0.1243 | -4 | c.104 others(25): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar |