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 | 148581447 | C | CACGT | intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0003 | a0001c0003t0079 | a0001c0003t0079g0161 | 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 | 148581469 | C | CACGT | intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0004 | a0001c0004t0095 | a0001c0004t0095g0113 | 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 | 148581530 | A | ACACG | intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0004 | a0001c0004t0095 | a0001c0004t0095g0113 | 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 | 148581592 | A | ATACG | 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 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148614693 | T | TTTTC | intron_variant | MODIFIER | HG01433.hp1 NA18943.hp1 NA18959.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0012a0001c0001t0014a0001c0001t0017others(5): Show | a0001c0001t0012g0168a0001c0001t0014g0055a0001c0001t0014g0058others(6): Show | 9 | 169 | 0.0533 | 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 | 148614726 | T | TTTCC | intron_variant | MODIFIER | NA19004.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0066 | 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 | T | TTTTC | intron_variant | MODIFIER | HG01952.hp1 HG02027.hp1 HG02071.hp1 others(9): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0009others(1): Show | a0001c0001t0008a0001c0001t0012a0001c0001t0017others(9): Show | a0001c0001t0008g0051a0001c0001t0012g0168a0001c0001t0017g0040others(9): Show | 12 | 169 | 0.0710 | 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 | 148614742 | C | CTTCT | intron_variant | MODIFIER | HG02809.hp1 NA19240.hp1 NA20129.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0035a0001c0001t0076a0001c0002t0018 | a0001c0001t0035g0078a0001c0001t0076g0153a0001c0002t0018g0156 | 3 | 169 | 0.0178 | 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 | 148614796 | T | TTCTC | intron_variant | MODIFIER | HG01109.hp1 HG01934.hp1 HG02280.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0010a0001c0001t0022a0001c0001t0037others(8): Show | a0001c0001t0010g0115a0001c0001t0010g0116a0001c0001t0010g0124others(10): Show | 13 | 169 | 0.0769 | 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 | 148623600 | A | AATAT | intron_variant | MODIFIER | HG01934.hp1 HG02451.hp2 HG03540.hp2 |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0098 | a0001c0001t0010g0115a0001c0001t0010g0116a0001c0001t0098g0119 | 3 | 169 | 0.0178 | 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 | 148629101 | T | TTGTG | intron_variant | MODIFIER | HG02895.hp1 NA18989.hp1 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0022a0001c0001t0085a0001c0001t0106 | a0001c0001t0022g0134a0001c0001t0085g0167a0001c0001t0106g0121 | 3 | 169 | 0.0178 | 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 | 148666585 | A | AAAAT | intron_variant | MODIFIER | HG02486.hp1 NA18986.hp1 NA18990.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0013a0001c0001t0059others(2): Show | a0001c0001t0004g0045a0001c0001t0013g0072a0001c0001t0059g0014others(2): Show | 5 | 169 | 0.0296 | 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 | 148682578 | G | GTGGA | intron_variant | MODIFIER | HG00642.hp1 HG01891.hp1 HG02896.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0041a0001c0001t0100others(6): Show | a0001c0001t0002g0020a0001c0001t0041g0071a0001c0001t0100g0140others(6): Show | 9 | 169 | 0.0533 | 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 | A | AGTGT | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(68): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(49): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(68): Show | 71 | 169 | 0.4201 | 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 | 148700985 | G | GGAGA | intron_variant | MODIFIER | HG00140.hp1 HG00621.hp1 HG01934.hp1 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0082others(16): Show | 19 | 169 | 0.1124 | 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 | 148701011 | A | AGAAT | intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0089 | a0001c0001t0089g0110 | 1 | 169 | 0.0059 | 4 | c.104 others(25): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148701012 | A | ATGTG | intron_variant | MODIFIER | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(65): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(65): Show | 68 | 169 | 0.4024 | 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 | 148701014 | G | GAGAA | intron_variant | MODIFIER | HG02451.hp1 HG03225.hp1 |
a0001 | a0001c0002 | a0001c0002t0078a0001c0002t0107 | a0001c0002t0078g0152a0001c0002t0107g0131 | 2 | 169 | 0.0118 | 4 | c.104 others(25): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | chrX | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148704460 | G | GTGTA | intron_variant | MODIFIER | HG01243.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0011a0001c0001t0044a0001c0001t0046others(3): Show | a0001c0001t0011g0128a0001c0001t0044g0127a0001c0001t0046g0165others(3): Show | 6 | 169 | 0.0355 | 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 | 148749947 | C | CTTTA | intron_variant | MODIFIER | HG00738.hp1 HG01978.hp2 HG02040.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(10): Show | a0001c0001t0001g0036a0001c0001t0004g0045a0001c0001t0005g0009others(10): Show | 13 | 169 | 0.0769 | 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 | 148762480 | A | ATGTG | intron_variant | MODIFIER | HG00738.hp1 HG01243.hp1 HG01255.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(9): Show | a0001c0001t0001g0036a0001c0001t0005g0009a0001c0001t0005g0022others(10): Show | 13 | 169 | 0.0769 | 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 | 148773651 | G | GAGGA | intron_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0001 | a0001c0001t0119 | a0001c0001t0119g0061 | 1 | 169 | 0.0059 | 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 | 148773669 | A | AGAAG | intron_variant | MODIFIER | HG01109.hp1 HG02622.hp2 |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0089 | a0001c0001t0010g0124a0001c0001t0089g0110 | 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 | 148773685 | G | GGAAA | intron_variant | MODIFIER | HG00639.hp2 HG01074.hp1 HG01099.hp1 others(20): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(17): Show | a0001c0001t0001g0019a0001c0001t0001g0082a0001c0001t0003g0065others(20): Show | 23 | 169 | 0.1361 | 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 | 148786613 | C | CAGTT | intron_variant | MODIFIER | HG01109.hp1 HG01934.hp1 HG02622.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0010a0001c0001t0020a0001c0001t0038others(4): Show | a0001c0001t0010g0115a0001c0001t0010g0116a0001c0001t0010g0124others(6): Show | 9 | 169 | 0.0533 | 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 | 148787312 | C | CTGTG | intron_variant | MODIFIER | HG01243.hp1 HG03486.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0044a0001c0002t0105 | a0001c0001t0044g0127a0001c0002t0105g0117 | 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 | 148792845 | A | AAAAG | intron_variant | MODIFIER | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0011a0001c0001t0066a0001c0002t0019others(4): Show | a0001c0001t0011g0128a0001c0001t0066g0015a0001c0002t0019g0123others(4): Show | 7 | 169 | 0.0414 | 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 | 148795800 | C | CAAAA | intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0002 | a0001c0002t0105 | a0001c0002t0105g0117 | 1 | 169 | 0.0059 | 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 | 148795832 | A | AATAT | intron_variant | MODIFIER | HG01069.hp1 HG01978.hp2 HG02280.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0006a0001c0001t0021a0001c0002t0091 | a0001c0001t0006g0163a0001c0001t0021g0150a0001c0002t0091g0136 | 3 | 169 | 0.0178 | 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 | 148795872 | T | TATAC | intron_variant | MODIFIER | HG00642.hp1 HG01258.hp1 HG01943.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0013others(9): Show | a0001c0001t0001g0068a0001c0001t0008g0059a0001c0001t0013g0034others(10): Show | 13 | 169 | 0.0769 | 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 | 148816933 | C | CAAAA | intron_variant | MODIFIER | HG02895.hp1 | a0001 | a0001c0001 | a0001c0001t0106 | a0001c0001t0106g0121 | 1 | 169 | 0.0059 | 4 | 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 | 148822704 | G | GGTGT | intron_variant | MODIFIER | HG02257.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0106a0001c0002t0009a0001c0002t0020others(4): Show | a0001c0001t0106g0121a0001c0002t0009g0126a0001c0002t0020g0132others(4): Show | 7 | 169 | 0.0414 | 4 | c.108 others(25): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148824060 | C | CCTCT | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(85): Show |
a0001a0002a0004 | a0001c0001a0001c0004a0002c0009others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(58): Show | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0039others(85): Show | 88 | 169 | 0.5207 | 4 | c.108 others(25): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148834505 | A | ATGTG | intron_variant | MODIFIER | HG01891.hp2 HG02615.hp2 HG03486.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0046a0001c0001t0110a0001c0002t0087 | a0001c0001t0046g0165a0001c0001t0110g0118a0001c0002t0087g0147 | 3 | 169 | 0.0178 | 4 | 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 | 148839894 | G | GGTGT | intron_variant | MODIFIER | HG01074.hp1 HG01099.hp1 HG01192.hp1 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(14): Show | a0001c0001t0001g0036a0001c0001t0001g0068a0001c0001t0006g0120others(17): Show | 20 | 169 | 0.1183 | 4 | c.117 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148845120 | T | TACAC | intron_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0116 | 1 | 169 | 0.0059 | 4 | 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 | 148849366 | T | TCCCC | intron_variant | MODIFIER | HG01978.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0021a0001c0002t0078a0001c0002t0082others(3): Show | a0001c0001t0021g0150a0001c0002t0078g0152a0001c0002t0082g0016others(3): Show | 6 | 169 | 0.0355 | 4 | 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 | 148852389 | G | GTTTT | intron_variant | MODIFIER | NA19079.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0051 | 1 | 169 | 0.0059 | 4 | 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 | 148862224 | T | TGCTA | intron_variant | MODIFIER | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0020a0001c0001t0037a0001c0001t0038others(7): Show | a0001c0001t0020g0109a0001c0001t0037g0037a0001c0001t0038g0102others(7): Show | 10 | 169 | 0.0592 | 4 | c.126 others(25): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148883980 | T | TACAC | intron_variant | MODIFIER | HG02895.hp1 | a0001 | a0001c0001 | a0001c0001t0106 | a0001c0001t0106g0121 | 1 | 169 | 0.0059 | 4 | 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 | 148894888 | G | GATAT | intron_variant | MODIFIER | HG02486.hp1 HG02615.hp1 |
a0001 | a0001c0001 | a0001c0001t0092a0001c0001t0093 | a0001c0001t0092g0008a0001c0001t0093g0007 | 2 | 169 | 0.0118 | 4 | c.135 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148894892 | G | GATAT | intron_variant | MODIFIER | HG02647.hp1 HG02809.hp1 HG03579.hp1 |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0035a0001c0001t0039 | a0001c0001t0011g0128a0001c0001t0035g0078a0001c0001t0039g0101 | 3 | 169 | 0.0178 | 4 | c.135 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148895570 | A | AGTGT | intron_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0002 | a0001c0002t0054 | a0001c0002t0054g0133 | 1 | 169 | 0.0059 | 4 | c.136 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148897221 | C | CTATA | intron_variant | MODIFIER | HG01243.hp1 NA18948.hp1 NA18984.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0044 | a0001c0001t0001g0039a0001c0001t0002g0062a0001c0001t0044g0127 | 3 | 169 | 0.0178 | 4 | c.136 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148911075 | T | TTATA | intron_variant | MODIFIER | HG02809.hp2 HG02976.hp1 HG06807.hp2 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0032a0001c0002t0040a0001c0005t0023 | a0001c0002t0032g0114a0001c0002t0040g0111a0001c0005t0023g0125 | 3 | 169 | 0.0178 | 4 | 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 | TACAC | intron_variant | MODIFIER | HG02647.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0011a0001c0005t0023 | a0001c0001t0011g0128a0001c0005t0023g0129 | 2 | 169 | 0.0118 | 4 | c.139 others(25): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148953798 | A | AACAC | intron_variant | MODIFIER | HG02451.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0018a0001c0002t0034a0001c0002t0078others(1): Show | a0001c0002t0018g0151a0001c0002t0018g0156a0001c0002t0034g0077others(2): Show | 5 | 169 | 0.0296 | 4 | c.155 others(19): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148971126 | G | GTTTT | intron_variant | MODIFIER | HG01891.hp2 HG02486.hp1 HG02615.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0035a0001c0001t0046a0001c0001t0092others(3): Show | a0001c0001t0035g0078a0001c0001t0046g0165a0001c0001t0092g0008others(3): Show | 6 | 169 | 0.0355 | 4 | c.326 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148975943 | C | CAAAA | intron_variant | MODIFIER | HG01891.hp2 HG03041.hp1 HG03486.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0046a0001c0001t0110a0001c0002t0094 | a0001c0001t0046g0165a0001c0001t0110g0118a0001c0002t0094g0106 | 3 | 169 | 0.0178 | 4 | c.340 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148977614 | G | GACAC | intron_variant | MODIFIER | HG01109.hp1 HG01934.hp1 HG02258.hp1 others(3): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0010a0001c0001t0022a0001c0001t0025others(1): Show | a0001c0001t0010g0115a0001c0001t0010g0116a0001c0001t0010g0124others(3): Show | 6 | 169 | 0.0355 | 4 | c.340 others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar |