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 | 87069271 | C | CTTTT | intron_variant | MODIFIER | HG02486.hp2 HG02622.hp2 HG02896.hp1 others(4): Show |
a0001a0010 | a0001c0001a0010c0032 | a0001c0001t0011a0001c0001t0017a0001c0001t0032others(1): Show | a0001c0001t0011g0096 a0001c0001t0011g0240 a0001c0001t0011g0265 others(4): Show |
7 | 57 | 0.1228 | 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 | 87081152 | A | ATTTT | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(34): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0270 a0001c0001t0002g0031 a0001c0001t0002g0246 others(34): Show |
37 | 67 | 0.5522 | 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 | C | CAATA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG01071.hp2 others(25): Show |
a0001a0007a0014 | a0001c0001a0001c0011a0001c0028others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(8): Show | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0143 others(25): Show |
28 | 97 | 0.2887 | 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 | 87085751 | C | CTTTT | intron_variant | MODIFIER | HG01071.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0012a0001c0001t0058 | a0001c0001t0001g0134 a0001c0001t0001g0177 a0001c0001t0012g0058 others(4): Show |
7 | 220 | 0.0318 | 4 | c.110 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87088775 | G | GTATT | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0003others(27): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(83): Show | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0045 others(243): Show |
246 | 292 | 0.8425 | 4 | c.110 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87122881 | T | TAAAA | intron_variant | MODIFIER | HG01175.hp2 HG01256.hp1 HG02080.hp1 others(9): Show |
a0001a0017 | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(7): Show | a0001c0001t0001g0033 a0001c0001t0001g0120 a0001c0001t0001g0142 others(9): Show |
12 | 35 | 0.3429 | 4 | c.246 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
AFF1_chr4_86930011_87146039 | 87138490 | G | GGTGT | 3_prime_UTR_variant | MODIFIER | HG00738.hp1 HG02572.hp2 NA18522.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0008 | a0001c0001t0025a0002c0008t0021 | a0001c0001t0025g0003 a0001c0001t0025g0190 a0002c0008t0021g0016 others(1): Show |
4 | 127 | 0.0315 | 4 | c.*28 others(15): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 21/21 | 2822 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87145999 | C | CAAAA | downstream_gene_variant | MODIFIER | HG00323.hp2 HG00621.hp2 HG00738.hp1 others(16): Show |
a0001 | a0001c0001a0001c0003a0001c0006 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(3): Show | a0001c0001t0003g0002 a0001c0001t0003g0005 a0001c0001t0003g0006 others(16): Show |
19 | 121 | 0.1570 | 4 | c.*10 others(17): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4961 | chr4 | TogoVar | |||||||
AFF2_chrX_148495617_149005663 | 148521374 | G | GCACA | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG01074.hp1 others(60): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0008others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(60): Show |
63 | 107 | 0.5888 | 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 | 148576793 | A | ATGTG | intron_variant | MODIFIER | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(19): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(17): Show | a0001c0001t0001g0122 a0001c0001t0005g0126 a0001c0001t0005g0130 others(19): Show |
22 | 40 | 0.5500 | 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 | 148581029 | A | ATATG | intron_variant | MODIFIER | HG01934.hp1 HG02451.hp2 HG02630.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0005a0001c0001t0008a0001c0002t0018others(1): Show | a0001c0001t0005g0117 a0001c0001t0005g0118 a0001c0001t0008g0121 others(2): Show |
5 | 167 | 0.0299 | 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 | 148581277 | C | CGTAT | intron_variant | MODIFIER | HG01109.hp1 HG01934.hp1 HG02145.hp1 others(15): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(13): Show | a0001c0001t0001g0020 a0001c0001t0005g0117 a0001c0001t0005g0118 others(15): Show |
18 | 167 | 0.1078 | 4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | |||||||
AFF2_chrX_148495617_149005663 | 148581356 | A | ACACG | intron_variant | MODIFIER | HG02056.hp1 HG02129.hp1 NA18967.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0015 a0001c0001t0001g0053 a0001c0001t0004g0010 |
3 | 81 | 0.0370 | 4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | |||||||
AFF2_chrX_148495617_149005663 | 148581417 | C | CACGT | intron_variant | MODIFIER | HG02056.hp1 HG02129.hp1 HG02602.hp1 others(7): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0053 others(7): Show |
10 | 162 | 0.0617 | 4 | c.48- others(21): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | chrX | TogoVar | |||||||
AFF2_chrX_148495617_149005663 | 148581418 | G | GTATA | intron_variant | MODIFIER | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0017a0001c0001t0046a0001c0001t0057others(2): Show | a0001c0001t0017g0136 a0001c0001t0046g0123 a0001c0001t0057g0166 others(2): Show |
5 | 146 | 0.0342 | 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 | 148581445 | T | TATAC | intron_variant | MODIFIER | HG02602.hp1 NA18966.hp1 NA19004.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0002g0033 others(3): Show |
6 | 65 | 0.0923 | 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 | 148581592 | A | ATACG | intron_variant | MODIFIER | HG02027.hp1 HG02735.hp1 HG02886.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011a0001c0001t0015others(1): Show | a0001c0001t0001g0078 a0001c0001t0001g0122 a0001c0001t0011g0072 others(3): Show |
6 | 139 | 0.0432 | 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 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0056 a0001c0001t0001g0146 a0001c0001t0001g0168 others(6): Show |
9 | 154 | 0.0584 | 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 |
a0001a0002 | a0001c0001a0001c0002a0002c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0084 a0001c0001t0001g0095 a0001c0001t0001g0168 others(9): Show |
12 | 81 | 0.1481 | 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 | a0001c0001t0029a0001c0001t0049a0001c0002t0019 | a0001c0001t0029g0153 a0001c0001t0049g0021 a0001c0002t0019g0157 |
3 | 154 | 0.0195 | 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 | a0001c0001t0005a0001c0001t0008a0001c0001t0017others(7): Show | a0001c0001t0005g0117 a0001c0001t0005g0118 a0001c0001t0005g0126 others(10): Show |
13 | 131 | 0.0992 | 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 | a0001c0001t0005a0001c0001t0008 | a0001c0001t0005g0117 a0001c0001t0005g0118 a0001c0001t0008g0121 |
3 | 137 | 0.0219 | 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 | a0001c0001t0011a0001c0001t0017a0001c0001t0046 | a0001c0001t0011g0088 a0001c0001t0017g0136 a0001c0001t0046g0123 |
3 | 143 | 0.0210 | 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 | a0001c0001t0001a0001c0001t0002a0001c0001t0016others(2): Show | a0001c0001t0001g0044 a0001c0001t0002g0073 a0001c0001t0016g0076 others(2): Show |
5 | 131 | 0.0382 | 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 | a0001c0001t0001a0001c0001t0011a0001c0001t0034others(6): Show | a0001c0001t0001g0018 a0001c0001t0011g0072 a0001c0001t0034g0140 others(6): Show |
9 | 129 | 0.0698 | 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 |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0034 others(68): Show |
71 | 89 | 0.7978 | 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(15): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(6): Show | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0030 others(15): Show |
18 | 167 | 0.1078 | 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 | 148701012 | A | ATGTG | intron_variant | MODIFIER | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(65): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(65): Show |
68 | 97 | 0.7010 | 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 | a0001c0002t0004a0001c0002t0050 | a0001c0002t0004g0156 a0001c0002t0050g0133 |
2 | 164 | 0.0122 | 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 | a0001c0001t0005a0001c0001t0031a0001c0001t0046others(3): Show | a0001c0001t0005g0130 a0001c0001t0031g0129 a0001c0001t0046g0123 others(3): Show |
6 | 21 | 0.2857 | 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(9): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(6): Show | a0001c0001t0001g0034 a0001c0001t0001g0044 a0001c0001t0001g0146 others(9): Show |
12 | 122 | 0.0984 | 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(9): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(4): Show | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0003g0027 others(9): Show |
12 | 38 | 0.3158 | 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 | a0001c0001t0005a0001c0001t0009 | a0001c0001t0005g0126 a0001c0001t0009g0112 |
2 | 164 | 0.0122 | 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 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0019 others(20): Show |
23 | 65 | 0.3538 | 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 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(4): Show | a0001c0001t0004g0111 a0001c0001t0005g0117 a0001c0001t0005g0118 others(6): Show |
9 | 167 | 0.0539 | 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 | a0001c0001t0031a0001c0002t0045 | a0001c0001t0031g0129 a0001c0002t0045g0119 |
2 | 166 | 0.0120 | 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 | a0001c0001t0005a0001c0001t0008a0001c0002t0009others(4): Show | a0001c0001t0005g0130 a0001c0001t0008g0013 a0001c0002t0009g0125 others(4): Show |
7 | 167 | 0.0419 | 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 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0056 a0001c0001t0001g0069 a0001c0001t0001g0093 others(10): Show |
13 | 61 | 0.2131 | 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 | 148822704 | G | GGTGT | intron_variant | MODIFIER | HG02257.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0046a0001c0002t0002a0001c0002t0004others(3): Show | a0001c0001t0046g0123 a0001c0002t0002g0128 a0001c0002t0004g0116 others(4): Show |
7 | 48 | 0.1458 | 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(84): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0002c0008others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(84): Show |
87 | 96 | 0.9063 | 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 | a0001c0001t0056a0001c0001t0057a0001c0002t0032 | a0001c0001t0056g0120 a0001c0001t0057g0166 a0001c0002t0032g0148 |
3 | 10 | 0.3000 | 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 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0034 a0001c0001t0001g0069 a0001c0001t0001g0090 others(17): Show |
20 | 36 | 0.5556 | 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 | 148862224 | T | TGCTA | intron_variant | MODIFIER | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0004a0001c0001t0008a0001c0001t0009others(7): Show | a0001c0001t0004g0111 a0001c0001t0008g0035 a0001c0001t0009g0112 others(7): Show |
10 | 167 | 0.0599 | 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 | 148894888 | G | GATAT | intron_variant | MODIFIER | HG02486.hp1 HG02615.hp1 |
a0001 | a0001c0001 | a0001c0001t0047a0001c0001t0048 | a0001c0001t0047g0008 a0001c0001t0048g0007 |
2 | 164 | 0.0122 | 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 | a0001c0001t0005a0001c0001t0049 | a0001c0001t0005g0062 a0001c0001t0005g0130 a0001c0001t0049g0021 |
3 | 145 | 0.0207 | 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 | 148897221 | C | CTATA | intron_variant | MODIFIER | HG01243.hp1 NA18948.hp1 NA18984.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0031 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0031g0129 |
3 | 150 | 0.0200 | 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 | a0001c0002t0004a0001c0002t0060a0001c0005t0020 | a0001c0002t0004g0116 a0001c0002t0060g0113 a0001c0005t0020g0127 |
3 | 131 | 0.0229 | 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 | a0001c0001t0005a0001c0005t0020 | a0001c0001t0005g0130 a0001c0005t0020g0131 |
2 | 29 | 0.0690 | 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 | a0001c0002t0004a0001c0002t0019a0001c0002t0045others(1): Show | a0001c0002t0004g0156 a0001c0002t0019g0152 a0001c0002t0019g0157 others(2): Show |
5 | 161 | 0.0311 | 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 | a0001c0001t0047a0001c0001t0048a0001c0001t0049others(3): Show | a0001c0001t0047g0008 a0001c0001t0048g0007 a0001c0001t0049g0021 others(3): Show |
6 | 156 | 0.0385 | 4 | c.326 others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar |