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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AEBP2_chr12_19434492_19527227 | 19508772 | AACAAAT | A | intron_variant | MODIFIER | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0016a0001c0001t0019a0001c0001t0046 | a0001c0001t0016g0035a0001c0001t0016g0036a0001c0001t0016g0038others(5): Show | 8 | 404 | 0.0198 | -6 | c.130 others(25): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | TogoVar | ||||||
AEBP2_chr12_19434492_19527227 | 19525458 | CTTTCCT | C | downstream_gene_variant | MODIFIER | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0233a0001c0001t0015g0234a0001c0001t0015g0235 | 3 | 404 | 0.0074 | -6 | c.*73 others(17): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3232 | chr12 | TogoVar | ||||||
AFAP1L1_chr5_149266859_149348637 | 149275455 | TTCTTCC | T | intron_variant | MODIFIER | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(38): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0032others(37): Show | 41 | 286 | 0.1434 | -6 | c.16+ others(21): Show |
AFAP1L1 | ENSG00000157510.14 | transcript | ENST00000296721.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
AFAP1L1_chr5_149266859_149348637 | 149305878 | CCACACA | C | intron_variant | MODIFIER | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(44): Show |
a0001a0003a0004others(3): Show | a0001c0001a0003c0005a0003c0008others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0082others(44): Show | 47 | 286 | 0.1643 | -6 | c.437 others(21): Show |
AFAP1L1 | ENSG00000157510.14 | transcript | ENST00000296721.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
AFAP1L2_chr10_114289824_114409502 | 114368767 | AACACAC | A | intron_variant | MODIFIER | HG00639.hp1 HG00741.hp1 HG01261.hp1 others(24): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0003others(10): Show | a0001c0001t0001g0067a0001c0001t0001g0071a0001c0001t0001g0094others(24): Show | 27 | 262 | 0.1031 | -6 | c.17- others(23): Show |
AFAP1L2 | ENSG00000169129.16 | transcript | ENST00000304129.9 | protein_coding | 1/18 | chr10 | TogoVar | ||||||
AFAP1_chr4_7753714_7944861 | 7795405 | CTTTTTT | C | intron_variant | MODIFIER | HG00140.hp1 HG01069.hp2 HG01099.hp1 others(9): Show |
a0001a0002 | a0001c0004a0001c0007a0001c0009others(2): Show | a0001c0004t0006a0001c0004t0008a0001c0004t0011others(5): Show | a0001c0004t0006g0063a0001c0004t0008g0293a0001c0004t0011g0253others(9): Show | 12 | 318 | 0.0377 | -6 | c.126 others(25): Show |
AFAP1 | ENSG00000196526.11 | transcript | ENST00000420658.6 | protein_coding | 10/17 | chr4 | TogoVar | ||||||
AFAP1_chr4_7753714_7944861 | 7840305 | GGTGTGT | G | intron_variant | MODIFIER | HG01433.hp1 HG02258.hp2 HG02572.hp2 others(14): Show |
a0001a0006 | a0001c0002a0001c0004a0001c0010others(3): Show | a0001c0002t0024a0001c0002t0034a0001c0002t0048others(7): Show | a0001c0002t0024g0291a0001c0002t0034g0268a0001c0002t0034g0292others(14): Show | 17 | 318 | 0.0535 | -6 | c.547 others(23): Show |
AFAP1 | ENSG00000196526.11 | transcript | ENST00000420658.6 | protein_coding | 5/17 | chr4 | TogoVar | ||||||
AFAP1_chr4_7753714_7944861 | 7840822 | CGGAAAG | C | intron_variant | MODIFIER | HG02257.hp1 HG02630.hp1 HG02922.hp2 others(2): Show |
a0002 | a0002c0005 | a0002c0005t0004 | a0002c0005t0004g0012a0002c0005t0004g0213a0002c0005t0004g0266others(2): Show | 5 | 318 | 0.0157 | -6 | c.547 others(23): Show |
AFAP1 | ENSG00000196526.11 | transcript | ENST00000420658.6 | protein_coding | 5/17 | chr4 | TogoVar | ||||||
AFAP1_chr4_7753714_7944861 | 7869144 | AGAAAGG | A | intron_variant | MODIFIER | HG02040.hp1 HG04184.hp2 NA19007.hp1 |
a0001a0003 | a0001c0003a0003c0006 | a0001c0003t0002a0003c0006t0005 | a0001c0003t0002g0176a0001c0003t0002g0256a0003c0006t0005g0143 | 3 | 318 | 0.0094 | -6 | c.128 others(21): Show |
AFAP1 | ENSG00000196526.11 | transcript | ENST00000420658.6 | protein_coding | 2/17 | chr4 | TogoVar | ||||||
AFAP1_chr4_7753714_7944861 | 7891184 | ATCTGAC | A | intron_variant | MODIFIER | HG00140.hp1 HG00735.hp1 HG01433.hp1 others(17): Show |
a0001a0002 | a0001c0002a0001c0004a0001c0007others(4): Show | a0001c0002t0032a0001c0002t0034a0001c0004t0011others(9): Show | a0001c0002t0032g0252a0001c0002t0034g0268a0001c0002t0034g0292others(17): Show | 20 | 318 | 0.0629 | -6 | c.-2- others(23): Show |
AFAP1 | ENSG00000196526.11 | transcript | ENST00000420658.6 | protein_coding | 1/17 | chr4 | TogoVar | ||||||
AFAP1_chr4_7753714_7944861 | 7908987 | CAATTGA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(41): Show | a0001c0001t0001a0001c0001t0010a0001c0001t0014others(96): Show | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0027others(270): Show | 273 | 318 | 0.8585 | -6 | c.-3+ others(23): Show |
AFAP1 | ENSG00000196526.11 | transcript | ENST00000420658.6 | protein_coding | 1/17 | chr4 | TogoVar | ||||||
AFDN_chr6_167821911_167977023 | 167844177 | AGTGTGT | A | intron_variant | MODIFIER | HG01074.hp2 HG01099.hp1 HG01106.hp2 others(17): Show |
a0001a0014 | a0001c0002a0001c0004a0014c0015 | a0001c0002t0001a0001c0004t0001a0001c0004t0010others(1): Show | a0001c0002t0001g0193a0001c0004t0001g0104a0001c0004t0001g0110others(17): Show | 20 | 326 | 0.0614 | -6 | c.105 others(25): Show |
AFDN | ENSG00000130396.22 | transcript | ENST00000683244.1 | protein_coding | 1/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
AFDN_chr6_167821911_167977023 | 167860159 | CTTTTTT | C | intron_variant | MODIFIER | HG00140.hp2 HG01167.hp1 HG02145.hp1 others(21): Show |
a0001a0002 | a0001c0002a0001c0004a0001c0006others(2): Show | a0001c0002t0001a0001c0004t0001a0001c0004t0010others(6): Show | a0001c0002t0001g0122a0001c0004t0001g0092a0001c0004t0001g0120others(20): Show | 24 | 326 | 0.0736 | -6 | c.106 others(23): Show |
AFDN | ENSG00000130396.22 | transcript | ENST00000683244.1 | protein_coding | 1/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
AFDN_chr6_167821911_167977023 | 167860193 | CCTTTGT | C | intron_variant | MODIFIER | HG02615.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
a0001a0002 | a0001c0006a0002c0029 | a0001c0006t0001a0001c0006t0017a0002c0029t0001 | a0001c0006t0001g0312a0001c0006t0001g0314a0001c0006t0017g0322others(1): Show | 4 | 326 | 0.0123 | -6 | c.106 others(23): Show |
AFDN | ENSG00000130396.22 | transcript | ENST00000683244.1 | protein_coding | 1/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
AFDN_chr6_167821911_167977023 | 167891404 | GGTGGGT | G | intron_variant | MODIFIER | HG01081.hp1 HG01099.hp1 HG02129.hp1 others(15): Show |
a0001a0009 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0003a0001c0002t0001a0001c0004t0001others(5): Show | a0001c0001t0003g0282a0001c0002t0001g0113a0001c0002t0001g0126others(15): Show | 18 | 326 | 0.0552 | -6 | c.117 others(23): Show |
AFDN | ENSG00000130396.22 | transcript | ENST00000683244.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
AFDN_chr6_167821911_167977023 | 167891408 | GGTGTGT | G | intron_variant | MODIFIER | HG02155.hp2 NA18971.hp1 NA19064.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0223a0001c0001t0002g0234a0001c0001t0002g0235 | 3 | 326 | 0.0092 | -6 | c.117 others(23): Show |
AFDN | ENSG00000130396.22 | transcript | ENST00000683244.1 | protein_coding | 8/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
AFDN_chr6_167821911_167977023 | 167897642 | CTTTTTT | C | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
a0001a0002a0014others(1): Show | a0001c0003a0001c0005a0001c0024others(6): Show | a0001c0003t0001a0001c0003t0021a0001c0005t0001others(8): Show | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0009others(85): Show | 89 | 326 | 0.2730 | -6 | c.131 others(23): Show |
AFDN | ENSG00000130396.22 | transcript | ENST00000683244.1 | protein_coding | 10/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
AFDN_chr6_167821911_167977023 | 167918454 | ATTTCTT | A | intron_variant | MODIFIER | HG02647.hp1 HG02896.hp1 HG03516.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0045a0001c0003t0001g0050a0001c0003t0001g0051 | 3 | 326 | 0.0092 | -6 | c.271 others(23): Show |
AFDN | ENSG00000130396.22 | transcript | ENST00000683244.1 | protein_coding | 20/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
AFDN_chr6_167821911_167977023 | 167964614 | CTGTGTG | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
a0001a0002a0003 | a0001c0002a0001c0003a0001c0004others(7): Show | a0001c0002t0001a0001c0003t0001a0001c0004t0001others(11): Show | a0001c0002t0001g0117a0001c0002t0001g0131a0001c0002t0001g0132others(54): Show | 58 | 326 | 0.1779 | -6 | c.496 others(25): Show |
AFDN | ENSG00000130396.22 | transcript | ENST00000683244.1 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86939124 | AAGAAAG | A | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(56): Show |
a0001a0006a0009others(2): Show | a0001c0001a0001c0003a0001c0011others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0124others(56): Show | 59 | 294 | 0.2007 | -6 | c.-37 others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86951617 | TTTTTTC | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(49): Show |
a0001a0009a0016 | a0001c0001a0001c0011a0001c0016others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(13): Show | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0132others(49): Show | 52 | 294 | 0.1769 | -6 | 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 | 86982388 | CTTTTTT | C | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(8): Show |
a0001a0010 | a0001c0001a0001c0002a0010c0015 | a0001c0001t0003a0001c0002t0005a0001c0002t0044others(2): Show | a0001c0001t0003g0192a0001c0002t0005g0185a0001c0002t0005g0193others(8): Show | 11 | 294 | 0.0374 | -6 | c.38+ others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86985181 | CTATATA | C | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0028a0002c0008others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0090others(73): Show | 76 | 294 | 0.2585 | -6 | c.38+ others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 86987254 | CTTATTA | C | 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 | -6 | c.38+ others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87000605 | CTGTGTG | C | intron_variant | MODIFIER | HG01884.hp1 HG02572.hp1 HG03516.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0008a0001c0001t0015a0001c0002t0005 | a0001c0001t0008g0115a0001c0001t0015g0114a0001c0002t0005g0117 | 3 | 294 | 0.0102 | -6 | c.39- others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87000987 | ATAATTC | A | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0005a0001c0002t0044others(1): Show | a0001c0001t0003g0192a0001c0002t0005g0193a0001c0002t0005g0194others(7): Show | 10 | 294 | 0.0340 | -6 | c.39- others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87005953 | ATGTCTT | A | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(13): Show |
a0001a0002a0007others(1): Show | a0001c0001a0001c0002a0002c0008others(2): Show | a0001c0001t0003a0001c0002t0005a0001c0002t0044others(5): Show | a0001c0001t0003g0192a0001c0002t0005g0185a0001c0002t0005g0193others(13): Show | 16 | 294 | 0.0544 | -6 | c.39- others(23): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87037992 | AAATTAT | A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(99): Show |
a0001a0003a0004others(4): Show | a0001c0001a0001c0028a0003c0012others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0221others(99): Show | 102 | 294 | 0.3469 | -6 | 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 | 87065036 | AAAAAAT | A | intron_variant | MODIFIER | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(7): Show |
a0001a0005 | a0001c0001a0005c0032 | a0001c0001t0011a0001c0001t0017a0001c0001t0032others(1): Show | a0001c0001t0011g0094a0001c0001t0011g0240a0001c0001t0011g0265others(7): Show | 10 | 294 | 0.0340 | -6 | c.105 others(27): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87066588 | CAAAACA | C | intron_variant | MODIFIER | HG01074.hp1 HG01109.hp1 HG01496.hp1 others(10): Show |
a0001a0012 | a0001c0001a0012c0021 | a0001c0001t0001a0001c0001t0009a0001c0001t0029others(2): Show | a0001c0001t0001g0270a0001c0001t0009g0208a0001c0001t0009g0216others(10): Show | 13 | 294 | 0.0442 | -6 | c.106 others(27): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
AFF1_chr4_86930011_87146039 | 87138490 | GGTGTGT | G | 3_prime_UTR_variant | MODIFIER | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(9): Show |
a0001a0005a0010 | a0001c0001a0005c0032a0010c0015 | a0001c0001t0011a0001c0001t0017a0001c0001t0032others(3): Show | a0001c0001t0011g0094a0001c0001t0011g0240a0001c0001t0011g0265others(9): Show | 12 | 294 | 0.0408 | -6 | c.*28 others(17): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 21/21 | 2816 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||
AFF1_chr4_86930011_87146039 | 87145999 | CAAAAAA | C | downstream_gene_variant | MODIFIER | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(13): Show |
a0001 | a0001c0002a0001c0014a0001c0017others(1): Show | a0001c0002t0005a0001c0002t0044a0001c0002t0049others(3): Show | a0001c0002t0005g0116a0001c0002t0005g0117a0001c0002t0005g0118others(13): Show | 16 | 294 | 0.0544 | -6 | c.*10 others(19): Show |
AFF1 | ENSG00000172493.23 | transcript | ENST00000395146.9 | protein_coding | 4961 | chr4 | TogoVar | ||||||
AFF2_chrX_148495617_149005663 | 148500637 | TGCCGCC | T | 5_prime_UTR_variant | MODIFIER | HG01358.hp1 NA19082.hp1 |
a0001 | a0001c0001 | a0001c0001t0116a0001c0001t0117 | a0001c0001t0116g0075a0001c0001t0117g0164 | 2 | 169 | 0.0118 | -6 | c.-41 others(15): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/21 | 414 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||
AFF2_chrX_148495617_149005663 | 148500679 | CGCCGCT | C | 5_prime_UTR_variant | MODIFIER | HG01884.hp1 HG01884.hp2 HG02630.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0029a0001c0002t0031a0001c0003t0030 | a0001c0002t0029g0149a0001c0002t0031g0148a0001c0003t0030g0158 | 3 | 169 | 0.0178 | -6 | c.-41 others(15): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/21 | 408 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||
AFF2_chrX_148495617_149005663 | 148521406 | ACACACT | A | intron_variant | MODIFIER | HG02145.hp1 HG02280.hp1 HG02895.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0022a0001c0001t0038a0001c0001t0106others(3): Show | a0001c0001t0022g0134a0001c0001t0038g0102a0001c0001t0106g0121others(3): Show | 6 | 169 | 0.0355 | -6 | c.47+ others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148524097 | TTCTCTC | T | intron_variant | MODIFIER | HG01934.hp1 HG02615.hp1 |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0092 | a0001c0001t0010g0116a0001c0001t0092g0008 | 2 | 169 | 0.0118 | -6 | c.47+ others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148524119 | CTCTCTG | C | intron_variant | MODIFIER | HG02486.hp1 HG03540.hp2 |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0093 | a0001c0001t0010g0115a0001c0001t0093g0007 | 2 | 169 | 0.0118 | -6 | c.47+ others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148524121 | CTCTGTG | C | intron_variant | MODIFIER | NA18940.hp1 NA19056.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0048 | a0001c0001t0001g0070a0001c0001t0048g0013 | 2 | 169 | 0.0118 | -6 | c.47+ others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148574943 | GGTGTGT | G | intron_variant | MODIFIER | HG01109.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(13): Show | a0001c0001t0001g0082a0001c0001t0004g0041a0001c0001t0006g0120others(13): Show | 16 | 169 | 0.0947 | -6 | c.47+ others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148574981 | TGTGTGA | T | intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0002 | a0001c0002t0091 | a0001c0002t0091g0136 | 1 | 169 | 0.0059 | -6 | c.47+ others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148581184 | CACATAT | C | intron_variant | MODIFIER | HG01934.hp1 HG02451.hp2 HG03540.hp2 |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0098 | a0001c0001t0010g0115a0001c0001t0010g0116a0001c0001t0098g0119 | 3 | 169 | 0.0178 | -6 | c.48- others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148581420 | ATACGTC | A | intron_variant | MODIFIER | HG02818.hp1 HG06807.hp2 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0009a0001c0005t0023 | a0001c0002t0009g0126a0001c0005t0023g0125 | 2 | 169 | 0.0118 | -6 | c.48- others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148581472 | ATATACG | A | intron_variant | MODIFIER | NA18967.hp1 | a0001 | a0001c0001 | a0001c0001t0042 | a0001c0001t0042g0012 | 1 | 169 | 0.0059 | -6 | c.48- others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148581540 | ATACGTC | A | intron_variant | MODIFIER | HG02735.hp1 NA18989.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0085 | a0001c0001t0001g0076a0001c0001t0085g0167 | 2 | 169 | 0.0118 | -6 | c.48- others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148581562 | ATATACG | A | intron_variant | MODIFIER | HG02040.hp1 HG02055.hp1 HG02257.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0011a0001c0001t0020others(9): Show | a0001c0001t0002g0029a0001c0001t0002g0062a0001c0001t0011g0112others(10): Show | 13 | 169 | 0.0769 | -6 | c.48- others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148614711 | TTCTTTC | T | intron_variant | MODIFIER | HG01243.hp1 HG01934.hp1 HG02647.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0011a0001c0001t0044 | a0001c0001t0010g0115a0001c0001t0010g0116a0001c0001t0011g0128others(1): Show | 4 | 169 | 0.0237 | -6 | c.48- others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148614790 | CTTCCTT | C | intron_variant | MODIFIER | HG02572.hp1 HG02886.hp1 HG03098.hp1 |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0066a0001c0002t0082a0001c0004t0075 | a0001c0001t0066g0015a0001c0002t0082g0016a0001c0004t0075g0004 | 3 | 169 | 0.0178 | -6 | c.48- others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148629101 | TTGTGTG | T | intron_variant | MODIFIER | HG02818.hp1 HG03486.hp2 |
a0001 | a0001c0002 | a0001c0002t0009a0001c0002t0105 | a0001c0002t0009g0126a0001c0002t0105g0117 | 2 | 169 | 0.0118 | -6 | c.48- others(23): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148681536 | ATGTGTG | A | intron_variant | MODIFIER | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0082others(25): Show | 28 | 169 | 0.1657 | -6 | c.104 others(27): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
AFF2_chrX_148495617_149005663 | 148700419 | AGTGTGT | A | intron_variant | MODIFIER | HG02976.hp2 | a0001 | a0001c0003 | a0001c0003t0026 | a0001c0003t0026g0157 | 1 | 169 | 0.0059 | -6 | c.104 others(27): Show |
AFF2 | ENSG00000155966.14 | transcript | ENST00000370460.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chrX | TogoVar |