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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ATP8B4_chr15_49853238_50124233 | 50113838 | CAAAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(106): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0002a0002c0021others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(106): Show | 109 | 254 | 0.4291 | -4 | c.-43 others(21): Show |
ATP8B4 | ENSG00000104043.15 | transcript | ENST00000284509.11 | protein_coding | 1/27 | chr15 | TogoVar | ||||||
ATP8B4_chr15_49853238_50124233 | 50119752 | CTTTT | C | upstream_gene_variant | MODIFIER | HG00642.hp2 HG01109.hp2 HG01168.hp1 others(14): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0003others(6): Show | a0001c0001t0001g0144a0002c0002t0001g0128a0002c0002t0001g0130others(14): Show | 17 | 254 | 0.0669 | -4 | c.-67 others(13): Show |
ATP8B4 | ENSG00000104043.15 | transcript | ENST00000284509.11 | protein_coding | 520 | chr15 | TogoVar | ||||||
ATP8B4_chr15_49853238_50124233 | 50122525 | GTGTT | G | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0002a0002c0021others(8): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(21): Show | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0008others(81): Show | 84 | 254 | 0.3307 | -4 | c.-34 others(15): Show |
ATP8B4 | ENSG00000104043.15 | transcript | ENST00000284509.11 | protein_coding | 3293 | chr15 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51600805 | AAAAC | A | 3_prime_UTR_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(12): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0005a0001c0002t0028a0001c0003t0028 | a0001c0002t0005g0048a0001c0002t0005g0054a0001c0002t0005g0065others(12): Show | 15 | 312 | 0.0481 | -4 | c.*40 others(13): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 28/28 | 402 | chr20 | TogoVar | |||||
ATP9A_chr20_51591514_51773390 | 51600807 | AACAC | A | 3_prime_UTR_variant | MODIFIER | HG01069.hp2 HG02818.hp1 HG02818.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0025a0001c0001t0061a0001c0001t0062others(5): Show | a0001c0001t0025g0019a0001c0001t0061g0014a0001c0001t0062g0292others(5): Show | 8 | 312 | 0.0256 | -4 | c.*40 others(13): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 28/28 | 400 | chr20 | TogoVar | |||||
ATP9A_chr20_51591514_51773390 | 51603771 | ATTAT | A | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(85): Show | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0037others(211): Show | 214 | 312 | 0.6859 | -4 | c.300 others(23): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 27/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51611534 | TCTAA | T | intron_variant | MODIFIER | HG01884.hp2 HG02976.hp2 HG03098.hp1 others(1): Show |
a0001 | a0001c0003 | a0001c0003t0012a0001c0003t0060 | a0001c0003t0012g0085a0001c0003t0012g0086a0001c0003t0012g0087others(1): Show | 4 | 312 | 0.0128 | -4 | c.257 others(23): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 23/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51617387 | ATTCT | A | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0009a0001c0001t0012a0001c0001t0013others(38): Show | a0001c0001t0009g0004a0001c0001t0009g0009a0001c0001t0012g0080others(69): Show | 72 | 312 | 0.2308 | -4 | c.241 others(20): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 22/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51620325 | AACAG | A | intron_variant | MODIFIER | HG02258.hp1 HG02630.hp1 NA18522.hp2 others(1): Show |
a0001 | a0001c0003 | a0001c0003t0015a0001c0003t0031 | a0001c0003t0015g0121a0001c0003t0015g0138a0001c0003t0015g0151others(1): Show | 4 | 312 | 0.0128 | -4 | c.211 others(23): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 19/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51635822 | AAGGG | A | intron_variant | MODIFIER | HG02145.hp1 HG02280.hp1 HG02630.hp2 others(8): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0009a0001c0001t0012a0001c0001t0013others(3): Show | a0001c0001t0009g0004a0001c0001t0009g0009a0001c0001t0012g0080others(8): Show | 11 | 312 | 0.0353 | -4 | c.166 others(23): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 15/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51635861 | AAGGG | A | intron_variant | MODIFIER | HG00423.hp1 HG00735.hp1 HG01070.hp2 others(17): Show |
a0001 | a0001c0001a0001c0003a0001c0009others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(7): Show | a0001c0001t0001g0026a0001c0001t0001g0287a0001c0001t0003g0012others(17): Show | 20 | 312 | 0.0641 | -4 | c.166 others(23): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 15/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51638069 | TTTTA | T | intron_variant | MODIFIER | HG01433.hp2 HG02630.hp2 NA21309.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0009a0001c0001t0036 | a0001c0001t0003g0057a0001c0001t0009g0004a0001c0001t0036g0096 | 3 | 312 | 0.0096 | -4 | c.166 others(23): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 15/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51638071 | TTATA | T | intron_variant | MODIFIER | HG00642.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0007a0001c0002t0015a0001c0002t0032others(2): Show | a0001c0002t0007g0207a0001c0002t0015g0047a0001c0002t0032g0044others(2): Show | 5 | 312 | 0.0160 | -4 | c.166 others(23): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 15/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51642003 | CTTCT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(42): Show |
a0001 | a0001c0002a0001c0003a0001c0014 | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(15): Show | a0001c0002t0001g0200a0001c0002t0002g0005a0001c0002t0002g0161others(42): Show | 45 | 312 | 0.1442 | -4 | c.150 others(23): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 14/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51642725 | CCAAA | C | intron_variant | MODIFIER | HG01071.hp2 HG01168.hp1 HG01175.hp1 others(9): Show |
a0001 | a0001c0002 | a0001c0002t0005a0001c0002t0007a0001c0002t0013others(4): Show | a0001c0002t0005g0048a0001c0002t0005g0054a0001c0002t0005g0189others(9): Show | 12 | 312 | 0.0385 | -4 | c.150 others(23): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 14/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51655713 | AACAG | A | intron_variant | MODIFIER | HG02145.hp1 HG02280.hp1 HG02630.hp2 others(8): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0009a0001c0001t0012a0001c0001t0013others(3): Show | a0001c0001t0009g0004a0001c0001t0009g0009a0001c0001t0012g0080others(8): Show | 11 | 312 | 0.0353 | -4 | c.150 others(23): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 14/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51678069 | GGAGT | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(23): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0003a0001c0002t0005others(7): Show | a0001c0002t0002g0005a0001c0002t0003g0066a0001c0002t0005g0048others(23): Show | 26 | 312 | 0.0833 | -4 | c.800 others(21): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 9/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51702365 | CGTGT | C | intron_variant | MODIFIER | HG00140.hp1 HG00438.hp2 HG00673.hp1 others(28): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0077a0001c0001t0001g0268a0001c0001t0001g0273others(28): Show | 31 | 312 | 0.0994 | -4 | c.437 others(21): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 4/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51723563 | CTTTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(92): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(49): Show | a0001c0001t0001g0287a0001c0001t0003g0166a0001c0001t0004g0297others(92): Show | 95 | 312 | 0.3045 | -4 | c.327 others(21): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 3/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51735341 | CACAG | C | intron_variant | MODIFIER | HG01106.hp1 HG01175.hp2 HG01515.hp1 others(16): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0012a0001c0001t0024a0001c0003t0007others(11): Show | a0001c0001t0012g0080a0001c0001t0024g0045a0001c0003t0007g0224others(16): Show | 19 | 312 | 0.0609 | -4 | c.69- others(19): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 1/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51741055 | TTTAA | T | intron_variant | MODIFIER | HG01891.hp1 HG02622.hp1 NA20129.hp1 |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0009a0001c0001t0039 | a0001c0001t0008g0072a0001c0001t0009g0078a0001c0001t0039g0122 | 3 | 312 | 0.0096 | -4 | c.69- others(21): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 1/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51748907 | TTAGA | T | intron_variant | MODIFIER | HG02257.hp2 NA18968.hp1 NA19060.hp1 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0001a0001c0001t0039a0001c0003t0051others(2): Show | a0001c0001t0001g0287a0001c0001t0039g0122a0001c0003t0051g0118others(2): Show | 5 | 312 | 0.0160 | -4 | c.69- others(21): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 1/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51749198 | GTAAA | G | intron_variant | MODIFIER | HG02622.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0039a0001c0001t0066a0001c0002t0052others(3): Show | a0001c0001t0039g0122a0001c0001t0066g0117a0001c0002t0052g0091others(3): Show | 6 | 312 | 0.0192 | -4 | c.68+ others(21): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 1/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51756271 | CTCTG | C | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0027others(131): Show | 134 | 312 | 0.4295 | -4 | c.68+ others(21): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 1/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51762660 | AAAAC | A | intron_variant | MODIFIER | HG02027.hp2 NA18957.hp2 NA18961.hp1 others(10): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(2): Show | a0001c0001t0001g0282a0001c0001t0002g0271a0001c0001t0002g0274others(10): Show | 13 | 312 | 0.0417 | -4 | c.68+ others(19): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 1/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51767073 | CTTTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(53): Show | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0027others(90): Show | 93 | 312 | 0.2981 | -4 | c.68+ others(19): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 1/27 | chr20 | TogoVar | ||||||
ATP9B_chr18_79064394_79383283 | 79072581 | CTCTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(85): Show |
a0001a0013a0017 | a0001c0001a0001c0004a0001c0014others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(85): Show | 88 | 298 | 0.2953 | -4 | c.119 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79084692 | GCTTC | G | intron_variant | MODIFIER | HG01106.hp2 HG01884.hp1 HG02572.hp2 others(1): Show |
a0001 | a0001c0004a0001c0037 | a0001c0004t0003a0001c0037t0003 | a0001c0004t0003g0101a0001c0004t0003g0102a0001c0004t0003g0103others(1): Show | 4 | 298 | 0.0134 | -4 | c.120 others(23): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79112039 | TAGAC | T | intron_variant | MODIFIER | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(8): Show |
a0001a0004 | a0001c0006a0004c0008a0004c0036 | a0001c0006t0003a0001c0006t0004a0004c0008t0001others(1): Show | a0001c0006t0003g0267a0001c0006t0003g0268a0001c0006t0004g0273others(7): Show | 11 | 298 | 0.0369 | -4 | c.445 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79119668 | CTGAG | C | intron_variant | MODIFIER | HG02970.hp1 HG03041.hp2 HG03195.hp2 |
a0002 | a0002c0002 | a0002c0002t0004a0002c0002t0009 | a0002c0002t0004g0253a0002c0002t0004g0258a0002c0002t0009g0255 | 3 | 298 | 0.0101 | -4 | c.558 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79120359 | TAAAA | T | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(5): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0158a0002c0002t0001g0159a0002c0002t0001g0160others(5): Show | 8 | 298 | 0.0269 | -4 | c.559 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 4/29 | chr18 | TogoVar | ||||||
ATP9B_chr18_79064394_79383283 | 79134710 | TTATC | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
a0002a0005a0006others(5): Show | a0002c0002a0002c0005a0002c0032others(9): Show | a0002c0002t0001a0002c0002t0002a0002c0002t0003others(16): Show | a0002c0002t0001g0158a0002c0002t0001g0159a0002c0002t0001g0160others(104): Show | 107 | 298 | 0.3591 | -4 | c.667 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79157207 | TACAC | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
a0002a0007a0008others(3): Show | a0002c0002a0002c0005a0007c0031others(4): Show | a0002c0002t0001a0002c0002t0002a0002c0002t0003others(10): Show | a0002c0002t0001g0158a0002c0002t0001g0159a0002c0002t0001g0160others(56): Show | 59 | 298 | 0.1980 | -4 | c.778 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79170428 | GTTAC | G | intron_variant | MODIFIER | HG01952.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
a0001 | a0001c0001a0001c0004a0001c0014 | a0001c0001t0001a0001c0004t0002a0001c0004t0003others(1): Show | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(6): Show | 9 | 298 | 0.0302 | -4 | c.779 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79174577 | CTCTT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
a0001a0002a0005others(6): Show | a0001c0004a0002c0002a0002c0005others(10): Show | a0001c0004t0002a0002c0002t0001a0002c0002t0002others(17): Show | a0001c0004t0002g0095a0002c0002t0001g0158a0002c0002t0001g0159others(105): Show | 108 | 298 | 0.3624 | -4 | c.779 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79185346 | ACTTT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0003a0001c0004others(29): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0002others(46): Show | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0037others(202): Show | 206 | 298 | 0.6913 | -4 | c.874 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79190511 | TACAC | T | intron_variant | MODIFIER | HG02300.hp2 HG04115.hp2 HG04184.hp2 others(2): Show |
a0001 | a0001c0001a0001c0025 | a0001c0001t0001a0001c0025t0001 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0052others(2): Show | 5 | 298 | 0.0168 | -4 | c.874 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79190543 | CACAT | C | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(54): Show |
a0002a0006a0009others(1): Show | a0002c0002a0002c0005a0002c0032others(4): Show | a0002c0002t0002a0002c0002t0003a0002c0002t0004others(9): Show | a0002c0002t0002g0175a0002c0002t0002g0180a0002c0002t0002g0181others(54): Show | 57 | 298 | 0.1913 | -4 | c.874 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79201241 | ATAGT | A | intron_variant | MODIFIER | HG01952.hp2 HG02055.hp2 HG02630.hp2 others(1): Show |
a0001 | a0001c0004 | a0001c0004t0002a0001c0004t0003 | a0001c0004t0002g0095a0001c0004t0002g0096a0001c0004t0002g0097others(1): Show | 4 | 298 | 0.0134 | -4 | c.955 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79206623 | CATAA | C | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(27): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0004others(8): Show | a0001c0001t0001a0001c0003t0003a0001c0004t0002others(9): Show | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0100others(27): Show | 30 | 298 | 0.1007 | -4 | c.955 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79208722 | TTACA | T | intron_variant | MODIFIER | HG02155.hp2 HG02293.hp1 NA18943.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 10 | 298 | 0.0336 | -4 | c.103 others(23): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79208792 | TACAA | T | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp2 others(65): Show |
a0001a0002a0006others(3): Show | a0001c0003a0001c0004a0001c0006others(8): Show | a0001c0003t0001a0001c0003t0003a0001c0003t0011others(17): Show | a0001c0003t0001g0136a0001c0003t0001g0137a0001c0003t0003g0112others(65): Show | 68 | 298 | 0.2282 | -4 | c.103 others(23): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79231778 | GTATA | G | intron_variant | MODIFIER | HG01952.hp2 HG02055.hp2 HG02630.hp2 others(1): Show |
a0001 | a0001c0004 | a0001c0004t0002a0001c0004t0003 | a0001c0004t0002g0095a0001c0004t0002g0096a0001c0004t0002g0097others(1): Show | 4 | 298 | 0.0134 | -4 | c.110 others(25): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79245791 | TACTG | T | intron_variant | MODIFIER | HG02572.hp1 HG02809.hp1 HG02970.hp2 |
a0001 | a0001c0011 | a0001c0011t0006 | a0001c0011t0006g0105a0001c0011t0006g0106a0001c0011t0006g0107 | 3 | 298 | 0.0101 | -4 | c.110 others(23): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79256248 | TCTAG | T | intron_variant | MODIFIER | HG01952.hp2 HG02055.hp2 HG02630.hp2 others(1): Show |
a0001 | a0001c0004 | a0001c0004t0002a0001c0004t0003 | a0001c0004t0002g0095a0001c0004t0002g0096a0001c0004t0002g0097others(1): Show | 4 | 298 | 0.0134 | -4 | c.126 others(23): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79256257 | CTATA | C | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(2): Show |
a0005 | a0005c0009 | a0005c0009t0005 | a0005c0009t0005g0165a0005c0009t0005g0166a0005c0009t0005g0167others(2): Show | 5 | 298 | 0.0168 | -4 | c.126 others(23): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79287983 | AGTTT | A | intron_variant | MODIFIER | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
a0001 | a0001c0011a0001c0014 | a0001c0011t0006a0001c0014t0006 | a0001c0011t0006g0105a0001c0011t0006g0106a0001c0011t0006g0107others(2): Show | 5 | 298 | 0.0168 | -4 | c.141 others(25): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79292118 | CTTTA | C | intron_variant | MODIFIER | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(3): Show |
a0002a0005 | a0002c0032a0005c0009 | a0002c0032t0005a0005c0009t0005 | a0002c0032t0005g0195a0005c0009t0005g0165a0005c0009t0005g0166others(3): Show | 6 | 298 | 0.0201 | -4 | c.141 others(25): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79329422 | TTTTG | T | intron_variant | MODIFIER | NA18982.hp1 NA19085.hp1 NA19086.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0008a0002c0002t0002 | a0001c0001t0008g0055a0001c0001t0008g0057a0002c0002t0002g0218 | 3 | 298 | 0.0101 | -4 | c.193 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79342604 | ATAAT | A | intron_variant | MODIFIER | HG01168.hp2 HG01169.hp2 HG01243.hp2 others(15): Show |
a0001a0002a0005 | a0001c0001a0001c0004a0001c0006others(4): Show | a0001c0001t0001a0001c0004t0004a0001c0006t0004others(4): Show | a0001c0001t0001g0011a0001c0004t0004g0117a0001c0004t0004g0119others(15): Show | 18 | 298 | 0.0604 | -4 | c.238 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar |