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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ATP9A_chr20_51591514_51773390 | 51760274 | GTT | G | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(61): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0030others(61): Show | 64 | 312 | 0.2051 | -2 | c.68+ others(17): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 1/27 | chr20 | TogoVar | ||||||
ATP9A_chr20_51591514_51773390 | 51767073 | CTT | C | intron_variant | MODIFIER | HG00323.hp1 HG01515.hp1 HG02630.hp1 others(8): Show |
a0001 | a0001c0001a0001c0003a0001c0008others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0303a0001c0001t0002g0305a0001c0001t0003g0302others(8): Show | 11 | 312 | 0.0353 | -2 | c.68+ others(17): Show |
ATP9A | ENSG00000054793.14 | transcript | ENST00000338821.6 | protein_coding | 1/27 | chr20 | TogoVar | ||||||
ATP9B_chr18_79064394_79383283 | 79070691 | CAT | C | 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 | -2 | c.119 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 1/29 | chr18 | TogoVar | ||||||
ATP9B_chr18_79064394_79383283 | 79071887 | TTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
a0001a0002a0003others(8): Show | a0001c0006a0001c0010a0002c0002others(15): Show | a0001c0006t0003a0001c0006t0004a0001c0006t0007others(25): Show | a0001c0006t0003g0267a0001c0006t0003g0268a0001c0006t0003g0281others(119): Show | 123 | 298 | 0.4128 | -2 | c.119 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79078565 | CTT | C | intron_variant | MODIFIER | HG00280.hp1 HG00673.hp2 HG01106.hp1 others(43): Show |
a0001a0012a0015others(1): Show | a0001c0001a0001c0003a0001c0004others(5): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0002others(11): Show | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0140others(43): Show | 46 | 298 | 0.1544 | -2 | c.119 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79097292 | CCT | C | intron_variant | MODIFIER | HG00280.hp1 HG00673.hp2 HG01106.hp1 others(48): Show |
a0001a0012a0015others(1): Show | a0001c0001a0001c0003a0001c0004others(7): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0002others(14): Show | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0140others(48): Show | 51 | 298 | 0.1711 | -2 | c.293 others(17): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79101639 | TAC | 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 | -2 | c.293 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79108826 | GAC | G | intron_variant | MODIFIER | HG02109.hp1 HG02293.hp2 HG03540.hp2 |
a0001 | a0001c0006 | a0001c0006t0007 | a0001c0006t0007g0285a0001c0006t0007g0286a0001c0006t0007g0290 | 3 | 298 | 0.0101 | -2 | c.294 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79116307 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(30): Show |
a0001a0003a0004others(1): Show | a0001c0006a0001c0010a0003c0007others(5): Show | a0001c0006t0003a0001c0006t0004a0001c0006t0007others(8): Show | a0001c0006t0003g0267a0001c0006t0003g0268a0001c0006t0003g0281others(29): Show | 33 | 298 | 0.1107 | -2 | c.558 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79116937 | AAT | A | intron_variant | MODIFIER | HG01358.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0003t0003a0001c0006t0007others(3): Show | a0001c0001t0001g0013a0001c0001t0001g0140a0001c0001t0001g0141others(11): Show | 14 | 298 | 0.0470 | -2 | c.558 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 4/29 | chr18 | TogoVar | ||||||
ATP9B_chr18_79064394_79383283 | 79116940 | TAA | T | intron_variant | MODIFIER | HG02040.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0003t0003a0001c0003t0011others(3): Show | a0001c0001t0001g0116a0001c0003t0003g0123a0001c0003t0003g0131others(4): Show | 7 | 298 | 0.0235 | -2 | c.558 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79118388 | TTG | T | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG02723.hp2 others(6): Show |
a0001a0003a0004 | a0001c0006a0003c0007a0003c0021others(1): Show | a0001c0006t0003a0003c0007t0004a0003c0021t0004others(1): Show | a0001c0006t0003g0268a0001c0006t0003g0281a0003c0007t0004g0279others(5): Show | 9 | 298 | 0.0302 | -2 | c.558 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79119108 | CTG | C | intron_variant | MODIFIER | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(30): Show |
a0001a0003a0004others(1): Show | a0001c0006a0001c0010a0003c0007others(5): Show | a0001c0006t0003a0001c0006t0004a0001c0006t0007others(8): Show | a0001c0006t0003g0267a0001c0006t0003g0268a0001c0006t0003g0281others(29): Show | 33 | 298 | 0.1107 | -2 | c.558 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79124164 | CAG | C | intron_variant | MODIFIER | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(30): Show |
a0001a0003a0004others(1): Show | a0001c0006a0001c0010a0003c0007others(5): Show | a0001c0006t0003a0001c0006t0004a0001c0006t0007others(8): Show | a0001c0006t0003g0267a0001c0006t0003g0268a0001c0006t0003g0281others(29): Show | 33 | 298 | 0.1107 | -2 | c.559 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79133508 | AAC | A | intron_variant | MODIFIER | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(50): Show |
a0001a0012a0015others(1): Show | a0001c0001a0001c0003a0001c0004others(7): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0002others(14): Show | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0051others(50): Show | 53 | 298 | 0.1779 | -2 | c.667 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79133737 | GAT | G | intron_variant | MODIFIER | HG00733.hp2 HG00741.hp1 HG01361.hp2 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0188a0002c0002t0002g0246a0002c0002t0002g0247others(1): Show | 4 | 298 | 0.0134 | -2 | c.667 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 5/29 | chr18 | TogoVar | ||||||
ATP9B_chr18_79064394_79383283 | 79149476 | GAA | G | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(5): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0158a0002c0002t0001g0159a0002c0002t0001g0160others(5): Show | 8 | 298 | 0.0269 | -2 | c.727 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79153653 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0003a0001c0004others(31): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0002others(48): Show | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(204): Show | 208 | 298 | 0.6980 | -2 | c.727 others(17): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79155753 | CTT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0001c0004others(17): Show | a0001c0001t0001a0001c0003t0003a0001c0003t0013others(30): Show | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(124): Show | 127 | 298 | 0.4262 | -2 | c.778 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79157207 | TAC | T | intron_variant | MODIFIER | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(36): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0026others(4): Show | a0001c0001t0001a0001c0004t0001a0001c0004t0003others(9): Show | a0001c0001t0001g0003a0001c0004t0001g0016a0001c0004t0003g0041others(36): Show | 39 | 298 | 0.1309 | -2 | c.778 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79157396 | CAA | C | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
a0001a0003a0005 | a0001c0003a0003c0020a0005c0009others(1): Show | a0001c0003t0003a0003c0020t0004a0005c0009t0005others(1): Show | a0001c0003t0003g0124a0001c0003t0003g0125a0003c0020t0004g0289others(7): Show | 10 | 298 | 0.0336 | -2 | c.778 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79162674 | CAG | C | intron_variant | MODIFIER | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
a0001a0004 | a0001c0006a0001c0038a0001c0039others(2): Show | a0001c0006t0003a0001c0006t0004a0001c0038t0001others(3): Show | a0001c0006t0003g0267a0001c0006t0003g0268a0001c0006t0004g0273others(9): Show | 13 | 298 | 0.0436 | -2 | c.778 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79163869 | TAC | T | intron_variant | MODIFIER | HG01071.hp2 HG01109.hp1 HG01934.hp2 others(12): Show |
a0001a0004 | a0001c0001a0001c0004a0001c0006others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(6): Show | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0059others(12): Show | 15 | 298 | 0.0503 | -2 | c.778 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79190511 | TAC | T | intron_variant | MODIFIER | HG01069.hp2 HG02155.hp2 HG02293.hp1 others(8): Show |
a0001a0017 | a0001c0001a0017c0019 | a0001c0001t0001a0017c0019t0002 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 11 | 298 | 0.0369 | -2 | c.874 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79190545 | CAT | C | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(29): Show |
a0001a0002a0007others(1): Show | a0001c0006a0002c0002a0007c0031others(1): Show | a0001c0006t0007a0002c0002t0002a0002c0002t0003others(4): Show | a0001c0006t0007g0285a0001c0006t0007g0286a0001c0006t0007g0290others(29): Show | 32 | 298 | 0.1074 | -2 | c.874 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79214977 | GTC | G | intron_variant | MODIFIER | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
a0001 | a0001c0011a0001c0014 | a0001c0011t0006a0001c0014t0006 | a0001c0011t0006g0105a0001c0011t0006g0106a0001c0011t0006g0107others(2): Show | 5 | 298 | 0.0168 | -2 | c.110 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79221928 | TAA | T | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(11): Show |
a0001a0002 | a0001c0006a0001c0011a0001c0014others(1): Show | a0001c0006t0004a0001c0011t0006a0001c0014t0006others(1): Show | a0001c0006t0004g0294a0001c0011t0006g0105a0001c0011t0006g0106others(11): Show | 14 | 298 | 0.0470 | -2 | c.110 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79231766 | ATG | A | intron_variant | MODIFIER | HG00544.hp2 HG01243.hp2 HG01884.hp2 others(5): Show |
a0002a0005 | a0002c0002a0002c0032a0005c0009 | a0002c0002t0002a0002c0032t0005a0005c0009t0005 | a0002c0002t0002g0191a0002c0002t0002g0232a0002c0032t0005g0195others(5): Show | 8 | 298 | 0.0269 | -2 | 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 | 79237689 | TGG | T | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp2 others(43): Show |
a0001a0002a0006others(3): Show | a0001c0003a0001c0004a0001c0006others(5): Show | a0001c0003t0001a0001c0003t0003a0001c0003t0011others(8): Show | a0001c0003t0001g0136a0001c0003t0001g0137a0001c0003t0003g0112others(43): Show | 46 | 298 | 0.1544 | -2 | 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 | 79245723 | CTG | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(89): Show |
a0001a0002a0005 | a0001c0001a0001c0004a0001c0010others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(89): Show | 92 | 298 | 0.3087 | -2 | c.110 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79246216 | GAC | G | intron_variant | MODIFIER | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0006a0001c0024others(6): Show | a0001c0001t0001a0001c0006t0007a0001c0024t0004others(6): Show | a0001c0001t0001g0100a0001c0001t0001g0118a0001c0006t0007g0290others(18): Show | 22 | 298 | 0.0738 | -2 | c.110 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 11/29 | chr18 | TogoVar | ||||||
ATP9B_chr18_79064394_79383283 | 79246289 | CTG | C | intron_variant | MODIFIER | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
a0001a0003a0010 | a0001c0006a0003c0007a0003c0020others(2): Show | a0001c0006t0007a0003c0007t0004a0003c0020t0004others(2): Show | a0001c0006t0007g0285a0001c0006t0007g0286a0001c0006t0007g0290others(10): Show | 13 | 298 | 0.0436 | -2 | c.110 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79256257 | CTA | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(75): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0003a0001c0015others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(75): Show | 78 | 298 | 0.2617 | -2 | c.126 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79259413 | CAG | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0006a0001c0024others(7): Show | a0001c0001t0001a0001c0006t0007a0001c0024t0004others(7): Show | a0001c0001t0001g0100a0001c0001t0001g0118a0001c0006t0007g0285others(27): Show | 31 | 298 | 0.1040 | -2 | c.126 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79270299 | GCT | G | intron_variant | MODIFIER | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
a0001a0002a0005 | a0001c0011a0001c0014a0002c0032others(1): Show | a0001c0011t0006a0001c0014t0006a0002c0032t0005others(1): Show | a0001c0011t0006g0105a0001c0011t0006g0106a0001c0011t0006g0107others(8): Show | 11 | 298 | 0.0369 | -2 | c.126 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79275259 | CCA | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(100): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0010others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(100): Show | 103 | 298 | 0.3456 | -2 | c.126 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79295111 | GAC | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
a0001a0002a0005others(11): Show | a0001c0001a0001c0003a0001c0004others(29): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(50): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(274): Show | 277 | 298 | 0.9295 | -2 | c.141 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79309064 | CAG | C | intron_variant | MODIFIER | HG02109.hp1 HG02293.hp2 HG03540.hp2 |
a0001 | a0001c0006 | a0001c0006t0007 | a0001c0006t0007g0285a0001c0006t0007g0286a0001c0006t0007g0290 | 3 | 298 | 0.0101 | -2 | c.177 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 15/29 | chr18 | TogoVar | ||||||
ATP9B_chr18_79064394_79383283 | 79316708 | CAT | C | intron_variant | MODIFIER | HG00639.hp2 HG01496.hp1 HG01934.hp1 others(2): Show |
a0001 | a0001c0003a0001c0004 | a0001c0003t0003a0001c0004t0003 | a0001c0003t0003g0129a0001c0004t0003g0056a0001c0004t0003g0060others(2): Show | 5 | 298 | 0.0168 | -2 | c.177 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79321384 | ATT | A | intron_variant | MODIFIER | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
a0001a0002a0005 | a0001c0001a0001c0004a0001c0037others(4): Show | a0001c0001t0001a0001c0004t0002a0001c0004t0003others(5): Show | a0001c0001t0001g0013a0001c0004t0002g0095a0001c0004t0002g0096others(12): Show | 15 | 298 | 0.0503 | -2 | c.177 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79327703 | GCT | G | intron_variant | MODIFIER | HG00140.hp1 HG00544.hp1 HG00673.hp2 others(59): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0014a0001c0015others(9): Show | a0001c0001t0001a0001c0014t0006a0001c0015t0001others(9): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 62 | 298 | 0.2081 | -2 | c.177 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79337186 | CCT | C | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp2 others(41): Show |
a0001a0002a0006others(3): Show | a0001c0003a0001c0004a0001c0006others(6): Show | a0001c0003t0003a0001c0003t0011a0001c0003t0013others(10): Show | a0001c0003t0003g0112a0001c0003t0003g0115a0001c0003t0003g0121others(41): Show | 44 | 298 | 0.1477 | -2 | c.211 others(17): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79347222 | GAC | G | intron_variant | MODIFIER | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(3): Show |
a0002a0005 | a0002c0032a0005c0009 | a0002c0032t0005a0005c0009t0005 | a0002c0032t0005g0195a0005c0009t0005g0165a0005c0009t0005g0166others(3): Show | 6 | 298 | 0.0201 | -2 | c.268 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79348248 | GAA | G | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
a0001a0002a0003others(9): Show | a0001c0003a0001c0004a0001c0006others(18): Show | a0001c0003t0002a0001c0003t0003a0001c0003t0011others(28): Show | a0001c0003t0002g0135a0001c0003t0003g0112a0001c0003t0003g0115others(142): Show | 145 | 298 | 0.4866 | -2 | c.290 others(17): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79354568 | CAA | C | intron_variant | MODIFIER | HG01106.hp1 HG01261.hp1 HG01934.hp1 others(17): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0001c0004others(4): Show | a0001c0001t0001a0001c0003t0003a0001c0003t0013others(5): Show | a0001c0001t0001g0071a0001c0003t0003g0121a0001c0003t0003g0127others(17): Show | 20 | 298 | 0.0671 | -2 | c.290 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79358109 | GGT | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(75): Show |
a0001a0002a0007others(4): Show | a0001c0001a0001c0003a0001c0004others(8): Show | a0001c0001t0002a0001c0003t0002a0001c0004t0002others(8): Show | a0001c0001t0002g0079a0001c0003t0002g0135a0001c0003t0002g0149others(75): Show | 78 | 298 | 0.2617 | -2 | c.290 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79367177 | CAG | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0003a0001c0004others(24): Show | a0001c0001t0002a0001c0001t0003a0001c0003t0002others(36): Show | a0001c0001t0002g0079a0001c0001t0003g0072a0001c0003t0002g0135others(160): Show | 163 | 298 | 0.5470 | -2 | c.301 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79367533 | CAG | C | intron_variant | MODIFIER | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
a0002 | a0002c0005 | a0002c0005t0001a0002c0005t0004 | a0002c0005t0001g0179a0002c0005t0001g0190a0002c0005t0001g0194others(2): Show | 5 | 298 | 0.0168 | -2 | c.301 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79371370 | TAA | T | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(7): Show |
a0001a0002 | a0001c0006a0001c0011a0002c0002 | a0001c0006t0007a0001c0011t0006a0002c0002t0001 | a0001c0006t0007g0290a0001c0011t0006g0105a0001c0011t0006g0107others(7): Show | 10 | 298 | 0.0336 | -2 | c.301 others(21): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ATP9B_chr18_79064394_79383283 | 79376172 | AAC | A | intron_variant | MODIFIER | HG00408.hp2 HG01243.hp2 HG02129.hp1 others(2): Show |
a0001a0002 | a0001c0003a0002c0002a0002c0032 | a0001c0003t0003a0002c0002t0002a0002c0002t0014others(1): Show | a0001c0003t0003g0146a0002c0002t0002g0182a0002c0002t0002g0189others(2): Show | 5 | 298 | 0.0168 | -2 | c.330 others(19): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar |