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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ACACB_chr12_109111587_109273226 | 109162605 | AG | A | intron_variant | MODIFIER | HG01168.hp1 HG01169.hp2 HG01891.hp2 others(6): Show |
a0001a0002a0007others(3): Show | a0001c0105a0001c0106a0001c0109others(5): Show | a0001c0105t0004a0001c0106t0001a0001c0109t0002others(5): Show | a0001c0105t0004g0296a0001c0106t0001g0293a0001c0109t0002g0276others(6): Show | 9 | 308 | 0.0292 | -1 | c.654 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109164717 | AT | A | intron_variant | MODIFIER | HG01891.hp1 HG01943.hp2 HG02622.hp2 others(3): Show |
a0001a0007 | a0001c0010a0001c0032a0001c0054others(2): Show | a0001c0010t0001a0001c0010t0009a0001c0032t0004others(3): Show | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0032t0004g0292others(3): Show | 6 | 308 | 0.0195 | -1 | c.654 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109166677 | AC | A | intron_variant | MODIFIER | HG00323.hp1 HG01167.hp2 HG01433.hp1 others(9): Show |
a0001a0006a0008others(2): Show | a0001c0058a0006c0026a0006c0078others(7): Show | a0001c0058t0016a0006c0026t0002a0006c0026t0016others(8): Show | a0001c0058t0016g0187a0006c0026t0002g0156a0006c0026t0016g0066others(9): Show | 12 | 308 | 0.0390 | -1 | c.654 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109169142 | CA | C | intron_variant | MODIFIER | HG00323.hp1 HG00642.hp2 HG01109.hp2 others(39): Show |
a0001a0002a0004others(9): Show | a0001c0038a0002c0007a0002c0070others(22): Show | a0001c0038t0001a0002c0007t0006a0002c0070t0005others(26): Show | a0001c0038t0001g0201a0002c0007t0006g0017a0002c0070t0005g0199others(39): Show | 42 | 308 | 0.1364 | -1 | c.925 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109170793 | GT | G | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
a0001a0002a0003others(21): Show | a0001c0004a0001c0010a0001c0011others(52): Show | a0001c0004t0002a0001c0004t0017a0001c0010t0001others(64): Show | a0001c0004t0002g0054a0001c0004t0017g0003a0001c0010t0001g0188others(135): Show | 138 | 308 | 0.4481 | -1 | c.926 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109175222 | GT | G | intron_variant | MODIFIER | HG01074.hp1 HG01109.hp2 HG01175.hp1 others(4): Show |
a0001a0002a0006 | a0001c0050a0001c0109a0001c0111others(3): Show | a0001c0050t0001a0001c0109t0002a0001c0111t0001others(3): Show | a0001c0050t0001g0277a0001c0050t0001g0278a0001c0109t0002g0276others(4): Show | 7 | 308 | 0.0227 | -1 | c.121 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 7/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109188240 | TC | T | intron_variant | MODIFIER | HG03490.hp2 NA18950.hp1 NA18950.hp2 others(2): Show |
a0001a0003a0005others(1): Show | a0001c0002a0001c0003a0003c0001others(2): Show | a0001c0002t0021a0001c0003t0002a0003c0001t0001others(2): Show | a0001c0002t0021g0243a0001c0003t0002g0112a0003c0001t0001g0145others(2): Show | 5 | 308 | 0.0162 | -1 | c.214 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109191215 | CT | C | intron_variant | MODIFIER | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(38): Show |
a0001a0002a0003others(9): Show | a0001c0004a0001c0010a0001c0016others(24): Show | a0001c0004t0017a0001c0010t0001a0001c0010t0009others(28): Show | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0009g0186others(38): Show | 41 | 308 | 0.1331 | -1 | c.214 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109193217 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
a0001a0002a0003others(37): Show | a0001c0002a0001c0003a0001c0004others(114): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(144): Show | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0081others(278): Show | 282 | 308 | 0.9156 | -1 | c.240 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 15/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109200031 | CA | C | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp1 HG01261.hp1 others(7): Show |
a0001a0002a0014 | a0001c0002a0001c0010a0001c0022others(2): Show | a0001c0002t0001a0001c0010t0002a0001c0022t0004others(2): Show | a0001c0002t0001g0081a0001c0010t0002g0261a0001c0022t0004g0004others(7): Show | 10 | 308 | 0.0325 | -1 | c.277 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 18/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109202226 | TG | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
a0001a0002a0007others(8): Show | a0001c0002a0001c0003a0001c0016others(31): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(41): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(91): Show | 94 | 308 | 0.3052 | -1 | c.291 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109204271 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
a0001a0002a0004others(18): Show | a0001c0002a0001c0003a0001c0004others(63): Show | a0001c0002t0001a0001c0002t0021a0001c0003t0002others(77): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(136): Show | 139 | 308 | 0.4513 | -1 | c.291 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109208217 | AT | A | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
a0001a0002a0003others(20): Show | a0001c0002a0001c0003a0001c0010others(42): Show | a0001c0002t0001a0001c0003t0002a0001c0003t0004others(52): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(99): Show | 102 | 308 | 0.3312 | -1 | c.306 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 20/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109210752 | TA | T | intron_variant | MODIFIER | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(10): Show |
a0001a0005a0007others(5): Show | a0001c0016a0005c0009a0007c0037others(7): Show | a0001c0016t0011a0005c0009t0006a0007c0037t0004others(7): Show | a0001c0016t0011g0274a0005c0009t0006g0257a0007c0037t0004g0200others(10): Show | 13 | 308 | 0.0422 | -1 | c.324 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109211342 | CT | C | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(83): Show |
a0001a0002a0003others(20): Show | a0001c0002a0001c0003a0001c0010others(44): Show | a0001c0002t0001a0001c0003t0002a0001c0010t0001others(48): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(83): Show | 86 | 308 | 0.2792 | -1 | c.325 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109211901 | GT | G | intron_variant | MODIFIER | HG00673.hp1 HG02040.hp1 HG02738.hp2 others(8): Show |
a0001a0002a0003 | a0001c0012a0001c0013a0001c0029others(4): Show | a0001c0012t0002a0001c0013t0001a0001c0029t0002others(4): Show | a0001c0012t0002g0045a0001c0012t0002g0250a0001c0012t0002g0251others(8): Show | 11 | 308 | 0.0357 | -1 | c.325 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109215104 | GA | G | intron_variant | MODIFIER | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(7): Show |
a0001a0002 | a0001c0002a0001c0010a0001c0016others(3): Show | a0001c0002t0001a0001c0010t0009a0001c0016t0009others(3): Show | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0009g0186others(7): Show | 10 | 308 | 0.0325 | -1 | c.335 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109216219 | CT | C | intron_variant | MODIFIER | HG00323.hp1 HG01070.hp2 HG01168.hp1 others(4): Show |
a0001a0003a0005others(2): Show | a0001c0003a0001c0018a0001c0046others(4): Show | a0001c0003t0004a0001c0018t0002a0001c0046t0002others(4): Show | a0001c0003t0004g0074a0001c0018t0002g0048a0001c0046t0002g0190others(4): Show | 7 | 308 | 0.0227 | -1 | c.335 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109216566 | AG | A | intron_variant | MODIFIER | HG02280.hp2 HG02559.hp1 HG06807.hp2 |
a0001a0007a0015 | a0001c0064a0007c0037a0015c0119 | a0001c0064t0009a0007c0037t0004a0015c0119t0004 | a0001c0064t0009g0184a0007c0037t0004g0073a0015c0119t0004g0169 | 3 | 308 | 0.0097 | -1 | c.335 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109218652 | AT | A | intron_variant | MODIFIER | HG01175.hp2 HG02280.hp2 HG02965.hp2 others(5): Show |
a0001a0002a0003others(1): Show | a0001c0002a0001c0003a0001c0064others(4): Show | a0001c0002t0008a0001c0003t0002a0001c0064t0009others(4): Show | a0001c0002t0008g0306a0001c0003t0002g0104a0001c0003t0002g0193others(5): Show | 8 | 308 | 0.0260 | -1 | c.356 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109218771 | CT | C | intron_variant | MODIFIER | HG01168.hp1 HG01169.hp2 HG03017.hp2 others(3): Show |
a0001a0005a0012others(1): Show | a0001c0046a0005c0009a0012c0035others(1): Show | a0001c0046t0002a0005c0009t0003a0005c0009t0006others(2): Show | a0001c0046t0002g0190a0005c0009t0003g0164a0005c0009t0006g0148others(3): Show | 6 | 308 | 0.0195 | -1 | c.356 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109226951 | CT | C | intron_variant | MODIFIER | HG01069.hp1 HG01433.hp1 HG01515.hp1 others(8): Show |
a0001a0003a0009others(1): Show | a0001c0011a0001c0022a0001c0055others(4): Show | a0001c0011t0001a0001c0022t0004a0001c0055t0001others(4): Show | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0022t0004g0004others(8): Show | 11 | 308 | 0.0357 | -1 | c.388 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 27/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109228033 | CA | C | intron_variant | MODIFIER | HG01109.hp2 HG01433.hp1 HG02280.hp2 others(14): Show |
a0001a0002a0005others(4): Show | a0001c0004a0001c0011a0001c0022others(10): Show | a0001c0004t0020a0001c0011t0001a0001c0022t0004others(10): Show | a0001c0004t0020g0023a0001c0011t0001g0056a0001c0011t0001g0157others(14): Show | 17 | 308 | 0.0552 | -1 | c.400 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109228658 | CA | C | intron_variant | MODIFIER | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(8): Show |
a0001a0002a0004others(1): Show | a0001c0010a0001c0016a0001c0032others(4): Show | a0001c0010t0002a0001c0010t0009a0001c0016t0009others(5): Show | a0001c0010t0002g0261a0001c0010t0009g0186a0001c0016t0009g0287others(8): Show | 11 | 308 | 0.0357 | -1 | c.400 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109238342 | AT | A | intron_variant | MODIFIER | HG01074.hp2 HG01106.hp2 HG01168.hp1 others(15): Show |
a0001a0002a0003others(8): Show | a0001c0003a0001c0013a0002c0014others(12): Show | a0001c0003t0002a0001c0013t0001a0002c0014t0003others(12): Show | a0001c0003t0002g0068a0001c0013t0001g0237a0002c0014t0003g0015others(15): Show | 18 | 308 | 0.0584 | -1 | c.466 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109238570 | TA | T | intron_variant | MODIFIER | HG00673.hp1 HG02040.hp1 HG02738.hp2 others(8): Show |
a0001a0002a0003 | a0001c0010a0001c0012a0001c0029others(4): Show | a0001c0010t0002a0001c0012t0002a0001c0029t0002others(4): Show | a0001c0010t0002g0021a0001c0012t0002g0045a0001c0012t0002g0250others(8): Show | 11 | 308 | 0.0357 | -1 | c.466 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109247539 | GA | G | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(12): Show |
a0001a0006a0009others(2): Show | a0001c0003a0001c0004a0001c0039others(8): Show | a0001c0003t0004a0001c0004t0017a0001c0039t0004others(9): Show | a0001c0003t0004g0074a0001c0003t0004g0300a0001c0004t0017g0003others(12): Show | 15 | 308 | 0.0487 | -1 | c.557 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 39/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109252440 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
a0001a0002a0003others(9): Show | a0001c0002a0001c0011a0001c0013others(24): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(32): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(81): Show | 84 | 308 | 0.2727 | -1 | c.590 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 42/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109257319 | TA | T | intron_variant | MODIFIER | HG02080.hp2 HG02109.hp2 HG02717.hp1 others(9): Show |
a0001a0002a0003others(1): Show | a0001c0003a0001c0010a0001c0016others(6): Show | a0001c0003t0002a0001c0010t0009a0001c0016t0009others(7): Show | a0001c0003t0002g0078a0001c0010t0009g0186a0001c0016t0009g0287others(9): Show | 12 | 308 | 0.0390 | -1 | c.626 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 45/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109264154 | CA | C | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
a0001a0002a0003others(13): Show | a0001c0003a0001c0004a0001c0010others(33): Show | a0001c0003t0002a0001c0004t0002a0001c0010t0002others(37): Show | a0001c0003t0002g0068a0001c0003t0002g0077a0001c0003t0002g0078others(78): Show | 81 | 308 | 0.2630 | -1 | c.678 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111681583 | CA | C | upstream_gene_variant | MODIFIER | HG01099.hp1 HG01175.hp2 HG01978.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0013a0001c0001t0001g0221a0001c0001t0001g0238others(4): Show | 7 | 336 | 0.0208 | -1 | c.-46 others(6): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4469 | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111682497 | CA | C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(238): Show |
a0001a0002a0004others(5): Show | a0001c0001a0001c0002a0001c0006others(8): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(9): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(229): Show | 241 | 336 | 0.7173 | -1 | c.-37 others(6): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3555 | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111688810 | AC | A | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | 336 | 0.0238 | -1 | c.-14 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111690780 | CA | C | intron_variant | MODIFIER | HG01099.hp2 HG01256.hp1 HG01975.hp2 others(18): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(18): Show | 21 | 336 | 0.0625 | -1 | c.-13 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111691594 | AT | A | intron_variant | MODIFIER | HG01993.hp1 HG02074.hp1 HG02135.hp2 others(22): Show |
a0001a0007 | a0001c0001a0001c0002a0007c0007 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(1): Show | a0001c0001t0001g0160a0001c0001t0001g0210a0001c0001t0001g0211others(22): Show | 25 | 336 | 0.0744 | -1 | c.-13 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111696013 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
a0001a0004a0005others(5): Show | a0001c0001a0001c0002a0001c0006others(8): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(9): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(201): Show | 213 | 336 | 0.6339 | -1 | c.187 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111697362 | CT | C | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0002a0002c0003t0003 | a0001c0001t0001g0038a0001c0002t0002g0092a0002c0003t0003g0318others(7): Show | 10 | 336 | 0.0298 | -1 | c.187 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111698297 | CT | C | intron_variant | MODIFIER | HG01175.hp1 HG01943.hp2 HG02257.hp2 others(6): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0003 | a0001c0001t0001g0089a0002c0003t0003g0318a0002c0003t0003g0319others(6): Show | 9 | 336 | 0.0268 | -1 | c.188 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111698404 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(123): Show |
a0001a0002a0005others(4): Show | a0001c0001a0001c0002a0001c0006others(7): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(8): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(119): Show | 126 | 336 | 0.3750 | -1 | c.188 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111700748 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG01168.hp1 others(28): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0002c0003t0003others(1): Show | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0040others(28): Show | 31 | 336 | 0.0923 | -1 | c.188 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111711522 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG01943.hp2 HG02074.hp1 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0002a0002c0003t0003 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0058others(17): Show | 20 | 336 | 0.0595 | -1 | c.691 others(8): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111713316 | GA | G | intron_variant | MODIFIER | HG00544.hp2 HG01943.hp2 HG02257.hp2 others(7): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0003 | a0001c0001t0001g0195a0001c0001t0001g0264a0002c0003t0003g0318others(7): Show | 10 | 336 | 0.0298 | -1 | c.850 others(8): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111713624 | CA | C | intron_variant | MODIFIER | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(16): Show |
a0001a0008 | a0001c0001a0001c0006a0008c0009 | a0001c0001t0001a0001c0001t0005a0001c0006t0001others(1): Show | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0184others(15): Show | 19 | 336 | 0.0566 | -1 | c.850 others(8): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111717346 | CA | C | intron_variant | MODIFIER | HG00140.hp2 HG01168.hp1 HG01256.hp1 others(11): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0002a0002c0003t0003 | a0001c0001t0001g0185a0001c0001t0001g0297a0001c0001t0001g0302others(11): Show | 14 | 336 | 0.0417 | -1 | c.992 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111718036 | CT | C | intron_variant | MODIFIER | HG00597.hp2 HG00735.hp2 HG01099.hp2 others(38): Show |
a0001a0003a0012 | a0001c0001a0001c0008a0003c0004others(1): Show | a0001c0001t0001a0001c0008t0001a0003c0004t0001others(1): Show | a0001c0001t0001g0040a0001c0001t0001g0057a0001c0001t0001g0063others(38): Show | 41 | 336 | 0.1220 | -1 | c.992 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111723684 | AC | A | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
a0001a0005a0009 | a0001c0001a0001c0002a0005c0016others(1): Show | a0001c0001t0001a0001c0002t0002a0005c0016t0001others(1): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(79): Show | 85 | 336 | 0.2530 | -1 | c.106 others(10): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111724820 | GA | G | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | 336 | 0.0238 | -1 | c.106 others(10): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111736185 | GT | G | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | 336 | 0.0238 | -1 | c.154 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111743369 | GT | G | intron_variant | MODIFIER | HG01167.hp1 HG02896.hp2 NA18946.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0214others(4): Show | 7 | 336 | 0.0208 | -1 | c.171 others(10): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111745835 | CT | C | intron_variant | MODIFIER | HG01167.hp1 HG01934.hp1 HG02622.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0140others(8): Show | 11 | 336 | 0.0327 | -1 | c.211 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |