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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ACACA_chr17_37079992_37411836 | 37406473 | C | CA | 5_prime_UTR_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(40): Show | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0053others(260): Show | 263 | 299 | 0.8796 | 1 | c.-17 others(10): Show |
ACACA | ENSG00000278540.5 | transcript | ENST00000616317.5 | protein_coding | 1/56 | 175 | chr17 | TogoVar | |||||
ACACA_chr17_37079992_37411836 | 37409767 | C | CA | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(178): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(33): Show | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0053others(178): Show | 181 | 299 | 0.6054 | 1 | c.-34 others(6): Show |
ACACA | ENSG00000278540.5 | transcript | ENST00000616317.5 | protein_coding | 2932 | chr17 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109112688 | C | CA | upstream_gene_variant | MODIFIER | HG01175.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
a0001a0002a0003others(3): Show | a0001c0003a0001c0074a0002c0006others(4): Show | a0001c0003t0002a0001c0074t0004a0002c0006t0005others(4): Show | a0001c0003t0002g0193a0001c0074t0004g0229a0002c0006t0005g0123others(5): Show | 8 | 308 | 0.0260 | 1 | c.-40 others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3898 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109115589 | A | AC | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
a0001a0002a0003others(31): Show | a0001c0002a0001c0003a0001c0004others(100): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(119): Show | a0001c0002t0001g0235a0001c0002t0001g0241a0001c0002t0001g0242others(205): Show | 208 | 308 | 0.6753 | 1 | c.-11 others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 997 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109117047 | C | CT | intron_variant | MODIFIER | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(72): Show |
a0001a0002a0003others(15): Show | a0001c0002a0001c0003a0001c0010others(39): Show | a0001c0002t0001a0001c0003t0002a0001c0010t0001others(44): Show | a0001c0002t0001g0191a0001c0003t0002g0193a0001c0010t0001g0188others(72): Show | 75 | 308 | 0.2435 | 1 | c.-10 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109118412 | C | CT | intron_variant | MODIFIER | HG01433.hp1 HG01884.hp2 HG02630.hp1 others(5): Show |
a0001a0002a0004others(2): Show | a0001c0002a0001c0004a0001c0011others(5): Show | a0001c0002t0008a0001c0004t0002a0001c0011t0001others(5): Show | a0001c0002t0008g0306a0001c0004t0002g0054a0001c0011t0001g0056others(5): Show | 8 | 308 | 0.0260 | 1 | c.-10 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109119589 | C | CA | intron_variant | MODIFIER | HG02145.hp2 HG02717.hp2 HG03195.hp1 others(3): Show |
a0001a0002a0003others(3): Show | a0001c0038a0002c0070a0003c0001others(3): Show | a0001c0038t0001a0002c0070t0005a0003c0001t0008others(3): Show | a0001c0038t0001g0201a0002c0070t0005g0199a0003c0001t0008g0128others(3): Show | 6 | 308 | 0.0195 | 1 | c.-10 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109122572 | C | CA | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
a0001a0002a0004others(9): Show | a0001c0002a0001c0003a0001c0004others(38): Show | a0001c0002t0001a0001c0003t0002a0001c0004t0007others(41): Show | a0001c0002t0001g0079a0001c0002t0001g0081a0001c0002t0001g0282others(53): Show | 56 | 308 | 0.1818 | 1 | c.-10 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109123180 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(78): Show |
a0001a0002a0003others(12): Show | a0001c0002a0001c0003a0001c0010others(43): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(51): Show | a0001c0002t0001g0085a0001c0002t0001g0241a0001c0002t0001g0242others(78): Show | 81 | 308 | 0.2630 | 1 | c.-10 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109124075 | G | GT | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(30): Show |
a0001a0002a0003others(7): Show | a0001c0002a0001c0003a0001c0010others(17): Show | a0001c0002t0001a0001c0002t0021a0001c0003t0002others(19): Show | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(30): Show | 33 | 308 | 0.1071 | 1 | c.-10 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109127421 | G | GA | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(106): Show |
a0001a0002a0003others(17): Show | a0001c0002a0001c0003a0001c0011others(53): Show | a0001c0002t0001a0001c0003t0004a0001c0011t0001others(59): Show | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0300others(106): Show | 109 | 308 | 0.3539 | 1 | c.-10 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109127597 | T | TA | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(36): Show |
a0001a0002a0003others(10): Show | a0001c0002a0001c0003a0001c0010others(23): Show | a0001c0002t0001a0001c0002t0021a0001c0003t0002others(25): Show | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(36): Show | 39 | 308 | 0.1266 | 1 | c.-10 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109128326 | C | CT | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(28): Show |
a0001a0002a0003others(6): Show | a0001c0002a0001c0003a0001c0010others(15): Show | a0001c0002t0001a0001c0002t0021a0001c0003t0002others(17): Show | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0021g0243others(28): Show | 31 | 308 | 0.1007 | 1 | c.-9- others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109132171 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
a0001a0002a0003others(17): Show | a0001c0010a0001c0012a0001c0013others(41): Show | a0001c0010t0001a0001c0010t0002a0001c0010t0009others(47): Show | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(74): Show | 77 | 308 | 0.2500 | 1 | c.-9- others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109133864 | T | TA | intron_variant | MODIFIER | HG00597.hp1 HG01070.hp2 HG01074.hp1 others(20): Show |
a0001a0002a0005others(2): Show | a0001c0004a0001c0010a0001c0011others(7): Show | a0001c0004t0002a0001c0004t0007a0001c0004t0020others(11): Show | a0001c0004t0002g0050a0001c0004t0002g0052a0001c0004t0007g0001others(19): Show | 23 | 308 | 0.0747 | 1 | c.-9- others(16): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109133901 | G | GT | intron_variant | MODIFIER | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
a0001a0002a0007others(4): Show | a0001c0004a0001c0016a0001c0038others(9): Show | a0001c0004t0017a0001c0016t0011a0001c0038t0001others(9): Show | a0001c0004t0017g0003a0001c0016t0011g0274a0001c0038t0001g0201others(11): Show | 14 | 308 | 0.0455 | 1 | c.-9- others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109135808 | C | CT | intron_variant | MODIFIER | HG01433.hp1 HG01884.hp1 HG02559.hp2 others(7): Show |
a0001a0010a0014others(3): Show | a0001c0016a0001c0032a0001c0038others(6): Show | a0001c0016t0009a0001c0032t0004a0001c0038t0001others(6): Show | a0001c0016t0009g0287a0001c0016t0009g0305a0001c0032t0004g0291others(7): Show | 10 | 308 | 0.0325 | 1 | c.-9- others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109137899 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
a0001a0002a0003others(13): Show | a0001c0010a0001c0013a0001c0016others(36): Show | a0001c0010t0001a0001c0010t0009a0001c0013t0001others(43): Show | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0013t0001g0153others(86): Show | 89 | 308 | 0.2890 | 1 | c.-9- others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109138570 | T | TA | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
a0001a0002a0004others(10): Show | a0001c0002a0001c0003a0001c0023others(34): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(44): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(89): Show | 92 | 308 | 0.2987 | 1 | c.-9- others(7): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109140890 | C | CT | intron_variant | MODIFIER | HG00597.hp1 HG01081.hp1 HG01167.hp2 others(22): Show |
a0001a0002a0007others(5): Show | a0001c0003a0001c0004a0001c0010others(17): Show | a0001c0003t0002a0001c0004t0002a0001c0010t0001others(18): Show | a0001c0003t0002g0077a0001c0003t0002g0078a0001c0003t0002g0099others(22): Show | 25 | 308 | 0.0812 | 1 | c.653 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109142082 | T | TA | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(72): Show |
a0001a0002a0003others(16): Show | a0001c0010a0001c0012a0001c0013others(40): Show | a0001c0010t0001a0001c0010t0002a0001c0010t0009others(46): Show | a0001c0010t0001g0188a0001c0010t0002g0261a0001c0010t0009g0186others(72): Show | 75 | 308 | 0.2435 | 1 | c.653 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109143462 | C | CA | intron_variant | MODIFIER | HG01109.hp2 HG01123.hp1 HG01168.hp1 others(9): Show |
a0001a0002a0006others(2): Show | a0001c0002a0001c0003a0001c0018others(7): Show | a0001c0002t0001a0001c0003t0002a0001c0018t0011others(8): Show | a0001c0002t0001g0283a0001c0003t0002g0094a0001c0018t0011g0046others(9): Show | 12 | 308 | 0.0390 | 1 | c.653 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109144750 | C | CT | intron_variant | MODIFIER | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(77): Show |
a0001a0002a0006others(11): Show | a0001c0002a0001c0003a0001c0004others(35): Show | a0001c0002t0001a0001c0003t0002a0001c0003t0004others(42): Show | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0081others(77): Show | 80 | 308 | 0.2597 | 1 | c.653 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109144757 | T | TC | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(13): Show |
a0001a0002a0028others(1): Show | a0001c0002a0001c0003a0002c0006others(3): Show | a0001c0002t0001a0001c0002t0021a0001c0003t0002others(5): Show | a0001c0002t0001g0035a0001c0002t0001g0191a0001c0002t0001g0235others(13): Show | 16 | 308 | 0.0520 | 1 | c.653 others(18): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109145252 | A | AG | intron_variant | MODIFIER | HG02109.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
a0001 | a0001c0016a0001c0032a0001c0062 | a0001c0016t0009a0001c0032t0004a0001c0062t0019 | a0001c0016t0009g0287a0001c0016t0009g0290a0001c0016t0009g0305others(3): Show | 6 | 308 | 0.0195 | 1 | c.653 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109145836 | T | TA | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp2 HG02630.hp1 others(9): Show |
a0001a0002a0003others(1): Show | a0001c0002a0001c0004a0001c0011others(6): Show | a0001c0002t0008a0001c0004t0002a0001c0011t0001others(6): Show | a0001c0002t0008g0306a0001c0004t0002g0054a0001c0011t0001g0056others(9): Show | 12 | 308 | 0.0390 | 1 | c.653 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109147391 | C | CT | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG01109.hp2 others(12): Show |
a0001a0006a0007others(3): Show | a0001c0002a0001c0003a0001c0004others(12): Show | a0001c0002t0008a0001c0003t0002a0001c0004t0007others(12): Show | a0001c0002t0008g0306a0001c0003t0002g0097a0001c0004t0007g0011others(12): Show | 15 | 308 | 0.0487 | 1 | c.653 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109150982 | C | CT | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(36): Show |
a0001a0002a0005others(8): Show | a0001c0002a0001c0012a0001c0013others(21): Show | a0001c0002t0008a0001c0012t0002a0001c0013t0001others(22): Show | a0001c0002t0008g0306a0001c0012t0002g0045a0001c0012t0002g0250others(36): Show | 39 | 308 | 0.1266 | 1 | c.653 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109152640 | C | CT | intron_variant | MODIFIER | HG01123.hp1 HG01261.hp2 HG01891.hp1 others(11): Show |
a0001a0003a0006others(4): Show | a0001c0011a0001c0018a0001c0074others(8): Show | a0001c0011t0008a0001c0018t0011a0001c0074t0004others(8): Show | a0001c0011t0008g0018a0001c0018t0011g0046a0001c0074t0004g0229others(11): Show | 14 | 308 | 0.0455 | 1 | c.653 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109155585 | C | CT | intron_variant | MODIFIER | HG00438.hp2 HG01175.hp1 HG04184.hp2 others(3): Show |
a0001a0002a0012 | a0001c0003a0001c0087a0001c0089others(3): Show | a0001c0003t0002a0001c0087t0001a0001c0089t0002others(3): Show | a0001c0003t0002g0077a0001c0087t0001g0236a0001c0089t0002g0162others(3): Show | 6 | 308 | 0.0195 | 1 | c.654 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109160089 | C | CA | intron_variant | MODIFIER | HG00423.hp1 HG00558.hp2 HG01109.hp1 others(24): Show |
a0001a0002a0003others(2): Show | a0001c0002a0001c0003a0001c0004others(17): Show | a0001c0002t0001a0001c0003t0002a0001c0004t0007others(18): Show | a0001c0002t0001g0235a0001c0003t0002g0099a0001c0003t0002g0103others(24): Show | 27 | 308 | 0.0877 | 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 | 109161980 | C | CT | intron_variant | MODIFIER | HG00735.hp2 HG01074.hp1 HG01175.hp1 others(12): Show |
a0001a0002a0003others(5): Show | a0001c0002a0001c0023a0001c0050others(11): Show | a0001c0002t0001a0001c0023t0004a0001c0050t0001others(11): Show | a0001c0002t0001g0235a0001c0023t0004g0121a0001c0050t0001g0277others(12): Show | 15 | 308 | 0.0487 | 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 | A | AT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
a0001a0002a0003others(19): Show | a0001c0002a0001c0003a0001c0012others(59): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(69): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(131): Show | 134 | 308 | 0.4351 | 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 | 109166649 | C | CA | intron_variant | MODIFIER | HG00597.hp1 HG01074.hp1 HG01109.hp2 others(35): Show |
a0001a0002a0004others(7): Show | a0001c0004a0001c0010a0001c0011others(21): Show | a0001c0004t0002a0001c0004t0007a0001c0010t0002others(24): Show | a0001c0004t0002g0052a0001c0004t0007g0011a0001c0004t0007g0019others(35): Show | 38 | 308 | 0.1234 | 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 | 109171013 | A | AT | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp2 HG01070.hp1 others(73): Show |
a0001a0002a0003others(15): Show | a0001c0002a0001c0003a0001c0004others(52): Show | a0001c0002t0001a0001c0003t0002a0001c0003t0004others(59): Show | a0001c0002t0001g0091a0001c0002t0001g0282a0001c0003t0002g0103others(73): Show | 76 | 308 | 0.2468 | 1 | c.926 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109171353 | C | CT | intron_variant | MODIFIER | HG00323.hp1 HG01109.hp2 HG01167.hp2 others(30): Show |
a0001a0002a0006others(6): Show | a0001c0016a0001c0039a0001c0054others(21): Show | a0001c0016t0011a0001c0039t0004a0001c0054t0001others(24): Show | a0001c0016t0011g0274a0001c0039t0004g0116a0001c0054t0001g0203others(30): Show | 33 | 308 | 0.1071 | 1 | c.926 others(8): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109174548 | G | GA | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
a0001a0002a0003others(15): Show | a0001c0004a0001c0012a0001c0013others(39): Show | a0001c0004t0017a0001c0012t0002a0001c0013t0001others(48): Show | a0001c0004t0017g0003a0001c0012t0002g0045a0001c0012t0002g0250others(104): Show | 107 | 308 | 0.3474 | 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 | 109174706 | T | TA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
a0001a0002a0007others(8): Show | a0001c0002a0001c0003a0001c0016others(33): Show | a0001c0002t0001a0001c0002t0008a0001c0003t0002others(42): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(91): Show | 94 | 308 | 0.3052 | 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 | 109175222 | G | GT | intron_variant | MODIFIER | HG00673.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
a0001a0002a0008others(1): Show | a0001c0029a0002c0007a0002c0017others(2): Show | a0001c0029t0002a0002c0007t0003a0002c0017t0003others(3): Show | a0001c0029t0002g0096a0002c0007t0003g0037a0002c0007t0003g0041others(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 | 109181229 | C | CT | intron_variant | MODIFIER | HG00323.hp1 HG01109.hp2 HG01167.hp2 others(41): Show |
a0001a0002a0006others(6): Show | a0001c0002a0001c0010a0001c0011others(28): Show | a0001c0002t0001a0001c0010t0001a0001c0010t0009others(32): Show | a0001c0002t0001g0075a0001c0010t0001g0188a0001c0010t0009g0186others(41): Show | 44 | 308 | 0.1429 | 1 | c.181 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109181840 | C | CT | intron_variant | MODIFIER | HG01074.hp1 HG01081.hp1 HG01175.hp1 others(13): Show |
a0001a0002a0004others(5): Show | a0001c0022a0001c0050a0001c0064others(12): Show | a0001c0022t0004a0001c0050t0001a0001c0064t0009others(12): Show | a0001c0022t0004g0004a0001c0050t0001g0277a0001c0050t0001g0278others(13): Show | 16 | 308 | 0.0520 | 1 | c.181 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109184706 | A | AT | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp2 HG01109.hp2 others(22): Show |
a0001a0004a0006others(3): Show | a0001c0058a0001c0087a0004c0008others(13): Show | a0001c0058t0016a0001c0087t0001a0004c0008t0001others(16): Show | a0001c0058t0016g0187a0001c0087t0001g0236a0004c0008t0001g0198others(22): Show | 25 | 308 | 0.0812 | 1 | c.181 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109190626 | G | GT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
a0001a0002a0003others(29): Show | a0001c0002a0001c0003a0001c0004others(93): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(116): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(234): Show | 237 | 308 | 0.7695 | 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 | 109191215 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
a0001a0002a0007others(10): Show | a0001c0002a0001c0003a0001c0018others(29): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(39): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(84): Show | 87 | 308 | 0.2825 | 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 | 109195726 | G | GT | intron_variant | MODIFIER | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(35): Show |
a0001a0002a0004others(8): Show | a0001c0004a0001c0010a0001c0016others(22): Show | a0001c0004t0017a0001c0010t0001a0001c0010t0009others(25): Show | a0001c0004t0017g0003a0001c0010t0001g0188a0001c0010t0009g0186others(35): Show | 38 | 308 | 0.1234 | 1 | c.248 others(10): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109200031 | C | CA | intron_variant | MODIFIER | HG00323.hp1 HG00609.hp2 HG01169.hp2 others(28): Show |
a0001a0002a0003others(10): Show | a0001c0003a0001c0023a0002c0006others(19): Show | a0001c0003t0002a0001c0023t0001a0002c0006t0003others(21): Show | a0001c0003t0002g0103a0001c0003t0002g0244a0001c0023t0001g0100others(28): Show | 31 | 308 | 0.1007 | 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 | 109200952 | T | TG | intron_variant | MODIFIER | HG00621.hp2 NA18946.hp1 NA18955.hp1 others(2): Show |
a0003a0005 | a0003c0001a0003c0005a0005c0019 | a0003c0001t0001a0003c0005t0002a0005c0019t0003 | a0003c0001t0001g0145a0003c0001t0001g0154a0003c0001t0001g0297others(2): Show | 5 | 308 | 0.0162 | 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 | 109204271 | C | CT | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
a0001a0002a0003others(13): Show | a0001c0011a0001c0012a0001c0013others(28): Show | a0001c0011t0001a0001c0012t0002a0001c0013t0001others(35): Show | a0001c0011t0001g0008a0001c0011t0001g0013a0001c0012t0002g0045others(82): Show | 85 | 308 | 0.2760 | 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 | 109205454 | C | CT | intron_variant | MODIFIER | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(7): Show |
a0001a0006a0007others(3): Show | a0001c0002a0001c0003a0001c0074others(6): Show | a0001c0002t0001a0001c0003t0004a0001c0074t0004others(6): Show | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0003t0004g0300others(7): Show | 10 | 308 | 0.0325 | 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 | 109206428 | C | CA | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(11): Show |
a0001a0002a0003others(4): Show | a0001c0002a0001c0012a0001c0046others(9): Show | a0001c0002t0001a0001c0012t0002a0001c0046t0002others(10): Show | a0001c0002t0001g0081a0001c0012t0002g0262a0001c0046t0002g0067others(11): Show | 14 | 308 | 0.0455 | 1 | c.291 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |