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 | 109137899 | C | CTT | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(50): Show |
a0001a0002a0003others(16): Show | a0001c0010a0001c0012a0001c0013others(31): Show | a0001c0010t0002a0001c0012t0002a0001c0013t0001others(33): Show | a0001c0010t0002g0261a0001c0012t0002g0045a0001c0012t0002g0250others(50): Show | 53 | 308 | 0.1721 | 2 | c.-9- others(17): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 1/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109143462 | C | CAA | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(77): Show |
a0001a0002a0006others(10): Show | a0001c0002a0001c0003a0001c0023others(33): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(41): Show | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0081others(77): Show | 80 | 308 | 0.2597 | 2 | c.653 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109144750 | C | CTT | intron_variant | MODIFIER | HG00323.hp1 HG01884.hp1 HG02074.hp2 others(10): Show |
a0001a0002a0003others(4): Show | a0001c0002a0001c0060a0001c0108others(8): Show | a0001c0002t0008a0001c0060t0002a0001c0108t0001others(9): Show | a0001c0002t0008g0306a0001c0060t0002g0272a0001c0108t0001g0010others(10): Show | 13 | 308 | 0.0422 | 2 | c.653 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109150982 | C | CTT | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(43): Show |
a0001a0002a0003others(10): Show | a0001c0010a0001c0022a0001c0034others(27): Show | a0001c0010t0001a0001c0010t0009a0001c0022t0004others(29): Show | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0022t0004g0004others(43): Show | 46 | 308 | 0.1494 | 2 | c.653 others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109161731 | T | TTG | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
a0001a0002a0007others(10): Show | a0001c0002a0001c0003a0001c0010others(34): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(45): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(92): Show | 95 | 308 | 0.3084 | 2 | c.654 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109164717 | A | ATT | intron_variant | MODIFIER | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(66): Show |
a0001a0002a0003others(9): Show | a0001c0002a0001c0003a0001c0013others(21): Show | a0001c0002t0001a0001c0003t0004a0001c0013t0001others(28): Show | a0001c0002t0001g0114a0001c0003t0004g0300a0001c0013t0001g0153others(66): Show | 69 | 308 | 0.2240 | 2 | c.654 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109167617 | A | ATG | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG03710.hp1 |
a0001 | a0001c0034a0001c0048 | a0001c0034t0001a0001c0048t0002 | a0001c0034t0001g0211a0001c0034t0001g0212a0001c0048t0002g0281 | 3 | 308 | 0.0097 | 2 | c.787 others(17): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109167621 | G | GTA | intron_variant | MODIFIER | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(19): Show |
a0001a0002a0006others(2): Show | a0001c0002a0001c0003a0001c0010others(10): Show | a0001c0002t0001a0001c0003t0002a0001c0010t0002others(11): Show | a0001c0002t0001g0098a0001c0002t0001g0109a0001c0002t0001g0191others(19): Show | 22 | 308 | 0.0714 | 2 | c.787 others(17): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109171013 | A | ATT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(58): Show |
a0001a0002a0006others(7): Show | a0001c0002a0001c0003a0001c0023others(21): Show | a0001c0002t0001a0001c0003t0002a0001c0003t0004others(26): Show | a0001c0002t0001g0035a0001c0002t0001g0079a0001c0002t0001g0081others(58): Show | 61 | 308 | 0.1981 | 2 | c.926 others(17): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109181840 | C | CTT | intron_variant | MODIFIER | HG01515.hp1 HG01943.hp2 HG02717.hp1 others(13): Show |
a0001a0002a0003others(3): Show | a0001c0010a0001c0022a0001c0029others(11): Show | a0001c0010t0001a0001c0010t0009a0001c0022t0004others(12): Show | a0001c0010t0001g0188a0001c0010t0009g0186a0001c0022t0004g0005others(13): Show | 16 | 308 | 0.0520 | 2 | c.181 others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 11/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109194511 | C | CGT | intron_variant | MODIFIER | HG00609.hp2 HG02080.hp2 NA19010.hp1 |
a0003a0019a0022 | a0003c0001a0019c0093a0022c0084 | a0003c0001t0001a0019c0093t0001a0022c0084t0004 | a0003c0001t0001g0137a0019c0093t0001g0159a0022c0084t0004g0254 | 3 | 308 | 0.0097 | 2 | c.248 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109194512 | A | ATG | intron_variant | MODIFIER | HG01943.hp1 HG02896.hp2 HG02922.hp2 others(3): Show |
a0001a0002a0036 | a0001c0069a0002c0007a0002c0017others(3): Show | a0001c0069t0002a0002c0007t0003a0002c0017t0024others(3): Show | a0001c0069t0002g0204a0002c0007t0003g0014a0002c0017t0024g0044others(3): Show | 6 | 308 | 0.0195 | 2 | c.248 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109194610 | C | CTG | intron_variant | MODIFIER | HG00609.hp1 HG00735.hp2 HG01258.hp1 others(17): Show |
a0001a0002a0006others(2): Show | a0001c0011a0001c0016a0001c0022others(12): Show | a0001c0011t0001a0001c0016t0009a0001c0022t0004others(13): Show | a0001c0011t0001g0056a0001c0016t0009g0287a0001c0022t0004g0004others(17): Show | 20 | 308 | 0.0649 | 2 | c.248 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109209767 | A | ATG | intron_variant | MODIFIER | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
a0001a0002a0007others(2): Show | a0001c0002a0001c0010a0001c0064others(4): Show | a0001c0002t0001a0001c0010t0001a0001c0064t0009others(4): Show | a0001c0002t0001g0075a0001c0010t0001g0188a0001c0064t0009g0184others(4): Show | 7 | 308 | 0.0227 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109209912 | C | CGT | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(76): Show |
a0001a0002a0003others(17): Show | a0001c0002a0001c0003a0001c0010others(41): Show | a0001c0002t0001a0001c0003t0002a0001c0003t0004others(47): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(76): Show | 79 | 308 | 0.2565 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109209944 | C | CGT | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(55): Show |
a0001a0002a0003others(8): Show | a0001c0002a0001c0003a0001c0010others(19): Show | a0001c0002t0001a0001c0003t0002a0001c0010t0002others(22): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(55): Show | 58 | 308 | 0.1883 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109209946 | C | CAT | intron_variant | MODIFIER | HG01891.hp1 HG02257.hp1 HG02615.hp1 others(12): Show |
a0001a0002a0006others(4): Show | a0001c0039a0001c0069a0001c0074others(10): Show | a0001c0039t0004a0001c0069t0002a0001c0074t0004others(11): Show | a0001c0039t0004g0116a0001c0069t0002g0204a0001c0074t0004g0229others(12): Show | 15 | 308 | 0.0487 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109209947 | G | GTA | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(59): Show |
a0001a0002a0003others(9): Show | a0001c0002a0001c0003a0001c0010others(20): Show | a0001c0002t0001a0001c0003t0002a0001c0010t0002others(23): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(59): Show | 62 | 308 | 0.2013 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109209967 | A | ATG | intron_variant | MODIFIER | HG01884.hp1 HG02559.hp2 HG03579.hp1 others(2): Show |
a0001a0002a0006others(2): Show | a0001c0003a0002c0017a0006c0113others(2): Show | a0001c0003t0004a0002c0017t0003a0006c0113t0004others(2): Show | a0001c0003t0004g0074a0002c0017t0003g0042a0006c0113t0004g0031others(2): Show | 5 | 308 | 0.0162 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109209981 | A | ATG | intron_variant | MODIFIER | HG00280.hp2 HG02723.hp2 HG02965.hp1 others(3): Show |
a0001a0002a0019 | a0001c0010a0001c0011a0001c0013others(3): Show | a0001c0010t0001a0001c0011t0001a0001c0013t0001others(3): Show | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(3): Show | 6 | 308 | 0.0195 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109210116 | T | TAC | intron_variant | MODIFIER | HG01891.hp1 HG02056.hp2 HG03225.hp1 others(3): Show |
a0001a0002a0003others(1): Show | a0001c0069a0001c0074a0001c0124others(3): Show | a0001c0069t0002a0001c0074t0004a0001c0124t0012others(3): Show | a0001c0069t0002g0204a0001c0074t0004g0229a0001c0124t0012g0197others(3): Show | 6 | 308 | 0.0195 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109210118 | C | CGT | intron_variant | MODIFIER | HG00280.hp2 HG02723.hp2 HG03669.hp1 others(1): Show |
a0001a0002 | a0001c0010a0001c0011a0001c0013others(1): Show | a0001c0010t0001a0001c0011t0001a0001c0013t0001others(1): Show | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(1): Show | 4 | 308 | 0.0130 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109210127 | G | GTA | intron_variant | MODIFIER | HG00642.hp2 HG00741.hp2 HG01255.hp1 |
a0002a0003a0004 | a0002c0024a0003c0001a0004c0008 | a0002c0024t0003a0003c0001t0001a0004c0008t0001 | a0002c0024t0003g0302a0003c0001t0001g0143a0004c0008t0001g0221 | 3 | 308 | 0.0097 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109210141 | A | ATG | intron_variant | MODIFIER | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
a0001a0002a0006others(3): Show | a0001c0003a0001c0010a0001c0016others(8): Show | a0001c0003t0004a0001c0010t0009a0001c0016t0009others(8): Show | a0001c0003t0004g0074a0001c0010t0009g0186a0001c0016t0009g0287others(11): Show | 14 | 308 | 0.0455 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109210143 | G | GTA | intron_variant | MODIFIER | HG02145.hp2 HG03098.hp2 HG03225.hp2 |
a0007a0033a0035 | a0007c0037a0033c0063a0035c0076 | a0007c0037t0004a0033c0063t0010a0035c0076t0010 | a0007c0037t0004g0200a0033c0063t0010g0117a0035c0076t0010g0267 | 3 | 308 | 0.0097 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109210150 | T | TAC | intron_variant | MODIFIER | HG01192.hp2 HG01891.hp1 HG01943.hp1 others(6): Show |
a0001a0002a0003others(3): Show | a0001c0069a0001c0074a0001c0124others(6): Show | a0001c0069t0002a0001c0074t0004a0001c0124t0012others(6): Show | a0001c0069t0002g0204a0001c0074t0004g0229a0001c0124t0012g0197others(6): Show | 9 | 308 | 0.0292 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109210182 | T | TAC | intron_variant | MODIFIER | HG00099.hp2 HG01192.hp2 HG01891.hp1 others(20): Show |
a0001a0002a0003others(6): Show | a0001c0002a0001c0039a0001c0069others(17): Show | a0001c0002t0001a0001c0039t0004a0001c0069t0002others(18): Show | a0001c0002t0001g0085a0001c0039t0004g0039a0001c0039t0004g0116others(20): Show | 23 | 308 | 0.0747 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109210186 | C | CGT | intron_variant | MODIFIER | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(4): Show |
a0001a0009 | a0001c0002a0001c0016a0009c0025 | a0001c0002t0001a0001c0016t0011a0009c0025t0001 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0016t0011g0274others(4): Show | 7 | 308 | 0.0227 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109210188 | C | CAT | intron_variant | MODIFIER | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(11): Show |
a0001a0004a0007others(4): Show | a0001c0002a0001c0003a0001c0018others(7): Show | a0001c0002t0001a0001c0002t0021a0001c0003t0002others(8): Show | a0001c0002t0001g0114a0001c0002t0001g0126a0001c0002t0021g0243others(11): Show | 14 | 308 | 0.0455 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109210205 | A | ATG | intron_variant | MODIFIER | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(4): Show |
a0001a0007a0009others(1): Show | a0001c0016a0007c0057a0009c0025others(1): Show | a0001c0016t0011a0007c0057t0004a0009c0025t0001others(1): Show | a0001c0016t0011g0274a0007c0057t0004g0207a0009c0025t0001g0105others(4): Show | 7 | 308 | 0.0227 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109210231 | A | ATG | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG02523.hp1 others(3): Show |
a0001a0002a0006 | a0001c0010a0001c0013a0002c0061others(1): Show | a0001c0010t0001a0001c0013t0001a0002c0061t0003others(2): Show | a0001c0010t0001g0188a0001c0013t0001g0256a0002c0061t0003g0062others(3): Show | 6 | 308 | 0.0195 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109210253 | A | ATG | intron_variant | MODIFIER | HG00323.hp1 HG02257.hp1 HG02523.hp1 others(11): Show |
a0001a0006a0007others(2): Show | a0001c0039a0001c0095a0001c0107others(6): Show | a0001c0039t0004a0001c0095t0001a0001c0107t0012others(8): Show | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0095t0001g0133others(11): Show | 14 | 308 | 0.0455 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109210261 | G | GTA | intron_variant | MODIFIER | HG00280.hp2 HG01261.hp2 HG02056.hp1 others(2): Show |
a0001a0004a0011others(2): Show | a0001c0013a0004c0112a0011c0027others(2): Show | a0001c0013t0001a0004c0112t0001a0011c0027t0004others(2): Show | a0001c0013t0001g0256a0004c0112t0001g0119a0011c0027t0004g0150others(2): Show | 5 | 308 | 0.0162 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109210289 | G | GTA | intron_variant | MODIFIER | HG02145.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
a0007a0009a0033others(1): Show | a0007c0037a0009c0096a0033c0063others(1): Show | a0007c0037t0004a0009c0096t0009a0033c0063t0010others(1): Show | a0007c0037t0004g0200a0009c0096t0009g0295a0033c0063t0010g0117others(1): Show | 4 | 308 | 0.0130 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109210307 | A | ACG | intron_variant | MODIFIER | HG01074.hp1 HG01169.hp1 HG02486.hp2 others(8): Show |
a0001a0004a0006others(1): Show | a0001c0004a0001c0038a0001c0048others(7): Show | a0001c0004t0017a0001c0038t0001a0001c0048t0004others(7): Show | a0001c0004t0017g0003a0001c0038t0001g0201a0001c0048t0004g0307others(8): Show | 11 | 308 | 0.0357 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109210310 | C | CGT | intron_variant | MODIFIER | HG00280.hp2 HG02723.hp2 HG03669.hp1 others(1): Show |
a0001a0002 | a0001c0010a0001c0011a0001c0013others(1): Show | a0001c0010t0001a0001c0011t0001a0001c0013t0001others(1): Show | a0001c0010t0001g0188a0001c0011t0001g0013a0001c0013t0001g0256others(1): Show | 4 | 308 | 0.0130 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109210313 | A | ATG | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(49): Show |
a0001a0002a0003others(7): Show | a0001c0002a0001c0003a0001c0010others(17): Show | a0001c0002t0001a0001c0003t0002a0001c0010t0002others(20): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0191others(49): Show | 52 | 308 | 0.1688 | 2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109210383 | A | ATC | intron_variant | MODIFIER | HG03098.hp2 HG03225.hp2 NA18992.hp2 others(2): Show |
a0003a0006a0008others(2): Show | a0003c0001a0006c0078a0008c0044others(2): Show | a0003c0001t0001a0006c0078t0001a0008c0044t0003others(2): Show | a0003c0001t0001g0145a0006c0078t0001g0181a0008c0044t0003g0182others(2): Show | 5 | 308 | 0.0162 | 2 | c.324 others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109216219 | C | CTT | intron_variant | MODIFIER | HG01168.hp2 HG01261.hp2 HG02015.hp1 others(7): Show |
a0002a0011a0012others(4): Show | a0002c0061a0002c0086a0011c0027others(5): Show | a0002c0061t0003a0002c0086t0003a0011c0027t0004others(6): Show | a0002c0061t0003g0062a0002c0086t0003g0260a0011c0027t0004g0150others(7): Show | 10 | 308 | 0.0325 | 2 | c.335 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 22/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109228033 | C | CAA | intron_variant | MODIFIER | HG00323.hp1 HG01891.hp1 HG02145.hp2 others(17): Show |
a0001a0002a0006others(3): Show | a0001c0039a0001c0074a0001c0095others(12): Show | a0001c0039t0004a0001c0074t0004a0001c0095t0001others(14): Show | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0074t0004g0229others(17): Show | 20 | 308 | 0.0649 | 2 | c.400 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 28/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109243893 | A | ATT | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
a0001a0002a0003others(12): Show | a0001c0002a0001c0003a0001c0004others(32): Show | a0001c0002t0001a0001c0002t0021a0001c0003t0002others(40): Show | a0001c0002t0001g0081a0001c0002t0001g0109a0001c0002t0001g0114others(84): Show | 87 | 308 | 0.2825 | 2 | c.517 others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109255095 | T | TAC | intron_variant | MODIFIER | HG02630.hp1 HG02922.hp1 HG02976.hp2 others(2): Show |
a0001 | a0001c0011a0001c0048a0001c0055others(1): Show | a0001c0011t0001a0001c0048t0004a0001c0055t0001others(1): Show | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0048t0004g0307others(2): Show | 5 | 308 | 0.0162 | 2 | c.616 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 44/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109262950 | T | TTA | intron_variant | MODIFIER | HG01433.hp1 HG02698.hp1 HG03098.hp1 others(2): Show |
a0001a0002a0014 | a0001c0098a0001c0124a0002c0020others(2): Show | a0001c0098t0001a0001c0124t0012a0002c0020t0003others(2): Show | a0001c0098t0001g0286a0001c0124t0012g0197a0002c0020t0003g0232others(2): Show | 5 | 308 | 0.0162 | 2 | c.678 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 49/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109266905 | A | ATT | 3_prime_UTR_variant | MODIFIER | HG00735.hp2 HG01123.hp1 HG01168.hp2 others(58): Show |
a0001a0003a0006others(10): Show | a0001c0003a0001c0004a0001c0010others(33): Show | a0001c0003t0004a0001c0004t0007a0001c0004t0017others(37): Show | a0001c0003t0004g0074a0001c0003t0004g0300a0001c0004t0007g0001others(57): Show | 61 | 308 | 0.1981 | 2 | c.*55 others(11): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 561 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||
ACAD10_chr12_111681053_111762099 | 111694662 | A | ACT | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | 336 | 0.0238 | 2 | c.187 others(19): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111697080 | C | CAA | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
a0001a0004a0005others(3): Show | a0001c0001a0001c0002a0001c0008others(5): Show | a0001c0001t0001a0001c0002t0002a0001c0008t0001others(5): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(173): Show | 184 | 336 | 0.5476 | 2 | c.187 others(19): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111697584 | C | CTT | intron_variant | MODIFIER | HG02074.hp2 HG02738.hp1 HG03486.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(6): Show | 9 | 336 | 0.0268 | 2 | c.188 others(19): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111703083 | C | CAA | intron_variant | MODIFIER | HG01943.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0003 | a0001c0001t0001g0042a0002c0003t0003g0318a0002c0003t0003g0319others(5): Show | 8 | 336 | 0.0238 | 2 | c.336 others(17): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111703905 | T | TTA | intron_variant | MODIFIER | HG00140.hp1 HG00738.hp1 HG01099.hp1 others(38): Show |
a0001a0003 | a0001c0001a0001c0006a0003c0004 | a0001c0001t0001a0001c0001t0004a0001c0006t0001others(1): Show | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(38): Show | 41 | 336 | 0.1220 | 2 | c.336 others(19): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111704688 | C | CTT | intron_variant | MODIFIER | HG00597.hp2 HG00735.hp2 HG01071.hp2 others(87): Show |
a0001a0005a0009others(1): Show | a0001c0001a0001c0002a0001c0008others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0008t0001others(3): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(83): Show | 90 | 336 | 0.2679 | 2 | c.337 others(19): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |