view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 | 109140890 | C | CT | intron_variant | MODIFIER | HG00597.hp1 HG01081.hp1 HG01167.hp2 others(22): Show |
a0001a0002a0007others(5): Show | a0001c0003a0001c0004a0001c0010others(17): Show | a0001c0003t0002a0001c0004t0002a0001c0010t0001others(18): Show | a0001c0003t0002g0077 a0001c0003t0002g0078 a0001c0003t0002g0109 others(22): Show |
25 | 163 | 0.1534 | 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 | a0001c0010t0001g0187 a0001c0010t0002g0259 a0001c0010t0009g0188 others(72): Show |
75 | 306 | 0.2451 | 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 | a0001c0002t0001g0282 a0001c0003t0002g0092 a0001c0018t0011g0048 others(9): Show |
12 | 77 | 0.1558 | 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(76): Show |
a0001a0002a0006others(11): Show | a0001c0002a0001c0003a0001c0004others(35): Show | a0001c0002t0001a0001c0003t0002a0001c0003t0004others(41): Show | a0001c0002t0001g0074 a0001c0002t0001g0079 a0001c0002t0001g0081 others(76): Show |
79 | 152 | 0.5197 | 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 |
a0001a0002a0037others(1): Show | a0001c0002a0001c0003a0002c0006others(3): Show | a0001c0002t0001a0001c0002t0021a0001c0003t0002others(5): Show | a0001c0002t0001g0002 a0001c0002t0001g0035 a0001c0002t0001g0191 others(12): Show |
16 | 306 | 0.0523 | 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 | a0001c0016t0009g0287 a0001c0016t0009g0288 a0001c0016t0009g0303 others(3): Show |
6 | 306 | 0.0196 | 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 | a0001c0002t0008g0304 a0001c0004t0002g0055 a0001c0011t0001g0054 others(9): Show |
12 | 304 | 0.0395 | 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 | a0001c0002t0008g0304 a0001c0003t0002g0100 a0001c0004t0007g0013 others(12): Show |
15 | 245 | 0.0612 | 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 | a0001c0002t0008g0304 a0001c0012t0002g0045 a0001c0012t0002g0248 others(36): Show |
39 | 196 | 0.1990 | 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 | a0001c0011t0008g0019 a0001c0018t0011g0048 a0001c0074t0004g0229 others(11): Show |
14 | 178 | 0.0787 | 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 |
a0001a0002a0015 | a0001c0003a0001c0087a0001c0089others(3): Show | a0001c0003t0002a0001c0087t0001a0001c0089t0002others(3): Show | a0001c0003t0002g0077 a0001c0087t0001g0236 a0001c0089t0002g0163 others(3): Show |
6 | 306 | 0.0196 | 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 | a0001c0002t0001g0235 a0001c0003t0002g0102 a0001c0003t0002g0109 others(24): Show |
27 | 304 | 0.0888 | 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 | a0001c0002t0001g0235 a0001c0023t0004g0121 a0001c0050t0001g0274 others(12): Show |
15 | 302 | 0.0497 | 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(130): Show |
a0001a0002a0003others(19): Show | a0001c0002a0001c0003a0001c0012others(58): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(68): Show | a0001c0002t0001g0002 a0001c0002t0001g0035 a0001c0002t0001g0074 others(129): Show |
133 | 228 | 0.5833 | 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 | a0001c0004t0002g0052 a0001c0004t0007g0013 a0001c0004t0007g0024 others(35): Show |
38 | 209 | 0.1818 | 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 | a0001c0002t0001g0091 a0001c0002t0001g0280 a0001c0003t0002g0102 others(73): Show |
76 | 231 | 0.3290 | 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 | a0001c0016t0011g0272 a0001c0039t0004g0116 a0001c0054t0001g0203 others(30): Show |
33 | 303 | 0.1089 | 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 | a0001c0004t0017g0004 a0001c0012t0002g0045 a0001c0012t0002g0248 others(104): Show |
107 | 299 | 0.3579 | 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(90): Show |
a0001a0002a0007others(8): Show | a0001c0002a0001c0003a0001c0016others(33): Show | a0001c0002t0001a0001c0002t0008a0001c0003t0002others(41): Show | a0001c0002t0001g0035 a0001c0002t0001g0074 a0001c0002t0001g0079 others(90): Show |
93 | 306 | 0.3039 | 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 | a0001c0029t0002g0098 a0002c0007t0003g0038 a0002c0007t0003g0042 others(4): Show |
7 | 299 | 0.0234 | 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 | a0001c0002t0001g0074 a0001c0010t0001g0187 a0001c0010t0009g0188 others(41): Show |
44 | 304 | 0.1447 | 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 | a0001c0022t0004g0006 a0001c0050t0001g0274 a0001c0050t0001g0276 others(13): Show |
16 | 90 | 0.1778 | 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 | a0001c0058t0016g0186 a0001c0087t0001g0236 a0004c0008t0001g0198 others(22): Show |
25 | 300 | 0.0833 | 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(233): Show |
a0001a0002a0003others(29): Show | a0001c0002a0001c0003a0001c0004others(93): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(115): Show | a0001c0002t0001g0002 a0001c0002t0001g0035 a0001c0002t0001g0074 others(232): Show |
236 | 297 | 0.7946 | 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(83): Show |
a0001a0002a0007others(10): Show | a0001c0002a0001c0003a0001c0018others(29): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(38): Show | a0001c0002t0001g0002 a0001c0002t0001g0035 a0001c0002t0001g0074 others(82): Show |
86 | 264 | 0.3258 | 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 | a0001c0004t0017g0004 a0001c0010t0001g0187 a0001c0010t0009g0188 others(35): Show |
38 | 305 | 0.1246 | 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 | a0001c0003t0002g0102 a0001c0003t0002g0241 a0001c0023t0001g0093 others(28): Show |
31 | 294 | 0.1054 | 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 | a0003c0001t0001g0141 a0003c0001t0001g0154 a0003c0001t0001g0295 others(2): Show |
5 | 306 | 0.0163 | 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 | a0001c0011t0001g0009 a0001c0011t0001g0014 a0001c0012t0002g0045 others(82): Show |
85 | 159 | 0.5346 | 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 | a0001c0002t0001g0280 a0001c0002t0001g0282 a0001c0003t0004g0298 others(7): Show |
10 | 303 | 0.0330 | 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 | a0001c0002t0001g0081 a0001c0012t0002g0260 a0001c0046t0002g0067 others(11): Show |
14 | 187 | 0.0749 | 1 | c.291 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109206598 | A | AG | intron_variant | MODIFIER | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(8): Show |
a0001a0002a0009 | a0001c0010a0001c0016a0001c0032others(2): Show | a0001c0010t0009a0001c0016t0009a0001c0032t0004others(2): Show | a0001c0010t0009g0188 a0001c0016t0009g0287 a0001c0016t0009g0288 others(8): Show |
11 | 306 | 0.0359 | 1 | c.291 others(18): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | chr12 | TogoVar | |||||||
ACACB_chr12_109111587_109273226 | 109210948 | T | TA | intron_variant | MODIFIER | HG00280.hp2 HG01081.hp1 HG01884.hp1 others(3): Show |
a0001a0006a0018others(2): Show | a0001c0003a0001c0013a0006c0113others(3): Show | a0001c0003t0004a0001c0013t0001a0006c0113t0004others(3): Show | a0001c0003t0004g0075 a0001c0013t0001g0255 a0006c0113t0004g0031 others(3): Show |
6 | 301 | 0.0199 | 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 | C | CT | intron_variant | MODIFIER | HG00597.hp1 HG02027.hp1 HG02080.hp1 others(11): Show |
a0001a0002a0003others(3): Show | a0001c0003a0001c0004a0001c0022others(9): Show | a0001c0003t0002a0001c0004t0002a0001c0022t0004others(9): Show | a0001c0003t0002g0241 a0001c0004t0002g0052 a0001c0022t0004g0008 others(11): Show |
14 | 213 | 0.0657 | 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 | 109214091 | C | CA | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(70): Show |
a0001a0002a0003others(9): Show | a0001c0002a0001c0003a0001c0010others(26): Show | a0001c0002t0001a0001c0003t0002a0001c0010t0001others(31): Show | a0001c0002t0001g0035 a0001c0002t0001g0074 a0001c0002t0001g0079 others(70): Show |
73 | 305 | 0.2393 | 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 | 109214102 | G | GA | intron_variant | MODIFIER | HG00323.hp1 HG01891.hp1 HG02257.hp1 others(17): Show |
a0001a0002a0006others(4): Show | a0001c0039a0001c0069a0001c0074others(12): Show | a0001c0039t0004a0001c0069t0002a0001c0074t0004others(14): Show | a0001c0039t0004g0037 a0001c0039t0004g0116 a0001c0069t0002g0204 others(17): Show |
20 | 305 | 0.0656 | 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 | 109214726 | C | CA | intron_variant | MODIFIER | HG02145.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
a0007a0028a0029others(1): Show | a0007c0037a0007c0057a0028c0076others(2): Show | a0007c0037t0004a0007c0057t0004a0028c0076t0010others(2): Show | a0007c0037t0004g0201 a0007c0057t0004g0207 a0028c0076t0010g0265 others(2): Show |
5 | 306 | 0.0163 | 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 | 109215765 | C | CA | intron_variant | MODIFIER | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(7): Show |
a0001a0002 | a0001c0002a0001c0010a0001c0016others(3): Show | a0001c0002t0001a0001c0010t0009a0001c0016t0009others(3): Show | a0001c0002t0001g0280 a0001c0002t0001g0282 a0001c0010t0009g0188 others(7): Show |
10 | 305 | 0.0328 | 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 | 109216219 | C | CT | intron_variant | MODIFIER | HG00438.hp2 HG01069.hp1 HG01106.hp2 others(5): Show |
a0001a0003a0009others(1): Show | a0001c0010a0001c0016a0001c0087others(3): Show | a0001c0010t0001a0001c0016t0011a0001c0087t0001others(3): Show | a0001c0010t0001g0187 a0001c0016t0011g0272 a0001c0087t0001g0236 others(5): Show |
8 | 288 | 0.0278 | 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 | 109218652 | A | AT | intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG02080.hp1 others(7): Show |
a0001a0002a0003others(2): Show | a0001c0003a0001c0010a0001c0011others(6): Show | a0001c0003t0002a0001c0010t0002a0001c0011t0001others(7): Show | a0001c0003t0002g0241 a0001c0010t0002g0020 a0001c0011t0001g0014 others(7): Show |
10 | 298 | 0.0336 | 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 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
a0001a0002a0003others(10): Show | a0001c0002a0001c0003a0001c0010others(25): Show | a0001c0002t0001a0001c0003t0002a0001c0010t0001others(28): Show | a0001c0002t0001g0035 a0001c0002t0001g0074 a0001c0002t0001g0079 others(63): Show |
66 | 300 | 0.2200 | 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 | 109221879 | C | CT | intron_variant | MODIFIER | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
a0001a0002a0003others(5): Show | a0001c0002a0001c0003a0001c0010others(8): Show | a0001c0002t0001a0001c0002t0021a0001c0003t0002others(9): Show | a0001c0002t0001g0079 a0001c0002t0001g0091 a0001c0002t0021g0242 others(11): Show |
14 | 306 | 0.0458 | 1 | c.356 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 24/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109226699 | C | CA | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
a0001a0002a0003others(23): Show | a0001c0002a0001c0003a0001c0010others(51): Show | a0001c0002t0001a0001c0003t0002a0001c0003t0004others(59): Show | a0001c0002t0001g0035 a0001c0002t0001g0126 a0001c0002t0001g0191 others(107): Show |
110 | 301 | 0.3654 | 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 | C | CA | intron_variant | MODIFIER | HG02965.hp1 NA18952.hp1 NA18952.hp2 others(6): Show |
a0001a0002a0004others(1): Show | a0001c0002a0001c0004a0001c0016others(3): Show | a0001c0002t0008a0001c0004t0007a0001c0016t0011others(3): Show | a0001c0002t0008g0304 a0001c0004t0007g0027 a0001c0016t0011g0272 others(6): Show |
9 | 269 | 0.0335 | 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 | C | CA | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(34): Show |
a0001a0002a0004others(14): Show | a0001c0003a0001c0004a0001c0012others(28): Show | a0001c0003t0004a0001c0004t0002a0001c0012t0002others(29): Show | a0001c0003t0004g0075 a0001c0004t0002g0052 a0001c0012t0002g0260 others(34): Show |
37 | 293 | 0.1263 | 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 | 109228964 | A | AT | intron_variant | MODIFIER | HG03098.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
a0009a0028a0029others(1): Show | a0009c0096a0028c0076a0029c0080others(1): Show | a0009c0096t0009a0028c0076t0010a0029c0080t0010others(1): Show | a0009c0096t0009g0294 a0028c0076t0010g0265 a0029c0080t0010g0071 others(1): Show |
4 | 306 | 0.0131 | 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 | 109234935 | G | GA | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(31): Show |
a0001a0002a0003others(6): Show | a0001c0002a0001c0010a0001c0011others(21): Show | a0001c0002t0001a0001c0010t0001a0001c0011t0001others(22): Show | a0001c0002t0001g0074 a0001c0002t0001g0079 a0001c0002t0001g0085 others(31): Show |
34 | 306 | 0.1111 | 1 | c.434 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 31/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109236744 | A | AT | intron_variant | MODIFIER | HG01109.hp2 HG01433.hp1 HG02630.hp1 others(8): Show |
a0001a0002a0006others(1): Show | a0001c0011a0001c0022a0001c0055others(4): Show | a0001c0011t0001a0001c0022t0004a0001c0055t0001others(4): Show | a0001c0011t0001g0054 a0001c0011t0001g0157 a0001c0022t0004g0005 others(8): Show |
11 | 305 | 0.0361 | 1 | c.444 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 33/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109238011 | C | CA | intron_variant | MODIFIER | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(21): Show |
a0001a0003a0004others(4): Show | a0001c0002a0001c0011a0001c0013others(10): Show | a0001c0002t0001a0001c0011t0008a0001c0013t0001others(10): Show | a0001c0002t0001g0191 a0001c0002t0001g0235 a0001c0011t0008g0019 others(21): Show |
24 | 301 | 0.0797 | 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 | 109251587 | T | TC | intron_variant | MODIFIER | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(5): Show |
a0001 | a0001c0004 | a0001c0004t0007a0001c0004t0020 | a0001c0004t0007g0001 a0001c0004t0007g0013 a0001c0004t0007g0024 others(3): Show |
8 | 306 | 0.0261 | 1 | c.579 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |