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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ACACA_chr17_37079992_37411836 | 37410340 | CTT | C | upstream_gene_variant | MODIFIER | HG00323.hp1 HG00544.hp2 HG01891.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0001g0053 a0001c0001t0001g0136 a0001c0001t0001g0143 others(13): Show |
16 | 121 | 0.1322 | -2 | c.-40 others(13): Show |
ACACA | ENSG00000278540.5 | transcript | ENST00000616317.5 | protein_coding | 3505 | chr17 | TogoVar | |||||||
ACACB_chr12_109111587_109273226 | 109112688 | CAA | C | upstream_gene_variant | MODIFIER | HG01167.hp2 HG01168.hp1 HG01169.hp2 others(10): Show |
a0001a0002a0006others(3): Show | a0001c0003a0001c0010a0001c0045others(7): Show | a0001c0003t0004a0001c0010t0001a0001c0010t0009others(8): Show | a0001c0003t0004g0298 a0001c0010t0001g0187 a0001c0010t0009g0188 others(10): Show |
13 | 114 | 0.1140 | -2 | c.-40 others(13): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 3898 | chr12 | TogoVar | |||||||
ACACB_chr12_109111587_109273226 | 109133240 | TTC | T | intron_variant | MODIFIER | HG00408.hp1 HG01081.hp1 HG01168.hp1 others(11): Show |
a0001a0002a0007others(7): Show | a0001c0004a0001c0038a0002c0070others(9): Show | a0001c0004t0017a0001c0038t0001a0002c0070t0005others(9): Show | a0001c0004t0017g0004 a0001c0038t0001g0199 a0002c0070t0005g0200 others(11): Show |
14 | 171 | 0.0819 | -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 | CAA | C | intron_variant | MODIFIER | HG00280.hp2 HG02145.hp2 HG02717.hp2 others(3): Show |
a0001a0002a0003others(2): Show | a0001c0013a0001c0038a0002c0070others(3): Show | a0001c0013t0001a0001c0038t0001a0002c0070t0005others(3): Show | a0001c0013t0001g0255 a0001c0038t0001g0199 a0002c0070t0005g0200 others(3): Show |
6 | 71 | 0.0845 | -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 | 109156587 | GTT | G | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(60): Show |
a0001a0002a0005others(13): Show | a0001c0010a0001c0012a0001c0013others(37): Show | a0001c0010t0001a0001c0010t0002a0001c0010t0009others(41): Show | a0001c0010t0001g0187 a0001c0010t0002g0259 a0001c0010t0009g0188 others(60): Show |
63 | 124 | 0.5081 | -2 | c.654 others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109158366 | ATT | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
a0001a0002a0004others(13): Show | a0001c0002a0001c0003a0001c0023others(41): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(51): Show | a0001c0002t0001g0002 a0001c0002t0001g0035 a0001c0002t0001g0074 others(103): Show |
107 | 154 | 0.6948 | -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 | 109166676 | AAC | A | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG01069.hp2 others(21): Show |
a0001a0002a0003others(3): Show | a0001c0010a0001c0016a0001c0045others(12): Show | a0001c0010t0001a0001c0010t0009a0001c0016t0009others(15): Show | a0001c0010t0001g0187 a0001c0010t0009g0188 a0001c0016t0009g0287 others(21): Show |
24 | 306 | 0.0784 | -2 | c.654 others(17): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 2/52 | chr12 | TogoVar | |||||||
ACACB_chr12_109111587_109273226 | 109167621 | GTA | G | intron_variant | MODIFIER | HG01255.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
a0001 | a0001c0002a0001c0004a0001c0010others(1): Show | a0001c0002t0008a0001c0004t0017a0001c0010t0001others(2): Show | a0001c0002t0008g0304 a0001c0004t0017g0004 a0001c0010t0001g0187 others(2): Show |
5 | 96 | 0.0521 | -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 | 109170785 | TTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
a0001a0002a0006others(14): Show | a0001c0002a0001c0003a0001c0016others(54): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(67): Show | a0001c0002t0001g0002 a0001c0002t0001g0035 a0001c0002t0001g0074 others(123): Show |
127 | 306 | 0.4150 | -2 | c.926 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109190626 | GTT | G | intron_variant | MODIFIER | HG01433.hp1 HG03139.hp1 HG03471.hp1 others(5): Show |
a0001a0006a0013others(1): Show | a0001c0022a0006c0113a0013c0077others(2): Show | a0001c0022t0004a0006c0113t0004a0013c0077t0004others(2): Show | a0001c0022t0004g0005 a0001c0022t0004g0006 a0001c0022t0004g0007 others(5): Show |
8 | 69 | 0.1159 | -2 | c.214 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 13/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109194510 | GCA | G | intron_variant | MODIFIER | HG01069.hp1 HG01192.hp1 HG01515.hp2 others(10): Show |
a0001a0002a0009 | a0001c0002a0001c0023a0001c0048others(5): Show | a0001c0002t0001a0001c0002t0008a0001c0023t0001others(6): Show | a0001c0002t0001g0002 a0001c0002t0001g0110 a0001c0002t0008g0304 others(9): Show |
13 | 251 | 0.0518 | -2 | c.248 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | TogoVar | |||||||
ACACB_chr12_109111587_109273226 | 109194511 | CAT | C | intron_variant | MODIFIER | HG01433.hp1 NA18522.hp2 NA19030.hp2 |
a0006a0013a0014 | a0006c0113a0013c0079a0014c0114 | a0006c0113t0004a0013c0079t0004a0014c0114t0004 | a0006c0113t0004g0031 a0013c0079t0004g0180 a0014c0114t0004g0010 |
3 | 227 | 0.0132 | -2 | c.248 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 16/52 | chr12 | TogoVar | |||||||
ACACB_chr12_109111587_109273226 | 109194610 | CTG | C | intron_variant | MODIFIER | HG00673.hp1 HG01884.hp1 HG02572.hp1 others(10): Show |
a0001a0002a0019 | a0001c0004a0001c0012a0001c0013others(6): Show | a0001c0004t0002a0001c0012t0002a0001c0013t0001others(6): Show | a0001c0004t0002g0047 a0001c0012t0002g0045 a0001c0012t0002g0248 others(10): Show |
13 | 158 | 0.0823 | -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 | 109204271 | CTT | C | intron_variant | MODIFIER | HG01070.hp2 HG01168.hp1 HG02965.hp1 others(3): Show |
a0001a0012a0035others(1): Show | a0001c0016a0001c0018a0001c0062others(3): Show | a0001c0016t0011a0001c0018t0002a0001c0062t0019others(3): Show | a0001c0016t0011g0272 a0001c0018t0002g0050 a0001c0062t0019g0286 others(3): Show |
6 | 80 | 0.0750 | -2 | c.291 others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 19/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109209819 | ATG | A | 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 | -2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | TogoVar | |||||||
ACACB_chr12_109111587_109273226 | 109209936 | CAT | C | intron_variant | MODIFIER | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
a0006 | a0006c0026 | a0006c0026t0002a0006c0026t0016 | a0006c0026t0002g0155 a0006c0026t0002g0156 a0006c0026t0016g0066 |
3 | 217 | 0.0138 | -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 | 109209946 | CGT | C | intron_variant | MODIFIER | HG02280.hp2 HG02559.hp1 HG03098.hp2 others(1): Show |
a0001a0007a0014others(1): Show | a0001c0064a0007c0037a0014c0119others(1): Show | a0001c0064t0009a0007c0037t0004a0014c0119t0004others(1): Show | a0001c0064t0009g0184 a0007c0037t0004g0073 a0014c0119t0004g0171 others(1): Show |
4 | 283 | 0.0141 | -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 | 109209972 | CAT | C | intron_variant | MODIFIER | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
a0006 | a0006c0026 | a0006c0026t0002a0006c0026t0016 | a0006c0026t0002g0155 a0006c0026t0002g0156 a0006c0026t0016g0066 |
3 | 272 | 0.0110 | -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 | 109210039 | ATG | A | intron_variant | MODIFIER | HG00323.hp1 HG02523.hp1 NA19009.hp2 |
a0006 | a0006c0026 | a0006c0026t0002a0006c0026t0016 | a0006c0026t0002g0155 a0006c0026t0002g0156 a0006c0026t0016g0066 |
3 | 306 | 0.0098 | -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 | 109210095 | ATG | A | intron_variant | MODIFIER | HG03831.hp2 HG04204.hp1 NA19240.hp2 |
a0002a0004a0005 | a0002c0053a0004c0040a0005c0056 | a0002c0053t0005a0004c0040t0002a0005c0056t0003 | a0002c0053t0005g0033 a0004c0040t0002g0213 a0005c0056t0003g0053 |
3 | 233 | 0.0129 | -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 | 109210175 | GTA | G | intron_variant | MODIFIER | HG01433.hp1 HG02922.hp1 NA20129.hp2 |
a0001a0013 | a0001c0011a0001c0055a0013c0079 | a0001c0011t0001a0001c0055t0001a0013c0079t0004 | a0001c0011t0001g0157 a0001c0055t0001g0226 a0013c0079t0004g0180 |
3 | 306 | 0.0098 | -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 | 109210207 | GTA | G | intron_variant | MODIFIER | HG01258.hp1 HG01515.hp2 NA18994.hp2 others(2): Show |
a0001a0002 | a0001c0023a0002c0007a0002c0017others(1): Show | a0001c0023t0001a0002c0007t0003a0002c0017t0003others(1): Show | a0001c0023t0001g0093 a0001c0023t0001g0123 a0002c0007t0003g0021 others(2): Show |
5 | 305 | 0.0164 | -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 | 109210220 | CAT | C | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(61): Show |
a0001a0002a0003others(8): Show | a0001c0002a0001c0004a0001c0010others(30): Show | a0001c0002t0008a0001c0004t0002a0001c0004t0007others(36): Show | a0001c0002t0008g0304 a0001c0004t0002g0047 a0001c0004t0002g0052 others(59): Show |
64 | 306 | 0.2092 | -2 | c.324 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | chr12 | TogoVar | |||||||
ACACB_chr12_109111587_109273226 | 109210227 | GTA | G | intron_variant | MODIFIER | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(1): Show |
a0009 | a0009c0025 | a0009c0025t0001 | a0009c0025t0001g0105 a0009c0025t0001g0267 a0009c0025t0001g0268 others(1): Show |
4 | 286 | 0.0140 | -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 | 109210268 | TAC | T | intron_variant | MODIFIER | HG00558.hp2 HG00642.hp1 HG01884.hp1 others(12): Show |
a0001a0002a0003others(7): Show | a0001c0003a0001c0010a0001c0064others(11): Show | a0001c0003t0004a0001c0010t0002a0001c0064t0009others(11): Show | a0001c0003t0004g0298 a0001c0010t0002g0020 a0001c0064t0009g0184 others(12): Show |
15 | 306 | 0.0490 | -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 | 109210282 | CAT | C | intron_variant | MODIFIER | HG02723.hp2 HG03669.hp1 HG04115.hp1 |
a0001a0002 | a0001c0010a0001c0011a0002c0061 | a0001c0010t0001a0001c0011t0001a0002c0061t0003 | a0001c0010t0001g0187 a0001c0011t0001g0014 a0002c0061t0003g0061 |
3 | 250 | 0.0120 | -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 | 109210287 | CTG | C | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp2 HG02083.hp1 others(13): Show |
a0001a0002a0006others(4): Show | a0001c0004a0002c0017a0002c0024others(6): Show | a0001c0004t0007a0001c0004t0020a0002c0017t0003others(7): Show | a0001c0004t0007g0001 a0001c0004t0007g0013 a0001c0004t0007g0024 others(11): Show |
16 | 215 | 0.0744 | -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 | 109210306 | TAC | T | intron_variant | MODIFIER | HG03195.hp1 HG03471.hp2 HG03540.hp1 |
a0001a0007a0029 | a0001c0004a0007c0057a0029c0080 | a0001c0004t0002a0007c0057t0004a0029c0080t0010 | a0001c0004t0002g0055 a0007c0057t0004g0207 a0029c0080t0010g0071 |
3 | 289 | 0.0104 | -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 | 109210339 | ACG | A | intron_variant | MODIFIER | HG00642.hp1 HG00673.hp1 HG01109.hp2 others(15): Show |
a0001a0002a0003others(4): Show | a0001c0012a0001c0013a0001c0016others(11): Show | a0001c0012t0002a0001c0013t0001a0001c0016t0011others(12): Show | a0001c0012t0002g0045 a0001c0012t0002g0248 a0001c0012t0002g0250 others(15): Show |
18 | 306 | 0.0588 | -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 | 109210447 | GTA | G | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(61): Show |
a0001a0002a0003others(9): Show | a0001c0002a0001c0003a0001c0010others(22): Show | a0001c0002t0001a0001c0003t0002a0001c0010t0001others(26): Show | a0001c0002t0001g0035 a0001c0002t0001g0074 a0001c0002t0001g0079 others(61): Show |
64 | 306 | 0.2092 | -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 | 109211342 | CTT | C | intron_variant | MODIFIER | HG00323.hp2 HG00597.hp2 HG02809.hp1 others(5): Show |
a0001a0003a0006others(2): Show | a0001c0002a0001c0011a0001c0016others(5): Show | a0001c0002t0001a0001c0011t0001a0001c0016t0011others(5): Show | a0001c0002t0001g0191 a0001c0011t0001g0009 a0001c0016t0011g0272 others(5): Show |
8 | 207 | 0.0386 | -2 | c.325 others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 21/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109233211 | CAT | C | intron_variant | MODIFIER | HG01081.hp1 HG01168.hp2 HG01261.hp2 others(10): Show |
a0001a0002a0006others(6): Show | a0001c0003a0001c0064a0002c0043others(8): Show | a0001c0003t0004a0001c0064t0009a0002c0043t0003others(9): Show | a0001c0003t0004g0075 a0001c0064t0009g0184 a0002c0043t0003g0012 others(10): Show |
13 | 306 | 0.0425 | -2 | c.413 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 29/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109238471 | AAT | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
a0001a0002a0003others(14): Show | a0001c0002a0001c0003a0001c0010others(43): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(58): Show | a0001c0002t0001g0002 a0001c0002t0001g0035 a0001c0002t0001g0081 others(152): Show |
156 | 306 | 0.5098 | -2 | c.466 others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 34/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACACB_chr12_109111587_109273226 | 109240821 | TCA | T | intron_variant | MODIFIER | HG01168.hp2 HG01261.hp2 HG01884.hp1 others(8): Show |
a0001a0002a0006others(5): Show | a0001c0003a0002c0043a0002c0061others(6): Show | a0001c0003t0004a0002c0043t0003a0002c0061t0003others(7): Show | a0001c0003t0004g0075 a0002c0043t0003g0012 a0002c0061t0003g0061 others(8): Show |
11 | 306 | 0.0359 | -2 | c.481 others(19): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 35/52 | chr12 | TogoVar | |||||||
ACACB_chr12_109111587_109273226 | 109244373 | TCA | T | intron_variant | MODIFIER | HG00609.hp1 HG02015.hp2 HG02027.hp1 others(4): Show |
a0001a0002a0005others(2): Show | a0001c0089a0002c0028a0005c0019others(2): Show | a0001c0089t0002a0002c0028t0003a0005c0019t0003others(2): Show | a0001c0089t0002g0163 a0002c0028t0003g0161 a0002c0028t0003g0179 others(4): Show |
7 | 306 | 0.0229 | -2 | c.517 others(21): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 37/52 | chr12 | TogoVar | |||||||
ACACB_chr12_109111587_109273226 | 109262950 | TTA | T | intron_variant | MODIFIER | HG02145.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
a0001a0007a0013 | a0001c0002a0007c0030a0007c0037others(2): Show | a0001c0002t0008a0007c0030t0004a0007c0037t0004others(2): Show | a0001c0002t0008g0304 a0007c0030t0004g0278 a0007c0030t0004g0284 others(3): Show |
6 | 30 | 0.2000 | -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 | 109269044 | TAG | T | downstream_gene_variant | MODIFIER | HG00673.hp1 HG02040.hp1 HG02109.hp1 others(12): Show |
a0001a0003a0004 | a0001c0003a0001c0004a0001c0010others(7): Show | a0001c0003t0002a0001c0004t0002a0001c0010t0002others(7): Show | a0001c0003t0002g0077 a0001c0003t0002g0102 a0001c0004t0002g0055 others(12): Show |
15 | 306 | 0.0490 | -2 | c.*26 others(13): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 819 | chr12 | TogoVar | |||||||
ACAD10_chr12_111681053_111762099 | 111682497 | CAA | C | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(12): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0001a0001c0002t0002a0003c0004t0001 | a0001c0001t0001g0059 a0001c0001t0001g0076 a0001c0001t0001g0204 others(12): Show |
15 | 85 | 0.1765 | -2 | c.-37 others(13): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3555 | chr12 | TogoVar | |||||||
ACAD10_chr12_111681053_111762099 | 111686697 | CAA | C | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0318 a0002c0003t0003g0319 a0002c0003t0003g0320 others(5): Show |
8 | 334 | 0.0240 | -2 | c.-14 others(17): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | TogoVar | |||||||
ACAD10_chr12_111681053_111762099 | 111687512 | CAT | C | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0318 a0002c0003t0003g0319 a0002c0003t0003g0320 others(5): Show |
8 | 334 | 0.0240 | -2 | c.-14 others(19): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111689720 | CTT | C | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0318 a0002c0003t0003g0319 a0002c0003t0003g0320 others(5): Show |
8 | 330 | 0.0242 | -2 | c.-13 others(19): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111698404 | CTT | C | intron_variant | MODIFIER | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(95): Show |
a0001a0004a0010 | a0001c0001a0001c0002a0004c0005others(1): Show | a0001c0001t0001a0001c0002t0002a0004c0005t0002others(1): Show | a0001c0001t0001g0015 a0001c0002t0002g0001 a0001c0002t0002g0004 others(90): Show |
98 | 187 | 0.5241 | -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 | 111703102 | ATT | A | intron_variant | MODIFIER | HG02074.hp2 HG04204.hp1 NA19000.hp1 |
a0001a0004 | a0001c0002a0004c0005 | a0001c0002t0002a0004c0005t0002 | a0001c0002t0002g0100 a0001c0002t0002g0138 a0004c0005t0002g0099 |
3 | 334 | 0.0090 | -2 | c.336 others(17): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | TogoVar | |||||||
ACAD10_chr12_111681053_111762099 | 111703905 | TTA | T | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(11): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0003 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0045 others(11): Show |
14 | 290 | 0.0483 | -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 | 111718036 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(80): Show |
a0001a0003a0005others(1): Show | a0001c0001a0003c0004a0005c0016others(1): Show | a0001c0001t0001a0001c0001t0004a0003c0004t0001others(2): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(77): Show |
83 | 138 | 0.6014 | -2 | c.992 others(19): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111723684 | ACC | A | intron_variant | MODIFIER | HG00544.hp1 HG01071.hp2 HG01123.hp2 others(91): Show |
a0001a0004a0006others(1): Show | a0001c0001a0001c0002a0004c0005others(2): Show | a0001c0001t0001a0001c0002t0002a0004c0005t0002others(2): Show | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0315 others(86): Show |
94 | 198 | 0.4747 | -2 | c.106 others(21): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111735459 | ATT | A | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0318 a0002c0003t0003g0319 a0002c0003t0003g0320 others(5): Show |
8 | 326 | 0.0245 | -2 | c.154 others(21): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111737841 | GGT | G | intron_variant | MODIFIER | NA18959.hp1 NA18971.hp2 NA18980.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | 303 | 0.0132 | -2 | c.171 others(19): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111740782 | CAA | C | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0318 a0002c0003t0003g0319 a0002c0003t0003g0320 others(5): Show |
8 | 224 | 0.0357 | -2 | c.171 others(21): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111745835 | CTT | C | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(6): Show |
a0002a0006 | a0002c0003a0006c0015 | a0002c0003t0003a0006c0015t0001 | a0002c0003t0003g0318 a0002c0003t0003g0319 a0002c0003t0003g0320 others(6): Show |
9 | 294 | 0.0306 | -2 | c.211 others(19): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |