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 | 109206598 | A | AG | intron_variant | MODIFIER | HG01069.hp1 HG01074.hp2 HG01106.hp2 others(8): Show |
a0001a0002a0009 | a0001c0010a0001c0016a0001c0032others(2): Show | a0001c0010t0009a0001c0016t0009a0001c0032t0004others(2): Show | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(8): Show | 11 | 308 | 0.0357 | 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 |
a0001a0006a0017others(2): Show | a0001c0003a0001c0013a0006c0113others(3): Show | a0001c0003t0004a0001c0013t0001a0006c0113t0004others(3): Show | a0001c0003t0004g0074a0001c0013t0001g0256a0006c0113t0004g0031others(3): Show | 6 | 308 | 0.0195 | 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 | a0001c0003t0002g0244a0001c0004t0002g0052a0001c0022t0004g0007others(11): Show | 14 | 308 | 0.0455 | 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 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(70): Show | 73 | 308 | 0.2370 | 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 | a0001c0039t0004g0039a0001c0039t0004g0116a0001c0069t0002g0204others(17): Show | 20 | 308 | 0.0649 | 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 |
a0007a0033a0035others(1): Show | a0007c0037a0007c0057a0033c0063others(2): Show | a0007c0037t0004a0007c0057t0004a0033c0063t0010others(2): Show | a0007c0037t0004g0200a0007c0057t0004g0207a0033c0063t0010g0117others(2): Show | 5 | 308 | 0.0162 | 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 | a0001c0002t0001g0282a0001c0002t0001g0283a0001c0010t0009g0186others(7): Show | 10 | 308 | 0.0325 | 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 | a0001c0010t0001g0188a0001c0016t0011g0274a0001c0087t0001g0236others(5): Show | 8 | 308 | 0.0260 | 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 | a0001c0003t0002g0244a0001c0010t0002g0016a0001c0011t0001g0013others(7): Show | 10 | 308 | 0.0325 | 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 | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(63): Show | 66 | 308 | 0.2143 | 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 | a0001c0002t0001g0079a0001c0002t0001g0091a0001c0002t0021g0243others(11): Show | 14 | 308 | 0.0455 | 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 | a0001c0002t0001g0035a0001c0002t0001g0126a0001c0002t0001g0191others(107): Show | 110 | 308 | 0.3571 | 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 | a0001c0002t0008g0306a0001c0004t0007g0020a0001c0016t0011g0274others(6): Show | 9 | 308 | 0.0292 | 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 | a0001c0003t0004g0074a0001c0004t0002g0052a0001c0012t0002g0262others(34): Show | 37 | 308 | 0.1201 | 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 |
a0009a0033a0035others(1): Show | a0009c0096a0033c0063a0035c0076others(1): Show | a0009c0096t0009a0033c0063t0010a0035c0076t0010others(1): Show | a0009c0096t0009g0295a0033c0063t0010g0117a0035c0076t0010g0267others(1): Show | 4 | 308 | 0.0130 | 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 | a0001c0002t0001g0075a0001c0002t0001g0079a0001c0002t0001g0085others(31): Show | 34 | 308 | 0.1104 | 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 | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0022t0004g0004others(8): Show | 11 | 308 | 0.0357 | 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 | a0001c0002t0001g0191a0001c0002t0001g0235a0001c0011t0008g0018others(21): Show | 24 | 308 | 0.0779 | 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 | a0001c0004t0007g0001a0001c0004t0007g0011a0001c0004t0007g0019others(4): Show | 8 | 308 | 0.0260 | 1 | c.579 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 41/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109252322 | G | GA | intron_variant | MODIFIER | HG02630.hp1 HG02922.hp1 HG03098.hp2 others(4): Show |
a0001a0002a0033others(2): Show | a0001c0011a0001c0055a0002c0092others(3): Show | a0001c0011t0001a0001c0055t0001a0002c0092t0010others(3): Show | a0001c0011t0001g0056a0001c0011t0001g0157a0001c0055t0001g0226others(4): Show | 7 | 308 | 0.0227 | 1 | c.590 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 42/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109259563 | C | CA | intron_variant | MODIFIER | HG00642.hp2 HG01168.hp2 HG01261.hp2 others(19): Show |
a0001a0004a0005others(6): Show | a0001c0003a0001c0004a0001c0010others(15): Show | a0001c0003t0002a0001c0004t0007a0001c0010t0002others(16): Show | a0001c0003t0002g0094a0001c0004t0007g0019a0001c0010t0002g0261others(19): Show | 22 | 308 | 0.0714 | 1 | c.649 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109259583 | C | CA | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(69): Show |
a0001a0003a0004others(11): Show | a0001c0003a0001c0004a0001c0010others(29): Show | a0001c0003t0002a0001c0004t0002a0001c0010t0002others(32): Show | a0001c0003t0002g0068a0001c0003t0002g0077a0001c0003t0002g0078others(69): Show | 72 | 308 | 0.2338 | 1 | c.649 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 47/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109261869 | T | TA | intron_variant | MODIFIER | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(5): Show |
a0001a0002a0009 | a0001c0010a0001c0016a0001c0064others(2): Show | a0001c0010t0009a0001c0016t0009a0001c0016t0011others(3): Show | a0001c0010t0009g0186a0001c0016t0009g0287a0001c0016t0009g0290others(5): Show | 8 | 308 | 0.0260 | 1 | c.667 others(9): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 48/52 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACACB_chr12_109111587_109273226 | 109266905 | A | AT | 3_prime_UTR_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
a0001a0002a0003others(15): Show | a0001c0003a0001c0004a0001c0010others(36): Show | a0001c0003t0002a0001c0004t0002a0001c0004t0020others(38): Show | a0001c0003t0002g0068a0001c0003t0002g0077a0001c0003t0002g0078others(82): Show | 85 | 308 | 0.2760 | 1 | c.*56 others(5): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 53/53 | 561 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||
ACACB_chr12_109111587_109273226 | 109273045 | G | GA | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
a0001a0002a0003others(20): Show | a0001c0002a0001c0003a0001c0004others(62): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(76): Show | a0001c0002t0001g0035a0001c0002t0001g0075a0001c0002t0001g0079others(149): Show | 153 | 308 | 0.4968 | 1 | c.*66 others(12): Show |
ACACB | ENSG00000076555.16 | transcript | ENST00000338432.12 | protein_coding | 4820 | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111681583 | C | CA | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(99): Show |
a0001a0005a0008others(1): Show | a0001c0001a0001c0002a0001c0008others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0008t0001others(3): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(96): Show | 102 | 336 | 0.3036 | 1 | c.-46 others(12): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4469 | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111682497 | C | CA | upstream_gene_variant | MODIFIER | HG00741.hp1 HG02683.hp2 HG03516.hp2 others(5): Show |
a0001a0011 | a0001c0001a0011c0012 | a0001c0001t0001a0011c0012t0001 | a0001c0001t0001g0166a0001c0001t0001g0179a0001c0001t0001g0229others(5): Show | 8 | 336 | 0.0238 | 1 | c.-37 others(12): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3555 | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111684663 | G | GT | upstream_gene_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0003 | a0001c0001t0001g0075a0002c0003t0003g0318a0002c0003t0003g0319others(6): Show | 9 | 336 | 0.0268 | 1 | c.-15 others(12): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1389 | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111690780 | C | CA | intron_variant | MODIFIER | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(9): Show |
a0001a0010 | a0001c0001a0001c0002a0010c0011 | a0001c0001t0001a0001c0002t0002a0010c0011t0002 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(9): Show | 12 | 336 | 0.0357 | 1 | c.-13 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111691594 | A | AT | intron_variant | MODIFIER | HG00140.hp2 HG00544.hp1 HG00735.hp2 others(44): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0002a0002c0003t0003 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(40): Show | 47 | 336 | 0.1399 | 1 | c.-13 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111694488 | C | CT | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | 336 | 0.0238 | 1 | c.187 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111697584 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(188): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0008others(6): Show | a0001c0001t0001a0001c0002t0002a0001c0008t0001others(6): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(180): Show | 191 | 336 | 0.5685 | 1 | c.188 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111697938 | C | CT | intron_variant | MODIFIER | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
a0001a0008 | a0001c0001a0001c0002a0008c0009 | a0001c0001t0001a0001c0002t0002a0008c0009t0006 | a0001c0001t0001g0079a0001c0001t0001g0295a0001c0001t0001g0298others(3): Show | 6 | 336 | 0.0179 | 1 | c.188 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111697999 | C | CT | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(13): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0002a0002c0003t0003 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(13): Show | 16 | 336 | 0.0476 | 1 | c.188 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111698297 | C | CT | intron_variant | MODIFIER | HG01433.hp1 HG02559.hp1 HG02738.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0166others(10): Show | 13 | 336 | 0.0387 | 1 | c.188 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111698404 | C | CT | intron_variant | MODIFIER | HG01993.hp1 HG02074.hp1 HG02135.hp2 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(17): Show | 20 | 336 | 0.0595 | 1 | c.188 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111700748 | C | CT | intron_variant | MODIFIER | HG01361.hp2 HG01952.hp1 HG02027.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0037a0001c0001t0001g0073a0001c0001t0001g0074others(18): Show | 21 | 336 | 0.0625 | 1 | c.188 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111703083 | C | CA | intron_variant | MODIFIER | HG01106.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
a0001a0006 | a0001c0001a0001c0002a0006c0014 | a0001c0001t0001a0001c0002t0002a0006c0014t0001 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0230others(12): Show | 15 | 336 | 0.0446 | 1 | c.336 others(8): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111704134 | C | CT | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0003 | a0001c0001t0001g0235a0002c0003t0003g0318a0002c0003t0003g0319others(6): Show | 9 | 336 | 0.0268 | 1 | c.337 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111704688 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
a0001a0004a0007 | a0001c0001a0001c0002a0004c0005others(1): Show | a0001c0001t0001a0001c0002t0002a0004c0005t0002others(1): Show | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0041others(94): Show | 101 | 336 | 0.3006 | 1 | c.337 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111706778 | A | AT | intron_variant | MODIFIER | HG01167.hp2 HG02273.hp1 HG02723.hp1 others(15): Show |
a0001a0010 | a0001c0001a0001c0002a0010c0011 | a0001c0001t0001a0001c0002t0002a0010c0011t0002 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0039others(15): Show | 18 | 336 | 0.0536 | 1 | c.531 others(8): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111706780 | A | AT | intron_variant | MODIFIER | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(128): Show |
a0001a0004a0012 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0008t0001others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0019others(121): Show | 131 | 336 | 0.3899 | 1 | c.531 others(8): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111706782 | A | AT | intron_variant | MODIFIER | HG01884.hp1 HG01934.hp1 HG01934.hp2 others(14): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(14): Show | 17 | 336 | 0.0506 | 1 | c.531 others(8): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111707417 | G | GT | intron_variant | MODIFIER | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | 336 | 0.0238 | 1 | c.531 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111708471 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG01175.hp1 HG01361.hp2 others(8): Show |
a0001a0010 | a0001c0001a0001c0002a0010c0011 | a0001c0001t0001a0001c0002t0002a0010c0011t0002 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0073others(8): Show | 11 | 336 | 0.0327 | 1 | c.532 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111709045 | C | CA | intron_variant | MODIFIER | HG01175.hp2 HG02071.hp2 HG02132.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(10): Show | 13 | 336 | 0.0387 | 1 | c.532 others(8): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111710497 | A | AT | intron_variant | MODIFIER | HG02027.hp1 HG02055.hp2 HG02698.hp1 others(7): Show |
a0001a0011 | a0001c0001a0001c0002a0011c0012 | a0001c0001t0001a0001c0002t0002a0011c0012t0001 | a0001c0001t0001g0084a0001c0001t0001g0186a0001c0001t0001g0189others(7): Show | 10 | 336 | 0.0298 | 1 | c.690 others(8): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111711522 | A | AT | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0079others(12): Show | 15 | 336 | 0.0446 | 1 | c.691 others(8): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ACAD10_chr12_111681053_111762099 | 111713937 | C | CA | intron_variant | MODIFIER | HG01496.hp2 NA18950.hp1 NA19083.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0235a0001c0001t0001g0265a0001c0002t0002g0107 | 3 | 336 | 0.0089 | 1 | c.850 others(18): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | TogoVar | ||||||
ACAD10_chr12_111681053_111762099 | 111713938 | C | CA | intron_variant | MODIFIER | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(4): Show | 7 | 336 | 0.0208 | 1 | c.850 others(9): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |