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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ACOXL_chr2_110727573_111123548 | 110803985 | C | CTT | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(8): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0004others(3): Show | a0001c0001t0001a0002c0002t0003a0002c0002t0004others(5): Show | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | 150 | 0.0733 | 2 | c.621 others(19): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110811730 | T | TAC | intron_variant | MODIFIER | HG01257.hp2 HG01258.hp2 HG01891.hp1 others(8): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0002others(2): Show | a0001c0001t0001g0055a0001c0001t0001g0113a0001c0001t0002g0006others(8): Show | 11 | 150 | 0.0733 | 2 | c.753 others(19): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110818451 | G | GTA | intron_variant | MODIFIER | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
a0001a0008 | a0001c0001a0008c0008 | a0001c0001t0006a0008c0008t0001 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | 150 | 0.0200 | 2 | c.753 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110846641 | G | GCA | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(18): Show |
a0001a0003a0007 | a0001c0001a0003c0004a0007c0009 | a0001c0001t0001a0001c0001t0002a0003c0004t0001others(2): Show | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0049others(18): Show | 21 | 150 | 0.1400 | 2 | c.788 others(19): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110881891 | G | GTT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0017a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(11): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(35): Show | 38 | 150 | 0.2533 | 2 | c.789 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110900086 | T | TAC | intron_variant | MODIFIER | HG01255.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
a0000a0001a0002others(1): Show | a0000c0013a0000c0014a0001c0001others(2): Show | a0000c0013t0001a0000c0014t0001a0001c0001t0001others(5): Show | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(14): Show | 17 | 150 | 0.1133 | 2 | c.789 others(19): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110901642 | C | CCA | intron_variant | MODIFIER | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
a0001a0002a0006others(3): Show | a0001c0001a0001c0012a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0006a0001c0012t0002others(6): Show | a0001c0001t0001g0012a0001c0001t0006g0017a0001c0012t0002g0131others(8): Show | 11 | 150 | 0.0733 | 2 | c.789 others(19): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110906586 | C | CAA | intron_variant | MODIFIER | HG01081.hp1 HG02280.hp2 HG02723.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0067others(3): Show | 6 | 150 | 0.0400 | 2 | c.789 others(19): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110915336 | T | TTA | intron_variant | MODIFIER | HG01891.hp1 HG02109.hp1 HG02145.hp2 |
a0004a0008 | a0004c0005a0008c0008 | a0004c0005t0002a0008c0008t0001 | a0004c0005t0002g0124a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | 150 | 0.0200 | 2 | c.905 others(19): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110915350 | A | ATG | intron_variant | MODIFIER | HG01081.hp1 HG02723.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0067a0001c0001t0002g0123 | 2 | 150 | 0.0133 | 2 | c.905 others(19): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110915407 | C | CAT | intron_variant | MODIFIER | HG01175.hp1 HG02886.hp1 |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0004c0005t0002 | a0001c0001t0001g0042a0004c0005t0002g0127 | 2 | 150 | 0.0133 | 2 | c.905 others(19): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110921388 | A | ACC | intron_variant | MODIFIER | HG01175.hp2 HG01496.hp2 HG01517.hp2 others(10): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0003a0001c0012others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0002others(5): Show | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0088others(10): Show | 13 | 150 | 0.0867 | 2 | c.906 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110925853 | C | CTT | intron_variant | MODIFIER | HG02258.hp1 HG03669.hp1 NA18950.hp2 others(2): Show |
a0001a0011 | a0001c0001a0011c0010 | a0001c0001t0001a0001c0001t0002a0011c0010t0002 | a0001c0001t0001g0011a0001c0001t0001g0138a0001c0001t0002g0076others(2): Show | 5 | 150 | 0.0333 | 2 | c.906 others(19): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110937379 | A | ATC | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(55): Show |
a0000a0001a0002others(5): Show | a0000c0014a0001c0001a0001c0017others(6): Show | a0000c0014t0001a0001c0001t0001a0001c0001t0002others(16): Show | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0012others(55): Show | 58 | 150 | 0.3867 | 2 | c.105 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 110950810 | G | GGA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0012a0001c0017others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0012t0002others(6): Show | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0028others(28): Show | 31 | 150 | 0.2067 | 2 | c.105 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110955933 | A | ATT | intron_variant | MODIFIER | HG00438.hp2 HG01167.hp1 HG01257.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0035a0001c0001t0001g0110a0001c0001t0002g0033others(2): Show | 5 | 150 | 0.0333 | 2 | c.105 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110963565 | A | ATG | intron_variant | MODIFIER | HG02451.hp2 HG02717.hp2 HG02723.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0002g0006others(1): Show | 4 | 150 | 0.0267 | 2 | c.106 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110972649 | G | GCA | intron_variant | MODIFIER | HG01257.hp2 HG01258.hp2 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0147a0002c0002t0002g0148 | 2 | 150 | 0.0133 | 2 | c.106 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110975415 | A | AGT | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(30): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0012others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(11): Show | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0063others(30): Show | 33 | 150 | 0.2200 | 2 | c.106 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110979101 | A | AAC | intron_variant | MODIFIER | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(32): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0012others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(11): Show | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0067others(32): Show | 35 | 150 | 0.2333 | 2 | c.106 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 110988857 | T | TTG | intron_variant | MODIFIER | HG00423.hp2 HG00673.hp2 HG01081.hp2 others(8): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(2): Show | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0082others(8): Show | 11 | 150 | 0.0733 | 2 | c.116 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110994447 | G | GTT | intron_variant | MODIFIER | HG01243.hp1 HG02080.hp1 HG03195.hp2 others(2): Show |
a0001a0002a0006 | a0001c0001a0001c0012a0002c0002others(1): Show | a0001c0001t0001a0001c0012t0002a0002c0002t0001others(1): Show | a0001c0001t0001g0031a0001c0012t0002g0131a0002c0002t0001g0114others(2): Show | 5 | 150 | 0.0333 | 2 | c.117 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111002029 | T | TTC | intron_variant | MODIFIER | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0024others(5): Show | 8 | 150 | 0.0533 | 2 | c.128 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111016108 | A | ATT | intron_variant | MODIFIER | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0017a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(13): Show | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0018others(54): Show | 57 | 150 | 0.3800 | 2 | c.128 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111018708 | T | TGG | intron_variant | MODIFIER | HG00438.hp2 HG01255.hp1 HG02027.hp1 others(3): Show |
a0001a0013 | a0001c0001a0013c0011 | a0001c0001t0001a0001c0001t0002a0013c0011t0001 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0110others(3): Show | 6 | 150 | 0.0400 | 2 | c.128 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111022421 | T | TCA | intron_variant | MODIFIER | HG01167.hp1 HG01168.hp2 HG02615.hp2 others(5): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(3): Show | a0001c0001t0001g0145a0001c0001t0002g0052a0001c0003t0001g0075others(5): Show | 8 | 150 | 0.0533 | 2 | c.128 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111053375 | T | TTG | intron_variant | MODIFIER | HG01081.hp1 HG01175.hp1 HG01257.hp2 others(24): Show |
a0000a0001a0002others(1): Show | a0000c0014a0001c0001a0002c0002others(1): Show | a0000c0014t0001a0001c0001t0001a0001c0001t0002others(4): Show | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0018others(24): Show | 27 | 150 | 0.1800 | 2 | c.144 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111056200 | T | TAA | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp2 HG01517.hp1 others(4): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0001c0001t0002a0004c0005t0002 | a0001c0001t0001g0028a0001c0001t0001g0110a0001c0001t0001g0122others(4): Show | 7 | 150 | 0.0467 | 2 | c.144 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111056788 | C | CAA | intron_variant | MODIFIER | HG02080.hp2 HG02145.hp1 HG03195.hp2 others(4): Show |
a0001a0002a0003 | a0001c0001a0001c0012a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0012t0002others(2): Show | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0126others(4): Show | 7 | 150 | 0.0467 | 2 | c.144 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111057977 | C | CAG | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
a0000a0001a0002others(11): Show | a0000c0014a0001c0001a0001c0003others(14): Show | a0000c0014t0001a0001c0001t0001a0001c0001t0002others(28): Show | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(123): Show | 126 | 150 | 0.8400 | 2 | c.144 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 111059768 | G | GAA | intron_variant | MODIFIER | HG01175.hp1 HG02257.hp1 HG02622.hp1 others(5): Show |
a0000a0001 | a0000c0014a0001c0001 | a0000c0014t0001a0001c0001t0001a0001c0001t0002 | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0042others(5): Show | 8 | 150 | 0.0533 | 2 | c.144 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111073299 | G | GAA | intron_variant | MODIFIER | HG03139.hp1 HG03516.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045a0001c0001t0001g0129 | 2 | 150 | 0.0133 | 2 | c.144 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 111079872 | C | CAA | intron_variant | MODIFIER | HG00673.hp2 HG02027.hp2 HG02258.hp1 others(16): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0002others(5): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0029others(16): Show | 19 | 150 | 0.1267 | 2 | c.144 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111084258 | T | TAC | intron_variant | MODIFIER | HG01081.hp2 HG01167.hp2 HG01168.hp2 others(10): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0012others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(4): Show | a0001c0001t0001g0011a0001c0001t0001g0082a0001c0001t0001g0138others(10): Show | 13 | 150 | 0.0867 | 2 | c.144 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111095222 | G | GAA | intron_variant | MODIFIER | HG01496.hp1 HG02145.hp2 HG02735.hp1 others(2): Show |
a0001a0003a0007others(1): Show | a0001c0001a0003c0004a0007c0009others(1): Show | a0001c0001t0001a0003c0004t0001a0007c0009t0001others(1): Show | a0001c0001t0001g0080a0001c0001t0001g0113a0003c0004t0001g0064others(2): Show | 5 | 150 | 0.0333 | 2 | c.154 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111109671 | A | ATT | intron_variant | MODIFIER | HG00544.hp1 HG01255.hp1 HG01257.hp2 others(15): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0012others(1): Show | a0001c0001t0002a0001c0003t0002a0001c0012t0002others(1): Show | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0047others(15): Show | 18 | 150 | 0.1200 | 2 | c.154 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACP1_chr2_259947_283283 | 271555 | C | CTG | intron_variant | MODIFIER | HG02738.hp2 HG03704.hp1 HG03831.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0025a0001c0001t0002g0073 | 3 | 390 | 0.0077 | 2 | c.44- others(15): Show |
ACP1 | ENSG00000143727.16 | transcript | ENST00000272065.10 | protein_coding | 1/5 | chr2 | TogoVar | ||||||
ACP2_chr11_47234302_47253814 | 47235926 | C | CTT | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(69): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0003t0003a0002c0002t0001others(4): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(19): Show | 72 | 358 | 0.2011 | 2 | c.*41 others(13): Show |
ACP2 | ENSG00000134575.13 | transcript | ENST00000672073.1 | protein_coding | 3375 | chr11 | TogoVar | ||||||
ACP2_chr11_47234302_47253814 | 47235959 | G | GTC | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00621.hp2 HG01433.hp2 others(15): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0003 | a0001c0001t0001g0043a0001c0003t0003g0008a0001c0003t0003g0024others(1): Show | 18 | 358 | 0.0503 | 2 | c.*41 others(13): Show |
ACP2 | ENSG00000134575.13 | transcript | ENST00000672073.1 | protein_coding | 3342 | chr11 | TogoVar | ||||||
ACP2_chr11_47234302_47253814 | 47245857 | C | CGT | intron_variant | MODIFIER | HG00099.hp1 HG00609.hp2 HG01071.hp2 others(29): Show |
a0001a0002a0007 | a0001c0001a0002c0002a0007c0009 | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(1): Show | a0001c0001t0001g0025a0002c0002t0001g0026a0002c0002t0002g0005others(5): Show | 32 | 358 | 0.0894 | 2 | c.298 others(15): Show |
ACP2 | ENSG00000134575.13 | transcript | ENST00000672073.1 | protein_coding | 3/10 | chr11 | TogoVar | ||||||
ACP2_chr11_47234302_47253814 | 47252959 | C | CTT | upstream_gene_variant | MODIFIER | HG00280.hp2 HG00642.hp2 HG01070.hp1 others(29): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0005a0002c0002t0001 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(4): Show | 32 | 358 | 0.0894 | 2 | c.-41 others(13): Show |
ACP2 | ENSG00000134575.13 | transcript | ENST00000672073.1 | protein_coding | 4146 | chr11 | TogoVar | ||||||
ACP3_chr3_132312407_132363841 | 132315391 | A | ATT | upstream_gene_variant | MODIFIER | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(5): Show | a0001c0001t0001g0032a0001c0001t0009g0111a0001c0001t0010g0014others(9): Show | 13 | 368 | 0.0353 | 2 | c.-20 others(13): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 2015 | chr3 | TogoVar | ||||||
ACP3_chr3_132312407_132363841 | 132320652 | G | GTT | intron_variant | MODIFIER | HG01175.hp1 HG03710.hp1 HG03831.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(3): Show | a0001c0001t0002g0025a0001c0001t0005g0025a0001c0001t0005g0229others(4): Show | 7 | 368 | 0.0190 | 2 | c.120 others(19): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132324218 | C | CAA | intron_variant | MODIFIER | HG01358.hp1 HG01978.hp2 HG02148.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0012a0001c0002t0011others(1): Show | a0001c0001t0001g0087a0001c0001t0012g0079a0001c0002t0011g0089others(4): Show | 7 | 368 | 0.0190 | 2 | c.121 others(19): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132325595 | A | AAC | intron_variant | MODIFIER | HG02896.hp1 HG03831.hp1 HG04184.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(3): Show | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0002g0202others(7): Show | 10 | 368 | 0.0272 | 2 | c.121 others(19): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132327514 | G | GAA | intron_variant | MODIFIER | HG01261.hp2 HG02148.hp2 HG02622.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0007a0001c0001t0008a0001c0001t0009others(5): Show | a0001c0001t0007g0160a0001c0001t0008g0162a0001c0001t0008g0234others(10): Show | 13 | 368 | 0.0353 | 2 | c.121 others(17): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132327793 | C | CAA | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(63): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(18): Show | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0102others(57): Show | 66 | 368 | 0.1794 | 2 | c.121 others(17): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132328679 | C | CAA | intron_variant | MODIFIER | HG01175.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0012a0001c0001t0016a0001c0001t0019others(1): Show | a0001c0001t0012g0009a0001c0001t0016g0084a0001c0001t0019g0228others(1): Show | 6 | 368 | 0.0163 | 2 | c.216 others(17): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132332612 | C | CAG | intron_variant | MODIFIER | HG02647.hp2 HG02717.hp1 HG02895.hp1 others(6): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0007a0001c0001t0009a0001c0001t0014others(3): Show | a0001c0001t0007g0134a0001c0001t0009g0133a0001c0001t0014g0136others(5): Show | 9 | 368 | 0.0245 | 2 | c.456 others(17): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132337063 | G | GGT | intron_variant | MODIFIER | HG00280.hp1 HG01255.hp1 HG01255.hp2 others(37): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(13): Show | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041others(33): Show | 40 | 368 | 0.1087 | 2 | c.457 others(17): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar |