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 | 111018710 | GA | G | intron_variant | MODIFIER | HG00438.hp1 HG00673.hp2 HG01175.hp2 others(30): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(10): Show | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0038others(30): Show | 33 | 150 | 0.2200 | -1 | c.128 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 111027325 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(43): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(7): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 46 | 150 | 0.3067 | -1 | c.128 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111032251 | CG | C | intron_variant | MODIFIER | HG01243.hp1 HG02258.hp1 HG03195.hp2 others(2): Show |
a0002a0006a0011others(1): Show | a0002c0002a0006c0006a0011c0010others(1): Show | a0002c0002t0001a0006c0006t0001a0011c0010t0002others(1): Show | a0002c0002t0001g0114a0002c0002t0001g0132a0006c0006t0001g0136others(2): Show | 5 | 150 | 0.0333 | -1 | c.136 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 111034922 | CT | C | intron_variant | MODIFIER | HG00673.hp2 HG01175.hp1 HG01257.hp2 others(26): Show |
a0000a0001a0002others(2): Show | a0000c0013a0000c0014a0001c0001others(4): Show | a0000c0013t0001a0000c0014t0001a0001c0001t0001others(8): Show | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0021others(26): Show | 29 | 150 | 0.1933 | -1 | c.136 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111046864 | CG | C | intron_variant | MODIFIER | HG01243.hp2 HG01891.hp1 HG02258.hp1 others(3): Show |
a0001a0004a0011 | a0001c0001a0004c0005a0011c0010 | a0001c0001t0001a0001c0001t0006a0004c0005t0001others(2): Show | a0001c0001t0001g0045a0001c0001t0001g0129a0001c0001t0006g0017others(3): Show | 6 | 150 | 0.0400 | -1 | c.137 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111050262 | TA | T | intron_variant | MODIFIER | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
a0001a0004a0008 | a0001c0001a0004c0005a0008c0008 | a0001c0001t0001a0004c0005t0002a0008c0008t0001 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0108others(7): Show | 10 | 150 | 0.0667 | -1 | c.144 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111050479 | TC | T | intron_variant | MODIFIER | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | 150 | 0.0267 | -1 | c.144 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111063648 | CA | C | intron_variant | MODIFIER | HG01081.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0005 | a0001c0001t0001a0001c0001t0006a0002c0002t0001others(1): Show | a0001c0001t0001g0067a0001c0001t0006g0017a0002c0002t0001g0099others(1): Show | 4 | 150 | 0.0267 | -1 | c.144 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111064445 | AC | A | intron_variant | MODIFIER | HG01243.hp1 HG03195.hp2 HG03225.hp1 others(1): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0004 | a0001c0001t0001a0002c0002t0001a0003c0004t0002 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132others(1): Show | 4 | 150 | 0.0267 | -1 | c.144 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 111074165 | GT | G | intron_variant | MODIFIER | HG02027.hp2 HG02451.hp2 HG02615.hp1 others(13): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(3): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 16 | 150 | 0.1067 | -1 | c.144 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111079823 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00544.hp2 HG01167.hp1 others(26): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(5): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(26): Show | 29 | 150 | 0.1933 | -1 | c.144 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111079872 | CA | C | intron_variant | MODIFIER | HG01517.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
a0001a0004a0006others(1): Show | a0001c0001a0004c0005a0006c0006others(1): Show | a0001c0001t0001a0004c0005t0002a0006c0006t0001others(1): Show | a0001c0001t0001g0097a0004c0005t0002g0020a0004c0005t0002g0022others(3): Show | 6 | 150 | 0.0400 | -1 | c.144 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111084730 | TA | T | intron_variant | MODIFIER | HG00673.hp2 HG02027.hp2 NA18950.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0002g0076others(1): Show | 4 | 150 | 0.0267 | -1 | c.144 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111084899 | GA | G | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(15): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(3): Show | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 18 | 150 | 0.1200 | -1 | c.144 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111085666 | GA | G | intron_variant | MODIFIER | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | 150 | 0.0200 | -1 | c.144 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111093226 | CA | C | intron_variant | MODIFIER | HG00140.hp1 HG00673.hp2 HG02027.hp2 others(6): Show |
a0001a0003a0004 | a0001c0001a0003c0004a0004c0005 | a0001c0001t0001a0001c0001t0002a0003c0004t0002others(1): Show | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0077others(6): Show | 9 | 150 | 0.0600 | -1 | c.154 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111095391 | CT | C | intron_variant | MODIFIER | HG00673.hp2 HG01517.hp1 HG02027.hp2 others(5): Show |
a0001a0014 | a0001c0001a0014c0020 | a0001c0001t0001a0001c0001t0002a0014c0020t0001 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0077others(5): Show | 8 | 150 | 0.0533 | -1 | c.154 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111095580 | AG | A | intron_variant | MODIFIER | HG00673.hp2 HG02027.hp2 HG02257.hp2 others(4): Show |
a0001a0014 | a0001c0001a0014c0020 | a0001c0001t0001a0001c0001t0002a0014c0020t0001 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0077others(4): Show | 7 | 150 | 0.0467 | -1 | c.154 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111102646 | CA | C | intron_variant | MODIFIER | HG00673.hp1 HG01081.hp2 HG01168.hp2 others(21): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0002c0002others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(11): Show | a0001c0001t0001g0082a0001c0001t0002g0052a0001c0001t0002g0094others(21): Show | 24 | 150 | 0.1600 | -1 | c.154 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111103764 | AT | A | intron_variant | MODIFIER | HG00673.hp1 HG01175.hp2 HG01981.hp1 others(16): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0002c0002others(5): Show | a0001c0001t0002a0001c0001t0006a0001c0003t0002others(8): Show | a0001c0001t0002g0052a0001c0001t0002g0094a0001c0001t0002g0101others(16): Show | 19 | 150 | 0.1267 | -1 | c.154 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111104100 | CT | C | intron_variant | MODIFIER | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(17): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0002c0002others(5): Show | a0001c0001t0002a0001c0001t0006a0001c0003t0002others(9): Show | a0001c0001t0002g0052a0001c0001t0002g0094a0001c0001t0002g0101others(17): Show | 20 | 150 | 0.1333 | -1 | c.154 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111106417 | CT | C | intron_variant | MODIFIER | HG00140.hp2 HG01168.hp1 HG03688.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0017a0002c0002 | a0001c0001t0002a0001c0017t0002a0002c0002t0002 | a0001c0001t0002g0060a0001c0001t0002g0107a0001c0001t0002g0125others(2): Show | 5 | 150 | 0.0333 | -1 | c.154 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111108371 | CT | C | intron_variant | MODIFIER | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(17): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0002others(9): Show | a0001c0001t0001g0145a0001c0001t0002g0052a0001c0001t0002g0094others(17): Show | 20 | 150 | 0.1333 | -1 | c.154 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111109444 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0001c0012others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(14): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(46): Show | 49 | 150 | 0.3267 | -1 | c.154 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111116817 | TA | T | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp1 HG01243.hp2 others(17): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0002c0002others(6): Show | a0001c0001t0001a0001c0001t0005a0001c0003t0001others(8): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 20 | 150 | 0.1333 | -1 | c.154 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111118222 | GA | G | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(47): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0001c0012others(7): Show | a0001c0001t0002a0001c0001t0006a0001c0003t0002others(11): Show | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0002g0033others(47): Show | 50 | 150 | 0.3333 | -1 | c.*41 others(5): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 18/18 | 418 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||
ACOXL_chr2_110727573_111123548 | 111120096 | GT | G | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(49): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0001c0012others(8): Show | a0001c0001t0002a0001c0001t0006a0001c0003t0002others(13): Show | a0001c0001t0002g0006a0001c0001t0002g0032a0001c0001t0002g0033others(49): Show | 52 | 150 | 0.3467 | -1 | c.*22 others(6): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1549 | chr2 | TogoVar | ||||||
ACP1_chr2_259947_283283 | 261513 | AT | A | upstream_gene_variant | MODIFIER | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0003a0001c0001t0002g0064a0001c0001t0002g0068others(1): Show | 10 | 390 | 0.0256 | -1 | c.-34 others(6): Show |
ACP1 | ENSG00000143727.16 | transcript | ENST00000272065.10 | protein_coding | 3433 | chr2 | TogoVar | ||||||
ACP1_chr2_259947_283283 | 264117 | AC | A | upstream_gene_variant | MODIFIER | HG00642.hp1 HG01109.hp1 HG03098.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033a0001c0001t0001g0075 | 3 | 390 | 0.0077 | -1 | c.-84 others(5): Show |
ACP1 | ENSG00000143727.16 | transcript | ENST00000272065.10 | protein_coding | 829 | chr2 | TogoVar | ||||||
ACP1_chr2_259947_283283 | 264604 | CG | C | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(1): Show | a0001c0001t0001g0076a0002c0002t0001g0002a0002c0002t0001g0006others(13): Show | 95 | 390 | 0.2436 | -1 | c.-36 others(5): Show |
ACP1 | ENSG00000143727.16 | transcript | ENST00000272065.10 | protein_coding | 342 | chr2 | TogoVar | ||||||
ACP1_chr2_259947_283283 | 265591 | AT | A | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(127): Show |
a0001a0003 | a0001c0001a0001c0004a0001c0006others(1): Show | a0001c0001t0001a0001c0004t0001a0001c0006t0001others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(24): Show | 130 | 390 | 0.3333 | -1 | c.43+ others(7): Show |
ACP1 | ENSG00000143727.16 | transcript | ENST00000272065.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACP1_chr2_259947_283283 | 267297 | CA | C | intron_variant | MODIFIER | NA18967.hp2 NA18977.hp1 NA19059.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0011 | 3 | 390 | 0.0077 | -1 | c.43+ others(8): Show |
ACP1 | ENSG00000143727.16 | transcript | ENST00000272065.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACP1_chr2_259947_283283 | 271998 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0033others(52): Show | 214 | 390 | 0.5487 | -1 | c.118 others(7): Show |
ACP1 | ENSG00000143727.16 | transcript | ENST00000272065.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACP1_chr2_259947_283283 | 280785 | GC | G | downstream_gene_variant | MODIFIER | HG00642.hp1 HG01109.hp1 HG03098.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033a0001c0001t0001g0075 | 3 | 390 | 0.0077 | -1 | c.*34 others(6): Show |
ACP1 | ENSG00000143727.16 | transcript | ENST00000272065.10 | protein_coding | 2503 | chr2 | TogoVar | ||||||
ACP2_chr11_47234302_47253814 | 47235765 | TA | T | downstream_gene_variant | MODIFIER | HG02965.hp1 HG02976.hp2 HG03139.hp1 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0004a0002c0002t0002g0077 | 3 | 358 | 0.0084 | -1 | c.*43 others(6): Show |
ACP2 | ENSG00000134575.13 | transcript | ENST00000672073.1 | protein_coding | 3536 | chr11 | TogoVar | ||||||
ACP2_chr11_47234302_47253814 | 47240820 | CA | C | intron_variant | MODIFIER | HG01515.hp1 HG02698.hp1 HG02809.hp2 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0050others(3): Show | 8 | 358 | 0.0224 | -1 | c.113 others(9): Show |
ACP2 | ENSG00000134575.13 | transcript | ENST00000672073.1 | protein_coding | 10/10 | chr11 | TogoVar | ||||||
ACP2_chr11_47234302_47253814 | 47252068 | GA | G | upstream_gene_variant | MODIFIER | HG00741.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001a0002c0002t0002 | a0001c0001t0001g0056a0001c0001t0001g0066a0002c0002t0001g0001others(2): Show | 7 | 358 | 0.0196 | -1 | c.-32 others(6): Show |
ACP2 | ENSG00000134575.13 | transcript | ENST00000672073.1 | protein_coding | 3255 | chr11 | TogoVar | ||||||
ACP2_chr11_47234302_47253814 | 47252959 | CT | C | upstream_gene_variant | MODIFIER | HG00733.hp1 HG02451.hp2 HG02965.hp1 others(3): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0026others(1): Show | 6 | 358 | 0.0168 | -1 | c.-41 others(6): Show |
ACP2 | ENSG00000134575.13 | transcript | ENST00000672073.1 | protein_coding | 4146 | chr11 | TogoVar | ||||||
ACP3_chr3_132312407_132363841 | 132317125 | CA | C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(37): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(204): Show | 230 | 368 | 0.6250 | -1 | c.-33 others(5): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 281 | chr3 | TogoVar | ||||||
ACP3_chr3_132312407_132363841 | 132318374 | AT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(21): Show | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0102others(60): Show | 71 | 368 | 0.1929 | -1 | c.120 others(8): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132318501 | CT | C | intron_variant | MODIFIER | HG01123.hp2 HG01433.hp2 HG02602.hp2 others(11): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0003a0001c0002t0004others(2): Show | a0001c0001t0001g0118a0001c0001t0001g0123a0001c0002t0003g0121others(11): Show | 14 | 368 | 0.0380 | -1 | c.120 others(8): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132318700 | GA | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(21): Show | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0102others(60): Show | 71 | 368 | 0.1929 | -1 | c.120 others(9): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132319547 | AT | A | intron_variant | MODIFIER | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(5): Show | a0001c0001t0001g0154a0001c0001t0008g0146a0001c0001t0008g0153others(11): Show | 14 | 368 | 0.0380 | -1 | c.120 others(9): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132320035 | TG | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(15): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(78): Show | 94 | 368 | 0.2554 | -1 | c.120 others(9): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | chr3 | TogoVar | ||||||
ACP3_chr3_132312407_132363841 | 132320652 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(37): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(179): Show | 202 | 368 | 0.5489 | -1 | c.120 others(9): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132321322 | GA | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(42): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(11): Show | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0102others(38): Show | 45 | 368 | 0.1223 | -1 | c.120 others(9): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132324633 | AT | A | intron_variant | MODIFIER | HG02055.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0008a0001c0001t0021others(1): Show | a0001c0001t0002g0157a0001c0001t0008g0234a0001c0001t0021g0035others(3): Show | 6 | 368 | 0.0163 | -1 | c.121 others(9): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132327514 | GA | G | intron_variant | MODIFIER | HG02647.hp2 HG02717.hp1 HG02895.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0007a0001c0001t0009a0001c0001t0014others(2): Show | a0001c0001t0007g0134a0001c0001t0009g0133a0001c0001t0014g0136others(4): Show | 8 | 368 | 0.0217 | -1 | c.121 others(8): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132328679 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(71): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(22): Show | a0001c0001t0001g0032a0001c0001t0001g0091a0001c0001t0001g0102others(66): Show | 74 | 368 | 0.2011 | -1 | c.216 others(8): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132329913 | CT | C | intron_variant | MODIFIER | HG01123.hp1 HG01257.hp1 HG02109.hp1 others(23): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(11): Show | a0001c0001t0001g0040a0001c0001t0002g0213a0001c0001t0007g0134others(22): Show | 26 | 368 | 0.0707 | -1 | c.216 others(9): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar |