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 | 110736619 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
a0000a0001a0002others(10): Show | a0000c0013a0000c0014a0001c0001others(14): Show | a0000c0013t0001a0000c0014t0001a0001c0001t0001others(22): Show | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0008others(91): Show | 94 | 150 | 0.6267 | -1 | c.-23 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110751298 | CA | C | intron_variant | MODIFIER | HG01257.hp2 HG01258.hp2 HG01517.hp2 others(10): Show |
a0001a0002a0007others(1): Show | a0001c0001a0002c0002a0007c0009others(1): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0002others(2): Show | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | 150 | 0.0867 | -1 | c.-22 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110752023 | CT | C | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(16): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0003t0001others(9): Show | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(16): Show | 19 | 150 | 0.1267 | -1 | c.-22 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110756032 | AT | A | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(47): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0003c0004others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(15): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 50 | 150 | 0.3333 | -1 | c.-22 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110769914 | AC | A | intron_variant | MODIFIER | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0004c0005t0002 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | 150 | 0.0200 | -1 | c.75+ others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110776568 | GC | G | intron_variant | MODIFIER | HG02976.hp1 HG03195.hp1 NA18906.hp1 |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0001a0006c0006t0002 | a0001c0001t0001g0145a0001c0001t0001g0150a0006c0006t0002g0146 | 3 | 150 | 0.0200 | -1 | c.75+ others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 110777552 | CT | C | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(3): Show |
a0002a0003a0005 | a0002c0002a0003c0004a0005c0007 | a0002c0002t0003a0002c0002t0004a0003c0004t0003others(2): Show | a0002c0002t0003g0139a0002c0002t0003g0142a0002c0002t0004g0141others(3): Show | 6 | 150 | 0.0400 | -1 | c.76- others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110787533 | CA | C | intron_variant | MODIFIER | HG01168.hp1 HG01168.hp2 HG01257.hp2 others(3): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0002a0001c0003t0001a0002c0002t0002others(2): Show | a0001c0001t0002g0060a0001c0003t0001g0041a0001c0003t0001g0087others(3): Show | 6 | 150 | 0.0400 | -1 | c.159 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110798258 | CT | C | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0004others(4): Show | a0001c0001t0001a0001c0001t0005a0002c0002t0002others(8): Show | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(15): Show | 18 | 150 | 0.1200 | -1 | c.346 others(8): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110812309 | CT | C | intron_variant | MODIFIER | HG02109.hp1 HG02145.hp2 HG02280.hp1 |
a0001a0008 | a0001c0001a0008c0008 | a0001c0001t0006a0008c0008t0001 | a0001c0001t0006g0017a0008c0008t0001g0015a0008c0008t0001g0016 | 3 | 150 | 0.0200 | -1 | c.753 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110817952 | CT | C | intron_variant | MODIFIER | HG01175.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0001a0002c0002t0002 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0003t0001g0036others(2): Show | 5 | 150 | 0.0333 | -1 | c.753 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110818393 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
a0000a0001a0002others(11): Show | a0000c0014a0001c0001a0001c0003others(15): Show | a0000c0014t0001a0001c0001t0001a0001c0001t0002others(29): Show | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0011others(117): Show | 120 | 150 | 0.8000 | -1 | c.753 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110834671 | TC | T | intron_variant | MODIFIER | HG06807.hp2 NA19043.hp2 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0013a0002c0002t0002g0014 | 2 | 150 | 0.0133 | -1 | c.754 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 110835350 | CT | C | intron_variant | MODIFIER | HG02451.hp1 HG02818.hp1 HG06807.hp1 |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0004c0005t0002 | a0001c0001t0001g0021a0004c0005t0002g0020a0004c0005t0002g0022 | 3 | 150 | 0.0200 | -1 | c.754 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 110837451 | TA | T | intron_variant | MODIFIER | HG00544.hp1 HG01081.hp2 HG01167.hp2 others(14): Show |
a0001a0003 | a0001c0001a0001c0003a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(2): Show | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0080others(14): Show | 17 | 150 | 0.1133 | -1 | c.754 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110844550 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(25): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0017a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0017t0002others(10): Show | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0031others(25): Show | 28 | 150 | 0.1867 | -1 | c.788 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110853913 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(91): Show |
a0000a0001a0002others(10): Show | a0000c0013a0001c0001a0001c0003others(14): Show | a0000c0013t0001a0001c0001t0001a0001c0001t0002others(28): Show | a0000c0013t0001g0046a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 94 | 150 | 0.6267 | -1 | c.788 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110855461 | GA | G | intron_variant | MODIFIER | HG02027.hp2 HG03688.hp1 NA18950.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0137others(2): Show | 5 | 150 | 0.0333 | -1 | c.788 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110865835 | GT | G | intron_variant | MODIFIER | HG00423.hp1 HG00673.hp1 HG01175.hp2 others(21): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(8): Show | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0077others(21): Show | 24 | 150 | 0.1600 | -1 | c.788 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110874392 | TC | T | intron_variant | MODIFIER | HG02145.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
a0000a0001a0002 | a0000c0013a0001c0001a0002c0002 | a0000c0013t0001a0001c0001t0001a0001c0001t0002others(1): Show | a0000c0013t0001g0046a0001c0001t0001g0024a0001c0001t0001g0039others(7): Show | 10 | 150 | 0.0667 | -1 | c.788 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110880153 | CA | C | intron_variant | MODIFIER | HG01168.hp2 HG02145.hp1 HG02622.hp2 others(10): Show |
a0000a0001a0002 | a0000c0013a0001c0001a0001c0003others(1): Show | a0000c0013t0001a0001c0001t0001a0001c0001t0002others(2): Show | a0000c0013t0001g0046a0001c0001t0001g0024a0001c0001t0001g0039others(10): Show | 13 | 150 | 0.0867 | -1 | c.789 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110886914 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0017a0002c0002others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(12): Show | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 41 | 150 | 0.2733 | -1 | c.789 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110889313 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0017a0003c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(8): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(29): Show | 32 | 150 | 0.2133 | -1 | c.789 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110904172 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0017a0002c0002others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(12): Show | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0018others(40): Show | 43 | 150 | 0.2867 | -1 | c.789 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 110906537 | CA | C | intron_variant | MODIFIER | HG01167.hp1 HG01167.hp2 HG01517.hp2 others(14): Show |
a0000a0001a0002others(1): Show | a0000c0013a0001c0001a0001c0003others(2): Show | a0000c0013t0001a0001c0001t0001a0001c0001t0002others(4): Show | a0000c0013t0001g0046a0001c0001t0001g0011a0001c0001t0001g0024others(14): Show | 17 | 150 | 0.1133 | -1 | c.789 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110906586 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0017a0003c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0017t0002others(4): Show | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(18): Show | 21 | 150 | 0.1400 | -1 | c.789 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110915062 | CA | C | intron_variant | MODIFIER | HG02257.hp1 HG02615.hp1 HG04115.hp1 others(3): Show |
a0000a0002a0005others(1): Show | a0000c0014a0002c0002a0005c0007others(1): Show | a0000c0014t0001a0002c0002t0001a0002c0002t0002others(2): Show | a0000c0014t0001g0072a0002c0002t0001g0061a0002c0002t0002g0014others(3): Show | 6 | 150 | 0.0400 | -1 | c.905 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 110915419 | TA | T | intron_variant | MODIFIER | HG02280.hp2 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0018a0001c0001t0001g0150 | 2 | 150 | 0.0133 | -1 | c.905 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 110915427 | TA | T | intron_variant | MODIFIER | HG01081.hp1 HG03831.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0067a0001c0001t0001g0113 | 2 | 150 | 0.0133 | -1 | c.905 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 110916239 | CT | C | intron_variant | MODIFIER | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(18): Show |
a0000a0001a0002others(7): Show | a0000c0014a0001c0001a0002c0002others(7): Show | a0000c0014t0001a0001c0001t0001a0001c0001t0005others(11): Show | a0000c0014t0001g0072a0001c0001t0001g0011a0001c0001t0001g0018others(18): Show | 21 | 150 | 0.1400 | -1 | c.905 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110921388 | AC | A | intron_variant | MODIFIER | HG01243.hp2 HG02622.hp1 HG02886.hp2 others(10): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(3): Show | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0049others(10): Show | 13 | 150 | 0.0867 | -1 | c.906 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110921400 | CT | C | intron_variant | MODIFIER | HG02280.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0001c0001t0005a0004c0005t0002 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0005g0149others(2): Show | 5 | 150 | 0.0333 | -1 | c.906 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110925853 | CT | C | intron_variant | MODIFIER | HG01243.hp2 HG02280.hp2 HG02451.hp1 others(11): Show |
a0001a0004a0006others(1): Show | a0001c0001a0004c0005a0006c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(5): Show | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0021others(11): Show | 14 | 150 | 0.0933 | -1 | c.906 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110926159 | AG | A | intron_variant | MODIFIER | HG02258.hp1 NA19030.hp1 |
a0001a0011 | a0001c0001a0011c0010 | a0001c0001t0001a0011c0010t0002 | a0001c0001t0001g0008a0011c0010t0002g0009 | 2 | 150 | 0.0133 | -1 | c.906 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 110936850 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
a0000a0001a0002others(3): Show | a0000c0014a0001c0001a0001c0012others(5): Show | a0000c0014t0001a0001c0001t0001a0001c0001t0002others(14): Show | a0000c0014t0001g0072a0001c0001t0001g0012a0001c0001t0001g0018others(53): Show | 56 | 150 | 0.3733 | -1 | c.105 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110938839 | CT | C | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(27): Show |
a0000a0001a0002others(3): Show | a0000c0013a0000c0014a0001c0001others(5): Show | a0000c0013t0001a0000c0014t0001a0001c0001t0001others(12): Show | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0029others(27): Show | 30 | 150 | 0.2000 | -1 | c.105 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110942726 | TA | T | intron_variant | MODIFIER | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0001c0001t0005a0004c0005t0002 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | 150 | 0.0533 | -1 | c.105 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110943162 | GA | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(42): Show |
a0000a0001a0002others(2): Show | a0000c0014a0001c0001a0001c0017others(3): Show | a0000c0014t0001a0001c0001t0001a0001c0001t0002others(11): Show | a0000c0014t0001g0072a0001c0001t0001g0028a0001c0001t0001g0029others(42): Show | 45 | 150 | 0.3000 | -1 | c.105 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110948703 | TA | T | intron_variant | MODIFIER | HG00323.hp1 HG00544.hp1 HG01081.hp1 others(37): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(13): Show | a0001c0001t0001g0067a0001c0001t0001g0077a0001c0001t0001g0096others(37): Show | 40 | 150 | 0.2667 | -1 | c.105 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110955933 | AT | A | intron_variant | MODIFIER | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(23): Show |
a0000a0001a0002others(4): Show | a0000c0014a0001c0001a0002c0002others(4): Show | a0000c0014t0001a0001c0001t0001a0001c0001t0002others(6): Show | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0018others(23): Show | 26 | 150 | 0.1733 | -1 | c.105 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110958049 | CA | C | intron_variant | MODIFIER | HG00544.hp1 HG00544.hp2 HG01081.hp1 others(30): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0002c0002others(5): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0002others(8): Show | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(30): Show | 33 | 150 | 0.2200 | -1 | c.105 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110960666 | GT | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
a0000a0001a0002others(6): Show | a0000c0013a0001c0001a0002c0002others(6): Show | a0000c0013t0001a0001c0001t0001a0001c0001t0002others(11): Show | a0000c0013t0001g0046a0001c0001t0001g0011a0001c0001t0001g0012others(53): Show | 56 | 150 | 0.3733 | -1 | c.106 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110975808 | CA | C | intron_variant | MODIFIER | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(15): Show |
a0000a0001a0002others(3): Show | a0000c0013a0000c0014a0001c0001others(4): Show | a0000c0013t0001a0000c0014t0001a0001c0001t0001others(7): Show | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0010others(15): Show | 18 | 150 | 0.1200 | -1 | c.106 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110985170 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
a0000a0001a0002others(10): Show | a0000c0013a0000c0014a0001c0001others(14): Show | a0000c0013t0001a0000c0014t0001a0001c0001t0001others(28): Show | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | 150 | 0.8533 | -1 | c.106 others(10): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110995080 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(60): Show |
a0000a0001a0002others(6): Show | a0000c0014a0001c0001a0001c0003others(8): Show | a0000c0014t0001a0001c0001t0001a0001c0001t0002others(13): Show | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(60): Show | 63 | 150 | 0.4200 | -1 | c.117 others(9): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | chr2 | TogoVar | ||||||
ACOXL_chr2_110727573_111123548 | 111002258 | AT | A | intron_variant | MODIFIER | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
a0000a0001a0002others(5): Show | a0000c0013a0000c0014a0001c0001others(7): Show | a0000c0013t0001a0000c0014t0001a0001c0001t0001others(11): Show | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0012others(54): Show | 57 | 150 | 0.3800 | -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 | 111004315 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
a0000a0001a0002others(10): Show | a0000c0013a0000c0014a0001c0001others(14): Show | a0000c0013t0001a0000c0014t0001a0001c0001t0001others(28): Show | a0000c0013t0001g0046a0000c0014t0001g0072a0001c0001t0001g0005others(125): Show | 128 | 150 | 0.8533 | -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 | 111005383 | AG | A | intron_variant | MODIFIER | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
a0004a0008 | a0004c0005a0008c0008 | a0004c0005t0001a0004c0005t0002a0008c0008t0001 | a0004c0005t0001g0134a0004c0005t0002g0020a0004c0005t0002g0022others(3): Show | 6 | 150 | 0.0400 | -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 | 111009513 | CA | C | intron_variant | MODIFIER | HG00438.hp1 HG01175.hp2 HG01243.hp1 others(14): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(2): Show | a0001c0001t0001a0002c0002t0001a0003c0004t0001others(6): Show | a0001c0001t0001g0010a0001c0001t0001g0086a0002c0002t0001g0061others(14): Show | 17 | 150 | 0.1133 | -1 | c.128 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111013522 | CA | C | intron_variant | MODIFIER | HG00323.hp2 HG01081.hp1 HG03516.hp2 others(2): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0006 | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(1): Show | a0001c0001t0001g0028a0001c0001t0001g0067a0002c0002t0001g0099others(2): Show | 5 | 150 | 0.0333 | -1 | c.128 others(11): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |