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 | 110846641 | G | GCACA | intron_variant | MODIFIER | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0003t0001 | a0001c0001t0001g0117a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | 150 | 0.0467 | 4 | c.788 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110849749 | A | AAAAC | intron_variant | MODIFIER | HG01167.hp1 HG01981.hp1 HG02109.hp1 others(20): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0003c0004others(6): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(9): Show | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0113others(20): Show | 23 | 150 | 0.1533 | 4 | c.788 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110854473 | T | TTCCC | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0017a0003c0004others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0017t0002others(7): Show | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(25): Show | 28 | 150 | 0.1867 | 4 | c.788 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110883107 | G | GTTTT | intron_variant | MODIFIER | HG00423.hp2 HG00673.hp2 HG01243.hp2 others(2): Show |
a0001a0003a0004others(1): Show | a0001c0001a0003c0004a0004c0005others(1): Show | a0001c0001t0001a0003c0004t0001a0004c0005t0001others(1): Show | a0001c0001t0001g0029a0001c0001t0001g0150a0003c0004t0001g0027others(2): Show | 5 | 150 | 0.0333 | 4 | c.789 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110891059 | A | AATTC | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0017a0003c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(8): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(30): Show | 33 | 150 | 0.2200 | 4 | c.789 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110895667 | T | TAGAG | intron_variant | MODIFIER | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
a0001a0004a0014 | a0001c0001a0004c0005a0014c0020 | a0001c0001t0001a0001c0001t0005a0004c0005t0002others(1): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(6): Show | 9 | 150 | 0.0600 | 4 | c.789 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110900086 | T | TACAC | intron_variant | MODIFIER | HG00673.hp1 HG01257.hp2 HG01258.hp2 others(6): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(2): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(4): Show | a0001c0001t0001g0056a0001c0001t0001g0068a0002c0002t0001g0051others(6): Show | 9 | 150 | 0.0600 | 4 | 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 | 110901642 | C | CCACA | intron_variant | MODIFIER | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(4): Show |
a0001a0002a0014 | a0001c0001a0002c0002a0014c0020 | a0001c0001t0001a0001c0001t0005a0002c0002t0002others(1): Show | a0001c0001t0001g0018a0001c0001t0001g0145a0001c0001t0001g0150others(4): Show | 7 | 150 | 0.0467 | 4 | 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 | 110915336 | T | TTATA | intron_variant | MODIFIER | HG02280.hp1 HG02897.hp2 NA20300.hp2 others(1): Show |
a0001a0004a0006 | a0001c0001a0004c0005a0006c0006 | a0001c0001t0001a0001c0001t0006a0004c0005t0002others(1): Show | a0001c0001t0001g0011a0001c0001t0006g0017a0004c0005t0002g0004others(1): Show | 4 | 150 | 0.0267 | 4 | c.905 others(21): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110938707 | A | AAATG | intron_variant | MODIFIER | HG01891.hp1 HG03195.hp2 NA21309.hp2 |
a0002a0004 | a0002c0002a0004c0005 | a0002c0002t0001a0004c0005t0002 | a0002c0002t0001g0132a0004c0005t0002g0004a0004c0005t0002g0124 | 3 | 150 | 0.0200 | 4 | 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 | 110943321 | A | AAAAG | intron_variant | MODIFIER | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0001c0001t0005a0004c0005t0002 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(5): Show | 8 | 150 | 0.0533 | 4 | 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 | 110949391 | C | CTTTT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
a0000a0001a0002others(8): Show | a0000c0014a0001c0001a0001c0003others(12): Show | a0000c0014t0001a0001c0001t0001a0001c0001t0002others(25): Show | a0000c0014t0001g0072a0001c0001t0001g0008a0001c0001t0001g0010others(96): Show | 99 | 150 | 0.6600 | 4 | c.105 others(25): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110963565 | A | ATGTG | intron_variant | MODIFIER | HG00438.hp2 HG02027.hp1 NA18946.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0002g0101 | 3 | 150 | 0.0200 | 4 | c.106 others(25): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110968778 | C | CAAAA | intron_variant | MODIFIER | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(31): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(12): Show | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0067others(31): Show | 34 | 150 | 0.2267 | 4 | c.106 others(25): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110970497 | A | AAAAG | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(42): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0001c0012others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(13): Show | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0055others(42): Show | 45 | 150 | 0.3000 | 4 | c.106 others(25): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110975415 | A | AGTGT | intron_variant | MODIFIER | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(8): Show |
a0001a0013 | a0001c0001a0001c0017a0013c0011 | a0001c0001t0001a0001c0001t0002a0001c0017t0002others(1): Show | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0082others(8): Show | 11 | 150 | 0.0733 | 4 | c.106 others(25): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 110988857 | T | TTGTG | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(30): Show |
a0000a0001a0002 | a0000c0014a0001c0001a0002c0002 | a0000c0014t0001a0001c0001t0001a0001c0001t0002others(4): Show | a0000c0014t0001g0072a0001c0001t0001g0005a0001c0001t0001g0007others(30): Show | 33 | 150 | 0.2200 | 4 | c.116 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111003550 | C | CAAAA | intron_variant | MODIFIER | HG00140.hp2 HG01168.hp1 HG01255.hp1 others(8): Show |
a0001a0002a0013others(1): Show | a0001c0001a0001c0017a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(4): Show | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0088others(8): Show | 11 | 150 | 0.0733 | 4 | 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 | TCACA | intron_variant | MODIFIER | HG00438.hp2 HG01243.hp2 HG01891.hp1 others(16): Show |
a0001a0004a0008 | a0001c0001a0004c0005a0008c0008 | a0001c0001t0001a0001c0001t0002a0004c0005t0001others(2): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0024others(16): Show | 19 | 150 | 0.1267 | 4 | 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 | 111050019 | C | CACTG | intron_variant | MODIFIER | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(34): Show |
a0000a0001a0002others(6): Show | a0000c0014a0001c0001a0001c0017others(7): Show | a0000c0014t0001a0001c0001t0001a0001c0001t0002others(10): Show | a0000c0014t0001g0072a0001c0001t0001g0010a0001c0001t0001g0011others(34): Show | 37 | 150 | 0.2467 | 4 | 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 | 111068897 | A | AATAC | intron_variant | MODIFIER | HG01243.hp1 HG03195.hp2 HG03225.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0010a0002c0002t0001g0114a0002c0002t0001g0132 | 3 | 150 | 0.0200 | 4 | c.144 others(25): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111075465 | G | GTCTT | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0003a0001c0012others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(20): Show | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0024others(66): Show | 69 | 150 | 0.4600 | 4 | c.144 others(25): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACOXL_chr2_110727573_111123548 | 111089298 | A | AAAAC | intron_variant | MODIFIER | HG02257.hp2 HG03579.hp2 HG04115.hp1 others(2): Show |
a0001a0004a0009others(1): Show | a0001c0001a0004c0005a0009c0016others(1): Show | a0001c0001t0001a0001c0001t0002a0004c0005t0002others(2): Show | a0001c0001t0001g0049a0001c0001t0002g0048a0004c0005t0002g0004others(2): Show | 5 | 150 | 0.0333 | 4 | 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 | 111109671 | A | ATTTT | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp1 HG01168.hp1 others(16): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(7): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(16): Show | 19 | 150 | 0.1267 | 4 | c.154 others(23): Show |
ACOXL | ENSG00000153093.21 | transcript | ENST00000439055.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACP1_chr2_259947_283283 | 270849 | T | TTTTG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0001c0006others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(81): Show | 345 | 390 | 0.8846 | 4 | c.44- others(18): Show |
ACP1 | ENSG00000143727.16 | transcript | ENST00000272065.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACP2_chr11_47234302_47253814 | 47245857 | C | CGTGT | intron_variant | MODIFIER | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(17): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0058a0001c0001t0001g0059a0002c0002t0002g0004 | 20 | 358 | 0.0559 | 4 | c.298 others(17): Show |
ACP2 | ENSG00000134575.13 | transcript | ENST00000672073.1 | protein_coding | 3/10 | chr11 | TogoVar | ||||||
ACP3_chr3_132312407_132363841 | 132328679 | C | CAAAA | intron_variant | MODIFIER | HG00423.hp2 HG01074.hp2 HG01433.hp1 others(28): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(4): Show | a0001c0001t0001g0215a0001c0001t0001g0219a0001c0001t0002g0001others(21): Show | 31 | 368 | 0.0842 | 4 | c.216 others(19): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132337063 | G | GGTGT | intron_variant | MODIFIER | HG00323.hp2 HG01175.hp1 HG02273.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(7): Show | a0001c0001t0001g0118a0001c0001t0005g0294a0001c0001t0008g0162others(11): Show | 16 | 368 | 0.0435 | 4 | c.457 others(19): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132358033 | C | CAATA | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(88): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0003c0006others(1): Show | a0001c0001t0002a0001c0001t0012a0001c0001t0017others(4): Show | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0006others(76): Show | 91 | 368 | 0.2473 | 4 | c.*11 others(15): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 10/10 | 1202 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||
ACP3_chr3_132312407_132363841 | 132358076 | T | TAAAA | 3_prime_UTR_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0007others(1): Show | a0001c0001t0001a0001c0001t0015a0001c0001t0016others(5): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(63): Show | 76 | 368 | 0.2065 | 4 | c.*12 others(15): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 10/10 | 1204 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||
ACP3_chr3_132312407_132363841 | 132359505 | C | CTAAA | downstream_gene_variant | MODIFIER | HG02109.hp1 HG02258.hp2 NA19030.hp2 |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0012a0001c0001t0035 | a0001c0001t0009g0156a0001c0001t0012g0297a0001c0001t0035g0159 | 3 | 368 | 0.0082 | 4 | c.*26 others(15): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 665 | chr3 | TogoVar | ||||||
ACP5_chr19_11569660_11582645 | 11579344 | T | TTTGG | upstream_gene_variant | MODIFIER | HG01255.hp1 HG02074.hp1 HG02080.hp1 others(25): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(7): Show | 28 | 444 | 0.0631 | 4 | c.-17 others(15): Show |
ACP5 | ENSG00000102575.14 | transcript | ENST00000648477.1 | protein_coding | 1700 | chr19 | TogoVar | ||||||
ACP6_chr1_147637230_147675524 | 147652753 | G | GAAAA | intron_variant | MODIFIER | HG00673.hp2 HG01952.hp1 HG02145.hp2 others(5): Show |
a0001a0003a0004 | a0001c0001a0001c0003a0003c0013others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(3): Show | a0001c0001t0001g0150a0001c0001t0001g0167a0001c0001t0004g0086others(4): Show | 8 | 404 | 0.0198 | 4 | c.781 others(19): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 6/9 | chr1 | TogoVar | ||||||
ACP6_chr1_147637230_147675524 | 147671242 | C | CAAAA | upstream_gene_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(59): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(11): Show | a0001c0001t0004g0002a0001c0001t0004g0014a0001c0001t0004g0035others(41): Show | 62 | 404 | 0.1535 | 4 | c.-11 others(15): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 719 | chr1 | TogoVar | ||||||
ACP6_chr1_147637230_147675524 | 147671411 | T | TCAAA | upstream_gene_variant | MODIFIER | HG01169.hp1 HG01175.hp1 HG01978.hp1 others(19): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0011a0001c0001t0059others(6): Show | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0017others(14): Show | 22 | 404 | 0.0545 | 4 | c.-13 others(15): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 888 | chr1 | TogoVar | ||||||
ACP7_chr19_39079368_39116493 | 39088726 | G | GGTTT | intron_variant | MODIFIER | HG01255.hp1 HG02165.hp1 NA18949.hp1 others(3): Show |
a0001 | a0001c0002a0001c0003a0001c0004 | a0001c0002t0022a0001c0003t0003a0001c0004t0004 | a0001c0002t0022g0188a0001c0003t0003g0013a0001c0003t0003g0259others(3): Show | 6 | 402 | 0.0149 | 4 | c.121 others(21): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP7_chr19_39079368_39116493 | 39092370 | G | GTATA | intron_variant | MODIFIER | HG01361.hp1 HG01978.hp1 NA21309.hp1 |
a0001 | a0001c0003 | a0001c0003t0003a0001c0003t0032 | a0001c0003t0003g0279a0001c0003t0003g0298a0001c0003t0032g0113 | 3 | 402 | 0.0075 | 4 | c.122 others(21): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP7_chr19_39079368_39116493 | 39093090 | T | TTTTC | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
a0001a0003a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(24): Show | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(141): Show | 144 | 402 | 0.3582 | 4 | c.122 others(21): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP7_chr19_39079368_39116493 | 39093099 | T | TTTCC | intron_variant | MODIFIER | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(82): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0015a0001c0002t0002others(13): Show | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0083others(82): Show | 85 | 402 | 0.2114 | 4 | c.122 others(21): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP7_chr19_39079368_39116493 | 39093141 | C | CTGCT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(33): Show | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(212): Show | 215 | 402 | 0.5348 | 4 | c.122 others(21): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP7_chr19_39079368_39116493 | 39102118 | T | TCACA | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0015a0001c0002t0002others(17): Show | a0001c0001t0001g0353a0001c0001t0001g0398a0001c0001t0015g0199others(88): Show | 91 | 402 | 0.2264 | 4 | c.111 others(21): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP7_chr19_39079368_39116493 | 39102120 | T | TCACA | intron_variant | MODIFIER | HG01934.hp2 HG02622.hp2 NA18940.hp2 others(10): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0006a0001c0003t0003a0001c0003t0006others(1): Show | a0001c0001t0006g0136a0001c0003t0003g0277a0001c0003t0003g0303others(10): Show | 13 | 402 | 0.0323 | 4 | c.111 others(21): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP7_chr19_39079368_39116493 | 39102715 | T | TTTTC | intron_variant | MODIFIER | HG00621.hp2 HG00738.hp1 HG01069.hp2 others(10): Show |
a0001 | a0001c0003 | a0001c0003t0003a0001c0003t0006 | a0001c0003t0003g0001a0001c0003t0003g0003a0001c0003t0003g0222others(8): Show | 13 | 402 | 0.0323 | 4 | c.111 others(23): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP7_chr19_39079368_39116493 | 39102785 | C | CTCTT | intron_variant | MODIFIER | HG00597.hp2 HG02976.hp1 HG03139.hp2 others(3): Show |
a0001 | a0001c0002a0001c0009a0001c0017 | a0001c0002t0002a0001c0002t0005a0001c0009t0005others(2): Show | a0001c0002t0002g0011a0001c0002t0005g0031a0001c0002t0005g0227others(3): Show | 6 | 402 | 0.0149 | 4 | c.111 others(23): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP7_chr19_39079368_39116493 | 39103441 | G | GTGTT | intron_variant | MODIFIER | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
a0001 | a0001c0006a0001c0010 | a0001c0006t0008a0001c0006t0009a0001c0006t0010others(1): Show | a0001c0006t0008g0019a0001c0006t0008g0020a0001c0006t0008g0022others(11): Show | 14 | 402 | 0.0348 | 4 | c.111 others(23): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP7_chr19_39079368_39116493 | 39113773 | C | CAATT | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(54): Show | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(395): Show | 401 | 402 | 0.9975 | 4 | c.*36 others(15): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2281 | chr19 | TogoVar | ||||||
ACP7_chr19_39079368_39116493 | 39115096 | C | CAAAA | downstream_gene_variant | MODIFIER | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(26): Show |
a0001 | a0001c0001a0001c0004a0001c0006others(2): Show | a0001c0001t0001a0001c0001t0013a0001c0004t0004others(8): Show | a0001c0001t0001g0313a0001c0001t0001g0346a0001c0001t0001g0380others(26): Show | 29 | 402 | 0.0721 | 4 | c.*49 others(15): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 3604 | chr19 | TogoVar | ||||||
ACRV1_chr11_125666522_125685847 | 125678978 | T | TTATA | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
a0001a0005a0006others(1): Show | a0001c0001a0005c0009a0006c0007others(1): Show | a0001c0001t0001a0001c0001t0002a0005c0009t0001others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(17): Show | 116 | 426 | 0.2723 | 4 | c.53- others(17): Show |
ACRV1 | ENSG00000134940.14 | transcript | ENST00000533904.6 | protein_coding | 1/3 | chr11 | TogoVar | ||||||
ACRV1_chr11_125666522_125685847 | 125682789 | T | TTGGG | upstream_gene_variant | MODIFIER | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0036others(4): Show | 13 | 426 | 0.0305 | 4 | c.-20 others(15): Show |
ACRV1 | ENSG00000134940.14 | transcript | ENST00000533904.6 | protein_coding | 1943 | chr11 | TogoVar | ||||||
ACSBG1_chr15_78162468_78239565 | 78179815 | T | TCACA | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp2 HG01496.hp1 others(20): Show |
a0001a0002 | a0001c0001a0001c0013a0001c0021others(1): Show | a0001c0001t0001a0001c0001t0029a0001c0013t0001others(3): Show | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0026others(20): Show | 23 | 350 | 0.0657 | 4 | c.125 others(19): Show |
ACSBG1 | ENSG00000103740.10 | transcript | ENST00000258873.9 | protein_coding | 9/13 | chr15 | TogoVar |