view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ACSBG2_chr19_6130667_6198091 | 6161099 | C | CA | intron_variant | MODIFIER | HG01934.hp1 HG02145.hp1 HG02615.hp1 others(19): Show |
a0001a0002a0006others(1): Show | a0001c0001a0002c0002a0006c0006others(1): Show | a0001c0001t0003a0002c0002t0001a0006c0006t0001others(1): Show | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0143 others(19): Show |
22 | 116 | 0.1897 | 1 | c.508 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6162264 | C | CA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0017a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0017t0001others(10): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
118 | 248 | 0.4758 | 1 | c.588 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6162566 | C | CA | intron_variant | MODIFIER | HG00140.hp1 HG01978.hp2 HG02145.hp1 others(6): Show |
a0001a0002a0005others(2): Show | a0001c0001a0002c0002a0005c0007others(2): Show | a0001c0001t0003a0002c0002t0001a0002c0002t0004others(3): Show | a0001c0001t0003g0163 a0002c0002t0001g0042 a0002c0002t0001g0076 others(6): Show |
9 | 113 | 0.0796 | 1 | c.588 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6163783 | C | CA | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
a0001a0002a0005others(4): Show | a0001c0001a0001c0017a0001c0024others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0017t0001others(7): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(62): Show |
65 | 189 | 0.3439 | 1 | c.589 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6164434 | C | CT | intron_variant | MODIFIER | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(24): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(3): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0004others(4): Show | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0155 others(24): Show |
27 | 237 | 0.1139 | 1 | c.589 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6164913 | C | CT | intron_variant | MODIFIER | HG01884.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
a0007a0008 | a0007c0008a0008c0009 | a0007c0008t0002a0008c0009t0002 | a0007c0008t0002g0145 a0007c0008t0002g0161 a0007c0008t0002g0162 others(2): Show |
5 | 260 | 0.0192 | 1 | c.589 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6167988 | C | CA | intron_variant | MODIFIER | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0001 a0003c0005t0001g0133 a0003c0005t0001g0198 others(3): Show |
7 | 260 | 0.0269 | 1 | c.738 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6173937 | A | AT | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp1 HG01433.hp1 others(16): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0005 | a0001c0001t0001a0002c0002t0001a0003c0005t0001 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0056 others(15): Show |
19 | 215 | 0.0884 | 1 | c.739 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6179293 | A | AT | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
a0001a0002a0006others(3): Show | a0001c0001a0001c0024a0002c0002others(4): Show | a0001c0001t0001a0001c0024t0001a0002c0002t0001others(5): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
105 | 224 | 0.4688 | 1 | c.906 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6181221 | C | CA | intron_variant | MODIFIER | HG01175.hp1 HG01175.hp2 HG01255.hp2 others(5): Show |
a0001a0002a0006others(1): Show | a0001c0001a0002c0002a0006c0006others(1): Show | a0001c0001t0001a0002c0002t0001a0006c0006t0001others(1): Show | a0001c0001t0001g0002 a0001c0001t0001g0177 a0001c0001t0001g0194 others(5): Show |
8 | 215 | 0.0372 | 1 | c.907 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6182210 | T | TA | intron_variant | MODIFIER | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(18): Show |
a0001a0003a0006others(2): Show | a0001c0001a0003c0004a0003c0012others(3): Show | a0001c0001t0001a0001c0001t0003a0003c0004t0002others(4): Show | a0001c0001t0001g0015 a0001c0001t0003g0141 a0001c0001t0003g0142 others(18): Show |
21 | 255 | 0.0824 | 1 | c.907 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6184614 | G | GA | intron_variant | MODIFIER | HG01255.hp1 HG01255.hp2 NA18952.hp1 others(5): Show |
a0001a0002a0011 | a0001c0001a0002c0002a0011c0014 | a0001c0001t0001a0002c0002t0001a0011c0014t0001 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0001g0182 others(5): Show |
8 | 260 | 0.0308 | 1 | c.132 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6184832 | G | GA | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(47): Show |
a0001a0002a0011others(2): Show | a0001c0001a0001c0017a0002c0002others(3): Show | a0001c0001t0001a0001c0017t0001a0002c0002t0001others(4): Show | a0001c0001t0001g0130 a0001c0001t0001g0151 a0001c0001t0001g0153 others(47): Show |
50 | 111 | 0.4505 | 1 | c.132 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6186058 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0017a0001c0024others(7): Show | a0001c0001t0001a0001c0017t0001a0001c0024t0001others(8): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0034 others(119): Show |
122 | 245 | 0.4980 | 1 | c.154 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6186555 | G | GA | intron_variant | MODIFIER | HG01433.hp1 HG01891.hp1 NA18973.hp2 others(6): Show |
a0003a0013 | a0003c0005a0003c0011a0013c0016 | a0003c0005t0001a0003c0011t0001a0013c0016t0001 | a0003c0005t0001g0001 a0003c0005t0001g0133 a0003c0005t0001g0198 others(5): Show |
9 | 259 | 0.0347 | 1 | c.154 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6187002 | G | GT | intron_variant | MODIFIER | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(11): Show |
a0001a0002a0016 | a0001c0001a0002c0002a0016c0018 | a0001c0001t0001a0002c0002t0001a0002c0002t0004others(1): Show | a0001c0001t0001g0158 a0001c0001t0001g0180 a0001c0001t0001g0191 others(11): Show |
14 | 204 | 0.0686 | 1 | c.154 others(9): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6192071 | C | CA | intron_variant | MODIFIER | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(12): Show |
a0001a0002a0005others(2): Show | a0001c0001a0002c0002a0005c0007others(2): Show | a0001c0001t0001a0002c0002t0001a0005c0007t0001others(2): Show | a0001c0001t0001g0204 a0002c0002t0001g0079 a0002c0002t0001g0081 others(12): Show |
15 | 112 | 0.1339 | 1 | c.*36 others(8): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6193709 | C | CA | downstream_gene_variant | MODIFIER | HG00673.hp1 HG01884.hp2 HG02027.hp1 others(24): Show |
a0002a0003a0004others(4): Show | a0002c0002a0003c0004a0003c0012others(6): Show | a0002c0002t0001a0003c0004t0002a0003c0012t0002others(6): Show | a0002c0002t0001g0115 a0003c0004t0002g0006 a0003c0004t0002g0007 others(24): Show |
27 | 260 | 0.1038 | 1 | c.*10 others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 619 | chr19 | TogoVar | |||||||
ACSBG2_chr19_6130667_6198091 | 6195648 | C | CA | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
a0001a0002a0004others(7): Show | a0001c0001a0001c0017a0001c0020others(10): Show | a0001c0001t0001a0001c0017t0001a0001c0020t0001others(14): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
205 | 232 | 0.8836 | 1 | c.*30 others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2558 | chr19 | TogoVar | |||||||
ACSBG2_chr19_6130667_6198091 | 6197275 | C | CA | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(44): Show |
a0001a0002a0005others(3): Show | a0001c0001a0002c0002a0005c0007others(3): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0004others(5): Show | a0001c0001t0001g0017 a0001c0001t0001g0053 a0001c0001t0001g0132 others(44): Show |
47 | 136 | 0.3456 | 1 | c.*46 others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4185 | chr19 | TogoVar | |||||||
ACSBG2_chr19_6130667_6198091 | 6197508 | C | CT | downstream_gene_variant | MODIFIER | HG00597.hp1 HG00735.hp2 HG01074.hp2 others(11): Show |
a0001a0002a0012 | a0001c0001a0002c0002a0012c0025 | a0001c0001t0001a0002c0002t0001a0012c0025t0001 | a0001c0001t0001g0150 a0001c0001t0001g0159 a0001c0001t0001g0175 others(11): Show |
14 | 123 | 0.1138 | 1 | c.*48 others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4418 | chr19 | TogoVar | |||||||
ACSBG2_chr19_6130667_6198091 | 6197815 | C | CT | downstream_gene_variant | MODIFIER | HG00408.hp1 HG01433.hp2 HG01891.hp1 others(11): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0011others(3): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0005others(4): Show | a0001c0001t0001g0004 a0001c0001t0001g0186 a0001c0001t0001g0203 others(11): Show |
14 | 226 | 0.0619 | 1 | c.*51 others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4725 | chr19 | TogoVar | |||||||
ACSBG2_chr19_6130667_6198091 | 6197856 | A | AC | downstream_gene_variant | MODIFIER | HG03669.hp2 NA18973.hp2 NA18983.hp2 others(2): Show |
a0002a0003 | a0002c0002a0003c0005 | a0002c0002t0001a0003c0005t0001 | a0002c0002t0001g0124 a0003c0005t0001g0001 a0003c0005t0001g0243 others(1): Show |
5 | 260 | 0.0192 | 1 | c.*52 others(12): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4766 | chr19 | TogoVar | |||||||
ACSF2_chr17_50421218_50479837 | 50421507 | T | TA | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(27): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(2): Show | a0001c0001t0001g0035 a0001c0001t0001g0066 a0001c0001t0001g0077 others(20): Show |
30 | 268 | 0.1119 | 1 | c.-47 others(12): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4710 | chr17 | TogoVar | |||||||
ACSF2_chr17_50421218_50479837 | 50421646 | C | CT | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(44): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(6): Show | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0103 others(40): Show |
47 | 314 | 0.1497 | 1 | c.-46 others(12): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4571 | chr17 | TogoVar | |||||||
ACSF2_chr17_50421218_50479837 | 50422192 | C | CT | upstream_gene_variant | MODIFIER | HG00621.hp1 HG01106.hp1 HG01175.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(16): Show |
21 | 162 | 0.1296 | 1 | c.-40 others(12): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 4025 | chr17 | TogoVar | |||||||
ACSF2_chr17_50421218_50479837 | 50429521 | C | CT | intron_variant | MODIFIER | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(37): Show |
a0001a0002a0004 | a0001c0002a0001c0003a0002c0004others(2): Show | a0001c0002t0001a0001c0002t0002a0001c0003t0001others(4): Show | a0001c0002t0001g0027 a0001c0002t0001g0039 a0001c0002t0001g0130 others(33): Show |
40 | 318 | 0.1258 | 1 | c.128 others(9): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50433111 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
a0001a0003a0007 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(4): Show | a0001c0001t0001g0124 a0001c0001t0001g0158 a0001c0001t0001g0169 others(126): Show |
150 | 312 | 0.4808 | 1 | c.128 others(9): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50434695 | A | AT | intron_variant | MODIFIER | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0002 | a0001c0001t0001g0121 a0002c0004t0002g0012 a0002c0004t0002g0040 others(7): Show |
11 | 313 | 0.0351 | 1 | c.128 others(9): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50435358 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(2): Show | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0232 others(67): Show |
83 | 318 | 0.2610 | 1 | c.128 others(9): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50435601 | T | TG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(185): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(8): Show | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0001t0001g0228 others(159): Show |
188 | 318 | 0.5912 | 1 | c.128 others(9): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50436738 | C | CT | intron_variant | MODIFIER | HG01175.hp1 HG01255.hp1 HG02451.hp1 others(7): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(2): Show | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0093 others(6): Show |
10 | 316 | 0.0316 | 1 | c.128 others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50439232 | C | CT | intron_variant | MODIFIER | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(34): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(7): Show | a0001c0001t0001g0036 a0001c0001t0001g0060 a0001c0001t0001g0090 others(33): Show |
37 | 307 | 0.1205 | 1 | c.128 others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50439806 | T | TA | intron_variant | MODIFIER | HG00280.hp2 HG00733.hp2 HG01109.hp2 others(3): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0003a0001c0003t0001 | a0001c0002t0003g0031 a0001c0003t0001g0203 a0001c0003t0001g0204 others(3): Show |
6 | 318 | 0.0189 | 1 | c.128 others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50445806 | T | TA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(10): Show | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(154): Show |
183 | 315 | 0.5810 | 1 | c.129 others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50449010 | C | CT | intron_variant | MODIFIER | HG00741.hp2 HG01074.hp1 HG01109.hp1 others(18): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0060 others(17): Show |
21 | 313 | 0.0671 | 1 | c.129 others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50452526 | G | GC | intron_variant | MODIFIER | HG00423.hp2 HG02572.hp1 NA18987.hp2 others(1): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0049 a0001c0002t0002g0168 a0001c0003t0001g0236 others(1): Show |
4 | 318 | 0.0126 | 1 | c.129 others(9): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50453949 | T | TA | intron_variant | MODIFIER | HG01243.hp2 HG02145.hp1 HG02922.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0008 | a0001c0001t0001a0001c0002t0002a0002c0008t0001 | a0001c0001t0001g0049 a0001c0002t0002g0011 a0002c0008t0001g0263 others(1): Show |
6 | 315 | 0.0190 | 1 | c.129 others(9): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50454169 | A | AT | intron_variant | MODIFIER | HG00438.hp2 HG00738.hp1 HG01106.hp2 others(54): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(6): Show | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0037 others(49): Show |
57 | 240 | 0.2375 | 1 | c.129 others(9): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50460040 | A | AT | intron_variant | MODIFIER | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
a0001a0004 | a0001c0002a0004c0006 | a0001c0002t0002a0004c0006t0001 | a0001c0002t0002g0010 a0001c0002t0002g0241 a0001c0002t0002g0242 others(1): Show |
6 | 318 | 0.0189 | 1 | c.129 others(8): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50464769 | T | TG | intron_variant | MODIFIER | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0003c0005t0002 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0062 others(15): Show |
19 | 197 | 0.0964 | 1 | c.121 others(9): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50464771 | G | GT | intron_variant | MODIFIER | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0010 a0001c0002t0002g0241 a0001c0002t0002g0242 |
5 | 317 | 0.0158 | 1 | c.121 others(18): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | TogoVar | |||||||
ACSF2_chr17_50421218_50479837 | 50464778 | G | GT | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00738.hp1 others(47): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0002t0002a0001c0003t0001 | a0001c0002t0001g0108 a0001c0002t0002g0005 a0001c0002t0002g0006 others(41): Show |
50 | 315 | 0.1587 | 1 | c.121 others(18): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | chr17 | TogoVar | |||||||
ACSF2_chr17_50421218_50479837 | 50466091 | C | CT | intron_variant | MODIFIER | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(13): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002 | a0001c0002t0001g0027 a0001c0002t0001g0039 a0001c0002t0001g0239 others(12): Show |
16 | 318 | 0.0503 | 1 | c.121 others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50466263 | A | AT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
a0001a0007 | a0001c0001a0001c0003a0007c0010 | a0001c0001t0001a0001c0003t0001a0001c0003t0002others(1): Show | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0003t0001g0004 others(68): Show |
84 | 318 | 0.2642 | 1 | c.121 others(10): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50472019 | T | TC | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(6): Show |
a0001a0003 | a0001c0002a0003c0005 | a0001c0002t0002a0003c0005t0002 | a0001c0002t0002g0184 a0003c0005t0002g0021 a0003c0005t0002g0148 others(5): Show |
9 | 318 | 0.0283 | 1 | c.132 others(9): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ACSF2_chr17_50421218_50479837 | 50477023 | A | AT | downstream_gene_variant | MODIFIER | HG00423.hp2 HG00642.hp1 HG00738.hp1 others(61): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0082 others(54): Show |
64 | 314 | 0.2038 | 1 | c.*24 others(12): Show |
ACSF2 | ENSG00000167107.13 | transcript | ENST00000300441.9 | protein_coding | 2187 | chr17 | TogoVar | |||||||
ACSF3_chr16_89088852_89161233 | 89091161 | C | CG | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0005a0001c0014others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(37): Show | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0090 others(135): Show |
147 | 365 | 0.4027 | 1 | c.-30 others(12): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2690 | chr16 | TogoVar | |||||||
ACSF3_chr16_89088852_89161233 | 89092578 | A | AC | upstream_gene_variant | MODIFIER | HG01891.hp2 HG02109.hp2 HG02615.hp1 others(6): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0008others(2): Show | a0001c0001t0001a0001c0001t0011a0002c0002t0004others(3): Show | a0001c0001t0001g0016 a0001c0001t0011g0012 a0001c0001t0011g0013 others(6): Show |
9 | 366 | 0.0246 | 1 | c.-16 others(12): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1273 | chr16 | TogoVar | |||||||
ACSF3_chr16_89088852_89161233 | 89092817 | A | AT | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0005a0001c0014others(18): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(61): Show | a0001c0001t0001g0002 a0001c0001t0001g0089 a0001c0001t0001g0090 others(262): Show |
281 | 354 | 0.7938 | 1 | c.-13 others(12): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 1034 | chr16 | TogoVar |