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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ABAT_chr16_8669617_8789570 | 8731632 | C | CT | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG01081.hp2 others(55): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0021others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(26): Show | a0001c0001t0001g0068 a0001c0001t0001g0119 a0001c0001t0001g0141 others(55): Show |
58 | 357 | 0.1625 | 1 | c.-41 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8733127 | A | AC | intron_variant | MODIFIER | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(33): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(20): Show | a0001c0001t0001g0031 a0001c0001t0001g0101 a0001c0001t0001g0114 others(33): Show |
36 | 356 | 0.1011 | 1 | c.-41 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8733424 | C | CG | intron_variant | MODIFIER | HG00621.hp1 HG01255.hp1 HG02523.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0002a0001c0001t0004a0001c0003t0001others(3): Show | a0001c0001t0002g0062 a0001c0001t0002g0136 a0001c0001t0004g0320 others(4): Show |
7 | 360 | 0.0194 | 1 | c.-41 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8735046 | T | TA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0003a0001c0011others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | a0001c0001t0001g0011 a0001c0001t0001g0051 a0001c0001t0001g0070 others(205): Show |
208 | 334 | 0.6228 | 1 | c.-41 others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8735173 | C | CA | intron_variant | MODIFIER | HG00621.hp1 HG01978.hp1 HG02027.hp1 others(16): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0011 a0001c0001t0002g0062 a0001c0001t0002g0065 others(16): Show |
19 | 324 | 0.0586 | 1 | c.-41 others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8737314 | C | CA | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(55): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0002c0002others(6): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(24): Show | a0001c0001t0002g0027 a0001c0001t0002g0347 a0001c0001t0006g0298 others(55): Show |
58 | 359 | 0.1616 | 1 | c.70+ others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8737768 | C | CA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(165): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0003a0001c0011others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(59): Show | a0001c0001t0001g0031 a0001c0001t0001g0070 a0001c0001t0001g0091 others(165): Show |
168 | 360 | 0.4667 | 1 | c.70+ others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8737920 | T | TA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0003a0001c0011others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(72): Show | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0060 others(250): Show |
253 | 358 | 0.7067 | 1 | c.70+ others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8737945 | G | GA | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp1 HG02055.hp1 |
a0003 | a0003c0010 | a0003c0010t0001a0003c0010t0010 | a0003c0010t0001g0234 a0003c0010t0010g0338 a0003c0010t0010g0339 |
3 | 360 | 0.0083 | 1 | c.70+ others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8737989 | G | GA | intron_variant | MODIFIER | HG00609.hp1 HG02818.hp1 HG02896.hp1 |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0001a0002c0002t0001a0002c0002t0007 | a0001c0003t0001g0090 a0002c0002t0001g0340 a0002c0002t0007g0010 |
3 | 74 | 0.0405 | 1 | c.70+ others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8738615 | T | TG | intron_variant | MODIFIER | HG02145.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
a0001a0006 | a0001c0001a0006c0014 | a0001c0001t0002a0001c0001t0006a0006c0014t0001 | a0001c0001t0002g0291 a0001c0001t0006g0298 a0001c0001t0006g0307 others(1): Show |
4 | 359 | 0.0111 | 1 | c.70+ others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8740011 | C | CA | intron_variant | MODIFIER | HG02818.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0002c0002t0001a0002c0002t0002others(1): Show | a0001c0001t0003g0353 a0002c0002t0001g0340 a0002c0002t0002g0006 others(1): Show |
4 | 360 | 0.0111 | 1 | c.70+ others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8742865 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0011others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(65): Show | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0060 others(235): Show |
238 | 342 | 0.6959 | 1 | c.71- others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8743007 | T | TA | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0023others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(33): Show | a0001c0001t0001g0267 a0001c0001t0001g0278 a0001c0001t0001g0318 others(85): Show |
88 | 124 | 0.7097 | 1 | c.71- others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8748686 | G | GC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0011others(20): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(94): Show | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0051 others(352): Show |
355 | 360 | 0.9861 | 1 | c.198 others(16): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 4/15 | chr16 | TogoVar | |||||||
ABAT_chr16_8669617_8789570 | 8749090 | C | CT | intron_variant | MODIFIER | HG01169.hp1 HG01192.hp2 HG01891.hp2 others(9): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0009others(1): Show | a0001c0001t0003a0002c0002t0001a0002c0002t0006others(5): Show | a0001c0001t0003g0164 a0002c0002t0001g0009 a0002c0002t0001g0292 others(9): Show |
12 | 356 | 0.0337 | 1 | c.198 others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8749386 | C | CT | intron_variant | MODIFIER | HG00673.hp1 HG00673.hp2 HG01168.hp1 others(29): Show |
a0001a0002a0005 | a0001c0013a0002c0002a0002c0004others(4): Show | a0001c0013t0002a0002c0002t0003a0002c0002t0006others(14): Show | a0001c0013t0002g0196 a0001c0013t0002g0197 a0002c0002t0003g0239 others(29): Show |
32 | 74 | 0.4324 | 1 | c.199 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8750943 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(97): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | a0001c0001t0001g0068 a0001c0001t0001g0166 a0001c0001t0001g0322 others(97): Show |
100 | 289 | 0.3460 | 1 | c.316 others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8753092 | C | CT | intron_variant | MODIFIER | HG00438.hp1 HG00673.hp1 HG00673.hp2 others(41): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0013others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0003t0001others(18): Show | a0001c0001t0001g0233 a0001c0001t0003g0041 a0001c0003t0001g0028 others(41): Show |
44 | 348 | 0.1264 | 1 | c.316 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8754179 | T | TA | intron_variant | MODIFIER | HG01106.hp1 HG01496.hp1 HG02559.hp1 others(6): Show |
a0002 | a0002c0002a0002c0004a0002c0005others(2): Show | a0002c0002t0001a0002c0002t0002a0002c0004t0001others(5): Show | a0002c0002t0001g0340 a0002c0002t0002g0006 a0002c0004t0001g0079 others(6): Show |
9 | 56 | 0.1607 | 1 | c.317 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8755140 | G | GT | intron_variant | MODIFIER | HG00099.hp1 HG01106.hp2 HG02055.hp2 others(12): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0002c0017others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0316 a0001c0001t0001g0319 a0001c0001t0001g0333 others(12): Show |
15 | 360 | 0.0417 | 1 | c.317 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8755756 | C | CA | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(7): Show | a0001c0001t0002a0001c0001t0003a0001c0003t0003others(29): Show | a0001c0001t0002g0138 a0001c0001t0003g0131 a0001c0003t0003g0084 others(75): Show |
78 | 320 | 0.2438 | 1 | c.317 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8756048 | C | CA | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(73): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(7): Show | a0001c0001t0002a0001c0001t0003a0001c0003t0001others(29): Show | a0001c0001t0002g0138 a0001c0001t0003g0131 a0001c0003t0001g0099 others(73): Show |
76 | 359 | 0.2117 | 1 | c.317 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8756416 | C | CT | intron_variant | MODIFIER | HG02055.hp2 HG02572.hp1 HG03041.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0017 | a0001c0001t0002a0002c0002t0001a0002c0002t0045others(1): Show | a0001c0001t0002g0291 a0002c0002t0001g0329 a0002c0002t0045g0306 others(1): Show |
4 | 360 | 0.0111 | 1 | c.317 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8765706 | C | CA | intron_variant | MODIFIER | HG01106.hp2 HG02004.hp2 HG02109.hp1 others(32): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0002c0008others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0011 a0001c0001t0001g0148 a0001c0001t0001g0233 others(32): Show |
35 | 360 | 0.0972 | 1 | c.541 others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8767990 | T | TA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(49): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0021others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(20): Show | a0001c0001t0001g0361 a0001c0001t0002g0043 a0001c0001t0006g0298 others(49): Show |
52 | 357 | 0.1457 | 1 | c.604 others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8769557 | C | CA | intron_variant | MODIFIER | HG00621.hp2 HG01168.hp2 HG01346.hp1 others(24): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0269 a0001c0001t0002g0125 a0001c0001t0003g0036 others(24): Show |
27 | 203 | 0.1330 | 1 | c.816 others(8): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8769576 | A | AG | intron_variant | MODIFIER | HG01516.hp1 HG03669.hp2 NA19000.hp1 |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0001a0001c0001t0004a0002c0005t0003 | a0001c0001t0001g0119 a0001c0001t0004g0097 a0002c0005t0003g0173 |
3 | 349 | 0.0086 | 1 | c.816 others(16): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 11/15 | chr16 | TogoVar | |||||||
ABAT_chr16_8669617_8789570 | 8773159 | T | TA | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00733.hp2 others(11): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0043others(6): Show | a0001c0001t0001g0051 a0001c0001t0001g0221 a0001c0001t0001g0267 others(11): Show |
14 | 360 | 0.0389 | 1 | c.954 others(16): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 12/15 | chr16 | TogoVar | |||||||
ABAT_chr16_8669617_8789570 | 8778599 | A | AC | intron_variant | MODIFIER | HG01106.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
a0002a0003 | a0002c0002a0002c0009a0003c0010 | a0002c0002t0019a0002c0002t0020a0002c0002t0032others(3): Show | a0002c0002t0019g0002 a0002c0002t0020g0238 a0002c0002t0032g0149 others(4): Show |
7 | 360 | 0.0194 | 1 | c.127 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8778776 | C | CA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0011others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | a0001c0001t0001g0031 a0001c0001t0001g0104 a0001c0001t0001g0194 others(103): Show |
106 | 359 | 0.2953 | 1 | c.127 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8779368 | T | TG | intron_variant | MODIFIER | HG01106.hp2 HG01346.hp1 HG02630.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0021a0002c0002t0019a0002c0002t0020others(4): Show | a0001c0001t0021g0323 a0002c0002t0019g0002 a0002c0002t0020g0238 others(4): Show |
7 | 360 | 0.0194 | 1 | c.127 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8780763 | T | TA | intron_variant | MODIFIER | HG01175.hp1 HG02572.hp2 HG02622.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0003t0003others(3): Show | a0001c0001t0001g0166 a0001c0001t0004g0126 a0001c0001t0004g0325 others(5): Show |
8 | 220 | 0.0364 | 1 | c.138 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8780823 | T | TG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0011others(18): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(63): Show | a0001c0001t0002g0027 a0001c0001t0002g0042 a0001c0001t0002g0043 others(218): Show |
221 | 360 | 0.6139 | 1 | c.138 others(9): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8784813 | C | CT | downstream_gene_variant | MODIFIER | HG00438.hp1 HG02055.hp2 HG02976.hp2 others(6): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0012others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(4): Show | a0001c0001t0001g0166 a0001c0001t0001g0275 a0001c0001t0002g0096 others(6): Show |
9 | 255 | 0.0353 | 1 | c.*33 others(12): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 244 | chr16 | TogoVar | |||||||
ABAT_chr16_8669617_8789570 | 8785107 | C | CT | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(142): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0011others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(35): Show | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0060 others(142): Show |
145 | 335 | 0.4328 | 1 | c.*36 others(12): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 538 | chr16 | TogoVar | |||||||
ABAT_chr16_8669617_8789570 | 8785460 | C | CA | downstream_gene_variant | MODIFIER | HG01168.hp1 HG01169.hp2 HG01515.hp2 others(8): Show |
a0001a0002 | a0001c0013a0002c0002a0002c0004others(3): Show | a0001c0013t0002a0002c0002t0001a0002c0002t0007others(4): Show | a0001c0013t0002g0196 a0001c0013t0002g0197 a0002c0002t0001g0026 others(8): Show |
11 | 358 | 0.0307 | 1 | c.*40 others(12): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 891 | chr16 | TogoVar | |||||||
ABAT_chr16_8669617_8789570 | 8787695 | C | CT | downstream_gene_variant | MODIFIER | HG01074.hp1 HG01258.hp1 HG01515.hp2 others(19): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0022others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(12): Show | a0001c0001t0001g0011 a0001c0001t0001g0221 a0001c0001t0002g0152 others(19): Show |
22 | 350 | 0.0629 | 1 | c.*62 others(12): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 3126 | chr16 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69143833 | G | GA | downstream_gene_variant | MODIFIER | HG01346.hp2 HG02451.hp2 HG03098.hp2 others(4): Show |
a0002a0008a0016 | a0002c0002a0008c0009a0016c0037 | a0002c0002t0001a0008c0009t0009a0016c0037t0007 | a0002c0002t0001g0020 a0008c0009t0009g0005 a0008c0009t0009g0227 others(3): Show |
7 | 78 | 0.0897 | 1 | c.*49 others(12): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 4173 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69146320 | T | TA | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
a0002a0003a0005others(5): Show | a0002c0002a0002c0015a0003c0003others(8): Show | a0002c0002t0001a0002c0002t0005a0002c0015t0001others(11): Show | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0017 others(128): Show |
135 | 346 | 0.3902 | 1 | c.*25 others(12): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1686 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69146594 | C | CA | downstream_gene_variant | MODIFIER | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0002a0002c0002t0001a0003c0003t0001others(4): Show | a0001c0001t0002g0029 a0002c0002t0001g0064 a0002c0002t0001g0101 others(18): Show |
21 | 345 | 0.0609 | 1 | c.*22 others(12): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1412 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69147216 | G | GT | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
a0001a0002a0003others(18): Show | a0001c0001a0001c0034a0002c0002others(25): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(36): Show | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0029 others(256): Show |
266 | 281 | 0.9466 | 1 | c.*16 others(6): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 790 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69150219 | T | TA | intron_variant | MODIFIER | HG02451.hp2 HG03098.hp2 HG03225.hp1 others(2): Show |
a0008 | a0008c0009 | a0008c0009t0009 | a0008c0009t0009g0005 a0008c0009t0009g0227 a0008c0009t0009g0245 others(1): Show |
5 | 346 | 0.0145 | 1 | c.439 others(9): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 36/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69154420 | C | CT | intron_variant | MODIFIER | HG00609.hp2 HG00639.hp1 HG01070.hp1 others(65): Show |
a0001a0004a0005others(4): Show | a0001c0001a0004c0004a0004c0006others(6): Show | a0001c0001t0002a0001c0001t0006a0004c0004t0003others(11): Show | a0001c0001t0002g0299 a0001c0001t0006g0012 a0001c0001t0006g0013 others(64): Show |
68 | 130 | 0.5231 | 1 | c.369 others(8): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 30/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69165332 | C | CA | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
a0007 | a0007c0008 | a0007c0008t0004a0007c0008t0007 | a0007c0008t0004g0197 a0007c0008t0007g0009 a0007c0008t0007g0330 others(5): Show |
9 | 346 | 0.0260 | 1 | c.316 others(9): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69166339 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
a0001a0002a0003others(9): Show | a0001c0001a0002c0002a0002c0015others(12): Show | a0001c0001t0002a0002c0002t0001a0002c0002t0005others(16): Show | a0001c0001t0002g0031 a0001c0001t0002g0032 a0002c0002t0001g0002 others(141): Show |
148 | 344 | 0.4302 | 1 | c.316 others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69171934 | C | CA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
a0001a0003a0004others(11): Show | a0001c0001a0001c0034a0001c0035others(17): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(23): Show | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0015 others(143): Show |
149 | 330 | 0.4515 | 1 | c.316 others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 25/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69177973 | A | AT | intron_variant | MODIFIER | HG02735.hp2 NA18612.hp1 NA18984.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0030 a0001c0001t0002g0038 a0001c0001t0002g0109 others(5): Show |
8 | 108 | 0.0741 | 1 | c.277 others(20): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69179205 | C | CA | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
a0002a0003a0005others(9): Show | a0002c0002a0002c0015a0003c0003others(12): Show | a0002c0002t0001a0002c0002t0005a0002c0015t0001others(15): Show | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0011 others(142): Show |
150 | 344 | 0.4360 | 1 | c.276 others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69179626 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
a0002a0003a0005others(7): Show | a0002c0002a0002c0015a0003c0003others(10): Show | a0002c0002t0001a0002c0002t0005a0002c0015t0001others(13): Show | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0011 others(138): Show |
145 | 346 | 0.4191 | 1 | c.276 others(10): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | TogoVar |