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 | 8681458 | C | CTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0001c0021others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | a0001c0001t0001g0031 a0001c0001t0001g0051 a0001c0001t0001g0060 others(187): Show |
190 | 326 | 0.5828 | 2 | c.-42 others(19): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8682186 | T | TAC | intron_variant | MODIFIER | HG00280.hp2 HG00544.hp2 HG00639.hp2 others(81): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0001c0011others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0211 others(81): Show |
84 | 289 | 0.2907 | 2 | c.-42 others(19): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8683551 | T | TAA | intron_variant | MODIFIER | HG02818.hp1 HG02896.hp1 HG03239.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0005a0001c0003t0001others(4): Show | a0001c0001t0001g0011 a0001c0001t0005g0056 a0001c0003t0001g0028 others(5): Show |
8 | 153 | 0.0523 | 2 | c.-42 others(19): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8700911 | C | CTT | intron_variant | MODIFIER | HG01192.hp2 HG01243.hp2 HG02055.hp1 others(13): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0007others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(10): Show | a0001c0001t0001g0233 a0001c0001t0001g0240 a0001c0001t0003g0036 others(13): Show |
16 | 284 | 0.0563 | 2 | c.-42 others(21): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8706238 | A | AAT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(3): Show | a0001c0001t0003a0001c0003t0002a0002c0002t0001others(5): Show | a0001c0001t0003g0041 a0001c0003t0002g0170 a0002c0002t0001g0021 others(7): Show |
10 | 331 | 0.0302 | 2 | c.-41 others(21): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8706404 | C | CAA | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0011others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0031 a0001c0001t0001g0101 a0001c0001t0001g0104 others(87): Show |
90 | 219 | 0.4110 | 2 | c.-41 others(21): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8709826 | C | CTT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(223): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0003a0001c0011others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(68): Show | a0001c0001t0001g0031 a0001c0001t0001g0068 a0001c0001t0001g0070 others(223): Show |
226 | 329 | 0.6869 | 2 | c.-41 others(21): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8710713 | A | AGG | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00733.hp2 others(44): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0001c0021others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0119 others(44): Show |
47 | 359 | 0.1309 | 2 | c.-41 others(21): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8712005 | C | CGG | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(78): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0001c0021others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(38): Show | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0119 others(78): Show |
81 | 183 | 0.4426 | 2 | c.-41 others(21): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8713283 | T | TAA | intron_variant | MODIFIER | HG02155.hp2 HG02451.hp1 NA18979.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0003t0015a0002c0002t0001others(2): Show | a0001c0001t0001g0068 a0001c0001t0001g0151 a0001c0003t0015g0063 others(3): Show |
6 | 168 | 0.0357 | 2 | c.-41 others(21): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8729828 | T | TAA | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG01167.hp2 others(50): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(30): Show | a0001c0001t0001g0011 a0001c0001t0001g0233 a0001c0001t0001g0240 others(50): Show |
53 | 105 | 0.5048 | 2 | c.-41 others(19): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8732025 | T | TTA | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
a0002 | a0002c0007a0002c0008a0002c0009others(1): Show | a0002c0007t0003a0002c0007t0007a0002c0007t0011others(5): Show | a0002c0007t0003g0005 a0002c0007t0007g0242 a0002c0007t0011g0004 others(7): Show |
10 | 360 | 0.0278 | 2 | c.-41 others(19): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8736241 | C | CAT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(351): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0011others(20): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(95): Show | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0051 others(351): Show |
354 | 360 | 0.9833 | 2 | c.70+ others(15): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | chr16 | TogoVar | |||||||
ABAT_chr16_8669617_8789570 | 8737947 | A | AAG | intron_variant | MODIFIER | HG00673.hp1 HG03710.hp2 NA18942.hp2 |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0001a0001c0001t0003a0002c0005t0003 | a0001c0001t0001g0313 a0001c0001t0003g0092 a0002c0005t0003g0200 |
3 | 360 | 0.0083 | 2 | c.70+ others(17): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | chr16 | TogoVar | |||||||
ABAT_chr16_8669617_8789570 | 8742865 | C | CAA | intron_variant | MODIFIER | HG00733.hp2 HG02055.hp2 HG02257.hp2 others(12): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0051 a0001c0001t0001g0219 a0001c0001t0001g0240 others(12): Show |
15 | 119 | 0.1261 | 2 | c.71- others(17): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8743007 | T | TAA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0011others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(38): Show | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0051 others(165): Show |
168 | 204 | 0.8235 | 2 | c.71- others(17): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8743318 | C | CTG | intron_variant | MODIFIER | HG01123.hp1 HG01123.hp2 HG01243.hp1 others(27): Show |
a0002 | a0002c0002a0002c0004a0002c0006others(1): Show | a0002c0002t0001a0002c0002t0002a0002c0002t0003others(15): Show | a0002c0002t0001g0026 a0002c0002t0001g0266 a0002c0002t0002g0046 others(27): Show |
30 | 74 | 0.4054 | 2 | c.71- others(17): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8743423 | T | TTA | intron_variant | MODIFIER | NA18948.hp2 NA18979.hp2 NA18983.hp2 |
a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0284 a0001c0003t0004g0285 a0001c0003t0004g0289 |
3 | 276 | 0.0109 | 2 | c.71- others(17): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8743442 | T | TAC | intron_variant | MODIFIER | HG00544.hp1 HG02109.hp1 HG02559.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0155 a0001c0001t0002g0096 a0001c0001t0003g0036 others(4): Show |
7 | 360 | 0.0194 | 2 | c.71- others(17): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8743444 | T | TAC | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0011others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0051 others(165): Show |
168 | 266 | 0.6316 | 2 | c.71- others(17): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8743704 | T | TAA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0011others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(68): Show | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0051 others(259): Show |
262 | 356 | 0.7360 | 2 | c.71- others(17): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8749386 | C | CTT | intron_variant | MODIFIER | HG01433.hp1 HG01496.hp1 HG02523.hp2 others(7): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0005others(1): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0003others(5): Show | a0001c0001t0001g0278 a0001c0003t0001g0094 a0001c0003t0003g0262 others(7): Show |
10 | 52 | 0.1923 | 2 | c.199 others(19): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8750943 | C | CTT | intron_variant | MODIFIER | HG00408.hp1 HG02630.hp2 NA18946.hp2 others(4): Show |
a0002 | a0002c0002a0002c0004a0002c0007 | a0002c0002t0001a0002c0002t0002a0002c0002t0029others(2): Show | a0002c0002t0001g0081 a0002c0002t0002g0046 a0002c0002t0002g0047 others(4): Show |
7 | 196 | 0.0357 | 2 | c.316 others(17): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8759363 | T | TAA | intron_variant | MODIFIER | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(62): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0240 a0001c0001t0002g0138 a0001c0001t0003g0131 others(62): Show |
65 | 345 | 0.1884 | 2 | c.366 others(19): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8759369 | A | AAT | intron_variant | MODIFIER | HG00673.hp1 HG00673.hp2 HG00735.hp2 others(45): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0001c0013others(6): Show | a0001c0001t0002a0001c0003t0001a0001c0003t0003others(18): Show | a0001c0001t0002g0291 a0001c0003t0001g0028 a0001c0003t0003g0089 others(45): Show |
48 | 150 | 0.3200 | 2 | c.366 others(19): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 6/15 | chr16 | TogoVar | |||||||
ABAT_chr16_8669617_8789570 | 8764843 | G | GCA | intron_variant | MODIFIER | HG00609.hp2 HG00621.hp2 HG01123.hp1 others(43): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0003t0003others(14): Show | a0001c0001t0001g0267 a0001c0001t0003g0131 a0001c0003t0003g0084 others(43): Show |
46 | 340 | 0.1353 | 2 | c.540 others(15): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8772248 | G | GTC | intron_variant | MODIFIER | HG01099.hp1 NA18946.hp1 NA19009.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0002 | a0001c0001t0001g0180 a0001c0001t0002g0050 a0002c0002t0002g0047 |
3 | 360 | 0.0083 | 2 | c.817 others(17): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8773105 | T | TAC | intron_variant | MODIFIER | HG00544.hp1 HG00609.hp2 HG00733.hp1 others(25): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0119 others(25): Show |
28 | 55 | 0.5091 | 2 | c.954 others(17): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8775565 | T | TAC | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00733.hp2 others(36): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0006others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0051 a0001c0001t0001g0221 a0001c0001t0001g0316 others(36): Show |
39 | 55 | 0.7091 | 2 | c.112 others(19): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABAT_chr16_8669617_8789570 | 8785107 | C | CTT | downstream_gene_variant | MODIFIER | HG00733.hp2 HG00735.hp2 HG01106.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0004 | a0001c0001t0001a0001c0003t0001a0001c0003t0036others(1): Show | a0001c0001t0001g0051 a0001c0001t0001g0267 a0001c0003t0001g0235 others(4): Show |
7 | 197 | 0.0355 | 2 | c.*36 others(13): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 538 | chr16 | TogoVar | |||||||
ABAT_chr16_8669617_8789570 | 8787695 | C | CTT | downstream_gene_variant | MODIFIER | HG02280.hp1 HG02559.hp1 HG02683.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0008a0001c0003t0035a0002c0002t0008others(2): Show | a0001c0001t0008g0034 a0001c0003t0035g0261 a0002c0002t0008g0111 others(4): Show |
7 | 335 | 0.0209 | 2 | c.*62 others(13): Show |
ABAT | ENSG00000183044.12 | transcript | ENST00000268251.13 | protein_coding | 3126 | chr16 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69146164 | A | ACT | downstream_gene_variant | MODIFIER | HG00639.hp1 HG01109.hp2 HG01361.hp2 others(21): Show |
a0005a0006 | a0005c0005a0006c0007a0006c0016 | a0005c0005t0004a0005c0005t0015a0006c0007t0004others(2): Show | a0005c0005t0004g0185 a0005c0005t0004g0200 a0005c0005t0004g0214 others(21): Show |
24 | 196 | 0.1224 | 2 | c.*26 others(13): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1842 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69146206 | G | GGA | downstream_gene_variant | MODIFIER | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(45): Show |
a0004a0008 | a0004c0004a0004c0006a0008c0009 | a0004c0004t0003a0004c0004t0011a0004c0006t0003others(2): Show | a0004c0004t0003g0007 a0004c0004t0003g0010 a0004c0004t0003g0077 others(43): Show |
48 | 346 | 0.1387 | 2 | c.*26 others(13): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1800 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69146222 | A | AAT | downstream_gene_variant | MODIFIER | HG01346.hp2 HG01891.hp2 HG02922.hp2 |
a0001a0010a0016 | a0001c0001a0010c0022a0016c0037 | a0001c0001t0002a0010c0022t0012a0016c0037t0007 | a0001c0001t0002g0168 a0010c0022t0012g0139 a0016c0037t0007g0328 |
3 | 346 | 0.0087 | 2 | c.*26 others(13): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1784 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69146368 | A | AAT | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(74): Show |
a0001a0010a0011others(5): Show | a0001c0001a0001c0034a0001c0035others(7): Show | a0001c0001t0002a0001c0001t0008a0001c0001t0013others(9): Show | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0015 others(72): Show |
77 | 299 | 0.2575 | 2 | c.*24 others(13): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 1638 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69147216 | G | GTT | downstream_gene_variant | MODIFIER | HG00609.hp2 HG00733.hp2 HG01069.hp2 others(52): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0035a0002c0002others(7): Show | a0001c0001t0002a0001c0035t0002a0002c0002t0001others(9): Show | a0001c0001t0002g0015 a0001c0001t0002g0159 a0001c0001t0002g0298 others(52): Show |
55 | 70 | 0.7857 | 2 | c.*16 others(13): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 790 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69179208 | A | AAC | intron_variant | MODIFIER | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(37): Show |
a0004 | a0004c0004a0004c0006 | a0004c0004t0003a0004c0004t0011a0004c0006t0003others(1): Show | a0004c0004t0003g0007 a0004c0004t0003g0010 a0004c0004t0003g0077 others(36): Show |
40 | 346 | 0.1156 | 2 | c.276 others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69180600 | T | TTA | intron_variant | MODIFIER | HG02451.hp2 HG02572.hp1 HG03098.hp2 others(3): Show |
a0008 | a0008c0009 | a0008c0009t0009 | a0008c0009t0009g0005 a0008c0009t0009g0201 a0008c0009t0009g0227 others(2): Show |
6 | 346 | 0.0173 | 2 | c.276 others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 22/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69184849 | A | ATG | intron_variant | MODIFIER | HG02451.hp2 HG03098.hp2 HG03225.hp1 others(5): Show |
a0001a0008a0014 | a0001c0001a0008c0009a0014c0020 | a0001c0001t0002a0008c0009t0009a0014c0020t0006 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0008c0009t0009g0005 others(4): Show |
8 | 189 | 0.0423 | 2 | c.249 others(19): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69184871 | G | GTA | intron_variant | MODIFIER | HG00639.hp1 HG01069.hp1 HG01070.hp1 others(35): Show |
a0004a0005a0006others(1): Show | a0004c0004a0005c0005a0006c0007others(2): Show | a0004c0004t0003a0005c0005t0004a0005c0005t0015others(5): Show | a0004c0004t0003g0077 a0004c0004t0003g0209 a0004c0004t0003g0210 others(34): Show |
38 | 157 | 0.2420 | 2 | c.249 others(19): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69184916 | T | TAC | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(20): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(6): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(9): Show | a0001c0001t0002g0161 a0001c0001t0002g0257 a0001c0001t0006g0225 others(20): Show |
23 | 236 | 0.0975 | 2 | c.249 others(19): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 20/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69191657 | A | ATG | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(241): Show |
a0001a0002a0003others(16): Show | a0001c0001a0002c0002a0002c0015others(25): Show | a0001c0001t0006a0001c0001t0017a0002c0002t0001others(34): Show | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0014 others(234): Show |
244 | 346 | 0.7052 | 2 | c.187 others(19): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 16/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69195554 | C | CTT | intron_variant | MODIFIER | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(36): Show |
a0001a0004a0013 | a0001c0001a0004c0004a0004c0006others(1): Show | a0001c0001t0006a0004c0004t0003a0004c0006t0003others(2): Show | a0001c0001t0006g0226 a0004c0004t0003g0007 a0004c0004t0003g0010 others(35): Show |
39 | 51 | 0.7647 | 2 | c.123 others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 11/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69198086 | A | ACT | intron_variant | MODIFIER | HG00609.hp2 HG00733.hp2 HG01070.hp1 others(45): Show |
a0004a0008 | a0004c0004a0004c0006a0008c0009 | a0004c0004t0003a0004c0004t0011a0004c0006t0003others(2): Show | a0004c0004t0003g0007 a0004c0004t0003g0010 a0004c0004t0003g0077 others(43): Show |
48 | 346 | 0.1387 | 2 | c.117 others(19): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 10/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69202778 | C | CTT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
a0002a0003a0004others(15): Show | a0002c0002a0002c0015a0003c0003others(24): Show | a0002c0002t0001a0002c0002t0005a0002c0015t0001others(32): Show | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0011 others(228): Show |
238 | 346 | 0.6879 | 2 | c.100 others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69207534 | G | GAT | intron_variant | MODIFIER | HG02055.hp2 HG02129.hp1 HG02280.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006 | a0001c0001t0002g0029 a0001c0001t0002g0070 a0001c0001t0002g0265 others(3): Show |
6 | 346 | 0.0173 | 2 | c.100 others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69210847 | C | CAT | intron_variant | MODIFIER | HG02027.hp1 HG02451.hp1 HG03516.hp1 others(6): Show |
a0001a0014 | a0001c0001a0014c0020a0014c0021 | a0001c0001t0002a0001c0001t0013a0014c0020t0006others(1): Show | a0001c0001t0002g0149 a0001c0001t0002g0156 a0001c0001t0002g0158 others(6): Show |
9 | 252 | 0.0357 | 2 | c.100 others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69211314 | G | GAT | intron_variant | MODIFIER | HG02040.hp1 NA18971.hp2 NA19054.hp2 others(1): Show |
a0001 | a0001c0001a0001c0035 | a0001c0001t0002a0001c0035t0002 | a0001c0001t0002g0038 a0001c0001t0002g0163 a0001c0001t0002g0165 others(1): Show |
4 | 246 | 0.0163 | 2 | c.100 others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69211360 | T | TAC | intron_variant | MODIFIER | HG01074.hp1 HG01192.hp1 NA18945.hp2 others(6): Show |
a0001a0004a0012 | a0001c0001a0004c0004a0004c0006others(1): Show | a0001c0001t0002a0004c0004t0003a0004c0006t0003others(1): Show | a0001c0001t0002g0156 a0001c0001t0002g0158 a0001c0001t0002g0159 others(6): Show |
9 | 311 | 0.0289 | 2 | c.100 others(21): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | TogoVar | |||||||
ABCA10_chr17_69143007_69233824 | 69214390 | C | CTG | intron_variant | MODIFIER | HG01099.hp2 HG02559.hp1 HG02965.hp1 |
a0005 | a0005c0005 | a0005c0005t0004 | a0005c0005t0004g0214 a0005c0005t0004g0215 a0005c0005t0004g0262 |
3 | 346 | 0.0087 | 2 | c.100 others(19): Show |
ABCA10 | ENSG00000154263.18 | transcript | ENST00000690296.1 | protein_coding | 9/38 | chr17 | TogoVar |