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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TRIM24_chr7_138455259_138594996 | 138508690 | T | TGC | intron_variant | MODIFIER | HG01106.hp2 HG01168.hp1 HG01243.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0008a0001c0001t0012others(2): Show | a0001c0001t0003g0270 a0001c0001t0003g0273 a0001c0001t0003g0274 others(15): Show |
18 | 312 | 0.0577 | 2 | c.483 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138508692 | T | TGC | intron_variant | MODIFIER | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0012others(6): Show | a0001c0001t0002g0107 a0001c0001t0002g0170 a0001c0001t0002g0214 others(23): Show |
27 | 312 | 0.0865 | 2 | c.483 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138508708 | C | CGT | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(12): Show | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(86): Show |
89 | 312 | 0.2853 | 2 | c.483 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138508720 | C | CGT | intron_variant | MODIFIER | HG02109.hp2 HG02622.hp2 HG02818.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0003a0001c0003t0014 | a0001c0001t0003g0273 a0001c0003t0014g0079 a0001c0003t0014g0096 |
3 | 312 | 0.0096 | 2 | c.483 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138508722 | T | TGC | intron_variant | MODIFIER | HG02109.hp1 HG02630.hp2 HG03540.hp2 |
a0001 | a0001c0001 | a0001c0001t0026a0001c0001t0035 | a0001c0001t0026g0266 a0001c0001t0026g0267 a0001c0001t0035g0265 |
3 | 312 | 0.0096 | 2 | c.483 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138509701 | C | CAA | intron_variant | MODIFIER | HG01256.hp2 HG02055.hp1 HG02257.hp2 others(11): Show |
a0001a0003 | a0001c0001a0003c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0027others(2): Show | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0059 others(11): Show |
14 | 312 | 0.0449 | 2 | c.483 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138515403 | C | CCT | intron_variant | MODIFIER | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0010a0001c0001t0017a0001c0004t0056others(1): Show | a0001c0001t0010g0186 a0001c0001t0010g0187 a0001c0001t0010g0188 others(7): Show |
10 | 312 | 0.0321 | 2 | c.631 others(15): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | chr7 | TogoVar | |||||||
TRIM24_chr7_138455259_138594996 | 138516813 | G | GTT | intron_variant | MODIFIER | HG02647.hp1 HG02683.hp1 HG02735.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0011 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0256 others(7): Show |
10 | 312 | 0.0321 | 2 | c.631 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138523750 | C | CAA | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(7): Show | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(85): Show |
88 | 312 | 0.2821 | 2 | c.765 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138537379 | G | GTT | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(58): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(58): Show |
61 | 312 | 0.1955 | 2 | c.997 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138539801 | C | CTT | intron_variant | MODIFIER | HG02055.hp1 HG02155.hp1 HG02976.hp1 others(4): Show |
a0001a0003 | a0001c0001a0003c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0049others(1): Show | a0001c0001t0001g0041 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
7 | 312 | 0.0224 | 2 | c.114 others(21): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138543831 | G | GTT | intron_variant | MODIFIER | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0010a0001c0004t0056a0001c0004t0057 | a0001c0001t0010g0187 a0001c0001t0010g0188 a0001c0001t0010g0244 others(3): Show |
6 | 312 | 0.0192 | 2 | c.114 others(21): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138545163 | C | CGT | intron_variant | MODIFIER | HG00140.hp2 HG01891.hp1 HG02083.hp1 others(25): Show |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0043 a0001c0001t0002g0125 a0001c0001t0002g0144 others(25): Show |
28 | 312 | 0.0897 | 2 | c.114 others(21): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138550318 | G | GGT | intron_variant | MODIFIER | HG01496.hp1 HG01891.hp1 HG02630.hp1 others(9): Show |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(4): Show | a0001c0001t0001g0074 a0001c0001t0002g0147 a0001c0001t0006g0177 others(9): Show |
12 | 312 | 0.0385 | 2 | c.114 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138560275 | C | CTA | intron_variant | MODIFIER | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0010a0001c0004t0056a0001c0004t0057 | a0001c0001t0010g0186 a0001c0001t0010g0187 a0001c0001t0010g0188 others(4): Show |
7 | 312 | 0.0224 | 2 | c.153 others(21): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138570644 | G | GTT | intron_variant | MODIFIER | HG02027.hp1 HG02055.hp2 HG02165.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0056a0001c0004t0057 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0059 others(3): Show |
6 | 312 | 0.0192 | 2 | c.170 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138575459 | A | ATT | intron_variant | MODIFIER | HG01891.hp1 HG03139.hp2 HG03225.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0006a0001c0001t0058a0002c0006t0006 | a0001c0001t0006g0177 a0001c0001t0006g0178 a0001c0001t0006g0179 others(5): Show |
8 | 312 | 0.0256 | 2 | c.201 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138578532 | T | TTG | intron_variant | MODIFIER | HG01891.hp2 HG02027.hp2 HG02083.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0012a0001c0001t0024others(3): Show | a0001c0001t0002g0107 a0001c0001t0002g0126 a0001c0001t0002g0140 others(13): Show |
16 | 312 | 0.0513 | 2 | c.225 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138578559 | T | TGC | intron_variant | MODIFIER | HG01346.hp1 HG01978.hp2 HG01993.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(4): Show |
7 | 312 | 0.0224 | 2 | c.225 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138578563 | T | TGC | intron_variant | MODIFIER | HG01175.hp1 HG02647.hp1 HG02683.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0011a0001c0001t0021 | a0001c0001t0005g0253 a0001c0001t0005g0254 a0001c0001t0005g0259 others(8): Show |
11 | 312 | 0.0353 | 2 | c.225 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138578920 | G | GTA | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(2): Show | a0001c0001t0003g0001 a0001c0001t0003g0289 a0001c0001t0004g0281 others(4): Show |
8 | 312 | 0.0256 | 2 | c.225 others(19): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
TRIM24_chr7_138455259_138594996 | 138591048 | A | AGT | downstream_gene_variant | MODIFIER | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0005 a0001c0001t0017g0006 a0001c0001t0017g0007 |
3 | 312 | 0.0096 | 2 | c.*60 others(13): Show |
TRIM24 | ENSG00000122779.18 | transcript | ENST00000343526.9 | protein_coding | 1053 | chr7 | TogoVar | |||||||
TRIM25_chr17_56882909_56919049 | 56887322 | G | GCA | downstream_gene_variant | MODIFIER | HG02015.hp1 HG02132.hp1 HG02895.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0001 a0001c0001t0002g0151 |
3 | 384 | 0.0078 | 2 | c.*43 others(13): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 586 | chr17 | TogoVar | |||||||
TRIM25_chr17_56882909_56919049 | 56910168 | A | AAC | intron_variant | MODIFIER | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(14): Show |
a0001a0003 | a0001c0001a0003c0003a0003c0007 | a0001c0001t0002a0001c0001t0006a0003c0003t0007others(6): Show | a0001c0001t0002g0016 a0001c0001t0002g0075 a0001c0001t0002g0077 others(9): Show |
17 | 384 | 0.0443 | 2 | c.598 others(19): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | TogoVar | |||||||
TRIM25_chr17_56882909_56919049 | 56915711 | C | CAA | upstream_gene_variant | MODIFIER | HG00735.hp2 HG01168.hp1 HG01358.hp2 others(3): Show |
a0001a0002 | a0001c0008a0002c0002 | a0001c0008t0006a0002c0002t0003a0002c0002t0012 | a0001c0008t0006g0058 a0002c0002t0003g0002 a0002c0002t0012g0064 |
6 | 384 | 0.0156 | 2 | c.-17 others(13): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1663 | chr17 | TogoVar | |||||||
TRIM26_chr6_30179455_30218406 | 30182970 | C | CTT | downstream_gene_variant | MODIFIER | HG00733.hp2 HG01081.hp1 HG01358.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0161 a0001c0001t0001g0290 a0001c0001t0001g0291 others(11): Show |
14 | 441 | 0.0318 | 2 | c.*29 others(13): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1484 | chr6 | TogoVar | |||||||
TRIM26_chr6_30179455_30218406 | 30183968 | C | CAA | downstream_gene_variant | MODIFIER | NA18955.hp1 NA18990.hp2 NA18999.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0332 others(1): Show |
6 | 441 | 0.0136 | 2 | c.*19 others(13): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 486 | chr6 | TogoVar | |||||||
TRIM26_chr6_30179455_30218406 | 30186573 | G | GAA | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0003a0001c0002t0005a0001c0002t0006others(4): Show | a0001c0001t0003g0105 a0001c0002t0005g0004 a0001c0002t0005g0025 others(44): Show |
59 | 441 | 0.1338 | 2 | c.938 others(15): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | TogoVar | |||||||
TRIM26_chr6_30179455_30218406 | 30188217 | C | CAA | intron_variant | MODIFIER | HG00621.hp2 HG00639.hp2 HG01106.hp1 others(19): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0025 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(14): Show |
22 | 441 | 0.0499 | 2 | c.937 others(17): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 9/9 | chr6 | TogoVar | |||||||
TRIM26_chr6_30179455_30218406 | 30193062 | G | GTA | intron_variant | MODIFIER | HG02074.hp2 HG03017.hp2 HG04228.hp2 |
a0003 | a0003c0006 | a0003c0006t0005 | a0003c0006t0005g0044 a0003c0006t0005g0047 a0003c0006t0005g0050 |
3 | 441 | 0.0068 | 2 | c.766 others(19): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | TogoVar | |||||||
TRIM26_chr6_30179455_30218406 | 30193158 | G | GTA | intron_variant | MODIFIER | NA18612.hp1 NA18956.hp2 NA18989.hp1 others(5): Show |
a0002 | a0002c0004 | a0002c0004t0001a0002c0004t0023 | a0002c0004t0001g0168 a0002c0004t0001g0200 a0002c0004t0001g0204 others(5): Show |
8 | 441 | 0.0181 | 2 | c.766 others(19): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | TogoVar | |||||||
TRIM26_chr6_30179455_30218406 | 30193160 | G | GTA | intron_variant | MODIFIER | HG00673.hp1 HG01167.hp2 HG01168.hp1 others(8): Show |
a0001a0002 | a0001c0003a0002c0004 | a0001c0003t0025a0002c0004t0001 | a0001c0003t0025g0362 a0002c0004t0001g0196 a0002c0004t0001g0197 others(8): Show |
11 | 441 | 0.0249 | 2 | c.766 others(19): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | TogoVar | |||||||
TRIM26_chr6_30179455_30218406 | 30193182 | A | ATT | intron_variant | MODIFIER | HG01071.hp2 HG01516.hp1 HG02015.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0188 others(9): Show |
18 | 441 | 0.0408 | 2 | c.766 others(19): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | TogoVar | |||||||
TRIM26_chr6_30179455_30218406 | 30193193 | T | TTC | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
a0001 | a0001c0002 | a0001c0002t0005a0001c0002t0006 | a0001c0002t0005g0004 a0001c0002t0005g0005 a0001c0002t0005g0025 others(8): Show |
18 | 441 | 0.0408 | 2 | c.766 others(19): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 6/9 | chr6 | TogoVar | |||||||
TRIM26_chr6_30179455_30218406 | 30203798 | C | CTT | intron_variant | MODIFIER | HG00741.hp2 HG01074.hp1 HG01106.hp2 others(68): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0005a0001c0002t0006others(4): Show | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(48): Show |
71 | 441 | 0.1610 | 2 | c.-26 others(19): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 2/9 | chr6 | TogoVar | |||||||
TRIM26_chr6_30179455_30218406 | 30208904 | A | ATC | intron_variant | MODIFIER | HG00609.hp2 HG00738.hp1 HG01109.hp2 others(32): Show |
a0001a0003 | a0001c0002a0001c0003a0003c0006 | a0001c0002t0005a0001c0002t0006a0001c0002t0008others(5): Show | a0001c0002t0005g0004 a0001c0002t0005g0005 a0001c0002t0005g0025 others(24): Show |
35 | 441 | 0.0794 | 2 | c.-37 others(21): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | TogoVar | |||||||
TRIM26_chr6_30179455_30218406 | 30208904 | A | ATG | intron_variant | MODIFIER | HG00597.hp1 HG01516.hp1 HG01928.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0005t0001others(1): Show | a0001c0001t0001g0241 a0001c0001t0001g0324 a0001c0001t0002g0242 others(10): Show |
13 | 441 | 0.0295 | 2 | c.-37 others(21): Show |
TRIM26 | ENSG00000234127.9 | transcript | ENST00000454678.7 | protein_coding | 1/9 | chr6 | TogoVar | |||||||
TRIM27_chr6_28898002_28928985 | 28910123 | G | GAA | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(43): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(2): Show | a0001c0001t0002g0031 a0001c0001t0002g0062 a0001c0001t0002g0067 others(31): Show |
46 | 409 | 0.1125 | 2 | c.771 others(19): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | TogoVar | |||||||
TRIM27_chr6_28898002_28928985 | 28911339 | G | GAA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(201): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
204 | 409 | 0.4988 | 2 | c.770 others(17): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | TogoVar | |||||||
TRIM27_chr6_28898002_28928985 | 28913267 | A | AAT | intron_variant | MODIFIER | HG00673.hp2 HG01255.hp1 HG01255.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(1): Show | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(7): Show |
10 | 409 | 0.0245 | 2 | c.748 others(19): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | TogoVar | |||||||
TRIM27_chr6_28898002_28928985 | 28913269 | A | AAT | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(39): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0186 a0001c0001t0002g0094 a0001c0001t0002g0113 others(29): Show |
42 | 409 | 0.1027 | 2 | c.748 others(19): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | TogoVar | |||||||
TRIM27_chr6_28898002_28928985 | 28914581 | T | TGG | intron_variant | MODIFIER | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0001g0182 others(28): Show |
36 | 409 | 0.0880 | 2 | c.748 others(19): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | TogoVar | |||||||
TRIM27_chr6_28898002_28928985 | 28915293 | T | TAA | intron_variant | MODIFIER | HG00642.hp2 HG01123.hp2 HG02818.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0002t0002 | a0001c0001t0002g0128 a0001c0001t0003g0237 a0001c0001t0003g0238 others(6): Show |
9 | 409 | 0.0220 | 2 | c.748 others(19): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | TogoVar | |||||||
TRIM27_chr6_28898002_28928985 | 28928837 | C | CAA | upstream_gene_variant | MODIFIER | HG00621.hp2 HG00642.hp2 HG01243.hp1 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0020 others(15): Show |
20 | 409 | 0.0489 | 2 | c.-52 others(13): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4853 | chr6 | TogoVar | |||||||
TRIM28_chr19_58539064_58555715 | 58540341 | C | CAG | upstream_gene_variant | MODIFIER | HG01069.hp1 HG02258.hp1 HG02258.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0014 a0001c0001t0003g0040 |
5 | 402 | 0.0124 | 2 | c.-44 others(13): Show |
TRIM28 | ENSG00000130726.12 | transcript | ENST00000253024.10 | protein_coding | 3722 | chr19 | TogoVar | |||||||
TRIM28_chr19_58539064_58555715 | 58540443 | G | GAT | upstream_gene_variant | MODIFIER | HG01069.hp1 HG02258.hp1 HG02258.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0005 | a0001c0001t0002g0048 a0001c0001t0003g0014 a0001c0001t0003g0040 others(1): Show |
9 | 402 | 0.0224 | 2 | c.-43 others(13): Show |
TRIM28 | ENSG00000130726.12 | transcript | ENST00000253024.10 | protein_coding | 3620 | chr19 | TogoVar | |||||||
TRIM28_chr19_58539064_58555715 | 58541306 | C | CCA | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(103): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0001others(5): Show | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(17): Show |
106 | 402 | 0.2637 | 2 | c.-34 others(13): Show |
TRIM28 | ENSG00000130726.12 | transcript | ENST00000253024.10 | protein_coding | 2757 | chr19 | TogoVar | |||||||
TRIM28_chr19_58539064_58555715 | 58541311 | C | CAT | upstream_gene_variant | MODIFIER | HG01069.hp1 HG02258.hp1 HG02258.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0005 a0001c0001t0003g0014 a0001c0001t0003g0040 |
6 | 402 | 0.0149 | 2 | c.-34 others(13): Show |
TRIM28 | ENSG00000130726.12 | transcript | ENST00000253024.10 | protein_coding | 2752 | chr19 | TogoVar | |||||||
TRIM28_chr19_58539064_58555715 | 58541411 | G | GAT | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(115): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(20): Show |
118 | 402 | 0.2935 | 2 | c.-33 others(13): Show |
TRIM28 | ENSG00000130726.12 | transcript | ENST00000253024.10 | protein_coding | 2652 | chr19 | TogoVar | |||||||
TRIM28_chr19_58539064_58555715 | 58546291 | C | CTT | intron_variant | MODIFIER | HG01069.hp1 HG02258.hp1 HG02258.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0014 a0001c0001t0003g0040 |
5 | 402 | 0.0124 | 2 | c.586 others(17): Show |
TRIM28 | ENSG00000130726.12 | transcript | ENST00000253024.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |