view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TRIM3_chr11_6443613_6478941 | 6455267 | CAT | C | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(109): Show |
a0001a0005a0007others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(12): Show | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0049others(88): Show | 112 | 384 | 0.2917 | -2 | c.153 others(19): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 7/11 | chr11 | TogoVar | |||||||
TRIM3_chr11_6443613_6478941 | 6460370 | AAG | A | intron_variant | MODIFIER | HG02040.hp2 HG02155.hp1 NA18981.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005a0001c0001t0001g0116a0001c0001t0001g0163 | 7 | 384 | 0.0182 | -2 | c.132 others(19): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | TogoVar | |||||||
TRIM3_chr11_6443613_6478941 | 6464986 | CAA | C | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(6): Show | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(46): Show | 61 | 384 | 0.1589 | -2 | c.131 others(17): Show |
TRIM3 | ENSG00000110171.21 | transcript | ENST00000345851.8 | protein_coding | 2/11 | chr11 | TogoVar | |||||||
TRIM40_chr6_30131140_30153728 | 30132911 | CTT | C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00621.hp2 HG00735.hp2 others(28): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(6): Show | 31 | 459 | 0.0675 | -2 | c.-35 others(13): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 3228 | chr6 | TogoVar | |||||||
TRIM40_chr6_30131140_30153728 | 30135216 | CAA | C | upstream_gene_variant | MODIFIER | HG02074.hp2 HG02630.hp1 HG02723.hp1 others(11): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0011a0004c0004t0010 | a0001c0001t0011g0024a0001c0001t0011g0033a0001c0001t0011g0043others(4): Show | 14 | 459 | 0.0305 | -2 | c.-12 others(13): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 923 | chr6 | TogoVar | |||||||
TRIM40_chr6_30131140_30153728 | 30138066 | TAC | T | intron_variant | MODIFIER | HG00738.hp2 HG01109.hp1 HG01975.hp1 others(19): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0001c0001t0011a0003c0003t0009 | a0001c0001t0001g0022a0001c0001t0001g0098a0001c0001t0001g0099others(5): Show | 22 | 459 | 0.0479 | -2 | c.345 others(17): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
TRIM40_chr6_30131140_30153728 | 30139337 | TTC | T | intron_variant | MODIFIER | HG02145.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0022 | a0001c0001t0007g0025a0001c0001t0007g0035a0001c0001t0007g0052others(3): Show | 9 | 459 | 0.0196 | -2 | c.345 others(19): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
TRIM40_chr6_30131140_30153728 | 30139339 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0012 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0012g0056 | 6 | 459 | 0.0131 | -2 | c.345 others(19): Show |
TRIM40 | ENSG00000204614.9 | transcript | ENST00000396581.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
TRIM41_chr5_181218281_181240808 | 181221139 | TAA | T | upstream_gene_variant | MODIFIER | HG00438.hp1 HG00597.hp1 HG00735.hp2 others(82): Show |
a0001a0002a0004others(3): Show | a0001c0001a0002c0002a0002c0014others(4): Show | a0001c0001t0005a0002c0002t0002a0002c0002t0007others(7): Show | a0001c0001t0005g0031a0002c0002t0002g0003a0002c0002t0002g0007others(51): Show | 85 | 398 | 0.2136 | -2 | c.-28 others(13): Show |
TRIM41 | ENSG00000146063.20 | transcript | ENST00000315073.10 | protein_coding | 2141 | chr5 | TogoVar | |||||||
TRIM41_chr5_181218281_181240808 | 181225541 | GAT | G | intron_variant | MODIFIER | HG02809.hp1 HG02896.hp1 HG02897.hp2 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0139a0001c0001t0005g0140a0001c0001t0005g0141 | 3 | 398 | 0.0075 | -2 | c.813 others(17): Show |
TRIM41 | ENSG00000146063.20 | transcript | ENST00000315073.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
TRIM41_chr5_181218281_181240808 | 181228558 | CAA | C | intron_variant | MODIFIER | HG00408.hp2 HG01106.hp2 HG01243.hp2 others(26): Show |
a0001a0002a0005 | a0001c0003a0002c0002a0005c0010 | a0001c0003t0003a0001c0003t0008a0001c0003t0016others(2): Show | a0001c0003t0003g0016a0001c0003t0003g0017a0001c0003t0003g0029others(22): Show | 29 | 398 | 0.0729 | -2 | c.814 others(19): Show |
TRIM41 | ENSG00000146063.20 | transcript | ENST00000315073.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
TRIM41_chr5_181218281_181240808 | 181235148 | CTT | C | 3_prime_UTR_variant | MODIFIER | HG00735.hp2 HG01106.hp2 HG01257.hp2 others(23): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0018others(3): Show | a0001c0001t0006a0001c0003t0008a0001c0003t0016others(6): Show | a0001c0001t0006g0031a0001c0001t0006g0109a0001c0001t0006g0136others(22): Show | 26 | 398 | 0.0653 | -2 | c.*37 others(11): Show |
TRIM41 | ENSG00000146063.20 | transcript | ENST00000315073.10 | protein_coding | 6/6 | 375 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
TRIM41_chr5_181218281_181240808 | 181239373 | CAA | C | downstream_gene_variant | MODIFIER | HG02055.hp2 HG02257.hp1 HG02922.hp2 others(2): Show |
a0001a0002 | a0001c0007a0002c0002 | a0001c0007t0005a0001c0007t0010a0002c0002t0002 | a0001c0007t0005g0055a0001c0007t0010g0027a0001c0007t0010g0054others(1): Show | 5 | 398 | 0.0126 | -2 | c.*45 others(13): Show |
TRIM41 | ENSG00000146063.20 | transcript | ENST00000315073.10 | protein_coding | 3566 | chr5 | TogoVar | |||||||
TRIM42_chr3_140673064_140706150 | 140673862 | CTA | C | upstream_gene_variant | MODIFIER | HG03490.hp2 HG03831.hp1 HG04204.hp1 others(1): Show |
a0001 | a0001c0001a0001c0016 | a0001c0001t0001a0001c0016t0001 | a0001c0001t0001g0057a0001c0001t0001g0200a0001c0001t0001g0212others(1): Show | 4 | 410 | 0.0098 | -2 | c.-43 others(13): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4201 | chr3 | TogoVar | |||||||
TRIM42_chr3_140673064_140706150 | 140686430 | CAT | C | intron_variant | MODIFIER | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(35): Show |
a0001a0005 | a0001c0001a0005c0006 | a0001c0001t0001a0005c0006t0001 | a0001c0001t0001g0009a0001c0001t0001g0048a0001c0001t0001g0049others(26): Show | 38 | 410 | 0.0927 | -2 | c.104 others(21): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 2/4 | chr3 | TogoVar | |||||||
TRIM42_chr3_140673064_140706150 | 140692530 | TAC | T | intron_variant | MODIFIER | HG02258.hp2 HG02717.hp2 HG03195.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0059a0001c0001t0001g0201a0001c0001t0001g0204others(1): Show | 5 | 410 | 0.0122 | -2 | c.208 others(21): Show |
TRIM42 | ENSG00000155890.4 | transcript | ENST00000286349.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TRIM43B_chr2_95472008_95489754 | 95474133 | TAC | T | downstream_gene_variant | MODIFIER | HG00673.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 6 | 424 | 0.0142 | -2 | c.*30 others(13): Show |
TRIM43B | ENSG00000144010.11 | transcript | ENST00000639673.3 | protein_coding | 2874 | chr2 | TogoVar | |||||||
TRIM43B_chr2_95472008_95489754 | 95481768 | ATC | A | intron_variant | MODIFIER | HG00733.hp1 HG03927.hp2 HG06807.hp2 |
a0001a0007a0008 | a0001c0002a0007c0011a0008c0010 | a0001c0002t0001a0007c0011t0002a0008c0010t0001 | a0001c0002t0001g0078a0007c0011t0002g0082a0008c0010t0001g0044 | 3 | 424 | 0.0071 | -2 | c.412 others(15): Show |
TRIM43B | ENSG00000144010.11 | transcript | ENST00000639673.3 | protein_coding | 2/6 | chr2 | TogoVar | |||||||
TRIM43_chr2_95587001_95604778 | 95594724 | AAT | A | intron_variant | MODIFIER | HG01891.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0028a0001c0001t0001g0074a0001c0001t0001g0075others(1): Show | 5 | 394 | 0.0127 | -2 | c.411 others(17): Show |
TRIM43 | ENSG00000144015.5 | transcript | ENST00000272395.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TRIM43_chr2_95587001_95604778 | 95595392 | CAG | C | intron_variant | MODIFIER | HG02055.hp2 HG02602.hp2 HG03471.hp2 others(1): Show |
a0005a0006a0008 | a0005c0013a0005c0017a0006c0015others(1): Show | a0005c0013t0001a0005c0017t0004a0006c0015t0001others(1): Show | a0005c0013t0001g0040a0005c0017t0004g0032a0006c0015t0001g0042others(1): Show | 4 | 394 | 0.0102 | -2 | c.507 others(17): Show |
TRIM43 | ENSG00000144015.5 | transcript | ENST00000272395.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
TRIM43_chr2_95587001_95604778 | 95602569 | TTG | T | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(30): Show |
a0001a0002 | a0001c0001a0001c0016a0002c0003 | a0001c0001t0001a0001c0001t0003a0001c0016t0001others(1): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0030others(8): Show | 33 | 394 | 0.0838 | -2 | c.*29 others(13): Show |
TRIM43 | ENSG00000144015.5 | transcript | ENST00000272395.3 | protein_coding | 2792 | chr2 | TogoVar | |||||||
TRIM44_chr11_35657775_35823007 | 35665586 | GTT | G | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(95): Show |
a0001a0003 | a0001c0001a0003c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(29): Show | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0105others(94): Show | 98 | 392 | 0.2500 | -2 | c.669 others(19): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM44_chr11_35657775_35823007 | 35680911 | CAG | C | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0018a0001c0001t0021a0001c0001t0028others(4): Show | a0001c0001t0018g0376a0001c0001t0018g0377a0001c0001t0018g0379others(10): Show | 13 | 392 | 0.0332 | -2 | c.670 others(19): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | chr11 | TogoVar | |||||||
TRIM44_chr11_35657775_35823007 | 35681952 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00738.hp1 HG01071.hp1 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(13): Show | a0001c0001t0003g0226a0001c0001t0003g0265a0001c0001t0004g0065others(18): Show | 21 | 392 | 0.0536 | -2 | c.670 others(19): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM44_chr11_35657775_35823007 | 35715404 | ATG | A | intron_variant | MODIFIER | HG02132.hp1 NA19002.hp2 NA19011.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0020a0001c0001t0054 | a0001c0001t0003g0239a0001c0001t0003g0251a0001c0001t0020g0222others(1): Show | 4 | 392 | 0.0102 | -2 | c.748 others(21): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM44_chr11_35657775_35823007 | 35718883 | CTT | C | intron_variant | MODIFIER | HG00423.hp1 HG00609.hp1 HG00639.hp2 others(79): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(21): Show | a0001c0001t0002g0295a0001c0001t0003g0013a0001c0001t0003g0148others(77): Show | 82 | 392 | 0.2092 | -2 | c.748 others(19): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM44_chr11_35657775_35823007 | 35725066 | TCA | T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00738.hp2 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0097a0001c0001t0001g0174a0001c0001t0001g0233others(17): Show | 21 | 392 | 0.0536 | -2 | c.748 others(17): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM44_chr11_35657775_35823007 | 35726683 | TAA | T | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(77): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0010others(16): Show | a0001c0001t0001g0093a0001c0001t0001g0138a0001c0001t0001g0141others(76): Show | 80 | 392 | 0.2041 | -2 | c.987 others(17): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM44_chr11_35657775_35823007 | 35740142 | ATT | A | intron_variant | MODIFIER | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0045 | a0001c0001t0011g0156a0001c0001t0011g0157a0001c0001t0011g0159others(4): Show | 7 | 392 | 0.0179 | -2 | c.100 others(21): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM44_chr11_35657775_35823007 | 35742773 | TAC | T | intron_variant | MODIFIER | HG02559.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0020a0001c0001t0108 | a0001c0001t0020g0222a0001c0001t0020g0223a0001c0001t0020g0224others(2): Show | 5 | 392 | 0.0128 | -2 | c.100 others(21): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM44_chr11_35657775_35823007 | 35766643 | CCT | C | intron_variant | MODIFIER | HG01884.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0014a0001c0001t0071 | a0001c0001t0014g0096a0001c0001t0014g0103a0001c0001t0014g0119others(1): Show | 4 | 392 | 0.0102 | -2 | c.100 others(23): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | chr11 | TogoVar | |||||||
TRIM44_chr11_35657775_35823007 | 35790561 | ATG | A | intron_variant | MODIFIER | HG00735.hp2 HG01361.hp2 HG01934.hp2 others(33): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0013a0001c0001t0025others(4): Show | a0001c0001t0005g0001a0001c0001t0005g0014a0001c0001t0005g0015others(33): Show | 36 | 392 | 0.0918 | -2 | c.100 others(23): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM44_chr11_35657775_35823007 | 35792072 | TAC | T | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0021a0001c0001t0028a0001c0001t0085others(1): Show | a0001c0001t0021g0370a0001c0001t0021g0371a0001c0001t0021g0380others(5): Show | 8 | 392 | 0.0204 | -2 | c.100 others(23): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM44_chr11_35657775_35823007 | 35793180 | AAG | A | intron_variant | MODIFIER | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(23): Show |
a0001 | a0001c0001 | a0001c0001t0014a0001c0001t0020a0001c0001t0033others(11): Show | a0001c0001t0014g0096a0001c0001t0014g0103a0001c0001t0014g0106others(23): Show | 26 | 392 | 0.0663 | -2 | c.100 others(23): Show |
TRIM44 | ENSG00000166326.7 | transcript | ENST00000299413.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM45_chr1_117106060_117126749 | 117110000 | CAG | C | downstream_gene_variant | MODIFIER | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(73): Show |
a0002a0003a0008 | a0002c0002a0002c0014a0003c0003others(1): Show | a0002c0002t0002a0002c0002t0011a0002c0002t0026others(4): Show | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(14): Show | 76 | 354 | 0.2147 | -2 | c.*23 others(13): Show |
TRIM45 | ENSG00000134253.10 | transcript | ENST00000256649.9 | protein_coding | 1059 | chr1 | TogoVar | |||||||
TRIM45_chr1_117106060_117126749 | 117118909 | CCT | C | intron_variant | MODIFIER | HG03490.hp1 HG03492.hp1 HG03669.hp1 others(1): Show |
a0005 | a0005c0005 | a0005c0005t0003 | a0005c0005t0003g0011 | 4 | 354 | 0.0113 | -2 | c.489 others(17): Show |
TRIM45 | ENSG00000134253.10 | transcript | ENST00000256649.9 | protein_coding | 1/5 | chr1 | TogoVar | |||||||
TRIM45_chr1_117106060_117126749 | 117123041 | GAA | G | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0010a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0009a0001c0001t0019others(16): Show | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(36): Show | 187 | 354 | 0.5283 | -2 | c.-18 others(13): Show |
TRIM45 | ENSG00000134253.10 | transcript | ENST00000256649.9 | protein_coding | 1293 | chr1 | TogoVar | |||||||
TRIM46_chr1_155168849_155189970 | 155171808 | CCT | C | upstream_gene_variant | MODIFIER | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(10): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0002a0001c0002t0001g0009a0001c0002t0001g0020 | 13 | 348 | 0.0374 | -2 | c.-21 others(13): Show |
TRIM46 | ENSG00000163462.19 | transcript | ENST00000334634.9 | protein_coding | 2040 | chr1 | TogoVar | |||||||
TRIM46_chr1_155168849_155189970 | 155182843 | CAA | C | intron_variant | MODIFIER | HG01081.hp2 HG01255.hp1 HG02486.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0072others(2): Show | 9 | 348 | 0.0259 | -2 | c.188 others(19): Show |
TRIM46 | ENSG00000163462.19 | transcript | ENST00000334634.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
TRIM47_chr17_75869164_75883581 | 75870657 | TCA | T | downstream_gene_variant | MODIFIER | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0011 | 5 | 374 | 0.0134 | -2 | c.*38 others(13): Show |
TRIM47 | ENSG00000132481.7 | transcript | ENST00000254816.6 | protein_coding | 3506 | chr17 | TogoVar | |||||||
TRIM47_chr17_75869164_75883581 | 75880334 | CTT | C | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(31): Show |
a0002 | a0002c0002a0002c0006a0002c0017 | a0002c0002t0001a0002c0002t0004a0002c0002t0007others(2): Show | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0012others(5): Show | 34 | 374 | 0.0909 | -2 | c.-17 others(13): Show |
TRIM47 | ENSG00000132481.7 | transcript | ENST00000254816.6 | protein_coding | 1754 | chr17 | TogoVar | |||||||
TRIM48_chr11_55257155_55276114 | 55273180 | TTA | T | downstream_gene_variant | MODIFIER | HG01109.hp1 HG02717.hp2 HG03098.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0025a0001c0001t0002g0055 | 3 | 272 | 0.0110 | -2 | c.*27 others(13): Show |
TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2067 | chr11 | TogoVar | |||||||
TRIM48_chr11_55257155_55276114 | 55273202 | TAA | T | downstream_gene_variant | MODIFIER | HG02615.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0011a0001c0001t0002g0025 | 6 | 272 | 0.0221 | -2 | c.*27 others(13): Show |
TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2089 | chr11 | TogoVar | |||||||
TRIM48_chr11_55257155_55276114 | 55273213 | TAA | T | downstream_gene_variant | MODIFIER | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0012 | 4 | 272 | 0.0147 | -2 | c.*27 others(13): Show |
TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2100 | chr11 | TogoVar | |||||||
TRIM48_chr11_55257155_55276114 | 55273271 | TTA | T | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(18): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0012 | a0001c0001t0002a0002c0002t0002a0002c0002t0003others(1): Show | a0001c0001t0002g0055a0002c0002t0002g0053a0002c0002t0002g0054others(4): Show | 21 | 272 | 0.0772 | -2 | c.*28 others(13): Show |
TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2158 | chr11 | TogoVar | |||||||
TRIM48_chr11_55257155_55276114 | 55273384 | TAA | T | downstream_gene_variant | MODIFIER | HG02129.hp1 HG02970.hp1 NA21309.hp1 |
a0000a0001 | a0000c0005a0001c0001 | a0000c0005t0004a0001c0001t0001 | a0000c0005t0004g0056a0000c0005t0004g0057a0001c0001t0001g0002 | 3 | 272 | 0.0110 | -2 | c.*29 others(13): Show |
TRIM48 | ENSG00000150244.12 | transcript | ENST00000417545.5 | protein_coding | 2271 | chr11 | TogoVar | |||||||
TRIM49B_chr11_49023823_49043155 | 49028971 | CAG | C | splice_region_variant | LOW | HG01884.hp2 HG02055.hp1 HG02559.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0016 | 5 | 430 | 0.0116 | -2 | c.-8_ others(7): Show |
TRIM49B | ENSG00000182053.13 | transcript | ENST00000332682.9 | protein_coding | 1/7 | chr11 | TogoVar | |||||||
TRIM49B_chr11_49023823_49043155 | 49035999 | GTC | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
a0001 | a0001c0001a0001c0003a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(7): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(89): Show | 289 | 430 | 0.6721 | -2 | c.762 others(17): Show |
TRIM49B | ENSG00000182053.13 | transcript | ENST00000332682.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM49C_chr11_90026106_90047025 | 90039263 | AAG | A | intron_variant | MODIFIER | HG00639.hp2 HG01099.hp2 HG01192.hp2 others(8): Show |
a0002a0004 | a0002c0002a0004c0006 | a0002c0002t0002a0002c0002t0007a0004c0006t0003 | a0002c0002t0002g0004a0002c0002t0002g0009a0002c0002t0002g0014others(4): Show | 11 | 120 | 0.0917 | -2 | c.761 others(17): Show |
TRIM49C | ENSG00000204449.3 | transcript | ENST00000448984.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TRIM49C_chr11_90026106_90047025 | 90041029 | CTT | C | splice_region_variant others(1): Show |
LOW | HG00639.hp2 HG00738.hp2 HG01099.hp2 others(7): Show |
a0002a0004a0005 | a0002c0002a0004c0006a0005c0005 | a0002c0002t0002a0002c0002t0007a0004c0006t0003others(1): Show | a0002c0002t0002g0004a0002c0002t0002g0014a0002c0002t0002g0015others(4): Show | 10 | 120 | 0.0833 | -2 | c.860 others(13): Show |
TRIM49C | ENSG00000204449.3 | transcript | ENST00000448984.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |