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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
IQSEC3_chr12_61767_183455 | 163240 | C | CCCCTCCA others(4063): Show |
intron_variant | MODIFIER | HG02027.hp2 HG02165.hp1 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0001 | 2 | 218 | 0.0092 | 4070 | c.258 others(4087): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
LRRFIP1_chr2_237622587_237786643 | 237655102 | C | CTATGTGA others(4063): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0004 | a0001c0004t0022 | a0001c0004t0022g0108 | 1 | 140 | 0.0071 | 4070 | c.96+ others(4087): Show |
LRRFIP1 | ENSG00000124831.20 | transcript | ENST00000308482.14 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
LRRFIP1_chr2_237622587_237786643 | 237655102 | C | CTATGTGA others(4064): Show |
intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0231 | 1 | 140 | 0.0071 | 4071 | c.96+ others(4088): Show |
LRRFIP1 | ENSG00000124831.20 | transcript | ENST00000308482.14 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(4064): Show |
upstream_gene_variant | MODIFIER | HG01255.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0176 | 1 | 8 | 0.1250 | 4071 | c.-45 others(4080): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
IFNAR1_chr21_33319970_33364864 | 33323046 | A | ATGGAATA others(4065): Show |
upstream_gene_variant | MODIFIER | NA19060.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0001 | 1 | 321 | 0.0031 | 4072 | c.-20 others(4083): Show |
IFNAR1 | ENSG00000142166.15 | transcript | ENST00000270139.8 | protein_coding | 1923 | chr21 | TogoVar | |||||||
LRRFIP1_chr2_237622587_237786643 | 237655114 | T | TAAAAGTC others(4066): Show |
intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0140 | 1 | 274 | 0.0036 | 4073 | c.96+ others(4090): Show |
LRRFIP1 | ENSG00000124831.20 | transcript | ENST00000308482.14 | protein_coding | 1/23 | chr2 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63693687 | A | ACCTCCAC others(4067): Show |
downstream_gene_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0001 | 1 | 221 | 0.0045 | 4074 | c.*67 others(4085): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4959 | chr20 | TogoVar | |||||||
ARHGEF16_chr1_3449665_3486113 | 3477303 | G | GTCACCCC others(4068): Show |
intron_variant | MODIFIER | HG03942.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0184 | 1 | 50 | 0.0200 | 4075 | c.147 others(4092): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
LAMA5_chr20_62304065_62372312 | 62318240 | G | GGAAGGGG others(4068): Show |
intron_variant | MODIFIER | HG02602.hp1 | a0013 | a0013c0019 | a0013c0019t0002 | a0013c0019t0002g0115 | 1 | 8 | 0.1250 | 4075 | c.723 others(4092): Show |
LAMA5 | ENSG00000130702.15 | transcript | ENST00000252999.7 | protein_coding | 53/79 | chr20 | TogoVar | |||||||
MORN1_chr1_2316253_2396554 | 2325140 | C | CTCCCTCC others(4069): Show |
intron_variant | MODIFIER | HG04199.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0056 | 1 | 2 | 0.5000 | 4076 | c.125 others(4093): Show |
MORN1 | ENSG00000116151.14 | transcript | ENST00000378531.8 | protein_coding | 12/13 | chr1 | TogoVar | |||||||
MORN1_chr1_2316253_2396554 | 2325140 | C | CTCCCTCC others(4069): Show |
intron_variant | MODIFIER | NA18747.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052 | 1 | 2 | 0.5000 | 4076 | c.125 others(4093): Show |
MORN1 | ENSG00000116151.14 | transcript | ENST00000378531.8 | protein_coding | 12/13 | chr1 | TogoVar | |||||||
FOXK2_chr17_82514732_82609602 | 82586258 | G | GGGGGAAA others(4070): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0081 | 1 | 285 | 0.0035 | 4077 | c.157 others(4092): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
CRTC3_chr15_90524923_90650345 | 90647402 | C | CCCTCCTC others(4071): Show |
downstream_gene_variant | MODIFIER | HG02129.hp2 | a0001 | a0001c0001 | a0001c0001t0039 | a0001c0001t0039g0172 | 1 | 69 | 0.0145 | 4078 | c.*52 others(4089): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2058 | chr15 | TogoVar | |||||||
FOXK2_chr17_82514732_82609602 | 82586538 | C | CAAAGGTG others(4071): Show |
intron_variant | MODIFIER | NA18959.hp1 | a0001 | a0001c0003 | a0001c0003t0047 | a0001c0003t0047g0286 | 1 | 198 | 0.0051 | 4078 | c.157 others(4095): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
LAMA5_chr20_62304065_62372312 | 62318240 | G | GGAAGGGG others(4071): Show |
intron_variant | MODIFIER | HG02129.hp1 | a0056 | a0056c0101 | a0056c0101t0001 | a0056c0101t0001g0143 | 1 | 8 | 0.1250 | 4078 | c.723 others(4095): Show |
LAMA5 | ENSG00000130702.15 | transcript | ENST00000252999.7 | protein_coding | 53/79 | chr20 | TogoVar | |||||||
CELSR1_chr22_46356174_46542620 | 46469974 | A | AGGGAGGA others(4072): Show |
intron_variant | MODIFIER | HG02647.hp1 | a0002 | a0002c0050 | a0002c0050t0003 | a0002c0050t0003g0053 | 1 | 13 | 0.0769 | 4079 | c.354 others(4098): Show |
CELSR1 | ENSG00000075275.18 | transcript | ENST00000674500.2 | protein_coding | 1/34 | chr22 | TogoVar | |||||||
LRRFIP1_chr2_237622587_237786643 | 237655112 | T | TCTAAAAG others(4072): Show |
intron_variant | MODIFIER | HG04184.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0027 | 1 | 274 | 0.0036 | 4079 | c.96+ others(4096): Show |
LRRFIP1 | ENSG00000124831.20 | transcript | ENST00000308482.14 | protein_coding | 1/23 | chr2 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63693732 | T | TCCACCTC others(4073): Show |
downstream_gene_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0014 | 1 | 99 | 0.0101 | 4080 | c.*67 others(4091): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4914 | chr20 | TogoVar | |||||||
BRF1_chr14_105204286_105306001 | 105238843 | T | CGTGGCAC others(4073): Show |
intron_variant | MODIFIER | HG00621.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019 | 1 | 38 | 0.0263 | 4080 | c.694 others(4097): Show |
BRF1 | ENSG00000185024.18 | transcript | ENST00000547530.7 | protein_coding | 6/17 | chr14 | TogoVar | |||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(4073): Show |
upstream_gene_variant | MODIFIER | HG01433.hp2 | a0001 | a0001c0001 | a0001c0001t0036 | a0001c0001t0036g0153 | 1 | 8 | 0.1250 | 4080 | c.-45 others(4089): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
RTEL1_chr20_63653312_63701245 | 63693732 | T | TCCACCTC others(4073): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0022 | 1 | 9 | 0.1111 | 4080 | c.299 others(4097): Show |
RTEL1 | ENSG00000258366.12 | transcript | ENST00000360203.11 | protein_coding | 30/34 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
TNFRSF6B_chr20_63691652_63703684 | 63693732 | T | TCCACCTC others(4073): Show |
upstream_gene_variant | MODIFIER | NA18906.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0002 | 1 | 3 | 0.3333 | 4080 | c.-30 others(4091): Show |
TNFRSF6B | ENSG00000243509.6 | transcript | ENST00000369996.3 | protein_coding | 2919 | chr20 | TogoVar | |||||||
GALNT9_chr12_132191372_132334589 | 132242969 | C | CCCCTTCC others(4074): Show |
intron_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0098 | 1 | 176 | 0.0057 | 4081 | c.107 others(4100): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar | |||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(4074): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0016 | a0016c0019 | a0016c0019t0006 | a0016c0019t0006g0018 | 1 | 34 | 0.0294 | 4081 | c.299 others(4096): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4076): Show |
intron_variant | MODIFIER | HG04204.hp2 | a0009 | a0009c0021 | a0009c0021t0023 | a0009c0021t0023g0099 | 1 | 7 | 0.1429 | 4083 | c.-17 others(4102): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
TSHB_chr1_115024826_115039302 | 115035215 | C | CAAAAAGT others(4076): Show |
downstream_gene_variant | MODIFIER | NA18959.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 426 | 0.0023 | 4083 | c.*98 others(4092): Show |
TSHB | ENSG00000134200.4 | transcript | ENST00000256592.3 | protein_coding | 914 | chr1 | TogoVar | |||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4077): Show |
intron_variant | MODIFIER | HG02572.hp2 | a0022 | a0022c0024 | a0022c0024t0010 | a0022c0024t0010g0044 | 1 | 7 | 0.1429 | 4084 | c.-17 others(4103): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4077): Show |
intron_variant | MODIFIER | HG01891.hp1 NA18986.hp1 NA19060.hp1 others(1): Show |
a0001a0002a0012 | a0001c0005a0002c0003a0012c0023 | a0001c0005t0017a0002c0003t0021a0002c0003t0077others(1): Show | a0001c0005t0017g0088 a0002c0003t0021g0043 a0002c0003t0077g0008 others(1): Show |
4 | 10 | 0.4000 | 4084 | c.-17 others(4103): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4077): Show |
intron_variant | MODIFIER | NA19009.hp1 | a0001 | a0001c0002 | a0001c0002t0082 | a0001c0002t0082g0002 | 1 | 7 | 0.1429 | 4084 | c.-17 others(4103): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(4077): Show |
upstream_gene_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0090 | 1 | 8 | 0.1250 | 4084 | c.-45 others(4093): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(4077): Show |
upstream_gene_variant | MODIFIER | HG01433.hp1 | a0001 | a0001c0001 | a0001c0001t0035 | a0001c0001t0035g0145 | 1 | 8 | 0.1250 | 4084 | c.-45 others(4093): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4078): Show |
intron_variant | MODIFIER | HG03927.hp1 | a0001 | a0001c0002 | a0001c0002t0081 | a0001c0002t0081g0011 | 1 | 7 | 0.1429 | 4085 | c.-17 others(4104): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4078): Show |
intron_variant | MODIFIER | HG01978.hp2 | a0008 | a0008c0007 | a0008c0007t0048 | a0008c0007t0048g0047 | 1 | 7 | 0.1429 | 4085 | c.-17 others(4104): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4078): Show |
intron_variant | MODIFIER | HG01069.hp2 | a0001 | a0001c0005 | a0001c0005t0018 | a0001c0005t0018g0089 | 1 | 7 | 0.1429 | 4085 | c.-17 others(4104): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4078): Show |
intron_variant | MODIFIER | HG02004.hp1 HG02698.hp2 NA19065.hp2 |
a0004a0012a0017 | a0004c0009a0012c0022a0017c0070 | a0004c0009t0001a0012c0022t0003a0017c0070t0001 | a0004c0009t0001g0070 a0012c0022t0003g0072 a0017c0070t0001g0029 |
3 | 9 | 0.3333 | 4085 | c.-17 others(4104): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4078): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0002 | a0002c0029 | a0002c0029t0022 | a0002c0029t0022g0049 | 1 | 7 | 0.1429 | 4085 | c.-17 others(4104): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4078): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0005 | a0001c0005t0065 | a0001c0005t0065g0006 | 1 | 7 | 0.1429 | 4085 | c.-17 others(4104): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4078): Show |
intron_variant | MODIFIER | HG02683.hp2 | a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0041 | 1 | 7 | 0.1429 | 4085 | c.-17 others(4104): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4079): Show |
intron_variant | MODIFIER | HG01978.hp1 | a0001 | a0001c0005 | a0001c0005t0066 | a0001c0005t0066g0004 | 1 | 7 | 0.1429 | 4086 | c.-17 others(4105): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4079): Show |
intron_variant | MODIFIER | HG02004.hp2 | a0001 | a0001c0025 | a0001c0025t0011 | a0001c0025t0011g0077 | 1 | 7 | 0.1429 | 4086 | c.-17 others(4105): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4079): Show |
intron_variant | MODIFIER | HG02258.hp2 NA19030.hp2 |
a0001a0005 | a0001c0006a0005c0008 | a0001c0006t0028a0005c0008t0010 | a0001c0006t0028g0034 a0005c0008t0010g0067 |
2 | 8 | 0.2500 | 4086 | c.-17 others(4105): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4079): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0033 | a0033c0026 | a0033c0026t0054 | a0033c0026t0054g0074 | 1 | 7 | 0.1429 | 4086 | c.-17 others(4105): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4079): Show |
intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0003 | a0002c0003t0069 | a0002c0003t0069g0010 | 1 | 7 | 0.1429 | 4086 | c.-17 others(4105): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
LAMA5_chr20_62304065_62372312 | 62318240 | G | GGAAGGGG others(4079): Show |
intron_variant | MODIFIER | HG02004.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0127 | 1 | 8 | 0.1250 | 4086 | c.723 others(4103): Show |
LAMA5 | ENSG00000130702.15 | transcript | ENST00000252999.7 | protein_coding | 53/79 | chr20 | TogoVar | |||||||
RPTOR_chr17_80539838_80971368 | 80744469 | C | CCCTGGCT others(4079): Show |
intron_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0003 | a0001c0003t0013 | a0001c0003t0013g0045 | 1 | 147 | 0.0068 | 4086 | c.655 others(4103): Show |
RPTOR | ENSG00000141564.16 | transcript | ENST00000306801.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
DOCK8_chr9_209865_470255 | 321164 | T | TCAGAGAT others(4080): Show |
intron_variant | MODIFIER | HG03831.hp2 | a0001 | a0001c0060 | a0001c0060t0001 | a0001c0060t0001g0080 | 1 | 253 | 0.0040 | 4087 | c.827 others(4104): Show |
DOCK8 | ENSG00000107099.18 | transcript | ENST00000432829.7 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4080): Show |
intron_variant | MODIFIER | HG02015.hp2 | a0008 | a0008c0007 | a0008c0007t0004 | a0008c0007t0004g0092 | 1 | 7 | 0.1429 | 4087 | c.-17 others(4106): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4080): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0004 | a0004c0009 | a0004c0009t0001 | a0004c0009t0001g0094 | 1 | 7 | 0.1429 | 4087 | c.-17 others(4106): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4080): Show |
intron_variant | MODIFIER | HG01099.hp2 | a0008 | a0008c0007 | a0008c0007t0004 | a0008c0007t0004g0071 | 1 | 7 | 0.1429 | 4087 | c.-17 others(4106): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4080): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0036 | a0036c0027 | a0036c0027t0020 | a0036c0027t0020g0075 | 1 | 7 | 0.1429 | 4087 | c.-17 others(4106): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |