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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4104): Show |
intron_variant | MODIFIER | HG00673.hp1 HG02922.hp1 |
a0001a0013 | a0001c0053a0013c0018 | a0001c0053t0039a0013c0018t0064 | a0001c0053t0039g0055 a0013c0018t0064g0012 |
2 | 8 | 0.2500 | 4111 | c.-17 others(4130): 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(4105): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0003 | a0003c0010 | a0003c0010t0025 | a0003c0010t0025g0048 | 1 | 7 | 0.1429 | 4112 | c.-17 others(4131): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181045891 | G | GACACCTC others(4106): Show |
intron_variant | MODIFIER | HG04199.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0168 | 1 | 29 | 0.0345 | 4113 | c.109 others(4128): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DLEC1_chr3_38034208_38129025 | 38084579 | G | GGGGGGTG others(4106): Show |
intron_variant | MODIFIER | HG02135.hp1 | a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0116 | 1 | 2 | 0.5000 | 4113 | c.126 others(4130): Show |
DLEC1 | ENSG00000008226.20 | transcript | ENST00000308059.11 | protein_coding | 7/36 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4106): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0003 | a0003c0010 | a0003c0010t0070 | a0003c0010t0070g0026 | 1 | 7 | 0.1429 | 4113 | c.-17 others(4132): 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(4106): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0052 | a0001c0052t0014 | a0001c0052t0014g0030 | 1 | 7 | 0.1429 | 4113 | c.-17 others(4132): 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(4106): Show |
intron_variant | MODIFIER | HG00741.hp2 | a0002 | a0002c0001 | a0002c0001t0019 | a0002c0001t0019g0066 | 1 | 7 | 0.1429 | 4113 | c.-17 others(4132): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
GNPDA1_chr5_141995671_142018027 | 142000088 | A | ATGCTTGG others(4106): Show |
downstream_gene_variant | MODIFIER | HG01099.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0132 | 1 | 30 | 0.0333 | 4113 | c.*19 others(4124): Show |
GNPDA1 | ENSG00000113552.16 | transcript | ENST00000311337.11 | protein_coding | 582 | chr5 | TogoVar | |||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4107): Show |
intron_variant | MODIFIER | NA19065.hp1 | a0001 | a0001c0002 | a0001c0002t0052 | a0001c0002t0052g0090 | 1 | 7 | 0.1429 | 4114 | c.-17 others(4133): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CTU2_chr16_88701503_88720396 | 88712912 | C | CCCCGAGA others(4108): Show |
intron_variant | MODIFIER | NA20905.hp1 | a0001 | a0001c0013 | a0001c0013t0001 | a0001c0013t0001g0150 | 1 | 409 | 0.0024 | 4115 | c.737 others(4128): Show |
CTU2 | ENSG00000174177.13 | transcript | ENST00000453996.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4108): Show |
intron_variant | MODIFIER | HG03927.hp2 | a0004 | a0004c0046 | a0004c0046t0001 | a0004c0046t0001g0095 | 1 | 7 | 0.1429 | 4115 | c.-17 others(4134): 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(4108): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0027 | a0027c0017 | a0027c0017t0001 | a0027c0017t0001g0037 | 1 | 7 | 0.1429 | 4115 | c.-17 others(4134): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FOXK2_chr17_82514732_82609602 | 82586449 | C | CGGAGGGG others(4108): Show |
intron_variant | MODIFIER | HG02080.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0057 | 1 | 244 | 0.0041 | 4115 | c.157 others(4132): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | chr17 | TogoVar | |||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(4108): Show |
intron_variant | MODIFIER | HG04184.hp2 | a0003 | a0003c0017 | a0003c0017t0002 | a0003c0017t0002g0234 | 1 | 34 | 0.0294 | 4115 | c.299 others(4130): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
ADGRA1_chr10_133082924_133136675 | 133111767 | A | ACACCTCC others(4110): Show |
intron_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0004 | a0001c0004t0052 | a0001c0004t0052g0338 | 1 | 172 | 0.0058 | 4117 | c.401 others(4134): Show |
ADGRA1 | ENSG00000197177.16 | transcript | ENST00000392607.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585418 | C | CCTTTCCA others(4110): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0087 | 1 | 174 | 0.0057 | 4117 | c.215 others(4134): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585418 | C | CCTTTCCA others(4110): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0003 | a0003c0004 | a0003c0004t0003 | a0003c0004t0003g0165 | 1 | 174 | 0.0057 | 4117 | c.215 others(4134): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PIEZO1_chr16_88710338_88790220 | 88712963 | G | GCCCCCCT others(4110): Show |
downstream_gene_variant | MODIFIER | NA20905.hp2 | a0087 | a0087c0149 | a0087c0149t0001 | a0087c0149t0001g0155 | 1 | 120 | 0.0083 | 4117 | c.*26 others(4128): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 2374 | chr16 | TogoVar | |||||||
ATP9B_chr18_79064394_79383283 | 79200703 | T | TGTCAGAG others(4112): Show |
intron_variant | MODIFIER | NA19074.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0109 | 1 | 76 | 0.0132 | 4119 | c.955 others(4136): Show |
ATP9B | ENSG00000166377.21 | transcript | ENST00000426216.6 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4112): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02965.hp1 |
a0001 | a0001c0005 | a0001c0005t0003 | a0001c0005t0003g0159 a0001c0005t0003g0168 |
2 | 63 | 0.0317 | 4119 | c.286 others(4136): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4112): Show |
intron_variant | MODIFIER | HG02717.hp1 HG02886.hp2 |
a0001 | a0001c0005 | a0001c0005t0003 | a0001c0005t0003g0162 a0001c0005t0003g0163 |
2 | 63 | 0.0317 | 4119 | c.286 others(4136): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4112): Show |
intron_variant | MODIFIER | HG02257.hp1 HG03195.hp2 NA19240.hp1 |
a0001 | a0001c0005 | a0001c0005t0003 | a0001c0005t0003g0158 a0001c0005t0003g0160 a0001c0005t0003g0161 |
3 | 64 | 0.0469 | 4119 | c.286 others(4136): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
AP2A2_chr11_920870_1017240 | 964867 | A | ATGGAAAG others(4113): Show |
intron_variant | MODIFIER | HG00597.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0240 | 1 | 23 | 0.0435 | 4120 | c.137 others(4137): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
RILPL2_chr12_123410039_123441684 | 123425654 | C | CTTTTTTT others(4113): Show |
intron_variant | MODIFIER | NA19084.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0311 | 1 | 241 | 0.0041 | 4120 | c.492 others(4137): Show |
RILPL2 | ENSG00000150977.11 | transcript | ENST00000280571.10 | protein_coding | 2/3 | chr12 | TogoVar | |||||||
RILPL2_chr12_123410039_123441684 | 123429150 | T | TTATTTTT others(4113): Show |
intron_variant | MODIFIER | HG02300.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0096 | 1 | 222 | 0.0045 | 4120 | c.491 others(4137): Show |
RILPL2 | ENSG00000150977.11 | transcript | ENST00000280571.10 | protein_coding | 2/3 | chr12 | TogoVar | |||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4114): Show |
intron_variant | MODIFIER | HG02300.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0021 | 1 | 62 | 0.0161 | 4121 | c.286 others(4138): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4114): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0003 | a0001c0003t0009 | a0001c0003t0009g0006 | 1 | 62 | 0.0161 | 4121 | c.286 others(4138): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
RILPL2_chr12_123410039_123441684 | 123425654 | C | CTTTTTTT others(4114): Show |
intron_variant | MODIFIER | HG01123.hp2 HG01975.hp1 HG02083.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0005g0033 |
6 | 246 | 0.0244 | 4121 | c.492 others(4138): Show |
RILPL2 | ENSG00000150977.11 | transcript | ENST00000280571.10 | protein_coding | 2/3 | chr12 | TogoVar | |||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4115): Show |
intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0005 | a0001c0005t0007 | a0001c0005t0007g0045 | 1 | 62 | 0.0161 | 4122 | c.286 others(4139): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4115): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0032 | 1 | 62 | 0.0161 | 4122 | c.286 others(4139): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4115): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(29): Show |
a0001 | a0001c0003 | a0001c0003t0003a0001c0003t0014 | a0001c0003t0003g0007 a0001c0003t0003g0008 a0001c0003t0003g0009 others(29): Show |
32 | 93 | 0.3441 | 4122 | c.286 others(4139): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4115): Show |
intron_variant | MODIFIER | HG02895.hp2 HG02897.hp2 HG03098.hp1 others(2): Show |
a0001a0003 | a0001c0003a0003c0007 | a0001c0003t0003a0003c0007t0003 | a0001c0003t0003g0046 a0003c0007t0003g0164 a0003c0007t0003g0165 others(2): Show |
5 | 66 | 0.0758 | 4122 | c.286 others(4139): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4115): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0053 | 1 | 62 | 0.0161 | 4122 | c.286 others(4139): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4115): Show |
intron_variant | MODIFIER | HG02280.hp1 HG03225.hp2 |
a0001 | a0001c0005a0001c0015 | a0001c0005t0003a0001c0015t0007 | a0001c0005t0003g0043 a0001c0015t0007g0044 |
2 | 63 | 0.0317 | 4122 | c.286 others(4139): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4115): Show |
intron_variant | MODIFIER | HG01993.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0022 | 1 | 62 | 0.0161 | 4122 | c.286 others(4139): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4115): Show |
intron_variant | MODIFIER | HG02622.hp2 HG02896.hp2 HG03516.hp2 |
a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0048 a0001c0003t0003g0049 a0001c0003t0003g0281 |
3 | 64 | 0.0469 | 4122 | c.286 others(4139): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4115): Show |
intron_variant | MODIFIER | HG03486.hp1 HG03516.hp1 NA20129.hp2 |
a0001a0006 | a0001c0004a0006c0016 | a0001c0004t0003a0006c0016t0003 | a0001c0004t0003g0051 a0001c0004t0003g0052 a0006c0016t0003g0050 |
3 | 64 | 0.0469 | 4122 | c.286 others(4139): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4115): Show |
intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0014 | 1 | 62 | 0.0161 | 4122 | c.286 others(4139): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
RILPL2_chr12_123410039_123441684 | 123425654 | C | CTTTTTTT others(4115): Show |
intron_variant | MODIFIER | NA19088.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0093 | 1 | 241 | 0.0041 | 4122 | c.492 others(4139): Show |
RILPL2 | ENSG00000150977.11 | transcript | ENST00000280571.10 | protein_coding | 2/3 | chr12 | TogoVar | |||||||
SIGIRR_chr11_400716_419999 | 412377 | C | CCAGCTCT others(4115): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0106 | 1 | 217 | 0.0046 | 4122 | c.-15 others(4141): Show |
SIGIRR | ENSG00000185187.13 | transcript | ENST00000431843.7 | protein_coding | 1/9 | chr11 | TogoVar | |||||||
GALNT9_chr12_132191372_132334589 | 132241883 | A | ACACACCC others(4116): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0040 | a0001c0040t0007 | a0001c0040t0007g0002 | 1 | 64 | 0.0156 | 4123 | c.107 others(4142): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar | |||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(4116): Show |
upstream_gene_variant | MODIFIER | HG01168.hp1 | a0002 | a0002c0006 | a0002c0006t0001 | a0002c0006t0001g0138 | 1 | 8 | 0.1250 | 4123 | c.-45 others(4132): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
DISC1_chr1_231621790_232046272 | 231799889 | T | TTCCCTCC others(4118): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0003 | a0003c0002 | a0003c0002t0020 | a0003c0002t0020g0022 | 1 | 3 | 0.3333 | 4125 | c.169 others(4142): Show |
DISC1 | ENSG00000162946.24 | transcript | ENST00000439617.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PAK2_chr3_196734857_196837647 | 196811228 | C | CCCTCCCT others(4120): Show |
intron_variant | MODIFIER | HG02818.hp1 | a0001 | a0001c0001 | a0001c0001t0039 | a0001c0001t0039g0130 | 1 | 173 | 0.0058 | 4127 | c.773 others(4142): Show |
PAK2 | ENSG00000180370.10 | transcript | ENST00000327134.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(4122): Show |
intron_variant | MODIFIER | HG01346.hp2 | a0022 | a0022c0052 | a0022c0052t0001 | a0022c0052t0001g0100 | 1 | 34 | 0.0294 | 4129 | c.299 others(4144): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
PTPRK_chr6_127963785_128525599 | 128005705 | A | ATGTCCCA others(4122): Show |
intron_variant | MODIFIER | HG02647.hp2 HG02723.hp2 |
a0001 | a0001c0005 | a0001c0005t0003 | a0001c0005t0003g0028 a0001c0005t0003g0036 |
2 | 30 | 0.0667 | 4129 | c.233 others(4146): Show |
PTPRK | ENSG00000152894.15 | transcript | ENST00000368226.9 | protein_coding | 14/29 | chr6 | TogoVar | |||||||
ZNF117_chr7_64966772_64996036 | 64981942 | T | TAAAACCT others(4123): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0005 | a0005c0005 | a0005c0005t0014 | a0005c0005t0014g0100 | 1 | 439 | 0.0023 | 4130 | c.-63 others(4143): Show |
ZNF117 | ENSG00000152926.16 | transcript | ENST00000282869.11 | protein_coding | 2/3 | chr7 | TogoVar | |||||||
ZNF117_chr7_64966772_64996036 | 64981942 | T | TAAAACCT others(4123): Show |
intron_variant | MODIFIER | HG02818.hp1 | a0005 | a0005c0005 | a0005c0005t0014 | a0005c0005t0014g0099 | 1 | 439 | 0.0023 | 4130 | c.-63 others(4143): Show |
ZNF117 | ENSG00000152926.16 | transcript | ENST00000282869.11 | protein_coding | 2/3 | chr7 | TogoVar | |||||||
ZNF117_chr7_64966772_64996036 | 64981942 | T | TAAAACCT others(4123): Show |
intron_variant | MODIFIER | HG01243.hp2 HG03471.hp2 |
a0005 | a0005c0005 | a0005c0005t0014 | a0005c0005t0014g0036 | 2 | 440 | 0.0045 | 4130 | c.-63 others(4143): Show |
ZNF117 | ENSG00000152926.16 | transcript | ENST00000282869.11 | protein_coding | 2/3 | chr7 | TogoVar | |||||||
LRRC27_chr10_132327193_132386508 | 132364372 | C | CCCACACT others(4125): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0028 | 1 | 283 | 0.0035 | 4132 | c.129 others(4151): Show |
LRRC27 | ENSG00000148814.18 | transcript | ENST00000368614.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar |