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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
COL4A2_chr13_110302284_110518209 | 110385906 | T | TTACAGTG others(497): Show |
intron_variant | MODIFIER | HG02155.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0359 | 1 | 245 | 0.0041 | 504 | c.180 others(523): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110385906 | T | TTACAGTG others(497): Show |
intron_variant | MODIFIER | HG01515.hp2 HG02559.hp2 HG02717.hp2 |
a0001a0002a0007 | a0001c0045a0002c0019a0007c0059 | a0001c0045t0003a0002c0019t0037a0007c0059t0024 | a0001c0045t0003g0021 a0002c0019t0037g0026 a0007c0059t0024g0252 |
3 | 247 | 0.0121 | 504 | c.180 others(523): Show |
COL4A2 | ENSG00000134871.19 | transcript | ENST00000360467.7 | protein_coding | 4/47 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
COL5A1_chr9_134636803_134849843 | 134729517 | T | TGTGTGTG others(497): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0001 | a0001c0005 | a0001c0005t0022 | a0001c0005t0022g0086 | 1 | 177 | 0.0056 | 504 | c.925 others(519): Show |
COL5A1 | ENSG00000130635.17 | transcript | ENST00000371817.8 | protein_coding | 6/65 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
COL9A3_chr20_62812050_62846159 | 62825130 | A | AGGGAGGG others(497): Show |
intron_variant | MODIFIER | HG02300.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054 | 1 | 220 | 0.0045 | 504 | c.630 others(519): Show |
COL9A3 | ENSG00000092758.18 | transcript | ENST00000649368.1 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
COL9A3_chr20_62812050_62846159 | 62825154 | A | AGGGAGGG others(497): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0116 | 1 | 235 | 0.0043 | 504 | c.630 others(519): Show |
COL9A3 | ENSG00000092758.18 | transcript | ENST00000649368.1 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
CTU2_chr16_88701503_88720396 | 88712921 | C | CCCCCTTC others(497): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00621.hp2 HG02056.hp2 others(8): Show |
a0002 | a0002c0003 | a0002c0003t0001a0002c0003t0005 | a0002c0003t0001g0012 a0002c0003t0001g0064 a0002c0003t0001g0084 others(5): Show |
11 | 262 | 0.0420 | 504 | c.737 others(517): Show |
CTU2 | ENSG00000174177.13 | transcript | ENST00000453996.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102260343 | T | TCTCCCAA others(497): Show |
intron_variant | MODIFIER | HG00735.hp1 | a0002 | a0002c0004 | a0002c0004t0001 | a0002c0004t0001g0084 | 1 | 15 | 0.0667 | 504 | c.125 others(525): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102260343 | T | TCTCCCAA others(497): Show |
intron_variant | MODIFIER | HG01258.hp2 HG02280.hp2 HG03669.hp1 |
a0002 | a0002c0004 | a0002c0004t0001 | a0002c0004t0001g0052 a0002c0004t0001g0083 a0002c0004t0001g0100 |
3 | 17 | 0.1765 | 504 | c.125 others(525): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102260343 | T | TCTCCCAA others(497): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0087 | 1 | 15 | 0.0667 | 504 | c.125 others(525): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102260343 | T | TCTCCCAA others(497): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0013others(8): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(19): Show | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(106): Show |
109 | 123 | 0.8862 | 504 | c.125 others(525): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CUX1_chr7_101811007_102288958 | 102260343 | T | TCTCCCAA others(497): Show |
intron_variant | MODIFIER | HG01884.hp2 HG03195.hp1 |
a0002a0003 | a0002c0004a0003c0006 | a0002c0004t0001a0003c0006t0001 | a0002c0004t0001g0018 a0003c0006t0001g0120 |
2 | 16 | 0.1250 | 504 | c.125 others(525): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000622516.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
CUX1_chr7_101812626_102263233 | 102260343 | T | TCTCCCAA others(497): Show |
downstream_gene_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0050 | 1 | 16 | 0.0625 | 504 | c.*11 others(517): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2111 | chr7 | TogoVar | |||||||
CUX1_chr7_101812626_102263233 | 102260343 | T | TCTCCCAA others(497): Show |
downstream_gene_variant | MODIFIER | HG01258.hp2 HG02280.hp1 HG03669.hp2 |
a0001a0005 | a0001c0002a0005c0014 | a0001c0002t0001a0005c0014t0001 | a0001c0002t0001g0049 a0001c0002t0001g0089 a0005c0014t0001g0067 |
3 | 18 | 0.1667 | 504 | c.*11 others(517): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2111 | chr7 | TogoVar | |||||||
CUX1_chr7_101812626_102263233 | 102260343 | T | TCTCCCAA others(497): Show |
downstream_gene_variant | MODIFIER | NA18906.hp2 NA20129.hp1 |
a0001a0007 | a0001c0001a0007c0015 | a0001c0001t0010a0007c0015t0027 | a0001c0001t0010g0053 a0007c0015t0027g0133 |
2 | 17 | 0.1176 | 504 | c.*11 others(517): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2111 | chr7 | TogoVar | |||||||
CUX1_chr7_101812626_102263233 | 102260343 | T | TCTCCCAA others(497): Show |
downstream_gene_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(108): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(70): Show | a0001c0001t0002g0105 a0001c0001t0003g0008 a0001c0001t0003g0048 others(108): Show |
111 | 126 | 0.8810 | 504 | c.*11 others(517): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2111 | chr7 | TogoVar | |||||||
CUX1_chr7_101812626_102263233 | 102260343 | T | TCTCCCAA others(497): Show |
downstream_gene_variant | MODIFIER | HG01884.hp1 HG03195.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0047a0001c0004t0002 | a0001c0001t0047g0085 a0001c0004t0002g0082 |
2 | 17 | 0.1176 | 504 | c.*11 others(517): Show |
CUX1 | ENSG00000257923.12 | transcript | ENST00000292535.12 | protein_coding | 2111 | chr7 | TogoVar | |||||||
CUX2_chr12_111029165_111355554 | 111326120 | G | GTTTTGTT others(497): Show |
intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0087 | 1 | 47 | 0.0213 | 504 | c.292 others(523): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
DLGAP2_chr8_732628_1713476 | 798487 | C | CGTTGGCA others(497): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0009 | a0001c0009t0012 | a0001c0009t0012g0006 | 1 | 21 | 0.0476 | 504 | c.18+ others(521): Show |
DLGAP2 | ENSG00000198010.13 | transcript | ENST00000637795.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
DLGAP2_chr8_732628_1713476 | 1206333 | G | GTGAGCGG others(497): Show |
intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0003 | a0001c0003t0014 | a0001c0003t0014g0020 | 1 | 33 | 0.0303 | 504 | c.74- others(521): Show |
DLGAP2 | ENSG00000198010.13 | transcript | ENST00000637795.2 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
DNAI7_chr12_25103289_25200160 | 25174520 | C | CATATATA others(497): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00642.hp2 HG01099.hp1 others(13): Show |
a0001a0003a0011 | a0001c0001a0003c0003a0011c0013 | a0001c0001t0002a0003c0003t0002a0011c0013t0002 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0006 others(13): Show |
16 | 203 | 0.0788 | 504 | c.22- others(521): Show |
DNAI7 | ENSG00000118307.20 | transcript | ENST00000395987.8 | protein_coding | 2/15 | chr12 | TogoVar | |||||||
DOCK8_chr9_209865_470255 | 400967 | T | TCCTCCAC others(497): Show |
intron_variant | MODIFIER | HG02071.hp1 | a0001 | a0001c0058 | a0001c0058t0001 | a0001c0058t0001g0100 | 1 | 153 | 0.0065 | 504 | c.323 others(523): Show |
DOCK8 | ENSG00000107099.18 | transcript | ENST00000432829.7 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
EXD3_chr9_137301896_137428162 | 137322959 | C | CTCTGCCG others(497): Show |
intron_variant | MODIFIER | HG00741.hp2 | a0014 | a0014c0025 | a0014c0025t0001 | a0014c0025t0001g0072 | 1 | 51 | 0.0196 | 504 | c.218 others(521): Show |
EXD3 | ENSG00000187609.16 | transcript | ENST00000340951.9 | protein_coding | 19/21 | chr9 | TogoVar | |||||||
FAM171A1_chr10_15206643_15376289 | 15229788 | A | ACTATCAC others(497): Show |
intron_variant | MODIFIER | HG00609.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0106 | 1 | 258 | 0.0039 | 504 | c.755 others(521): Show |
FAM171A1 | ENSG00000148468.17 | transcript | ENST00000378116.9 | protein_coding | 5/7 | chr10 | TogoVar | |||||||
FGFR2_chr10_121473332_121603444 | 121584822 | C | CCCCAACC others(497): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0004 | a0001c0004t0004 | a0001c0004t0004g0202 | 1 | 3 | 0.3333 | 504 | c.109 others(521): Show |
FGFR2 | ENSG00000066468.24 | transcript | ENST00000358487.10 | protein_coding | 2/17 | chr10 | TogoVar | |||||||
GAL3ST2_chr2_241771822_241809287 | 241807891 | C | CTCCCCCC others(497): Show |
downstream_gene_variant | MODIFIER | NA19091.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0168 | 1 | 306 | 0.0033 | 504 | c.*37 others(515): Show |
GAL3ST2 | ENSG00000154252.12 | transcript | ENST00000192314.7 | protein_coding | 3605 | chr2 | TogoVar | |||||||
GNA15_chr19_3131033_3168749 | 3145577 | T | TCTCACTC others(497): Show |
intron_variant | MODIFIER | HG02723.hp2 HG02965.hp2 HG03098.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0011a0001c0002t0001a0001c0003t0001 | a0001c0001t0011g0267 a0001c0002t0001g0242 a0001c0002t0001g0268 others(2): Show |
5 | 92 | 0.0543 | 504 | c.146 others(521): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
GNA15_chr19_3131033_3168749 | 3145577 | T | TCTCACTC others(497): Show |
intron_variant | MODIFIER | HG01070.hp1 NA20129.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0001 | a0001c0002t0001g0097 a0001c0003t0001g0219 |
2 | 89 | 0.0225 | 504 | c.146 others(521): Show |
GNA15 | ENSG00000060558.4 | transcript | ENST00000262958.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
GNG13_chr16_793041_805734 | 795580 | G | GCCCTTCT others(497): Show |
downstream_gene_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 1 | 243 | 0.0041 | 504 | c.*31 others(515): Show |
GNG13 | ENSG00000127588.5 | transcript | ENST00000248150.5 | protein_coding | 2460 | chr16 | TogoVar | |||||||
GPR173_chrX_53043789_53085615 | 53073903 | A | ATATATAT others(497): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0194 | 1 | 133 | 0.0075 | 504 | c.-97 others(521): Show |
GPR173 | ENSG00000184194.6 | transcript | ENST00000332582.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
GPR173_chrX_53043789_53085615 | 53074425 | T | TATATATT others(497): Show |
intron_variant | MODIFIER | HG02056.hp1 HG02132.hp1 HG03492.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0006a0001c0001t0031 | a0001c0001t0004g0114 a0001c0001t0006g0200 a0001c0001t0031g0131 |
3 | 87 | 0.0345 | 504 | c.-97 others(521): Show |
GPR173 | ENSG00000184194.6 | transcript | ENST00000332582.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
GPR173_chrX_53043789_53085615 | 53074425 | T | TATATATT others(497): Show |
intron_variant | MODIFIER | HG02896.hp2 | a0001 | a0001c0006 | a0001c0006t0020 | a0001c0006t0020g0177 | 1 | 85 | 0.0118 | 504 | c.-97 others(521): Show |
GPR173 | ENSG00000184194.6 | transcript | ENST00000332582.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643092 | C | CATCCATC others(497): Show |
intron_variant | MODIFIER | HG00438.hp2 HG02083.hp2 NA18939.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0242 a0001c0001t0001g0256 a0001c0001t0002g0301 others(6): Show |
9 | 319 | 0.0282 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643147 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0064 | 1 | 307 | 0.0033 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643151 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | NA18946.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0228 | 1 | 296 | 0.0034 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643151 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | NA18969.hp2 NA19056.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0034 | a0001c0001t0006g0264 a0001c0001t0034g0270 |
2 | 297 | 0.0067 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643155 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | NA18952.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0227 | 1 | 242 | 0.0041 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643155 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | HG02683.hp2 HG03491.hp1 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0195 a0001c0001t0003g0215 a0001c0001t0003g0216 |
3 | 244 | 0.0123 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643155 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0206 | 1 | 242 | 0.0041 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643155 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0001 | a0001c0001t0030 | a0001c0001t0030g0030 | 1 | 242 | 0.0041 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643159 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | HG01516.hp1 HG03831.hp2 NA19065.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0057 | a0001c0001t0003g0231 a0001c0001t0003g0267 a0001c0001t0057g0278 |
3 | 124 | 0.0242 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643159 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | HG01255.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0213 | 1 | 122 | 0.0082 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643159 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | HG01952.hp2 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0031 | 1 | 122 | 0.0082 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643159 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | NA18948.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0142 | 1 | 122 | 0.0082 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643159 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0187 | 1 | 122 | 0.0082 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643159 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0001 | a0001c0007 | a0001c0007t0019 | a0001c0007t0019g0182 | 1 | 122 | 0.0082 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643159 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | NA19064.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0282 | 1 | 122 | 0.0082 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643159 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | NA18995.hp2 | a0001 | a0001c0001 | a0001c0001t0044 | a0001c0001t0044g0316 | 1 | 122 | 0.0082 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643159 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0059 | a0001c0001t0059g0280 | 1 | 122 | 0.0082 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
GRAMD4_chr22_46615386_46684785 | 46643163 | C | CCATCCAT others(497): Show |
intron_variant | MODIFIER | HG01192.hp2 HG02293.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0023 | a0001c0001t0001g0073 a0001c0001t0023g0121 |
2 | 315 | 0.0063 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
IL17REL_chr22_49986811_50017765 | 50009894 | T | TGGCGGCA others(497): Show |
intron_variant | MODIFIER | HG00642.hp1 HG01081.hp1 HG01081.hp2 others(24): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0017others(2): Show | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0081 others(21): Show |
27 | 129 | 0.2093 | 504 | c.103 others(521): Show |
IL17REL | ENSG00000188263.11 | transcript | ENST00000695950.1 | protein_coding | 1/14 | chr22 | TogoVar |