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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNOT1_chr16_58514951_58634826 | 58586397 | G | GGGGAGGG others(497): Show |
intron_variant | MODIFIER | NA19065.hp1 | a0001 | a0001c0014 | a0001c0014t0001 | a0001c0014t0001g0060 | 1 | 308 | 0.0033 | 504 | c.637 others(519): Show |
CNOT1 | ENSG00000125107.19 | transcript | ENST00000317147.10 | protein_coding | 7/48 | chr16 | TogoVar | ||||||
COL4A2_chr13_110302284_110518209 | 110385546 | T | TTACAGTG others(497): Show |
intron_variant | MODIFIER | NA19084.hp2 | a0001 | a0001c0008 | a0001c0008t0002 | a0001c0008t0002g0276 | 1 | 372 | 0.0027 | 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 | HG00099.hp2 HG00597.hp2 HG01167.hp1 others(13): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0010a0001c0002t0001a0001c0002t0002others(12): Show | a0001c0001t0010g0033a0001c0002t0001g0152a0001c0002t0002g0286others(13): Show | 16 | 372 | 0.0430 | 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 | HG01168.hp2 HG01261.hp1 HG01975.hp2 others(15): Show |
a0001a0002a0006others(3): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(13): Show | a0001c0001t0001g0231a0001c0001t0003g0064a0001c0001t0006g0083others(15): Show | 18 | 372 | 0.0484 | 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 | HG02155.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0359 | 1 | 372 | 0.0027 | 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 | a0001c0045t0003g0021a0002c0019t0037g0026a0007c0059t0024g0252 | 3 | 372 | 0.0081 | 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 | a0001c0005t0022g0085 | 1 | 272 | 0.0037 | 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 | 412 | 0.0024 | 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 | a0001c0010 | a0001c0010t0002 | a0001c0010t0002g0134 | 1 | 412 | 0.0024 | 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 | a0002c0003t0001g0011a0002c0003t0001g0071a0002c0003t0001g0111others(5): Show | 11 | 418 | 0.0263 | 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 | a0002c0004t0001g0086 | 1 | 132 | 0.0076 | 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 others(1): Show |
a0002 | a0002c0004 | a0002c0004t0001 | a0002c0004t0001g0051a0002c0004t0001g0085a0002c0004t0001g0101others(1): Show | 4 | 132 | 0.0303 | 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 | a0001c0002t0001g0078 | 1 | 132 | 0.0076 | 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 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(106): Show | 109 | 132 | 0.8258 | 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 | a0002c0004t0001g0018a0003c0006t0001g0119 | 2 | 132 | 0.0152 | 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 | a0001c0002t0001g0055 | 1 | 136 | 0.0074 | 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 others(1): Show |
a0001a0006 | a0001c0002a0006c0014 | a0001c0002t0001a0006c0014t0001 | a0001c0002t0001g0054a0001c0002t0001g0081a0001c0002t0001g0100others(1): Show | 4 | 136 | 0.0294 | 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 |
a0001a0003 | a0001c0001a0003c0015 | a0001c0001t0010a0003c0015t0027 | a0001c0001t0010g0045a0003c0015t0027g0133 | 2 | 136 | 0.0147 | 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 |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(70): Show | a0001c0001t0002g0105a0001c0001t0003g0008a0001c0001t0003g0047others(108): Show | 111 | 136 | 0.8162 | 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 | a0001c0001t0047g0084a0001c0004t0002g0049 | 2 | 136 | 0.0147 | 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 | a0001c0003t0001g0088 | 1 | 100 | 0.0100 | 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 | 40 | 0.0250 | 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 | 40 | 0.0250 | 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 |
a0001a0003a0010 | a0001c0001a0003c0003a0010c0013 | a0001c0001t0002a0003c0003t0002a0010c0013t0002 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(13): Show | 16 | 336 | 0.0476 | 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 | a0001c0059 | a0001c0059t0001 | a0001c0059t0001g0100 | 1 | 256 | 0.0039 | 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 | a0026 | a0026c0025 | a0026c0025t0001 | a0026c0025t0001g0071 | 1 | 82 | 0.0122 | 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 | 303 | 0.0033 | 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 | 240 | 0.0042 | 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 | a0001c0001t0001g0204 | 1 | 314 | 0.0032 | 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 | a0001c0001t0011g0274a0001c0002t0001g0248a0001c0002t0001g0273others(2): Show | 5 | 450 | 0.0111 | 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 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0003a0001c0002t0001a0001c0003t0001 | a0001c0001t0003g0233a0001c0002t0001g0090a0001c0003t0001g0226 | 3 | 450 | 0.0067 | 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 | 422 | 0.0024 | 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 | a0001c0002t0002g0191 | 1 | 208 | 0.0048 | 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 | a0001c0001t0004a0001c0001t0006a0001c0001t0042 | a0001c0001t0004g0117a0001c0001t0006g0201a0001c0001t0042g0129 | 3 | 208 | 0.0144 | 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 | a0001c0014 | a0001c0014t0027 | a0001c0014t0027g0176 | 1 | 208 | 0.0048 | 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 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0002g0301others(6): Show | 9 | 328 | 0.0274 | 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 | a0001c0001t0019g0062 | 1 | 328 | 0.0031 | 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 | a0001c0001t0003g0239 | 1 | 328 | 0.0031 | 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 | a0001c0001t0006g0198a0001c0001t0034g0201 | 2 | 328 | 0.0061 | 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 | a0001c0001t0003g0238 | 1 | 328 | 0.0031 | 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 | a0001c0001t0003g0207a0001c0001t0003g0228a0001c0001t0003g0229 | 3 | 328 | 0.0092 | 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 | homoSapiens_chm13v2.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0223 | 1 | 328 | 0.0031 | 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 | a0001c0001t0003g0218 | 1 | 328 | 0.0031 | 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 | a0001c0001t0030g0044 | 1 | 328 | 0.0031 | 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 | a0001c0001t0003a0001c0001t0058 | a0001c0001t0003g0244a0001c0001t0003g0283a0001c0001t0058g0277 | 3 | 328 | 0.0092 | 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 | a0001c0001t0003g0226 | 1 | 328 | 0.0031 | 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 | a0001c0001t0017g0045 | 1 | 328 | 0.0031 | 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 | a0001c0001t0001g0141 | 1 | 328 | 0.0031 | 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 | 328 | 0.0031 | 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 | 328 | 0.0031 | 504 | c.283 others(521): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar |