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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP35_chr19_46855997_47010077 | 47007643 | C | CTTT | downstream_gene_variant | MODIFIER | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(35): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(12): Show | a0001c0001t0004g0070a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 38 | 298 | 0.1275 | 3 | c.*69 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2567 | chr19 | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131077881 | G | GAAT | intron_variant | MODIFIER | HG02809.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0208 | 1 | 302 | 0.0033 | 3 | c.-14 others(22): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131079562 | G | GTTT | intron_variant | MODIFIER | HG01074.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0178 | 1 | 302 | 0.0033 | 3 | c.-14 others(22): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131080398 | T | TAAA | intron_variant | MODIFIER | HG01167.hp1 HG02630.hp1 NA20300.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0029a0001c0001t0004g0150a0001c0001t0004g0223 | 3 | 302 | 0.0099 | 3 | c.-14 others(22): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131092704 | C | CTTT | downstream_gene_variant | MODIFIER | HG00438.hp1 HG00741.hp2 HG01928.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0001g0094a0001c0001t0003g0002a0001c0001t0003g0194others(3): Show | 7 | 302 | 0.0232 | 3 | c.*39 others(14): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 2820 | chrX | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144542384 | C | CGAT | intron_variant | MODIFIER | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
a0001 | a0001c0004a0001c0007 | a0001c0004t0006a0001c0007t0003 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(3): Show | 6 | 246 | 0.0244 | 3 | c.252 others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144559354 | C | CAAA | intron_variant | MODIFIER | HG02145.hp1 HG02572.hp1 HG02572.hp2 others(3): Show |
a0001 | a0001c0001a0001c0014 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(2): Show | a0001c0001t0001g0238a0001c0001t0004g0237a0001c0001t0007g0239others(3): Show | 6 | 246 | 0.0244 | 3 | c.513 others(20): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144568333 | C | CAAA | intron_variant | MODIFIER | HG01175.hp2 HG01891.hp2 HG02004.hp2 others(4): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(2): Show | a0001c0001t0001g0175a0001c0001t0001g0190a0001c0001t0001g0198others(4): Show | 7 | 246 | 0.0285 | 3 | c.512 others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144603687 | C | CAAA | intron_variant | MODIFIER | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
a0001 | a0001c0001a0001c0018 | a0001c0001t0001a0001c0018t0001 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | 246 | 0.0407 | 3 | c.80+ others(18): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144614354 | A | ATTT | intron_variant | MODIFIER | HG02572.hp1 HG02615.hp2 HG02976.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0014 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(2): Show | a0001c0001t0001g0024a0001c0001t0001g0228a0001c0001t0004g0237others(3): Show | 6 | 246 | 0.0244 | 3 | c.-81 others(20): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144624363 | A | AAAG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(213): Show | 216 | 246 | 0.8781 | 3 | c.-81 others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144627554 | C | CAAA | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(73): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(73): Show | 76 | 246 | 0.3089 | 3 | c.-81 others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144656807 | C | CAAA | intron_variant | MODIFIER | HG00323.hp1 HG00558.hp2 HG01167.hp1 others(24): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0016others(4): Show | a0001c0001t0001g0107a0001c0001t0001g0122a0001c0001t0001g0136others(24): Show | 27 | 246 | 0.1098 | 3 | c.-82 others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669506 | C | CAAA | intron_variant | MODIFIER | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002a0001c0007others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(3): Show | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(12): Show | 15 | 246 | 0.0610 | 3 | c.-82 others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38608226 | A | ACTC | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(320): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0002a0001c0004others(36): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(66): Show | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(289): Show | 323 | 350 | 0.9229 | 3 | c.137 others(20): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38653341 | G | GCGT | downstream_gene_variant | MODIFIER | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(32): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0005a0001c0002t0004a0001c0004t0004others(10): Show | a0001c0001t0005g0187a0001c0001t0005g0219a0001c0001t0005g0236others(28): Show | 35 | 350 | 0.1000 | 3 | c.*34 others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2689 | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38653358 | G | GGCA | downstream_gene_variant | MODIFIER | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(32): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0005a0001c0002t0004a0001c0004t0004others(10): Show | a0001c0001t0005g0187a0001c0001t0005g0219a0001c0001t0005g0236others(28): Show | 35 | 350 | 0.1000 | 3 | c.*35 others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2706 | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100699506 | A | ATTT | intron_variant | MODIFIER | HG01496.hp1 HG01928.hp2 HG02071.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0022a0002c0002t0002 | a0001c0001t0001g0185a0001c0001t0001g0210a0001c0001t0001g0211others(3): Show | 6 | 286 | 0.0210 | 3 | c.154 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100704997 | C | CCAA | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0008others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(28): Show | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0026others(109): Show | 112 | 286 | 0.3916 | 3 | c.154 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100710538 | G | GTTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(58): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0008others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(19): Show | a0001c0001t0001g0062a0001c0001t0001g0076a0001c0001t0001g0095others(58): Show | 61 | 286 | 0.2133 | 3 | c.154 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100717636 | C | CAAA | intron_variant | MODIFIER | HG00099.hp1 HG00597.hp2 HG00673.hp2 others(26): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0015others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0266a0001c0001t0001g0271a0001c0001t0001g0276others(26): Show | 29 | 286 | 0.1014 | 3 | c.154 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100717923 | T | TGAA | intron_variant | MODIFIER | HG00735.hp2 HG01346.hp1 HG01433.hp2 others(9): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0014a0002c0002t0002others(4): Show | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0003t0014g0234others(9): Show | 12 | 286 | 0.0420 | 3 | c.154 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100725934 | C | CAAA | intron_variant | MODIFIER | HG01109.hp2 HG01175.hp1 HG02486.hp1 others(5): Show |
a0001a0002 | a0001c0010a0002c0002a0002c0006 | a0001c0010t0001a0002c0002t0002a0002c0006t0008others(2): Show | a0001c0010t0001g0238a0002c0002t0002g0019a0002c0006t0008g0240others(5): Show | 8 | 286 | 0.0280 | 3 | c.154 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100733825 | G | GAAA | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(59): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0008others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(18): Show | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0027others(59): Show | 62 | 286 | 0.2168 | 3 | c.155 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100735002 | A | AAAC | intron_variant | MODIFIER | HG00735.hp2 HG01346.hp1 HG01433.hp2 others(7): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0014a0002c0002t0002others(4): Show | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0003t0014g0234others(7): Show | 10 | 286 | 0.0350 | 3 | c.155 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100735023 | C | CAAA | intron_variant | MODIFIER | HG01433.hp1 HG02280.hp1 HG02615.hp2 others(3): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0001a0002c0002t0002a0002c0004t0007 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0015others(3): Show | 6 | 286 | 0.0210 | 3 | c.155 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100751773 | C | CTTT | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(9): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0001a0002c0002t0002a0002c0002t0004others(3): Show | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0068others(9): Show | 12 | 286 | 0.0420 | 3 | c.155 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100764005 | C | CTCT | intron_variant | MODIFIER | HG02055.hp1 HG02559.hp2 HG03139.hp1 others(1): Show |
a0002 | a0002c0002a0002c0011 | a0002c0002t0018a0002c0002t0039a0002c0011t0017 | a0002c0002t0018g0193a0002c0002t0018g0194a0002c0002t0039g0195others(1): Show | 4 | 286 | 0.0140 | 3 | c.155 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | C | CAAA | intron_variant | MODIFIER | HG00738.hp2 HG01358.hp2 HG02897.hp2 others(4): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0002c0004others(2): Show | a0001c0001t0001a0002c0002t0020a0002c0004t0007others(2): Show | a0001c0001t0001g0095a0001c0001t0001g0184a0001c0001t0001g0210others(4): Show | 7 | 286 | 0.0245 | 3 | c.251 others(18): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837662 | C | CATT | intron_variant | MODIFIER | HG00423.hp1 HG00738.hp1 HG00741.hp1 others(17): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0031a0001c0003t0006others(6): Show | a0001c0001t0001g0047a0001c0001t0001g0062a0001c0001t0001g0066others(17): Show | 20 | 286 | 0.0699 | 3 | c.313 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875761 | C | CGGG | intron_variant | MODIFIER | HG00544.hp2 HG01928.hp2 HG02056.hp2 others(33): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0030a0001c0003t0006others(5): Show | a0001c0001t0001g0023a0001c0001t0001g0091a0001c0001t0001g0126others(33): Show | 36 | 286 | 0.1259 | 3 | c.384 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100876005 | T | TTAA | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(34): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(6): Show | a0001c0001t0001g0135a0001c0001t0001g0266a0001c0001t0001g0279others(34): Show | 37 | 286 | 0.1294 | 3 | c.384 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100895493 | C | CTTT | intron_variant | MODIFIER | HG00423.hp1 HG00733.hp1 HG01070.hp1 others(18): Show |
a0001a0002 | a0001c0003a0002c0002a0002c0005 | a0001c0003t0001a0001c0003t0006a0001c0003t0014others(4): Show | a0001c0003t0001g0157a0001c0003t0001g0158a0001c0003t0001g0170others(18): Show | 21 | 286 | 0.0734 | 3 | c.385 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100899669 | C | CTTT | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(30): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(4): Show | a0001c0003t0001g0157a0001c0003t0001g0158a0001c0003t0001g0170others(30): Show | 33 | 286 | 0.1154 | 3 | c.385 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100904247 | C | CTCT | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(29): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(4): Show | a0001c0003t0001g0157a0001c0003t0001g0158a0001c0003t0003g0118others(29): Show | 32 | 286 | 0.1119 | 3 | c.385 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100914509 | G | GAAC | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(34): Show |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(5): Show | a0001c0003t0001g0157a0001c0003t0001g0158a0001c0003t0001g0170others(34): Show | 37 | 286 | 0.1294 | 3 | c.486 others(18): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980550 | T | TTTC | intron_variant | MODIFIER | HG00408.hp2 HG02630.hp1 HG03130.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0002a0002c0002t0035 | a0001c0001t0002g0025a0002c0002t0002g0139a0002c0002t0002g0222others(1): Show | 4 | 286 | 0.0140 | 3 | c.245 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100996996 | C | CTTT | downstream_gene_variant | MODIFIER | HG00735.hp1 HG01496.hp2 NA18959.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0041a0001c0003t0001 | a0001c0001t0001g0196a0001c0001t0001g0220a0001c0001t0041g0116others(1): Show | 4 | 286 | 0.0140 | 3 | c.*81 others(14): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3056 | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12804971 | T | TCTG | intron_variant | MODIFIER | HG02622.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | 230 | 0.0217 | 3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12814235 | G | GTTT | intron_variant | MODIFIER | HG02451.hp1 HG02559.hp1 HG02647.hp1 others(4): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(2): Show | a0001c0001t0001a0001c0004t0010a0001c0005t0001others(2): Show | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0004t0010g0031others(4): Show | 7 | 230 | 0.0304 | 3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12818335 | G | GAAA | intron_variant | MODIFIER | HG00423.hp1 HG00733.hp1 HG00738.hp2 others(39): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(39): Show | 42 | 230 | 0.1826 | 3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12828628 | T | TTTC | intron_variant | MODIFIER | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0003 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | 230 | 0.0217 | 3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12828636 | C | CTTT | intron_variant | MODIFIER | HG02145.hp1 HG02622.hp2 HG02647.hp2 others(5): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(3): Show | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0001t0001g0189others(5): Show | 8 | 230 | 0.0348 | 3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12842148 | T | TAAA | intron_variant | MODIFIER | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0003 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | 230 | 0.0217 | 3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12845506 | C | CAAA | intron_variant | MODIFIER | HG02559.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0010 | a0001c0001t0001g0033a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | 230 | 0.0217 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12846098 | G | GAAA | intron_variant | MODIFIER | HG00423.hp1 HG00733.hp1 HG01243.hp1 others(17): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(5): Show | a0001c0001t0001g0194a0001c0001t0001g0202a0001c0001t0001g0209others(17): Show | 20 | 230 | 0.0870 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12847510 | C | CTTT | intron_variant | MODIFIER | HG02258.hp1 HG02622.hp2 NA18906.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0009a0001c0005t0007 | a0001c0001t0001g0027a0001c0001t0009g0151a0001c0005t0007g0039 | 3 | 230 | 0.0130 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12849568 | C | CTTT | intron_variant | MODIFIER | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(4): Show | a0001c0001t0001g0136a0001c0001t0001g0174a0001c0001t0001g0225others(7): Show | 10 | 230 | 0.0435 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12849594 | T | TTTG | intron_variant | MODIFIER | HG00423.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0008a0001c0001t0019others(1): Show | a0001c0001t0001g0209a0001c0001t0001g0214a0001c0001t0008g0042others(5): Show | 8 | 230 | 0.0348 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12852277 | C | CTTT | intron_variant | MODIFIER | HG00423.hp2 HG02027.hp2 HG02145.hp2 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0002g0015others(6): Show | 9 | 230 | 0.0391 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar |