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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP42_chr11_100682288_100998941 | 100699506 | A | ATATT | intron_variant | MODIFIER | HG00735.hp1 HG02083.hp2 HG02895.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0011 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | 286 | 0.0245 | 4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100705015 | A | ACAAC | intron_variant | MODIFIER | HG02723.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0003a0002c0002t0002a0002c0002t0011 | a0001c0003t0003g0274a0002c0002t0002g0006a0002c0002t0011g0207others(1): Show | 4 | 286 | 0.0140 | 4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100710538 | G | GTTTT | intron_variant | MODIFIER | HG01081.hp1 HG01192.hp1 HG01346.hp1 others(14): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0003t0003a0001c0003t0006others(8): Show | a0001c0001t0001g0011a0001c0001t0001g0276a0001c0003t0003g0264others(14): Show | 17 | 286 | 0.0594 | 4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100714389 | T | TTGTG | intron_variant | MODIFIER | HG01433.hp1 HG02280.hp1 HG02970.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0135a0002c0002t0001g0012a0002c0002t0001g0013others(2): Show | 5 | 286 | 0.0175 | 4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100729054 | C | CCACT | intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
a0001a0002 | a0001c0010a0002c0006 | a0001c0010t0001a0002c0006t0008a0002c0006t0011others(1): Show | a0001c0010t0001g0238a0002c0006t0008g0240a0002c0006t0008g0243others(4): Show | 7 | 286 | 0.0245 | 4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100733825 | G | GAAAA | intron_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG00733.hp2 others(26): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0030others(7): Show | a0001c0001t0001g0023a0001c0001t0001g0080a0001c0001t0001g0177others(26): Show | 29 | 286 | 0.1014 | 4 | c.155 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100744557 | T | TGTGC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(158): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0008others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(35): Show | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0026others(158): Show | 161 | 286 | 0.5629 | 4 | c.155 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100751773 | C | CTTTT | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(18): Show | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0079others(36): Show | 39 | 286 | 0.1364 | 4 | c.155 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100764025 | C | CTTCT | intron_variant | MODIFIER | HG01433.hp1 HG02280.hp1 HG02615.hp2 others(3): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0001a0002c0002t0002a0002c0004t0007 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0015others(3): Show | 6 | 286 | 0.0210 | 4 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100766222 | G | GGTGT | intron_variant | MODIFIER | HG00099.hp1 HG00597.hp2 HG00673.hp2 others(23): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0015others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0266a0001c0001t0001g0271a0001c0001t0001g0276others(23): Show | 26 | 286 | 0.0909 | 4 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100770918 | G | GTGTT | intron_variant | MODIFIER | HG00738.hp2 HG01081.hp1 HG01891.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0005others(1): Show | a0001c0001t0001a0002c0002t0002a0002c0002t0008others(3): Show | a0001c0001t0001g0002a0002c0002t0002g0139a0002c0002t0008g0028others(5): Show | 8 | 286 | 0.0280 | 4 | c.250 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100779483 | T | TACAC | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(12): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0037a0001c0003t0003others(8): Show | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0037g0041others(12): Show | 15 | 286 | 0.0525 | 4 | c.250 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | C | CAAAA | intron_variant | MODIFIER | HG03195.hp1 HG04228.hp1 NA19005.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0091a0001c0001t0001g0198a0001c0001t0001g0199others(3): Show | 6 | 286 | 0.0210 | 4 | c.251 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100818756 | T | TTTTG | intron_variant | MODIFIER | HG00738.hp2 HG02818.hp1 HG03017.hp2 |
a0002 | a0002c0002a0002c0006a0002c0009 | a0002c0002t0002a0002c0006t0008a0002c0009t0004 | a0002c0002t0002g0102a0002c0006t0008g0240a0002c0009t0004g0237 | 3 | 286 | 0.0105 | 4 | c.312 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837663 | A | ATTAT | intron_variant | MODIFIER | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(51): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0008others(4): Show | a0001c0001t0001a0001c0001t0019a0001c0001t0024others(13): Show | a0001c0001t0001g0023a0001c0001t0001g0072a0001c0001t0001g0079others(51): Show | 54 | 286 | 0.1888 | 4 | c.313 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100845076 | G | GATAT | intron_variant | MODIFIER | HG02622.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002 | a0001c0001t0001a0001c0001t0031a0001c0008t0001others(3): Show | a0001c0001t0001g0047a0001c0001t0031g0251a0001c0008t0001g0004others(4): Show | 7 | 286 | 0.0245 | 4 | c.313 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | G | GGTGT | intron_variant | MODIFIER | HG01081.hp1 HG01243.hp2 HG01346.hp1 others(14): Show |
a0002 | a0002c0002a0002c0005 | a0002c0002t0002a0002c0002t0004a0002c0002t0008others(4): Show | a0002c0002t0002g0010a0002c0002t0002g0050a0002c0002t0002g0225others(14): Show | 17 | 286 | 0.0594 | 4 | c.313 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875073 | G | GTCTC | intron_variant | MODIFIER | HG01081.hp2 HG01106.hp1 HG01175.hp2 others(3): Show |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0018a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | 286 | 0.0210 | 4 | c.384 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100881829 | T | TTTTG | intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0010a0002c0006 | a0001c0001t0001a0001c0010t0001a0002c0006t0008others(1): Show | a0001c0001t0001g0076a0001c0010t0001g0238a0002c0006t0008g0240others(3): Show | 6 | 286 | 0.0210 | 4 | c.384 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100893158 | G | GGTGT | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(15): Show |
a0002 | a0002c0002a0002c0004a0002c0009 | a0002c0002t0002a0002c0002t0005a0002c0002t0008others(8): Show | a0002c0002t0002g0034a0002c0002t0002g0222a0002c0002t0002g0245others(15): Show | 18 | 286 | 0.0629 | 4 | c.385 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903114 | T | TGCGC | intron_variant | MODIFIER | HG00408.hp2 HG00639.hp1 HG01261.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0026a0001c0001t0001g0093a0001c0001t0001g0095others(7): Show | 10 | 286 | 0.0350 | 4 | c.385 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCACA | intron_variant | MODIFIER | HG00642.hp1 HG00673.hp2 HG01928.hp2 others(23): Show |
a0001a0002 | a0001c0003a0002c0002a0002c0011 | a0001c0003t0003a0001c0003t0022a0001c0003t0033others(8): Show | a0001c0003t0003g0119a0001c0003t0003g0155a0001c0003t0003g0219others(23): Show | 26 | 286 | 0.0909 | 4 | c.385 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903706 | C | CAAAA | intron_variant | MODIFIER | HG01243.hp2 HG02818.hp2 HG02895.hp2 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0008a0002c0002t0011a0002c0002t0018others(1): Show | a0002c0002t0008g0005a0002c0002t0011g0231a0002c0002t0018g0193others(2): Show | 5 | 286 | 0.0175 | 4 | c.385 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AATAT | intron_variant | MODIFIER | HG00741.hp1 HG01346.hp2 HG01928.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0007 | a0001c0001t0001g0069a0001c0001t0001g0141a0001c0001t0001g0145others(4): Show | 7 | 286 | 0.0245 | 4 | c.385 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100917015 | T | TTGTG | intron_variant | MODIFIER | HG00741.hp2 HG01069.hp1 HG02145.hp2 others(2): Show |
a0001a0002 | a0001c0008a0002c0002 | a0001c0008t0010a0002c0002t0004a0002c0002t0008others(1): Show | a0001c0008t0010g0253a0002c0002t0004g0108a0002c0002t0004g0109others(2): Show | 5 | 286 | 0.0175 | 4 | c.486 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100935656 | T | TCACA | intron_variant | MODIFIER | HG01346.hp1 HG02055.hp2 HG02056.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0014a0002c0002others(1): Show | a0001c0001t0001a0001c0014t0001a0002c0002t0002others(1): Show | a0001c0001t0001g0144a0001c0014t0001g0132a0002c0002t0002g0010others(1): Show | 4 | 286 | 0.0140 | 4 | c.703 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100935673 | C | CAGAG | intron_variant | MODIFIER | HG00423.hp1 HG00733.hp1 HG01070.hp1 others(11): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0006a0001c0003t0014others(1): Show | a0001c0003t0001g0157a0001c0003t0001g0158a0001c0003t0001g0170others(11): Show | 14 | 286 | 0.0490 | 4 | c.703 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100935677 | C | CACAG | intron_variant | MODIFIER | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(48): Show |
a0001a0002 | a0001c0008a0002c0002a0002c0005others(1): Show | a0001c0008t0010a0002c0002t0001a0002c0002t0002others(11): Show | a0001c0008t0010g0253a0002c0002t0001g0012a0002c0002t0001g0013others(48): Show | 51 | 286 | 0.1783 | 4 | c.703 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100935677 | C | CAGAG | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(34): Show |
a0002a0003 | a0002c0002a0002c0006a0003c0007 | a0002c0002t0002a0002c0002t0004a0002c0002t0005others(8): Show | a0002c0002t0002g0019a0002c0002t0002g0034a0002c0002t0002g0139others(34): Show | 37 | 286 | 0.1294 | 4 | c.703 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100972516 | T | TTGGA | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(80): Show |
a0001a0002 | a0001c0001a0001c0008a0001c0010others(4): Show | a0001c0001t0001a0001c0001t0019a0001c0001t0024others(11): Show | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0023others(80): Show | 83 | 286 | 0.2902 | 4 | c.155 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCT | intron_variant | MODIFIER | HG01243.hp1 HG01361.hp1 HG02280.hp2 others(9): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0024a0001c0001t0032others(1): Show | a0001c0001t0001g0123a0001c0001t0001g0133a0001c0001t0001g0154others(9): Show | 12 | 286 | 0.0420 | 4 | c.245 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTT | intron_variant | MODIFIER | HG00423.hp1 HG01256.hp1 HG02004.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0006a0001c0003t0001others(2): Show | a0001c0001t0001g0047a0001c0001t0006g0081a0001c0003t0001g0170others(4): Show | 7 | 286 | 0.0245 | 4 | c.245 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100987806 | A | AAAAT | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(104): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0014others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0024others(20): Show | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0047others(104): Show | 107 | 286 | 0.3741 | 4 | c.253 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100993327 | C | CATAT | 3_prime_UTR_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01516.hp1 others(5): Show |
a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0016a0002c0004t0007g0060a0002c0004t0007g0074others(5): Show | 8 | 286 | 0.0280 | 4 | c.*45 others(15): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 24/24 | 4540 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||
ARHGAP42_chr11_100682288_100998941 | 100995655 | G | GAATA | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(13): Show | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0023others(76): Show | 79 | 286 | 0.2762 | 4 | c.*68 others(15): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1715 | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12818335 | G | GAAAA | intron_variant | MODIFIER | HG02109.hp1 HG02145.hp2 HG02258.hp2 others(14): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0033a0001c0001t0001g0176a0001c0001t0001g0225others(14): Show | 17 | 230 | 0.0739 | 4 | c.53+ others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12825416 | T | TTGTG | intron_variant | MODIFIER | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | 230 | 0.0217 | 4 | c.53+ others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12828636 | C | CTTTT | intron_variant | MODIFIER | HG00738.hp2 HG02132.hp2 HG02145.hp2 others(7): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0007others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0154a0001c0001t0001g0163a0001c0001t0002g0108others(7): Show | 10 | 230 | 0.0435 | 4 | c.53+ others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12841637 | C | CAAAA | intron_variant | MODIFIER | HG01891.hp2 HG02647.hp1 HG02922.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0003t0001others(2): Show | a0001c0001t0001g0009a0001c0001t0003g0074a0001c0001t0003g0090others(3): Show | 6 | 230 | 0.0261 | 4 | c.53+ others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12849214 | C | CGTGT | intron_variant | MODIFIER | HG01884.hp2 HG01934.hp1 HG02280.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(1): Show | a0001c0001t0001g0214a0001c0001t0001g0227a0001c0001t0001g0228others(6): Show | 9 | 230 | 0.0391 | 4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12849568 | C | CTTTT | intron_variant | MODIFIER | HG00673.hp1 HG02559.hp1 HG02559.hp2 others(4): Show |
a0001 | a0001c0001a0001c0004a0001c0006 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0001g0033a0001c0001t0001g0112a0001c0001t0001g0137others(4): Show | 7 | 230 | 0.0304 | 4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12849594 | T | TTTTG | intron_variant | MODIFIER | HG01934.hp1 HG02145.hp2 HG03225.hp2 others(3): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(2): Show | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0007g0038others(3): Show | 6 | 230 | 0.0261 | 4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12868591 | T | TTATA | intron_variant | MODIFIER | HG01070.hp1 HG01074.hp1 HG02071.hp2 others(9): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0101others(9): Show | 12 | 230 | 0.0522 | 4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12870048 | C | CTTTT | intron_variant | MODIFIER | HG00735.hp1 HG01192.hp1 HG01192.hp2 others(19): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0035others(19): Show | 22 | 230 | 0.0957 | 4 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12894227 | T | TGAGA | intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0013a0001c0001t0001g0183a0001c0001t0002g0019others(5): Show | 8 | 230 | 0.0348 | 4 | c.54- others(17): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12894241 | A | AGAGT | intron_variant | MODIFIER | HG00639.hp2 HG01928.hp1 HG02027.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0111others(11): Show | 14 | 230 | 0.0609 | 4 | c.54- others(17): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12894241 | A | AGTGT | intron_variant | MODIFIER | HG02559.hp1 HG02895.hp1 HG02895.hp2 others(5): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0005t0001a0001c0005t0005others(2): Show | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | 230 | 0.0348 | 4 | c.54- others(17): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12894308 | G | GGAGA | intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0013a0001c0001t0001g0183a0001c0001t0002g0019others(6): Show | 9 | 230 | 0.0391 | 4 | c.54- others(17): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12898956 | G | GATTT | intron_variant | MODIFIER | HG00642.hp1 HG01192.hp2 HG01258.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0033others(3): Show | a0001c0001t0002g0008a0001c0001t0006g0099a0001c0001t0033g0029others(3): Show | 6 | 230 | 0.0261 | 4 | c.198 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903083 | T | TGAGA | intron_variant | MODIFIER | HG00642.hp1 HG02572.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0183a0001c0001t0006g0099 | 2 | 230 | 0.0087 | 4 | c.199 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar |