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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP6_chrX_11132544_11670920 | 11558836 | C | CAAA | intron_variant | MODIFIER | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(9): Show |
a0001a0002a0004 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0007t0001others(2): Show | a0001c0001t0001g0020a0001c0001t0001g0039a0001c0001t0001g0040others(9): Show | 12 | 144 | 0.0833 | 3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11559929 | A | AAAT | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG01934.hp1 others(14): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(3): Show | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0027others(14): Show | 17 | 144 | 0.1181 | 3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11571709 | A | AAAT | intron_variant | MODIFIER | HG01167.hp1 HG01243.hp1 HG01358.hp1 others(7): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(2): Show | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0033others(7): Show | 10 | 144 | 0.0694 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590847 | A | AAGG | intron_variant | MODIFIER | HG03654.hp1 NA19056.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0056a0001c0001t0001g0081 | 2 | 144 | 0.0139 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590852 | A | AAGG | intron_variant | MODIFIER | HG02135.hp1 NA18961.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0088a0001c0001t0001g0099 | 2 | 144 | 0.0139 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590857 | A | AAGG | intron_variant | MODIFIER | HG01515.hp1 HG02027.hp1 HG03130.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0007t0001a0002c0002t0003 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0007t0001g0021others(1): Show | 4 | 144 | 0.0278 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590862 | A | AAAG | intron_variant | MODIFIER | HG00673.hp1 HG01515.hp1 HG02027.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0001t0001g0082others(4): Show | 7 | 144 | 0.0486 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590862 | A | AAGG | intron_variant | MODIFIER | HG01109.hp1 HG02040.hp1 NA18970.hp1 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0009 | a0001c0001t0001a0001c0003t0001a0001c0009t0001 | a0001c0001t0001g0028a0001c0001t0001g0068a0001c0001t0001g0087others(2): Show | 5 | 144 | 0.0347 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590921 | A | AAAG | intron_variant | MODIFIER | HG02809.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0124 | 1 | 144 | 0.0069 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11629962 | A | AAGT | intron_variant | MODIFIER | HG01261.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0080 | 1 | 144 | 0.0069 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | C | CAAA | intron_variant | MODIFIER | HG01258.hp1 HG01928.hp1 HG01943.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0021 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(11): Show | 14 | 144 | 0.0972 | 3 | c.588 others(20): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44767984 | C | CTTT | intron_variant | MODIFIER | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
a0001a0002a0005others(2): Show | a0001c0007a0001c0008a0002c0023others(3): Show | a0001c0007t0001a0001c0008t0001a0002c0023t0005others(3): Show | a0001c0007t0001g0069a0001c0008t0001g0038a0002c0023t0005g0071others(6): Show | 9 | 390 | 0.0231 | 3 | c.-72 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44771242 | A | ATTT | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0007others(25): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(32): Show | a0001c0001t0001g0042a0001c0001t0001g0161a0001c0001t0003g0023others(61): Show | 64 | 390 | 0.1641 | 3 | c.-71 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44778953 | T | TGCC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
a0001a0002a0003others(25): Show | a0001c0001a0001c0004a0001c0007others(71): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(85): Show | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0042others(306): Show | 309 | 390 | 0.7923 | 3 | c.-71 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44779564 | A | ATTT | intron_variant | MODIFIER | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(76): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0004a0001c0007others(34): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(41): Show | a0001c0001t0001g0017a0001c0001t0003g0063a0001c0001t0010g0198others(76): Show | 79 | 390 | 0.2026 | 3 | c.-71 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44787919 | C | CTTT | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
a0001a0002a0006others(1): Show | a0001c0007a0002c0011a0002c0016others(3): Show | a0001c0007t0001a0002c0011t0005a0002c0016t0004others(3): Show | a0001c0007t0001g0058a0001c0007t0001g0202a0002c0011t0005g0061others(5): Show | 8 | 390 | 0.0205 | 3 | c.79+ others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44790676 | C | CAAA | intron_variant | MODIFIER | HG00423.hp1 HG00673.hp2 HG00735.hp2 others(20): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0007others(12): Show | a0001c0001t0003a0001c0004t0001a0001c0004t0003others(13): Show | a0001c0001t0003g0063a0001c0001t0003g0080a0001c0004t0001g0335others(20): Show | 23 | 390 | 0.0590 | 3 | c.79+ others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44795040 | C | CAAA | intron_variant | MODIFIER | HG02074.hp1 HG02809.hp1 HG03130.hp2 others(3): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0007a0002c0011others(3): Show | a0001c0001t0003a0001c0007t0001a0002c0011t0005others(3): Show | a0001c0001t0003g0305a0001c0007t0001g0069a0002c0011t0005g0016others(3): Show | 6 | 390 | 0.0154 | 3 | c.80- others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44797217 | C | CTTT | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0007others(22): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(28): Show | a0001c0001t0001g0097a0001c0001t0001g0200a0001c0001t0001g0370others(96): Show | 99 | 390 | 0.2539 | 3 | c.80- others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44797979 | A | ATTT | intron_variant | MODIFIER | HG02602.hp1 HG03017.hp1 HG03704.hp1 others(7): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0003a0002c0016others(3): Show | a0001c0001t0003a0001c0001t0010a0002c0003t0004others(4): Show | a0001c0001t0003g0293a0001c0001t0010g0198a0002c0003t0004g0021others(7): Show | 10 | 390 | 0.0256 | 3 | c.80- others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44816803 | C | CAAA | intron_variant | MODIFIER | HG01496.hp2 HG01516.hp2 HG01891.hp2 others(17): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0007others(8): Show | a0001c0001t0003a0001c0004t0010a0001c0007t0001others(8): Show | a0001c0001t0003g0074a0001c0001t0003g0201a0001c0004t0010g0302others(17): Show | 20 | 390 | 0.0513 | 3 | c.386 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | G | GTTT | intron_variant | MODIFIER | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(78): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0007others(16): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(20): Show | a0001c0001t0001g0024a0001c0001t0001g0370a0001c0001t0003g0080others(78): Show | 81 | 390 | 0.2077 | 3 | c.596 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44829118 | C | CAAA | intron_variant | MODIFIER | HG00738.hp2 HG01496.hp2 HG02559.hp1 others(26): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0007a0001c0010others(18): Show | a0001c0001t0003a0001c0007t0001a0001c0010t0001others(18): Show | a0001c0001t0003g0109a0001c0001t0003g0110a0001c0007t0001g0058others(26): Show | 29 | 390 | 0.0744 | 3 | c.596 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44830024 | C | CTTT | intron_variant | MODIFIER | HG02257.hp2 HG02559.hp2 HG02647.hp1 others(6): Show |
a0001a0002a0012 | a0001c0007a0002c0003a0002c0006others(4): Show | a0001c0007t0001a0002c0003t0004a0002c0006t0004others(4): Show | a0001c0007t0001g0202a0001c0007t0001g0324a0002c0003t0004g0011others(6): Show | 9 | 390 | 0.0231 | 3 | c.596 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | C | CTTT | intron_variant | MODIFIER | HG00741.hp1 HG01891.hp1 HG02074.hp2 others(12): Show |
a0001a0006a0011others(2): Show | a0001c0001a0001c0004a0001c0007others(6): Show | a0001c0001t0001a0001c0004t0001a0001c0007t0001others(6): Show | a0001c0001t0001g0017a0001c0001t0001g0097a0001c0004t0001g0136others(12): Show | 15 | 390 | 0.0385 | 3 | c.878 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44858533 | C | CTTT | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0008others(12): Show | a0001c0001t0003a0001c0001t0011a0001c0004t0003others(14): Show | a0001c0001t0003g0023a0001c0001t0003g0028a0001c0001t0003g0063others(76): Show | 79 | 390 | 0.2026 | 3 | c.878 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44863816 | G | GCCT | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0004a0001c0008others(39): Show | a0001c0001t0003a0001c0001t0011a0001c0004t0003others(42): Show | a0001c0001t0003g0006a0001c0001t0003g0023a0001c0001t0003g0028others(178): Show | 181 | 390 | 0.4641 | 3 | c.*12 others(14): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1033 | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44867113 | C | CAAA | downstream_gene_variant | MODIFIER | HG00099.hp2 HG01109.hp2 HG01192.hp2 others(18): Show |
a0002a0008a0010others(1): Show | a0002c0011a0002c0013a0002c0020others(9): Show | a0002c0011t0005a0002c0011t0007a0002c0013t0007others(10): Show | a0002c0011t0005g0333a0002c0011t0007g0031a0002c0011t0007g0182others(18): Show | 21 | 390 | 0.0539 | 3 | c.*45 others(14): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4330 | chr22 | TogoVar | ||||||
ARHGDIB_chr12_14937031_14966601 | 14939333 | C | CAAA | downstream_gene_variant | MODIFIER | HG00099.hp1 HG01175.hp1 HG01934.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0002t0001 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0066others(8): Show | 13 | 464 | 0.0280 | 3 | c.*31 others(14): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 2697 | chr12 | TogoVar | ||||||
ARHGDIB_chr12_14937031_14966601 | 14952277 | C | CAAA | intron_variant | MODIFIER | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0086a0001c0002t0001g0009a0001c0002t0001g0087others(4): Show | 10 | 464 | 0.0216 | 3 | c.-12 others(20): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17611987 | C | CCAT | intron_variant | MODIFIER | HG00642.hp1 HG03225.hp1 HG03471.hp1 |
a0002 | a0002c0007 | a0002c0007t0002 | a0002c0007t0002g0013a0002c0007t0002g0104a0002c0007t0002g0111 | 3 | 168 | 0.0179 | 3 | c.610 others(20): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17666990 | G | GGAA | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(24): Show |
a0001a0002a0004others(4): Show | a0001c0011a0001c0017a0001c0020others(11): Show | a0001c0011t0001a0001c0017t0002a0001c0020t0001others(11): Show | a0001c0011t0001g0004a0001c0011t0001g0138a0001c0011t0001g0152others(24): Show | 27 | 168 | 0.1607 | 3 | c.300 others(22): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17695790 | T | TCTG | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(122): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0006a0001c0011others(30): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(35): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(122): Show | 125 | 168 | 0.7441 | 3 | c.330 others(20): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17696212 | C | CAAA | intron_variant | MODIFIER | HG00738.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
a0001a0010a0018 | a0001c0001a0001c0013a0001c0044others(2): Show | a0001c0001t0001a0001c0013t0001a0001c0044t0004others(2): Show | a0001c0001t0001g0124a0001c0013t0001g0008a0001c0044t0004g0161others(2): Show | 5 | 168 | 0.0298 | 3 | c.330 others(20): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1841892 | G | GACC | intron_variant | MODIFIER | HG03942.hp1 NA18960.hp1 NA19000.hp2 |
a0001a0002 | a0001c0003a0001c0115a0002c0061 | a0001c0003t0001a0001c0115t0005a0002c0061t0025 | a0001c0003t0001g0306a0001c0115t0005g0286a0002c0061t0025g0292 | 3 | 363 | 0.0083 | 3 | c.-47 others(20): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841910 | G | GACC | intron_variant | MODIFIER | HG00738.hp2 HG02074.hp2 NA19012.hp1 |
a0001a0002 | a0001c0003a0002c0034a0002c0152 | a0001c0003t0001a0002c0034t0004a0002c0152t0002 | a0001c0003t0001g0183a0002c0034t0004g0148a0002c0152t0002g0019 | 3 | 363 | 0.0083 | 3 | c.-47 others(20): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1871112 | C | CAAA | intron_variant | MODIFIER | HG01515.hp1 HG01517.hp2 HG02083.hp2 others(10): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0005others(6): Show | a0001c0001t0012a0001c0001t0019a0001c0003t0051others(8): Show | a0001c0001t0012g0207a0001c0001t0019g0320a0001c0003t0051g0118others(10): Show | 13 | 363 | 0.0358 | 3 | c.679 others(20): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889168 | G | GGAT | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01346.hp1 others(4): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0019a0001c0002t0001a0001c0002t0010others(4): Show | a0001c0001t0019g0278a0001c0002t0001g0037a0001c0002t0010g0212others(4): Show | 7 | 363 | 0.0193 | 3 | c.118 others(22): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889281 | G | GTGA | intron_variant | MODIFIER | NA18941.hp2 NA18943.hp2 NA18966.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0010 | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0002g0271a0001c0002t0001g0270a0001c0002t0002g0002others(2): Show | 5 | 363 | 0.0138 | 3 | c.118 others(22): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1893092 | C | CAAA | intron_variant | MODIFIER | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(44): Show |
a0001a0003a0006others(3): Show | a0001c0002a0001c0003a0001c0004others(30): Show | a0001c0002t0001a0001c0003t0001a0001c0003t0008others(40): Show | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0068others(44): Show | 47 | 363 | 0.1295 | 3 | c.118 others(20): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1894171 | C | CAAA | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp2 HG02717.hp1 others(5): Show |
a0001a0009 | a0001c0005a0001c0016a0001c0047others(1): Show | a0001c0005t0003a0001c0005t0016a0001c0005t0018others(4): Show | a0001c0005t0003g0359a0001c0005t0016g0101a0001c0005t0018g0337others(5): Show | 8 | 363 | 0.0220 | 3 | c.126 others(20): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156979361 | C | CTTT | intron_variant | MODIFIER | HG01175.hp2 HG02148.hp1 HG02486.hp2 others(5): Show |
a0001a0002a0010 | a0001c0001a0002c0002a0010c0014 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(2): Show | a0001c0001t0001g0278a0001c0001t0004g0151a0001c0001t0004g0179others(5): Show | 8 | 362 | 0.0221 | 3 | c.274 others(16): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156994392 | G | GTGT | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0004others(2): Show | a0001c0001t0004a0001c0001t0006a0002c0002t0002others(10): Show | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(82): Show | 86 | 362 | 0.2376 | 3 | c.33- others(18): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156994392 | G | GTTT | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(76): Show |
a0001a0002a0003 | a0001c0001a0001c0005a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(5): Show | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(76): Show | 79 | 362 | 0.2182 | 3 | c.33- others(18): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156996772 | C | CAAA | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0004others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(9): Show | a0001c0001t0001g0301a0001c0001t0001g0302a0001c0001t0004g0130others(64): Show | 68 | 362 | 0.1879 | 3 | c.33- others(20): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156996859 | A | ATTT | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(83): Show |
a0001a0002a0003 | a0001c0001a0001c0005a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(6): Show | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(83): Show | 86 | 362 | 0.2376 | 3 | c.33- others(20): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157029261 | T | TTTG | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(81): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0004 | a0001c0001t0001a0001c0001t0010a0001c0001t0034others(3): Show | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(81): Show | 84 | 362 | 0.2320 | 3 | c.32+ others(20): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157048957 | C | CTTT | upstream_gene_variant | MODIFIER | HG01952.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
a0002a0005 | a0002c0002a0002c0004a0005c0006 | a0002c0002t0002a0002c0002t0012a0002c0002t0017others(2): Show | a0002c0002t0002g0005a0002c0002t0002g0029a0002c0002t0002g0033others(8): Show | 11 | 362 | 0.0304 | 3 | c.-46 others(14): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3216 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120332520 | T | TTTG | upstream_gene_variant | MODIFIER | HG01123.hp2 HG01884.hp1 HG03239.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0014a0001c0002t0007 | a0001c0001t0001g0196a0001c0001t0014g0254a0001c0002t0007g0041others(1): Show | 4 | 308 | 0.0130 | 3 | c.-47 others(14): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 3892 | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120345701 | C | CAAA | intron_variant | MODIFIER | HG00597.hp2 HG02602.hp2 HG03239.hp2 others(4): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0022a0001c0004t0005a0001c0004t0012 | a0001c0001t0022g0158a0001c0004t0005g0046a0001c0004t0005g0047others(4): Show | 7 | 308 | 0.0227 | 3 | c.32+ others(18): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |