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 | 11169709 | CTGT | C | intron_variant | MODIFIER | HG03492.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0034 | 1 | 144 | 0.0069 | -3 | c.163 others(18): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174628 | TTTC | T | intron_variant | MODIFIER | HG00738.hp1 HG01167.hp1 HG02647.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0036a0001c0001t0002g0129a0001c0001t0002g0132others(1): Show | 4 | 144 | 0.0278 | -3 | c.162 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174632 | TTTC | T | intron_variant | MODIFIER | HG00280.hp1 HG00609.hp1 HG02055.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0015a0001c0001t0019others(3): Show | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0061others(9): Show | 12 | 144 | 0.0833 | -3 | c.162 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11302277 | GTAC | G | intron_variant | MODIFIER | NA19055.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 144 | 0.0069 | -3 | c.589 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11310160 | CAAA | C | intron_variant | MODIFIER | HG01106.hp1 HG02451.hp2 HG02965.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007a0001c0001t0008 | a0001c0001t0001g0020a0001c0001t0001g0043a0001c0001t0001g0046others(3): Show | 6 | 144 | 0.0417 | -3 | c.589 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11310771 | CCTT | C | intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0126 | 1 | 144 | 0.0069 | -3 | c.589 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11344678 | CAAA | C | intron_variant | MODIFIER | HG01109.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0028 | 1 | 144 | 0.0069 | -3 | c.589 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11354294 | TTTC | T | intron_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023 | 1 | 144 | 0.0069 | -3 | c.589 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11358482 | TTTC | T | intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0005 | a0002c0005t0006 | a0002c0005t0006g0018 | 1 | 144 | 0.0069 | -3 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11370893 | AAAC | A | intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0005 | a0002c0005t0006 | a0002c0005t0006g0018 | 1 | 144 | 0.0069 | -3 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11427815 | AGAG | A | intron_variant | MODIFIER | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(49): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(6): Show | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0024others(49): Show | 52 | 144 | 0.3611 | -3 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11443291 | ATTG | A | intron_variant | MODIFIER | HG01109.hp1 HG01258.hp1 HG01934.hp1 others(14): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0007t0001a0002c0002t0003others(1): Show | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0027others(14): Show | 17 | 144 | 0.1181 | -3 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11454110 | ATTT | A | intron_variant | MODIFIER | HG01109.hp1 HG01258.hp1 HG01934.hp1 others(15): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0007t0001others(2): Show | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0028others(15): Show | 18 | 144 | 0.1250 | -3 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11477172 | AAAC | A | intron_variant | MODIFIER | HG01109.hp1 HG01258.hp1 HG01934.hp1 others(15): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0007t0001a0002c0002t0003others(1): Show | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0027others(15): Show | 18 | 144 | 0.1250 | -3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11484429 | AAAG | A | intron_variant | MODIFIER | HG01256.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0019 | 1 | 144 | 0.0069 | -3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11498942 | TGAG | T | intron_variant | MODIFIER | HG03492.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0034 | 1 | 144 | 0.0069 | -3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11500663 | CAAA | C | intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0005 | a0002c0005t0006 | a0002c0005t0006g0018 | 1 | 144 | 0.0069 | -3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11500976 | TTGA | T | intron_variant | MODIFIER | HG02735.hp1 NA19240.hp1 |
a0002 | a0002c0002a0002c0005 | a0002c0002t0003a0002c0005t0006 | a0002c0002t0003g0016a0002c0005t0006g0018 | 2 | 144 | 0.0139 | -3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11514161 | CAAA | C | intron_variant | MODIFIER | NA20129.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0012 | 1 | 144 | 0.0069 | -3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11518462 | CTTT | C | intron_variant | MODIFIER | HG01109.hp1 NA18955.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0028a0001c0001t0001g0122 | 2 | 144 | 0.0139 | -3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11520130 | TTTA | T | intron_variant | MODIFIER | HG03942.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0135 | 1 | 144 | 0.0069 | -3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11559929 | AAAT | A | intron_variant | MODIFIER | HG02132.hp1 NA19056.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0081a0001c0001t0011g0001 | 2 | 144 | 0.0139 | -3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11589413 | CCTT | C | intron_variant | MODIFIER | HG02735.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0016 | 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 | 11590848 | AAAG | A | intron_variant | MODIFIER | HG01167.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0132 | 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 | 11592823 | TTGG | T | intron_variant | MODIFIER | NA18966.hp1 NA19058.hp1 NA19088.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0096a0001c0001t0001g0100a0001c0001t0001g0107 | 3 | 144 | 0.0208 | -3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11623696 | CAAA | C | intron_variant | MODIFIER | HG03486.hp2 NA19063.hp1 NA19082.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0016 | a0001c0001t0001g0014a0001c0001t0001g0026a0002c0002t0016g0007 | 3 | 144 | 0.0208 | -3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11628477 | TTTC | T | intron_variant | MODIFIER | HG02055.hp1 HG02809.hp1 NA19043.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126 | 3 | 144 | 0.0208 | -3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11636033 | CCTT | C | intron_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0125 | 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 | 11637762 | ATTT | A | intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0013 | 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 | 11645713 | AAAG | A | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG01256.hp1 others(23): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0001t0008a0001c0001t0022others(4): Show | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(23): Show | 26 | 144 | 0.1806 | -3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11659449 | AAAG | A | intron_variant | MODIFIER | HG00280.hp1 HG01515.hp1 HG02698.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003a0002c0002t0016 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(7): Show | 10 | 144 | 0.0694 | -3 | c.588 others(20): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | CAAA | C | intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0049 | 1 | 144 | 0.0069 | -3 | c.588 others(20): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44754981 | CCTT | C | intron_variant | MODIFIER | HG00323.hp2 HG00597.hp1 HG00621.hp2 others(17): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0002c0003others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(8): Show | a0001c0001t0001g0192a0001c0001t0001g0200a0001c0001t0003g0081others(17): Show | 20 | 390 | 0.0513 | -3 | c.-72 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44757805 | ATTT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(160): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0004a0001c0007others(47): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(58): Show | a0001c0001t0001g0024a0001c0001t0003g0006a0001c0001t0003g0023others(160): Show | 163 | 390 | 0.4180 | -3 | c.-72 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44772223 | CTTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0004a0001c0007others(38): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(45): Show | a0001c0001t0001g0024a0001c0001t0003g0109a0001c0001t0003g0110others(104): Show | 107 | 390 | 0.2744 | -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 | 44786441 | ATCT | A | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(79): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0004a0001c0007others(33): Show | a0001c0001t0001a0001c0001t0010a0001c0004t0001others(40): Show | a0001c0001t0001g0017a0001c0001t0010g0198a0001c0004t0001g0007others(79): Show | 82 | 390 | 0.2103 | -3 | c.-71 others(15): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44791182 | ATGT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0004a0001c0007others(37): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(44): Show | a0001c0001t0001g0200a0001c0001t0003g0006a0001c0001t0003g0023others(135): Show | 138 | 390 | 0.3539 | -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 | 44794287 | CATT | C | intron_variant | MODIFIER | HG02135.hp1 HG02258.hp2 HG02559.hp1 others(17): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0007a0002c0003others(11): Show | a0001c0001t0003a0001c0001t0010a0001c0007t0001others(12): Show | a0001c0001t0003g0006a0001c0001t0003g0293a0001c0001t0010g0198others(17): Show | 20 | 390 | 0.0513 | -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 | 44802985 | CCTG | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0007a0001c0018others(35): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(44): Show | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0097others(166): Show | 169 | 390 | 0.4333 | -3 | c.167 others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | GTTT | G | intron_variant | MODIFIER | HG01099.hp1 HG02897.hp1 HG03041.hp2 others(4): Show |
a0001a0002a0003 | a0001c0004a0001c0007a0002c0011others(2): Show | a0001c0004t0011a0001c0007t0001a0002c0011t0005others(2): Show | a0001c0004t0011g0190a0001c0007t0001g0069a0001c0007t0001g0107others(4): Show | 7 | 390 | 0.0180 | -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 | 44828425 | ATTT | A | intron_variant | MODIFIER | HG00609.hp2 HG00738.hp1 HG01106.hp2 others(38): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0007others(15): Show | a0001c0001t0003a0001c0004t0001a0001c0007t0001others(18): Show | a0001c0001t0003g0260a0001c0004t0001g0136a0001c0007t0001g0058others(38): Show | 41 | 390 | 0.1051 | -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 | 44838908 | CTTG | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0004a0001c0007others(44): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(52): Show | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0161others(156): Show | 159 | 390 | 0.4077 | -3 | c.597 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44850899 | GGTT | G | intron_variant | MODIFIER | HG01496.hp2 HG01891.hp1 HG01943.hp2 others(22): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0007a0001c0008others(10): Show | a0001c0001t0001a0001c0007t0001a0001c0008t0001others(10): Show | a0001c0001t0001g0017a0001c0007t0001g0058a0001c0007t0001g0069others(22): Show | 25 | 390 | 0.0641 | -3 | c.877 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44852189 | CAAA | C | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(90): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0004a0001c0007others(27): Show | a0001c0001t0001a0001c0004t0001a0001c0007t0001others(29): Show | a0001c0001t0001g0097a0001c0001t0001g0370a0001c0004t0001g0136others(90): Show | 93 | 390 | 0.2385 | -3 | c.877 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTTT | C | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(29): Show |
a0001a0003a0004others(2): Show | a0001c0001a0003c0002a0003c0005others(6): Show | a0001c0001t0001a0001c0001t0003a0003c0002t0002others(8): Show | a0001c0001t0001g0192a0001c0001t0003g0074a0001c0001t0003g0201others(29): Show | 32 | 390 | 0.0821 | -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 | 44860996 | TCTC | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0004a0001c0008others(37): Show | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(42): Show | a0001c0001t0003g0006a0001c0001t0003g0023a0001c0001t0003g0028others(177): Show | 180 | 390 | 0.4615 | -3 | c.981 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44864878 | ACTG | A | downstream_gene_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG01070.hp2 others(28): Show |
a0001a0005a0011others(1): Show | a0001c0001a0001c0004a0001c0007others(8): Show | a0001c0001t0001a0001c0004t0001a0001c0007t0001others(9): Show | a0001c0001t0001g0097a0001c0001t0001g0370a0001c0004t0001g0136others(28): Show | 31 | 390 | 0.0795 | -3 | c.*22 others(14): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2095 | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44865300 | TAGA | T | downstream_gene_variant | MODIFIER | HG01070.hp2 HG01071.hp2 HG02738.hp1 |
a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0012a0001c0009t0001g0076a0001c0009t0001g0077 | 3 | 390 | 0.0077 | -3 | c.*27 others(14): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2517 | chr22 | TogoVar | ||||||
ARHGDIB_chr12_14937031_14966601 | 14964219 | TAAG | T | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(48): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0003others(2): Show | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(36): Show | 51 | 464 | 0.1099 | -3 | c.-26 others(14): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 2619 | chr12 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 278439 | ACTC | A | upstream_gene_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG02572.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0005a0001c0001t0013others(1): Show | a0001c0001t0003g0005a0001c0001t0005g0005a0001c0001t0013g0020others(1): Show | 5 | 442 | 0.0113 | -3 | c.-22 others(14): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2151 | chr16 | TogoVar |