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 | 11320766 | T | TACAC | intron_variant | MODIFIER | HG00609.hp1 HG01069.hp1 HG01192.hp1 others(28): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0036others(28): Show | 31 | 144 | 0.2153 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11340727 | T | TCAAA | intron_variant | MODIFIER | HG02735.hp1 HG03130.hp1 NA19240.hp1 others(1): Show |
a0001a0002 | a0001c0007a0002c0002a0002c0005 | a0001c0007t0001a0002c0002t0003a0002c0005t0006 | a0001c0007t0001g0021a0002c0002t0003g0012a0002c0002t0003g0016others(1): Show | 4 | 144 | 0.0278 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11346719 | A | AAAAG | intron_variant | MODIFIER | HG01243.hp1 HG02027.hp1 HG02056.hp1 others(9): Show |
a0001a0003 | a0001c0001a0001c0004a0001c0009others(1): Show | a0001c0001t0001a0001c0001t0014a0001c0004t0005others(2): Show | a0001c0001t0001g0058a0001c0001t0001g0068a0001c0001t0001g0071others(9): Show | 12 | 144 | 0.0833 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11346922 | A | AAAAC | intron_variant | MODIFIER | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(18): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(6): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0042others(18): Show | 21 | 144 | 0.1458 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11351047 | T | TACAC | intron_variant | MODIFIER | HG01069.hp1 HG02622.hp2 HG03579.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0019 | a0001c0001t0001g0003a0001c0001t0001g0044a0001c0001t0001g0045others(4): Show | 7 | 144 | 0.0486 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11353549 | A | AGTGT | intron_variant | MODIFIER | HG02132.hp1 HG02717.hp1 NA19086.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0061a0001c0001t0001g0114a0001c0001t0011g0001 | 3 | 144 | 0.0208 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11354295 | T | TTCTC | intron_variant | MODIFIER | NA20752.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0128 | 1 | 144 | 0.0069 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11354321 | C | CTATA | intron_variant | MODIFIER | HG00280.hp1 NA19058.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008a0001c0001t0001g0100 | 2 | 144 | 0.0139 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11354351 | A | ATATG | intron_variant | MODIFIER | NA18747.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0121 | 1 | 144 | 0.0069 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11358431 | A | ATCTT | intron_variant | MODIFIER | HG02486.hp1 HG02965.hp1 HG03486.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0038others(6): Show | 9 | 144 | 0.0625 | 4 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11411183 | T | TTATA | intron_variant | MODIFIER | HG02717.hp1 HG02922.hp1 HG03209.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(1): Show | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0046others(5): Show | 8 | 144 | 0.0556 | 4 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11417059 | C | CATAT | intron_variant | MODIFIER | HG00621.hp1 HG02738.hp1 HG03471.hp1 others(6): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0010a0001c0003t0001others(1): Show | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0062others(6): Show | 9 | 144 | 0.0625 | 4 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11442336 | A | ATTCT | intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0114 | 1 | 144 | 0.0069 | 4 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11450203 | A | AGTGT | intron_variant | MODIFIER | HG01074.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0015 | a0001c0001t0001g0024a0001c0001t0001g0115a0001c0001t0002g0136others(1): Show | 4 | 144 | 0.0278 | 4 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11453222 | C | CTATA | intron_variant | MODIFIER | HG02735.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0016 | 1 | 144 | 0.0069 | 4 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11467988 | G | GAATA | intron_variant | MODIFIER | NA19056.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081 | 1 | 144 | 0.0069 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11467992 | G | GAATA | intron_variant | MODIFIER | NA18995.hp1 | a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0070 | 1 | 144 | 0.0069 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11485016 | A | AAAAC | intron_variant | MODIFIER | HG02735.hp1 HG03098.hp1 NA19240.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0005 | a0001c0001t0001a0002c0002t0003a0002c0002t0006others(1): Show | a0001c0001t0001g0024a0002c0002t0003g0012a0002c0002t0003g0016others(2): Show | 5 | 144 | 0.0347 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11492058 | G | GTTGT | intron_variant | MODIFIER | HG01109.hp1 HG01258.hp1 HG01934.hp1 others(19): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0007t0001a0002c0002t0003others(3): Show | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(19): Show | 22 | 144 | 0.1528 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11493835 | C | CTTTT | intron_variant | MODIFIER | HG01109.hp1 HG01258.hp1 HG01934.hp1 others(15): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0007t0001a0002c0002t0003others(2): Show | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 18 | 144 | 0.1250 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11497559 | T | TTCTC | intron_variant | MODIFIER | HG01109.hp1 HG01258.hp1 HG01934.hp1 others(16): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0007t0001others(2): Show | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0027others(16): Show | 19 | 144 | 0.1319 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11508852 | T | TACAC | intron_variant | MODIFIER | NA20129.hp1 NA20752.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0003 | a0001c0001t0002g0128a0002c0002t0003g0012 | 2 | 144 | 0.0139 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11514838 | G | GCACA | intron_variant | MODIFIER | NA18960.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0063 | 1 | 144 | 0.0069 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11514841 | C | CACAA | intron_variant | MODIFIER | HG01106.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0030 | 1 | 144 | 0.0069 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11519479 | G | GTTGT | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0003t0001others(5): Show | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0023others(22): Show | 25 | 144 | 0.1736 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11520131 | T | TTATA | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG01109.hp1 others(8): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0019a0001c0003t0001 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0052others(8): Show | 11 | 144 | 0.0764 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11527011 | A | AGTGT | intron_variant | MODIFIER | HG00140.hp1 HG01192.hp1 HG01255.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0019 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0044others(15): Show | 18 | 144 | 0.1250 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11552555 | C | CATAT | intron_variant | MODIFIER | HG01261.hp1 HG02027.hp1 HG02300.hp2 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0009 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0001t0001g0055others(8): Show | 11 | 144 | 0.0764 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11558836 | C | CAAAA | intron_variant | MODIFIER | HG02258.hp1 HG02572.hp1 NA18982.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(1): Show | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0004g0095others(2): Show | 5 | 144 | 0.0347 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11563348 | T | TAAAG | intron_variant | MODIFIER | HG00280.hp1 HG01106.hp1 HG01109.hp1 others(45): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(10): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(45): Show | 48 | 144 | 0.3333 | 4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11576833 | A | ATGTT | intron_variant | MODIFIER | HG00280.hp1 HG01106.hp1 HG01109.hp1 others(40): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(9): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(40): Show | 43 | 144 | 0.2986 | 4 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590869 | G | GGAAA | intron_variant | MODIFIER | HG01109.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0028 | 1 | 144 | 0.0069 | 4 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11599064 | C | CATAA | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG02258.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0008a0002c0002t0018 | a0001c0001t0001g0028a0001c0001t0008g0030a0002c0002t0018g0029 | 3 | 144 | 0.0208 | 4 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11625286 | A | AGTGT | intron_variant | MODIFIER | HG02895.hp1 | a0003 | a0003c0010 | a0003c0010t0017 | a0003c0010t0017g0119 | 1 | 144 | 0.0069 | 4 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11628984 | C | CGTGT | intron_variant | MODIFIER | HG00280.hp1 HG01243.hp1 HG03486.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0004t0005a0002c0002t0003others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0014others(4): Show | 7 | 144 | 0.0486 | 4 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | C | CAAAA | intron_variant | MODIFIER | HG00738.hp1 HG01069.hp1 HG02074.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | 144 | 0.0556 | 4 | c.588 others(21): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44754338 | T | TTGTG | intron_variant | MODIFIER | HG01891.hp2 HG02129.hp1 HG02523.hp1 others(2): Show |
a0001a0002 | a0001c0004a0002c0003a0002c0006others(1): Show | a0001c0004t0001a0002c0003t0001a0002c0003t0004others(2): Show | a0001c0004t0001g0181a0002c0003t0001g0387a0002c0003t0004g0180others(2): Show | 5 | 390 | 0.0128 | 4 | c.-72 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44754373 | T | TGTGA | intron_variant | MODIFIER | HG02273.hp2 HG03225.hp1 NA18988.hp2 |
a0001a0002a0003 | a0001c0004a0002c0019a0003c0005 | a0001c0004t0003a0002c0019t0008a0003c0005t0002 | a0001c0004t0003g0363a0002c0019t0008g0313a0003c0005t0002g0083 | 3 | 390 | 0.0077 | 4 | c.-72 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44767984 | C | CTTTT | intron_variant | MODIFIER | HG00099.hp2 HG01109.hp2 HG01256.hp2 others(17): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0007a0001c0018others(10): Show | a0001c0001t0003a0001c0007t0001a0001c0018t0001others(10): Show | a0001c0001t0003g0063a0001c0001t0003g0153a0001c0001t0003g0344others(17): Show | 20 | 390 | 0.0513 | 4 | c.-72 others(23): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44771242 | A | ATTTT | intron_variant | MODIFIER | HG00597.hp2 HG02055.hp2 HG02135.hp1 others(3): Show |
a0001a0002a0003 | a0001c0001a0001c0021a0002c0013others(2): Show | a0001c0001t0003a0001c0001t0009a0001c0021t0001others(3): Show | a0001c0001t0003g0006a0001c0001t0009g0173a0001c0021t0001g0033others(3): Show | 6 | 390 | 0.0154 | 4 | c.-71 others(23): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44777998 | T | TTTTA | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(26): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0004a0001c0008others(11): Show | a0001c0001t0003a0001c0004t0001a0001c0004t0003others(14): Show | a0001c0001t0003g0159a0001c0001t0003g0305a0001c0004t0001g0136others(26): Show | 29 | 390 | 0.0744 | 4 | c.-71 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44779564 | A | ATTTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0004a0001c0007others(50): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(59): Show | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0097others(213): Show | 216 | 390 | 0.5539 | 4 | c.-71 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44783054 | C | CCCCT | intron_variant | MODIFIER | HG02896.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
a0001a0002a0003 | a0001c0007a0002c0023a0003c0005 | a0001c0007t0001a0002c0023t0005a0003c0005t0012 | a0001c0007t0001g0069a0002c0023t0005g0071a0002c0023t0005g0072others(1): Show | 4 | 390 | 0.0103 | 4 | c.-71 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44792021 | C | CTTTT | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG01256.hp1 others(32): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0007others(16): Show | a0001c0001t0001a0001c0001t0010a0001c0004t0003others(18): Show | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0010g0198others(32): Show | 35 | 390 | 0.0897 | 4 | c.79+ others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44795040 | C | CAAAA | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp2 HG02615.hp2 others(12): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0007a0002c0011others(6): Show | a0001c0001t0009a0001c0007t0001a0002c0011t0005others(6): Show | a0001c0001t0009g0173a0001c0001t0009g0321a0001c0007t0001g0058others(12): Show | 15 | 390 | 0.0385 | 4 | c.80- others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44813790 | C | CACTT | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(137): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0004a0001c0007others(32): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(38): Show | a0001c0001t0001g0024a0001c0001t0001g0134a0001c0001t0001g0161others(137): Show | 140 | 390 | 0.3590 | 4 | c.300 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44816803 | C | CAAAA | intron_variant | MODIFIER | HG01517.hp2 HG02027.hp2 HG02055.hp2 others(4): Show |
a0001a0002a0003 | a0001c0001a0001c0009a0001c0018others(3): Show | a0001c0001t0003a0001c0009t0001a0001c0018t0001others(3): Show | a0001c0001t0003g0260a0001c0009t0001g0317a0001c0018t0001g0125others(4): Show | 7 | 390 | 0.0180 | 4 | c.386 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44818705 | C | CTCTT | intron_variant | MODIFIER | HG01496.hp2 HG02258.hp2 HG02280.hp1 others(22): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0007a0001c0008others(11): Show | a0001c0001t0003a0001c0007t0001a0001c0008t0001others(11): Show | a0001c0001t0003g0063a0001c0007t0001g0058a0001c0007t0001g0202others(22): Show | 25 | 390 | 0.0641 | 4 | c.387 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44821914 | T | TAGAG | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(144): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0004a0001c0007others(22): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(28): Show | a0001c0001t0001g0024a0001c0001t0001g0097a0001c0001t0001g0370others(144): Show | 147 | 390 | 0.3769 | 4 | c.387 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | G | GGTTT | intron_variant | MODIFIER | HG02559.hp2 HG02809.hp1 HG03516.hp1 |
a0001a0002 | a0001c0007a0002c0011a0002c0019 | a0001c0007t0001a0002c0011t0005a0002c0019t0008 | a0001c0007t0001g0324a0002c0011t0005g0016a0002c0019t0008g0046 | 3 | 390 | 0.0077 | 4 | c.596 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | chr22 | TogoVar |