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 | 11465134 | AACTT | A | intron_variant | MODIFIER | HG02735.hp1 HG03098.hp1 NA20129.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003a0002c0002t0006 | a0001c0001t0001g0024a0002c0002t0003g0016a0002c0002t0006g0031 | 3 | 144 | 0.0208 | -4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11467980 | AAATG | A | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG00738.hp1 others(57): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(8): Show | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0014others(57): Show | 60 | 144 | 0.4167 | -4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11467992 | GAATA | G | intron_variant | MODIFIER | HG01106.hp1 HG02055.hp1 HG02074.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(1): Show | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0057others(6): Show | 9 | 144 | 0.0625 | -4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11475560 | TACAC | T | intron_variant | MODIFIER | HG00621.hp1 HG00673.hp1 HG02572.hp1 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0044others(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 | 11500681 | AAAAG | A | intron_variant | MODIFIER | HG03098.hp1 NA20129.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0006 | a0001c0001t0001g0024a0002c0002t0006g0031 | 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 | 11508852 | TACAC | T | intron_variant | MODIFIER | NA19009.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0032 | 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 | 11514838 | GCACA | G | intron_variant | MODIFIER | HG01074.hp1 NA18943.hp1 NA18986.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0016 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0104others(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 | 11520131 | TTATA | T | intron_variant | MODIFIER | HG02922.hp2 HG03516.hp1 NA18962.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0002c0002t0003others(1): Show | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0004g0095others(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 | 11527011 | AGTGT | A | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG01258.hp1 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0008a0001c0001t0015others(1): Show | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0035others(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 | 11552555 | CATAT | C | intron_variant | MODIFIER | HG00673.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0015a0001c0003t0001others(1): Show | a0001c0001t0001g0027a0001c0001t0001g0085a0001c0001t0001g0094others(4): Show | 7 | 144 | 0.0486 | -4 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11558836 | CAAAA | C | intron_variant | MODIFIER | HG02735.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0016 | 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 | 11566906 | TCAAA | T | intron_variant | MODIFIER | HG02300.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0084 | 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 | 11592627 | ATATT | A | intron_variant | MODIFIER | HG03098.hp1 NA20129.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0006 | a0001c0001t0001g0024a0002c0002t0006g0031 | 2 | 144 | 0.0139 | -4 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11623696 | CAAAA | C | intron_variant | MODIFIER | HG00280.hp1 HG01515.hp1 HG02698.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(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 | 11623776 | ATAAT | A | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG01256.hp1 others(24): Show |
a0001a0002a0003 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0022others(5): Show | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(24): Show | 27 | 144 | 0.1875 | -4 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11628300 | CACAG | C | intron_variant | MODIFIER | HG01243.hp1 HG03486.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0005 | a0001c0001t0001g0014a0001c0004t0005g0015 | 2 | 144 | 0.0139 | -4 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11628984 | CGTGT | C | intron_variant | MODIFIER | HG01074.hp1 HG01106.hp1 HG01256.hp1 others(27): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0007a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(8): Show | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(27): Show | 30 | 144 | 0.2083 | -4 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11629017 | GTGTA | G | intron_variant | MODIFIER | HG02735.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0016 | 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 | 11630010 | AGTGT | A | intron_variant | MODIFIER | HG00280.hp1 HG01515.hp1 HG02698.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003a0002c0002t0016 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(5): Show | 8 | 144 | 0.0556 | -4 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11630618 | AGGAT | A | intron_variant | MODIFIER | HG00280.hp1 HG01515.hp1 HG02698.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003a0002c0002t0016 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(5): Show | 8 | 144 | 0.0556 | -4 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11655239 | TTGAG | T | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG01256.hp1 others(23): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0001t0008a0001c0001t0022others(4): Show | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(23): Show | 26 | 144 | 0.1806 | -4 | c.588 others(21): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44757805 | ATTTT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0004a0001c0007others(36): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(44): Show | a0001c0001t0001g0017a0001c0001t0001g0097a0001c0001t0001g0134others(118): Show | 121 | 390 | 0.3103 | -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 | 44766099 | GGTCT | G | intron_variant | MODIFIER | HG00323.hp2 HG01243.hp1 HG01891.hp1 others(29): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0007others(16): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(19): Show | a0001c0001t0001g0017a0001c0001t0001g0192a0001c0001t0003g0081others(29): Show | 32 | 390 | 0.0821 | -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 | 44772223 | CTTTT | C | intron_variant | MODIFIER | HG00438.hp2 HG01167.hp1 HG01358.hp2 others(23): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0007others(12): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(13): Show | a0001c0001t0001g0200a0001c0001t0003g0028a0001c0004t0003g0339others(23): Show | 26 | 390 | 0.0667 | -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 | TTTTA | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0004a0001c0007others(39): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(47): Show | a0001c0001t0001g0024a0001c0001t0001g0097a0001c0001t0001g0134others(135): Show | 138 | 390 | 0.3539 | -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 | 44813320 | CACAT | C | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp2 HG02615.hp2 others(7): Show |
a0001a0002a0006others(3): Show | a0001c0007a0002c0011a0006c0027others(4): Show | a0001c0007t0001a0002c0011t0005a0006c0027t0001others(4): Show | a0001c0007t0001g0058a0001c0007t0001g0202a0002c0011t0005g0061others(7): Show | 10 | 390 | 0.0256 | -4 | c.300 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44813328 | TACAG | T | intron_variant | MODIFIER | NA18947.hp1 NA19004.hp1 NA19058.hp2 others(2): Show |
a0001a0002a0004 | a0001c0001a0002c0003a0002c0016others(1): Show | a0001c0001t0001a0002c0003t0004a0002c0016t0004others(1): Show | a0001c0001t0001g0097a0002c0003t0004g0253a0002c0016t0004g0199others(2): Show | 5 | 390 | 0.0128 | -4 | c.300 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | GTTTT | G | intron_variant | MODIFIER | HG01255.hp1 HG01516.hp2 HG01517.hp2 others(21): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0004a0001c0007others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(13): Show | a0001c0001t0001g0161a0001c0001t0003g0293a0001c0001t0010g0198others(21): Show | 24 | 390 | 0.0615 | -4 | c.596 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44828425 | ATTTT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0007others(24): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(30): Show | a0001c0001t0001g0024a0001c0001t0001g0097a0001c0001t0001g0370others(130): Show | 133 | 390 | 0.3410 | -4 | c.596 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44829721 | TATGA | T | intron_variant | MODIFIER | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0007others(13): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(15): Show | a0001c0001t0001g0024a0001c0001t0003g0080a0001c0001t0003g0081others(66): Show | 69 | 390 | 0.1769 | -4 | c.596 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44843972 | TAGAG | T | intron_variant | MODIFIER | NA18906.hp2 NA18961.hp2 NA18982.hp1 |
a0002a0003 | a0002c0020a0003c0002 | a0002c0020t0005a0003c0002t0002 | a0002c0020t0005g0355a0003c0002t0002g0026a0003c0002t0002g0032 | 3 | 390 | 0.0077 | -4 | c.597 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44850963 | CAAAA | C | intron_variant | MODIFIER | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(12): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0004a0002c0016others(4): Show | a0001c0001t0001a0001c0004t0001a0002c0016t0004others(5): Show | a0001c0001t0001g0097a0001c0001t0001g0370a0001c0004t0001g0136others(12): Show | 15 | 390 | 0.0385 | -4 | c.877 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44851393 | ATATT | A | intron_variant | MODIFIER | HG00280.hp1 HG00544.hp1 HG00609.hp1 others(142): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0004a0001c0007others(34): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(40): Show | a0001c0001t0001g0017a0001c0001t0003g0074a0001c0001t0003g0113others(142): Show | 145 | 390 | 0.3718 | -4 | c.877 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTTTT | C | intron_variant | MODIFIER | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(7): Show |
a0001a0003a0004others(1): Show | a0001c0004a0003c0002a0003c0005others(3): Show | a0001c0004t0010a0003c0002t0002a0003c0005t0002others(4): Show | a0001c0004t0010g0302a0003c0002t0002g0269a0003c0005t0002g0330others(7): Show | 10 | 390 | 0.0256 | -4 | c.878 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44857907 | TCCTG | T | intron_variant | MODIFIER | HG02055.hp1 HG02809.hp2 HG02976.hp1 others(1): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0009a0001c0001t0010a0001c0004t0010 | a0001c0001t0009g0173a0001c0001t0009g0321a0001c0001t0010g0198others(1): Show | 4 | 390 | 0.0103 | -4 | c.878 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44858548 | TTTTA | T | intron_variant | MODIFIER | HG00099.hp2 HG01255.hp1 HG01516.hp1 others(9): Show |
a0002a0008a0009others(1): Show | a0002c0011a0002c0013a0008c0014others(3): Show | a0002c0011t0005a0002c0013t0005a0008c0014t0005others(3): Show | a0002c0011t0005g0086a0002c0011t0005g0319a0002c0013t0005g0043others(9): Show | 12 | 390 | 0.0308 | -4 | c.878 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44862250 | TTTAC | T | intron_variant | MODIFIER | HG02630.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
a0002 | a0002c0011a0002c0020a0002c0023 | a0002c0011t0005a0002c0020t0005a0002c0023t0005 | a0002c0011t0005g0333a0002c0020t0005g0047a0002c0020t0005g0355others(3): Show | 6 | 390 | 0.0154 | -4 | c.982 others(17): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44862611 | GTATA | G | 3_prime_UTR_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(96): Show |
a0003a0004a0007others(4): Show | a0003c0002a0003c0005a0003c0034others(16): Show | a0003c0002t0002a0003c0005t0002a0003c0005t0014others(18): Show | a0003c0002t0002g0008a0003c0002t0002g0026a0003c0002t0002g0032others(96): Show | 99 | 390 | 0.2539 | -4 | c.*18 others(11): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 12/12 | 18 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||
ARHGAP8_chr22_44747575_44867784 | 44867299 | CAAAA | C | downstream_gene_variant | MODIFIER | HG02165.hp2 HG02630.hp1 HG02717.hp2 others(7): Show |
a0002a0010 | a0002c0011a0002c0013a0002c0020others(3): Show | a0002c0011t0005a0002c0011t0007a0002c0013t0007others(4): Show | a0002c0011t0005g0333a0002c0011t0007g0031a0002c0013t0007g0187others(7): Show | 10 | 390 | 0.0256 | -4 | c.*47 others(15): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4516 | chr22 | TogoVar | ||||||
ARHGDIA_chr17_81862721_81876337 | 81868078 | GAGAC | G | 3_prime_UTR_variant | MODIFIER | HG02615.hp1 HG03471.hp2 HG03540.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0010 | a0001c0001t0006g0011a0001c0001t0010g0023 | 3 | 384 | 0.0078 | -4 | c.*79 others(13): Show |
ARHGDIA | ENSG00000141522.12 | transcript | ENST00000269321.12 | protein_coding | 6/6 | 794 | chr17 | TogoVar | |||||
ARHGDIB_chr12_14937031_14966601 | 14948100 | GCACA | G | intron_variant | MODIFIER | HG00140.hp2 HG00733.hp1 HG01071.hp2 others(18): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0003 | a0001c0001t0001g0079a0001c0002t0001g0009a0001c0002t0001g0010others(8): Show | 21 | 464 | 0.0453 | -4 | c.266 others(19): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | TogoVar | ||||||
ARHGDIB_chr12_14937031_14966601 | 14953818 | GCTCT | G | intron_variant | MODIFIER | HG00609.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0006 | a0001c0001t0001g0157a0001c0002t0001g0081a0001c0002t0001g0217others(1): Show | 5 | 464 | 0.0108 | -4 | c.-12 others(21): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | TogoVar | ||||||
ARHGDIB_chr12_14937031_14966601 | 14953954 | TTTCC | T | intron_variant | MODIFIER | HG01891.hp2 HG02109.hp2 HG02135.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0007a0001c0002t0001 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0269others(7): Show | 14 | 464 | 0.0302 | -4 | c.-12 others(21): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | TogoVar | ||||||
ARHGDIB_chr12_14937031_14966601 | 14966220 | CGTGT | C | upstream_gene_variant | MODIFIER | HG02615.hp2 NA18946.hp2 NA18972.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | 464 | 0.0151 | -4 | c.-47 others(15): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 4620 | chr12 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 282999 | GTCTC | G | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(75): Show | 357 | 442 | 0.8077 | -4 | c.*19 others(13): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 6/6 | 190 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||
ARHGDIG_chr16_275591_288010 | 287491 | ATAAT | A | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(90): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(41): Show | 93 | 442 | 0.2104 | -4 | c.*46 others(15): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 4482 | chr16 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17552571 | GTTTT | G | intron_variant | MODIFIER | HG02572.hp1 HG02602.hp1 HG02896.hp2 others(6): Show |
a0001a0002 | a0001c0001a0002c0007a0002c0008others(1): Show | a0001c0001t0001a0001c0001t0003a0002c0007t0002others(2): Show | a0001c0001t0001g0010a0001c0001t0001g0062a0001c0001t0001g0124others(6): Show | 9 | 168 | 0.0536 | -4 | c.-44 others(23): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17562415 | TCAAA | T | intron_variant | MODIFIER | HG02109.hp1 HG02280.hp1 |
a0001a0019 | a0001c0006a0019c0029 | a0001c0006t0007a0019c0029t0001 | a0001c0006t0007g0150a0019c0029t0001g0121 | 2 | 168 | 0.0119 | -4 | c.-43 others(23): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17566024 | GTGTT | G | intron_variant | MODIFIER | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0008a0002c0041 | a0001c0001t0001a0001c0001t0003a0002c0008t0002others(1): Show | a0001c0001t0001g0062a0001c0001t0001g0124a0001c0001t0001g0127others(4): Show | 7 | 168 | 0.0417 | -4 | c.-43 others(23): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17584857 | GCACA | G | intron_variant | MODIFIER | HG00738.hp1 HG02071.hp1 HG02809.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0011a0001c0013others(1): Show | a0001c0001t0003a0001c0011t0001a0001c0013t0001others(1): Show | a0001c0001t0003g0168a0001c0011t0001g0004a0001c0013t0001g0008others(2): Show | 5 | 168 | 0.0298 | -4 | c.38- others(19): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar |