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 | 11411183 | T | TTATATA | intron_variant | MODIFIER | HG00642.hp1 HG01167.hp1 HG01192.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0036others(9): Show | 12 | 144 | 0.0833 | 6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11411222 | T | TATATAA | intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0043 | 1 | 144 | 0.0069 | 6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11417059 | C | CATATAT | intron_variant | MODIFIER | HG00673.hp1 HG02451.hp2 HG03017.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0003 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0038others(7): Show | 10 | 144 | 0.0694 | 6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11417105 | T | TATATAC | intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0142 | 1 | 144 | 0.0069 | 6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11427815 | A | AGAGGAG | intron_variant | MODIFIER | HG00642.hp1 HG01074.hp1 HG02698.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0045others(6): Show | 9 | 144 | 0.0625 | 6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11450203 | A | AGTGTGT | intron_variant | MODIFIER | HG03486.hp1 HG06807.hp2 NA19043.hp1 |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0007a0001c0003t0001a0001c0004t0005 | a0001c0001t0007g0013a0001c0003t0001g0126a0001c0004t0005g0047 | 3 | 144 | 0.0208 | 6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11497559 | T | TTCTCTC | intron_variant | MODIFIER | HG00140.hp1 HG01255.hp1 HG02486.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0005 | a0001c0001t0001a0001c0001t0002a0002c0002t0003others(2): Show | a0001c0001t0001g0120a0001c0001t0002g0130a0001c0001t0002g0133others(6): Show | 9 | 144 | 0.0625 | 6 | c.588 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11500663 | C | CAAAAAA | intron_variant | MODIFIER | HG02258.hp1 | a0002 | a0002c0002 | a0002c0002t0018 | a0002c0002t0018g0029 | 1 | 144 | 0.0069 | 6 | c.588 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11508852 | T | TACACAC | intron_variant | MODIFIER | HG01109.hp1 HG01258.hp1 HG01934.hp1 others(13): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0007t0001a0002c0002t0003others(1): Show | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0027others(13): Show | 16 | 144 | 0.1111 | 6 | c.588 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11520131 | T | TTATATA | intron_variant | MODIFIER | HG01928.hp1 HG01952.hp1 HG02040.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0021others(1): Show | a0001c0001t0001g0027a0001c0001t0001g0087a0001c0001t0001g0088others(4): Show | 7 | 144 | 0.0486 | 6 | c.588 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11527011 | A | AGTGTGT | intron_variant | MODIFIER | HG02074.hp1 HG02083.hp1 HG02135.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0063a0001c0001t0001g0086a0001c0001t0001g0098others(2): Show | 5 | 144 | 0.0347 | 6 | c.588 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11552555 | C | CATATAT | intron_variant | MODIFIER | HG01074.hp1 HG01167.hp1 HG01243.hp1 others(9): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0038a0001c0001t0001g0062a0001c0001t0001g0067others(9): Show | 12 | 144 | 0.0833 | 6 | c.588 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11552599 | T | TATAGAC | intron_variant | MODIFIER | HG02922.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0011 | 1 | 144 | 0.0069 | 6 | c.588 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11552599 | T | TATATAG | intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052 | 1 | 144 | 0.0069 | 6 | c.588 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11552601 | G | GACACAC | intron_variant | MODIFIER | HG01106.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0030 | 1 | 144 | 0.0069 | 6 | c.588 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11559929 | A | AAATAAT | intron_variant | MODIFIER | HG01258.hp1 HG02071.hp1 HG03098.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0005 | a0001c0001t0001a0001c0007t0001a0002c0005t0006 | a0001c0001t0001g0024a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | 144 | 0.0556 | 6 | c.588 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11571709 | A | AAATAAT | intron_variant | MODIFIER | HG02922.hp1 NA18962.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0040a0001c0001t0002g0138 | 2 | 144 | 0.0139 | 6 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590910 | G | GAAAAGA | intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0005 | a0002c0005t0006 | a0002c0005t0006g0018 | 1 | 144 | 0.0069 | 6 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11628984 | C | CGTGTGT | intron_variant | MODIFIER | HG02135.hp1 HG02922.hp2 NA18906.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003 | a0001c0001t0001g0004a0001c0001t0001g0099a0002c0002t0003g0010others(1): Show | 4 | 144 | 0.0278 | 6 | c.588 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | C | CAAAAAA | intron_variant | MODIFIER | HG01192.hp1 HG02602.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | 144 | 0.0139 | 6 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44754338 | T | TTGTGTG | intron_variant | MODIFIER | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(13): Show |
a0001a0002a0003 | a0001c0001a0001c0007a0001c0008others(8): Show | a0001c0001t0001a0001c0007t0001a0001c0008t0001others(8): Show | a0001c0001t0001g0097a0001c0007t0001g0382a0001c0008t0001g0098others(13): Show | 16 | 390 | 0.0410 | 6 | 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 | 44754373 | T | TGTGTGA | intron_variant | MODIFIER | HG02602.hp1 HG02622.hp2 HG02896.hp2 others(12): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0004a0002c0003others(7): Show | a0001c0001t0003a0001c0004t0003a0002c0003t0004others(9): Show | a0001c0001t0003g0089a0001c0004t0003g0085a0001c0004t0003g0088others(12): Show | 15 | 390 | 0.0385 | 6 | 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 | 44767984 | C | CTTTTTT | intron_variant | MODIFIER | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(14): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0004a0002c0003others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(8): Show | a0001c0001t0001g0200a0001c0001t0003g0006a0001c0001t0003g0224others(14): Show | 17 | 390 | 0.0436 | 6 | c.-72 others(25): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44787032 | A | AAAAAAC | intron_variant | MODIFIER | HG00099.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
a0002a0003a0008 | a0002c0023a0003c0005a0008c0014 | a0002c0023t0005a0003c0005t0012a0008c0014t0005 | a0002c0023t0005g0071a0002c0023t0005g0072a0003c0005t0012g0087others(1): Show | 4 | 390 | 0.0103 | 6 | 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 | 44787047 | A | AAAAAAC | intron_variant | MODIFIER | HG01243.hp2 HG02486.hp2 HG02572.hp2 others(9): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0007a0002c0011others(6): Show | a0001c0001t0001a0001c0001t0009a0001c0007t0001others(7): Show | a0001c0001t0001g0042a0001c0001t0009g0173a0001c0001t0009g0321others(9): Show | 12 | 390 | 0.0308 | 6 | 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 | 44801038 | C | CTGTCCG | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(63): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0004a0001c0007others(26): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(31): Show | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0003g0074others(63): Show | 66 | 390 | 0.1692 | 6 | c.80- others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44806945 | C | CAGAATG | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG00673.hp1 others(38): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0007a0001c0018others(18): Show | a0001c0001t0001a0001c0001t0003a0001c0007t0001others(20): Show | a0001c0001t0001g0024a0001c0001t0003g0211a0001c0001t0003g0260others(38): Show | 41 | 390 | 0.1051 | 6 | c.168 others(23): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | G | GTTTTTT | intron_variant | MODIFIER | HG01167.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0007others(14): Show | a0001c0001t0003a0001c0004t0001a0001c0007t0001others(15): Show | a0001c0001t0003g0028a0001c0004t0001g0007a0001c0007t0001g0356others(18): Show | 21 | 390 | 0.0539 | 6 | c.596 others(23): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44833096 | C | CTTTTCT | intron_variant | MODIFIER | HG00423.hp2 HG01256.hp1 HG03834.hp2 others(8): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0004a0001c0007others(5): Show | a0001c0001t0001a0001c0004t0001a0001c0007t0001others(5): Show | a0001c0001t0001g0097a0001c0001t0001g0370a0001c0004t0001g0340others(8): Show | 11 | 390 | 0.0282 | 6 | c.596 others(23): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44858369 | G | GTTTTCT | intron_variant | MODIFIER | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0003others(1): Show | a0001c0001t0009a0001c0001t0010a0001c0004t0010others(2): Show | a0001c0001t0009g0173a0001c0001t0009g0321a0001c0001t0010g0198others(6): Show | 9 | 390 | 0.0231 | 6 | c.878 others(23): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGDIB_chr12_14937031_14966601 | 14948099 | T | TGCGCGC | intron_variant | MODIFIER | HG02602.hp1 NA19030.hp2 NA19070.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0090a0001c0001t0001g0148a0001c0001t0001g0179 | 3 | 464 | 0.0065 | 6 | c.266 others(21): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | TogoVar | ||||||
ARHGDIB_chr12_14937031_14966601 | 14948100 | G | GCACACA | intron_variant | MODIFIER | HG01109.hp1 HG02523.hp2 NA19091.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0248a0001c0002t0001g0097a0001c0002t0001g0125 | 3 | 464 | 0.0065 | 6 | c.266 others(21): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | TogoVar | ||||||
ARHGDIB_chr12_14937031_14966601 | 14948100 | G | GCGCGCA | intron_variant | MODIFIER | HG00438.hp1 HG02886.hp1 HG03579.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0047a0001c0001t0001g0084a0001c0001t0001g0135others(1): Show | 5 | 464 | 0.0108 | 6 | c.266 others(21): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285790 | C | CCCCCTG | downstream_gene_variant | MODIFIER | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0006a0001c0001t0013others(1): Show | a0001c0001t0004g0006a0001c0001t0006g0016a0001c0001t0013g0020others(1): Show | 5 | 442 | 0.0113 | 6 | c.*29 others(17): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2781 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285925 | T | TCCCAAC | downstream_gene_variant | MODIFIER | HG00738.hp1 HG01168.hp2 HG01169.hp1 others(16): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(8): Show | 19 | 442 | 0.0430 | 6 | c.*31 others(17): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2916 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285983 | T | TCCCAAC | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(51): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(10): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(19): Show | 54 | 442 | 0.1222 | 6 | c.*31 others(17): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2974 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 286000 | T | TCCCAAC | downstream_gene_variant | MODIFIER | HG01891.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(1): Show | a0001c0001t0001g0008a0001c0001t0003g0008a0001c0001t0005g0008others(2): Show | 7 | 442 | 0.0158 | 6 | c.*31 others(17): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2991 | chr16 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17588849 | A | AGTGTGT | intron_variant | MODIFIER | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(12): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0011a0001c0012others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0011t0001others(7): Show | a0001c0001t0001g0043a0001c0001t0001g0057a0001c0001t0001g0088others(12): Show | 15 | 168 | 0.0893 | 6 | c.257 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17588880 | G | GTGTGTC | intron_variant | MODIFIER | HG00558.hp2 HG00642.hp2 HG01074.hp1 others(33): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0011a0001c0019others(14): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(16): Show | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(33): Show | 36 | 168 | 0.2143 | 6 | c.257 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17696045 | A | AAAAAAT | intron_variant | MODIFIER | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
a0002a0005 | a0002c0007a0005c0024 | a0002c0007t0002a0005c0024t0002 | a0002c0007t0002g0013a0002c0007t0002g0058a0002c0007t0002g0085others(3): Show | 6 | 168 | 0.0357 | 6 | c.330 others(23): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1824901 | T | TCCCCCC | intron_variant | MODIFIER | HG00323.hp2 HG00558.hp2 HG01070.hp1 others(31): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0003a0001c0004others(23): Show | a0001c0001t0006a0001c0003t0007a0001c0003t0029others(29): Show | a0001c0001t0006g0098a0001c0001t0006g0115a0001c0003t0007g0102others(30): Show | 34 | 363 | 0.0937 | 6 | c.-48 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1832506 | G | GCAGAGA | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(54): Show |
a0001a0002a0003others(7): Show | a0001c0002a0001c0003a0001c0004others(41): Show | a0001c0002t0026a0001c0003t0001a0001c0003t0008others(50): Show | a0001c0002t0026g0192a0001c0003t0001g0306a0001c0003t0008g0288others(54): Show | 57 | 363 | 0.1570 | 6 | c.-48 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1832999 | G | GAGAGAT | intron_variant | MODIFIER | NA18939.hp1 NA18982.hp2 NA19002.hp2 |
a0001 | a0001c0002a0001c0010a0001c0067 | a0001c0002t0001a0001c0010t0001a0001c0067t0001 | a0001c0002t0001g0064a0001c0010t0001g0065a0001c0067t0001g0063 | 3 | 363 | 0.0083 | 6 | c.-48 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1833035 | G | GACAGAC | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(59): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0019others(84): Show | a0001c0001t0002g0030a0001c0001t0002g0053a0001c0001t0002g0066others(115): Show | 118 | 363 | 0.3251 | 6 | c.-48 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1871112 | C | CAAAAAA | intron_variant | MODIFIER | HG00438.hp1 HG00673.hp1 HG02895.hp1 others(11): Show |
a0001a0002a0025 | a0001c0046a0001c0047a0001c0063others(10): Show | a0001c0046t0001a0001c0047t0009a0001c0063t0002others(10): Show | a0001c0046t0001g0332a0001c0046t0001g0333a0001c0047t0009g0334others(11): Show | 14 | 363 | 0.0386 | 6 | c.679 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1892277 | C | CTGTGTG | intron_variant | MODIFIER | HG00323.hp1 HG00673.hp2 HG00735.hp1 others(20): Show |
a0001a0003a0007 | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0003others(18): Show | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0004g0022others(20): Show | 23 | 363 | 0.0634 | 6 | c.118 others(25): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1918460 | C | CTGTGTG | intron_variant | MODIFIER | HG00140.hp2 HG02717.hp2 HG03540.hp1 |
a0001a0002a0012 | a0001c0020a0002c0017a0012c0084 | a0001c0020t0016a0002c0017t0002a0012c0084t0003 | a0001c0020t0016g0092a0002c0017t0002g0041a0012c0084t0003g0356 | 3 | 363 | 0.0083 | 6 | c.214 others(25): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156936493 | A | AATATAT | intron_variant | MODIFIER | HG02015.hp2 HG02258.hp1 HG02698.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0275a0001c0001t0001g0294a0001c0001t0001g0295others(3): Show | 6 | 362 | 0.0166 | 6 | c.463 others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | AATATAT | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(24): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0032others(2): Show | a0001c0001t0001g0279a0001c0001t0001g0282a0001c0001t0001g0292others(23): Show | 27 | 362 | 0.0746 | 6 | c.463 others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AAAATAT | intron_variant | MODIFIER | HG00642.hp2 HG02451.hp1 HG02735.hp2 others(5): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0008 | a0001c0001t0001a0002c0002t0002a0002c0008t0002 | a0001c0001t0001g0315a0002c0002t0002g0028a0002c0002t0002g0039others(5): Show | 8 | 362 | 0.0221 | 6 | c.463 others(23): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar |