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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP8_chr22_44747575_44867784 | 44827336 | G | GTTTT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(95): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0007others(20): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(23): Show | a0001c0001t0001g0097a0001c0001t0001g0192a0001c0001t0001g0200others(95): Show | 98 | 390 | 0.2513 | 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 | 44829118 | C | CAAAA | intron_variant | MODIFIER | HG02451.hp2 HG02630.hp2 HG03492.hp1 others(3): Show |
a0001a0002a0003 | a0001c0007a0001c0008a0002c0006others(2): Show | a0001c0007t0001a0001c0008t0001a0002c0006t0001others(2): Show | a0001c0007t0001g0304a0001c0007t0001g0382a0001c0008t0001g0038others(3): Show | 6 | 390 | 0.0154 | 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 | 44833097 | T | TTTTC | intron_variant | MODIFIER | HG01109.hp2 HG02258.hp1 HG02559.hp1 others(7): Show |
a0002a0006a0009others(1): Show | a0002c0064a0006c0027a0006c0030others(3): Show | a0002c0064t0005a0006c0027t0001a0006c0030t0001others(3): Show | a0002c0064t0005g0067a0006c0027t0001g0314a0006c0027t0001g0346others(7): Show | 10 | 390 | 0.0256 | 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 | 44833344 | G | GTGGT | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(61): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0004a0001c0007others(10): Show | a0001c0001t0003a0001c0004t0001a0001c0004t0003others(13): Show | a0001c0001t0003g0089a0001c0001t0003g0157a0001c0001t0003g0159others(61): Show | 64 | 390 | 0.1641 | 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 | 44835231 | C | CTATA | intron_variant | MODIFIER | HG01109.hp2 HG02809.hp2 HG02976.hp1 others(2): Show |
a0001a0002a0006 | a0001c0001a0002c0064a0006c0027 | a0001c0001t0003a0001c0001t0009a0002c0064t0005others(1): Show | a0001c0001t0003g0063a0001c0001t0009g0173a0001c0001t0009g0321others(2): Show | 5 | 390 | 0.0128 | 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 | 44842357 | A | AAAAC | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp2 NA18906.hp2 |
a0002a0011 | a0002c0020a0011c0035 | a0002c0020t0005a0011c0035t0001 | a0002c0020t0005g0355a0011c0035t0001g0001a0011c0035t0001g0045 | 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 | 44851393 | A | ATATT | intron_variant | MODIFIER | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(15): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0004a0002c0016others(5): Show | a0001c0001t0001a0001c0004t0001a0001c0004t0003others(7): Show | a0001c0001t0001g0097a0001c0001t0001g0370a0001c0004t0001g0136others(15): Show | 18 | 390 | 0.0462 | 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 | C | CTTTT | intron_variant | MODIFIER | HG01934.hp1 HG02572.hp1 HG02818.hp2 others(6): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0007a0001c0018others(4): Show | a0001c0001t0001a0001c0007t0001a0001c0018t0001others(4): Show | a0001c0001t0001g0370a0001c0007t0001g0324a0001c0007t0001g0356others(6): Show | 9 | 390 | 0.0231 | 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 | 44857929 | A | ATTTC | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0004a0001c0008others(30): Show | a0001c0001t0003a0001c0001t0009a0001c0001t0010others(38): Show | a0001c0001t0003g0006a0001c0001t0003g0023a0001c0001t0003g0028others(124): Show | 127 | 390 | 0.3256 | 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 | 44857945 | C | CAGTG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
a0001a0002a0003others(23): Show | a0001c0001a0001c0004a0001c0007others(66): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(83): Show | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0097others(301): Show | 304 | 390 | 0.7795 | 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 | 44858533 | C | CTTTT | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(131): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0037others(25): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(29): Show | a0001c0001t0001g0042a0001c0001t0003g0156a0001c0004t0003g0118others(131): Show | 134 | 390 | 0.3436 | 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 | 44861545 | G | GCCTC | intron_variant | MODIFIER | HG03490.hp1 HG03492.hp2 NA18939.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0003a0001c0004t0003 | a0001c0001t0003g0080a0001c0001t0003g0109a0001c0001t0003g0110others(3): Show | 6 | 390 | 0.0154 | 4 | c.982 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGDIB_chr12_14937031_14966601 | 14940736 | T | TAAAC | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(6): Show | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0039others(73): Show | 94 | 464 | 0.2026 | 4 | c.*17 others(15): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1294 | chr12 | TogoVar | ||||||
ARHGDIB_chr12_14937031_14966601 | 14948099 | T | TGCGC | intron_variant | MODIFIER | HG00639.hp2 HG02155.hp1 HG03942.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0053a0001c0001t0001g0145a0001c0001t0001g0147others(1): Show | 5 | 464 | 0.0108 | 4 | c.266 others(19): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | TogoVar | ||||||
ARHGDIB_chr12_14937031_14966601 | 14948100 | G | GCACA | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG00741.hp1 others(54): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0005a0001c0002t0001others(2): Show | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0059others(31): Show | 57 | 464 | 0.1228 | 4 | c.266 others(19): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17544291 | T | TATGA | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(10): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0006a0001c0038others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0006t0001others(6): Show | a0001c0001t0001g0118a0001c0001t0001g0124a0001c0001t0001g0127others(10): Show | 13 | 168 | 0.0774 | 4 | c.-44 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17548646 | C | CTTTT | intron_variant | MODIFIER | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0017a0001c0033others(4): Show | a0001c0001t0003a0001c0017t0002a0001c0033t0002others(4): Show | a0001c0001t0003g0114a0001c0017t0002g0113a0001c0033t0002g0110others(4): Show | 7 | 168 | 0.0417 | 4 | c.-44 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17588849 | A | AGTGT | intron_variant | MODIFIER | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(7): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0012a0001c0013others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0012t0001others(6): Show | a0001c0001t0001g0002a0001c0001t0001g0096a0001c0001t0003g0168others(7): Show | 10 | 168 | 0.0595 | 4 | c.257 others(19): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17611533 | T | TATCC | intron_variant | MODIFIER | HG00323.hp1 HG01106.hp2 HG01169.hp1 others(21): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0012a0001c0019others(9): Show | a0001c0001t0001a0001c0012t0001a0001c0019t0001others(9): Show | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0033others(21): Show | 24 | 168 | 0.1429 | 4 | c.610 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17611977 | G | GTCCA | intron_variant | MODIFIER | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(39): Show |
a0001a0002a0004others(7): Show | a0001c0001a0001c0006a0001c0011others(20): Show | a0001c0001t0001a0001c0001t0003a0001c0006t0003others(21): Show | a0001c0001t0001g0095a0001c0001t0001g0140a0001c0001t0003g0114others(39): Show | 42 | 168 | 0.2500 | 4 | c.610 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17655437 | G | GTCCA | intron_variant | MODIFIER | HG00558.hp1 HG06807.hp2 NA18747.hp1 others(1): Show |
a0001 | a0001c0001a0001c0019 | a0001c0001t0001a0001c0019t0001 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0159others(1): Show | 4 | 168 | 0.0238 | 4 | c.248 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10L_chr1_17534698_17702869 | 17686078 | T | TTTTC | intron_variant | MODIFIER | HG00558.hp2 HG01257.hp2 HG01258.hp1 others(12): Show |
a0001a0003a0013others(1): Show | a0001c0001a0003c0002a0013c0039others(1): Show | a0001c0001t0001a0001c0001t0003a0003c0002t0001others(2): Show | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(12): Show | 15 | 168 | 0.0893 | 4 | c.301 others(23): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1821139 | C | CAAAA | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(19): Show |
a0001a0002a0003others(2): Show | a0001c0003a0001c0004a0001c0009others(15): Show | a0001c0003t0008a0001c0004t0005a0001c0009t0005others(18): Show | a0001c0003t0008g0288a0001c0004t0005g0299a0001c0009t0005g0287others(19): Show | 22 | 363 | 0.0606 | 4 | c.-30 others(15): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2786 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1824899 | C | CACCT | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0003a0001c0004others(25): Show | a0001c0001t0006a0001c0003t0007a0001c0003t0021others(32): Show | a0001c0001t0006g0098a0001c0001t0006g0115a0001c0003t0007g0102others(33): Show | 37 | 363 | 0.1019 | 4 | c.-48 others(19): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1832753 | C | CAGAG | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0001c0003others(64): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(95): Show | a0001c0001t0002g0030a0001c0001t0002g0053a0001c0001t0002g0066others(135): Show | 138 | 363 | 0.3802 | 4 | c.-48 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1832835 | C | CAGAG | intron_variant | MODIFIER | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
a0001a0002a0005others(4): Show | a0001c0001a0001c0002a0001c0003others(40): Show | a0001c0001t0004a0001c0001t0014a0001c0001t0019others(51): Show | a0001c0001t0004g0022a0001c0001t0004g0138a0001c0001t0004g0141others(67): Show | 70 | 363 | 0.1928 | 4 | c.-48 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1833021 | C | CAGAG | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0001c0003others(65): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(96): Show | a0001c0001t0002g0030a0001c0001t0002g0053a0001c0001t0002g0066others(134): Show | 137 | 363 | 0.3774 | 4 | c.-48 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1833119 | G | GAGAC | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(29): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0001c0004others(23): Show | a0001c0001t0006a0001c0003t0003a0001c0003t0035others(25): Show | a0001c0001t0006g0098a0001c0001t0006g0115a0001c0003t0003g0161others(28): Show | 32 | 363 | 0.0882 | 4 | c.-48 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1839677 | A | ACTGT | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(143): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0002a0001c0003others(79): Show | a0001c0001t0002a0001c0001t0019a0001c0002t0001others(102): Show | a0001c0001t0002g0224a0001c0001t0002g0239a0001c0001t0019g0278others(143): Show | 146 | 363 | 0.4022 | 4 | c.-47 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1857875 | G | GATCT | intron_variant | MODIFIER | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0001c0003others(36): Show | a0001c0001t0002a0001c0001t0014a0001c0002t0001others(44): Show | a0001c0001t0002g0239a0001c0001t0002g0271a0001c0001t0014g0361others(54): Show | 57 | 363 | 0.1570 | 4 | c.38- others(15): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1857879 | G | GATCT | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG01070.hp1 others(25): Show |
a0001a0002a0005others(3): Show | a0001c0001a0001c0002a0001c0041others(22): Show | a0001c0001t0002a0001c0002t0020a0001c0002t0049others(23): Show | a0001c0001t0002g0030a0001c0002t0020g0206a0001c0002t0049g0021others(24): Show | 28 | 363 | 0.0771 | 4 | c.38- others(15): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1871112 | C | CAAAA | intron_variant | MODIFIER | HG00408.hp1 HG02280.hp2 HG02615.hp2 others(12): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0002a0001c0009others(7): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0001others(9): Show | a0001c0001t0002g0271a0001c0001t0004g0354a0001c0002t0001g0211others(12): Show | 15 | 363 | 0.0413 | 4 | c.679 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1873510 | T | TTGCG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0002a0001c0003others(103): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0019others(144): Show | a0001c0001t0002g0069a0001c0001t0002g0239a0001c0001t0004g0354others(187): Show | 191 | 363 | 0.5262 | 4 | c.680 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1873510 | T | TTTCA | intron_variant | MODIFIER | HG00408.hp1 HG00621.hp2 HG02280.hp2 others(17): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0005others(8): Show | a0001c0001t0002a0001c0001t0012a0001c0002t0001others(10): Show | a0001c0001t0002g0224a0001c0001t0002g0271a0001c0001t0012g0207others(17): Show | 20 | 363 | 0.0551 | 4 | c.680 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888397 | C | CACTG | intron_variant | MODIFIER | HG01952.hp1 HG02074.hp2 NA18942.hp1 others(4): Show |
a0002 | a0002c0025a0002c0028a0002c0033others(4): Show | a0002c0025t0059a0002c0028t0001a0002c0033t0002others(4): Show | a0002c0025t0059g0105a0002c0028t0001g0223a0002c0033t0002g0006others(4): Show | 7 | 363 | 0.0193 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888410 | G | GGGGT | intron_variant | MODIFIER | HG01952.hp1 HG02074.hp2 NA18942.hp1 others(4): Show |
a0002 | a0002c0025a0002c0028a0002c0033others(4): Show | a0002c0025t0059a0002c0028t0001a0002c0033t0002others(4): Show | a0002c0025t0059g0105a0002c0028t0001g0223a0002c0033t0002g0006others(4): Show | 7 | 363 | 0.0193 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888919 | C | CACTG | intron_variant | MODIFIER | HG00621.hp2 HG02074.hp2 NA18942.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0028a0002c0033others(4): Show | a0001c0001t0002a0001c0001t0004a0002c0028t0001others(5): Show | a0001c0001t0002g0224a0001c0001t0004g0141a0002c0028t0001g0223others(5): Show | 8 | 363 | 0.0220 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888982 | A | AGTGG | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01346.hp1 others(4): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0019a0001c0002t0001a0001c0002t0010others(4): Show | a0001c0001t0019g0278a0001c0002t0001g0037a0001c0002t0010g0212others(4): Show | 7 | 363 | 0.0193 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889386 | C | CACTG | intron_variant | MODIFIER | HG01081.hp2 HG02647.hp2 HG02723.hp2 |
a0001a0010 | a0001c0016a0010c0097a0010c0098 | a0001c0016t0004a0010c0097t0014a0010c0098t0003 | a0001c0016t0004g0176a0010c0097t0014g0205a0010c0098t0003g0203 | 3 | 363 | 0.0083 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889386 | C | CGCTG | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(15): Show |
a0002a0014a0018 | a0002c0025a0002c0028a0002c0032others(14): Show | a0002c0025t0059a0002c0028t0001a0002c0032t0004others(14): Show | a0002c0025t0059g0105a0002c0028t0001g0223a0002c0032t0004g0173others(15): Show | 18 | 363 | 0.0496 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889688 | C | CACTG | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01346.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0019a0001c0002t0001others(4): Show | a0001c0001t0002g0271a0001c0001t0019g0278a0001c0002t0001g0037others(7): Show | 10 | 363 | 0.0276 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1892277 | C | CTGTG | intron_variant | MODIFIER | HG00280.hp2 HG01074.hp1 HG01106.hp1 others(13): Show |
a0001a0020a0022 | a0001c0001a0001c0002a0001c0008others(9): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0001others(11): Show | a0001c0001t0002g0069a0001c0001t0004g0158a0001c0001t0004g0159others(13): Show | 16 | 363 | 0.0441 | 4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1918460 | C | CTGTG | intron_variant | MODIFIER | HG00323.hp1 HG00738.hp1 HG01106.hp1 others(13): Show |
a0001a0004a0014 | a0001c0001a0001c0003a0001c0004others(9): Show | a0001c0001t0004a0001c0001t0012a0001c0001t0043others(12): Show | a0001c0001t0004g0141a0001c0001t0004g0158a0001c0001t0012g0207others(13): Show | 16 | 363 | 0.0441 | 4 | c.214 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1949018 | A | ATGTG | intron_variant | MODIFIER | HG00741.hp2 HG01109.hp2 HG03239.hp1 |
a0005a0017 | a0005c0039a0017c0126 | a0005c0039t0001a0005c0039t0030a0017c0126t0007 | a0005c0039t0001g0070a0005c0039t0030g0139a0017c0126t0007g0113 | 3 | 363 | 0.0083 | 4 | c.339 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1950519 | A | ATTAT | intron_variant | MODIFIER | HG01081.hp1 HG01261.hp1 HG02451.hp2 others(9): Show |
a0001a0002a0004others(3): Show | a0001c0002a0001c0003a0001c0052others(6): Show | a0001c0002t0001a0001c0003t0003a0001c0052t0032others(8): Show | a0001c0002t0001g0274a0001c0002t0001g0327a0001c0003t0003g0362others(9): Show | 12 | 363 | 0.0331 | 4 | c.339 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156930060 | T | TTCTC | downstream_gene_variant | MODIFIER | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
a0002 | a0002c0004 | a0002c0004t0005a0002c0004t0009a0002c0004t0025others(1): Show | a0002c0004t0005g0052a0002c0004t0005g0054a0002c0004t0005g0111others(15): Show | 19 | 362 | 0.0525 | 4 | c.*59 others(15): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4779 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | AATAT | intron_variant | MODIFIER | HG01167.hp1 HG02074.hp1 HG02602.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0035 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0290others(4): Show | 7 | 362 | 0.0193 | 4 | c.463 others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156992379 | T | TCCTG | intron_variant | MODIFIER | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(19): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0006a0002c0004t0005a0002c0004t0009others(1): Show | a0001c0001t0006g0110a0001c0001t0006g0112a0001c0001t0006g0122others(18): Show | 22 | 362 | 0.0608 | 4 | c.33- others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156996772 | C | CAAAA | intron_variant | MODIFIER | HG00642.hp2 HG01175.hp1 HG01952.hp2 others(20): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0006 | a0001c0001t0001a0002c0002t0002a0002c0002t0012others(3): Show | a0001c0001t0001g0347a0002c0002t0002g0034a0002c0002t0002g0035others(20): Show | 23 | 362 | 0.0635 | 4 | c.33- others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156996859 | A | ATTTT | intron_variant | MODIFIER | HG00621.hp2 HG01361.hp2 HG02083.hp1 others(9): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0001c0001t0010a0001c0001t0036others(2): Show | a0001c0001t0001g0279a0001c0001t0001g0310a0001c0001t0001g0312others(9): Show | 12 | 362 | 0.0332 | 4 | c.33- others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar |