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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF28_chr5_73621196_73946990 | 73652124 | G | GTAT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(75): Show |
a0001a0002a0003others(19): Show | a0001c0001a0001c0021a0001c0023others(39): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0008others(55): Show | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(75): Show | 78 | 188 | 0.4149 | 3 | c.-12 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73731011 | T | TAAA | intron_variant | MODIFIER | HG00280.hp2 HG01071.hp1 HG01106.hp1 others(17): Show |
a0002a0004a0005others(5): Show | a0002c0002a0002c0006a0004c0004others(12): Show | a0002c0002t0001a0002c0006t0003a0002c0006t0004others(15): Show | a0002c0002t0001g0003a0002c0006t0003g0111a0002c0006t0004g0109others(17): Show | 20 | 188 | 0.1064 | 3 | c.34- others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73778076 | T | TAAA | intron_variant | MODIFIER | HG01123.hp1 HG01934.hp2 HG02723.hp2 others(4): Show |
a0001a0016a0019others(1): Show | a0001c0028a0001c0077a0016c0027others(2): Show | a0001c0028t0001a0001c0077t0002a0016c0027t0001others(3): Show | a0001c0028t0001g0146a0001c0028t0001g0181a0001c0077t0002g0028others(4): Show | 7 | 188 | 0.0372 | 3 | c.840 others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73782132 | T | TAAA | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(49): Show |
a0001a0002a0004others(16): Show | a0001c0021a0002c0002a0002c0003others(24): Show | a0001c0021t0007a0002c0002t0001a0002c0002t0002others(37): Show | a0001c0021t0007g0178a0002c0002t0001g0003a0002c0002t0002g0086others(49): Show | 52 | 188 | 0.2766 | 3 | c.910 others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73794340 | A | AGTT | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
a0001a0002a0003others(31): Show | a0001c0021a0001c0028a0002c0002others(50): Show | a0001c0021t0007a0001c0021t0008a0001c0028t0001others(82): Show | a0001c0021t0007g0178a0001c0021t0008g0102a0001c0028t0001g0146others(125): Show | 128 | 188 | 0.6809 | 3 | c.911 others(16): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73801501 | G | GCAT | intron_variant | MODIFIER | HG02630.hp2 HG03225.hp2 NA21309.hp1 |
a0001a0008a0028 | a0001c0021a0008c0011a0028c0031 | a0001c0021t0008a0008c0011t0002a0028c0031t0004 | a0001c0021t0008g0102a0008c0011t0002g0142a0028c0031t0004g0113 | 3 | 188 | 0.0160 | 3 | c.102 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73803011 | G | GGCA | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG01891.hp2 others(11): Show |
a0002a0003a0004others(6): Show | a0002c0002a0002c0006a0003c0007others(8): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(10): Show | a0002c0002t0001g0096a0002c0002t0002g0086a0002c0006t0002g0018others(11): Show | 14 | 188 | 0.0745 | 3 | c.102 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73807487 | C | CTTT | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 HG02145.hp1 others(4): Show |
a0002a0007a0024others(2): Show | a0002c0002a0002c0006a0007c0009others(3): Show | a0002c0002t0001a0002c0002t0002a0002c0006t0002others(4): Show | a0002c0002t0001g0096a0002c0002t0002g0086a0002c0006t0002g0018others(4): Show | 7 | 188 | 0.0372 | 3 | c.102 others(24): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73869222 | T | TGGG | intron_variant | MODIFIER | HG01167.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
a0002a0004a0005others(1): Show | a0002c0002a0004c0004a0005c0022others(2): Show | a0002c0002t0001a0002c0002t0002a0004c0004t0001others(4): Show | a0002c0002t0001g0132a0002c0002t0002g0159a0004c0004t0001g0167others(4): Show | 7 | 188 | 0.0372 | 3 | c.242 others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73869222 | T | TTGG | intron_variant | MODIFIER | HG00140.hp2 HG01517.hp2 |
a0002a0025 | a0002c0002a0025c0033 | a0002c0002t0001a0025c0033t0007 | a0002c0002t0001g0096a0025c0033t0007g0174 | 2 | 188 | 0.0106 | 3 | c.242 others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 20/35 | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73910381 | C | CAAA | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(36): Show |
a0001a0002a0003others(13): Show | a0001c0021a0002c0003a0002c0032others(22): Show | a0001c0021t0008a0002c0003t0001a0002c0032t0002others(29): Show | a0001c0021t0008g0102a0002c0003t0001g0076a0002c0032t0002g0065others(36): Show | 39 | 188 | 0.2075 | 3 | c.464 others(20): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73932800 | C | CTTT | intron_variant | MODIFIER | HG00735.hp2 HG01167.hp2 HG01175.hp1 others(21): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0021a0002c0002others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0021t0008others(20): Show | a0001c0001t0001g0063a0001c0001t0002g0058a0001c0021t0008g0102others(21): Show | 24 | 188 | 0.1277 | 3 | c.494 others(22): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF33_chr2_38884875_38980454 | 38904707 | C | CAAA | intron_variant | MODIFIER | HG03942.hp2 NA18977.hp1 NA19001.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | 278 | 0.0216 | 3 | c.-86 others(20): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF33_chr2_38884875_38980454 | 38942468 | C | CTTT | intron_variant | MODIFIER | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(48): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(47): Show | 51 | 278 | 0.1835 | 3 | c.791 others(20): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF33_chr2_38884875_38980454 | 38955481 | C | CTTT | intron_variant | MODIFIER | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(142): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0003a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(15): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(138): Show | 145 | 278 | 0.5216 | 3 | c.122 others(22): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF33_chr2_38884875_38980454 | 38962849 | C | CAAA | intron_variant | MODIFIER | HG00597.hp1 HG00735.hp1 HG01106.hp1 others(30): Show |
a0001a0008 | a0001c0001a0001c0014a0008c0012 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(4): Show | a0001c0001t0001g0073a0001c0001t0001g0093a0001c0001t0001g0099others(30): Show | 33 | 278 | 0.1187 | 3 | c.234 others(22): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF35_chr7_144181083_144200833 | 144189806 | C | CTTT | intron_variant | MODIFIER | HG00558.hp1 HG02273.hp2 HG02735.hp2 others(6): Show |
a0001a0003 | a0001c0001a0001c0003a0003c0004 | a0001c0001t0001a0001c0003t0001a0001c0003t0019others(1): Show | a0001c0001t0001g0060a0001c0001t0001g0115a0001c0001t0001g0117others(6): Show | 9 | 383 | 0.0235 | 3 | c.-12 others(20): Show |
ARHGEF35 | ENSG00000213214.6 | transcript | ENST00000378115.3 | protein_coding | 1/1 | chr7 | TogoVar | ||||||
ARHGEF35_chr7_144181083_144200833 | 144197945 | C | CAAA | upstream_gene_variant | MODIFIER | HG01109.hp2 HG02055.hp2 HG02622.hp2 others(6): Show |
a0001a0002 | a0001c0003a0002c0002a0002c0009others(1): Show | a0001c0003t0001a0002c0002t0004a0002c0009t0009others(1): Show | a0001c0003t0001g0140a0002c0002t0004g0009a0002c0002t0004g0066others(3): Show | 9 | 383 | 0.0235 | 3 | c.-24 others(14): Show |
ARHGEF35 | ENSG00000213214.6 | transcript | ENST00000378115.3 | protein_coding | 2113 | chr7 | TogoVar | ||||||
ARHGEF37_chr5_149576498_149639968 | 149598262 | A | ACTC | intron_variant | MODIFIER | HG00558.hp2 HG02818.hp1 HG03041.hp2 others(5): Show |
a0001a0002a0005others(1): Show | a0001c0002a0002c0001a0005c0011others(1): Show | a0001c0002t0005a0001c0002t0006a0001c0002t0008others(5): Show | a0001c0002t0005g0370a0001c0002t0006g0088a0001c0002t0008g0255others(5): Show | 8 | 394 | 0.0203 | 3 | c.186 others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF37_chr5_149576498_149639968 | 149598263 | C | CTCT | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(26): Show |
a0001a0003a0004others(7): Show | a0001c0002a0001c0005a0003c0003others(10): Show | a0001c0002t0005a0001c0005t0005a0003c0003t0002others(10): Show | a0001c0002t0005g0374a0001c0005t0005g0002a0001c0005t0005g0174others(25): Show | 29 | 394 | 0.0736 | 3 | c.186 others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF37_chr5_149576498_149639968 | 149598363 | C | CTCT | intron_variant | MODIFIER | HG00280.hp2 HG01952.hp1 HG02630.hp2 others(1): Show |
a0003a0004a0005 | a0003c0003a0004c0004a0005c0035 | a0003c0003t0002a0004c0004t0004a0005c0035t0003 | a0003c0003t0002g0277a0004c0004t0004g0222a0004c0004t0004g0373others(1): Show | 4 | 394 | 0.0102 | 3 | c.186 others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF37_chr5_149576498_149639968 | 149624900 | G | GTTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
a0001a0003a0006others(5): Show | a0001c0002a0001c0005a0003c0003others(9): Show | a0001c0002t0005a0001c0002t0006a0001c0002t0008others(21): Show | a0001c0002t0005g0367a0001c0002t0005g0368a0001c0002t0005g0370others(108): Show | 117 | 394 | 0.2970 | 3 | c.146 others(20): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF37_chr5_149576498_149639968 | 149637262 | T | TTTA | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
a0001a0002a0003others(7): Show | a0001c0002a0002c0001a0003c0003others(9): Show | a0001c0002t0008a0001c0002t0015a0002c0001t0001others(16): Show | a0001c0002t0008g0004a0001c0002t0008g0167a0001c0002t0008g0173others(72): Show | 77 | 394 | 0.1954 | 3 | c.*50 others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2295 | chr5 | TogoVar | ||||||
ARHGEF38_chr4_105547620_105685914 | 105582164 | C | CAAA | intron_variant | MODIFIER | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(51): Show |
a0001a0002a0003others(6): Show | a0001c0002a0001c0003a0001c0009others(10): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(17): Show | a0001c0002t0001g0167a0001c0002t0001g0172a0001c0002t0002g0069others(51): Show | 54 | 186 | 0.2903 | 3 | c.197 others(20): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105585726 | C | CTTT | intron_variant | MODIFIER | HG01070.hp1 HG01981.hp1 HG02080.hp2 others(14): Show |
a0001a0002a0005 | a0001c0002a0001c0003a0001c0004others(4): Show | a0001c0002t0003a0001c0002t0007a0001c0003t0007others(8): Show | a0001c0002t0003g0101a0001c0002t0003g0150a0001c0002t0007g0147others(14): Show | 17 | 186 | 0.0914 | 3 | c.197 others(20): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105661474 | T | TTTA | intron_variant | MODIFIER | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
a0001a0002a0003others(1): Show | a0001c0002a0001c0003a0001c0004others(7): Show | a0001c0002t0002a0001c0002t0007a0001c0002t0008others(9): Show | a0001c0002t0002g0072a0001c0002t0002g0100a0001c0002t0007g0147others(13): Show | 16 | 186 | 0.0860 | 3 | c.154 others(22): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105668668 | A | AGAT | intron_variant | MODIFIER | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(3): Show |
a0001a0007 | a0001c0004a0007c0019 | a0001c0004t0005a0007c0019t0005 | a0001c0004t0005g0037a0001c0004t0005g0039a0001c0004t0005g0042others(3): Show | 6 | 186 | 0.0323 | 3 | c.214 others(20): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF3_chr3_56722420_56806949 | 56727357 | T | TCCC | downstream_gene_variant | MODIFIER | HG00621.hp1 HG00673.hp1 HG01099.hp1 others(42): Show |
a0001a0004 | a0001c0002a0001c0006a0004c0011 | a0001c0002t0002a0001c0002t0005a0001c0002t0006others(5): Show | a0001c0002t0002g0002a0001c0002t0002g0032a0001c0002t0002g0033others(41): Show | 45 | 358 | 0.1257 | 3 | c.*19 others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 62 | chr3 | TogoVar | ||||||
ARHGEF3_chr3_56722420_56806949 | 56733984 | C | CAAA | intron_variant | MODIFIER | HG01981.hp2 HG02083.hp2 HG02135.hp1 others(8): Show |
a0001 | a0001c0002a0001c0005a0001c0006 | a0001c0002t0002a0001c0005t0001a0001c0006t0002 | a0001c0002t0002g0019a0001c0002t0002g0123a0001c0002t0002g0128others(8): Show | 11 | 358 | 0.0307 | 3 | c.104 others(22): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | TogoVar | ||||||
ARHGEF3_chr3_56722420_56806949 | 56741184 | C | CCTT | intron_variant | MODIFIER | HG01884.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0094others(1): Show | 4 | 358 | 0.0112 | 3 | c.871 others(20): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | TogoVar | ||||||
ARHGEF3_chr3_56722420_56806949 | 56767583 | C | CAAA | intron_variant | MODIFIER | HG01361.hp2 HG01928.hp1 HG02074.hp2 others(6): Show |
a0001a0002a0005 | a0001c0002a0001c0007a0001c0008others(3): Show | a0001c0002t0002a0001c0007t0004a0001c0008t0004others(3): Show | a0001c0002t0002g0122a0001c0002t0002g0126a0001c0007t0004g0112others(6): Show | 9 | 358 | 0.0251 | 3 | c.204 others(20): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | TogoVar | ||||||
ARHGEF3_chr3_56722420_56806949 | 56789020 | A | ATGC | intron_variant | MODIFIER | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(31): Show |
a0001a0002 | a0001c0002a0001c0003a0001c0005others(4): Show | a0001c0002t0002a0001c0003t0001a0001c0005t0001others(6): Show | a0001c0002t0002g0126a0001c0002t0002g0157a0001c0002t0002g0215others(31): Show | 34 | 358 | 0.0950 | 3 | c.96+ others(20): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | TogoVar | ||||||
ARHGEF40_chr14_21065304_21095248 | 21077279 | A | ATTT | intron_variant | MODIFIER | HG00735.hp2 HG01123.hp1 HG02055.hp2 others(4): Show |
a0001a0004a0014 | a0001c0003a0004c0005a0014c0038 | a0001c0003t0001a0004c0005t0001a0014c0038t0001 | a0001c0003t0001g0027a0004c0005t0001g0081a0004c0005t0001g0082others(2): Show | 7 | 386 | 0.0181 | 3 | c.203 others(20): Show |
ARHGEF40 | ENSG00000165801.10 | transcript | ENST00000298694.9 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGEF40_chr14_21065304_21095248 | 21094726 | T | TGGG | downstream_gene_variant | MODIFIER | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(25): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0003a0003c0004others(6): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0002others(8): Show | a0001c0001t0001g0011a0001c0001t0001g0134a0001c0003t0001g0023others(15): Show | 28 | 386 | 0.0725 | 3 | c.*57 others(14): Show |
ARHGEF40 | ENSG00000165801.10 | transcript | ENST00000298694.9 | protein_coding | 4479 | chr14 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130833392 | A | AAAG | upstream_gene_variant | MODIFIER | HG02155.hp2 HG02965.hp2 |
a0001a0007 | a0001c0001a0007c0013 | a0001c0001t0001a0007c0013t0003 | a0001c0001t0001g0040a0007c0013t0003g0060 | 2 | 144 | 0.0139 | 3 | c.-35 others(14): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3521 | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130849556 | T | TTCA | intron_variant | MODIFIER | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(3): Show |
a0001a0008a0022 | a0001c0001a0001c0002a0008c0053others(1): Show | a0001c0001t0001a0001c0002t0001a0008c0053t0001others(1): Show | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | 144 | 0.0417 | 3 | c.39+ others(20): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130889811 | C | CAAA | intron_variant | MODIFIER | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0028 | a0001c0001t0001a0001c0002t0001a0002c0028t0001 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0137others(2): Show | 5 | 144 | 0.0347 | 3 | c.40- others(20): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF4_chr2_130831914_131052253 | 130902704 | T | TCGG | intron_variant | MODIFIER | HG01081.hp2 HG01975.hp2 HG02155.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0015others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0015t0001others(1): Show | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0114others(8): Show | 11 | 144 | 0.0764 | 3 | c.40- others(20): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF4_chr2_130831914_131052253 | 130927694 | G | GGTA | intron_variant | MODIFIER | HG00621.hp1 HG01109.hp2 HG01884.hp2 others(39): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0014a0002c0010others(16): Show | a0001c0001t0001a0001c0014t0001a0002c0010t0001others(20): Show | a0001c0001t0001g0017a0001c0014t0001g0036a0002c0010t0001g0003others(39): Show | 42 | 144 | 0.2917 | 3 | c.355 others(22): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF4_chr2_130831914_131052253 | 130979734 | T | TAAA | intron_variant | MODIFIER | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(4): Show |
a0001a0008a0014 | a0001c0001a0001c0002a0008c0012others(1): Show | a0001c0001t0001a0001c0002t0001a0008c0012t0001others(1): Show | a0001c0001t0001g0033a0001c0001t0001g0063a0001c0001t0001g0088others(4): Show | 7 | 144 | 0.0486 | 3 | c.398 others(24): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF4_chr2_130831914_131052253 | 130984688 | T | TAAA | intron_variant | MODIFIER | HG00621.hp1 HG01884.hp2 HG02630.hp2 others(22): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0010a0002c0011others(9): Show | a0001c0001t0001a0002c0010t0001a0002c0011t0001others(10): Show | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0043others(22): Show | 25 | 144 | 0.1736 | 3 | c.398 others(24): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF4_chr2_130831914_131052253 | 131001302 | C | CAAA | intron_variant | MODIFIER | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(15): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0007others(10): Show | a0001c0001t0001a0001c0002t0001a0001c0007t0004others(12): Show | a0001c0001t0001g0086a0001c0002t0001g0031a0001c0002t0001g0083others(15): Show | 18 | 144 | 0.1250 | 3 | c.398 others(24): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF4_chr2_130831914_131052253 | 131029551 | C | CTTT | intron_variant | MODIFIER | HG01884.hp2 HG02630.hp2 HG02895.hp2 others(8): Show |
a0001a0002a0005others(2): Show | a0001c0015a0001c0018a0002c0011others(5): Show | a0001c0015t0001a0001c0018t0005a0002c0011t0001others(5): Show | a0001c0015t0001g0078a0001c0015t0001g0079a0001c0018t0005g0106others(8): Show | 11 | 144 | 0.0764 | 3 | c.412 others(22): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF6_chrX_136660550_136785932 | 136668512 | T | TTTC | intron_variant | MODIFIER | HG00323.hp2 HG01243.hp1 HG02056.hp1 others(42): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0022others(41): Show | 45 | 247 | 0.1822 | 3 | c.219 others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136668527 | C | CTTA | intron_variant | MODIFIER | NA18987.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 | 1 | 247 | 0.0041 | 3 | c.219 others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136668533 | C | CTTA | intron_variant | MODIFIER | HG02055.hp1 HG03225.hp1 HG03492.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0071others(5): Show | 8 | 247 | 0.0324 | 3 | c.219 others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 21/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136694056 | C | CTTT | intron_variant | MODIFIER | HG01243.hp1 HG02886.hp1 HG03540.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0114a0001c0001t0002g0207a0001c0001t0002g0208 | 3 | 247 | 0.0122 | 3 | c.104 others(22): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136700528 | G | GGAA | intron_variant | MODIFIER | NA18987.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 | 1 | 247 | 0.0041 | 3 | c.104 others(22): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136701702 | C | CTTT | intron_variant | MODIFIER | NA18987.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 | 1 | 247 | 0.0041 | 3 | c.104 others(22): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 9/21 | chrX | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136727394 | T | TTTC | intron_variant | MODIFIER | HG01081.hp1 HG02004.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0156a0001c0001t0001g0192 | 2 | 247 | 0.0081 | 3 | c.732 others(20): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar |