view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP10_chr4_147727088_148077776 | 148017680 | A | ATATATAT others(19): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0063 | 1 | 66 | 0.0152 | 26 | c.171 others(45): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148039368 | A | ATTTTTTT others(19): Show |
intron_variant | MODIFIER | HG02818.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0087 | 1 | 44 | 0.0227 | 26 | c.186 others(45): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148043614 | A | AATATATA others(19): Show |
intron_variant | MODIFIER | NA19064.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0028 | 1 | 10 | 0.1000 | 26 | c.186 others(45): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31925262 | G | GCAGTACA others(19): Show |
intron_variant | MODIFIER | NA19063.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0202 | 1 | 320 | 0.0031 | 26 | c.-11 others(45): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143320403 | T | TCCCCCCC others(19): Show |
intron_variant | MODIFIER | NA18991.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033 | 1 | 141 | 0.0071 | 26 | c.474 others(45): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(19): Show |
intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0091 | 1 | 22 | 0.0455 | 26 | c.475 others(45): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(19): Show |
intron_variant | MODIFIER | HG02615.hp2 HG03491.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039 a0001c0001t0001g0067 |
2 | 23 | 0.0870 | 26 | c.475 others(45): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(19): Show |
intron_variant | MODIFIER | NA19085.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0051 | 1 | 22 | 0.0455 | 26 | c.475 others(45): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(19): Show |
intron_variant | MODIFIER | HG00642.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0107 | 1 | 22 | 0.0455 | 26 | c.475 others(45): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | G | GGTGTGTG others(19): Show |
intron_variant | MODIFIER | HG01255.hp1 HG02148.hp1 HG02965.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0073 |
3 | 12 | 0.2500 | 26 | c.113 others(47): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673756 | G | GTATATAT others(19): Show |
intron_variant | MODIFIER | HG03710.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068 | 1 | 87 | 0.0115 | 26 | c.113 others(47): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTATATAT others(19): Show |
intron_variant | MODIFIER | HG03490.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0090 | 1 | 18 | 0.0556 | 26 | c.113 others(47): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTATAT others(19): Show |
intron_variant | MODIFIER | HG03831.hp1 HG03831.hp2 NA18953.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0016 a0001c0001t0001g0072 a0001c0002t0001g0035 |
3 | 20 | 0.1500 | 26 | c.113 others(47): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTGTAT others(19): Show |
intron_variant | MODIFIER | HG03927.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 18 | 0.0556 | 26 | c.113 others(47): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTGTGT others(19): Show |
intron_variant | MODIFIER | NA18955.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034 | 1 | 18 | 0.0556 | 26 | c.113 others(47): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTGTGT others(19): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0100 | 1 | 18 | 0.0556 | 26 | c.113 others(47): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24950836 | C | CAAAAAAA others(19): Show |
intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0232 | 1 | 171 | 0.0058 | 26 | c.104 others(45): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24961911 | T | TTATATAT others(19): Show |
intron_variant | MODIFIER | HG02572.hp2 HG02922.hp1 HG02922.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0005a0001c0004t0002a0001c0004t0008 | a0001c0001t0005g0114 a0001c0004t0002g0115 a0001c0004t0008g0104 |
3 | 103 | 0.0291 | 26 | c.574 others(43): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129619345 | C | CAGGGGGA others(19): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0004 | a0004c0008 | a0004c0008t0004 | a0004c0008t0004g0055 | 1 | 232 | 0.0043 | 26 | c.787 others(41): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625219 | G | GATATATG others(19): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0137 | 1 | 170 | 0.0059 | 26 | c.786 others(43): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97251159 | G | GAGGAAGG others(19): Show |
intron_variant | MODIFIER | HG01952.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0037 | 1 | 240 | 0.0042 | 26 | c.928 others(43): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110648226 | T | TATATATA others(19): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0025 | 1 | 207 | 0.0048 | 26 | c.189 others(45): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110660064 | A | AAAAAAAA others(19): Show |
intron_variant | MODIFIER | HG02622.hp2 HG03540.hp2 |
a0005 | a0005c0007 | a0005c0007t0010 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | 165 | 0.0121 | 26 | c.189 others(45): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110687035 | C | CATATATA others(19): Show |
intron_variant | MODIFIER | HG02071.hp2 HG02132.hp1 HG02738.hp2 others(5): Show |
a0001a0003 | a0001c0001a0001c0009a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(2): Show | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0002g0162 others(5): Show |
8 | 133 | 0.0602 | 26 | c.188 others(43): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48577793 | C | CTTTTACT others(19): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0003 | a0003c0012 | a0003c0012t0005 | a0003c0012t0005g0266 | 1 | 237 | 0.0042 | 26 | c.234 others(43): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 2/9 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(19): Show |
downstream_gene_variant | MODIFIER | HG00642.hp1 HG01099.hp2 HG01106.hp2 others(12): Show |
a0001a0006a0011 | a0001c0001a0001c0004a0001c0005others(5): Show | a0001c0001t0001a0001c0004t0001a0001c0005t0006others(6): Show | a0001c0001t0001g0114 a0001c0001t0001g0149 a0001c0001t0001g0219 others(12): Show |
15 | 66 | 0.2273 | 26 | c.*21 others(37): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85487450 | T | TATATTAT others(19): Show |
intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0004 | a0001c0004t0004 | a0001c0004t0004g0033 | 1 | 94 | 0.0106 | 26 | c.-21 others(45): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85487726 | A | ATATTATA others(19): Show |
intron_variant | MODIFIER | HG01884.hp1 HG01884.hp2 HG02486.hp2 others(3): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(2): Show | a0001c0001t0005a0001c0004t0004a0001c0005t0004others(2): Show | a0001c0001t0005g0035 a0001c0001t0005g0075 a0001c0004t0004g0036 others(3): Show |
6 | 106 | 0.0566 | 26 | c.-21 others(45): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949221 | G | GAGAGAGG others(19): Show |
intron_variant | MODIFIER | HG02257.hp2 HG02922.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0028a0001c0003t0012 | a0001c0001t0028g0085 a0001c0003t0012g0093 |
2 | 77 | 0.0260 | 26 | c.110 others(47): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142949221 | G | GAGAGGAG others(19): Show |
intron_variant | MODIFIER | HG01167.hp1 NA18906.hp2 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0009a0001c0001t0016 | a0001c0001t0006g0088 a0001c0001t0009g0026 a0001c0001t0016g0040 |
3 | 78 | 0.0385 | 26 | c.110 others(47): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(19): Show |
intron_variant | MODIFIER | NA19068.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0018 | 1 | 144 | 0.0069 | 26 | c.110 others(47): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(19): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0001 | a0001c0001t0029 | a0001c0001t0029g0102 | 1 | 144 | 0.0069 | 26 | c.110 others(47): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATGT others(19): Show |
intron_variant | MODIFIER | NA18961.hp2 | a0001 | a0001c0001 | a0001c0001t0053 | a0001c0001t0053g0078 | 1 | 144 | 0.0069 | 26 | c.110 others(47): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATGTGT others(19): Show |
intron_variant | MODIFIER | NA18612.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0184 | 1 | 144 | 0.0069 | 26 | c.110 others(47): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012548 | C | CATATATA others(19): Show |
intron_variant | MODIFIER | HG02818.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0039 | 1 | 171 | 0.0058 | 26 | c.110 others(45): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATACATA others(19): Show |
intron_variant | MODIFIER | HG04228.hp2 NA18994.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0016 a0001c0001t0003g0191 |
2 | 49 | 0.0408 | 26 | c.110 others(45): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATATATA others(19): Show |
intron_variant | MODIFIER | HG02698.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0003a0001c0001t0006a0001c0001t0054others(2): Show | a0001c0001t0003g0188 a0001c0001t0006g0095 a0001c0001t0054g0082 others(2): Show |
5 | 52 | 0.0962 | 26 | c.110 others(45): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTTTTTT others(19): Show |
intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0142 | 1 | 46 | 0.0217 | 26 | c.153 others(47): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729674 | T | TGCCCGGG others(19): Show |
upstream_gene_variant | MODIFIER | HG00140.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0236 | 1 | 246 | 0.0041 | 26 | c.-14 others(35): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 41 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(19): Show |
intron_variant | MODIFIER | HG01099.hp1 HG01175.hp2 HG01243.hp1 others(4): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0005others(1): Show | a0001c0001t0001a0001c0003t0003a0002c0005t0002others(1): Show | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0003t0003g0104 others(4): Show |
7 | 127 | 0.0551 | 26 | c.122 others(41): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATGTAT others(19): Show |
intron_variant | MODIFIER | HG02602.hp1 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0118 | 1 | 121 | 0.0083 | 26 | c.122 others(41): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730234 | T | TATATATA others(19): Show |
intron_variant | MODIFIER | HG00621.hp2 | a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0093 | 1 | 246 | 0.0041 | 26 | c.122 others(41): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730236 | T | TATATATA others(19): Show |
intron_variant | MODIFIER | HG00741.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0099 | 1 | 240 | 0.0042 | 26 | c.122 others(41): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841186 | T | TCTCTCTC others(19): Show |
intron_variant | MODIFIER | HG02965.hp2 HG03130.hp1 HG03516.hp1 |
a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0087 a0001c0003t0003g0169 a0001c0003t0003g0170 |
3 | 245 | 0.0122 | 26 | c.543 others(43): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119293703 | A | AGTGTGTG others(19): Show |
upstream_gene_variant | MODIFIER | HG00597.hp1 HG02486.hp1 HG02486.hp2 others(10): Show |
a0001a0002a0007 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0005a0001c0001t0011a0001c0001t0020others(8): Show | a0001c0001t0005g0059 a0001c0001t0011g0299 a0001c0001t0020g0057 others(10): Show |
13 | 213 | 0.0610 | 26 | c.-12 others(37): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 679 | chr3 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119388306 | T | TTACATAT others(19): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02129.hp2 NA19000.hp2 others(3): Show |
a0001a0002a0013 | a0001c0001a0001c0004a0002c0003others(1): Show | a0001c0001t0005a0001c0001t0006a0001c0004t0003others(2): Show | a0001c0001t0005g0120 a0001c0001t0006g0103 a0001c0001t0006g0110 others(3): Show |
6 | 104 | 0.0577 | 26 | c.683 others(43): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(19): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(11): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0002others(5): Show | a0001c0001t0002g0094 a0001c0001t0002g0118 a0001c0001t0002g0133 others(11): Show |
14 | 116 | 0.1207 | 26 | c.226 others(45): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCACAC others(19): Show |
intron_variant | MODIFIER | HG01496.hp2 NA19000.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0041 | a0001c0001t0001g0198 a0001c0001t0041g0127 |
2 | 41 | 0.0488 | 26 | c.385 others(45): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(19): Show |
intron_variant | MODIFIER | HG00597.hp1 HG02698.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0104 a0002c0002t0002g0025 |
2 | 25 | 0.0800 | 26 | c.245 others(45): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTTTTT others(19): Show |
intron_variant | MODIFIER | NA18945.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0203 | 1 | 24 | 0.0417 | 26 | c.245 others(45): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |