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 | 147912548 | AATATATA others(19): Show |
A | intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0008 | 1 | 3 | 0.3333 | -26 | c.116 others(43): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148043614 | AATATATA others(19): Show |
A | intron_variant | MODIFIER | NA18979.hp2 NA18983.hp1 NA19064.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0054 |
3 | 12 | 0.2500 | -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 | 31905609 | AGAGCTTT others(19): Show |
A | intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0040 | a0001c0001t0040g0211 | 1 | 320 | 0.0031 | -26 | c.684 others(43): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143263907 | CTTTTTTT others(19): Show |
C | intron_variant | MODIFIER | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0055 others(9): Show |
12 | 32 | 0.3750 | -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 | 143330113 | AAAAAAAA others(19): Show |
A | intron_variant | MODIFIER | HG01255.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030 | 1 | 154 | 0.0065 | -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 | 143407987 | GTATATAT others(19): Show |
G | intron_variant | MODIFIER | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(34): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(34): Show |
37 | 93 | 0.3978 | -26 | c.475 others(45): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625292 | GATATATG others(19): Show |
G | intron_variant | MODIFIER | HG00741.hp2 HG01361.hp2 HG01981.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0232 |
3 | 234 | 0.0128 | -26 | c.786 others(43): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97218927 | GTGTGTGT others(19): Show |
G | downstream_gene_variant | MODIFIER | HG03017.hp1 | a0002 | a0002c0004 | a0002c0004t0002 | a0002c0004t0002g0149 | 1 | 221 | 0.0045 | -26 | c.*71 others(37): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3251 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97218941 | GTATATAT others(19): Show |
G | downstream_gene_variant | MODIFIER | HG01074.hp2 HG02155.hp1 HG02258.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0017 | a0001c0001t0001g0126 a0001c0001t0001g0138 a0001c0001t0001g0153 others(3): Show |
6 | 124 | 0.0484 | -26 | c.*71 others(37): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3237 | chr10 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110687061 | CACACACA others(19): Show |
C | intron_variant | MODIFIER | HG01346.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0102 | 1 | 224 | 0.0045 | -26 | c.188 others(43): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24583454 | TAAGAAAG others(19): Show |
T | downstream_gene_variant | MODIFIER | NA18957.hp1 NA18989.hp2 NA18992.hp1 others(3): Show |
a0001a0003 | a0001c0001a0003c0006 | a0001c0001t0016a0003c0006t0002a0003c0006t0003 | a0001c0001t0016g0351 a0003c0006t0002g0347 a0003c0006t0002g0348 others(3): Show |
6 | 350 | 0.0171 | -26 | c.*93 others(35): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 159 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24622433 | CATATATA others(19): Show |
C | intron_variant | MODIFIER | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
6 | 19 | 0.3158 | -26 | c.525 others(41): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38503749 | AGGAGGCC others(19): Show |
A | intron_variant | MODIFIER | NA18948.hp2 | a0001 | a0001c0006 | a0001c0006t0002 | a0001c0006t0002g0088 | 1 | 308 | 0.0032 | -26 | c.344 others(45): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85487450 | TATATTAT others(19): Show |
T | intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0063 | 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 | 85564924 | GTATATAT others(19): Show |
G | intron_variant | MODIFIER | HG01109.hp2 HG02723.hp2 HG02738.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0003t0005a0001c0003t0010others(1): Show | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0039 others(4): Show |
7 | 34 | 0.2059 | -26 | c.-20 others(43): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85669644 | AATATATA others(19): Show |
A | intron_variant | MODIFIER | HG02055.hp2 HG02717.hp1 HG03130.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0063 others(1): Show |
4 | 24 | 0.1667 | -26 | c.181 others(45): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85894975 | AAAAAAAA others(19): Show |
A | intron_variant | MODIFIER | HG00323.hp2 HG00642.hp2 HG01167.hp1 others(16): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0004t0003others(5): Show | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0021 others(16): Show |
19 | 108 | 0.1759 | -26 | c.269 others(45): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85997360 | TAGATGAT others(19): Show |
T | intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0005 | a0001c0005t0004 | a0001c0005t0004g0038 | 1 | 93 | 0.0108 | -26 | c.200 others(45): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 9/9 | chr4 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6832291 | TTTTGAAA others(19): Show |
T | intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0019 | a0001c0019t0021 | a0001c0019t0021g0073 | 1 | 246 | 0.0041 | -26 | c.326 others(43): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6909275 | CTTTTCTT others(19): Show |
C | intron_variant | MODIFIER | HG01081.hp2 HG02970.hp1 HG03453.hp1 |
a0001 | a0001c0010 | a0001c0010t0003 | a0001c0010t0003g0089 a0001c0010t0003g0098 a0001c0010t0003g0114 |
3 | 246 | 0.0122 | -26 | c.209 others(43): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064759 | GAGAAAGA others(19): Show |
G | intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0244 | 1 | 386 | 0.0026 | -26 | c.97+ others(41): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064805 | AAGAAAGA others(19): Show |
A | intron_variant | MODIFIER | HG01358.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
a0001a0010 | a0001c0001a0010c0011 | a0001c0001t0001a0010c0011t0001 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0166 others(12): Show |
15 | 388 | 0.0387 | -26 | c.97+ others(41): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129054175 | CTCATGGA others(19): Show |
C | intron_variant | MODIFIER | HG02559.hp1 | a0001 | a0001c0015 | a0001c0015t0036 | a0001c0015t0036g0197 | 1 | 396 | 0.0025 | -26 | c.963 others(43): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129193549 | AATATATA others(19): Show |
A | upstream_gene_variant | MODIFIER | HG02818.hp2 HG02965.hp1 HG03540.hp2 |
a0002 | a0002c0004 | a0002c0004t0001 | a0002c0004t0001g0212 a0002c0004t0001g0226 a0002c0004t0001g0228 |
3 | 262 | 0.0115 | -26 | c.-13 others(37): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1225 | chr11 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(19): Show |
A | intron_variant | MODIFIER | HG00642.hp1 HG02922.hp1 HG03195.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0029a0001c0001t0034a0001c0002t0005others(1): Show | a0001c0001t0029g0113 a0001c0001t0034g0252 a0001c0002t0005g0207 others(4): Show |
7 | 39 | 0.1795 | -26 | c.-18 others(47): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144684605 | ACAGCTGC others(19): Show |
A | intron_variant | MODIFIER | NA18997.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0241 | 1 | 244 | 0.0041 | -26 | c.-82 others(43): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144685114 | GGGGCACA others(19): Show |
G | intron_variant | MODIFIER | HG02280.hp1 HG02451.hp2 HG02647.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0001a0001c0001t0007a0001c0002t0001others(2): Show | a0001c0001t0001g0014 a0001c0001t0007g0017 a0001c0002t0001g0018 others(2): Show |
5 | 244 | 0.0205 | -26 | c.-82 others(41): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100728714 | GTATATAT others(19): Show |
G | intron_variant | MODIFIER | HG02970.hp1 | a0002 | a0002c0002 | a0002c0002t0040 | a0002c0002t0040g0102 | 1 | 164 | 0.0061 | -26 | c.154 others(45): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875101 | CTCTCTCT others(19): Show |
C | intron_variant | MODIFIER | NA18957.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0208 | 1 | 203 | 0.0049 | -26 | c.384 others(45): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921223 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG01346.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0046 a0001c0001t0001g0093 a0001c0001t0001g0095 others(1): Show |
4 | 280 | 0.0143 | -26 | c.487 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921225 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG02486.hp2 HG03225.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0037a0002c0002t0002 | a0001c0001t0037g0041 a0002c0002t0002g0248 |
2 | 274 | 0.0073 | -26 | c.487 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921227 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG01123.hp2 HG02602.hp2 NA18970.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0066 a0001c0001t0001g0143 a0001c0001t0001g0159 others(1): Show |
4 | 237 | 0.0169 | -26 | c.487 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921229 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG02602.hp1 HG04199.hp2 NA18952.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0124 others(1): Show |
4 | 250 | 0.0160 | -26 | c.487 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921231 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG02055.hp2 | a0002 | a0002c0005 | a0002c0005t0010 | a0002c0005t0010g0030 | 1 | 238 | 0.0042 | -26 | c.487 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921233 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | NA18940.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0099 | 1 | 261 | 0.0038 | -26 | c.487 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802945 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | NA18989.hp1 | a0001 | a0001c0009 | a0001c0009t0002 | a0001c0009t0002g0104 | 1 | 226 | 0.0044 | -26 | c.53+ others(43): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11176300 | CATATATA others(19): Show |
C | intron_variant | MODIFIER | NA18522.hp1 NA20129.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003 | a0001c0001t0001g0051 a0002c0002t0003g0012 |
2 | 14 | 0.1429 | -26 | c.162 others(45): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11353549 | AGTGTGTG others(19): Show |
A | intron_variant | MODIFIER | NA19082.hp1 | a0002 | a0002c0002 | a0002c0002t0014 | a0002c0002t0014g0006 | 1 | 51 | 0.0196 | -26 | c.589 others(45): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11503849 | CACACACA others(19): Show |
C | intron_variant | MODIFIER | HG02895.hp1 HG03209.hp1 |
a0001a0004 | a0001c0001a0004c0009 | a0001c0001t0001a0004c0009t0001 | a0001c0001t0001g0046 a0004c0009t0001g0119 |
2 | 144 | 0.0139 | -26 | c.588 others(47): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590836 | GAAAAGAA others(19): Show |
G | intron_variant | MODIFIER | HG00738.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0106 | 1 | 142 | 0.0070 | -26 | c.588 others(45): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44801017 | GGGGGCCG others(19): Show |
G | intron_variant | MODIFIER | HG01243.hp2 HG01891.hp1 HG03831.hp2 others(2): Show |
a0001a0002a0003 | a0001c0001a0001c0007a0002c0003others(2): Show | a0001c0001t0001a0001c0007t0001a0002c0003t0004others(2): Show | a0001c0001t0001g0017 a0001c0007t0001g0070 a0002c0003t0004g0168 others(2): Show |
5 | 371 | 0.0135 | -26 | c.80- others(41): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888823 | ATGAGGAG others(19): Show |
A | intron_variant | MODIFIER | HG00140.hp1 HG01243.hp1 HG04204.hp1 others(4): Show |
a0001 | a0001c0003a0001c0005a0001c0006others(3): Show | a0001c0003t0009a0001c0005t0001a0001c0006t0001others(4): Show | a0001c0003t0009g0282 a0001c0005t0001g0325 a0001c0006t0001g0239 others(4): Show |
7 | 190 | 0.0368 | -26 | c.118 others(45): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156954380 | CAAAAAAA others(19): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(10): Show |
13 | 28 | 0.4643 | -26 | c.179 others(43): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120351408 | AATATATA others(19): Show |
A | intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0029 | a0001c0001t0029g0190 | 1 | 277 | 0.0036 | -26 | c.32+ others(43): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120442437 | CACACACA others(19): Show |
C | intron_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0124 | 1 | 306 | 0.0033 | -26 | c.130 others(43): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 15/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7359744 | GGAGTTCA others(19): Show |
G | intron_variant | MODIFIER | HG00639.hp2 HG00673.hp2 HG01070.hp2 others(44): Show |
a0001a0003a0013others(1): Show | a0001c0001a0001c0013a0001c0016others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(13): Show | a0001c0001t0001g0104 a0001c0001t0002g0063 a0001c0001t0002g0067 others(44): Show |
47 | 296 | 0.1588 | -26 | c.-11 others(45): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF26_chr3_154116390_154262825 | 154239289 | AGAGAGAG others(19): Show |
A | intron_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0234 | 1 | 222 | 0.0045 | -26 | c.209 others(45): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73675848 | CATTTTCT others(19): Show |
C | intron_variant | MODIFIER | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(21): Show |
a0002a0003a0004others(7): Show | a0002c0002a0002c0006a0003c0007others(11): Show | a0002c0002t0001a0002c0006t0003a0002c0006t0004others(17): Show | a0002c0002t0001g0131 a0002c0006t0003g0111 a0002c0006t0004g0109 others(21): Show |
24 | 186 | 0.1290 | -26 | c.-11 others(43): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741377 | GTGTGTGT others(19): Show |
G | intron_variant | MODIFIER | HG02615.hp2 | a0002 | a0002c0002 | a0002c0002t0005 | a0002c0002t0005g0022 | 1 | 159 | 0.0063 | -26 | c.34- others(41): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741381 | GTGTGTAT others(19): Show |
G | intron_variant | MODIFIER | HG02155.hp2 HG03927.hp2 HG04115.hp2 others(6): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0071a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0071t0001others(5): Show | a0001c0001t0001g0003 a0001c0001t0002g0050 a0001c0071t0001g0073 others(6): Show |
9 | 163 | 0.0552 | -26 | c.34- others(41): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |