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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP10_chr4_147727088_148077776 | 147798765 | CTCTCTCT others(19): Show |
C | intron_variant | MODIFIER | HG02738.hp2 NA18522.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0081a0001c0002t0001g0078 | 2 | 106 | 0.0189 | -26 | c.155 others(45): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147912548 | AATATATA others(19): Show |
A | intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0008 | 1 | 106 | 0.0094 | -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 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0054 | 3 | 106 | 0.0283 | -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 | a0001c0001t0040g0212 | 1 | 322 | 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 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0055others(9): Show | 12 | 162 | 0.0741 | -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 | 162 | 0.0062 | -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 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(34): Show | 37 | 162 | 0.2284 | -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 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0232 | 3 | 238 | 0.0126 | -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 | 242 | 0.0041 | -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 | a0001c0001t0001g0126a0001c0001t0001g0138a0001c0001t0001g0155others(3): Show | 6 | 242 | 0.0248 | -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 | a0001c0001t0003g0091 | 1 | 226 | 0.0044 | -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 |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0016a0006c0006t0002a0006c0006t0003 | a0001c0001t0016g0352a0006c0006t0002g0348a0006c0006t0002g0349others(3): Show | 6 | 352 | 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 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 6 | 352 | 0.0171 | -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 | a0001c0006t0002g0084 | 1 | 309 | 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 | a0001c0001t0001g0062 | 1 | 108 | 0.0093 | -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 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0039others(4): Show | 7 | 108 | 0.0648 | -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 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0001g0065others(1): Show | 4 | 108 | 0.0370 | -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 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0025others(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 | 108 | 0.0093 | -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 | 248 | 0.0040 | -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 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114 | 3 | 248 | 0.0121 | -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 | a0001c0001t0001g0227 | 1 | 390 | 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 |
a0001a0007 | a0001c0001a0007c0011 | a0001c0001t0001a0007c0011t0001 | a0001c0001t0001g0020a0001c0001t0001g0161a0001c0001t0001g0166others(12): Show | 15 | 390 | 0.0385 | -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 | a0001c0015t0036g0195 | 1 | 398 | 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 | a0002c0004t0001g0206a0002c0004t0001g0220a0002c0004t0001g0222 | 3 | 398 | 0.0075 | -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 | a0001c0001t0034a0001c0001t0038a0001c0002t0006others(1): Show | a0001c0001t0034g0111a0001c0001t0038g0252a0001c0002t0006g0207others(4): Show | 7 | 298 | 0.0235 | -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 | a0001c0002t0001g0242 | 1 | 246 | 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 | a0001c0001t0001g0016a0001c0001t0007g0018a0001c0002t0001g0020others(2): Show | 5 | 246 | 0.0203 | -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 | a0002c0002t0040g0101 | 1 | 286 | 0.0035 | -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 | a0001c0001t0001g0204 | 1 | 286 | 0.0035 | -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 | a0001c0001t0001g0047a0001c0001t0001g0093a0001c0001t0001g0095others(1): Show | 4 | 286 | 0.0140 | -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 | a0001c0001t0037g0041a0002c0002t0002g0248 | 2 | 286 | 0.0070 | -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 | a0001c0001t0001g0068a0001c0001t0001g0141a0001c0001t0001g0166others(1): Show | 4 | 286 | 0.0140 | -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 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0113others(1): Show | 4 | 286 | 0.0140 | -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 | 286 | 0.0035 | -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 | 286 | 0.0035 | -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 | a0001c0009t0002g0110 | 1 | 230 | 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 | a0001c0001t0001g0051a0002c0002t0003g0012 | 2 | 144 | 0.0139 | -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 | a0002c0002t0016 | a0002c0002t0016g0007 | 1 | 144 | 0.0069 | -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 |
a0001a0003 | a0001c0001a0003c0010 | a0001c0001t0001a0003c0010t0017 | a0001c0001t0001g0046a0003c0010t0017g0119 | 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 | a0001c0001t0004g0101 | 1 | 144 | 0.0069 | -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 | a0001c0001t0001g0017a0001c0007t0001g0070a0002c0003t0004g0168others(2): Show | 5 | 390 | 0.0128 | -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 | a0001c0003t0008a0001c0005t0001a0001c0006t0001others(4): Show | a0001c0003t0008g0288a0001c0005t0001g0325a0001c0006t0001g0264others(4): Show | 7 | 363 | 0.0193 | -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 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(10): Show | 13 | 362 | 0.0359 | -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 | 308 | 0.0033 | -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 | 308 | 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(45): Show |
a0001a0003a0012others(1): Show | a0001c0001a0001c0013a0001c0016others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(13): Show | a0001c0001t0001g0216a0001c0001t0002g0181a0001c0001t0002g0182others(45): Show | 48 | 298 | 0.1611 | -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 | a0001c0001t0002g0236 | 1 | 283 | 0.0035 | -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 | a0002c0002t0001g0130a0002c0006t0003g0111a0002c0006t0004g0109others(21): Show | 24 | 188 | 0.1277 | -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 | 188 | 0.0053 | -26 | c.34- others(41): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |