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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
APBA2_chr15_28880974_29123315 | 28969128 | TTTTCTTT others(25): Show |
T | intron_variant | MODIFIER | HG00323.hp2 HG01081.hp2 HG01167.hp1 others(78): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0007a0001c0009others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(38): Show | a0001c0001t0001g0010 a0001c0001t0002g0006 a0001c0001t0002g0116 others(78): Show |
81 | 90 | 0.9000 | -32 | c.-94 others(51): Show |
APBA2 | ENSG00000034053.15 | transcript | ENST00000683413.1 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
APBB1_chr11_6390125_6424094 | 6410376 | CCAGTAAA others(25): Show |
C | intron_variant | MODIFIER | HG00544.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0133 | 1 | 414 | 0.0024 | -32 | c.721 others(47): Show |
APBB1 | ENSG00000166313.20 | transcript | ENST00000609360.6 | protein_coding | 2/14 | chr11 | TogoVar | |||||||
APBB2_chr4_40805027_41219542 | 40982265 | AGAAAGAA others(25): Show |
A | intron_variant | MODIFIER | HG01255.hp2 | a0001 | a0001c0004 | a0001c0004t0004 | a0001c0004t0004g0144 | 1 | 184 | 0.0054 | -32 | c.835 others(51): Show |
APBB2 | ENSG00000163697.18 | transcript | ENST00000508593.6 | protein_coding | 6/17 | chr4 | TogoVar | |||||||
APBB2_chr4_40805027_41219542 | 40982273 | AGAAAGAA others(25): Show |
A | intron_variant | MODIFIER | NA19043.hp2 | a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0148 | 1 | 174 | 0.0057 | -32 | c.835 others(51): Show |
APBB2 | ENSG00000163697.18 | transcript | ENST00000508593.6 | protein_coding | 6/17 | chr4 | TogoVar | |||||||
APLF_chr2_68462585_68585162 | 68518598 | TATAATAT others(25): Show |
T | intron_variant | MODIFIER | NA18969.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0159 | 1 | 153 | 0.0065 | -32 | c.622 others(49): Show |
APLF | ENSG00000169621.11 | transcript | ENST00000303795.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
APOO_chrX_23828353_23912938 | 23829569 | AAAAAATA others(25): Show |
A | downstream_gene_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0221 | 1 | 164 | 0.0061 | -32 | c.*40 others(43): Show |
APOO | ENSG00000184831.14 | transcript | ENST00000379226.9 | protein_coding | 3783 | chrX | TogoVar | |||||||
APPL2_chr12_105168300_105241174 | 105224070 | AATCAACA others(25): Show |
A | intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0256 | 1 | 390 | 0.0026 | -32 | c.153 others(49): Show |
APPL2 | ENSG00000136044.12 | transcript | ENST00000258530.8 | protein_coding | 2/20 | chr12 | TogoVar | |||||||
AQP8_chr16_25211947_25233932 | 25216203 | TTCTTTCT others(25): Show |
T | upstream_gene_variant | MODIFIER | HG02293.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0187 | 1 | 409 | 0.0024 | -32 | c.-84 others(41): Show |
AQP8 | ENSG00000103375.11 | transcript | ENST00000219660.6 | protein_coding | 743 | chr16 | TogoVar | |||||||
AREG_chr4_74440136_74460005 | 74441442 | TTATATAT others(25): Show |
T | upstream_gene_variant | MODIFIER | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0017 |
14 | 75 | 0.1867 | -32 | c.-39 others(43): Show |
AREG | ENSG00000109321.11 | transcript | ENST00000395748.8 | protein_coding | 3693 | chr4 | TogoVar | |||||||
ARF3_chr12_48930723_48962487 | 48932241 | ATATATAT others(25): Show |
A | downstream_gene_variant | MODIFIER | HG01358.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0073 | 1 | 338 | 0.0030 | -32 | c.*66 others(43): Show |
ARF3 | ENSG00000134287.10 | transcript | ENST00000256682.9 | protein_coding | 3481 | chr12 | TogoVar | |||||||
ARFGAP1_chr20_63267813_63294790 | 63292775 | GGGCATAC others(25): Show |
G | downstream_gene_variant | MODIFIER | HG02129.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 340 | 0.0029 | -32 | c.*49 others(43): Show |
ARFGAP1 | ENSG00000101199.13 | transcript | ENST00000370283.9 | protein_coding | 2986 | chr20 | TogoVar | |||||||
ARFGEF3_chr6_138156939_138349663 | 138345451 | TTATATAT others(25): Show |
T | downstream_gene_variant | MODIFIER | HG01071.hp1 HG02004.hp1 HG02148.hp2 |
a0001a0002a0010 | a0001c0001a0002c0002a0010c0024 | a0001c0001t0001a0002c0002t0001a0010c0024t0027 | a0001c0001t0001g0163 a0002c0002t0001g0064 a0010c0024t0027g0062 |
3 | 104 | 0.0288 | -32 | c.*89 others(43): Show |
ARFGEF3 | ENSG00000112379.9 | transcript | ENST00000251691.5 | protein_coding | 789 | chr6 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106570586 | GTCCCAGC others(25): Show |
G | upstream_gene_variant | MODIFIER | HG02809.hp1 HG02965.hp2 HG03471.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0018 a0001c0001t0006g0056 a0001c0001t0006g0057 |
5 | 374 | 0.0134 | -32 | c.-26 others(43): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 2450 | chr13 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147798755 | CTCTCTCT others(25): Show |
C | intron_variant | MODIFIER | HG01070.hp1 HG03492.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0035 a0001c0001t0002g0022 |
2 | 94 | 0.0213 | -32 | c.155 others(51): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143542806 | ATATATAT others(25): Show |
A | intron_variant | MODIFIER | HG02559.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061 | 1 | 160 | 0.0063 | -32 | c.926 others(51): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625138 | TATATTAT others(25): Show |
T | intron_variant | MODIFIER | HG02818.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0044 | 1 | 236 | 0.0042 | -32 | c.786 others(49): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625670 | TTATATTA others(25): Show |
T | intron_variant | MODIFIER | HG00733.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0178 | 1 | 236 | 0.0042 | -32 | c.786 others(49): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129714935 | ATAATTTG others(25): Show |
A | upstream_gene_variant | MODIFIER | NA18612.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0054 | 1 | 236 | 0.0042 | -32 | c.-48 others(43): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4759 | chr6 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97218925 | GTGTGTGT others(25): Show |
G | downstream_gene_variant | MODIFIER | HG02004.hp1 | a0002 | a0002c0004 | a0002c0004t0002 | a0002c0004t0002g0073 | 1 | 240 | 0.0042 | -32 | c.*71 others(43): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3253 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97218927 | GTGTGTGT others(25): Show |
G | downstream_gene_variant | MODIFIER | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(10): Show |
a0002 | a0002c0004 | a0002c0004t0002 | a0002c0004t0002g0060 a0002c0004t0002g0064 a0002c0004t0002g0065 others(10): Show |
13 | 233 | 0.0558 | -32 | c.*71 others(43): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3251 | chr10 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110572835 | GTTTGAGT others(25): Show |
G | downstream_gene_variant | MODIFIER | NA18999.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0175 | 1 | 224 | 0.0045 | -32 | c.*65 others(43): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4207 | chr11 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24689843 | TATGTATA others(25): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
a0001a0002a0005others(5): Show | a0001c0001a0002c0002a0002c0015others(10): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0004others(14): Show | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(134): Show |
137 | 350 | 0.3914 | -32 | c.64- others(49): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85570364 | CTCTTTCT others(25): Show |
C | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG01070.hp1 others(47): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(17): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(47): Show |
50 | 55 | 0.9091 | -32 | c.-20 others(47): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890143 | AAAAAAAA others(25): Show |
A | intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0167 | 1 | 196 | 0.0051 | -32 | c.487 others(49): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890145 | AAAAAAAA others(25): Show |
A | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG02155.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0005a0001c0001t0020others(3): Show | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(8): Show |
11 | 195 | 0.0564 | -32 | c.487 others(49): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142947151 | CTGAGCTG others(25): Show |
C | intron_variant | MODIFIER | NA18978.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0136 | 1 | 196 | 0.0051 | -32 | c.110 others(53): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729544 | GCACTCAC others(25): Show |
G | upstream_gene_variant | MODIFIER | HG00741.hp2 HG02602.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0003 | a0001c0001t0001g0026 a0001c0003t0003g0027 |
2 | 245 | 0.0082 | -32 | c.-27 others(41): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 171 | chr18 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(25): Show |
A | intron_variant | MODIFIER | NA18973.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0123 | 1 | 33 | 0.0303 | -32 | c.-18 others(53): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100728714 | GTATATAT others(25): Show |
G | intron_variant | MODIFIER | HG02622.hp2 HG02965.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0031 | a0001c0001t0001g0046 a0001c0001t0031g0249 |
2 | 165 | 0.0121 | -32 | c.154 others(51): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | AATATATA others(25): Show |
A | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(30): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0003a0001c0003t0006others(4): Show | a0001c0003t0001g0156 a0001c0003t0001g0163 a0001c0003t0001g0172 others(30): Show |
33 | 100 | 0.3300 | -32 | c.385 others(49): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11176300 | CATATATA others(25): Show |
C | intron_variant | MODIFIER | NA18982.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027 | 1 | 13 | 0.0769 | -32 | c.162 others(51): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44801077 | AGGGGCAC others(25): Show |
A | intron_variant | MODIFIER | HG03209.hp2 | a0023 | a0023c0077 | a0023c0077t0006 | a0023c0077t0006g0068 | 1 | 350 | 0.0029 | -32 | c.80- others(45): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44801459 | GTGTGTGG others(25): Show |
G | intron_variant | MODIFIER | HG01243.hp2 HG02809.hp1 |
a0002 | a0002c0011a0002c0068 | a0002c0011t0005a0002c0068t0008 | a0002c0011t0005g0016 a0002c0068t0008g0044 |
2 | 229 | 0.0087 | -32 | c.80- others(45): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1839535 | CTGTCTGG others(25): Show |
C | intron_variant | MODIFIER | HG01081.hp1 HG02615.hp1 HG02818.hp1 |
a0001a0003 | a0001c0002a0001c0007a0003c0044 | a0001c0002t0001a0001c0007t0008a0003c0044t0002 | a0001c0002t0001g0327 a0001c0007t0008g0362 a0003c0044t0002g0328 |
3 | 362 | 0.0083 | -32 | c.-47 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1840166 | CAAGCTGT others(25): Show |
C | intron_variant | MODIFIER | NA18964.hp2 | a0001 | a0001c0085 | a0001c0085t0001 | a0001c0085t0001g0207 | 1 | 326 | 0.0031 | -32 | c.-47 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1840307 | GTGGGGAC others(25): Show |
G | intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0020 | a0001c0020t0016 | a0001c0020t0016g0308 | 1 | 360 | 0.0028 | -32 | c.-47 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1840559 | TGATATGG others(25): Show |
T | intron_variant | MODIFIER | HG03831.hp1 | a0004 | a0004c0051 | a0004c0051t0005 | a0004c0051t0005g0318 | 1 | 362 | 0.0028 | -32 | c.-47 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889302 | GCATGGGG others(25): Show |
G | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01346.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0019a0001c0002t0001a0001c0002t0012others(1): Show | a0001c0001t0019g0245 a0001c0002t0001g0068 a0001c0002t0012g0190 others(1): Show |
4 | 362 | 0.0110 | -32 | c.118 others(51): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120334845 | GTATATGT others(25): Show |
G | upstream_gene_variant | MODIFIER | NA20752.hp2 | a0001 | a0001c0006 | a0001c0006t0002 | a0001c0006t0002g0303 | 1 | 306 | 0.0033 | -32 | c.-23 others(43): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1567 | chr11 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120351427 | ATATATAT others(25): Show |
A | intron_variant | MODIFIER | HG00673.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 | 1 | 256 | 0.0039 | -32 | c.32+ others(49): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120351429 | ATATATAT others(25): Show |
A | intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0146 | 1 | 299 | 0.0033 | -32 | c.32+ others(49): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7350763 | GGTGGGTG others(25): Show |
G | intron_variant | MODIFIER | HG02976.hp1 | a0021 | a0021c0030 | a0021c0030t0006 | a0021c0030t0006g0255 | 1 | 88 | 0.0114 | -32 | c.-11 others(51): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73671710 | ATATATAT others(25): Show |
A | intron_variant | MODIFIER | HG01934.hp2 HG03927.hp1 |
a0013a0018 | a0013c0016a0018c0019 | a0013c0016t0002a0018c0019t0002 | a0013c0016t0002g0059 a0018c0019t0002g0009 |
2 | 157 | 0.0127 | -32 | c.-11 others(51): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741375 | GTGTGTGT others(25): Show |
G | intron_variant | MODIFIER | NA21309.hp2 | a0003 | a0003c0007 | a0003c0007t0001 | a0003c0007t0001g0045 | 1 | 157 | 0.0064 | -32 | c.34- others(47): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741377 | GTGTGTGT others(25): Show |
G | intron_variant | MODIFIER | NA18988.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0058 | 1 | 159 | 0.0063 | -32 | c.34- others(47): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741379 | GTGTGTGT others(25): Show |
G | intron_variant | MODIFIER | HG00140.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0032 | 1 | 176 | 0.0057 | -32 | c.34- others(47): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF33_chr2_38884875_38980454 | 38951640 | TATATATA others(25): Show |
T | intron_variant | MODIFIER | NA18964.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0145 | 1 | 276 | 0.0036 | -32 | c.105 others(49): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF4_chr2_130831914_131052253 | 130988883 | TATATATA others(25): Show |
T | intron_variant | MODIFIER | NA18981.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035 | 1 | 139 | 0.0072 | -32 | c.398 others(53): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111133763 | TTATATAT others(25): Show |
T | intron_variant | MODIFIER | HG00741.hp2 HG01071.hp1 HG03195.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0009 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(1): Show | a0001c0001t0001g0123 a0001c0001t0005g0224 a0001c0001t0007g0031 others(1): Show |
4 | 93 | 0.0430 | -32 | c.165 others(51): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 156934912 | TTATATAT others(25): Show |
T | intron_variant | MODIFIER | HG00280.hp1 HG01516.hp1 HG02280.hp1 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0095 a0001c0002t0001g0104 a0001c0002t0001g0115 others(1): Show |
4 | 23 | 0.1739 | -32 | c.213 others(49): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar |