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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP19_chr10_97217179_97297637 | 97218937 | GTGTGTAT others(17): Show |
G | downstream_gene_variant | MODIFIER | NA18999.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0193 | 1 | 242 | 0.0041 | -24 | c.*71 others(35): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3241 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97218941 | GTATATAT others(17): Show |
G | downstream_gene_variant | MODIFIER | HG00609.hp2 HG00673.hp1 HG02015.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0125a0001c0001t0001g0134a0001c0001t0001g0141others(4): Show | 7 | 242 | 0.0289 | -24 | c.*71 others(35): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3237 | chr10 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110689740 | CGGGGAAA others(17): Show |
C | intron_variant | MODIFIER | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(4): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0002a0001c0001t0004a0003c0004t0017 | a0001c0001t0002g0008a0001c0001t0004g0009a0001c0001t0004g0010others(4): Show | 7 | 226 | 0.0310 | -24 | c.188 others(39): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24580886 | CAAAAAAA others(17): Show |
C | downstream_gene_variant | MODIFIER | HG00639.hp2 HG01257.hp1 HG01978.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(2): Show | 5 | 352 | 0.0142 | -24 | c.*35 others(35): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2727 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24622433 | CATATATA others(17): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
a0001a0002a0005others(3): Show | a0001c0001a0002c0002a0002c0015others(7): Show | a0001c0001t0001a0002c0002t0001a0002c0015t0001others(8): Show | a0001c0001t0001g0269a0002c0002t0001g0010a0002c0002t0001g0018others(84): Show | 87 | 352 | 0.2472 | -24 | c.525 others(39): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24695050 | CAAAAAAA others(17): Show |
C | intron_variant | MODIFIER | HG00609.hp1 HG01123.hp1 HG02004.hp1 others(17): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0001c0001t0004a0003c0003t0001others(1): Show | a0001c0001t0001g0177a0001c0001t0001g0190a0001c0001t0004g0296others(17): Show | 20 | 352 | 0.0568 | -24 | c.64- others(41): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48531650 | GGAGGGCA others(17): Show |
G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(38): Show | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(193): Show | 197 | 270 | 0.7296 | -24 | c.322 others(43): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38504978 | CTTTTTTT others(17): Show |
C | intron_variant | MODIFIER | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0004t0001g0057 | 3 | 309 | 0.0097 | -24 | c.344 others(43): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85485364 | AAAAAAAA others(17): Show |
A | intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0059 | 1 | 108 | 0.0093 | -24 | c.-21 others(41): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85564924 | GTATATAT others(17): Show |
G | intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0004 | a0001c0004t0004 | a0001c0004t0004g0033 | 1 | 108 | 0.0093 | -24 | c.-20 others(41): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85570364 | CTCTTTCT others(17): Show |
C | intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0007 | a0001c0007t0003 | a0001c0007t0003g0044 | 1 | 108 | 0.0093 | -24 | c.-20 others(39): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85655784 | TATATATA others(17): Show |
T | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0003 | a0001c0003t0010 | a0001c0003t0010g0083 | 1 | 108 | 0.0093 | -24 | c.181 others(43): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85669644 | AATATATA others(17): Show |
A | intron_variant | MODIFIER | HG04204.hp1 NA21309.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0010 | a0001c0001t0001g0018a0001c0003t0010g0083 | 2 | 108 | 0.0185 | -24 | c.181 others(43): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85743392 | CAAAAAAA others(17): Show |
C | intron_variant | MODIFIER | HG01167.hp2 HG02615.hp1 NA18906.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0007 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0002t0007g0056 | 3 | 108 | 0.0278 | -24 | c.268 others(43): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142908474 | TGGTCTCT others(17): Show |
T | intron_variant | MODIFIER | NA18948.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0061 | 1 | 198 | 0.0051 | -24 | c.933 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142950988 | TCTTTCCC others(17): Show |
T | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(63): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0034others(153): Show | 156 | 198 | 0.7879 | -24 | 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 | 142963163 | GGTATATA others(17): Show |
G | intron_variant | MODIFIER | HG01175.hp2 HG01192.hp1 HG03579.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0101a0001c0001t0005g0108a0001c0001t0005g0109 | 3 | 198 | 0.0152 | -24 | c.110 others(45): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161051967 | TCACCACC others(17): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(47): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0002c0002t0001others(2): Show | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0001g0042others(46): Show | 50 | 390 | 0.1282 | -24 | c.101 others(41): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 9/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | TTCTCTCT others(17): Show |
T | intron_variant | MODIFIER | HG02717.hp1 HG03540.hp2 |
a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0290a0002c0003t0001g0296 | 2 | 390 | 0.0051 | -24 | c.537 others(38): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46874620 | TCAGCCTC others(17): Show |
T | intron_variant | MODIFIER | HG00642.hp1 | a0001 | a0001c0002 | a0001c0002t0006 | a0001c0002t0006g0207 | 1 | 298 | 0.0034 | -24 | c.-18 others(45): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(17): Show |
A | intron_variant | MODIFIER | HG02451.hp2 HG02572.hp2 NA18969.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0032others(1): Show | a0001c0001t0003g0054a0001c0001t0004g0070a0001c0001t0004g0071others(3): Show | 6 | 298 | 0.0201 | -24 | c.-18 others(45): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | CATATATA others(17): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(119): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(85): Show | 122 | 302 | 0.4040 | -24 | c.-14 others(43): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP39_chr8_144524179_144690846 | 144558013 | ACTTACGT others(17): Show |
A | intron_variant | MODIFIER | HG02004.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0198 | 1 | 246 | 0.0041 | -24 | c.513 others(41): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144561707 | CTCCAGTG others(17): Show |
C | intron_variant | MODIFIER | HG00408.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050 | 1 | 246 | 0.0041 | -24 | c.513 others(41): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144561755 | ATCCAGTG others(17): Show |
A | intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0191 | 1 | 246 | 0.0041 | -24 | c.513 others(41): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144562021 | CACTCCAG others(17): Show |
C | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(44): Show |
a0001a0004a0005 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0213others(44): Show | 47 | 246 | 0.1911 | -24 | c.513 others(41): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144602773 | TATGTGCA others(17): Show |
T | intron_variant | MODIFIER | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0002t0001g0117others(1): Show | 4 | 246 | 0.0163 | -24 | c.80+ others(39): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38653334 | AGTGGTGG others(17): Show |
A | downstream_gene_variant | MODIFIER | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(29): Show |
a0001a0013a0015 | a0001c0001a0001c0002a0013c0015others(1): Show | a0001c0001t0004a0001c0002t0004a0001c0002t0005others(3): Show | a0001c0001t0004g0050a0001c0002t0004g0033a0001c0002t0004g0055others(29): Show | 32 | 350 | 0.0914 | -24 | c.*34 others(35): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2682 | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100728713 | CGTATATA others(17): Show |
C | intron_variant | MODIFIER | HG03540.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0222 | 1 | 286 | 0.0035 | -24 | c.154 others(43): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100728714 | GTATATAT others(17): Show |
G | intron_variant | MODIFIER | HG03492.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0152 | 1 | 286 | 0.0035 | -24 | c.154 others(43): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100763685 | TCCCCATG others(17): Show |
T | intron_variant | MODIFIER | HG01106.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0097 | 1 | 286 | 0.0035 | -24 | c.155 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100921225 | ATATATAT others(17): Show |
A | intron_variant | MODIFIER | HG02257.hp2 | a0002 | a0002c0002 | a0002c0002t0008 | a0002c0002t0008g0230 | 1 | 286 | 0.0035 | -24 | c.487 others(39): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921227 | ATATATAT others(17): Show |
A | intron_variant | MODIFIER | HG00408.hp2 HG01074.hp2 HG01433.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(1): Show | a0001c0001t0001g0128a0001c0001t0002g0003a0001c0001t0002g0025others(6): Show | 9 | 286 | 0.0315 | -24 | c.487 others(39): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921229 | ATATATAT others(17): Show |
A | intron_variant | MODIFIER | HG00323.hp2 HG00735.hp1 HG01257.hp2 others(13): Show |
a0001 | a0001c0001a0001c0015 | a0001c0001t0001a0001c0001t0032a0001c0001t0041others(1): Show | a0001c0001t0001g0007a0001c0001t0001g0080a0001c0001t0001g0086others(13): Show | 16 | 286 | 0.0559 | -24 | c.487 others(39): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921231 | ATATATAT others(17): Show |
A | intron_variant | MODIFIER | HG00673.hp1 HG01192.hp2 HG01358.hp1 others(26): Show |
a0001 | a0001c0001a0001c0012 | a0001c0001t0001a0001c0001t0019a0001c0001t0034others(2): Show | a0001c0001t0001g0066a0001c0001t0001g0084a0001c0001t0001g0087others(26): Show | 29 | 286 | 0.1014 | -24 | c.487 others(39): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921233 | ATATATAT others(17): Show |
A | intron_variant | MODIFIER | HG01928.hp1 HG03492.hp2 NA18522.hp2 |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0001a0002c0005t0010 | a0001c0001t0001g0152a0001c0001t0001g0165a0002c0005t0010g0056 | 3 | 286 | 0.0105 | -24 | c.487 others(39): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921235 | ATATATAT others(17): Show |
A | intron_variant | MODIFIER | HG01346.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 | 1 | 286 | 0.0035 | -24 | c.487 others(39): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802947 | ATATATAT others(17): Show |
A | intron_variant | MODIFIER | HG04204.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0229 | 1 | 230 | 0.0044 | -24 | c.53+ others(41): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11174623 | TTTTCTTT others(17): Show |
T | intron_variant | MODIFIER | HG01074.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0136 | 1 | 144 | 0.0069 | -24 | c.162 others(43): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11201989 | CTGTGTGT others(17): Show |
C | intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052 | 1 | 144 | 0.0069 | -24 | c.749 others(41): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17676428 | ATGGGTGC others(17): Show |
A | intron_variant | MODIFIER | HG02451.hp1 | a0003 | a0003c0002 | a0003c0002t0001 | a0003c0002t0001g0105 | 1 | 168 | 0.0060 | -24 | c.301 others(45): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1833267 | GGCAGAGA others(17): Show |
G | intron_variant | MODIFIER | HG01891.hp2 HG02145.hp2 NA19030.hp2 |
a0001a0015 | a0001c0005a0001c0106a0015c0072 | a0001c0005t0016a0001c0106t0042a0015c0072t0007 | a0001c0005t0016g0101a0001c0106t0042g0330a0015c0072t0007g0329 | 3 | 363 | 0.0083 | -24 | c.-48 others(41): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156954380 | CAAAAAAA others(17): Show |
C | intron_variant | MODIFIER | HG01978.hp1 | a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0267 | 1 | 362 | 0.0028 | -24 | c.179 others(41): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3471390 | TCTGCTGC others(17): Show |
T | intron_variant | MODIFIER | HG02004.hp2 | a0004 | a0004c0010 | a0004c0010t0002 | a0004c0010t0002g0060 | 1 | 334 | 0.0030 | -24 | c.102 others(43): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73304750 | CCCCGCAC others(17): Show |
C | upstream_gene_variant | MODIFIER | NA20905.hp2 | a0004 | a0004c0005 | a0004c0005t0009 | a0004c0005t0009g0020 | 1 | 228 | 0.0044 | -24 | c.-38 others(35): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 3525 | chr11 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73332350 | CGTGTGTG others(17): Show |
C | intron_variant | MODIFIER | HG00140.hp2 HG01928.hp1 NA20905.hp2 |
a0002a0004 | a0002c0004a0004c0005 | a0002c0004t0003a0004c0005t0009 | a0002c0004t0003g0144a0004c0005t0009g0016a0004c0005t0009g0020 | 3 | 228 | 0.0132 | -24 | c.319 others(45): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7346474 | CGTGTGTG others(17): Show |
C | upstream_gene_variant | MODIFIER | HG02015.hp2 HG02155.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082a0001c0001t0001g0090 | 2 | 298 | 0.0067 | -24 | c.-28 others(35): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2462 | chr19 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7350763 | GGTGGGTG others(17): Show |
G | intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0246 | 1 | 298 | 0.0034 | -24 | c.-11 others(43): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7362011 | AAGAAGGA others(17): Show |
A | intron_variant | MODIFIER | HG03834.hp1 | a0001 | a0001c0019 | a0001c0019t0006 | a0001c0019t0006g0063 | 1 | 298 | 0.0034 | -24 | c.-11 others(41): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7385443 | CATTATTA others(17): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
a0002a0003a0017 | a0002c0004a0003c0003a0017c0051 | a0002c0004t0004a0003c0003t0001a0017c0051t0006 | a0002c0004t0004g0018a0002c0004t0004g0019a0002c0004t0004g0064others(4): Show | 7 | 298 | 0.0235 | -24 | c.967 others(41): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |