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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP26_chr5_142765377_143234007 | 143222246 | TACACACA others(3): Show |
T | intron_variant | MODIFIER | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0007 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(12): Show | a0001c0001t0002g0036a0001c0001t0009g0026a0001c0001t0009g0039others(18): Show | 21 | 198 | 0.1061 | -10 | c.219 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP27_chr17_45388908_45437870 | 45399591 | CAAAGAAA others(3): Show |
C | intron_variant | MODIFIER | HG01074.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0197 | 1 | 347 | 0.0029 | -10 | c.174 others(29): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45419512 | GTATATAT others(3): Show |
G | intron_variant | MODIFIER | NA18982.hp2 NA19070.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0288a0001c0001t0002g0289 | 2 | 347 | 0.0058 | -10 | c.657 others(29): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729411 | AACACAGG others(3): Show |
A | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0003a0001c0010others(17): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(30): Show | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(130): Show | 133 | 248 | 0.5363 | -10 | c.-41 others(19): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 304 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6782592 | ATTTTTTT others(3): Show |
A | intron_variant | MODIFIER | HG01243.hp1 HG02109.hp1 HG02895.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(2): Show | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(4): Show | 7 | 248 | 0.0282 | -10 | c.123 others(29): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6802335 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | HG02630.hp2 | a0008 | a0008c0011 | a0008c0011t0005 | a0008c0011t0005g0016 | 1 | 248 | 0.0040 | -10 | c.123 others(29): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841198 | TCTCTCCT others(3): Show |
T | intron_variant | MODIFIER | NA19012.hp2 | a0002 | a0002c0005 | a0002c0005t0002 | a0002c0005t0002g0043 | 1 | 248 | 0.0040 | -10 | c.543 others(27): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6911393 | TTATATGC others(3): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0001c0010others(16): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(29): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 183 | 248 | 0.7379 | -10 | c.209 others(27): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP29_chr1_94163905_94242584 | 94168365 | CTTTTTTT others(3): Show |
C | downstream_gene_variant | MODIFIER | HG03831.hp2 NA20905.hp1 |
a0001 | a0001c0001 | a0001c0001t0042a0001c0001t0043 | a0001c0001t0042g0206a0001c0001t0043g0205 | 2 | 356 | 0.0056 | -10 | c.*54 others(21): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 539 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94182811 | TAAAACAA others(3): Show |
T | intron_variant | MODIFIER | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(7): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0001a0001c0001t0010a0001c0001t0041others(1): Show | a0001c0001t0001g0150a0001c0001t0010g0029a0001c0001t0010g0288others(6): Show | 10 | 356 | 0.0281 | -10 | c.224 others(29): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94221357 | GGTGTTTA others(3): Show |
G | intron_variant | MODIFIER | NA19240.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0046 | 1 | 356 | 0.0028 | -10 | c.206 others(25): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | TTCTCTCT others(3): Show |
T | intron_variant | MODIFIER | HG00741.hp1 HG01243.hp1 HG02040.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0033a0001c0001t0001g0096a0001c0001t0001g0098others(7): Show | 10 | 390 | 0.0256 | -10 | c.537 others(23): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055886 | TAAATAAA others(3): Show |
T | intron_variant | MODIFIER | HG01928.hp2 HG02040.hp1 HG02683.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0067others(5): Show | 8 | 390 | 0.0205 | -10 | c.345 others(25): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064769 | GAAAGAAA others(3): Show |
G | intron_variant | MODIFIER | HG00099.hp2 HG01433.hp1 HG01515.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0099others(4): Show | 7 | 390 | 0.0180 | -10 | c.97+ others(25): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064821 | AAGAAAGA others(3): Show |
A | intron_variant | MODIFIER | HG02622.hp1 HG02886.hp1 HG02922.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0013a0001c0001t0001g0164a0001c0001t0001g0191others(5): Show | 8 | 390 | 0.0205 | -10 | c.97+ others(25): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119332631 | TCTCTCAC others(3): Show |
T | intron_variant | MODIFIER | HG01361.hp1 HG02970.hp1 HG03654.hp1 |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0018a0001c0002t0001a0002c0003t0019 | a0001c0001t0018g0209a0001c0002t0001g0070a0002c0003t0019g0182 | 3 | 310 | 0.0097 | -10 | c.101 others(29): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119332633 | TCTCACAC others(3): Show |
T | intron_variant | MODIFIER | HG01081.hp2 HG01099.hp1 HG01358.hp1 others(13): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0011a0001c0001t0018a0001c0002t0012others(6): Show | a0001c0001t0011g0001a0001c0001t0011g0158a0001c0001t0011g0183others(12): Show | 16 | 310 | 0.0516 | -10 | c.101 others(29): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119332635 | TCACACAC others(3): Show |
T | intron_variant | MODIFIER | HG00639.hp1 HG00735.hp1 HG02559.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0018 | a0001c0001t0011a0001c0001t0045a0001c0001t0052others(2): Show | a0001c0001t0011g0186a0001c0001t0045g0286a0001c0001t0052g0283others(4): Show | 7 | 310 | 0.0226 | -10 | c.101 others(29): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119422923 | ACTATTCT others(3): Show |
A | downstream_gene_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
a0001a0003a0013others(1): Show | a0001c0001a0001c0002a0003c0006others(3): Show | a0001c0001t0006a0001c0001t0008a0001c0001t0017others(17): Show | a0001c0001t0006g0025a0001c0001t0006g0027a0001c0001t0006g0065others(95): Show | 98 | 310 | 0.3161 | -10 | c.*66 others(21): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2210 | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119424672 | ATTTTTTT others(3): Show |
A | downstream_gene_variant | MODIFIER | NA18975.hp2 NA19087.hp2 |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0004 | a0001c0002t0001g0023a0001c0002t0004g0230 | 2 | 310 | 0.0065 | -10 | c.*84 others(21): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3959 | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128963212 | TATTAACA others(3): Show |
T | downstream_gene_variant | MODIFIER | HG01123.hp1 HG06807.hp1 |
a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0384a0001c0003t0005g0385 | 2 | 398 | 0.0050 | -10 | c.*56 others(21): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1847 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129051953 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG01109.hp2 HG01891.hp1 HG02895.hp1 others(2): Show |
a0001 | a0001c0003 | a0001c0003t0006 | a0001c0003t0006g0199a0001c0003t0006g0200a0001c0003t0006g0201others(2): Show | 5 | 398 | 0.0126 | -10 | c.963 others(29): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129058213 | ACACACAC others(3): Show |
A | intron_variant | MODIFIER | HG02055.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
a0001 | a0001c0005 | a0001c0005t0001a0001c0005t0017 | a0001c0005t0001g0003a0001c0005t0001g0004a0001c0005t0001g0076others(4): Show | 7 | 398 | 0.0176 | -10 | c.963 others(27): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129082475 | GCAAATAA others(3): Show |
G | intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0310 | 1 | 398 | 0.0025 | -10 | c.531 others(29): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | ||||||
ARHGAP33_chr19_35770564_35793822 | 35790989 | AGGGGCAG others(3): Show |
A | downstream_gene_variant | MODIFIER | NA19072.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0063 | 1 | 420 | 0.0024 | -10 | c.*25 others(21): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 2168 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46869476 | TTGTGTGT others(3): Show |
T | intron_variant | MODIFIER | HG02886.hp1 HG02886.hp2 HG03130.hp2 others(5): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0007others(1): Show | a0001c0001t0015a0001c0001t0023a0001c0001t0040others(4): Show | a0001c0001t0015g0037a0001c0001t0023g0039a0001c0001t0023g0055others(5): Show | 8 | 298 | 0.0269 | -10 | c.-18 others(29): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(3): Show |
A | intron_variant | MODIFIER | HG00597.hp1 HG00738.hp1 HG01081.hp2 others(13): Show |
a0001a0005a0006 | a0001c0001a0005c0012a0006c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0186a0001c0001t0002g0267a0001c0001t0003g0021others(13): Show | 16 | 298 | 0.0537 | -10 | c.-18 others(31): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46888333 | TACACACA others(3): Show |
T | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0019a0001c0001t0029a0001c0001t0042 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | 298 | 0.0134 | -10 | c.-18 others(31): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46981825 | GTGTTTTG others(3): Show |
G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0007others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(38): Show | a0001c0001t0001g0204a0001c0001t0002g0136a0001c0001t0003g0001others(115): Show | 118 | 298 | 0.3960 | -10 | c.382 others(29): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47003913 | GACACGCA others(3): Show |
G | 3_prime_UTR_variant | MODIFIER | NA18970.hp1 | a0001 | a0001c0001 | a0001c0001t0044 | a0001c0001t0044g0063 | 1 | 298 | 0.0034 | -10 | c.*32 others(21): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||
ARHGAP35_chr19_46855997_47010077 | 47007073 | CTTTTTTT others(3): Show |
C | downstream_gene_variant | MODIFIER | HG00639.hp1 HG02135.hp1 HG02572.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0009others(1): Show | a0001c0001t0002g0131a0001c0001t0003g0011a0001c0001t0003g0061others(2): Show | 5 | 298 | 0.0168 | -10 | c.*63 others(21): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1997 | chr19 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144559354 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0017 | a0001c0017t0001 | a0001c0017t0001g0064 | 1 | 246 | 0.0041 | -10 | c.513 others(27): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144608156 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG00741.hp1 NA18946.hp1 NA19043.hp2 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0080a0001c0002t0001g0098a0001c0002t0001g0162 | 3 | 246 | 0.0122 | -10 | c.-81 others(27): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144650143 | GGAAAAAA others(3): Show |
G | intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0170 | 1 | 246 | 0.0041 | -10 | c.-82 others(29): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144673012 | TTCAAAAC others(3): Show |
T | intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0012 | a0001c0012t0002 | a0001c0012t0002g0128 | 1 | 246 | 0.0041 | -10 | c.-82 others(29): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38630072 | CTTTCTTT others(3): Show |
C | intron_variant | MODIFIER | HG02630.hp1 HG02809.hp2 |
a0004 | a0004c0011 | a0004c0011t0004 | a0004c0011t0004g0312a0004c0011t0004g0313 | 2 | 350 | 0.0057 | -10 | c.783 others(25): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100704964 | GGTGAGCC others(3): Show |
G | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(82): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0010a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(23): Show | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0026others(82): Show | 85 | 286 | 0.2972 | -10 | c.154 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100728713 | CGTATATA others(3): Show |
C | intron_variant | MODIFIER | HG01081.hp1 HG01106.hp2 HG01123.hp1 others(12): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0005others(2): Show | a0001c0001t0001a0001c0001t0037a0002c0002t0002others(7): Show | a0001c0001t0001g0088a0001c0001t0001g0186a0001c0001t0001g0211others(12): Show | 15 | 286 | 0.0525 | -10 | c.154 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100728714 | GTATATAT others(3): Show |
G | intron_variant | MODIFIER | HG01978.hp2 HG02723.hp1 NA19043.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0140a0002c0002t0002g0151a0002c0002t0002g0254 | 3 | 286 | 0.0105 | -10 | c.154 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG01891.hp1 | a0002 | a0002c0005 | a0002c0005t0010 | a0002c0005t0010g0044 | 1 | 286 | 0.0035 | -10 | c.251 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875099 | CTCTCTCT others(3): Show |
C | intron_variant | MODIFIER | HG01884.hp2 | a0002 | a0002c0002 | a0002c0002t0005 | a0002c0002t0005g0115 | 1 | 286 | 0.0035 | -10 | c.384 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875101 | CTCTCTCT others(3): Show |
C | intron_variant | MODIFIER | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(41): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(6): Show | a0001c0001t0001g0011a0001c0001t0001g0069a0001c0001t0001g0070others(41): Show | 44 | 286 | 0.1539 | -10 | c.384 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875103 | CTCTCTGT others(3): Show |
C | intron_variant | MODIFIER | HG02738.hp2 HG02970.hp1 NA19091.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0012a0002c0002 | a0001c0001t0001a0001c0012t0001a0002c0002t0025others(1): Show | a0001c0001t0001g0121a0001c0012t0001g0131a0002c0002t0025g0247others(1): Show | 4 | 286 | 0.0140 | -10 | c.384 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875105 | CTCTGTGT others(3): Show |
C | intron_variant | MODIFIER | HG00544.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0001a0001c0008t0001a0002c0002t0002others(2): Show | a0001c0001t0001g0023a0001c0008t0001g0004a0002c0002t0002g0254others(2): Show | 5 | 286 | 0.0175 | -10 | c.384 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875107 | CTGTGTGT others(3): Show |
C | intron_variant | MODIFIER | HG00423.hp1 HG00741.hp1 HG00741.hp2 others(37): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0030others(8): Show | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0068others(37): Show | 40 | 286 | 0.1399 | -10 | c.384 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | AATATATA others(3): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG01346.hp1 HG02074.hp2 others(9): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0006 | a0001c0001t0001a0002c0002t0002a0002c0002t0004others(4): Show | a0001c0001t0001g0178a0001c0001t0001g0224a0002c0002t0002g0010others(9): Show | 12 | 286 | 0.0420 | -10 | c.385 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100908170 | AGTAGTCT others(3): Show |
A | intron_variant | MODIFIER | NA18953.hp2 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0122 | 1 | 286 | 0.0035 | -10 | c.385 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100917015 | TTGTGTGT others(3): Show |
T | intron_variant | MODIFIER | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
a0001a0002 | a0001c0001a0001c0010a0002c0002others(1): Show | a0001c0001t0013a0001c0010t0001a0002c0002t0002others(3): Show | a0001c0001t0013g0122a0001c0001t0013g0168a0001c0001t0013g0283others(15): Show | 18 | 286 | 0.0629 | -10 | c.486 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921241 | ATATATTT others(3): Show |
A | intron_variant | MODIFIER | HG02004.hp1 | a0003 | a0003c0007 | a0003c0007t0005 | a0003c0007t0005g0078 | 1 | 286 | 0.0035 | -10 | c.487 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921243 | ATATTTTT others(3): Show |
A | intron_variant | MODIFIER | HG03540.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0222 | 1 | 286 | 0.0035 | -10 | c.487 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |