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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP20_chr11_110572043_110717437 | 110664727 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG01928.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068 | 1 | 226 | 0.0044 | -10 | c.188 others(29): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24580886 | CAAAAAAA others(3): Show |
C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0002c0015others(10): Show | a0001c0001t0001a0001c0001t0005a0002c0002t0001others(14): Show | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0170others(125): Show | 128 | 352 | 0.3636 | -10 | c.*35 others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2727 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24619054 | GTTAAATT others(3): Show |
G | intron_variant | MODIFIER | NA18974.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0304 | 1 | 352 | 0.0028 | -10 | c.242 others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24622433 | CATATATA others(3): Show |
C | intron_variant | MODIFIER | HG00597.hp2 HG01891.hp1 HG02615.hp2 others(7): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(4): Show | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0002g0326others(7): Show | 10 | 352 | 0.0284 | -10 | c.525 others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628896 | TACATATA others(3): Show |
T | intron_variant | MODIFIER | NA19002.hp2 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0223 | 1 | 352 | 0.0028 | -10 | c.495 others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628952 | CTATATAT others(3): Show |
C | intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0190 | 1 | 352 | 0.0028 | -10 | c.495 others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24639833 | GAGAAAGC others(3): Show |
G | intron_variant | MODIFIER | HG02109.hp1 HG03195.hp1 |
a0012 | a0012c0010 | a0012c0010t0001 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | 352 | 0.0057 | -10 | c.269 others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24695050 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG02109.hp1 NA19065.hp1 NA19080.hp2 |
a0001a0012 | a0001c0001a0012c0010 | a0001c0001t0001a0012c0010t0001 | a0001c0001t0001g0226a0001c0001t0001g0234a0012c0010t0001g0267 | 3 | 352 | 0.0085 | -10 | c.64- others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48578524 | ATGTGTGT others(3): Show |
A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(75): Show |
a0001a0003a0006others(2): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0040others(75): Show | 78 | 270 | 0.2889 | -10 | c.234 others(27): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 2/9 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38447437 | GAAAAAAA others(3): Show |
G | intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0263 | 1 | 309 | 0.0032 | -10 | c.64- others(27): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38453418 | CGTGCGTG others(3): Show |
C | intron_variant | MODIFIER | HG01081.hp1 HG02818.hp1 HG03471.hp2 |
a0001 | a0001c0004a0001c0020 | a0001c0004t0006a0001c0020t0005 | a0001c0004t0006g0008a0001c0020t0005g0009a0001c0020t0005g0141 | 3 | 309 | 0.0097 | -10 | c.64- others(25): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38453422 | CGTGTGTG others(3): Show |
C | intron_variant | MODIFIER | HG01169.hp1 HG01261.hp1 HG01433.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0002a0001c0003t0001 | a0001c0002t0002g0013a0001c0002t0002g0255a0001c0003t0001g0012 | 3 | 309 | 0.0097 | -10 | c.64- others(25): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38453452 | TGTGTGTG others(3): Show |
T | intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0150 | 1 | 309 | 0.0032 | -10 | c.64- others(25): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38504978 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | HG00323.hp1 HG00544.hp2 HG00733.hp1 others(20): Show |
a0001a0017 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0005t0001others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0083others(19): Show | 23 | 309 | 0.0744 | -10 | c.344 others(29): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38509021 | TGGGGAAG others(3): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0002a0001c0003others(55): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(69): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 308 | 309 | 0.9968 | -10 | c.344 others(27): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85485372 | AAAAAATA others(3): Show |
A | intron_variant | MODIFIER | HG01167.hp2 NA20300.hp2 |
a0001a0002 | a0001c0002a0002c0006 | a0001c0002t0007a0002c0006t0006 | a0001c0002t0007g0056a0002c0006t0006g0095 | 2 | 108 | 0.0185 | -10 | c.-21 others(27): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85485374 | AAAATATA others(3): Show |
A | intron_variant | MODIFIER | HG01168.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0092 | 1 | 108 | 0.0093 | -10 | c.-21 others(27): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85485376 | AATATATA others(3): Show |
A | intron_variant | MODIFIER | HG01978.hp1 HG02080.hp2 HG02451.hp2 others(12): Show |
a0001a0004a0005 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0015a0001c0002t0002others(5): Show | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0062others(12): Show | 15 | 108 | 0.1389 | -10 | c.-21 others(27): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85564924 | GTATATAT others(3): Show |
G | intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0049 | 1 | 108 | 0.0093 | -10 | c.-20 others(27): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85612083 | TACACACA others(3): Show |
T | intron_variant | MODIFIER | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(42): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(19): Show | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(42): Show | 45 | 108 | 0.4167 | -10 | c.180 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85643234 | GTTTTTTT others(3): Show |
G | intron_variant | MODIFIER | HG02145.hp1 HG02145.hp2 HG02622.hp1 others(5): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(4): Show | a0001c0001t0001g0048a0001c0001t0005g0101a0001c0002t0002g0005others(5): Show | 8 | 108 | 0.0741 | -10 | c.180 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85655808 | GAGAGAGA others(3): Show |
G | intron_variant | MODIFIER | HG01978.hp2 HG02080.hp1 NA18968.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0107 | 3 | 108 | 0.0278 | -10 | c.181 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85660794 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | NA19240.hp1 NA20300.hp2 |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0002c0006t0006 | a0001c0001t0001g0008a0002c0006t0006g0095 | 2 | 108 | 0.0185 | -10 | c.181 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85669644 | AATATATA others(3): Show |
A | intron_variant | MODIFIER | HG02145.hp1 HG04204.hp2 |
a0001a0002 | a0001c0002a0002c0006 | a0001c0002t0002a0002c0006t0006 | a0001c0002t0002g0076a0002c0006t0006g0031 | 2 | 108 | 0.0185 | -10 | c.181 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85700406 | AATAAATA others(3): Show |
A | intron_variant | MODIFIER | HG01167.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025 | 1 | 108 | 0.0093 | -10 | c.181 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85724489 | GTGTATAT others(3): Show |
G | intron_variant | MODIFIER | HG02622.hp1 HG03516.hp2 |
a0001 | a0001c0003a0001c0008 | a0001c0003t0001a0001c0008t0014 | a0001c0003t0001g0051a0001c0008t0014g0063 | 2 | 108 | 0.0185 | -10 | c.268 others(27): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85731019 | CACACACA others(3): Show |
C | intron_variant | MODIFIER | HG02155.hp2 HG03492.hp2 HG04204.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0018a0001c0001t0001g0066a0001c0003t0001g0014 | 3 | 108 | 0.0278 | -10 | c.268 others(27): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85743392 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(3): Show | a0001c0001t0001g0018a0001c0001t0001g0048a0001c0001t0001g0065others(11): Show | 14 | 108 | 0.1296 | -10 | c.268 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85745407 | GTATATAT others(3): Show |
G | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00639.hp1 others(24): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(9): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0019others(24): Show | 27 | 108 | 0.2500 | -10 | c.268 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85750485 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0003 | a0001c0003t0010 | a0001c0003t0010g0083 | 1 | 108 | 0.0093 | -10 | c.268 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85813816 | TTTTATAT others(3): Show |
T | intron_variant | MODIFIER | HG01884.hp1 HG02897.hp2 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0002a0001c0005t0004 | a0001c0002t0002g0005a0001c0005t0004g0034 | 2 | 108 | 0.0185 | -10 | c.268 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85827461 | CGTGTGTG others(3): Show |
C | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(1): Show | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0107others(3): Show | 6 | 108 | 0.0556 | -10 | c.269 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85839843 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | HG01167.hp2 HG02486.hp1 |
a0001 | a0001c0002a0001c0007 | a0001c0002t0007a0001c0007t0003 | a0001c0002t0007g0056a0001c0007t0003g0044 | 2 | 108 | 0.0185 | -10 | c.269 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85854135 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG01109.hp2 HG02109.hp1 HG02622.hp1 others(2): Show |
a0001 | a0001c0001a0001c0007a0001c0008 | a0001c0001t0001a0001c0007t0003a0001c0008t0014 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0048others(2): Show | 5 | 108 | 0.0463 | -10 | c.269 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85880519 | TTGTGTGT others(3): Show |
T | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(26): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(9): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0018others(26): Show | 29 | 108 | 0.2685 | -10 | c.269 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85898031 | GTGTATAT others(3): Show |
G | intron_variant | MODIFIER | HG00423.hp2 HG00639.hp1 HG01433.hp1 others(8): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0013others(1): Show | a0001c0001t0001a0001c0001t0021a0001c0003t0001others(4): Show | a0001c0001t0001g0032a0001c0001t0021g0054a0001c0003t0001g0004others(8): Show | 11 | 108 | 0.1019 | -10 | c.269 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85898033 | GTATATAT others(3): Show |
G | intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0059 | 1 | 108 | 0.0093 | -10 | c.269 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142796054 | CTGTGTGT others(3): Show |
C | intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0001 | a0001c0001t0030 | a0001c0001t0030g0102 | 1 | 198 | 0.0051 | -10 | c.154 others(29): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142806473 | ATGTGTGT others(3): Show |
A | intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0023 | a0001c0001t0023g0055 | 1 | 198 | 0.0051 | -10 | c.154 others(29): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142808236 | GAAAAAAA others(3): Show |
G | intron_variant | MODIFIER | HG02572.hp2 NA18990.hp2 |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0047 | a0001c0001t0011g0094a0001c0001t0047g0127 | 2 | 198 | 0.0101 | -10 | c.154 others(29): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142867288 | GGTGTGTG others(3): Show |
G | intron_variant | MODIFIER | HG02622.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0033 | a0001c0001t0002g0022a0001c0001t0033g0053 | 2 | 198 | 0.0101 | -10 | c.155 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | AATATATA others(3): Show |
A | intron_variant | MODIFIER | NA18971.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0179 | 1 | 198 | 0.0051 | -10 | c.487 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142963163 | GGTATATA others(3): Show |
G | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(42): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0012a0001c0001t0001g0153a0001c0001t0001g0196others(42): Show | 45 | 198 | 0.2273 | -10 | c.110 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142980352 | CTTTATTT others(3): Show |
C | intron_variant | MODIFIER | HG00323.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0034a0001c0001t0036others(1): Show | a0001c0001t0002g0023a0001c0001t0002g0027a0001c0001t0034g0192others(2): Show | 5 | 198 | 0.0253 | -10 | c.110 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143004017 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG02698.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0141a0001c0001t0002g0005a0001c0001t0002g0006others(13): Show | 16 | 198 | 0.0808 | -10 | c.110 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143029392 | GTTTTTTT others(3): Show |
G | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG02109.hp2 others(15): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(8): Show | a0001c0001t0004g0002a0001c0001t0004g0098a0001c0001t0004g0099others(15): Show | 18 | 198 | 0.0909 | -10 | c.114 others(29): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143072393 | CACTACTG others(3): Show |
C | intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0105 | 1 | 198 | 0.0051 | -10 | c.153 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | CTTTTTTT others(3): Show |
C | intron_variant | MODIFIER | HG02280.hp2 HG02622.hp2 HG02647.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010a0001c0001t0025 | a0001c0001t0002g0008a0001c0001t0010g0080a0001c0001t0025g0103 | 3 | 198 | 0.0152 | -10 | c.153 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143161004 | ATTTTTTT others(3): Show |
A | intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0045 | 1 | 198 | 0.0051 | -10 | c.198 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143167482 | CAAAAAAA others(3): Show |
C | intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0142 | 1 | 198 | 0.0051 | -10 | c.198 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |