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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP24_chr4_85470150_86007666 | 85578749 | T | TATC | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(29): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(98): Show |
101 | 108 | 0.9352 | 3 | c.180 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85596582 | C | CTGT | intron_variant | MODIFIER | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(42): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(19): Show | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
45 | 108 | 0.4167 | 3 | c.180 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85610451 | C | CAAA | intron_variant | MODIFIER | HG00423.hp1 HG01884.hp2 HG03492.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0013a0001c0003t0001others(1): Show | a0001c0001t0001g0003 a0001c0002t0013g0029 a0001c0003t0001g0022 others(1): Show |
4 | 17 | 0.2353 | 3 | c.180 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85647194 | A | AATT | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(6): Show | a0001c0001t0001g0032 a0001c0001t0001g0094 a0001c0001t0005g0035 others(9): Show |
12 | 81 | 0.1481 | 3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85647205 | T | TTAG | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00642.hp1 others(24): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0013others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(24): Show |
27 | 83 | 0.3253 | 3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85654720 | G | GGAA | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(42): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(13): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(42): Show |
45 | 108 | 0.4167 | 3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85657160 | C | CTTA | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(41): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0015a0001c0002t0002others(12): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(41): Show |
44 | 108 | 0.4074 | 3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85660794 | C | CAAA | intron_variant | MODIFIER | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0020 others(17): Show |
20 | 23 | 0.8696 | 3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85704725 | G | GGAC | intron_variant | MODIFIER | HG01243.hp1 HG03130.hp2 |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0005a0002c0006t0018 | a0001c0001t0005g0074 a0002c0006t0018g0040 |
2 | 108 | 0.0185 | 3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85734636 | A | ATTT | intron_variant | MODIFIER | HG02486.hp1 HG02622.hp1 HG02622.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0015a0001c0002t0007others(5): Show | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0042 others(8): Show |
11 | 28 | 0.3929 | 3 | c.268 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85738367 | T | TTTA | intron_variant | MODIFIER | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(17): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0020a0001c0001t0021others(10): Show | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0042 others(17): Show |
20 | 60 | 0.3333 | 3 | c.268 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85742251 | C | CAGT | intron_variant | MODIFIER | HG02055.hp2 HG02630.hp1 HG03486.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0003t0001a0001c0004t0003others(1): Show | a0001c0001t0001g0066 a0001c0003t0001g0089 a0001c0004t0003g0062 others(1): Show |
4 | 108 | 0.0370 | 3 | c.268 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85755626 | G | GTTT | intron_variant | MODIFIER | HG00323.hp1 HG01168.hp2 HG02080.hp2 others(6): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0013others(2): Show | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0064 others(6): Show |
9 | 47 | 0.1915 | 3 | c.268 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85784924 | T | TATC | intron_variant | MODIFIER | HG01109.hp2 NA21309.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0030 a0001c0002t0002g0060 |
2 | 108 | 0.0185 | 3 | c.268 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85872595 | C | CTTT | intron_variant | MODIFIER | HG01243.hp1 HG02055.hp2 HG02080.hp1 others(8): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(3): Show | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0066 others(8): Show |
11 | 41 | 0.2683 | 3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85893290 | C | CTGA | intron_variant | MODIFIER | HG00735.hp2 HG01069.hp1 HG01516.hp2 others(1): Show |
a0001a0003 | a0001c0001a0003c0012 | a0001c0001t0001a0003c0012t0001 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0102 others(1): Show |
4 | 108 | 0.0370 | 3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85894099 | T | TAAA | intron_variant | MODIFIER | HG00423.hp2 HG01433.hp1 HG02109.hp2 others(8): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0016a0001c0003t0001others(4): Show | a0001c0001t0001g0097 a0001c0002t0016g0055 a0001c0003t0001g0005 others(8): Show |
11 | 20 | 0.5500 | 3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85973839 | T | TTTG | intron_variant | MODIFIER | HG00642.hp2 HG00735.hp1 HG01070.hp1 others(21): Show |
a0001a0004 | a0001c0002a0001c0011a0004c0009 | a0001c0002t0002a0001c0002t0007a0001c0002t0008others(5): Show | a0001c0002t0002g0004 a0001c0002t0002g0009 a0001c0002t0002g0025 others(21): Show |
24 | 108 | 0.2222 | 3 | c.733 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 86000080 | C | CTTT | intron_variant | MODIFIER | HG01243.hp2 HG01884.hp1 HG02257.hp2 others(10): Show |
a0001 | a0001c0004a0001c0005a0001c0007 | a0001c0004t0003a0001c0004t0004a0001c0005t0003others(3): Show | a0001c0004t0003g0044 a0001c0004t0003g0051 a0001c0004t0003g0062 others(10): Show |
13 | 74 | 0.1757 | 3 | c.200 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 86000309 | T | TACA | intron_variant | MODIFIER | HG02145.hp1 HG03130.hp2 NA20300.hp2 |
a0002 | a0002c0006 | a0002c0006t0006a0002c0006t0018 | a0002c0006t0006g0031 a0002c0006t0006g0091 a0002c0006t0018g0040 |
3 | 108 | 0.0278 | 3 | c.200 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68798517 | G | GAAA | intron_variant | MODIFIER | HG00735.hp2 HG01123.hp2 HG02257.hp2 others(8): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0008others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(5): Show | a0001c0001t0001g0023 a0001c0001t0003g0341 a0001c0001t0004g0336 others(7): Show |
11 | 72 | 0.1528 | 3 | c.467 others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68815443 | C | CTTT | intron_variant | MODIFIER | HG00280.hp2 HG01109.hp1 HG01168.hp1 others(15): Show |
a0002a0003 | a0002c0002a0003c0003 | a0002c0002t0011a0003c0003t0001a0003c0003t0006others(1): Show | a0002c0002t0011g0141 a0002c0002t0011g0153 a0003c0003t0001g0103 others(15): Show |
18 | 46 | 0.3913 | 3 | c.808 others(18): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68821092 | C | CTTT | intron_variant | MODIFIER | HG00621.hp1 HG02647.hp2 HG02717.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0109 a0001c0001t0001g0118 a0001c0001t0001g0203 others(14): Show |
18 | 110 | 0.1636 | 3 | c.120 others(22): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68823298 | A | ACTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(139): Show |
a0001a0007a0010others(1): Show | a0001c0001a0007c0013a0010c0018others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(127): Show |
142 | 366 | 0.3880 | 3 | c.173 others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142768900 | T | TTGG | upstream_gene_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG02109.hp2 others(22): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0020 others(22): Show |
25 | 192 | 0.1302 | 3 | c.-18 others(14): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1476 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142791082 | G | GTTT | intron_variant | MODIFIER | HG02451.hp2 HG02622.hp1 HG02622.hp2 others(16): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0034 a0001c0001t0002g0008 a0001c0001t0002g0043 others(16): Show |
19 | 135 | 0.1407 | 3 | c.154 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142844051 | G | GTTT | intron_variant | MODIFIER | HG01175.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0002a0001c0001t0005a0001c0001t0013others(4): Show | a0001c0001t0002g0036 a0001c0001t0005g0109 a0001c0001t0013g0065 others(4): Show |
7 | 160 | 0.0438 | 3 | c.155 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142904525 | G | GAAA | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(58): Show | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0020 others(148): Show |
151 | 180 | 0.8389 | 3 | c.832 others(18): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142947095 | T | TAAA | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp1 HG02698.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0141 a0001c0001t0002g0005 a0001c0001t0002g0006 others(10): Show |
13 | 52 | 0.2500 | 3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949198 | A | AGAG | intron_variant | MODIFIER | HG02280.hp2 HG03579.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0024 | a0001c0001t0006g0064 a0001c0001t0024g0103 |
2 | 182 | 0.0110 | 3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949200 | A | AGAG | intron_variant | MODIFIER | NA18961.hp1 NA19010.hp1 |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0007 | a0001c0002t0001g0134 a0001c0002t0007g0067 |
2 | 182 | 0.0110 | 3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949214 | A | AGAG | intron_variant | MODIFIER | HG00609.hp1 HG02622.hp2 HG02886.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0020 a0001c0001t0002g0008 a0001c0001t0004g0099 others(2): Show |
5 | 191 | 0.0262 | 3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142958922 | A | AAAG | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(157): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(61): Show | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0020 others(157): Show |
160 | 189 | 0.8466 | 3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143004017 | C | CAAA | intron_variant | MODIFIER | HG01175.hp2 HG01192.hp1 HG02622.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0012a0001c0001t0032 | a0001c0001t0005g0101 a0001c0001t0005g0108 a0001c0001t0005g0109 others(2): Show |
5 | 31 | 0.1613 | 3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143006316 | C | CTGT | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG02698.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0005a0001c0001t0020others(4): Show | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0118 others(9): Show |
12 | 123 | 0.0976 | 3 | c.110 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143011303 | C | CTTT | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG00738.hp1 others(46): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0141 a0001c0001t0001g0196 a0001c0001t0002g0005 others(46): Show |
49 | 55 | 0.8909 | 3 | c.110 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012578 | A | ATGG | intron_variant | MODIFIER | NA18612.hp1 NA18972.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0158 a0001c0001t0002g0184 |
2 | 164 | 0.0122 | 3 | c.110 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143028165 | G | GGAT | intron_variant | MODIFIER | HG00544.hp1 HG01175.hp2 HG01192.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0005a0001c0002t0039a0001c0002t0047 | a0001c0001t0005g0108 a0001c0001t0005g0109 a0001c0002t0039g0155 others(1): Show |
4 | 195 | 0.0205 | 3 | c.114 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTT | intron_variant | MODIFIER | HG02155.hp2 HG03579.hp1 NA18944.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0001g0153 a0001c0001t0003g0019 a0001c0001t0004g0056 others(7): Show |
10 | 55 | 0.1818 | 3 | c.153 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143097821 | C | CAAA | intron_variant | MODIFIER | HG01069.hp1 HG02074.hp2 HG02897.hp2 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0034 a0001c0001t0001g0131 a0001c0001t0002g0036 others(6): Show |
9 | 30 | 0.3000 | 3 | c.153 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143106466 | C | CTTT | intron_variant | MODIFIER | HG01071.hp1 HG01175.hp1 HG03017.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0007a0001c0001t0040a0001c0002t0001others(2): Show | a0001c0001t0007g0107 a0001c0001t0040g0171 a0001c0002t0001g0136 others(3): Show |
6 | 53 | 0.1132 | 3 | c.153 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143144398 | T | TTTA | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(26): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0116 a0001c0001t0002g0007 a0001c0001t0002g0016 others(26): Show |
29 | 196 | 0.1480 | 3 | c.183 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143160474 | G | GTTT | intron_variant | MODIFIER | HG02451.hp2 HG02970.hp2 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0022 a0001c0001t0002g0043 a0001c0001t0002g0046 |
3 | 156 | 0.0192 | 3 | c.198 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | chr5 | TogoVar | |||||||
ARHGAP27_chr17_45388908_45437870 | 45412962 | C | CTTT | intron_variant | MODIFIER | HG00673.hp2 HG01361.hp2 HG02273.hp2 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(3): Show | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(11): Show |
14 | 94 | 0.1489 | 3 | c.658 others(20): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6782592 | A | ATTT | intron_variant | MODIFIER | HG00280.hp2 HG00558.hp2 HG01081.hp1 others(14): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0012others(3): Show | a0001c0001t0001a0001c0003t0003a0001c0012t0001others(4): Show | a0001c0001t0001g0042 a0001c0001t0001g0130 a0001c0001t0001g0190 others(14): Show |
17 | 29 | 0.5862 | 3 | c.123 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6802335 | C | CTTT | intron_variant | MODIFIER | HG01175.hp2 HG02109.hp2 HG02135.hp2 others(6): Show |
a0001a0006a0008 | a0001c0001a0001c0003a0006c0008others(1): Show | a0001c0001t0001a0001c0003t0003a0006c0008t0002others(1): Show | a0001c0001t0001g0124 a0001c0001t0001g0149 a0001c0001t0001g0185 others(6): Show |
9 | 162 | 0.0556 | 3 | c.123 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6805479 | C | CTTT | intron_variant | MODIFIER | HG01891.hp2 HG02559.hp1 HG02818.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0008a0001c0001t0018others(2): Show | a0001c0001t0001g0210 a0001c0001t0008g0074 a0001c0001t0018g0111 others(2): Show |
5 | 173 | 0.0289 | 3 | c.123 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6811116 | T | TTAC | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(20): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0018others(7): Show | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0026 others(20): Show |
23 | 246 | 0.0935 | 3 | c.123 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841180 | C | CTCT | intron_variant | MODIFIER | HG00735.hp1 HG01099.hp2 HG01106.hp1 others(4): Show |
a0001a0010 | a0001c0001a0001c0019a0010c0014 | a0001c0001t0001a0001c0019t0021a0010c0014t0001 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | 203 | 0.0345 | 3 | c.543 others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6841190 | T | TCTC | intron_variant | MODIFIER | HG02280.hp2 HG02559.hp1 HG02818.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0018a0002c0002t0004 | a0001c0001t0018g0111 a0002c0002t0004g0006 a0002c0002t0004g0147 |
3 | 237 | 0.0127 | 3 | c.543 others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar |