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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AQP8_chr16_25211947_25233932 | 25216207 | TTCTTTCT others(21): Show |
T | upstream_gene_variant | MODIFIER | HG01952.hp1 HG02273.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0027 |
2 | 413 | 0.0048 | -28 | c.-83 others(37): Show |
AQP8 | ENSG00000103375.11 | transcript | ENST00000219660.6 | protein_coding | 739 | chr16 | TogoVar | |||||||
ARAP2_chr4_36061004_36249514 | 36156419 | GAAAGAAA others(21): Show |
G | intron_variant | MODIFIER | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
a0001a0017 | a0001c0001a0017c0017 | a0001c0001t0002a0001c0001t0004a0017c0017t0002 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | 276 | 0.0109 | -28 | c.275 others(47): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | TogoVar | |||||||
ARFGEF3_chr6_138156939_138349663 | 138345448 | AAATTATA others(21): Show |
A | downstream_gene_variant | MODIFIER | HG02809.hp1 HG02818.hp2 |
a0001a0012 | a0001c0015a0012c0016 | a0001c0015t0013a0012c0016t0013 | a0001c0015t0013g0116 a0012c0016t0013g0099 |
2 | 182 | 0.0110 | -28 | c.*89 others(39): Show |
ARFGEF3 | ENSG00000112379.9 | transcript | ENST00000251691.5 | protein_coding | 786 | chr6 | TogoVar | |||||||
ARFIP1_chr4_152774954_152917357 | 152804093 | ATATATAT others(21): Show |
A | intron_variant | MODIFIER | HG04199.hp1 NA18906.hp2 NA20129.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0295 a0001c0001t0004g0331 a0001c0001t0004g0332 |
3 | 237 | 0.0127 | -28 | c.-10 others(47): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152804338 | ATATATAT others(21): Show |
A | intron_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0035 | 1 | 237 | 0.0042 | -28 | c.-10 others(47): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147741767 | TACACACA others(21): Show |
T | intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0093 | 1 | 101 | 0.0099 | -28 | c.154 others(45): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147783753 | AACACATT others(21): Show |
A | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG02258.hp2 others(12): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(1): Show | a0001c0001t0001a0001c0005t0001a0001c0006t0001others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(12): Show |
15 | 100 | 0.1500 | -28 | c.155 others(47): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147798765 | CTCTCTCT others(21): Show |
C | intron_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0072 | 1 | 94 | 0.0106 | -28 | c.155 others(47): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31862696 | GCACACAC others(21): Show |
G | intron_variant | MODIFIER | NA18993.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0145 | 1 | 251 | 0.0040 | -28 | c.685 others(45): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143379402 | AATTCATA others(21): Show |
A | intron_variant | MODIFIER | HG02129.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0084 | 1 | 160 | 0.0063 | -28 | c.475 others(47): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143679657 | GTGTGTGT others(21): Show |
G | intron_variant | MODIFIER | HG00621.hp1 NA18966.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0087 a0001c0001t0001g0139 |
2 | 160 | 0.0125 | -28 | c.113 others(49): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97218927 | GTGTGTGT others(21): Show |
G | downstream_gene_variant | MODIFIER | HG03490.hp2 HG03492.hp2 HG04184.hp1 |
a0002 | a0002c0004 | a0002c0004t0002 | a0002c0004t0002g0148 a0002c0004t0002g0151 a0002c0004t0002g0176 |
3 | 223 | 0.0135 | -28 | c.*71 others(39): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3251 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97218939 | GTGTATAT others(21): Show |
G | downstream_gene_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0129 | 1 | 234 | 0.0043 | -28 | c.*71 others(39): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3239 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97258749 | GAGACCCT others(21): Show |
G | intron_variant | MODIFIER | HG01346.hp1 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0136 | 1 | 240 | 0.0042 | -28 | c.840 others(43): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24622433 | CATATATA others(21): Show |
C | intron_variant | MODIFIER | HG02280.hp1 HG02486.hp1 NA19056.hp2 |
a0001a0006 | a0001c0001a0006c0007 | a0001c0001t0001a0006c0007t0006 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0006c0007t0006g0293 |
3 | 16 | 0.1875 | -28 | c.525 others(43): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48473516 | ATGAGGAC others(21): Show |
A | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
a0001a0003a0005others(5): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0058 others(99): Show |
103 | 268 | 0.3843 | -28 | c.451 others(45): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 4/9 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48473541 | ACGCTGAG others(21): Show |
A | intron_variant | MODIFIER | NA18945.hp1 NA18950.hp1 NA18979.hp2 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(2): Show |
5 | 131 | 0.0382 | -28 | c.451 others(45): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 4/9 | chr10 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85487463 | CATATATT others(21): Show |
C | intron_variant | MODIFIER | HG01167.hp2 HG01243.hp1 HG02145.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0006 | a0001c0001t0005a0001c0002t0007a0001c0002t0016others(1): Show | a0001c0001t0005g0074 a0001c0001t0005g0101 a0001c0002t0007g0056 others(2): Show |
5 | 72 | 0.0694 | -28 | c.-21 others(47): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85564924 | GTATATAT others(21): Show |
G | intron_variant | MODIFIER | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
a0001a0002 | a0001c0002a0001c0003a0001c0004others(2): Show | a0001c0002t0002a0001c0003t0011a0001c0004t0004others(3): Show | a0001c0002t0002g0060 a0001c0002t0002g0096 a0001c0003t0011g0095 others(4): Show |
7 | 34 | 0.2059 | -28 | c.-20 others(45): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85570364 | CTCTTTCT others(21): Show |
C | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(44): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(14): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(44): Show |
47 | 52 | 0.9038 | -28 | c.-20 others(43): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85669644 | AATATATA others(21): Show |
A | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(26): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0008others(7): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(26): Show |
29 | 49 | 0.5918 | -28 | c.181 others(47): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85874758 | TTATATAA others(21): Show |
T | intron_variant | MODIFIER | HG01109.hp2 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 a0001c0001t0001g0030 |
2 | 108 | 0.0185 | -28 | c.269 others(47): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45432814 | GTCCCGCG others(21): Show |
G | 5_prime_UTR_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0018 | 1 | 346 | 0.0029 | -28 | c.-37 others(37): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/20 | 2536 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729546 | ACTCACAC others(21): Show |
A | upstream_gene_variant | MODIFIER | HG02630.hp2 | a0008 | a0008c0011 | a0008c0011t0005 | a0008c0011t0005g0017 | 1 | 180 | 0.0056 | -28 | c.-27 others(37): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 169 | chr18 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(21): Show |
A | intron_variant | MODIFIER | HG01243.hp2 HG01255.hp1 HG02055.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0002a0001c0001t0004a0001c0001t0020others(2): Show | a0001c0001t0002g0019 a0001c0001t0004g0102 a0001c0001t0020g0032 others(9): Show |
12 | 44 | 0.2727 | -28 | c.-18 others(49): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | CATATATA others(21): Show |
C | intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0102 | 1 | 5 | 0.2000 | -28 | c.-14 others(47): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1066453 | TTAGCTAA others(21): Show |
T | upstream_gene_variant | MODIFIER | HG02897.hp2 | a0009 | a0009c0024 | a0009c0024t0002 | a0009c0024t0002g0148 | 1 | 416 | 0.0024 | -28 | c.-95 others(37): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 713 | chr19 | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11176300 | CATATATA others(21): Show |
C | intron_variant | MODIFIER | HG01243.hp1 HG02145.hp1 HG03098.hp1 others(3): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0008a0001c0004t0005others(2): Show | a0001c0001t0001g0024 a0001c0001t0008g0049 a0001c0004t0005g0015 others(3): Show |
6 | 18 | 0.3333 | -28 | c.162 others(47): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11275267 | AGGTATGT others(21): Show |
A | intron_variant | MODIFIER | HG01261.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0083 | 1 | 144 | 0.0069 | -28 | c.589 others(47): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11520129 | TTTTATAT others(21): Show |
T | intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0005 | a0002c0005t0006 | a0002c0005t0006g0018 | 1 | 144 | 0.0069 | -28 | c.588 others(49): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590773 | CTCGAAAA others(21): Show |
C | intron_variant | MODIFIER | HG02698.hp1 NA20905.hp1 |
a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0005 a0002c0002t0003g0009 |
2 | 123 | 0.0163 | -28 | c.588 others(47): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590842 | AAAAGAAA others(21): Show |
A | intron_variant | MODIFIER | NA18948.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0053 | 1 | 127 | 0.0079 | -28 | c.588 others(47): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGEF10L_chr1_17534698_17702869 | 17683088 | AGGGTGCT others(21): Show |
A | intron_variant | MODIFIER | HG01884.hp1 HG02622.hp2 |
a0001a0012 | a0001c0044a0012c0031 | a0001c0044t0004a0012c0031t0006 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | 166 | 0.0120 | -28 | c.301 others(47): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17683173 | TGGTGCTC others(21): Show |
T | intron_variant | MODIFIER | NA18982.hp1 | a0020 | a0020c0049 | a0020c0049t0004 | a0020c0049t0004g0075 | 1 | 131 | 0.0076 | -28 | c.301 others(47): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17683312 | CGGGTGCT others(21): Show |
C | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01074.hp1 others(9): Show |
a0001a0003a0012 | a0001c0011a0001c0013a0001c0020others(4): Show | a0001c0011t0001a0001c0013t0001a0001c0020t0001others(4): Show | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(9): Show |
12 | 165 | 0.0727 | -28 | c.301 others(47): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1832371 | CAGAGACA others(21): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0001c0003others(65): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(98): Show | a0001c0001t0002g0033 a0001c0001t0002g0054 a0001c0001t0002g0069 others(135): Show |
138 | 362 | 0.3812 | -28 | c.-48 others(45): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1838614 | GAGGCTAA others(21): Show |
G | intron_variant | MODIFIER | NA19082.hp1 | a0002 | a0002c0030 | a0002c0030t0002 | a0002c0030t0002g0081 | 1 | 362 | 0.0028 | -28 | c.-47 others(45): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888731 | GGTTTGTG others(21): Show |
G | intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0003 | a0001c0003t0058 | a0001c0003t0058g0338 | 1 | 347 | 0.0029 | -28 | c.118 others(47): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889372 | GGTATGTG others(21): Show |
G | intron_variant | MODIFIER | NA18941.hp2 NA18943.hp2 NA18966.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0010 | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0002g0249 a0001c0002t0001g0248 a0001c0002t0002g0002 others(2): Show |
5 | 343 | 0.0146 | -28 | c.118 others(47): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1889904 | AACTTTGT others(21): Show |
A | intron_variant | MODIFIER | HG01496.hp1 HG02486.hp1 HG02559.hp1 others(18): Show |
a0001a0004a0022 | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0003a0001c0002t0001a0001c0003t0001others(16): Show | a0001c0001t0003g0109 a0001c0002t0001g0053 a0001c0002t0001g0071 others(18): Show |
21 | 362 | 0.0580 | -28 | c.118 others(47): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157035883 | ATATATAT others(21): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0005a0001c0011others(5): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(28): Show | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0269 others(254): Show |
265 | 295 | 0.8983 | -28 | c.32+ others(43): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120351433 | ATATATAT others(21): Show |
A | intron_variant | MODIFIER | HG03490.hp1 | a0001 | a0001c0001 | a0001c0001t0025 | a0001c0001t0025g0235 | 1 | 303 | 0.0033 | -28 | c.32+ others(45): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7442124 | CCCTTCCT others(21): Show |
C | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(83): Show |
a0001a0002a0004others(8): Show | a0001c0001a0002c0004a0004c0040others(8): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(19): Show | a0001c0001t0002g0012 a0001c0001t0002g0028 a0001c0001t0002g0033 others(83): Show |
86 | 125 | 0.6880 | -28 | c.136 others(44): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73671694 | TTATATAT others(21): Show |
T | intron_variant | MODIFIER | HG01169.hp2 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0042 | 1 | 167 | 0.0060 | -28 | c.-11 others(47): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73671716 | ATATATAT others(21): Show |
A | intron_variant | MODIFIER | HG02155.hp2 HG03831.hp2 |
a0003a0005 | a0003c0005a0005c0008 | a0003c0005t0006a0005c0008t0001 | a0003c0005t0006g0173 a0005c0008t0001g0052 |
2 | 173 | 0.0116 | -28 | c.-11 others(47): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741363 | GTGTGTGT others(21): Show |
G | intron_variant | MODIFIER | HG00738.hp1 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0076 | 1 | 184 | 0.0054 | -28 | c.34- others(43): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741379 | GTGTGTGT others(21): Show |
G | intron_variant | MODIFIER | NA18962.hp2 | a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0029 | 1 | 176 | 0.0057 | -28 | c.34- others(43): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741381 | GTGTGTAT others(21): Show |
G | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp2 HG01346.hp1 others(10): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0023a0002c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0023t0002others(7): Show | a0001c0001t0001g0028 a0001c0001t0001g0100 a0001c0001t0002g0062 others(10): Show |
13 | 167 | 0.0778 | -28 | c.34- others(43): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73741383 | GTGTATAT others(21): Show |
G | intron_variant | MODIFIER | HG01074.hp1 HG01106.hp2 HG02258.hp1 others(1): Show |
a0001a0004a0014others(1): Show | a0001c0001a0004c0060a0014c0062others(1): Show | a0001c0001t0002a0004c0060t0003a0014c0062t0007others(1): Show | a0001c0001t0002g0033 a0004c0060t0003g0147 a0014c0062t0007g0171 others(1): Show |
4 | 173 | 0.0231 | -28 | c.34- others(43): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73806422 | ACTATATA others(21): Show |
A | intron_variant | MODIFIER | HG00735.hp2 HG02615.hp1 NA20300.hp2 |
a0001a0002 | a0001c0025a0002c0003 | a0001c0025t0005a0002c0003t0001a0002c0003t0002 | a0001c0025t0005g0130 a0002c0003t0001g0166 a0002c0003t0002g0092 |
3 | 76 | 0.0395 | -28 | c.102 others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |