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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARFGEF3_chr6_138156939_138349663 | 138156999 | G | GCTGAGA | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0004a0001c0005others(33): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(69): Show | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0070 others(120): Show |
124 | 188 | 0.6596 | 6 | c.-50 others(17): Show |
ARFGEF3 | ENSG00000112379.9 | transcript | ENST00000251691.5 | protein_coding | 4939 | chr6 | TogoVar | |||||||
ARFGEF3_chr6_138156939_138349663 | 138270427 | G | GACACAC | intron_variant | MODIFIER | HG01109.hp1 HG02027.hp1 HG02818.hp1 others(7): Show |
a0001a0002a0005others(1): Show | a0001c0005a0002c0002a0002c0003others(5): Show | a0001c0005t0007a0002c0002t0001a0002c0002t0017others(6): Show | a0001c0005t0007g0092 a0002c0002t0001g0011 a0002c0002t0017g0016 others(7): Show |
10 | 42 | 0.2381 | 6 | c.212 others(25): Show |
ARFGEF3 | ENSG00000112379.9 | transcript | ENST00000251691.5 | protein_coding | 12/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARFGEF3_chr6_138156939_138349663 | 138349084 | G | GTCCACT | downstream_gene_variant | MODIFIER | HG02258.hp1 HG02622.hp1 HG03579.hp1 others(1): Show |
a0001a0002 | a0001c0005a0002c0003a0002c0011 | a0001c0005t0023a0002c0003t0023a0002c0003t0048others(1): Show | a0001c0005t0023g0186 a0002c0003t0023g0155 a0002c0003t0048g0160 others(1): Show |
4 | 188 | 0.0213 | 6 | c.*12 others(19): Show |
ARFGEF3 | ENSG00000112379.9 | transcript | ENST00000251691.5 | protein_coding | 4422 | chr6 | TogoVar | |||||||
ARFIP1_chr4_152774954_152917357 | 152782223 | G | GGTGTGT | intron_variant | MODIFIER | HG02615.hp2 HG02723.hp1 HG02886.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004 | a0001c0001t0002g0180 a0001c0001t0002g0187 a0001c0001t0003g0050 others(11): Show |
14 | 48 | 0.2917 | 6 | c.-10 others(23): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152804366 | T | TATTTTA | intron_variant | MODIFIER | HG01243.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0002 | a0001c0001t0004g0174 a0001c0001t0004g0175 a0001c0001t0004g0176 others(8): Show |
11 | 340 | 0.0324 | 6 | c.-10 others(25): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | chr4 | TogoVar | |||||||
ARFIP1_chr4_152774954_152917357 | 152808283 | A | ATTTTTT | intron_variant | MODIFIER | HG01192.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0013 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0094 others(3): Show |
6 | 10 | 0.6000 | 6 | c.-9- others(23): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152889498 | C | CATATAT | intron_variant | MODIFIER | HG00408.hp2 HG00735.hp1 HG01070.hp1 others(32): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0016 others(32): Show |
35 | 239 | 0.1464 | 6 | c.966 others(23): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152908891 | A | AGTGTGT | intron_variant | MODIFIER | HG02027.hp1 HG02129.hp1 HG02257.hp1 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0002g0016 others(17): Show |
20 | 52 | 0.3846 | 6 | c.967 others(23): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARFRP1_chr20_63693647_63712976 | 63693654 | A | ACCACCT | downstream_gene_variant | MODIFIER | HG01168.hp2 HG01175.hp2 HG02717.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
5 | 251 | 0.0199 | 6 | c.*67 others(17): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4992 | chr20 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63693699 | A | ACCACCT | downstream_gene_variant | MODIFIER | HG01109.hp2 HG01516.hp2 HG02165.hp2 others(6): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0010 | a0001c0002t0002g0001 a0001c0002t0002g0011 a0001c0002t0002g0068 others(1): Show |
9 | 197 | 0.0457 | 6 | c.*67 others(17): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4947 | chr20 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63693708 | A | ACCACCT | downstream_gene_variant | MODIFIER | NA18951.hp1 NA19000.hp1 NA19057.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 | 3 | 226 | 0.0133 | 6 | c.*67 others(17): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4938 | chr20 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63693726 | A | ACCACCT | downstream_gene_variant | MODIFIER | HG02109.hp2 HG03209.hp2 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0019 a0001c0001t0005g0076 |
3 | 279 | 0.0108 | 6 | c.*67 others(17): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4920 | chr20 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63693732 | T | TCCACCA | downstream_gene_variant | MODIFIER | NA18951.hp1 NA19000.hp1 NA19057.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 | 3 | 101 | 0.0297 | 6 | c.*67 others(17): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4914 | chr20 | TogoVar | |||||||
ARG1_chr6_131568226_131589329 | 131578782 | G | GAGAGAC | intron_variant | MODIFIER | HG03486.hp2 NA18906.hp1 NA19043.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039 a0001c0001t0001g0082 |
3 | 418 | 0.0072 | 6 | c.131 others(21): Show |
ARG1 | ENSG00000118520.16 | transcript | ENST00000368087.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARG1_chr6_131568226_131589329 | 131584363 | A | AACACAC | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(32): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(13): Show |
35 | 321 | 0.1090 | 6 | c.*45 others(15): Show |
ARG1 | ENSG00000118520.16 | transcript | ENST00000368087.8 | protein_coding | 35 | chr6 | TogoVar | |||||||
ARG1_chr6_131568226_131589329 | 131584816 | T | TACACAC | downstream_gene_variant | MODIFIER | HG02698.hp1 HG03831.hp1 HG03834.hp2 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0001 | 4 | 187 | 0.0214 | 6 | c.*90 others(15): Show |
ARG1 | ENSG00000118520.16 | transcript | ENST00000368087.8 | protein_coding | 488 | chr6 | TogoVar | |||||||
ARG2_chr14_67614920_67656708 | 67627256 | G | GATATAT | intron_variant | MODIFIER | HG01081.hp1 HG01106.hp1 HG01257.hp1 others(13): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0030 a0001c0001t0001g0101 a0001c0001t0001g0102 others(12): Show |
16 | 49 | 0.3265 | 6 | c.184 others(23): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARG2_chr14_67614920_67656708 | 67642793 | C | CTTTTTT | intron_variant | MODIFIER | HG00597.hp2 HG00621.hp1 HG00642.hp2 others(42): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(30): Show |
45 | 76 | 0.5921 | 6 | c.362 others(21): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121571553 | A | ATATTAT | intron_variant | MODIFIER | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(27): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0002a0001c0001t0005a0001c0001t0030others(3): Show | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0051 others(23): Show |
30 | 278 | 0.1079 | 6 | c.103 others(21): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121576707 | T | TTCTTTC | intron_variant | MODIFIER | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0002a0003c0003t0008 | a0001c0001t0002g0052 a0003c0003t0008g0325 a0003c0003t0008g0326 others(2): Show |
5 | 133 | 0.0376 | 6 | c.104 others(19): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121577226 | C | CATATAT | intron_variant | MODIFIER | HG00738.hp2 HG01175.hp1 HG01175.hp2 others(8): Show |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0001a0001c0001t0006a0001c0001t0026others(3): Show | a0001c0001t0001g0023 a0001c0001t0001g0243 a0001c0001t0001g0246 others(7): Show |
11 | 355 | 0.0310 | 6 | c.220 others(21): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121577259 | A | ATATATT | intron_variant | MODIFIER | HG02056.hp2 HG02155.hp2 HG02647.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(1): Show | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(4): Show |
7 | 194 | 0.0361 | 6 | c.220 others(21): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121580567 | A | AGTGTGT | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(81): Show |
a0001a0003a0004others(2): Show | a0001c0001a0003c0003a0004c0004others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(13): Show | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0012 others(73): Show |
84 | 316 | 0.2658 | 6 | c.220 others(23): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121580606 | A | ATTTTTT | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(73): Show |
a0001a0004a0006others(2): Show | a0001c0001a0004c0004a0006c0010others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(12): Show | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0012 others(66): Show |
76 | 318 | 0.2390 | 6 | c.220 others(23): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147736120 | C | CTGTGTG | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG01891.hp2 others(15): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0034 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | 50 | 0.3600 | 6 | c.154 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147736150 | G | GTGTGTC | intron_variant | MODIFIER | HG03225.hp2 NA18522.hp1 |
a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0007 a0001c0009t0001g0008 |
2 | 98 | 0.0204 | 6 | c.154 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147783767 | T | TGTATTG | intron_variant | MODIFIER | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(3): Show | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0047 others(11): Show |
14 | 104 | 0.1346 | 6 | c.155 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147798777 | C | CTATATA | intron_variant | MODIFIER | HG01884.hp1 HG02145.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061 a0001c0001t0001g0088 |
2 | 82 | 0.0244 | 6 | c.155 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147837643 | G | GTTTTTT | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(1): Show | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0024 others(24): Show |
27 | 75 | 0.3600 | 6 | c.313 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147869996 | G | GTTTTTT | intron_variant | MODIFIER | HG01261.hp1 HG02056.hp2 HG02080.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0035 others(3): Show |
6 | 67 | 0.0896 | 6 | c.702 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147870928 | C | CTGTGTG | intron_variant | MODIFIER | HG02080.hp2 HG02818.hp1 HG03492.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0002t0001 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0003g0087 others(1): Show |
4 | 16 | 0.2500 | 6 | c.703 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147900819 | T | TCAACAA | intron_variant | MODIFIER | HG01243.hp1 HG02056.hp1 NA18522.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0081 |
3 | 78 | 0.0385 | 6 | c.103 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147911993 | A | ATATATG | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG02056.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0013 a0001c0001t0001g0033 a0001c0001t0001g0042 others(7): Show |
10 | 89 | 0.1124 | 6 | c.116 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147918133 | A | ATTTTTT | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(24): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(24): Show |
27 | 69 | 0.3913 | 6 | c.122 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148017652 | C | CTATATA | intron_variant | MODIFIER | HG00558.hp1 HG02976.hp1 NA18612.hp1 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0002c0003t0001g0073 |
3 | 56 | 0.0536 | 6 | c.171 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148017680 | A | ATATGAG | intron_variant | MODIFIER | HG02258.hp1 NA18522.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0076 a0001c0001t0001g0081 |
2 | 67 | 0.0299 | 6 | c.171 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148036066 | C | CTGTGTG | intron_variant | MODIFIER | HG01071.hp2 HG02055.hp2 HG02258.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0006others(1): Show | a0001c0001t0001a0001c0004t0001a0001c0006t0001others(1): Show | a0001c0001t0001g0027 a0001c0001t0001g0095 a0001c0004t0001g0045 others(3): Show |
6 | 46 | 0.1304 | 6 | c.186 others(27): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148043614 | A | AATATAT | intron_variant | MODIFIER | HG01169.hp2 HG02976.hp2 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0034 a0002c0003t0001g0009 |
2 | 11 | 0.1818 | 6 | c.186 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148065979 | C | CAAAAAA | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(7): Show |
a0001a0003 | a0001c0001a0001c0011a0003c0007 | a0001c0001t0001a0001c0011t0001a0003c0007t0001 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0076 others(7): Show |
10 | 40 | 0.2500 | 6 | c.227 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32629941 | A | AGTGTGT | intron_variant | MODIFIER | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(26): Show |
a0001a0007 | a0001c0001a0001c0002a0007c0009 | a0001c0001t0001a0001c0001t0003a0001c0001t0019others(2): Show | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0087 others(15): Show |
29 | 149 | 0.1946 | 6 | c.110 others(23): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30639971 | A | AGTGTGT | downstream_gene_variant | MODIFIER | HG01517.hp2 HG02083.hp2 HG02129.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(5): Show |
9 | 75 | 0.1200 | 6 | c.*12 others(17): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1162 | chr15 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31805648 | T | TCACACA | 3_prime_UTR_variant | MODIFIER | HG00280.hp1 HG00741.hp1 HG01106.hp1 others(23): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0009a0001c0001t0024others(2): Show | a0001c0001t0006g0148 a0001c0001t0006g0151 a0001c0001t0006g0156 others(23): Show |
26 | 55 | 0.4727 | 6 | c.*20 others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31816168 | C | CGTGTGT | intron_variant | MODIFIER | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(28): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0007others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(10): Show | a0001c0001t0001g0117 a0001c0001t0001g0133 a0001c0001t0001g0140 others(28): Show |
31 | 72 | 0.4306 | 6 | c.173 others(25): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31918315 | T | TCACACA | intron_variant | MODIFIER | HG00544.hp2 HG00621.hp2 HG01358.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0008a0001c0001t0012others(2): Show | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0120 others(6): Show |
9 | 68 | 0.1324 | 6 | c.-11 others(25): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31923132 | G | GAAAAAA | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(9): Show | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0216 others(23): Show |
26 | 164 | 0.1585 | 6 | c.-11 others(25): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31933207 | C | CATATAT | upstream_gene_variant | MODIFIER | HG00544.hp2 HG01358.hp1 HG02273.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0109 others(4): Show |
7 | 101 | 0.0693 | 6 | c.-46 others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4377 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31933240 | A | ATATATC | upstream_gene_variant | MODIFIER | HG01891.hp2 HG02572.hp2 HG02965.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(1): Show | a0001c0001t0004g0025 a0001c0001t0005g0045 a0001c0001t0011g0055 others(2): Show |
5 | 277 | 0.0181 | 6 | c.-46 others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4410 | chr10 | TogoVar | |||||||
ARHGAP15_chr2_143124419_143773352 | 143153777 | A | ATCTTCT | intron_variant | MODIFIER | HG01358.hp2 HG03491.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0147 a0001c0001t0001g0151 |
2 | 124 | 0.0161 | 6 | c.-14 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143153840 | T | TTCCTCC | intron_variant | MODIFIER | HG00609.hp1 HG00741.hp1 HG02145.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0002t0001g0093 |
3 | 73 | 0.0411 | 6 | c.-14 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143153843 | T | TTCCTCC | intron_variant | MODIFIER | HG01243.hp2 HG01255.hp1 HG02523.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0038 others(3): Show |
6 | 43 | 0.1395 | 6 | c.-14 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |