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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARFRP1_chr20_63693647_63712976 | 63693705 | T | TCCA | downstream_gene_variant | MODIFIER | HG02896.hp1 HG02970.hp1 HG06807.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0004a0001c0001t0006a0001c0003t0004 | a0001c0001t0004g0092 a0001c0001t0006g0020 a0001c0003t0004g0014 |
3 | 258 | 0.0116 | 3 | c.*67 others(14): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4941 | chr20 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63693723 | A | ACCT | downstream_gene_variant | MODIFIER | HG01258.hp2 HG02132.hp1 HG02602.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 |
3 | 219 | 0.0137 | 3 | c.*67 others(14): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4923 | chr20 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63693732 | T | TCCA | downstream_gene_variant | MODIFIER | HG02622.hp1 HG03654.hp1 HG03669.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(3): Show |
6 | 104 | 0.0577 | 3 | c.*67 others(14): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4914 | chr20 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63701998 | G | GCCC | intron_variant | MODIFIER | HG00544.hp2 HG00741.hp1 HG01099.hp2 others(33): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0018others(1): Show | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0026 others(10): Show |
36 | 50 | 0.7200 | 3 | c.347 others(17): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 5/7 | chr20 | TogoVar | |||||||
ARG2_chr14_67614920_67656708 | 67623534 | C | CTTT | intron_variant | MODIFIER | HG01175.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(8): Show |
11 | 76 | 0.1447 | 3 | c.184 others(20): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARG2_chr14_67614920_67656708 | 67625680 | C | CAAA | intron_variant | MODIFIER | HG01175.hp1 HG02145.hp2 HG02622.hp2 others(19): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0003g0177 others(19): Show |
22 | 382 | 0.0576 | 3 | c.184 others(20): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARG2_chr14_67614920_67656708 | 67631430 | C | CTTT | intron_variant | MODIFIER | HG00609.hp1 HG02080.hp1 HG02109.hp2 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0354 a0001c0001t0002g0002 a0001c0001t0002g0018 others(10): Show |
21 | 363 | 0.0579 | 3 | c.184 others(22): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARG2_chr14_67614920_67656708 | 67632808 | A | ATTT | intron_variant | MODIFIER | HG00639.hp1 HG00735.hp1 HG01106.hp1 others(12): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0001c0001t0002a0003c0004t0001 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0106 others(10): Show |
15 | 107 | 0.1402 | 3 | c.185 others(20): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARG2_chr14_67614920_67656708 | 67637410 | C | CAAA | intron_variant | MODIFIER | HG00423.hp1 HG00597.hp2 HG01256.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0296 a0001c0001t0001g0301 a0001c0001t0001g0308 others(6): Show |
9 | 114 | 0.0789 | 3 | c.185 others(20): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARG2_chr14_67614920_67656708 | 67642793 | C | CTTT | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(93): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0120 a0001c0001t0001g0230 a0001c0001t0002g0007 others(74): Show |
96 | 127 | 0.7559 | 3 | c.362 others(18): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARG2_chr14_67614920_67656708 | 67643852 | T | TAAA | intron_variant | MODIFIER | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(22): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0004a0002c0002t0002 | a0001c0001t0002g0007 a0001c0001t0002g0026 a0001c0001t0002g0027 others(17): Show |
25 | 45 | 0.5556 | 3 | c.362 others(20): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARG2_chr14_67614920_67656708 | 67655028 | C | CAAA | downstream_gene_variant | MODIFIER | HG00639.hp1 HG00735.hp1 HG01074.hp1 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0061 others(15): Show |
20 | 187 | 0.1070 | 3 | c.*41 others(14): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3321 | chr14 | TogoVar | |||||||
ARGFX_chr3_121562949_121595622 | 121563903 | A | AAAT | upstream_gene_variant | MODIFIER | HG01106.hp1 HG03471.hp1 NA18971.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0007a0001c0001t0033 | a0001c0001t0004g0313 a0001c0001t0007g0259 a0001c0001t0033g0009 |
3 | 19 | 0.1579 | 3 | c.-41 others(14): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 4045 | chr3 | TogoVar | |||||||
ARGFX_chr3_121562949_121595622 | 121571553 | A | ATAT | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(124): Show |
a0001a0007a0008 | a0001c0001a0007c0007a0008c0011 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(15): Show | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
127 | 375 | 0.3387 | 3 | c.103 others(18): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121576707 | T | TTTC | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(6): Show | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0010 others(42): Show |
48 | 176 | 0.2727 | 3 | c.104 others(16): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121577257 | A | ATTT | intron_variant | MODIFIER | HG02622.hp2 HG03209.hp2 HG03453.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005 | a0001c0001t0002g0076 a0001c0001t0002g0129 a0001c0001t0005g0128 |
3 | 361 | 0.0083 | 3 | c.220 others(18): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121577259 | A | ATTT | intron_variant | MODIFIER | HG01891.hp2 HG02165.hp1 HG03654.hp2 others(5): Show |
a0001a0004a0007 | a0001c0001a0004c0004a0007c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0266 a0001c0001t0002g0001 a0001c0001t0002g0012 others(5): Show |
8 | 195 | 0.0410 | 3 | c.220 others(18): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121577260 | T | TATA | intron_variant | MODIFIER | HG02486.hp2 NA18968.hp2 NA18982.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(1): Show | a0001c0001t0001g0248 a0001c0001t0002g0016 a0001c0001t0002g0141 others(2): Show |
6 | 388 | 0.0155 | 3 | c.220 others(18): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | chr3 | TogoVar | |||||||
ARGFX_chr3_121562949_121595622 | 121579945 | C | CTTT | intron_variant | MODIFIER | HG00735.hp2 HG01109.hp2 HG02145.hp2 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(3): Show | a0001c0001t0001g0023 a0001c0001t0001g0253 a0001c0001t0001g0265 others(16): Show |
20 | 275 | 0.0727 | 3 | c.220 others(20): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121580607 | T | TATA | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(10): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0362 a0002c0002t0001g0166 a0002c0002t0001g0167 others(10): Show |
13 | 381 | 0.0341 | 3 | c.220 others(20): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | chr3 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106541495 | C | CAAA | downstream_gene_variant | MODIFIER | HG00544.hp2 HG01928.hp2 HG02129.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0021 others(11): Show |
14 | 106 | 0.1321 | 3 | c.*25 others(14): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 177 | chr13 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106544554 | G | GATC | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(110): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(7): Show | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(68): Show |
113 | 374 | 0.3021 | 3 | c.658 others(18): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 3/3 | chr13 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147730885 | C | CTTT | upstream_gene_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG02258.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(1): Show | a0001c0001t0001g0040 a0001c0001t0001g0080 a0001c0001t0001g0084 others(7): Show |
10 | 39 | 0.2564 | 3 | c.-14 others(14): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1202 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147742476 | C | CTTT | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0023 a0001c0001t0001g0091 a0001c0001t0001g0099 others(3): Show |
6 | 35 | 0.1714 | 3 | c.154 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147762536 | A | ATTT | intron_variant | MODIFIER | HG03098.hp1 HG03471.hp1 NA19012.hp2 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0008t0001 | a0001c0001t0001g0070 a0001c0008t0001g0059 a0001c0008t0001g0060 |
3 | 103 | 0.0291 | 3 | c.154 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147765337 | T | TGTG | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp1 HG01167.hp1 others(31): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(5): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(31): Show |
34 | 73 | 0.4658 | 3 | c.154 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147765338 | G | GTGT | intron_variant | MODIFIER | HG00558.hp2 HG01071.hp2 HG01167.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0002t0001a0001c0009t0001 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(12): Show |
15 | 98 | 0.1531 | 3 | c.154 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147784746 | T | TATA | intron_variant | MODIFIER | HG00558.hp2 HG01070.hp1 HG01167.hp1 others(21): Show |
a0001 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(3): Show | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0023 others(21): Show |
24 | 102 | 0.2353 | 3 | c.155 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147784748 | T | TAAA | intron_variant | MODIFIER | HG02145.hp1 HG02615.hp1 HG02738.hp2 others(1): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(1): Show | a0001c0001t0001g0097 a0001c0002t0001g0078 a0001c0005t0001g0098 others(1): Show |
4 | 104 | 0.0385 | 3 | c.155 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147785083 | T | TAAA | intron_variant | MODIFIER | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(22): Show |
a0001 | a0001c0001a0001c0002a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(22): Show |
25 | 62 | 0.4032 | 3 | c.155 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147793321 | T | TATA | intron_variant | MODIFIER | HG01884.hp2 HG02451.hp2 |
a0001 | a0001c0002a0001c0011 | a0001c0002t0001a0001c0011t0001 | a0001c0002t0001g0090 a0001c0011t0001g0092 |
2 | 101 | 0.0198 | 3 | c.155 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147869998 | T | TTTG | intron_variant | MODIFIER | HG03098.hp1 HG03516.hp2 |
a0001 | a0001c0005a0001c0008 | a0001c0005t0001a0001c0008t0001 | a0001c0005t0001g0003 a0001c0008t0001g0060 |
2 | 65 | 0.0308 | 3 | c.702 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147872099 | C | CAAA | intron_variant | MODIFIER | HG02572.hp2 HG02886.hp1 HG03471.hp2 others(1): Show |
a0001 | a0001c0001a0001c0004a0001c0005 | a0001c0001t0001a0001c0004t0001a0001c0005t0001 | a0001c0001t0001g0081 a0001c0004t0001g0045 a0001c0004t0001g0105 others(1): Show |
4 | 45 | 0.0889 | 3 | c.703 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147877819 | C | CTTT | intron_variant | MODIFIER | HG01261.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
a0001 | a0001c0001a0001c0006a0001c0011 | a0001c0001t0001a0001c0006t0001a0001c0011t0001 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0006t0001g0039 others(2): Show |
5 | 47 | 0.1064 | 3 | c.833 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147882462 | C | CAAA | intron_variant | MODIFIER | HG01261.hp1 HG02056.hp2 HG02080.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(2): Show | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0035 others(8): Show |
11 | 34 | 0.3235 | 3 | c.103 others(20): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147898187 | T | TTGA | intron_variant | MODIFIER | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(44): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(44): Show |
47 | 104 | 0.4519 | 3 | c.103 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147900819 | T | TCAA | intron_variant | MODIFIER | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(23): Show |
26 | 101 | 0.2574 | 3 | c.103 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147922687 | C | CAAA | intron_variant | MODIFIER | HG00558.hp1 HG02165.hp2 HG02258.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0001a0001c0002t0001a0001c0006t0001 | a0001c0001t0001g0024 a0001c0002t0001g0020 a0001c0006t0001g0039 others(1): Show |
4 | 35 | 0.1143 | 3 | c.122 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148012924 | G | GTTT | intron_variant | MODIFIER | HG00558.hp2 HG01169.hp1 HG01261.hp1 others(13): Show |
a0001a0002a0003 | a0001c0001a0001c0011a0002c0003others(1): Show | a0001c0001t0001a0001c0011t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0052 others(13): Show |
16 | 78 | 0.2051 | 3 | c.171 others(24): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148052392 | C | CTTT | intron_variant | MODIFIER | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
a0001a0002a0004 | a0001c0001a0002c0003a0004c0010 | a0001c0001t0001a0001c0001t0003a0002c0003t0001others(1): Show | a0001c0001t0001g0069 a0001c0001t0001g0091 a0001c0001t0001g0094 others(3): Show |
6 | 39 | 0.1538 | 3 | c.202 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148065979 | C | CAAA | intron_variant | MODIFIER | HG02738.hp2 HG03239.hp1 HG03471.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0070 a0001c0001t0002g0030 a0001c0002t0001g0072 others(2): Show |
5 | 35 | 0.1429 | 3 | c.227 others(22): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32613813 | C | CAAA | upstream_gene_variant | MODIFIER | HG00642.hp1 HG01169.hp2 HG01975.hp2 others(7): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0098 others(6): Show |
10 | 143 | 0.0699 | 3 | c.-23 others(14): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1690 | chr15 | TogoVar | |||||||
ARHGAP11A_chr15_32610504_32644941 | 32617471 | C | CTTT | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(7): Show |
a0001a0007 | a0001c0001a0001c0002a0007c0009 | a0001c0001t0004a0001c0002t0005a0007c0009t0005 | a0001c0001t0004g0185 a0001c0001t0004g0186 a0001c0002t0005g0020 others(6): Show |
10 | 223 | 0.0448 | 3 | c.129 others(20): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32640121 | C | CTTT | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00558.hp1 HG02451.hp2 others(14): Show |
a0001a0004a0006 | a0001c0001a0001c0006a0004c0013others(1): Show | a0001c0001t0001a0001c0001t0009a0001c0001t0014others(3): Show | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0160 others(9): Show |
17 | 205 | 0.0829 | 3 | c.*22 others(14): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 181 | chr15 | TogoVar | |||||||
ARHGAP11A_chr15_32610504_32644941 | 32640123 | T | TTTC | downstream_gene_variant | MODIFIER | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
a0001a0007 | a0001c0001a0001c0002a0007c0009 | a0001c0001t0001a0001c0002t0005a0007c0009t0005 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0044 others(6): Show |
13 | 334 | 0.0389 | 3 | c.*22 others(14): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 183 | chr15 | TogoVar | |||||||
ARHGAP11B_chr15_30621128_30643810 | 30624418 | C | CAAA | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(16): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(11): Show |
19 | 92 | 0.2065 | 3 | c.-24 others(14): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1709 | chr15 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31804673 | C | CTTT | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(108): Show |
a0001a0002 | a0001c0001a0001c0007a0001c0010others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(20): Show | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(108): Show |
111 | 152 | 0.7303 | 3 | c.*29 others(14): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 724 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31823476 | C | CAAA | intron_variant | MODIFIER | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(11): Show |
a0001 | a0001c0003a0001c0005 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(2): Show | a0001c0003t0010g0006 a0001c0003t0010g0010 a0001c0003t0010g0011 others(11): Show |
14 | 315 | 0.0444 | 3 | c.153 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31829154 | A | AAAC | intron_variant | MODIFIER | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(101): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0004 | a0001c0001t0003a0001c0001t0009a0001c0001t0017others(18): Show | a0001c0001t0003g0118 a0001c0001t0003g0180 a0001c0001t0009g0026 others(101): Show |
104 | 319 | 0.3260 | 3 | c.144 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | TogoVar | |||||||
ARHGAP12_chr10_31800398_31933831 | 31874973 | C | CAAA | intron_variant | MODIFIER | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(36): Show |
a0002a0003 | a0002c0002a0003c0004 | a0002c0002t0002a0002c0002t0007a0002c0002t0014others(6): Show | a0002c0002t0002g0242 a0002c0002t0002g0249 a0002c0002t0002g0250 others(36): Show |
39 | 87 | 0.4483 | 3 | c.685 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar |