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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARFIP1_chr4_152774954_152917357 | 152904168 | ATGTG | A | intron_variant | MODIFIER | HG00408.hp1 HG02300.hp2 HG02717.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0002 | a0001c0001t0001g0276 a0001c0001t0001g0302 a0002c0003t0002g0040 others(3): Show |
6 | 342 | 0.0175 | -4 | c.967 others(21): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152908891 | AGTGT | A | intron_variant | MODIFIER | HG00099.hp2 HG00621.hp2 HG00741.hp1 others(37): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0084 a0001c0001t0001g0219 a0001c0001t0001g0241 others(37): Show |
40 | 342 | 0.1170 | -4 | c.967 others(21): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152914383 | TTATG | T | downstream_gene_variant | MODIFIER | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0002t0002 | a0001c0001t0002g0002 a0001c0001t0002g0191 a0001c0001t0002g0192 others(10): Show |
13 | 342 | 0.0380 | -4 | c.*41 others(15): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 2027 | chr4 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63701998 | GCCCC | G | intron_variant | MODIFIER | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(74): Show |
a0001a0002 | a0001c0002a0002c0005 | a0001c0002t0002a0001c0002t0010a0001c0002t0012others(1): Show | a0001c0002t0002g0001 a0001c0002t0002g0009 a0001c0002t0002g0021 others(17): Show |
77 | 296 | 0.2601 | -4 | c.347 others(18): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 5/7 | chr20 | TogoVar | |||||||
ARG1_chr6_131568226_131589329 | 131575888 | CTTTG | C | intron_variant | MODIFIER | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0031 others(2): Show |
12 | 420 | 0.0286 | -4 | c.58- others(17): Show |
ARG1 | ENSG00000118520.16 | transcript | ENST00000368087.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARG1_chr6_131568226_131589329 | 131584363 | AACAC | A | downstream_gene_variant | MODIFIER | HG00408.hp1 HG01069.hp2 HG02132.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(1): Show |
10 | 420 | 0.0238 | -4 | c.*45 others(13): Show |
ARG1 | ENSG00000118520.16 | transcript | ENST00000368087.8 | protein_coding | 35 | chr6 | TogoVar | |||||||
ARG1_chr6_131568226_131589329 | 131584816 | TACAC | T | downstream_gene_variant | MODIFIER | HG01168.hp2 HG01169.hp2 HG02723.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0033 |
4 | 420 | 0.0095 | -4 | c.*90 others(13): Show |
ARG1 | ENSG00000118520.16 | transcript | ENST00000368087.8 | protein_coding | 488 | chr6 | TogoVar | |||||||
ARG2_chr14_67614920_67656708 | 67623534 | CTTTT | C | intron_variant | MODIFIER | HG00609.hp1 HG02080.hp1 HG03486.hp1 others(22): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0047 a0001c0001t0001g0124 a0001c0001t0001g0125 others(16): Show |
25 | 438 | 0.0571 | -4 | c.184 others(21): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARG2_chr14_67614920_67656708 | 67627256 | GATAT | G | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(41): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0036 a0001c0001t0001g0135 a0001c0001t0001g0139 others(37): Show |
44 | 438 | 0.1005 | -4 | c.184 others(21): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121564244 | CTTTT | C | upstream_gene_variant | MODIFIER | HG00735.hp2 HG00741.hp2 HG01070.hp1 others(14): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0245 a0001c0001t0001g0250 a0001c0001t0001g0293 others(14): Show |
17 | 410 | 0.0415 | -4 | c.-37 others(15): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3704 | chr3 | TogoVar | |||||||
ARGFX_chr3_121562949_121595622 | 121565169 | TAAAC | T | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00735.hp1 HG01069.hp1 others(31): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(9): Show | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0247 others(29): Show |
34 | 410 | 0.0829 | -4 | c.-28 others(15): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2779 | chr3 | TogoVar | |||||||
ARGFX_chr3_121562949_121595622 | 121565800 | TATAC | T | upstream_gene_variant | MODIFIER | HG02280.hp2 HG02615.hp1 HG02809.hp1 others(2): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0005a0002c0002t0001others(2): Show | a0001c0001t0002g0102 a0001c0001t0005g0103 a0002c0002t0001g0166 others(2): Show |
5 | 410 | 0.0122 | -4 | c.-22 others(15): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2148 | chr3 | TogoVar | |||||||
ARGFX_chr3_121562949_121595622 | 121571730 | ATTTT | A | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(140): Show |
a0001a0004a0006others(3): Show | a0001c0001a0004c0004a0006c0011others(3): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(17): Show | a0001c0001t0002g0006 a0001c0001t0002g0029 a0001c0001t0002g0035 others(137): Show |
143 | 410 | 0.3488 | -4 | c.103 others(19): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121576707 | TTTTC | T | intron_variant | MODIFIER | HG00544.hp2 HG00735.hp1 HG01106.hp2 others(62): Show |
a0001a0002a0005others(3): Show | a0001c0001a0002c0002a0005c0005others(3): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(13): Show | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0022 others(61): Show |
65 | 410 | 0.1585 | -4 | c.104 others(17): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121577141 | CATAA | C | intron_variant | MODIFIER | NA18939.hp1 NA18954.hp2 NA18973.hp1 others(5): Show |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0001a0001c0001t0006a0006c0006t0006 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0280 others(5): Show |
8 | 410 | 0.0195 | -4 | c.220 others(19): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121578120 | CTTTT | C | intron_variant | MODIFIER | NA18946.hp2 NA18962.hp1 NA18973.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0032 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0099 others(3): Show |
6 | 410 | 0.0146 | -4 | 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 | 121579627 | AACAG | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(46): Show |
a0001a0002a0012 | a0001c0001a0002c0002a0012c0009 | a0001c0001t0001a0002c0002t0001a0002c0002t0006others(5): Show | a0001c0001t0001g0189 a0002c0002t0001g0002 a0002c0002t0001g0009 others(44): Show |
49 | 410 | 0.1195 | -4 | 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 | 121584204 | GAGGA | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(65): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | a0001c0001t0001g0011 a0001c0001t0001g0237 a0001c0001t0001g0239 others(64): Show |
68 | 410 | 0.1659 | -4 | c.221 others(19): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARGLU1_chr13_106536673_106573137 | 106539240 | CTATT | C | downstream_gene_variant | MODIFIER | HG04204.hp1 HG04228.hp2 NA20129.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015 a0001c0001t0001g0068 |
3 | 376 | 0.0080 | -4 | c.*47 others(15): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 2432 | chr13 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106540792 | CTGGA | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(49): Show |
91 | 376 | 0.2420 | -4 | c.*32 others(15): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 880 | chr13 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106546585 | TAATA | T | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010 | a0001c0001t0002g0022 a0001c0001t0002g0032 a0001c0001t0002g0105 others(3): Show |
9 | 376 | 0.0239 | -4 | c.658 others(21): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 3/3 | chr13 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106561424 | TACAC | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(81): Show |
170 | 376 | 0.4521 | -4 | c.348 others(21): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 1/3 | chr13 | TogoVar | |||||||
ARGLU1_chr13_106536673_106573137 | 106569333 | ATAAT | A | upstream_gene_variant | MODIFIER | HG01884.hp1 HG03130.hp2 NA20300.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002 a0001c0001t0002g0029 a0001c0001t0002g0083 |
4 | 376 | 0.0106 | -4 | c.-14 others(15): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 1197 | chr13 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147741788 | ACACG | A | intron_variant | MODIFIER | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
a0001a0003 | a0001c0001a0001c0004a0003c0007 | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(1): Show | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(12): Show |
15 | 106 | 0.1415 | -4 | c.154 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147766799 | CATAT | C | intron_variant | MODIFIER | HG02280.hp2 HG02886.hp1 NA18522.hp2 others(1): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0005t0001a0001c0006t0001 | a0001c0001t0001g0081 a0001c0001t0001g0094 a0001c0005t0001g0074 others(1): Show |
4 | 106 | 0.0377 | -4 | 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 | 147766836 | ATATT | A | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | 106 | 0.0377 | -4 | 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 | 147768587 | ATAAT | A | intron_variant | MODIFIER | HG02145.hp1 HG02615.hp1 HG03225.hp1 |
a0001a0002 | a0001c0001a0001c0005a0002c0003 | a0001c0001t0001a0001c0005t0001a0002c0003t0001 | a0001c0001t0001g0097 a0001c0005t0001g0098 a0002c0003t0001g0096 |
3 | 106 | 0.0283 | -4 | 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 | 147783792 | TTATG | T | intron_variant | MODIFIER | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(2): Show | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0047 others(10): Show |
13 | 106 | 0.1226 | -4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147783824 | TTGTG | T | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG02080.hp1 others(24): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(24): Show |
27 | 106 | 0.2547 | -4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147783888 | TTGTG | T | intron_variant | MODIFIER | HG02572.hp1 HG02895.hp1 HG03209.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0002t0001a0001c0009t0001 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0002t0001g0005 others(1): Show |
4 | 106 | 0.0377 | -4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147791569 | TTTTG | T | intron_variant | MODIFIER | HG02896.hp1 NA18522.hp1 |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0009t0001 | a0001c0001t0001g0002 a0001c0009t0001g0007 |
2 | 106 | 0.0189 | -4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147798722 | ACACT | A | intron_variant | MODIFIER | HG02895.hp1 HG02896.hp1 HG03209.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0002t0001g0005 |
3 | 106 | 0.0283 | -4 | c.155 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147820580 | GTTTT | G | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(19): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(19): Show |
22 | 106 | 0.2076 | -4 | c.155 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147839092 | GTATC | G | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(27): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(7): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(27): Show |
30 | 106 | 0.2830 | -4 | c.313 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147839142 | ATCTG | A | intron_variant | MODIFIER | HG02145.hp2 NA19087.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0055 a0001c0001t0001g0061 |
2 | 106 | 0.0189 | -4 | c.313 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147869998 | TTGTG | T | intron_variant | MODIFIER | HG02895.hp2 HG03209.hp1 NA19064.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
4 | 106 | 0.0377 | -4 | c.702 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147870928 | CTGTG | C | intron_variant | MODIFIER | HG00558.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0046 others(7): Show |
10 | 106 | 0.0943 | -4 | c.703 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147873681 | AACAC | A | intron_variant | MODIFIER | HG02818.hp2 HG02896.hp1 NA18979.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0002t0001g0066 |
3 | 106 | 0.0283 | -4 | c.703 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147890293 | TTTGA | T | intron_variant | MODIFIER | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(4): Show | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
36 | 106 | 0.3396 | -4 | c.103 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147911993 | ACGTG | A | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
a0001a0002a0003 | a0001c0001a0001c0011a0002c0003others(1): Show | a0001c0001t0001a0001c0011t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0083 a0001c0011t0001g0092 a0002c0003t0001g0096 others(2): Show |
5 | 106 | 0.0472 | -4 | c.116 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 147911994 | CGTGT | C | intron_variant | MODIFIER | HG01993.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0051 others(4): Show |
7 | 106 | 0.0660 | -4 | c.116 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147912548 | AATAT | A | intron_variant | MODIFIER | HG02818.hp2 HG02896.hp1 HG03209.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0053 others(2): Show |
5 | 106 | 0.0472 | -4 | c.116 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147921558 | CAGAG | C | intron_variant | MODIFIER | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
a0001a0002a0003 | a0001c0001a0001c0005a0002c0003others(1): Show | a0001c0001t0001a0001c0005t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0061 others(6): Show |
9 | 106 | 0.0849 | -4 | c.122 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147935343 | AAGAT | A | intron_variant | MODIFIER | HG02895.hp1 HG03516.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0001 | a0001c0001t0001g0006 a0001c0005t0001g0003 |
2 | 106 | 0.0189 | -4 | c.122 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147937236 | CCTCT | C | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0038 a0001c0001t0001g0076 a0001c0001t0001g0099 others(3): Show |
6 | 106 | 0.0566 | -4 | c.122 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147948314 | AAGTC | A | intron_variant | MODIFIER | HG02451.hp2 HG02818.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0011 | a0001c0001t0001a0001c0001t0003a0001c0011t0001 | a0001c0001t0001g0093 a0001c0001t0003g0087 a0001c0011t0001g0092 |
3 | 106 | 0.0283 | -4 | c.139 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147955217 | TTAAG | T | intron_variant | MODIFIER | HG01884.hp2 HG02572.hp2 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0004t0001 | a0001c0002t0001g0090 a0001c0004t0001g0105 |
2 | 106 | 0.0189 | -4 | c.139 others(19): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 15/22 | chr4 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 148005734 | TTCTC | T | intron_variant | MODIFIER | HG02056.hp2 HG02080.hp2 HG03098.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0002t0001a0001c0004t0001 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0034 others(4): Show |
7 | 106 | 0.0660 | -4 | 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 | 148017652 | CTATA | C | intron_variant | MODIFIER | HG01884.hp2 HG02165.hp2 HG02738.hp2 others(11): Show |
a0001a0004 | a0001c0002a0001c0004a0001c0008others(2): Show | a0001c0002t0001a0001c0004t0001a0001c0008t0001others(2): Show | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0019 others(11): Show |
14 | 106 | 0.1321 | -4 | c.171 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148032327 | TCCCC | T | intron_variant | MODIFIER | HG02056.hp1 HG02056.hp2 HG02080.hp1 others(10): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(2): Show | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0030 others(10): Show |
13 | 106 | 0.1226 | -4 | c.186 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar |