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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP18_chr6_129571132_129715177 | 129617459 | AATTCGGA others(13): Show |
A | intron_variant | MODIFIER | NA18963.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0038 | 1 | 236 | 0.0042 | -20 | c.953 others(37): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129676912 | CCTCTTTT others(13): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | 165 | 0.0545 | -20 | c.113 others(39): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129676915 | CTTTTTTT others(13): Show |
C | intron_variant | MODIFIER | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(2): Show |
5 | 96 | 0.0521 | -20 | c.113 others(39): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97218941 | GTATATAT others(13): Show |
G | downstream_gene_variant | MODIFIER | HG00597.hp1 HG03453.hp1 HG03834.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0127 a0001c0001t0001g0160 a0001c0001t0001g0162 others(2): Show |
5 | 123 | 0.0407 | -20 | c.*71 others(31): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3237 | chr10 | TogoVar | |||||||
ARHGAP19_chr10_97217179_97297637 | 97239547 | AGAGGGTG others(13): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(41): Show |
a0001a0003a0004others(2): Show | a0001c0001a0003c0005a0004c0006others(2): Show | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(5): Show | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(41): Show |
44 | 116 | 0.3793 | -20 | c.118 others(39): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110648154 | AATATATA others(13): Show |
A | intron_variant | MODIFIER | NA18972.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0020 | 1 | 221 | 0.0045 | -20 | c.189 others(39): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24622433 | CATATATA others(13): Show |
C | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp2 HG00673.hp1 others(27): Show |
a0001a0002a0004others(3): Show | a0001c0001a0001c0014a0002c0002others(4): Show | a0001c0001t0005a0001c0014t0004a0002c0002t0001others(7): Show | a0001c0001t0005g0002 a0001c0001t0005g0007 a0001c0014t0004g0287 others(27): Show |
30 | 43 | 0.6977 | -20 | c.525 others(35): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24695050 | CAAAAAAA others(13): Show |
C | intron_variant | MODIFIER | NA19087.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0301 | 1 | 3 | 0.3333 | -20 | c.64- others(37): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48472529 | TAAAATAA others(13): Show |
T | intron_variant | MODIFIER | HG03669.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0075 | 1 | 268 | 0.0037 | -20 | c.451 others(37): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 4/9 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38504976 | ATCTTTTT others(13): Show |
A | intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 | 1 | 307 | 0.0033 | -20 | c.344 others(39): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38504978 | CTTTTTTT others(13): Show |
C | intron_variant | MODIFIER | HG01081.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
a0001 | a0001c0003a0001c0020a0001c0027 | a0001c0003t0001a0001c0020t0005a0001c0027t0005 | a0001c0003t0001g0275 a0001c0020t0005g0011 a0001c0020t0005g0143 others(1): Show |
4 | 17 | 0.2353 | -20 | c.344 others(39): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85475685 | GGGGGGCG others(13): Show |
G | intron_variant | MODIFIER | HG02738.hp1 NA18968.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0105 a0001c0001t0001g0108 |
2 | 108 | 0.0185 | -20 | c.-21 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85590180 | GCCTGCCT others(13): Show |
G | intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0005 | a0001c0005t0004 | a0001c0005t0004g0038 | 1 | 108 | 0.0093 | -20 | c.180 others(39): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85590192 | GCCTTCCT others(13): Show |
G | intron_variant | MODIFIER | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0008a0001c0003t0001others(2): Show | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0094 others(5): Show |
8 | 39 | 0.2051 | -20 | c.180 others(39): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85724489 | GTGTATAT others(13): Show |
G | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(38): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(14): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(38): Show |
41 | 54 | 0.7593 | -20 | c.268 others(37): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85997371 | TATAGATA others(13): Show |
T | intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0008 | a0001c0008t0014 | a0001c0008t0014g0065 | 1 | 20 | 0.0500 | -20 | c.200 others(39): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142787294 | TAATTTAT others(13): Show |
T | intron_variant | MODIFIER | HG03209.hp2 | a0001 | a0001c0001 | a0001c0001t0031 | a0001c0001t0031g0051 | 1 | 196 | 0.0051 | -20 | c.154 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142867288 | GGTGTGTG others(13): Show |
G | intron_variant | MODIFIER | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(21): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(10): Show | a0001c0001t0002g0118 a0001c0001t0002g0195 a0001c0001t0003g0119 others(21): Show |
24 | 69 | 0.3478 | -20 | c.155 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890145 | AAAAAAAA others(13): Show |
A | intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0001 | a0001c0001t0030 | a0001c0001t0030g0003 | 1 | 185 | 0.0054 | -20 | c.487 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890147 | AAAAAATA others(13): Show |
A | intron_variant | MODIFIER | HG01069.hp2 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0010 | 1 | 189 | 0.0053 | -20 | c.487 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890149 | AAAATATA others(13): Show |
A | intron_variant | MODIFIER | HG01175.hp2 HG01192.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0108 a0001c0001t0005g0109 |
2 | 185 | 0.0108 | -20 | c.487 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45419508 | GTATGTAT others(13): Show |
G | intron_variant | MODIFIER | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
a0002a0003 | a0002c0002a0003c0003 | a0002c0002t0001a0003c0003t0001 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0040 others(8): Show |
11 | 342 | 0.0322 | -20 | c.657 others(39): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | |||||||
ARHGAP27_chr17_45388908_45437870 | 45419512 | GTATATAT others(13): Show |
G | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(69): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0002g0226 others(62): Show |
72 | 119 | 0.6050 | -20 | c.657 others(39): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | |||||||
ARHGAP27_chr17_45388908_45437870 | 45433915 | TGGCTAAC others(13): Show |
T | upstream_gene_variant | MODIFIER | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
a0004 | a0004c0004 | a0004c0004t0004a0004c0004t0014 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(9): Show |
20 | 336 | 0.0595 | -20 | c.-14 others(31): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1046 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6729315 | TGCGCGCG others(13): Show |
T | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0003a0001c0010others(17): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(30): Show | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0026 others(133): Show |
136 | 245 | 0.5551 | -20 | c.-50 others(29): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 400 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6729554 | AGGAGCGC others(13): Show |
A | upstream_gene_variant | MODIFIER | HG02976.hp2 NA20129.hp1 |
a0001 | a0001c0003a0001c0019 | a0001c0003t0003a0001c0019t0021 | a0001c0003t0003g0084 a0001c0019t0021g0073 |
2 | 243 | 0.0082 | -20 | c.-26 others(29): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 161 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6841265 | CCCTTGGT others(13): Show |
C | intron_variant | MODIFIER | HG02523.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0096 | 1 | 246 | 0.0041 | -20 | c.543 others(37): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161051967 | TCACCACC others(13): Show |
T | intron_variant | MODIFIER | HG03017.hp2 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0253 | 1 | 2 | 0.5000 | -20 | c.101 others(37): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 9/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | TTCTCTCT others(13): Show |
T | intron_variant | MODIFIER | HG03942.hp2 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0263 | 1 | 28 | 0.0357 | -20 | c.537 others(33): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161055886 | TAAATAAA others(13): Show |
T | intron_variant | MODIFIER | HG02129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0122 | 1 | 317 | 0.0032 | -20 | c.345 others(35): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064779 | AAAAGAAA others(13): Show |
A | intron_variant | MODIFIER | HG02040.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0108 | 1 | 307 | 0.0033 | -20 | c.97+ others(35): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119304894 | CAAAATAA others(13): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(123): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0001c0004others(13): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0011others(46): Show | a0001c0001t0005g0023 a0001c0001t0005g0059 a0001c0001t0005g0084 others(122): Show |
126 | 232 | 0.5431 | -20 | c.100 others(37): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119332627 | TCTCTCTC others(13): Show |
T | intron_variant | MODIFIER | HG02559.hp2 NA19070.hp1 NA19083.hp1 others(1): Show |
a0001a0004 | a0001c0001a0001c0004a0001c0005others(1): Show | a0001c0001t0005a0001c0004t0063a0001c0005t0001others(1): Show | a0001c0001t0005g0059 a0001c0004t0063g0062 a0001c0005t0001g0006 others(1): Show |
4 | 308 | 0.0130 | -20 | c.101 others(39): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(13): Show |
A | intron_variant | MODIFIER | HG00438.hp2 HG02071.hp1 HG02922.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0014 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0080 others(6): Show |
9 | 41 | 0.2195 | -20 | c.-18 others(41): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46981825 | GTGTTTTG others(13): Show |
G | intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0278 | 1 | 40 | 0.0250 | -20 | c.382 others(39): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | CATATATA others(13): Show |
C | intron_variant | MODIFIER | HG03704.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0186 | 1 | 5 | 0.2000 | -20 | c.-14 others(39): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144561253 | GTCCATCA others(13): Show |
G | intron_variant | MODIFIER | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(31): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0007others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(11): Show | a0001c0001t0001g0021 a0001c0001t0001g0157 a0001c0001t0001g0222 others(31): Show |
34 | 244 | 0.1393 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144561264 | CCCAGTGG others(13): Show |
C | intron_variant | MODIFIER | NA19087.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0042 | 1 | 234 | 0.0043 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144561397 | GTCCATCA others(13): Show |
G | intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0142 | 1 | 205 | 0.0049 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144561437 | GTCCATCA others(13): Show |
G | intron_variant | MODIFIER | HG00323.hp1 HG01192.hp2 HG02257.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002a0001c0014 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(2): Show | a0001c0001t0002g0129 a0001c0001t0004g0236 a0001c0001t0007g0167 others(12): Show |
15 | 229 | 0.0655 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144561628 | CCCAGTGG others(13): Show |
C | intron_variant | MODIFIER | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
a0001 | a0001c0004 | a0001c0004t0006 | a0001c0004t0006g0064 a0001c0004t0006g0065 a0001c0004t0006g0068 others(2): Show |
5 | 241 | 0.0207 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144561941 | CACTCCAG others(13): Show |
C | intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0092 | 1 | 243 | 0.0041 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144561984 | CCCAGTGG others(13): Show |
C | intron_variant | MODIFIER | HG02109.hp2 | a0001 | a0001c0001 | a0001c0001t0020 | a0001c0001t0020g0075 | 1 | 244 | 0.0041 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144562246 | ACTCCAGT others(13): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(69): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(6): Show | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0052 others(69): Show |
72 | 244 | 0.2951 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144562305 | GGCTCCAG others(13): Show |
G | intron_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0168 | 1 | 241 | 0.0041 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144562348 | TCCAGTGG others(13): Show |
T | intron_variant | MODIFIER | NA19082.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0144 | 1 | 242 | 0.0041 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144562408 | TCCAGTGG others(13): Show |
T | intron_variant | MODIFIER | NA18980.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0032 | 1 | 244 | 0.0041 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144562567 | CACACTCC others(13): Show |
C | intron_variant | MODIFIER | NA18971.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039 | 1 | 244 | 0.0041 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144562744 | CCCAGTGG others(13): Show |
C | intron_variant | MODIFIER | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0021a0001c0002t0019a0001c0004t0006 | a0001c0001t0021g0057 a0001c0002t0019g0123 a0001c0004t0006g0064 others(4): Show |
7 | 243 | 0.0288 | -20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100779541 | TATATATA others(13): Show |
T | intron_variant | MODIFIER | NA19002.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0225 | 1 | 284 | 0.0035 | -20 | c.250 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | chr11 | TogoVar |