regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | 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 | 238 | 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 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(6): Show | 9 | 238 | 0.0378 | -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 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(2): Show | 5 | 238 | 0.0210 | -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 | a0001c0001t0001g0127a0001c0001t0001g0162a0001c0001t0001g0164others(2): Show | 5 | 242 | 0.0207 | -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 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(41): Show | 44 | 242 | 0.1818 | -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 | a0001c0001t0011g0018 | 1 | 226 | 0.0044 | -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 | a0001c0001t0005g0001a0001c0001t0005g0006a0001c0014t0004g0286others(27): Show | 30 | 352 | 0.0852 | -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 | a0001c0001t0002g0300 | 1 | 352 | 0.0028 | -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 | 270 | 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 | a0001c0001t0001g0147 | 1 | 309 | 0.0032 | -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 | a0001c0003t0001g0279a0001c0020t0005g0009a0001c0020t0005g0141others(1): Show | 4 | 309 | 0.0129 | -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 | a0001c0001t0001g0107a0001c0001t0001g0108 | 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 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0090others(5): Show | 8 | 108 | 0.0741 | -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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(38): Show | 41 | 108 | 0.3796 | -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 | a0001c0008t0014g0063 | 1 | 108 | 0.0093 | -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 | a0001c0001t0032 | a0001c0001t0032g0051 | 1 | 198 | 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 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(10): Show | a0001c0001t0002g0118a0001c0001t0002g0195a0001c0001t0003g0119others(21): Show | 24 | 198 | 0.1212 | -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 | a0001c0001t0031 | a0001c0001t0031g0003 | 1 | 198 | 0.0051 | -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 | a0001c0001t0019 | a0001c0001t0019g0010 | 1 | 198 | 0.0051 | -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 | a0001c0001t0005g0108a0001c0001t0005g0109 | 2 | 198 | 0.0101 | -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 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0040others(8): Show | 11 | 347 | 0.0317 | -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 | a0001c0001t0001g0195a0001c0001t0001g0203a0001c0001t0002g0215others(62): Show | 72 | 347 | 0.2075 | -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 | a0004c0004t0004a0004c0004t0026 | a0004c0004t0004g0001a0004c0004t0004g0017a0004c0004t0004g0304others(9): Show | 20 | 347 | 0.0576 | -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(134): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0003a0001c0010others(17): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(30): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(134): Show | 137 | 248 | 0.5524 | -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 | a0001c0003t0003g0084a0001c0019t0021g0073 | 2 | 248 | 0.0081 | -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 | 248 | 0.0040 | -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 | a0002c0003t0001g0257 | 1 | 390 | 0.0026 | -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 | a0002c0003t0001g0267 | 1 | 390 | 0.0026 | -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 | a0001c0001t0001g0113 | 1 | 390 | 0.0026 | -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 | a0001c0001t0001g0098 | 1 | 390 | 0.0026 | -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 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(122): Show | 126 | 310 | 0.4065 | -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 | a0001c0001t0005a0001c0004t0064a0001c0005t0001others(1): Show | a0001c0001t0005g0058a0001c0004t0064g0061a0001c0005t0001g0005others(1): Show | 4 | 310 | 0.0129 | -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 | a0001c0001t0004a0001c0001t0016 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0078others(6): Show | 9 | 298 | 0.0302 | -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 | 298 | 0.0034 | -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 | a0001c0001t0004g0203 | 1 | 302 | 0.0033 | -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 |
a0001a0005 | a0001c0001a0001c0002a0001c0007others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(11): Show | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(31): Show | 34 | 246 | 0.1382 | -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 | a0001c0001t0001g0047 | 1 | 246 | 0.0041 | -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 | a0001c0001t0001g0144 | 1 | 246 | 0.0041 | -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 | a0001c0001t0002g0131a0001c0001t0004g0237a0001c0001t0007g0168others(12): Show | 15 | 246 | 0.0610 | -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 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | 246 | 0.0203 | -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 | a0001c0001t0016g0105 | 1 | 246 | 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 | a0001c0001t0020g0079 | 1 | 246 | 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(70): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(6): Show | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0029others(70): Show | 73 | 246 | 0.2968 | -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 | a0001c0002t0001g0169 | 1 | 246 | 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 | a0001c0001t0001g0146 | 1 | 246 | 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 | a0001c0002t0001g0038 | 1 | 246 | 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 | a0001c0001t0001g0045 | 1 | 246 | 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 | a0001c0001t0021g0062a0001c0002t0019g0125a0001c0004t0006g0069others(4): Show | 7 | 246 | 0.0285 | -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 | a0001c0001t0001g0224 | 1 | 286 | 0.0035 | -20 | c.250 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | chr11 | TogoVar |