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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ANTXR2_chr4_79896146_80078229 | 80015898 | AAGGAAAG others(33): Show |
A | intron_variant | MODIFIER | HG03098.hp1 NA19012.hp1 |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0002a0006c0006t0073 | a0001c0001t0002g0224a0006c0006t0073g0252 | 2 | 268 | 0.0075 | -40 | c.945 others(57): Show |
ANTXR2 | ENSG00000163297.18 | transcript | ENST00000403729.7 | protein_coding | 11/16 | chr4 | TogoVar | ||||||
ANTXR2_chr4_79896146_80078229 | 80015903 | AAGGAAAG others(33): Show |
A | intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0001 | a0001c0001t0074 | a0001c0001t0074g0228 | 1 | 268 | 0.0037 | -40 | c.945 others(57): Show |
ANTXR2 | ENSG00000163297.18 | transcript | ENST00000403729.7 | protein_coding | 11/16 | chr4 | TogoVar | ||||||
ANXA3_chr4_78546770_78615447 | 78548080 | CAGTGAGG others(33): Show |
C | upstream_gene_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0038 | 1 | 330 | 0.0030 | -40 | c.-38 others(51): Show |
ANXA3 | ENSG00000138772.13 | transcript | ENST00000264908.11 | protein_coding | 3689 | chr4 | TogoVar | ||||||
ANXA8L1_chr10_46370776_46396778 | 46370983 | CCTGAGCC others(33): Show |
C | upstream_gene_variant | MODIFIER | HG01261.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0116 | 1 | 390 | 0.0026 | -40 | c.-48 others(51): Show |
ANXA8L1 | ENSG00000264230.9 | transcript | ENST00000619162.5 | protein_coding | 4792 | chr10 | TogoVar | ||||||
AP3B1_chr5_77997326_78299698 | 78096739 | TGCCCCGT others(33): Show |
T | intron_variant | MODIFIER | HG00741.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0064 | 1 | 226 | 0.0044 | -40 | c.247 others(59): Show |
AP3B1 | ENSG00000132842.15 | transcript | ENST00000255194.11 | protein_coding | 21/26 | chr5 | TogoVar | ||||||
AP3D1_chr19_2095988_2156566 | 2128442 | GCACTGCA others(33): Show |
G | intron_variant | MODIFIER | HG00733.hp2 HG01243.hp2 HG01515.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(3): Show | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0120others(10): Show | 13 | 406 | 0.0320 | -40 | c.806 others(55): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | TogoVar | ||||||
AP3D1_chr19_2095988_2156566 | 2128553 | AGCTCCGA others(33): Show |
A | intron_variant | MODIFIER | HG01243.hp2 HG01978.hp1 HG02040.hp1 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(1): Show | a0001c0001t0001g0085a0001c0001t0001g0112a0001c0001t0002g0063others(3): Show | 6 | 406 | 0.0148 | -40 | c.806 others(55): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | TogoVar | ||||||
AP3D1_chr19_2095988_2156566 | 2128672 | AGCTCCGA others(33): Show |
A | intron_variant | MODIFIER | HG00140.hp2 HG01074.hp2 HG01109.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0002t0001a0001c0004t0002 | a0001c0001t0001g0002a0001c0001t0001g0134a0001c0002t0001g0003others(3): Show | 8 | 406 | 0.0197 | -40 | c.806 others(55): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | TogoVar | ||||||
AP3D1_chr19_2095988_2156566 | 2128751 | AGCTCCGA others(33): Show |
A | intron_variant | MODIFIER | HG01433.hp2 HG02129.hp1 HG02129.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(2): Show | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0132others(6): Show | 10 | 406 | 0.0246 | -40 | c.806 others(55): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | TogoVar | ||||||
AP3D1_chr19_2095988_2156566 | 2128823 | GCCCCACA others(33): Show |
G | intron_variant | MODIFIER | NA19057.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0222 | 1 | 406 | 0.0025 | -40 | c.806 others(55): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | TogoVar | ||||||
AP3D1_chr19_2095988_2156566 | 2128876 | GACACTGC others(33): Show |
G | intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0016 | a0001c0016t0002 | a0001c0016t0002g0097 | 1 | 406 | 0.0025 | -40 | c.806 others(55): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | TogoVar | ||||||
AP3S2_chr15_89825599_89898994 | 89844233 | TTCTTTCT others(33): Show |
T | intron_variant | MODIFIER | HG01109.hp1 HG03225.hp2 |
a0001 | a0001c0001 | a0001c0001t0043a0001c0001t0045 | a0001c0001t0043g0184a0001c0001t0045g0303 | 2 | 312 | 0.0064 | -40 | c.346 others(57): Show |
AP3S2 | ENSG00000157823.17 | transcript | ENST00000336418.9 | protein_coding | 4/5 | chr15 | TogoVar | ||||||
AP3S2_chr15_89825599_89898994 | 89858477 | AAGAAAGA others(33): Show |
A | intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0023 | a0001c0001t0023g0305 | 1 | 312 | 0.0032 | -40 | c.345 others(59): Show |
AP3S2 | ENSG00000157823.17 | transcript | ENST00000336418.9 | protein_coding | 4/5 | chr15 | TogoVar | ||||||
AP3S2_chr15_89825599_89898994 | 89858499 | GAGAGAGA others(33): Show |
G | intron_variant | MODIFIER | HG01243.hp2 HG01517.hp1 HG02145.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0168a0001c0001t0002g0177a0001c0001t0002g0179others(4): Show | 7 | 312 | 0.0224 | -40 | c.345 others(59): Show |
AP3S2 | ENSG00000157823.17 | transcript | ENST00000336418.9 | protein_coding | 4/5 | chr15 | TogoVar | ||||||
AP3S2_chr15_89825599_89898994 | 89867748 | CTGAGAAG others(33): Show |
C | intron_variant | MODIFIER | HG02004.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0114 | 1 | 312 | 0.0032 | -40 | c.345 others(57): Show |
AP3S2 | ENSG00000157823.17 | transcript | ENST00000336418.9 | protein_coding | 4/5 | chr15 | TogoVar | ||||||
APLP2_chr11_130064894_130149805 | 130091891 | GGCTGCCG others(33): Show |
G | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(58): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0005a0002c0002others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(12): Show | a0001c0001t0001g0152a0001c0001t0002g0002a0001c0001t0002g0003others(56): Show | 61 | 274 | 0.2226 | -40 | c.106 others(59): Show |
APLP2 | ENSG00000084234.18 | transcript | ENST00000338167.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
APOBEC3B_chr22_38977347_38997779 | 38981173 | AGCCCCCG others(33): Show |
A | upstream_gene_variant | MODIFIER | NA20300.hp1 NA21309.hp2 |
a0003a0012 | a0003c0017a0012c0032 | a0003c0017t0001a0012c0032t0001 | a0003c0017t0001g0174a0012c0032t0001g0136 | 2 | 354 | 0.0057 | -40 | c.-12 others(51): Show |
APOBEC3B | ENSG00000179750.16 | transcript | ENST00000333467.4 | protein_coding | 1173 | chr22 | TogoVar | ||||||
APOH_chr17_66207033_66234415 | 66224666 | GGGAAGGG others(33): Show |
G | intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0155 | 1 | 386 | 0.0026 | -40 | c.339 others(55): Show |
APOH | ENSG00000091583.11 | transcript | ENST00000205948.11 | protein_coding | 3/7 | chr17 | TogoVar | ||||||
APOH_chr17_66207033_66234415 | 66224671 | GGGAAGGG others(33): Show |
G | intron_variant | MODIFIER | NA19062.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0164 | 1 | 386 | 0.0026 | -40 | c.339 others(55): Show |
APOH | ENSG00000091583.11 | transcript | ENST00000205948.11 | protein_coding | 3/7 | chr17 | TogoVar | ||||||
APOH_chr17_66207033_66234415 | 66224676 | GGGAAGGG others(33): Show |
G | intron_variant | MODIFIER | HG01243.hp2 HG02280.hp2 HG03579.hp2 |
a0002 | a0002c0002a0002c0011 | a0002c0002t0001a0002c0011t0002 | a0002c0002t0001g0055a0002c0011t0002g0013 | 3 | 386 | 0.0078 | -40 | c.339 others(55): Show |
APOH | ENSG00000091583.11 | transcript | ENST00000205948.11 | protein_coding | 3/7 | chr17 | TogoVar | ||||||
ARAF_chrX_47556205_47576908 | 47576379 | CTTCCAGT others(33): Show |
C | downstream_gene_variant | MODIFIER | HG00609.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 318 | 0.0031 | -40 | c.*49 others(51): Show |
ARAF | ENSG00000078061.14 | transcript | ENST00000377045.9 | protein_coding | 4472 | chrX | TogoVar | ||||||
ARF3_chr12_48930723_48962487 | 48939225 | AACCCAGA others(33): Show |
A | intron_variant | MODIFIER | NA18985.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0115 | 1 | 348 | 0.0029 | -40 | c.385 others(55): Show |
ARF3 | ENSG00000134287.10 | transcript | ENST00000256682.9 | protein_coding | 4/4 | chr12 | TogoVar | ||||||
ARFGEF2_chr20_48916711_49041693 | 48936375 | AGGTGGCT others(33): Show |
A | intron_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0121 | 1 | 352 | 0.0028 | -40 | c.122 others(57): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARFIP1_chr4_152774954_152917357 | 152804298 | TATTATAT others(33): Show |
T | intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0103 | 1 | 342 | 0.0029 | -40 | c.-10 others(59): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | chr4 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152866723 | GCTCCTCA others(33): Show |
G | intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0167 | 1 | 342 | 0.0029 | -40 | c.202 others(57): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147798755 | CTCTCTCT others(33): Show |
C | intron_variant | MODIFIER | HG01169.hp2 homoSapiens_chm13v2.hp1 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0011a0002c0003t0001g0009 | 2 | 106 | 0.0189 | -40 | c.155 others(59): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143134114 | TCTATCTA others(33): Show |
T | intron_variant | MODIFIER | HG00621.hp1 HG00642.hp1 HG00642.hp2 others(45): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0108others(45): Show | 48 | 162 | 0.2963 | -40 | c.-15 others(57): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143555860 | AAGAATAG others(33): Show |
A | intron_variant | MODIFIER | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(50): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(50): Show | 53 | 162 | 0.3272 | -40 | c.926 others(55): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP21_chr10_24578614_24728887 | 24689894 | ATGTGTAT others(33): Show |
A | intron_variant | MODIFIER | HG02129.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
a0001a0007a0017others(1): Show | a0001c0001a0007c0007a0017c0029others(1): Show | a0001c0001t0001a0007c0007t0006a0007c0007t0015others(2): Show | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 10 | 352 | 0.0284 | -40 | c.64- others(57): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119422123 | CTAGAGGA others(33): Show |
C | downstream_gene_variant | MODIFIER | HG00280.hp2 HG00741.hp1 HG01258.hp2 others(3): Show |
a0002 | a0002c0003 | a0002c0003t0002a0002c0003t0009a0002c0003t0030others(1): Show | a0002c0003t0002g0118a0002c0003t0002g0152a0002c0003t0009g0167others(3): Show | 6 | 310 | 0.0194 | -40 | c.*58 others(51): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1410 | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129129198 | ACCGTCTG others(33): Show |
A | intron_variant | MODIFIER | HG01123.hp1 HG06807.hp1 |
a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0384a0001c0003t0005g0385 | 2 | 398 | 0.0050 | -40 | c.226 others(57): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129129297 | CCCCCTCC others(33): Show |
C | intron_variant | MODIFIER | NA18994.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0156 | 1 | 398 | 0.0025 | -40 | c.226 others(57): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(33): Show |
A | intron_variant | MODIFIER | HG02109.hp1 | a0001 | a0001c0001 | a0001c0001t0020 | a0001c0001t0020g0115 | 1 | 298 | 0.0034 | -40 | c.-18 others(61): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP39_chr8_144524179_144690846 | 144561388 | CCCAGTGG others(33): Show |
C | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
a0001a0004 | a0001c0003a0001c0005a0001c0010others(1): Show | a0001c0003t0001a0001c0003t0009a0001c0005t0001others(3): Show | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(7): Show | 10 | 246 | 0.0407 | -40 | c.513 others(57): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144561568 | CCCAGTGG others(33): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(66): Show |
a0001 | a0001c0001a0001c0002a0001c0007others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0018others(7): Show | a0001c0001t0001g0049a0001c0001t0001g0065a0001c0001t0001g0097others(66): Show | 69 | 246 | 0.2805 | -40 | c.513 others(57): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144620226 | TGTGTGTG others(33): Show |
T | intron_variant | MODIFIER | HG00280.hp2 HG00438.hp2 HG00735.hp2 others(21): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(8): Show | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0134others(21): Show | 24 | 246 | 0.0976 | -40 | c.-81 others(59): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144620468 | TGTGTGCC others(33): Show |
T | intron_variant | MODIFIER | NA18990.hp1 NA21309.hp1 |
a0001 | a0001c0002a0001c0017 | a0001c0002t0001a0001c0017t0001 | a0001c0002t0001g0214a0001c0017t0001g0064 | 2 | 246 | 0.0081 | -40 | c.-81 others(59): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285966 | TCCCAACC others(33): Show |
T | downstream_gene_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0001 | 1 | 442 | 0.0023 | -40 | c.*31 others(51): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2957 | chr16 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1823999 | CGCGGGGG others(33): Show |
C | 5_prime_UTR_variant | MODIFIER | NA19080.hp2 | a0001 | a0001c0006 | a0001c0006t0050 | a0001c0006t0050g0094 | 1 | 363 | 0.0028 | -40 | c.-14 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/29 | 19342 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||
ARHGEF10_chr8_1818926_1963641 | 1919378 | CTGGGTGA others(33): Show |
C | intron_variant | MODIFIER | HG03831.hp2 | a0002 | a0002c0108 | a0002c0108t0004 | a0002c0108t0004g0142 | 1 | 363 | 0.0028 | -40 | c.214 others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1919587 | GGAGCTGT others(33): Show |
G | intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0140 | a0001c0140t0005 | a0001c0140t0005g0297 | 1 | 363 | 0.0028 | -40 | c.214 others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 157035871 | ATATATAT others(33): Show |
A | intron_variant | MODIFIER | HG03654.hp2 HG03831.hp1 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0044a0002c0002t0002g0095 | 2 | 362 | 0.0055 | -40 | c.32+ others(55): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120351419 | ATATATAT others(33): Show |
A | intron_variant | MODIFIER | NA20805.hp2 | a0001 | a0001c0012 | a0001c0012t0001 | a0001c0012t0001g0296 | 1 | 308 | 0.0033 | -40 | c.32+ others(57): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7450257 | GTCCATTT others(33): Show |
G | intron_variant | MODIFIER | HG00639.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0237 | 1 | 298 | 0.0034 | -40 | c.173 others(57): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7450422 | GGGATCTT others(33): Show |
G | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(26): Show |
a0001a0002a0003others(6): Show | a0001c0018a0001c0047a0002c0005others(8): Show | a0001c0018t0001a0001c0047t0002a0002c0005t0001others(9): Show | a0001c0018t0001g0101a0001c0018t0001g0118a0001c0018t0001g0136others(26): Show | 29 | 298 | 0.0973 | -40 | c.173 others(57): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73671708 | ATATATAT others(33): Show |
A | intron_variant | MODIFIER | HG01243.hp2 HG02622.hp2 |
a0002a0012 | a0002c0002a0012c0072 | a0002c0002t0002a0012c0072t0005 | a0002c0002t0002g0133a0012c0072t0005g0144 | 2 | 188 | 0.0106 | -40 | c.-11 others(59): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73737439 | CTTCTTTT others(33): Show |
C | intron_variant | MODIFIER | HG02602.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
a0004a0008a0015others(1): Show | a0004c0018a0008c0011a0015c0038others(1): Show | a0004c0018t0001a0008c0011t0002a0015c0038t0001others(1): Show | a0004c0018t0001g0179a0008c0011t0002g0162a0015c0038t0001g0061others(1): Show | 4 | 188 | 0.0213 | -40 | c.34- others(57): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561424 | GGAATAGA others(33): Show |
G | intron_variant | MODIFIER | HG02015.hp2 HG02040.hp2 NA19072.hp1 |
a0001a0002 | a0001c0002a0002c0001 | a0001c0002t0001a0002c0001t0001 | a0001c0002t0001g0167a0002c0001t0001g0119a0002c0001t0001g0180 | 3 | 186 | 0.0161 | -40 | c.196 others(57): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARID2_chr12_45724706_45913037 | 45899655 | ATATATAT others(33): Show |
A | intron_variant | MODIFIER | HG02886.hp1 HG02965.hp1 NA18973.hp2 others(4): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0003c0004t0006 | a0001c0001t0001g0129a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | 318 | 0.0220 | -40 | c.536 others(59): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ARID4B_chr1_235161902_235333179 | 235173757 | AAAAAAAA others(33): Show |
A | intron_variant | MODIFIER | HG02486.hp1 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0128 | 1 | 272 | 0.0037 | -40 | c.366 others(58): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 22/23 | chr1 | TogoVar |