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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AOAH_chr7_36507941_36729494 | 36517262 | C | CTCTTTCT others(37): Show |
intron_variant | MODIFIER | HG01934.hp1 HG02970.hp1 HG03041.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0065 others(1): Show |
4 | 18 | 0.2222 | 44 | c.160 others(63): Show |
AOAH | ENSG00000136250.12 | transcript | ENST00000617537.5 | protein_coding | 20/20 | chr7 | TogoVar | |||||||
AOPEP_chr9_94721699_95092159 | 94728239 | G | GCGCGCGC others(37): Show |
intron_variant | MODIFIER | NA19079.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0150 | 1 | 44 | 0.0227 | 44 | c.-13 others(63): Show |
AOPEP | ENSG00000148120.19 | transcript | ENST00000375315.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
AP2A2_chr11_920870_1017240 | 974145 | A | AGGTGGCC others(37): Show |
intron_variant | MODIFIER | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(18): Show |
a0001a0002 | a0001c0002a0001c0003a0001c0008others(1): Show | a0001c0002t0002a0001c0002t0004a0001c0002t0011others(3): Show | a0001c0002t0002g0225 a0001c0002t0002g0232 a0001c0002t0002g0233 others(18): Show |
21 | 265 | 0.0792 | 44 | c.473 others(61): Show |
AP2A2 | ENSG00000183020.15 | transcript | ENST00000448903.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
APOA4_chr11_116815700_116828304 | 116818381 | T | TATATATA others(37): Show |
downstream_gene_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0005 | 1 | 350 | 0.0029 | 44 | c.*24 others(55): Show |
APOA4 | ENSG00000110244.7 | transcript | ENST00000357780.5 | protein_coding | 2318 | chr11 | TogoVar | |||||||
APOBEC1_chr12_7644400_7670908 | 7660375 | G | GGAAGGAA others(37): Show |
intron_variant | MODIFIER | HG00741.hp1 NA18999.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0335 a0001c0003t0001g0338 |
2 | 99 | 0.0202 | 44 | c.16+ others(59): Show |
APOBEC1 | ENSG00000111701.7 | transcript | ENST00000229304.5 | protein_coding | 1/4 | chr12 | TogoVar | |||||||
APOBEC1_chr12_7644400_7670908 | 7660375 | G | GGAAGGAA others(37): Show |
intron_variant | MODIFIER | HG03710.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0336 | 1 | 98 | 0.0102 | 44 | c.16+ others(59): Show |
APOBEC1 | ENSG00000111701.7 | transcript | ENST00000229304.5 | protein_coding | 1/4 | chr12 | TogoVar | |||||||
APOBEC1_chr12_7644400_7670908 | 7660375 | G | GGAAGGAA others(37): Show |
intron_variant | MODIFIER | HG03491.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0333 | 1 | 98 | 0.0102 | 44 | c.16+ others(59): Show |
APOBEC1 | ENSG00000111701.7 | transcript | ENST00000229304.5 | protein_coding | 1/4 | chr12 | TogoVar | |||||||
APOBEC3A_chr22_38952609_38968184 | 38958490 | T | TTCCTTCC others(37): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0005 | a0001c0005t0003 | a0001c0005t0003g0032 | 1 | 358 | 0.0028 | 44 | c.29+ others(57): Show |
APOBEC3A | ENSG00000128383.14 | transcript | ENST00000249116.7 | protein_coding | 1/4 | chr22 | TogoVar | |||||||
ARC_chr8_142606049_142619479 | 142607253 | A | AGGGGAGG others(37): Show |
downstream_gene_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(9): Show | a0001c0001t0001g0001 a0001c0001t0002g0002 a0001c0001t0002g0014 others(11): Show |
100 | 297 | 0.3367 | 44 | c.*53 others(55): Show |
ARC | ENSG00000198576.4 | transcript | ENST00000356613.4 | protein_coding | 3795 | chr8 | TogoVar | |||||||
ARGFX_chr3_121562949_121595622 | 121565791 | A | ATATATAT others(37): Show |
upstream_gene_variant | MODIFIER | HG03516.hp2 | a0003 | a0003c0003 | a0003c0003t0008 | a0003c0003t0008g0332 | 1 | 405 | 0.0025 | 44 | c.-22 others(55): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2157 | chr3 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625852 | T | TTATACAT others(37): Show |
intron_variant | MODIFIER | HG02896.hp1 HG02897.hp1 |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | 234 | 0.0085 | 44 | c.786 others(61): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24617724 | T | TAGCTTTA others(37): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0007 | a0002c0002t0001g0018 a0002c0002t0001g0118 a0002c0002t0001g0119 others(20): Show |
23 | 350 | 0.0657 | 44 | c.242 others(63): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24617740 | T | TCCGTAGA others(37): Show |
intron_variant | MODIFIER | HG00099.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0280 | 1 | 350 | 0.0029 | 44 | c.242 others(63): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(37): Show |
downstream_gene_variant | MODIFIER | HG01081.hp1 HG01257.hp1 NA19062.hp2 |
a0001a0002 | a0001c0001a0001c0020a0002c0022 | a0001c0001t0001a0001c0020t0005a0002c0022t0001 | a0001c0001t0001g0103 a0001c0020t0005g0011 a0002c0022t0001g0097 |
3 | 54 | 0.0556 | 44 | c.*21 others(55): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(37): Show |
downstream_gene_variant | MODIFIER | HG00735.hp2 HG01169.hp1 HG01433.hp1 others(7): Show |
a0001 | a0001c0002a0001c0040a0001c0048 | a0001c0002t0002a0001c0002t0012a0001c0040t0002others(1): Show | a0001c0002t0002g0015 a0001c0002t0002g0026 a0001c0002t0002g0110 others(7): Show |
10 | 61 | 0.1639 | 44 | c.*21 others(55): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATACATA others(37): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0008 | a0001c0008t0019 | a0001c0008t0019g0177 | 1 | 48 | 0.0208 | 44 | c.110 others(63): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6909301 | T | TTTTCTTT others(37): Show |
intron_variant | MODIFIER | HG01256.hp2 HG01884.hp2 HG02258.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0113 a0001c0001t0001g0175 a0001c0001t0006g0155 others(1): Show |
4 | 194 | 0.0206 | 44 | c.209 others(61): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129193703 | A | ATATATAA others(37): Show |
upstream_gene_variant | MODIFIER | HG02602.hp2 | a0001 | a0001c0010 | a0001c0010t0008 | a0001c0010t0008g0193 | 1 | 216 | 0.0046 | 44 | c.-15 others(55): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1379 | chr11 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531543 | A | AACACTAG others(37): Show |
intron_variant | MODIFIER | NA18967.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141 | 1 | 244 | 0.0041 | 44 | c.298 others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144561705 | C | CGCTCCAG others(37): Show |
intron_variant | MODIFIER | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
a0001 | a0001c0001a0001c0018 | a0001c0001t0001a0001c0018t0001 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(6): Show |
9 | 244 | 0.0369 | 44 | c.513 others(61): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11174573 | C | CCTTCCTT others(37): Show |
intron_variant | MODIFIER | HG02071.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0036 | 1 | 74 | 0.0135 | 44 | c.162 others(63): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11190473 | A | ATATATAT others(37): Show |
intron_variant | MODIFIER | HG02451.hp2 NA19240.hp1 |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0001a0002c0005t0006 | a0001c0001t0001g0020 a0002c0005t0006g0018 |
2 | 121 | 0.0165 | 44 | c.821 others(61): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 3/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44800030 | A | AGGCACGA others(37): Show |
intron_variant | MODIFIER | HG01109.hp2 | a0002 | a0002c0064 | a0002c0064t0005 | a0002c0064t0005g0067 | 1 | 237 | 0.0042 | 44 | c.80- others(59): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44800030 | A | AGGCACGG others(37): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0004a0001c0007others(27): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(32): Show | a0001c0001t0001g0101 a0001c0001t0001g0192 a0001c0001t0001g0200 others(110): Show |
113 | 349 | 0.3238 | 44 | c.80- others(59): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1849291 | C | CACAGCAA others(37): Show |
intron_variant | MODIFIER | HG01175.hp1 HG01192.hp1 HG02886.hp1 |
a0001 | a0001c0009a0001c0154 | a0001c0009t0004a0001c0154t0011 | a0001c0009t0004g0303 a0001c0009t0004g0326 a0001c0154t0011g0241 |
3 | 362 | 0.0083 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1849368 | A | ACGTGGAC others(37): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0003 | a0003c0064 | a0003c0064t0060 | a0003c0064t0060g0269 | 1 | 362 | 0.0028 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1849588 | C | CGTGGACA others(37): Show |
intron_variant | MODIFIER | NA18962.hp1 NA19091.hp1 |
a0001a0025 | a0001c0110a0025c0055 | a0001c0110t0005a0025c0055t0007 | a0001c0110t0005g0172 a0025c0055t0007g0173 |
2 | 362 | 0.0055 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1849714 | T | TGGCCACG others(37): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0003 | a0003c0064 | a0003c0064t0060 | a0003c0064t0060g0269 | 1 | 352 | 0.0028 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1849893 | T | TGTGGACA others(37): Show |
intron_variant | MODIFIER | HG00597.hp1 HG00597.hp2 HG01361.hp1 others(5): Show |
a0001a0006a0007 | a0001c0006a0001c0011a0001c0020others(3): Show | a0001c0006t0001a0001c0011t0001a0001c0011t0006others(4): Show | a0001c0006t0001g0009 a0001c0011t0001g0016 a0001c0011t0006g0121 others(5): Show |
8 | 322 | 0.0248 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1849894 | G | GTGGACAC others(37): Show |
intron_variant | MODIFIER | HG00140.hp2 HG01070.hp2 HG03831.hp2 others(3): Show |
a0001a0002 | a0001c0003a0002c0017a0002c0024others(1): Show | a0001c0003t0007a0002c0017t0002a0002c0017t0005others(2): Show | a0001c0003t0007g0169 a0002c0017t0002g0043 a0002c0017t0002g0044 others(3): Show |
6 | 340 | 0.0176 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1849937 | C | CATGGACA others(37): Show |
intron_variant | MODIFIER | HG02074.hp2 | a0002 | a0002c0034 | a0002c0034t0010 | a0002c0034t0010g0135 | 1 | 362 | 0.0028 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1849938 | G | GTGGACAC others(37): Show |
intron_variant | MODIFIER | HG01358.hp2 HG02148.hp1 HG03471.hp2 others(2): Show |
a0001a0004 | a0001c0005a0001c0007a0001c0010others(2): Show | a0001c0005t0001a0001c0007t0008a0001c0010t0001others(2): Show | a0001c0005t0001g0055 a0001c0007t0008g0347 a0001c0010t0001g0047 others(2): Show |
5 | 311 | 0.0161 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1849982 | A | ATGGACAC others(37): Show |
intron_variant | MODIFIER | HG04228.hp2 | a0001 | a0001c0018 | a0001c0018t0028 | a0001c0018t0028g0108 | 1 | 260 | 0.0038 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1849982 | A | ATGGACAC others(37): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01168.hp1 HG01175.hp1 others(12): Show |
a0001a0002a0013 | a0001c0004a0001c0006a0001c0009others(10): Show | a0001c0004t0002a0001c0006t0001a0001c0009t0004others(10): Show | a0001c0004t0002g0324 a0001c0006t0001g0239 a0001c0006t0001g0240 others(12): Show |
15 | 274 | 0.0547 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1850026 | A | ATGGACAC others(37): Show |
intron_variant | MODIFIER | NA19084.hp1 | a0007 | a0007c0148 | a0007c0148t0002 | a0007c0148t0002g0003 | 1 | 209 | 0.0048 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1850026 | A | ATGGACAC others(37): Show |
intron_variant | MODIFIER | HG03669.hp1 | a0001 | a0001c0009 | a0001c0009t0059 | a0001c0009t0059g0298 | 1 | 209 | 0.0048 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1850026 | A | ATGGACAC others(37): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0102 | a0001c0102t0012 | a0001c0102t0012g0119 | 1 | 209 | 0.0048 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1850057 | G | GTGGGCCG others(37): Show |
intron_variant | MODIFIER | NA18954.hp2 | a0002 | a0002c0149 | a0002c0149t0047 | a0002c0149t0047g0007 | 1 | 336 | 0.0030 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1850062 | C | CCGGCTGC others(37): Show |
intron_variant | MODIFIER | NA19080.hp2 | a0001 | a0001c0006 | a0001c0006t0039 | a0001c0006t0039g0160 | 1 | 345 | 0.0029 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1850068 | G | GCATGGAC others(37): Show |
intron_variant | MODIFIER | HG01496.hp1 HG02486.hp1 HG04184.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0053 a0001c0002t0001g0071 a0001c0002t0001g0341 |
3 | 345 | 0.0087 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1850070 | G | ATGGACAC others(37): Show |
intron_variant | MODIFIER | NA19086.hp2 | a0001 | a0001c0037 | a0001c0037t0009 | a0001c0037t0009g0305 | 1 | 262 | 0.0038 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1850070 | G | GTGGACAC others(37): Show |
intron_variant | MODIFIER | NA20752.hp2 | a0001 | a0001c0042 | a0001c0042t0034 | a0001c0042t0034g0021 | 1 | 262 | 0.0038 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1850113 | C | CGTGGACA others(37): Show |
intron_variant | MODIFIER | HG03491.hp1 HG03492.hp1 |
a0001 | a0001c0013 | a0001c0013t0001 | a0001c0013t0001g0223 a0001c0013t0001g0224 |
2 | 361 | 0.0055 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1850114 | A | ATGGACAC others(37): Show |
intron_variant | MODIFIER | HG03688.hp1 | a0001 | a0001c0001 | a0001c0001t0038 | a0001c0001t0038g0100 | 1 | 246 | 0.0041 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1850156 | A | ACGTGGAC others(37): Show |
intron_variant | MODIFIER | HG01074.hp1 HG01109.hp2 |
a0001a0005 | a0001c0001a0005c0039 | a0001c0001t0002a0005c0039t0001 | a0001c0001t0002g0072 a0005c0039t0001g0073 |
2 | 240 | 0.0083 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1850156 | A | ATGTGGAC others(37): Show |
intron_variant | MODIFIER | HG01106.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0197 | 1 | 239 | 0.0042 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1850158 | G | GTGGACAC others(37): Show |
intron_variant | MODIFIER | HG00597.hp2 HG01361.hp1 HG01978.hp1 others(14): Show |
a0001a0002a0007 | a0001c0002a0001c0003a0001c0006others(12): Show | a0001c0002t0001a0001c0003t0058a0001c0006t0001others(13): Show | a0001c0002t0001g0046 a0001c0003t0058g0338 a0001c0006t0001g0009 others(14): Show |
17 | 272 | 0.0625 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1850159 | T | TGGACACA others(37): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00597.hp1 HG00738.hp1 others(40): Show |
a0001a0002a0004others(7): Show | a0001c0001a0001c0002a0001c0003others(28): Show | a0001c0001t0005a0001c0002t0001a0001c0003t0007others(35): Show | a0001c0001t0005g0150 a0001c0002t0001g0244 a0001c0003t0007g0169 others(40): Show |
43 | 305 | 0.1410 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1850201 | C | CGTGGACA others(37): Show |
intron_variant | MODIFIER | HG03834.hp1 | a0002 | a0002c0027 | a0002c0027t0005 | a0002c0027t0005g0151 | 1 | 334 | 0.0030 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1850239 | C | CGGCCACG others(37): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0052 | a0001c0052t0045 | a0001c0052t0045g0336 | 1 | 360 | 0.0028 | 44 | c.37+ others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | chr8 | TogoVar |