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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
PNPLA7_chr9_137454952_137555402 | 137503756 | A | AGAAAGAA others(527): Show |
intron_variant | MODIFIER | NA19080.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045 | 1 | 188 | 0.0053 | 534 | c.147 others(553): Show |
PNPLA7 | ENSG00000130653.16 | transcript | ENST00000406427.6 | protein_coding | 14/34 | chr9 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2124224 | C | CGGCTATA others(527): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0031 | 1 | 286 | 0.0035 | 534 | c.335 others(553): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PWWP2B_chr10_132392200_132422859 | 132392564 | G | GTGATGAT others(527): Show |
upstream_gene_variant | MODIFIER | HG01891.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0105 | 1 | 374 | 0.0027 | 534 | c.-46 others(545): Show |
PWWP2B | ENSG00000171813.14 | transcript | ENST00000305233.6 | protein_coding | 4635 | chr10 | TogoVar | ||||||
RAP1GAP2_chr17_2791438_3042741 | 2831059 | C | CTCCCCTC others(527): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0002 | a0001c0002t0106 | a0001c0002t0106g0160 | 1 | 218 | 0.0046 | 534 | c.80+ others(551): Show |
RAP1GAP2 | ENSG00000132359.17 | transcript | ENST00000254695.13 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
RGS12_chr4_3288021_3444913 | 3310263 | T | TCTGAGGG others(527): Show |
intron_variant | MODIFIER | NA19090.hp1 | a0001 | a0001c0031 | a0001c0031t0001 | a0001c0031t0001g0035 | 1 | 312 | 0.0032 | 534 | c.-10 others(553): Show |
RGS12 | ENSG00000159788.20 | transcript | ENST00000336727.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
RGS12_chr4_3288021_3444913 | 3310263 | T | TCTGAGGG others(527): Show |
intron_variant | MODIFIER | HG01891.hp2 HG01975.hp1 HG02055.hp2 others(6): Show |
a0003 | a0003c0016a0003c0017a0003c0047 | a0003c0016t0001a0003c0017t0001a0003c0047t0001 | a0003c0016t0001g0204a0003c0016t0001g0205a0003c0016t0001g0207others(6): Show | 9 | 312 | 0.0289 | 534 | c.-10 others(553): Show |
RGS12 | ENSG00000159788.20 | transcript | ENST00000336727.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
RORA_chr15_60483284_61234302 | 60542566 | C | CAGCACGC others(527): Show |
intron_variant | MODIFIER | HG02572.hp1 HG02723.hp2 HG02965.hp1 others(2): Show |
a0001 | a0001c0005a0001c0006 | a0001c0005t0004a0001c0006t0004 | a0001c0005t0004g0024a0001c0005t0004g0082a0001c0005t0004g0107others(2): Show | 5 | 118 | 0.0424 | 534 | c.197 others(553): Show |
RORA | ENSG00000069667.16 | transcript | ENST00000335670.11 | protein_coding | 2/10 | chr15 | TogoVar | ||||||
SAMD11_chr1_918923_949574 | 934189 | G | GCGTTACA others(527): Show |
intron_variant | MODIFIER | HG00642.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0169 | 1 | 434 | 0.0023 | 534 | c.843 others(551): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
SAMD11_chr1_918923_949574 | 934657 | A | AGGCGGCT others(527): Show |
intron_variant | MODIFIER | HG01074.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0167 | 1 | 434 | 0.0023 | 534 | c.843 others(551): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
SEPTIN9_chr17_77276499_77505593 | 77485015 | G | GTGATTGT others(527): Show |
intron_variant | MODIFIER | HG03579.hp1 | a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0036 | 1 | 150 | 0.0067 | 534 | c.914 others(551): Show |
SEPTIN9 | ENSG00000184640.20 | transcript | ENST00000427177.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
SEPTIN9_chr17_77314518_77505593 | 77485015 | G | GTGATTGT others(527): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0139 | 1 | 158 | 0.0063 | 534 | c.860 others(551): Show |
SEPTIN9 | ENSG00000184640.20 | transcript | ENST00000329047.13 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
SHANK1_chr19_50654255_50724802 | 50678939 | A | ATGGGGAG others(527): Show |
intron_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0003 | a0001c0003t0023 | a0001c0003t0023g0078 | 1 | 316 | 0.0032 | 534 | c.257 others(553): Show |
SHANK1 | ENSG00000161681.17 | transcript | ENST00000293441.6 | protein_coding | 21/23 | chr19 | TogoVar | ||||||
SHANK1_chr19_50654255_50724802 | 50678939 | A | ATGGGGAG others(527): Show |
intron_variant | MODIFIER | HG02976.hp1 HG04228.hp2 |
a0001a0003 | a0001c0004a0003c0005 | a0001c0004t0028a0003c0005t0014 | a0001c0004t0028g0234a0003c0005t0014g0220 | 2 | 316 | 0.0063 | 534 | c.257 others(553): Show |
SHANK1 | ENSG00000161681.17 | transcript | ENST00000293441.6 | protein_coding | 21/23 | chr19 | TogoVar | ||||||
SIK3_chr11_116838402_117103428 | 116947170 | T | TATTATTT others(527): Show |
intron_variant | MODIFIER | NA19062.hp2 | a0002 | a0002c0004 | a0002c0004t0006 | a0002c0004t0006g0366 | 1 | 366 | 0.0027 | 534 | c.454 others(551): Show |
SIK3 | ENSG00000160584.17 | transcript | ENST00000445177.6 | protein_coding | 3/24 | chr11 | TogoVar | ||||||
SIMC1_chr5_176233424_176350989 | 176305290 | C | CCAGCCAC others(527): Show |
intron_variant | MODIFIER | HG03139.hp2 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0261a0001c0001t0001g0263 | 2 | 360 | 0.0056 | 534 | c.173 others(553): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
SIMC1_chr5_176233424_176350989 | 176305290 | C | CCAGCCAC others(527): Show |
intron_variant | MODIFIER | NA18998.hp2 | a0007 | a0007c0008 | a0007c0008t0001 | a0007c0008t0001g0178 | 1 | 360 | 0.0028 | 534 | c.173 others(553): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
SIMC1_chr5_176233424_176350989 | 176305290 | C | CCAGCCAC others(527): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(35): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004a0001c0001t0001g0175a0001c0001t0001g0176others(35): Show | 38 | 360 | 0.1056 | 534 | c.173 others(553): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
SIMC1_chr5_176233424_176350989 | 176305290 | C | CCAGCCAC others(527): Show |
intron_variant | MODIFIER | HG00733.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0260 | 1 | 360 | 0.0028 | 534 | c.173 others(553): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
SIMC1_chr5_176233424_176350989 | 176305290 | C | CCAGCCAC others(527): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0194 | 1 | 360 | 0.0028 | 534 | c.173 others(553): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
SIMC1_chr5_176233424_176350989 | 176305290 | C | CCAGCCAC others(527): Show |
intron_variant | MODIFIER | NA19009.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0250 | 1 | 360 | 0.0028 | 534 | c.173 others(553): Show |
SIMC1 | ENSG00000170085.18 | transcript | ENST00000429602.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
SLC6A3_chr5_1387794_1450440 | 1414424 | A | AGAAGGCA others(527): Show |
intron_variant | MODIFIER | NA18964.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0269 | 1 | 373 | 0.0027 | 534 | c.115 others(551): Show |
SLC6A3 | ENSG00000142319.18 | transcript | ENST00000270349.12 | protein_coding | 8/14 | chr5 | TogoVar | ||||||
SLC6A3_chr5_1387794_1450440 | 1423008 | A | ACGGTGCT others(527): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0006 | a0001c0006t0005 | a0001c0006t0005g0177 | 1 | 373 | 0.0027 | 534 | c.654 others(549): Show |
SLC6A3 | ENSG00000142319.18 | transcript | ENST00000270349.12 | protein_coding | 4/14 | chr5 | TogoVar | ||||||
SMIM36_chr17_55444856_55516452 | 55501087 | A | ATATTATA others(527): Show |
intron_variant | MODIFIER | NA19003.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0260 | 1 | 340 | 0.0029 | 534 | c.*17 others(553): Show |
SMIM36 | ENSG00000261873.3 | transcript | ENST00000636752.2 | protein_coding | 1/4 | chr17 | TogoVar | ||||||
SNX9_chr6_157818246_157950077 | 157827089 | C | CATATATT others(527): Show |
intron_variant | MODIFIER | NA19089.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0121 | 1 | 302 | 0.0033 | 534 | c.12+ others(549): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
SPATC1L_chr21_46156160_46189459 | 46161029 | A | AAGGGGAA others(527): Show |
downstream_gene_variant | MODIFIER | NA18970.hp1 NA19007.hp2 NA19087.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 3 | 251 | 0.0120 | 534 | c.*34 others(543): Show |
SPATC1L | ENSG00000160284.15 | transcript | ENST00000291672.6 | protein_coding | 130 | chr21 | TogoVar | ||||||
SPATC1L_chr21_46156160_46189459 | 46161029 | A | AAGGGGAA others(527): Show |
downstream_gene_variant | MODIFIER | NA18954.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0106 | 1 | 251 | 0.0040 | 534 | c.*34 others(543): Show |
SPATC1L | ENSG00000160284.15 | transcript | ENST00000291672.6 | protein_coding | 130 | chr21 | TogoVar | ||||||
SRXN1_chr20_641615_658200 | 642230 | T | TGGGGGGG others(527): Show |
downstream_gene_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0088 | 1 | 422 | 0.0024 | 534 | c.*64 others(545): Show |
SRXN1 | ENSG00000271303.2 | transcript | ENST00000381962.4 | protein_coding | 4384 | chr20 | TogoVar | ||||||
SULF2_chr20_47652406_47790481 | 47670707 | G | GGGGGTGG others(527): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0002 | a0001c0002t0011 | a0001c0002t0011g0002 | 1 | 364 | 0.0028 | 534 | c.157 others(553): Show |
SULF2 | ENSG00000196562.16 | transcript | ENST00000688720.1 | protein_coding | 11/20 | chr20 | TogoVar | ||||||
TBC1D22A_chr22_46757650_47180693 | 47128195 | T | TCCCTCCA others(527): Show |
intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0035 | 1 | 112 | 0.0089 | 534 | c.142 others(555): Show |
TBC1D22A | ENSG00000054611.14 | transcript | ENST00000337137.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
TBCD_chr17_82747065_82950914 | 82849190 | T | TCCACCTC others(527): Show |
intron_variant | MODIFIER | HG03130.hp2 HG03225.hp2 |
a0002 | a0002c0012 | a0002c0012t0008 | a0002c0012t0008g0170a0002c0012t0008g0171 | 2 | 318 | 0.0063 | 534 | c.131 others(555): Show |
TBCD | ENSG00000141556.22 | transcript | ENST00000355528.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
TBCD_chr17_82747065_82950914 | 82849190 | T | TCCACCTC others(527): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0020 | a0020c0042 | a0020c0042t0044 | a0020c0042t0044g0137 | 1 | 318 | 0.0031 | 534 | c.131 others(555): Show |
TBCD | ENSG00000141556.22 | transcript | ENST00000355528.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
TCF3_chr19_1604292_1657615 | 1628013 | A | ACGGGGTG others(527): Show |
intron_variant | MODIFIER | HG02135.hp2 | a0003 | a0003c0006 | a0003c0006t0002 | a0003c0006t0002g0150 | 1 | 352 | 0.0028 | 534 | c.299 others(549): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | TogoVar | ||||||
TCF3_chr19_1604292_1657615 | 1628734 | A | ACGGGGGT others(527): Show |
intron_variant | MODIFIER | HG01256.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0216 | 1 | 352 | 0.0028 | 534 | c.299 others(551): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | TogoVar | ||||||
TMEM255B_chr13_113754226_113821995 | 113816252 | G | GGGGAGAC others(527): Show |
3_prime_UTR_variant | MODIFIER | HG02004.hp2 | a0001 | a0001c0001 | a0001c0001t0116 | a0001c0001t0116g0074 | 1 | 260 | 0.0039 | 534 | c.*43 others(545): Show |
TMEM255B | ENSG00000184497.13 | transcript | ENST00000375353.5 | protein_coding | 9/9 | 4355 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||
TMEM255B_chr13_113754226_113821995 | 113816264 | G | GTGTTCGC others(527): Show |
3_prime_UTR_variant | MODIFIER | HG03704.hp2 | a0001 | a0001c0001 | a0001c0001t0107 | a0001c0001t0107g0210 | 1 | 260 | 0.0039 | 534 | c.*43 others(545): Show |
TMEM255B | ENSG00000184497.13 | transcript | ENST00000375353.5 | protein_coding | 9/9 | 4367 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||
TUBB2B_chr6_3219277_3232653 | 3222038 | C | CCACCACC others(527): Show |
downstream_gene_variant | MODIFIER | HG02818.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0016 | 1 | 360 | 0.0028 | 534 | c.*27 others(545): Show |
TUBB2B | ENSG00000137285.11 | transcript | ENST00000259818.8 | protein_coding | 2238 | chr6 | TogoVar | ||||||
TUBB2B_chr6_3219277_3232653 | 3222288 | T | TCACCATC others(527): Show |
downstream_gene_variant | MODIFIER | NA18947.hp2 NA18971.hp1 NA18983.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 3 | 360 | 0.0083 | 534 | c.*24 others(545): Show |
TUBB2B | ENSG00000137285.11 | transcript | ENST00000259818.8 | protein_coding | 1988 | chr6 | TogoVar | ||||||
ULK1_chr12_131889622_131928150 | 131917219 | C | CGGGTTCG others(527): Show |
intron_variant | MODIFIER | NA18975.hp2 | a0001 | a0001c0003 | a0001c0003t0007 | a0001c0003t0007g0226 | 1 | 344 | 0.0029 | 534 | c.218 others(551): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
UNC5D_chr8_35230475_35801540 | 35509493 | T | TCTCCCTC others(527): Show |
intron_variant | MODIFIER | HG02976.hp2 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0033 | 1 | 64 | 0.0156 | 534 | c.104 others(553): Show |
UNC5D | ENSG00000156687.11 | transcript | ENST00000404895.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
UNC5D_chr8_35230475_35801540 | 35509498 | T | TCTCCTCT others(527): Show |
intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0022 | 1 | 64 | 0.0156 | 534 | c.104 others(553): Show |
UNC5D | ENSG00000156687.11 | transcript | ENST00000404895.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
WDR64_chr1_241647281_241807777 | 241675123 | C | CCTTCCTT others(527): Show |
intron_variant | MODIFIER | NA18977.hp1 NA19058.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0164a0001c0002t0002g0195 | 2 | 326 | 0.0061 | 534 | c.483 others(549): Show |
WDR64 | ENSG00000162843.18 | transcript | ENST00000437684.7 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
WDR64_chr1_241647281_241807777 | 241675123 | C | CCTTCCTT others(527): Show |
intron_variant | MODIFIER | HG00558.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0284 | 1 | 326 | 0.0031 | 534 | c.483 others(549): Show |
WDR64 | ENSG00000162843.18 | transcript | ENST00000437684.7 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
WDR64_chr1_241647281_241807777 | 241675123 | C | CCTTCCTT others(527): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0007 | 1 | 326 | 0.0031 | 534 | c.483 others(549): Show |
WDR64 | ENSG00000162843.18 | transcript | ENST00000437684.7 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
WDR64_chr1_241647281_241807777 | 241675123 | C | CCTTCCTT others(527): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0312 | 1 | 326 | 0.0031 | 534 | c.483 others(549): Show |
WDR64 | ENSG00000162843.18 | transcript | ENST00000437684.7 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
WDR64_chr1_241647281_241807777 | 241675123 | C | CCTTCCTT others(527): Show |
intron_variant | MODIFIER | NA18977.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0198 | 1 | 326 | 0.0031 | 534 | c.483 others(549): Show |
WDR64 | ENSG00000162843.18 | transcript | ENST00000437684.7 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ACAP3_chr1_1287391_1312930 | 1289847 | G | GAGTCTCT others(528): Show |
downstream_gene_variant | MODIFIER | HG03927.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0032 | 1 | 295 | 0.0034 | 535 | c.*37 others(546): Show |
ACAP3 | ENSG00000131584.19 | transcript | ENST00000354700.10 | protein_coding | 2543 | chr1 | TogoVar | ||||||
ADPRHL1_chr13_113394611_113458488 | 113418984 | C | CTCCCTCC others(528): Show |
intron_variant | MODIFIER | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0020a0002c0002t0065a0002c0002t0068 | a0002c0002t0020g0065a0002c0002t0020g0220a0002c0002t0065g0219others(1): Show | 4 | 262 | 0.0153 | 535 | c.106 others(554): Show |
ADPRHL1 | ENSG00000153531.15 | transcript | ENST00000612156.3 | protein_coding | 7/7 | chr13 | TogoVar | ||||||
ADPRHL1_chr13_113394611_113458488 | 113419010 | C | CCCTCCCT others(528): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0002 | a0002c0002 | a0002c0002t0067 | a0002c0002t0067g0068 | 1 | 262 | 0.0038 | 535 | c.106 others(554): Show |
ADPRHL1 | ENSG00000153531.15 | transcript | ENST00000612156.3 | protein_coding | 7/7 | chr13 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97251792 | G | GGGAAGGG others(528): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0140 | 1 | 242 | 0.0041 | 535 | c.927 others(552): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144687797 | C | CCGTGACC others(528): Show |
upstream_gene_variant | MODIFIER | NA19087.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0047 | 1 | 246 | 0.0041 | 535 | c.-21 others(546): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1952 | chr8 | TogoVar |