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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CLPTM1L_chr5_1312752_1350099 | 1333251 | C | CGGATGAG others(975): Show |
intron_variant | MODIFIER | HG00733.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0297 | 1 | 370 | 0.0027 | 982 | c.891 others(999): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | ||||||
CLPTM1L_chr5_1312752_1350099 | 1333251 | C | CGGATGAG others(975): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01255.hp1 HG01358.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0299others(2): Show | 5 | 370 | 0.0135 | 982 | c.891 others(999): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | ||||||
CLPTM1L_chr5_1312752_1350099 | 1333251 | C | CGGATGAG others(975): Show |
intron_variant | MODIFIER | HG00544.hp1 HG00609.hp2 HG00621.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0248a0001c0001t0001g0256others(7): Show | 13 | 370 | 0.0351 | 982 | c.891 others(999): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | ||||||
CLPTM1L_chr5_1312752_1350099 | 1333251 | C | CGGATGAG others(975): Show |
intron_variant | MODIFIER | NA18955.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0287 | 1 | 370 | 0.0027 | 982 | c.891 others(999): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | ||||||
CNST_chr1_246561456_246673595 | 246613656 | T | TCTCTCCC others(975): Show |
intron_variant | MODIFIER | NA18978.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0112 | 1 | 320 | 0.0031 | 982 | c.380 others(999): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CNST_chr1_246561456_246673595 | 246613656 | T | TCTCTCCC others(975): Show |
intron_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0067 | 1 | 320 | 0.0031 | 982 | c.380 others(999): Show |
CNST | ENSG00000162852.14 | transcript | ENST00000366513.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ELL_chr19_18437663_18527070 | 18442449 | A | ACACACCC others(975): Show |
downstream_gene_variant | MODIFIER | HG00735.hp2 HG01433.hp2 HG02004.hp2 |
a0001a0003 | a0001c0001a0003c0006 | a0001c0001t0001a0003c0006t0001 | a0001c0001t0001g0222a0001c0001t0001g0238a0003c0006t0001g0221 | 3 | 244 | 0.0123 | 982 | c.*23 others(993): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 213 | chr19 | TogoVar | ||||||
ELL_chr19_18437663_18527070 | 18442449 | A | ACACACCC others(975): Show |
downstream_gene_variant | MODIFIER | HG03654.hp1 | a0003 | a0003c0006 | a0003c0006t0001 | a0003c0006t0001g0226 | 1 | 244 | 0.0041 | 982 | c.*23 others(993): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 213 | chr19 | TogoVar | ||||||
FBXL14_chr12_1560993_1599581 | 1574458 | C | CGTGTGGG others(975): Show |
intron_variant | MODIFIER | HG02258.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0263 | 1 | 418 | 0.0024 | 982 | c.119 others(1001): Show |
FBXL14 | ENSG00000171823.7 | transcript | ENST00000339235.4 | protein_coding | 1/1 | chr12 | TogoVar | ||||||
IFNAR1_chr21_33319970_33364864 | 33322909 | T | TAATATAT others(975): Show |
upstream_gene_variant | MODIFIER | HG03130.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039 | 1 | 323 | 0.0031 | 982 | c.-21 others(993): Show |
IFNAR1 | ENSG00000142166.15 | transcript | ENST00000270139.8 | protein_coding | 2060 | chr21 | TogoVar | ||||||
IQSEC3_chr12_61767_183455 | 103629 | G | GGGGGAGG others(975): Show |
intron_variant | MODIFIER | NA19004.hp1 | a0001 | a0001c0006 | a0001c0006t0002 | a0001c0006t0002g0092 | 1 | 282 | 0.0036 | 982 | c.623 others(999): Show |
IQSEC3 | ENSG00000120645.12 | transcript | ENST00000538872.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ISYNA1_chr19_18429388_18443133 | 18442449 | A | ACACACCC others(975): Show |
upstream_gene_variant | MODIFIER | NA18955.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0002 | 1 | 308 | 0.0033 | 982 | c.-43 others(993): Show |
ISYNA1 | ENSG00000105655.19 | transcript | ENST00000338128.13 | protein_coding | 4317 | chr19 | TogoVar | ||||||
ISYNA1_chr19_18429388_18443133 | 18442449 | A | ACACACCC others(975): Show |
upstream_gene_variant | MODIFIER | HG01433.hp1 HG02004.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0002 | 2 | 308 | 0.0065 | 982 | c.-43 others(993): Show |
ISYNA1 | ENSG00000105655.19 | transcript | ENST00000338128.13 | protein_coding | 4317 | chr19 | TogoVar | ||||||
ISYNA1_chr19_18429388_18443133 | 18442449 | A | ACACACCC others(975): Show |
upstream_gene_variant | MODIFIER | HG03654.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0002 | 1 | 308 | 0.0033 | 982 | c.-43 others(993): Show |
ISYNA1 | ENSG00000105655.19 | transcript | ENST00000338128.13 | protein_coding | 4317 | chr19 | TogoVar | ||||||
ITGB5_chr3_124756948_124892365 | 124805580 | C | CAGCTGGG others(975): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0006 | a0001c0006t0002 | a0001c0006t0002g0131 | 1 | 352 | 0.0028 | 982 | c.126 others(1001): Show |
ITGB5 | ENSG00000082781.12 | transcript | ENST00000296181.9 | protein_coding | 9/14 | chr3 | TogoVar | ||||||
LARS1_chr5_146108034_146187650 | 146174593 | T | TATATATC others(975): Show |
intron_variant | MODIFIER | HG03490.hp1 HG03492.hp2 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0278a0002c0002t0002g0279 | 2 | 284 | 0.0070 | 982 | c.126 others(999): Show |
LARS1 | ENSG00000133706.20 | transcript | ENST00000394434.7 | protein_coding | 2/31 | chr5 | TogoVar | ||||||
MGAT5B_chr17_76863404_76955393 | 76925235 | G | GCCCTCCC others(975): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0002 | a0002c0006 | a0002c0006t0007 | a0002c0006t0007g0073 | 1 | 278 | 0.0036 | 982 | c.115 others(999): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
PKD1L3_chr16_71924538_72005402 | 71946837 | T | TGGGGAGA others(975): Show |
intron_variant | MODIFIER | HG02293.hp2 | a0005 | a0005c0003 | a0005c0003t0001 | a0005c0003t0001g0169 | 1 | 308 | 0.0033 | 982 | c.371 others(999): Show |
PKD1L3 | ENSG00000277481.2 | transcript | ENST00000620267.2 | protein_coding | 22/29 | chr16 | TogoVar | ||||||
PKD1L3_chr16_71924538_72005402 | 71946837 | T | TGGGGAGA others(975): Show |
intron_variant | MODIFIER | HG03654.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0079 | 1 | 308 | 0.0033 | 982 | c.371 others(999): Show |
PKD1L3 | ENSG00000277481.2 | transcript | ENST00000620267.2 | protein_coding | 22/29 | chr16 | TogoVar | ||||||
PKD1L3_chr16_71924538_72005402 | 71946837 | T | TGGGGAGA others(975): Show |
intron_variant | MODIFIER | NA18971.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0226 | 1 | 308 | 0.0033 | 982 | c.371 others(999): Show |
PKD1L3 | ENSG00000277481.2 | transcript | ENST00000620267.2 | protein_coding | 22/29 | chr16 | TogoVar | ||||||
RPTOR_chr17_80539838_80971368 | 80748289 | G | GGGGGCTG others(975): Show |
intron_variant | MODIFIER | HG02145.hp1 HG02559.hp1 HG06807.hp2 |
a0001 | a0001c0011a0001c0046a0001c0050 | a0001c0011t0024a0001c0046t0024a0001c0050t0007 | a0001c0011t0024g0147a0001c0046t0024g0164a0001c0050t0007g0148 | 3 | 196 | 0.0153 | 982 | c.655 others(999): Show |
RPTOR | ENSG00000141564.16 | transcript | ENST00000306801.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
SEL1L2_chr20_13844247_13995614 | 13934358 | C | CATATATA others(975): Show |
intron_variant | MODIFIER | NA18949.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0068 | 1 | 324 | 0.0031 | 982 | c.115 others(999): Show |
SEL1L2 | ENSG00000101251.13 | transcript | ENST00000284951.10 | protein_coding | 2/19 | chr20 | TogoVar | ||||||
SRXN1_chr20_641615_658200 | 642230 | T | TGGGGGGG others(975): Show |
downstream_gene_variant | MODIFIER | NA18995.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0006 | 1 | 422 | 0.0024 | 982 | c.*64 others(993): Show |
SRXN1 | ENSG00000271303.2 | transcript | ENST00000381962.4 | protein_coding | 4384 | chr20 | TogoVar | ||||||
STK24_chr13_98440185_98582107 | 98473274 | G | GGAGAGGA others(975): Show |
intron_variant | MODIFIER | HG03710.hp2 | a0001 | a0001c0001 | a0001c0001t0032 | a0001c0001t0032g0006 | 1 | 322 | 0.0031 | 982 | c.597 others(999): Show |
STK24 | ENSG00000102572.15 | transcript | ENST00000539966.6 | protein_coding | 5/10 | chr13 | TogoVar | ||||||
TAOK3_chr12_118144801_118377907 | 118295131 | A | ACCGGGTT others(975): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02647.hp2 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0256a0001c0001t0003g0257a0001c0001t0003g0261 | 3 | 314 | 0.0096 | 982 | c.-19 others(1003): Show |
TAOK3 | ENSG00000135090.14 | transcript | ENST00000392533.8 | protein_coding | 1/20 | chr12 | TogoVar | ||||||
TAOK3_chr12_118144801_118377907 | 118295133 | C | CGGGTTCA others(975): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(1): Show | a0001c0001t0001g0245a0001c0001t0003g0244a0001c0001t0003g0246others(15): Show | 18 | 314 | 0.0573 | 982 | c.-19 others(1003): Show |
TAOK3 | ENSG00000135090.14 | transcript | ENST00000392533.8 | protein_coding | 1/20 | chr12 | TogoVar | ||||||
TBCD_chr17_82747065_82950914 | 82764737 | T | TCTCATAG others(975): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
a0002a0005a0021 | a0002c0007a0002c0026a0005c0013others(1): Show | a0002c0007t0011a0002c0026t0008a0005c0013t0011others(1): Show | a0002c0007t0011g0237a0002c0026t0008g0236a0005c0013t0011g0234others(3): Show | 6 | 318 | 0.0189 | 982 | c.333 others(997): Show |
TBCD | ENSG00000141556.22 | transcript | ENST00000355528.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
TMPRSS2_chr21_41459305_41513158 | 41474530 | G | GGTGAAGG others(975): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0008 | a0001c0008t0001 | a0001c0008t0001g0066 | 1 | 382 | 0.0026 | 982 | c.728 others(999): Show |
TMPRSS2 | ENSG00000184012.14 | transcript | ENST00000332149.10 | protein_coding | 8/13 | chr21 | TogoVar | ||||||
TWIST2_chr2_238843085_238915534 | 238870692 | C | CCCCACAC others(975): Show |
intron_variant | MODIFIER | HG02155.hp1 HG02165.hp1 HG03834.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0042a0001c0001t0001g0048a0001c0001t0001g0049others(5): Show | 8 | 338 | 0.0237 | 982 | c.*35 others(1001): Show |
TWIST2 | ENSG00000233608.5 | transcript | ENST00000612363.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
UCKL1_chr20_63934829_63961416 | 63948630 | G | GAGGGGGT others(975): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0047 | 1 | 356 | 0.0028 | 982 | c.114 others(999): Show |
UCKL1 | ENSG00000198276.16 | transcript | ENST00000354216.11 | protein_coding | 1/14 | chr20 | TogoVar | ||||||
UCN3_chr10_5359966_5379692 | 5370472 | C | CGTGTGTG others(975): Show |
intron_variant | MODIFIER | HG03688.hp1 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0401 | 1 | 468 | 0.0021 | 982 | c.-6- others(997): Show |
UCN3 | ENSG00000178473.7 | transcript | ENST00000380433.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
WDR25_chr14_100371485_100535303 | 100526932 | A | ATCACCAC others(975): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0178 | 1 | 228 | 0.0044 | 982 | c.127 others(999): Show |
WDR25 | ENSG00000176473.14 | transcript | ENST00000402312.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ADAMTS3_chr4_72275969_72574221 | 72456228 | G | GTACTATA others(976): Show |
intron_variant | MODIFIER | NA18974.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0107 | 1 | 182 | 0.0055 | 983 | c.505 others(1002): Show |
ADAMTS3 | ENSG00000156140.11 | transcript | ENST00000286657.10 | protein_coding | 3/21 | chr4 | TogoVar | ||||||
ADAMTS3_chr4_72275969_72574221 | 72456228 | G | GTACTATA others(976): Show |
intron_variant | MODIFIER | HG00140.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0034 | 1 | 182 | 0.0055 | 983 | c.505 others(1002): Show |
ADAMTS3 | ENSG00000156140.11 | transcript | ENST00000286657.10 | protein_coding | 3/21 | chr4 | TogoVar | ||||||
ADAMTS3_chr4_72275969_72574221 | 72456228 | G | GTACTATA others(976): Show |
intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0040 | 1 | 182 | 0.0055 | 983 | c.505 others(1002): Show |
ADAMTS3 | ENSG00000156140.11 | transcript | ENST00000286657.10 | protein_coding | 3/21 | chr4 | TogoVar | ||||||
ADPRHL1_chr13_113394611_113458488 | 113412889 | G | GCTCGGTT others(976): Show |
intron_variant | MODIFIER | HG01074.hp2 | a0007 | a0007c0009 | a0007c0009t0011 | a0007c0009t0011g0116 | 1 | 262 | 0.0038 | 983 | c.106 others(1002): Show |
ADPRHL1 | ENSG00000153531.15 | transcript | ENST00000612156.3 | protein_coding | 7/7 | chr13 | TogoVar | ||||||
ADPRHL1_chr13_113394611_113458488 | 113412889 | G | GCTCGGTT others(976): Show |
intron_variant | MODIFIER | HG00099.hp2 | a0010 | a0010c0010 | a0010c0010t0010 | a0010c0010t0010g0145 | 1 | 262 | 0.0038 | 983 | c.106 others(1002): Show |
ADPRHL1 | ENSG00000153531.15 | transcript | ENST00000612156.3 | protein_coding | 7/7 | chr13 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | HG04204.hp2 | a0001 | a0001c0007 | a0001c0007t0003 | a0001c0007t0003g0118 | 1 | 246 | 0.0041 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
a0001 | a0001c0001a0001c0014 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | 246 | 0.0203 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | HG00558.hp1 NA18940.hp2 NA18997.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | 246 | 0.0203 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(8): Show |
a0001a0004 | a0001c0002a0001c0003a0001c0005others(2): Show | a0001c0002t0001a0001c0003t0001a0001c0003t0009others(4): Show | a0001c0002t0001g0013a0001c0003t0001g0005a0001c0003t0001g0012others(8): Show | 11 | 246 | 0.0447 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | NA18995.hp2 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0192 | 1 | 246 | 0.0041 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | NA18945.hp1 NA18999.hp1 NA19012.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0047others(1): Show | 4 | 246 | 0.0163 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(41): Show |
a0001 | a0001c0001a0001c0002a0001c0007others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(8): Show | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0030others(41): Show | 44 | 246 | 0.1789 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0160 | 1 | 246 | 0.0041 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(146): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0001t0001g0065others(146): Show | 149 | 246 | 0.6057 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016 | 1 | 246 | 0.0041 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | HG01081.hp1 | a0001 | a0001c0016 | a0001c0016t0001 | a0001c0016t0001g0091 | 1 | 246 | 0.0041 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | HG02258.hp1 HG03209.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0018 | a0001c0001t0003g0023a0001c0001t0018g0022 | 2 | 246 | 0.0081 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669258 | A | ACACTTTG others(976): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0134 | 1 | 246 | 0.0041 | 983 | c.-82 others(1002): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar |