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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARID2_chr12_45724706_45913037 | 45781372 | T | TTGGCCAG others(1022): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0185 | 1 | 8 | 0.1250 | 1029 | c.285 others(1048): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ARID2_chr12_45724706_45913037 | 45781372 | T | TTGGCCAG others(1022): Show |
intron_variant | MODIFIER | HG02896.hp1 HG02897.hp2 NA18969.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0147 a0001c0001t0001g0270 a0001c0001t0001g0291 others(1): Show |
4 | 11 | 0.3636 | 1029 | c.285 others(1048): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ARID2_chr12_45724706_45913037 | 45781372 | T | TTGGCCAG others(1022): Show |
intron_variant | MODIFIER | HG03669.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0279 | 1 | 8 | 0.1250 | 1029 | c.285 others(1048): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ARID2_chr12_45724706_45913037 | 45781372 | T | TTGGCCAG others(1022): Show |
intron_variant | MODIFIER | HG01358.hp1 NA20752.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0130 a0001c0001t0011g0118 |
2 | 9 | 0.2222 | 1029 | c.285 others(1048): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ARID2_chr12_45724706_45913037 | 45781372 | T | TTGGCCAG others(1022): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0189 | 1 | 8 | 0.1250 | 1029 | c.285 others(1048): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ARID2_chr12_45724706_45913037 | 45781372 | T | TTGGCCAG others(1022): Show |
intron_variant | MODIFIER | HG01975.hp2 NA18612.hp1 NA18747.hp1 others(3): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0004c0005t0001 | a0001c0001t0001g0089 a0001c0001t0001g0153 a0001c0001t0001g0163 others(3): Show |
6 | 13 | 0.4615 | 1029 | c.285 others(1048): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ARID2_chr12_45724706_45913037 | 45781372 | T | TTGGCCAG others(1022): Show |
intron_variant | MODIFIER | NA18944.hp1 NA18977.hp2 NA19072.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 a0001c0001t0001g0084 a0001c0001t0001g0152 others(1): Show |
4 | 11 | 0.3636 | 1029 | c.285 others(1048): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ARID2_chr12_45724706_45913037 | 45781372 | T | TTGGCCAG others(1022): Show |
intron_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0256 | 1 | 8 | 0.1250 | 1029 | c.285 others(1048): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ARID2_chr12_45724706_45913037 | 45781372 | T | TTGGCCAG others(1022): Show |
intron_variant | MODIFIER | HG03669.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0234 | 1 | 8 | 0.1250 | 1029 | c.285 others(1048): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
C10orf67_chr10_23197696_23349797 | 23331540 | A | AAGGGAAA others(1022): Show |
intron_variant | MODIFIER | HG01255.hp2 HG01257.hp2 HG01952.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0204 |
3 | 221 | 0.0136 | 1029 | c.327 others(1046): Show |
C10orf67 | ENSG00000179133.15 | transcript | ENST00000636213.3 | protein_coding | 2/15 | chr10 | TogoVar | |||||||
CFAP61_chr20_20047532_20365698 | 20320483 | A | ATATTATA others(1022): Show |
intron_variant | MODIFIER | NA18945.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0028 | 1 | 174 | 0.0057 | 1029 | c.342 others(1050): Show |
CFAP61 | ENSG00000089101.19 | transcript | ENST00000245957.10 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
CUX2_chr12_111029165_111355554 | 111326188 | G | GTTTTGTT others(1022): Show |
intron_variant | MODIFIER | HG01069.hp2 | a0003 | a0003c0015 | a0003c0015t0001 | a0003c0015t0001g0067 | 1 | 35 | 0.0286 | 1029 | c.292 others(1048): Show |
CUX2 | ENSG00000111249.14 | transcript | ENST00000261726.11 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
DPEP1_chr16_89608642_89643433 | 89619124 | C | CCCCCCCG others(1022): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0248 | 1 | 216 | 0.0046 | 1029 | c.-10 others(1048): Show |
DPEP1 | ENSG00000015413.10 | transcript | ENST00000690203.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
DPEP1_chr16_89608642_89643433 | 89619428 | C | CCCCCCCT others(1022): Show |
intron_variant | MODIFIER | NA19084.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0131 | 1 | 233 | 0.0043 | 1029 | c.-10 others(1048): Show |
DPEP1 | ENSG00000015413.10 | transcript | ENST00000690203.1 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
EML1_chr14_99788413_99947060 | 99928137 | G | GTGGTGGT others(1022): Show |
intron_variant | MODIFIER | HG02630.hp1 HG02976.hp2 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0008 a0001c0003t0001g0009 |
2 | 258 | 0.0078 | 1029 | c.190 others(1048): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
EML1_chr14_99788413_99947060 | 99928137 | G | GTGGTGGT others(1022): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0175 | 1 | 257 | 0.0039 | 1029 | c.190 others(1048): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
FAM234A_chr16_229821_271096 | 239175 | C | CTGTAGTC others(1022): Show |
intron_variant | MODIFIER | HG02818.hp2 | a0001 | a0001c0005 | a0001c0005t0002 | a0001c0005t0002g0131 | 1 | 137 | 0.0073 | 1029 | c.-14 others(1048): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
FAM234A_chr16_229821_271096 | 239175 | C | CTGTAGTC others(1022): Show |
intron_variant | MODIFIER | HG02027.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0059 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
5 | 141 | 0.0355 | 1029 | c.-14 others(1048): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
FAM234A_chr16_229821_271096 | 239175 | C | CTGTAGTC others(1022): Show |
intron_variant | MODIFIER | HG01123.hp1 NA18967.hp2 NA18978.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0012a0001c0002t0002 | a0001c0001t0001g0076 a0001c0001t0001g0107 a0001c0001t0001g0109 others(2): Show |
5 | 141 | 0.0355 | 1029 | c.-14 others(1048): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
FAM234A_chr16_229821_271096 | 239175 | C | CTGTAGTC others(1022): Show |
intron_variant | MODIFIER | NA18940.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0123 | 1 | 137 | 0.0073 | 1029 | c.-14 others(1048): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
FAM234A_chr16_229821_271096 | 239175 | C | CTGTAGTC others(1022): Show |
intron_variant | MODIFIER | HG00140.hp2 HG02698.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0099 a0001c0002t0002g0125 |
2 | 138 | 0.0145 | 1029 | c.-14 others(1048): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
GALNT9_chr12_132191372_132334589 | 132241523 | C | CCACACAC others(1022): Show |
intron_variant | MODIFIER | HG02004.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0139 | 1 | 142 | 0.0070 | 1029 | c.107 others(1048): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar | |||||||
HAUS2_chr15_42543838_42574994 | 42557411 | T | TATATTTT others(1022): Show |
intron_variant | MODIFIER | HG02559.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0040 | 1 | 132 | 0.0076 | 1029 | c.94- others(1042): Show |
HAUS2 | ENSG00000137814.12 | transcript | ENST00000260372.8 | protein_coding | 1/5 | chr15 | TogoVar | |||||||
LHFPL3_chr7_104323603_104913561 | 104824176 | A | ATATATAT others(1022): Show |
intron_variant | MODIFIER | NA18612.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0053 | 1 | 71 | 0.0141 | 1029 | c.683 others(1048): Show |
LHFPL3 | ENSG00000187416.13 | transcript | ENST00000424859.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
MED16_chr19_862963_898187 | 871818 | A | AGTGAGCG others(1022): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0035 | 1 | 51 | 0.0196 | 1029 | c.209 others(1046): Show |
MED16 | ENSG00000175221.16 | transcript | ENST00000325464.6 | protein_coding | 12/15 | chr19 | TogoVar | |||||||
NME8_chr7_37843597_37905397 | 37848245 | G | GGAGACGG others(1022): Show |
upstream_gene_variant | MODIFIER | HG02055.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0143 | 1 | 294 | 0.0034 | 1029 | c.-72 others(1038): Show |
NME8 | ENSG00000086288.12 | transcript | ENST00000199447.9 | protein_coding | 351 | chr7 | TogoVar | |||||||
PKHD1_chr6_51610299_52092613 | 51982220 | A | ATCCGGGA others(1022): Show |
intron_variant | MODIFIER | HG01243.hp2 HG02683.hp1 |
a0002a0019 | a0002c0004a0019c0089 | a0002c0004t0011a0019c0089t0002 | a0002c0004t0011g0101 a0019c0089t0002g0116 |
2 | 94 | 0.0213 | 1029 | c.575 others(1050): Show |
PKHD1 | ENSG00000170927.15 | transcript | ENST00000371117.8 | protein_coding | 35/66 | chr6 | TogoVar | |||||||
RIN3_chr14_92508781_92693994 | 92547356 | T | TATTATAA others(1022): Show |
intron_variant | MODIFIER | HG01358.hp2 HG02735.hp1 |
a0002a0005 | a0002c0002a0005c0006 | a0002c0002t0001a0005c0006t0001 | a0002c0002t0001g0179 a0005c0006t0001g0284 |
2 | 101 | 0.0198 | 1029 | c.45- others(1044): Show |
RIN3 | ENSG00000100599.16 | transcript | ENST00000216487.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
RIN3_chr14_92508781_92693994 | 92547356 | T | TATTATAA others(1022): Show |
intron_variant | MODIFIER | HG03704.hp2 | a0012 | a0012c0016 | a0012c0016t0002 | a0012c0016t0002g0297 | 1 | 100 | 0.0100 | 1029 | c.45- others(1044): Show |
RIN3 | ENSG00000100599.16 | transcript | ENST00000216487.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
RXRA_chr9_134321455_134445585 | 134394154 | G | GGTGATGG others(1022): Show |
intron_variant | MODIFIER | NA19080.hp2 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0104 | 1 | 3 | 0.3333 | 1029 | c.29- others(1044): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
RXRA_chr9_134321455_134445585 | 134394154 | G | GGTGATGG others(1022): Show |
intron_variant | MODIFIER | HG01074.hp2 HG01928.hp2 HG02165.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0029a0001c0001t0030 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0107 others(2): Show |
5 | 7 | 0.7143 | 1029 | c.29- others(1044): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
RXRA_chr9_134321455_134445585 | 134394154 | G | GGTGATGG others(1022): Show |
intron_variant | MODIFIER | HG01255.hp1 | a0001 | a0001c0001 | a0001c0001t0032 | a0001c0001t0032g0017 | 1 | 3 | 0.3333 | 1029 | c.29- others(1044): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
RXRA_chr9_134321455_134445585 | 134394154 | G | GGTGATGG others(1022): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0204 | 1 | 3 | 0.3333 | 1029 | c.29- others(1044): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SEL1L2_chr20_13844247_13995614 | 13934476 | C | CATATATA others(1022): Show |
intron_variant | MODIFIER | HG04228.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0039 | 1 | 39 | 0.0256 | 1029 | c.115 others(1046): Show |
SEL1L2 | ENSG00000101251.13 | transcript | ENST00000284951.10 | protein_coding | 2/19 | chr20 | TogoVar | |||||||
SYNE3_chr14_95402266_95521650 | 95419899 | G | GGTGGTGG others(1022): Show |
intron_variant | MODIFIER | HG03927.hp1 | a0006 | a0006c0089 | a0006c0089t0019 | a0006c0089t0019g0038 | 1 | 90 | 0.0111 | 1029 | c.272 others(1048): Show |
SYNE3 | ENSG00000176438.13 | transcript | ENST00000682763.1 | protein_coding | 17/17 | chr14 | TogoVar | |||||||
TAF4_chr20_61969798_62070881 | 62058768 | C | CGGGGGCC others(1022): Show |
intron_variant | MODIFIER | HG01952.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0222 | 1 | 237 | 0.0042 | 1029 | c.136 others(1048): Show |
TAF4 | ENSG00000130699.20 | transcript | ENST00000252996.9 | protein_coding | 1/14 | chr20 | TogoVar | |||||||
TAFA5_chr22_48484553_48756932 | 48620724 | A | ACCATCCC others(1022): Show |
intron_variant | MODIFIER | HG02258.hp1 HG06807.hp1 |
a0001 | a0001c0001 | a0001c0001t0018a0001c0001t0038 | a0001c0001t0018g0028 a0001c0001t0038g0196 |
2 | 29 | 0.0690 | 1029 | c.113 others(1048): Show |
TAFA5 | ENSG00000219438.9 | transcript | ENST00000402357.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TXNDC16_chr14_52425596_52557505 | 52530465 | T | TAATAATA others(1022): Show |
intron_variant | MODIFIER | NA19004.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 83 | 0.0120 | 1029 | c.392 others(1046): Show |
TXNDC16 | ENSG00000087301.9 | transcript | ENST00000281741.9 | protein_coding | 6/20 | chr14 | TogoVar | |||||||
U2AF2_chr19_55650035_55679716 | 55670449 | C | CCCGTGCA others(1022): Show |
intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0242 | 1 | 149 | 0.0067 | 1029 | c.129 others(1046): Show |
U2AF2 | ENSG00000063244.14 | transcript | ENST00000308924.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
U2AF2_chr19_55650035_55679716 | 55670466 | C | CCGTGCAC others(1022): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0295 | 1 | 277 | 0.0036 | 1029 | c.129 others(1046): Show |
U2AF2 | ENSG00000063244.14 | transcript | ENST00000308924.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
U2AF2_chr19_55650035_55679716 | 55670515 | C | CCCGTGCA others(1022): Show |
intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0278 | 1 | 385 | 0.0026 | 1029 | c.129 others(1046): Show |
U2AF2 | ENSG00000063244.14 | transcript | ENST00000308924.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
U2AF2_chr19_55650035_55679716 | 55670515 | C | CCCGTGCA others(1022): Show |
intron_variant | MODIFIER | HG02896.hp1 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0289 a0001c0001t0001g0291 |
2 | 386 | 0.0052 | 1029 | c.129 others(1046): Show |
U2AF2 | ENSG00000063244.14 | transcript | ENST00000308924.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
U2AF2_chr19_55650035_55679716 | 55670515 | C | CCCGTGCA others(1022): Show |
intron_variant | MODIFIER | NA19090.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0273 | 1 | 385 | 0.0026 | 1029 | c.129 others(1046): Show |
U2AF2 | ENSG00000063244.14 | transcript | ENST00000308924.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
VCX2_chrX_8164944_8176267 | 8169829 | T | TCCCTCCC others(1022): Show |
downstream_gene_variant | MODIFIER | NA20805.hp1 | a0019 | a0019c0018 | a0019c0018t0002 | a0019c0018t0002g0024 | 1 | 96 | 0.0104 | 1029 | c.*20 others(1038): Show |
VCX2 | ENSG00000177504.10 | transcript | ENST00000317103.5 | protein_coding | 114 | chrX | TogoVar | |||||||
VCX_chrX_7838171_7849143 | 7844275 | A | AGGGAGGG others(1022): Show |
downstream_gene_variant | MODIFIER | HG02559.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0001 | 1 | 282 | 0.0035 | 1029 | c.*25 others(1038): Show |
VCX | ENSG00000182583.13 | transcript | ENST00000688183.1 | protein_coding | 133 | chrX | TogoVar | |||||||
ARHGEF10L_chr1_17534698_17702869 | 17689462 | C | CCTCCCTC others(1023): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0011 | a0011c0025 | a0011c0025t0002 | a0011c0025t0002g0049 | 1 | 166 | 0.0060 | 1030 | c.318 others(1049): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1833035 | G | GAGAGACA others(1023): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0144 | a0001c0144t0052 | a0001c0144t0052g0339 | 1 | 74 | 0.0135 | 1030 | c.-48 others(1047): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARID2_chr12_45724706_45913037 | 45781372 | T | TTGGCCAG others(1023): Show |
intron_variant | MODIFIER | NA19088.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0172 | 1 | 8 | 0.1250 | 1030 | c.285 others(1049): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ARID2_chr12_45724706_45913037 | 45781372 | T | TTGGCCAG others(1023): Show |
intron_variant | MODIFIER | HG03831.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0137 | 1 | 8 | 0.1250 | 1030 | c.285 others(1049): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
ARID2_chr12_45724706_45913037 | 45781372 | T | TTGGCCAG others(1023): Show |
intron_variant | MODIFIER | HG01109.hp1 NA18952.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0158 a0001c0001t0001g0300 |
2 | 9 | 0.2222 | 1030 | c.285 others(1049): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | TogoVar |