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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
FARP2_chr2_241351285_241499841 | 241457540 | G | GCACTAAG others(722): Show |
intron_variant | MODIFIER | HG00639.hp1 HG01175.hp2 HG01981.hp1 others(2): Show |
a0002a0017 | a0002c0002a0017c0017 | a0002c0002t0001a0017c0017t0001 | a0002c0002t0001g0254a0002c0002t0001g0260a0002c0002t0001g0261others(2): Show | 5 | 378 | 0.0132 | 729 | c.158 others(746): Show |
FARP2 | ENSG00000006607.14 | transcript | ENST00000264042.8 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
FHIT_chr3_59742277_61256452 | 60861215 | T | TATATGAT others(722): Show |
intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0010 | 1 | 46 | 0.0217 | 729 | c.-11 others(750): Show |
FHIT | ENSG00000189283.11 | transcript | ENST00000492590.6 | protein_coding | 3/9 | chr3 | TogoVar | ||||||
FMR1NB_chrX_147976337_148031665 | 147992469 | C | CCCCCCCC others(722): Show |
intron_variant | MODIFIER | NA18955.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0080 | 1 | 275 | 0.0036 | 729 | c.278 others(748): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
FTCD_chr21_46131779_46160579 | 46144485 | T | TCCCCTTT others(722): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0004 | a0004c0008 | a0004c0008t0001 | a0004c0008t0001g0168 | 1 | 230 | 0.0044 | 729 | c.126 others(746): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | TogoVar | ||||||
FTCD_chr21_46131779_46160579 | 46144485 | T | TCCCCTTT others(722): Show |
intron_variant | MODIFIER | HG02615.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0003 | a0001c0002t0001g0109a0001c0002t0001g0112a0001c0003t0003g0110others(1): Show | 4 | 230 | 0.0174 | 729 | c.126 others(746): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | TogoVar | ||||||
FTCD_chr21_46131779_46160579 | 46144485 | T | TCCCCTTT others(722): Show |
intron_variant | MODIFIER | HG00140.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0169 | 1 | 230 | 0.0044 | 729 | c.126 others(746): Show |
FTCD | ENSG00000160282.15 | transcript | ENST00000397746.8 | protein_coding | 10/13 | chr21 | TogoVar | ||||||
GAL3ST2_chr2_241771822_241809287 | 241807935 | T | TCCCCCCT others(722): Show |
downstream_gene_variant | MODIFIER | HG00642.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 314 | 0.0032 | 729 | c.*37 others(740): Show |
GAL3ST2 | ENSG00000154252.12 | transcript | ENST00000192314.7 | protein_coding | 3649 | chr2 | TogoVar | ||||||
GAS6_chr13_113815549_113869076 | 113824259 | C | CGGTCTGG others(722): Show |
intron_variant | MODIFIER | HG02135.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0034 | 1 | 143 | 0.0070 | 729 | c.147 others(746): Show |
GAS6 | ENSG00000183087.15 | transcript | ENST00000327773.7 | protein_coding | 12/14 | chr13 | TogoVar | ||||||
GRINA_chr8_143985056_143998415 | 143988242 | T | TGGGTTCA others(722): Show |
upstream_gene_variant | MODIFIER | NA19083.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0002 | 1 | 352 | 0.0028 | 729 | c.-19 others(740): Show |
GRINA | ENSG00000178719.17 | transcript | ENST00000395068.9 | protein_coding | 1813 | chr8 | TogoVar | ||||||
HNF4A_chr20_44350699_44437845 | 44404776 | T | TGTGTTTG others(722): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02451.hp1 HG02965.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0017a0001c0001t0047a0001c0001t0048 | a0001c0001t0017g0207a0001c0001t0017g0209a0001c0001t0017g0314others(2): Show | 5 | 322 | 0.0155 | 729 | c.50- others(744): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ICA1_chr7_8108184_8267167 | 8152796 | T | TCCACCAC others(722): Show |
intron_variant | MODIFIER | NA18954.hp1 NA18999.hp1 NA19056.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0018a0001c0001t0004g0172a0001c0001t0004g0173 | 3 | 274 | 0.0110 | 729 | c.804 others(746): Show |
ICA1 | ENSG00000003147.19 | transcript | ENST00000402384.8 | protein_coding | 8/13 | chr7 | TogoVar | ||||||
IFNAR1_chr21_33319970_33364864 | 33322909 | T | TAATATAT others(722): Show |
upstream_gene_variant | MODIFIER | NA19070.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 323 | 0.0031 | 729 | c.-21 others(740): Show |
IFNAR1 | ENSG00000142166.15 | transcript | ENST00000270139.8 | protein_coding | 2060 | chr21 | TogoVar | ||||||
IFT140_chr16_1505427_1617072 | 1599452 | G | GCCGTCCG others(722): Show |
intron_variant | MODIFIER | NA18941.hp1 NA18959.hp2 NA19079.hp1 others(1): Show |
a0002a0019a0020 | a0002c0003a0019c0033a0020c0035 | a0002c0003t0003a0019c0033t0003a0020c0035t0003 | a0002c0003t0003g0007a0002c0003t0003g0009a0019c0033t0003g0018others(1): Show | 4 | 334 | 0.0120 | 729 | c.369 others(746): Show |
IFT140 | ENSG00000187535.14 | transcript | ENST00000426508.7 | protein_coding | 4/30 | chr16 | TogoVar | ||||||
IQCB1_chr3_121764761_121840060 | 121786167 | T | TAAGAAAG others(722): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0138 | 1 | 308 | 0.0033 | 729 | c.127 others(748): Show |
IQCB1 | ENSG00000173226.17 | transcript | ENST00000310864.11 | protein_coding | 12/14 | chr3 | TogoVar | ||||||
KRT82_chr12_52388931_52411335 | 52409039 | T | TCCTCTCC others(722): Show |
upstream_gene_variant | MODIFIER | NA19004.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0001 | 1 | 370 | 0.0027 | 729 | c.-27 others(740): Show |
KRT82 | ENSG00000161850.3 | transcript | ENST00000257974.3 | protein_coding | 2705 | chr12 | TogoVar | ||||||
KRT82_chr12_52388931_52411335 | 52409039 | T | TCCTCTCC others(722): Show |
upstream_gene_variant | MODIFIER | HG00735.hp2 HG01943.hp2 HG01952.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0001 | 3 | 370 | 0.0081 | 729 | c.-27 others(740): Show |
KRT82 | ENSG00000161850.3 | transcript | ENST00000257974.3 | protein_coding | 2705 | chr12 | TogoVar | ||||||
KRT82_chr12_52388931_52411335 | 52409039 | T | TCCTCTCC others(722): Show |
upstream_gene_variant | MODIFIER | NA18955.hp2 NA19088.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0001 | a0001c0001t0002g0001a0002c0002t0001g0003 | 2 | 370 | 0.0054 | 729 | c.-27 others(740): Show |
KRT82 | ENSG00000161850.3 | transcript | ENST00000257974.3 | protein_coding | 2705 | chr12 | TogoVar | ||||||
LAMA5_chr20_62304065_62372312 | 62349805 | T | TGGCGGTG others(722): Show |
intron_variant | MODIFIER | HG01175.hp2 | a0000 | a0000c0096 | a0000c0096t0002 | a0000c0096t0002g0089 | 1 | 186 | 0.0054 | 729 | c.956 others(746): Show |
LAMA5 | ENSG00000130702.15 | transcript | ENST00000252999.7 | protein_coding | 6/79 | chr20 | TogoVar | ||||||
LHPP_chr10_124456823_124619141 | 124610989 | C | CGGGTGAG others(722): Show |
intron_variant | MODIFIER | HG00099.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0191 | 1 | 260 | 0.0039 | 729 | c.717 others(746): Show |
LHPP | ENSG00000107902.14 | transcript | ENST00000368842.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
MICAL3_chr22_17782649_18029561 | 17876951 | G | GTTAGGGA others(722): Show |
intron_variant | MODIFIER | HG02523.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033 | 1 | 274 | 0.0037 | 729 | c.224 others(748): Show |
MICAL3 | ENSG00000243156.9 | transcript | ENST00000441493.7 | protein_coding | 16/31 | chr22 | TogoVar | ||||||
MICAL3_chr22_17782649_18029561 | 17877288 | T | TGGAGGTT others(722): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0004 | a0004c0007 | a0004c0007t0005 | a0004c0007t0005g0204 | 1 | 274 | 0.0037 | 729 | c.224 others(748): Show |
MICAL3 | ENSG00000243156.9 | transcript | ENST00000441493.7 | protein_coding | 16/31 | chr22 | TogoVar | ||||||
MICAL3_chr22_17782649_18029561 | 17877441 | G | GGGAGGTT others(722): Show |
intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0080 | 1 | 274 | 0.0037 | 729 | c.224 others(748): Show |
MICAL3 | ENSG00000243156.9 | transcript | ENST00000441493.7 | protein_coding | 16/31 | chr22 | TogoVar | ||||||
NEU4_chr2_241804193_241822413 | 241807935 | T | TCCCCCCT others(722): Show |
upstream_gene_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0055 | 1 | 319 | 0.0031 | 729 | c.-13 others(740): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 1257 | chr2 | TogoVar | ||||||
NKAIN2_chr6_123798865_124830640 | 124687566 | T | TATATTCC others(722): Show |
intron_variant | MODIFIER | HG02602.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0043 | 1 | 66 | 0.0152 | 729 | c.474 others(748): Show |
NKAIN2 | ENSG00000188580.16 | transcript | ENST00000368417.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
NXN_chr17_794310_984776 | 841624 | G | GGGCGAGC others(722): Show |
intron_variant | MODIFIER | HG04199.hp2 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0002 | 1 | 242 | 0.0041 | 729 | c.361 others(748): Show |
NXN | ENSG00000167693.17 | transcript | ENST00000336868.8 | protein_coding | 1/7 | chr17 | TogoVar | ||||||
NXN_chr17_794310_984776 | 948839 | C | CCCCGCGG others(722): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0006 | a0001c0006t0005 | a0001c0006t0005g0080 | 1 | 242 | 0.0041 | 729 | c.360 others(748): Show |
NXN | ENSG00000167693.17 | transcript | ENST00000336868.8 | protein_coding | 1/7 | chr17 | TogoVar | ||||||
PCDH15_chr10_53797771_54806231 | 54332334 | A | ATATTATT others(722): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 1 | 102 | 0.0098 | 729 | c.595 others(746): Show |
PCDH15 | ENSG00000150275.20 | transcript | ENST00000644397.2 | protein_coding | 6/37 | chr10 | TogoVar | ||||||
PCDH15_chr10_53816099_54806231 | 54332334 | A | ATATTATT others(722): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 1 | 94 | 0.0106 | 729 | c.595 others(746): Show |
PCDH15 | ENSG00000150275.20 | transcript | ENST00000320301.11 | protein_coding | 6/32 | chr10 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984158 | T | TAACCACC others(722): Show |
intron_variant | MODIFIER | HG02723.hp2 HG03130.hp1 |
a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0160a0001c0004t0005g0161 | 2 | 300 | 0.0067 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0219 | 1 | 300 | 0.0033 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG02717.hp2 HG03041.hp1 HG03486.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0017 | a0001c0001t0001a0001c0001t0004a0001c0002t0006others(1): Show | a0001c0001t0001g0032a0001c0001t0001g0107a0001c0001t0004g0176others(2): Show | 5 | 300 | 0.0167 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG01934.hp2 HG02109.hp2 |
a0001 | a0001c0002 | a0001c0002t0009 | a0001c0002t0009g0004a0001c0002t0009g0005 | 2 | 300 | 0.0067 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG01106.hp2 HG04228.hp2 |
a0002 | a0002c0003 | a0002c0003t0012 | a0002c0003t0012g0220a0002c0003t0012g0221 | 2 | 300 | 0.0067 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG02572.hp2 NA19240.hp2 |
a0001 | a0001c0002 | a0001c0002t0006a0001c0002t0016 | a0001c0002t0006g0236a0001c0002t0016g0003 | 2 | 300 | 0.0067 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0222 | 1 | 300 | 0.0033 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02486.hp2 HG02622.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0016a0001c0002t0008a0001c0002t0009others(1): Show | a0001c0001t0016g0020a0001c0002t0008g0021a0001c0002t0009g0022others(1): Show | 4 | 300 | 0.0133 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00597.hp1 HG02523.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0034 | a0001c0001t0001g0213a0001c0001t0002g0184a0001c0001t0002g0192others(2): Show | 5 | 300 | 0.0167 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG02970.hp1 HG04228.hp1 |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0037a0002c0007t0009 | a0001c0001t0037g0066a0002c0007t0009g0001 | 2 | 300 | 0.0067 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | NA18980.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0085 | 1 | 300 | 0.0033 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG01255.hp2 HG02602.hp2 HG03927.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(1): Show | a0001c0001t0001g0199a0001c0001t0002g0200a0001c0001t0008g0024others(1): Show | 4 | 300 | 0.0133 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG00423.hp2 HG01099.hp2 HG01167.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0040a0001c0001t0001g0262a0001c0001t0001g0263others(9): Show | 12 | 300 | 0.0400 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0002 | a0001c0002t0036 | a0001c0002t0036g0240 | 1 | 300 | 0.0033 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0002 | a0002c0003 | a0002c0003t0011 | a0002c0003t0011g0237 | 1 | 300 | 0.0033 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | NA18944.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0196 | 1 | 300 | 0.0033 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF21B_chr22_44876162_45015005 | 44984159 | C | CACCACCA others(722): Show |
intron_variant | MODIFIER | HG02976.hp2 | a0002 | a0002c0007 | a0002c0007t0005 | a0002c0007t0005g0234 | 1 | 300 | 0.0033 | 729 | c.120 others(748): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PLCB1_chr20_8127266_8889900 | 8662119 | T | TAATTATA others(722): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0018 | a0001c0018t0017 | a0001c0018t0017g0018 | 1 | 106 | 0.0094 | 729 | c.862 others(746): Show |
PLCB1 | ENSG00000182621.19 | transcript | ENST00000338037.11 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
PLEKHG4B_chr5_87168_194966 | 141104 | C | CCCCCTGC others(722): Show |
intron_variant | MODIFIER | HG04204.hp2 | a0004 | a0004c0006 | a0004c0006t0125 | a0004c0006t0125g0048 | 1 | 210 | 0.0048 | 729 | c.147 others(746): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2124224 | C | CGGCTATA others(722): Show |
intron_variant | MODIFIER | NA18967.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069 | 1 | 286 | 0.0035 | 729 | c.335 others(748): 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(722): Show |
upstream_gene_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0250 | 1 | 374 | 0.0027 | 729 | c.-46 others(740): Show |
PWWP2B | ENSG00000171813.14 | transcript | ENST00000305233.6 | protein_coding | 4635 | chr10 | TogoVar | ||||||
ROBO2_chr3_77035099_77654964 | 77323064 | T | TATATTAT others(722): Show |
intron_variant | MODIFIER | NA18959.hp2 NA19077.hp2 |
a0001 | a0001c0002 | a0001c0002t0010 | a0001c0002t0010g0037a0001c0002t0010g0144 | 2 | 160 | 0.0125 | 729 | c.389 others(750): Show |
ROBO2 | ENSG00000185008.19 | transcript | ENST00000696593.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr3 | TogoVar |