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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
POLR3C_chr1_145819200_145849402 | 145842809 | A | AGATAGAT others(32): Show |
3_prime_UTR_variant | MODIFIER | HG01433.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0027a0001c0001t0032 | a0001c0001t0007g0008a0001c0001t0007g0054a0001c0001t0007g0055others(2): Show | 7 | 368 | 0.0190 | 39 | c.*39 others(48): Show |
POLR3C | ENSG00000186141.10 | transcript | ENST00000334163.4 | protein_coding | 15/15 | 398 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||
POTEC_chr18_14502339_14548600 | 14543600 | T | TGCGCGTG others(32): Show |
upstream_gene_variant | MODIFIER | HG01346.hp2 HG02135.hp1 HG02486.hp2 others(1): Show |
a0005a0006a0008others(1): Show | a0005c0005a0006c0008a0008c0010others(1): Show | a0005c0005t0005a0006c0008t0020a0008c0010t0014others(1): Show | a0005c0005t0005g0346a0006c0008t0020g0329a0008c0010t0014g0220others(1): Show | 4 | 388 | 0.0103 | 39 | c.-45 others(48): Show |
POTEC | ENSG00000183206.18 | transcript | ENST00000358970.10 | protein_coding | 1 | chr18 | TogoVar | ||||||
POTEC_chr18_14502339_14548600 | 14543632 | T | TGCGGGGC others(32): Show |
upstream_gene_variant | MODIFIER | NA19083.hp1 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0081 | 1 | 388 | 0.0026 | 39 | c.-48 others(48): Show |
POTEC | ENSG00000183206.18 | transcript | ENST00000358970.10 | protein_coding | 33 | chr18 | TogoVar | ||||||
POTEF_chr2_130068535_130134222 | 130071560 | A | AAGCTAGG others(32): Show |
downstream_gene_variant | MODIFIER | NA18979.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0138 | 1 | 165 | 0.0061 | 39 | c.*26 others(50): Show |
POTEF | ENSG00000196604.13 | transcript | ENST00000409914.7 | protein_coding | 1974 | chr2 | TogoVar | ||||||
POTEG_chr14_19397486_19439341 | 19434934 | C | CGCGCGTG others(32): Show |
upstream_gene_variant | MODIFIER | HG01071.hp2 HG01981.hp2 HG02647.hp1 others(1): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0002a0005c0007others(1): Show | a0001c0001t0001a0002c0002t0002a0005c0007t0003others(1): Show | a0001c0001t0001g0074a0002c0002t0002g0090a0005c0007t0003g0033others(1): Show | 4 | 111 | 0.0360 | 39 | c.-64 others(48): Show |
POTEG | ENSG00000187537.13 | transcript | ENST00000547848.5 | protein_coding | 594 | chr14 | TogoVar | ||||||
PP2D1_chr3_19980346_20017264 | 20012956 | G | GTATATAT others(32): Show |
upstream_gene_variant | MODIFIER | HG03710.hp1 | a0003 | a0003c0003 | a0003c0003t0004 | a0003c0003t0004g0165 | 1 | 396 | 0.0025 | 39 | c.-88 others(48): Show |
PP2D1 | ENSG00000183977.14 | transcript | ENST00000389050.5 | protein_coding | 693 | chr3 | TogoVar | ||||||
PPA2_chr4_105364077_105479062 | 105450601 | C | CTTTTTTT others(32): Show |
intron_variant | MODIFIER | HG01256.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0329 | 1 | 366 | 0.0027 | 39 | c.268 others(56): Show |
PPA2 | ENSG00000138777.20 | transcript | ENST00000341695.10 | protein_coding | 3/11 | chr4 | TogoVar | ||||||
PPARA_chr22_46145526_46248755 | 46205554 | A | ATATATAT others(32): Show |
intron_variant | MODIFIER | HG02109.hp1 | a0001 | a0001c0001 | a0001c0001t0026 | a0001c0001t0026g0152 | 1 | 200 | 0.0050 | 39 | c.208 others(56): Show |
PPARA | ENSG00000186951.17 | transcript | ENST00000407236.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
PPFIA1_chr11_70265690_70389396 | 70277060 | A | ATATATAT others(32): Show |
intron_variant | MODIFIER | NA19240.hp1 | a0001 | a0001c0005 | a0001c0005t0003 | a0001c0005t0003g0160 | 1 | 282 | 0.0036 | 39 | c.264 others(56): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
PPHLN1_chr12_42321167_42447181 | 42360110 | C | CAAAAAAA others(32): Show |
intron_variant | MODIFIER | HG01074.hp1 NA19058.hp2 NA20805.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0206 | 3 | 376 | 0.0080 | 39 | c.299 others(56): Show |
PPHLN1 | ENSG00000134283.18 | transcript | ENST00000358314.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
PPIL2_chr22_21661012_21702907 | 21682594 | G | GCTGCCTC others(32): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0002a0001c0001t0007a0001c0001t0015others(4): Show | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(68): Show | 98 | 378 | 0.2593 | 39 | c.477 others(52): Show |
PPIL2 | ENSG00000100023.20 | transcript | ENST00000398831.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
PPL_chr16_4877507_4942148 | 4920371 | G | GAAAGAAA others(32): Show |
intron_variant | MODIFIER | HG00639.hp2 HG00738.hp1 HG01074.hp2 others(13): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0007a0002c0016others(4): Show | a0001c0001t0001a0002c0007t0003a0002c0016t0009others(4): Show | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0180others(13): Show | 16 | 372 | 0.0430 | 39 | c.63- others(54): Show |
PPL | ENSG00000118898.16 | transcript | ENST00000345988.7 | protein_coding | 1/21 | chr16 | TogoVar | ||||||
PPM1E_chr17_58750854_58990179 | 58785458 | T | TATATATA others(32): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0210 | 1 | 312 | 0.0032 | 39 | c.464 others(58): Show |
PPM1E | ENSG00000175175.6 | transcript | ENST00000308249.4 | protein_coding | 1/6 | chr17 | TogoVar | ||||||
PPP1CB_chr2_28746830_28807940 | 28785065 | C | CTTTTTTT others(32): Show |
intron_variant | MODIFIER | HG03704.hp1 | a0001 | a0001c0002 | a0001c0002t0024 | a0001c0002t0024g0049 | 1 | 366 | 0.0027 | 39 | c.592 others(56): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
PPP1R16B_chr20_38800697_38928024 | 38855982 | A | AGAGAGAG others(32): Show |
intron_variant | MODIFIER | HG02165.hp1 HG03942.hp1 HG03942.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0003 | a0001c0001t0001g0232a0001c0002t0002g0024a0001c0002t0003g0018 | 3 | 244 | 0.0123 | 39 | c.250 others(58): Show |
PPP1R16B | ENSG00000101445.10 | transcript | ENST00000299824.6 | protein_coding | 2/10 | chr20 | TogoVar | ||||||
PPP2R2D_chr10_131896008_131964834 | 131952098 | A | AGGGGGGT others(32): Show |
intron_variant | MODIFIER | HG02165.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0149 | 1 | 394 | 0.0025 | 39 | c.108 others(58): Show |
PPP2R2D | ENSG00000175470.20 | transcript | ENST00000455566.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
PPP2R3B_chrX_328933_391907 | 339472 | G | GGGGGTGA others(32): Show |
intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0018 | 1 | 25 | 0.0400 | 39 | c.135 others(56): Show |
PPP2R3B | ENSG00000167393.18 | transcript | ENST00000390665.9 | protein_coding | 10/12 | chrX | TogoVar | ||||||
PPP2R5C_chr14_101756709_101932977 | 101918139 | A | ATTAAGTA others(32): Show |
intron_variant | MODIFIER | HG01243.hp1 HG01255.hp2 HG01258.hp1 others(22): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(4): Show | a0001c0001t0001g0096a0001c0001t0002g0028a0001c0001t0002g0029others(22): Show | 25 | 138 | 0.1812 | 39 | c.160 others(56): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
PPP2R5C_chr14_101756709_101932977 | 101924445 | C | CTTTTTTT others(32): Show |
intron_variant | MODIFIER | HG01433.hp1 HG02559.hp1 HG02735.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0007 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0040others(5): Show | 8 | 138 | 0.0580 | 39 | c.160 others(56): Show |
PPP2R5C | ENSG00000078304.20 | transcript | ENST00000694906.1 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
PPP3CA_chr4_101018418_101352526 | 101054554 | C | CCTTAGAA others(32): Show |
intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0142 | 1 | 192 | 0.0052 | 39 | c.115 others(58): Show |
PPP3CA | ENSG00000138814.17 | transcript | ENST00000394854.8 | protein_coding | 10/13 | chr4 | TogoVar | ||||||
PPP4R3A_chr14_91452508_91515310 | 91507418 | T | TATACTAT others(32): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0163 | 1 | 370 | 0.0027 | 39 | c.142 others(56): Show |
PPP4R3A | ENSG00000100796.18 | transcript | ENST00000554943.6 | protein_coding | 1/14 | chr14 | TogoVar | ||||||
PRAMEF14_chr1_13336892_13352134 | 13349251 | A | AGAAAGAA others(32): Show |
upstream_gene_variant | MODIFIER | NA19064.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0006 | 1 | 256 | 0.0039 | 39 | c.-22 others(50): Show |
PRAMEF14 | ENSG00000204481.8 | transcript | ENST00000334600.7 | protein_coding | 2118 | chr1 | TogoVar | ||||||
PRAMEF15_chr1_13310581_13327598 | 13327508 | T | TCCCGTCT others(32): Show |
downstream_gene_variant | MODIFIER | NA19078.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035 | 1 | 302 | 0.0033 | 39 | c.*52 others(50): Show |
PRAMEF15 | ENSG00000204501.7 | transcript | ENST00000376152.2 | protein_coding | 4911 | chr1 | TogoVar | ||||||
PRCC_chr1_156762535_156805815 | 156787650 | C | CTTTTTTT others(32): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0067 | 1 | 350 | 0.0029 | 39 | c.108 others(56): Show |
PRCC | ENSG00000143294.15 | transcript | ENST00000271526.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRCP_chr11_82817936_82905430 | 82841053 | A | AATATATA others(32): Show |
intron_variant | MODIFIER | HG00741.hp1 HG02145.hp2 HG02630.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0002a0001c0001t0011a0002c0003t0002 | a0001c0001t0002g0027a0001c0001t0011g0107a0001c0001t0011g0108others(4): Show | 7 | 320 | 0.0219 | 39 | c.922 others(56): Show |
PRCP | ENSG00000137509.12 | transcript | ENST00000313010.8 | protein_coding | 6/8 | chr11 | TogoVar | ||||||
PRDM16_chr1_3064203_3443621 | 3231375 | C | CCCGTCGT others(32): Show |
intron_variant | MODIFIER | HG01123.hp1 HG01255.hp1 HG02132.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0014 | a0001c0001t0001a0001c0001t0005a0001c0002t0001others(6): Show | a0001c0001t0001g0179a0001c0001t0005g0184a0001c0002t0001g0210others(6): Show | 9 | 210 | 0.0429 | 39 | c.388 others(58): Show |
PRDM16 | ENSG00000142611.17 | transcript | ENST00000270722.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRDM16_chr1_3064203_3443621 | 3231385 | T | TGGACAGC others(32): Show |
intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(54): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0055a0001c0001t0001g0119a0001c0001t0001g0125others(54): Show | 57 | 210 | 0.2714 | 39 | c.388 others(58): Show |
PRDM16 | ENSG00000142611.17 | transcript | ENST00000270722.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRDM16_chr1_3064203_3443621 | 3231406 | T | TCCCCTTC others(32): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00735.hp1 HG01070.hp1 others(20): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(18): Show | a0001c0001t0001g0096a0001c0001t0004g0046a0001c0001t0007g0054others(20): Show | 23 | 210 | 0.1095 | 39 | c.388 others(58): Show |
PRDM16 | ENSG00000142611.17 | transcript | ENST00000270722.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRDM16_chr1_3064203_3443621 | 3286837 | C | CGTGGGAC others(32): Show |
intron_variant | MODIFIER | HG01517.hp1 NA18990.hp1 NA19085.hp1 |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0003c0005t0009 | a0001c0001t0001g0179a0001c0002t0001g0114a0003c0005t0009g0010 | 3 | 210 | 0.0143 | 39 | c.438 others(58): Show |
PRDM16 | ENSG00000142611.17 | transcript | ENST00000270722.10 | protein_coding | 3/16 | chr1 | TogoVar | ||||||
PRDM16_chr1_3064203_3443621 | 3433482 | G | GCTGCCTG others(32): Show |
intron_variant | MODIFIER | HG02735.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0146 | 1 | 210 | 0.0048 | 39 | c.369 others(54): Show |
PRDM16 | ENSG00000142611.17 | transcript | ENST00000270722.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRDM16_chr1_3064203_3443621 | 3433541 | C | CGCCCTGC others(32): Show |
intron_variant | MODIFIER | HG02895.hp2 | a0001 | a0001c0001 | a0001c0001t0042 | a0001c0001t0042g0124 | 1 | 210 | 0.0048 | 39 | c.369 others(56): Show |
PRDM16 | ENSG00000142611.17 | transcript | ENST00000270722.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRDM16_chr1_3064203_3443621 | 3433570 | T | TGGGATGG others(32): Show |
intron_variant | MODIFIER | HG03579.hp1 HG03654.hp2 |
a0001a0002 | a0001c0008a0002c0003 | a0001c0008t0040a0002c0003t0006 | a0001c0008t0040g0021a0002c0003t0006g0050 | 2 | 210 | 0.0095 | 39 | c.369 others(54): Show |
PRDM16 | ENSG00000142611.17 | transcript | ENST00000270722.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRIMPOL_chr4_184644738_184699952 | 184676774 | C | CCCCCTTC others(32): Show |
intron_variant | MODIFIER | HG00733.hp2 HG01975.hp1 HG02145.hp1 others(15): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0001a0004c0004t0001 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0030others(14): Show | 18 | 328 | 0.0549 | 39 | c.845 others(56): Show |
PRIMPOL | ENSG00000164306.11 | transcript | ENST00000314970.11 | protein_coding | 7/13 | chr4 | TogoVar | ||||||
PRKCA_chr17_66297613_66815743 | 66799547 | G | GTGGTGGT others(32): Show |
intron_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0026 | 1 | 178 | 0.0056 | 39 | c.185 others(58): Show |
PRKCA | ENSG00000154229.12 | transcript | ENST00000413366.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
PRKCB_chr16_23830983_24225611 | 24117081 | A | AAACATTT others(32): Show |
intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02717.hp2 others(6): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0017a0001c0001t0069a0001c0003t0010others(6): Show | a0001c0001t0017g0082a0001c0001t0069g0049a0001c0003t0010g0143others(6): Show | 9 | 148 | 0.0608 | 39 | c.918 others(56): Show |
PRKCB | ENSG00000166501.14 | transcript | ENST00000643927.1 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
PRKCG_chr19_53877197_53912652 | 53906078 | C | CCTTCTTC others(32): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0328 | 1 | 362 | 0.0028 | 39 | c.176 others(56): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
PRKCG_chr19_53877197_53912652 | 53906081 | C | CCTTCTTC others(32): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0007 | a0001c0007t0004 | a0001c0007t0004g0027 | 1 | 362 | 0.0028 | 39 | c.176 others(56): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
PRKCG_chr19_53877197_53912652 | 53906084 | C | CCTCCTCC others(32): Show |
intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0354 | 1 | 362 | 0.0028 | 39 | c.176 others(56): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
PRKCG_chr19_53877197_53912652 | 53906084 | C | CCTCCTCC others(32): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0343 | 1 | 362 | 0.0028 | 39 | c.176 others(56): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122247 | G | GTCACGGC others(32): Show |
intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0277 | 1 | 286 | 0.0035 | 39 | c.335 others(58): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122314 | C | CACGGTGG others(32): Show |
intron_variant | MODIFIER | HG00438.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0103 | 1 | 286 | 0.0035 | 39 | c.335 others(58): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122363 | G | GTCACGGC others(32): Show |
intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0128 | 1 | 286 | 0.0035 | 39 | c.335 others(58): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122568 | C | CATGGTGG others(32): Show |
intron_variant | MODIFIER | HG02273.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0244 | 1 | 286 | 0.0035 | 39 | c.335 others(58): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122709 | G | GTTCATGG others(32): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02698.hp2 NA20752.hp1 |
a0001a0002 | a0001c0001a0001c0003a0002c0008 | a0001c0001t0001a0001c0003t0001a0002c0008t0001 | a0001c0001t0001g0277a0001c0003t0001g0196a0002c0008t0001g0282 | 3 | 286 | 0.0105 | 39 | c.335 others(58): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122842 | G | GTCATGGT others(32): Show |
intron_variant | MODIFIER | HG03209.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0239 | 1 | 286 | 0.0035 | 39 | c.335 others(58): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123271 | C | CACGGCTG others(32): Show |
intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0211 | 1 | 286 | 0.0035 | 39 | c.335 others(58): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123422 | G | GTCACGGC others(32): Show |
intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0211 | 1 | 286 | 0.0035 | 39 | c.335 others(58): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123455 | G | GTCACGGC others(32): Show |
intron_variant | MODIFIER | NA19011.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0197 | 1 | 286 | 0.0035 | 39 | c.335 others(58): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123536 | G | GTCACGGC others(32): Show |
intron_variant | MODIFIER | HG01169.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0201 | 1 | 286 | 0.0035 | 39 | c.335 others(58): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123797 | G | GTCATGGT others(32): Show |
intron_variant | MODIFIER | HG01978.hp2 HG03927.hp1 NA18967.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0004a0001c0003t0001 | a0001c0001t0001g0049a0001c0001t0004g0063a0001c0003t0001g0273 | 3 | 286 | 0.0105 | 39 | c.335 others(58): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar |