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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
PRKCB_chr16_23830983_24225611 | 24182902 | T | TGTGTGTG others(14): Show |
intron_variant | MODIFIER | HG01109.hp2 HG02615.hp1 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0069a0001c0006t0039 | a0001c0001t0069g0049a0001c0006t0039g0025 | 2 | 148 | 0.0135 | 21 | c.153 others(40): Show |
PRKCB | ENSG00000166501.14 | transcript | ENST00000643927.1 | protein_coding | 13/16 | chr16 | TogoVar | ||||||
PRKCD_chr3_53156209_53197717 | 53156244 | C | CTTTTTTT others(14): Show |
upstream_gene_variant | MODIFIER | HG02451.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
a0001 | a0001c0005a0001c0008 | a0001c0005t0003a0001c0008t0004 | a0001c0005t0003g0007a0001c0005t0003g0189a0001c0008t0004g0194 | 5 | 322 | 0.0155 | 21 | c.-53 others(32): Show |
PRKCD | ENSG00000163932.16 | transcript | ENST00000330452.8 | protein_coding | 4964 | chr3 | TogoVar | ||||||
PRKCE_chr2_45646675_46192990 | 45716687 | A | AGAAGGAA others(14): Show |
intron_variant | MODIFIER | HG02083.hp2 HG03453.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0071a0001c0001t0002g0080 | 2 | 168 | 0.0119 | 21 | c.348 others(40): Show |
PRKCE | ENSG00000171132.14 | transcript | ENST00000306156.8 | protein_coding | 1/14 | chr2 | TogoVar | ||||||
PRKCE_chr2_45646675_46192990 | 45751809 | A | ATTTTTTT others(14): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0010 | a0001c0010t0001 | a0001c0010t0001g0129 | 1 | 168 | 0.0060 | 21 | c.349 others(40): Show |
PRKCE | ENSG00000171132.14 | transcript | ENST00000306156.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
PRKCE_chr2_45646675_46192990 | 46061833 | C | CTTTTCTT others(14): Show |
intron_variant | MODIFIER | HG01081.hp2 HG01106.hp1 HG02300.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0116 | 3 | 168 | 0.0179 | 21 | c.143 others(42): Show |
PRKCE | ENSG00000171132.14 | transcript | ENST00000306156.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
PRKCE_chr2_45646675_46192990 | 46123214 | C | CTTTTTTT others(14): Show |
intron_variant | MODIFIER | HG00140.hp1 HG01074.hp1 HG01106.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003a0001c0010 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(2): Show | a0001c0001t0003g0056a0001c0001t0005g0083a0001c0001t0005g0109others(3): Show | 6 | 168 | 0.0357 | 21 | c.159 others(42): Show |
PRKCE | ENSG00000171132.14 | transcript | ENST00000306156.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
PRKCG_chr19_53877197_53912652 | 53878650 | A | AAAAAAAT others(14): Show |
upstream_gene_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0345 | 1 | 362 | 0.0028 | 21 | c.-38 others(32): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3546 | chr19 | TogoVar | ||||||
PRKCG_chr19_53877197_53912652 | 53906069 | C | CCTTCTTC others(14): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0270 | 1 | 362 | 0.0028 | 21 | c.176 others(38): 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(14): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0275 | 1 | 362 | 0.0028 | 21 | c.176 others(38): 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(14): Show |
intron_variant | MODIFIER | NA18952.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0108 | 1 | 362 | 0.0028 | 21 | c.176 others(38): 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(14): Show |
intron_variant | MODIFIER | HG02109.hp1 HG02723.hp2 HG04115.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0193 | 3 | 362 | 0.0083 | 21 | c.176 others(38): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
PRKCG_chr19_53877197_53912652 | 53906084 | C | CCTTCTTC others(14): Show |
intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0053 | 1 | 362 | 0.0028 | 21 | c.176 others(38): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
PRKCH_chr14_61316579_61555976 | 61505395 | C | CTTTTTTT others(14): Show |
intron_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054 | 1 | 208 | 0.0048 | 21 | c.143 others(42): Show |
PRKCH | ENSG00000027075.17 | transcript | ENST00000332981.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
PRKCI_chr3_170217424_170310977 | 170245945 | C | CTTTGTTT others(14): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0295 | 1 | 342 | 0.0029 | 21 | c.223 others(40): Show |
PRKCI | ENSG00000163558.13 | transcript | ENST00000295797.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
PRKCI_chr3_170217424_170310977 | 170245945 | C | CTTTGTTT others(14): Show |
intron_variant | MODIFIER | HG02647.hp2 HG03225.hp1 HG03471.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007a0001c0001t0010 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0007g0068others(2): Show | 5 | 342 | 0.0146 | 21 | c.223 others(40): Show |
PRKCI | ENSG00000163558.13 | transcript | ENST00000295797.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
PRKCI_chr3_170217424_170310977 | 170245950 | T | TTTTTTTT others(14): Show |
intron_variant | MODIFIER | NA19068.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0161 | 1 | 342 | 0.0029 | 21 | c.223 others(40): Show |
PRKCI | ENSG00000163558.13 | transcript | ENST00000295797.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122087 | C | CACGGCTG others(14): Show |
intron_variant | MODIFIER | HG02148.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0198 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122093 | G | GGTAGTTA others(14): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0024 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122144 | G | GGTAGTTA others(14): Show |
intron_variant | MODIFIER | HG02293.hp1 HG02698.hp1 NA18980.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050a0001c0001t0001g0082a0001c0001t0001g0085 | 3 | 286 | 0.0105 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122487 | G | GGTAGTTA others(14): Show |
intron_variant | MODIFIER | HG00438.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0103 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122568 | C | CACGGCTA others(14): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0047 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122574 | G | GGTAGTTA others(14): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0162 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122581 | G | GTCACAGC others(14): Show |
intron_variant | MODIFIER | HG00438.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0103 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122640 | G | GGTAGTTA others(14): Show |
intron_variant | MODIFIER | NA19004.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0260 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122647 | G | GTCACAGC others(14): Show |
intron_variant | MODIFIER | HG00639.hp1 HG00733.hp1 HG00733.hp2 others(6): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0201a0001c0002t0001g0233a0001c0002t0002g0035others(6): Show | 9 | 286 | 0.0315 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122703 | G | GGTAGTTA others(14): Show |
intron_variant | MODIFIER | HG00738.hp2 HG01261.hp2 HG01978.hp2 others(6): Show |
a0001 | a0001c0001a0001c0003a0001c0006 | a0001c0001t0001a0001c0001t0012a0001c0003t0001others(1): Show | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0060others(6): Show | 9 | 286 | 0.0315 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122729 | T | TGGCGGTG others(14): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0153 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122850 | G | GGTAGTTA others(14): Show |
intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0023 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2122865 | G | GGTAGTTA others(14): Show |
intron_variant | MODIFIER | HG00438.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0261 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123047 | C | CACGGCTG others(14): Show |
intron_variant | MODIFIER | HG01070.hp1 HG02055.hp2 HG03669.hp1 |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0006a0001c0002t0001a0001c0003t0001 | a0001c0001t0006g0016a0001c0002t0001g0233a0001c0003t0001g0132 | 3 | 286 | 0.0105 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123364 | G | GGTAGTTA others(14): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0130 | 1 | 286 | 0.0035 | 21 | c.335 others(40): 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(14): Show |
intron_variant | MODIFIER | HG02165.hp1 HG02300.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0251a0001c0003t0001g0133 | 2 | 286 | 0.0070 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123463 | G | GGTAGTTA others(14): Show |
intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0065 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123470 | G | GTCACGGC others(14): Show |
intron_variant | MODIFIER | NA19004.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0260 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123485 | G | GTCACGGC others(14): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0126 | 1 | 286 | 0.0035 | 21 | c.335 others(40): 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(14): Show |
intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0277 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123709 | G | GATCATGG others(14): Show |
intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0023 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123710 | G | GTCACGGC others(14): Show |
intron_variant | MODIFIER | NA18961.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123710 | G | GTCACGGC others(14): Show |
intron_variant | MODIFIER | HG03492.hp2 HG03654.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0001 | a0001c0002t0001g0203a0001c0003t0001g0141 | 2 | 286 | 0.0070 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123718 | G | GGTGGTTA others(14): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0130 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123796 | G | GGTCACGG others(14): Show |
intron_variant | MODIFIER | NA19011.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0197 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123797 | G | GTCACGGC others(14): Show |
intron_variant | MODIFIER | HG02976.hp1 NA18956.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0060a0001c0001t0001g0240 | 2 | 286 | 0.0070 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123848 | G | GTCACAGC others(14): Show |
intron_variant | MODIFIER | HG02132.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKCZ_chr1_2045411_2190395 | 2123856 | G | GGTAGTTA others(14): Show |
intron_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0072 | 1 | 286 | 0.0035 | 21 | c.335 others(40): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PRKD1_chr14_29571479_29932847 | 29762774 | A | ATTTTTTG others(14): Show |
intron_variant | MODIFIER | HG01071.hp1 HG01109.hp1 HG01358.hp2 others(24): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(11): Show | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0064others(24): Show | 27 | 156 | 0.1731 | 21 | c.265 others(40): Show |
PRKD1 | ENSG00000184304.17 | transcript | ENST00000331968.11 | protein_coding | 1/17 | chr14 | TogoVar | ||||||
PRKD1_chr14_29571479_29932847 | 29808373 | C | CTTTTTTT others(14): Show |
intron_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0062 | 1 | 156 | 0.0064 | 21 | c.265 others(40): Show |
PRKD1 | ENSG00000184304.17 | transcript | ENST00000331968.11 | protein_coding | 1/17 | chr14 | TogoVar | ||||||
PRKD2_chr19_46669316_46722114 | 46680946 | A | ATATATAT others(14): Show |
intron_variant | MODIFIER | HG01256.hp2 HG01258.hp1 HG01361.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0063a0001c0001t0001g0106a0001c0001t0001g0108others(1): Show | 4 | 378 | 0.0106 | 21 | c.207 others(38): Show |
PRKD2 | ENSG00000105287.13 | transcript | ENST00000291281.9 | protein_coding | 15/17 | chr19 | TogoVar | ||||||
PRKD2_chr19_46669316_46722114 | 46680946 | A | ATATATAT others(14): Show |
intron_variant | MODIFIER | HG02135.hp2 NA19085.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0043a0001c0001t0001g0069 | 2 | 378 | 0.0053 | 21 | c.207 others(38): Show |
PRKD2 | ENSG00000105287.13 | transcript | ENST00000291281.9 | protein_coding | 15/17 | chr19 | TogoVar | ||||||
PRKD2_chr19_46669316_46722114 | 46680946 | A | ATATATAT others(14): Show |
intron_variant | MODIFIER | HG04199.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0133 | 1 | 378 | 0.0027 | 21 | c.207 others(38): Show |
PRKD2 | ENSG00000105287.13 | transcript | ENST00000291281.9 | protein_coding | 15/17 | chr19 | TogoVar | ||||||
PRKD2_chr19_46669316_46722114 | 46680946 | A | ATATATAT others(14): Show |
intron_variant | MODIFIER | HG01517.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030 | 1 | 378 | 0.0027 | 21 | c.207 others(38): Show |
PRKD2 | ENSG00000105287.13 | transcript | ENST00000291281.9 | protein_coding | 15/17 | chr19 | TogoVar |