view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
PRKCG_chr19_53877197_53912652 | 53906084 | C | CCTCCTTC others(11): Show |
intron_variant | MODIFIER | HG02132.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0330 | 1 | 362 | 0.0028 | 18 | c.176 others(35): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
PRKCH_chr14_61316579_61555976 | 61428076 | T | TAGATAGA others(11): Show |
intron_variant | MODIFIER | HG01070.hp1 HG01175.hp2 NA18949.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0005others(1): Show | a0001c0001t0001a0001c0004t0004a0002c0005t0004others(1): Show | a0001c0001t0001g0095a0001c0004t0004g0053a0002c0005t0004g0043others(2): Show | 5 | 208 | 0.0240 | 18 | c.428 others(37): Show |
PRKCH | ENSG00000027075.17 | transcript | ENST00000332981.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
PRKCH_chr14_61316579_61555976 | 61428112 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG02976.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0063 | 1 | 208 | 0.0048 | 18 | c.428 others(37): Show |
PRKCH | ENSG00000027075.17 | transcript | ENST00000332981.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
PRKCH_chr14_61316579_61555976 | 61505395 | C | CTTTTCTT others(11): Show |
intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0132 | 1 | 208 | 0.0048 | 18 | c.143 others(39): Show |
PRKCH | ENSG00000027075.17 | transcript | ENST00000332981.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
PRKCH_chr14_61316579_61555976 | 61528151 | T | TACACACA others(11): Show |
intron_variant | MODIFIER | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(16): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0021others(7): Show | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070others(16): Show | 19 | 208 | 0.0914 | 18 | c.143 others(35): Show |
PRKCH | ENSG00000027075.17 | transcript | ENST00000332981.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
PRKCH_chr14_61316579_61555976 | 61528973 | C | CGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG00639.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0138 | 1 | 208 | 0.0048 | 18 | c.143 others(33): Show |
PRKCH | ENSG00000027075.17 | transcript | ENST00000332981.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
PRKCH_chr14_61316579_61555976 | 61529005 | T | TGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG02896.hp1 HG02897.hp2 HG02976.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0011a0001c0002t0002g0012a0001c0002t0002g0063 | 3 | 208 | 0.0144 | 18 | c.143 others(33): Show |
PRKCH | ENSG00000027075.17 | transcript | ENST00000332981.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2080321 | G | GGGCAGTG others(11): Show |
intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG02056.hp2 others(27): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(7): Show | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0001t0001g0242others(27): Show | 30 | 286 | 0.1049 | 18 | c.334 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2080325 | A | AGTGCGCG others(11): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00558.hp2 HG01884.hp2 others(21): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0163others(21): Show | 24 | 286 | 0.0839 | 18 | c.334 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2080337 | C | CGTGGCGG others(11): Show |
intron_variant | MODIFIER | HG03209.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0239 | 1 | 286 | 0.0035 | 18 | c.334 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122071 | C | CGGTGGTG others(11): Show |
intron_variant | MODIFIER | HG01069.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0214 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122168 | C | CGTGGTGG others(11): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0153 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122249 | T | TGTGGTGG others(11): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0153 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122249 | T | TGTGGTGG others(11): Show |
intron_variant | MODIFIER | HG02293.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0226 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122266 | C | CAGCGATA others(11): Show |
intron_variant | MODIFIER | NA18967.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2122365 | T | TGTGGTGG others(11): Show |
intron_variant | MODIFIER | HG03453.hp1 NA19030.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0153a0001c0001t0001g0280 | 2 | 286 | 0.0070 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122595 | G | GGTCACAG others(11): Show |
intron_variant | MODIFIER | HG01243.hp1 HG01256.hp1 HG02257.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(1): Show | a0001c0001t0001g0118a0001c0001t0001g0178a0001c0002t0001g0166others(8): Show | 11 | 286 | 0.0385 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122876 | C | CGGTGGTG others(11): Show |
intron_variant | MODIFIER | NA19064.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0278 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2122943 | G | GGTCATGG others(11): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0157 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123053 | G | GGTTAGGT others(11): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02809.hp1 HG02922.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0003t0001g0135 | 3 | 286 | 0.0105 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123082 | C | CAGCGATA others(11): Show |
intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0147 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2123082 | C | CGGCTATA others(11): Show |
intron_variant | MODIFIER | NA18961.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123100 | C | CGGCGATA others(11): Show |
intron_variant | MODIFIER | HG02622.hp2 NA19005.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0062a0001c0003t0001g0125 | 2 | 286 | 0.0070 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123118 | C | CGGCTGTA others(11): Show |
intron_variant | MODIFIER | HG04204.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0150 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123136 | C | CGGCTATA others(11): Show |
intron_variant | MODIFIER | HG02717.hp1 HG03579.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0172a0001c0003t0001g0130 | 2 | 286 | 0.0070 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123158 | G | GGTAGTTA others(11): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0262 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123176 | G | GGTAGTTA others(11): Show |
intron_variant | MODIFIER | HG01517.hp1 HG02896.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0205a0001c0002t0001g0211 | 2 | 286 | 0.0070 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123190 | C | CGGCTATA others(11): Show |
intron_variant | MODIFIER | HG01070.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0132 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123306 | C | CAGCGATA others(11): Show |
intron_variant | MODIFIER | NA18961.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2123310 | G | GGTAGTTA others(11): Show |
intron_variant | MODIFIER | HG04204.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0150 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123319 | G | GGTCACAG others(11): Show |
intron_variant | MODIFIER | HG02148.hp2 NA19005.hp1 |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0003 | a0001c0003t0001g0062a0001c0003t0003g0198 | 2 | 286 | 0.0070 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123342 | C | CGGCTGTA others(11): Show |
intron_variant | MODIFIER | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0256a0001c0002t0002g0035a0001c0003t0001g0059others(6): Show | 9 | 286 | 0.0315 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123385 | G | GGTCACAG others(11): Show |
intron_variant | MODIFIER | HG00558.hp2 HG02080.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0096a0001c0002t0001g0100 | 2 | 286 | 0.0070 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123472 | T | TATGGTGG others(11): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0015 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2123606 | C | CGGCTATA others(11): Show |
intron_variant | MODIFIER | HG02055.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0016 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123660 | C | CGGCTATA others(11): Show |
intron_variant | MODIFIER | HG01070.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0132 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123660 | C | CGGCTATA others(11): Show |
intron_variant | MODIFIER | HG02132.hp2 HG02148.hp2 HG02165.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0003 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0251others(1): Show | 4 | 286 | 0.0140 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123747 | C | CGGCTATA others(11): Show |
intron_variant | MODIFIER | HG02055.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0016 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123765 | C | CGGCTGTA others(11): Show |
intron_variant | MODIFIER | HG00738.hp2 HG02896.hp1 HG03209.hp2 |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0001a0001c0002t0001a0001c0006t0001 | a0001c0001t0001g0239a0001c0002t0001g0211a0001c0006t0001g0131 | 3 | 286 | 0.0105 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123805 | G | GGTTAGGT others(11): Show |
intron_variant | MODIFIER | NA18980.hp1 | a0001 | a0001c0003 | a0001c0003t0014 | a0001c0003t0014g0117 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123812 | G | GTCATGGT others(11): Show |
intron_variant | MODIFIER | NA19079.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0083 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2123888 | C | CTATAGTT others(11): Show |
intron_variant | MODIFIER | NA18980.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2123942 | C | CTATAGTT others(11): Show |
intron_variant | MODIFIER | HG02300.hp1 HG04228.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0133a0001c0003t0001g0283 | 2 | 286 | 0.0070 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2124029 | C | CTGTAGTT others(11): Show |
intron_variant | MODIFIER | HG01433.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0212 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2124101 | C | CTATAGTT others(11): Show |
intron_variant | MODIFIER | HG00140.hp2 HG01496.hp1 HG01978.hp1 others(5): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0002a0001c0003t0001a0001c0003t0003 | a0001c0002t0002g0031a0001c0003t0001g0062a0001c0003t0001g0125others(5): Show | 8 | 286 | 0.0280 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2124134 | C | CAGCGATA others(11): Show |
intron_variant | MODIFIER | HG02056.hp1 NA19088.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0061a0001c0001t0004g0079 | 2 | 286 | 0.0070 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2124199 | A | AGGGTCAT others(11): Show |
intron_variant | MODIFIER | HG01070.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0132 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2124263 | C | CTGTAGTT others(11): Show |
intron_variant | MODIFIER | NA19240.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0161 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | chr1 | TogoVar | |||||||
PRKCZ_chr1_2045411_2190395 | 2124314 | C | CGGCTGTA others(11): Show |
intron_variant | MODIFIER | HG02148.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0198 | 1 | 286 | 0.0035 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PRKCZ_chr1_2045411_2190395 | 2124417 | G | GGTCACGG others(11): Show |
intron_variant | MODIFIER | HG01934.hp2 HG02735.hp1 HG02895.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0257a0001c0002t0001g0154a0001c0002t0001g0207others(1): Show | 4 | 286 | 0.0140 | 18 | c.335 others(37): Show |
PRKCZ | ENSG00000067606.17 | transcript | ENST00000378567.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | TogoVar |