Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5582 |
| ensemblid | ENSG00000126583.12 |
| hgncid | 9402 |
| symbol | PRKCG |
| name | protein kinase C gamma |
| refseq_nuc | NM_002739.5 |
| refseq_prot | NP_002730.1 |
| ensembl_nuc | ENST00000263431.4 |
| ensembl_prot | ENSP00000263431.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 53882197 |
| end | 53907652 |
| strand | + |
| ver | v1.2 |
| region | chr19:53882197-53907652 |
| region5000 | chr19:53877197-53912652 |
| regionname0 | PRKCG_chr19_53882197_53907652 |
| regionname5000 | PRKCG_chr19_53877197_53912652 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 697 | 357 | 92 | 70 | 133 | 14 | 46 | 97 | PRKCG_chr19_53877197_53912652 | PRKCG | MAGLG others(692): Show |
chr19 | 53877197 | 53912652 |
| a0002 | 0/0 | 697 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | MAGLG others(692): Show |
chr19 | 53877197 | 53912652 |
| a0003 | 0/0 | 697 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | MAGLG others(692): Show |
chr19 | 53877197 | 53912652 |
| a0004 | 0/0 | 528 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | MAGLG others(523): Show |
chr19 | 53877197 | 53912652 |
| a0005 | 0/0 | 697 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | MAGLG others(692): Show |
chr19 | 53877197 | 53912652 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2091 | 147 | 33 | 28 | 54 | 5 | 27 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0002 | 0/0 | 2091 | 111 | 19 | 31 | 38 | 9 | 14 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0003 | 0/0 | 2091 | 33 | 2 | 1 | 30 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0004 | 0/0 | 2091 | 16 | 12 | 4 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0005 | 1/1 | 2091 | 10 | 5 | 2 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0006 | 0/0 | 2091 | 7 | 6 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0007 | 0/0 | 2091 | 7 | 6 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0008 | 0/0 | 2091 | 4 | 0 | 0 | 4 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0009 | 0/0 | 2091 | 3 | 0 | 0 | 3 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0010 | 0/0 | 2091 | 3 | 3 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0011 | 0/0 | 2091 | 3 | 0 | 0 | 0 | 0 | 3 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0012 | 0/0 | 2091 | 2 | 2 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0014 | 0/0 | 2091 | 2 | 0 | 0 | 2 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0016 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0017 | 0/0 | 2091 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0018 | 0/0 | 2091 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0020 | 0/0 | 2091 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0021 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0023 | 0/0 | 2091 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0024 | 0/0 | 2091 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0025 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0001c0026 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0002c0013 | 0/0 | 2091 | 2 | 2 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0003c0022 | 0/0 | 2091 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0004c0019 | 0/0 | 2091 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 | ||
| a0005c0015 | 0/0 | 2091 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ATGGC others(2086): Show |
chr19 | 53877197 | 53912652 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3149 | 132 | 20 | 26 | 54 | 5 | 27 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0001t0003 | 0/0 | 3149 | 9 | 8 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0001t0004 | 0/0 | 3149 | 4 | 4 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0001t0005 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0001t0007 | 0/0 | 3134 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3129): Show |
chr19 | 53877197 | 53912652 |
| a0001c0002t0001 | 0/0 | 3149 | 110 | 18 | 31 | 38 | 9 | 14 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0002t0002 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3145): Show |
chr19 | 53877197 | 53912652 |
| a0001c0003t0001 | 0/0 | 3149 | 31 | 0 | 1 | 30 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0003t0002 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3145): Show |
chr19 | 53877197 | 53912652 |
| a0001c0003t0005 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0004t0001 | 0/0 | 3149 | 6 | 4 | 2 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0004t0002 | 0/0 | 3150 | 10 | 8 | 2 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3145): Show |
chr19 | 53877197 | 53912652 |
| a0001c0005t0001 | 1/1 | 3149 | 5 | 1 | 1 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0005t0004 | 0/0 | 3149 | 3 | 2 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0005t0006 | 0/0 | 3149 | 2 | 2 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0006t0001 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0006t0003 | 0/0 | 3149 | 6 | 5 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0007t0001 | 0/0 | 3149 | 5 | 4 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0007t0004 | 0/0 | 3149 | 2 | 2 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0008t0001 | 0/0 | 3149 | 4 | 0 | 0 | 4 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0009t0001 | 0/0 | 3149 | 3 | 0 | 0 | 3 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0010t0002 | 0/0 | 3150 | 3 | 3 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3145): Show |
chr19 | 53877197 | 53912652 |
| a0001c0011t0001 | 0/0 | 3149 | 3 | 0 | 0 | 0 | 0 | 3 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0012t0001 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0012t0002 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3145): Show |
chr19 | 53877197 | 53912652 |
| a0001c0014t0001 | 0/0 | 3149 | 2 | 0 | 0 | 2 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0016t0001 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0017t0001 | 0/0 | 3149 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0018t0001 | 0/0 | 3149 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0020t0001 | 0/0 | 3149 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0021t0001 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0023t0001 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0024t0001 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0025t0005 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0001c0026t0005 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0002c0013t0002 | 0/0 | 3150 | 2 | 2 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3145): Show |
chr19 | 53877197 | 53912652 |
| a0003c0022t0001 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0004c0019t0001 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| a0005c0015t0001 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | ACATT others(3144): Show |
chr19 | 53877197 | 53912652 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0001t0007g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0002t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0003t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0004t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0005t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0005t0001g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0005t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0005t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0005t0001g0331 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0005t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0005t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0005t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0005t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0005t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0006t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0006t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0006t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0006t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0006t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0006t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0006t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0007t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0007t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0007t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0007t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0007t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0007t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0007t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0008t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0008t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0008t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0008t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0009t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0009t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0009t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0010t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0010t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0010t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0011t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0011t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0011t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0012t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0012t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0014t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0014t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0016t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0017t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0018t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0020t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0021t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0023t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0024t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0025t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0001c0026t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0002c0013t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0002c0013t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0003c0022t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0004c0019t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| a0005c0015t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0086 | EUR | GBR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0296 | EUR | GBR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0118 | EUR | FIN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0294 | EUR | FIN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | FIN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0298 | EUR | FIN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00423 | hp2 | a0001 | c0009 | t0001 | g0167 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00544 | hp2 | a0001 | c0009 | t0001 | g0007 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00597 | hp1 | a0001 | c0003 | t0001 | g0303 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0330 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | CHS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0295 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00738 | hp1 | a0001 | c0005 | t0001 | g0325 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00738 | hp2 | a0001 | c0020 | t0001 | g0102 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0307 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG00741 | hp2 | a0001 | c0004 | t0001 | g0155 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0297 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01070 | hp2 | a0001 | c0017 | t0001 | g0019 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01109 | hp1 | a0001 | c0004 | t0002 | g0339 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01109 | hp2 | a0001 | c0005 | t0004 | g0038 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0156 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0292 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01243 | hp2 | a0001 | c0004 | t0002 | g0343 | AMR | PUR | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0264 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0306 | EUR | IBS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0119 | EUR | IBS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0066 | EUR | IBS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0099 | EUR | IBS | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01891 | hp2 | a0001 | c0012 | t0002 | g0055 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01943 | hp1 | a0001 | c0006 | t0003 | g0032 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0200 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01981 | hp1 | a0001 | c0001 | t0007 | g0127 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02004 | hp2 | a0001 | c0018 | t0001 | g0103 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0283 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02145 | hp2 | a0001 | c0004 | t0002 | g0348 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0282 | EAS | CDX | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0349 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | PEL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0336 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | KHV | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02615 | hp1 | a0001 | c0004 | t0002 | g0345 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02615 | hp2 | a0002 | c0013 | t0002 | g0017 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02622 | hp1 | a0001 | c0006 | t0003 | g0147 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0043 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02647 | hp1 | a0001 | c0004 | t0002 | g0338 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02698 | hp1 | a0001 | c0005 | t0001 | g0231 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02717 | hp2 | a0001 | c0004 | t0002 | g0347 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0136 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02809 | hp1 | a0001 | c0006 | t0003 | g0146 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0341 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02818 | hp1 | a0001 | c0007 | t0001 | g0150 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0342 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02886 | hp1 | a0001 | c0025 | t0005 | g0151 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02895 | hp1 | a0001 | c0010 | t0002 | g0036 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02896 | hp2 | a0001 | c0005 | t0006 | g0039 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02897 | hp2 | a0001 | c0005 | t0006 | g0040 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02922 | hp2 | a0001 | c0010 | t0002 | g0037 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0275 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02965 | hp2 | a0001 | c0006 | t0003 | g0148 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02970 | hp1 | a0001 | c0005 | t0004 | g0041 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02976 | hp2 | a0001 | c0006 | t0003 | g0143 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0030 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0316 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0340 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0065 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03130 | hp1 | a0001 | c0012 | t0001 | g0056 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03139 | hp2 | a0001 | c0007 | t0004 | g0035 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0270 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03209 | hp1 | a0001 | c0004 | t0002 | g0335 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03209 | hp2 | a0002 | c0013 | t0002 | g0018 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03225 | hp2 | a0001 | c0003 | t0005 | g0205 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0115 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03453 | hp1 | a0001 | c0026 | t0005 | g0053 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03453 | hp2 | a0001 | c0016 | t0001 | g0016 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0165 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03491 | hp2 | a0001 | c0011 | t0001 | g0159 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03492 | hp2 | a0001 | c0011 | t0001 | g0158 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03540 | hp1 | a0001 | c0004 | t0002 | g0344 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03540 | hp2 | a0001 | c0010 | t0002 | g0211 | AFR | GWD | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0212 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03654 | hp1 | a0001 | c0011 | t0001 | g0157 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | STU | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | STU | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | BEB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | BEB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | BEB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | BEB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | BEB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0293 | SAS | STU | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0031 | SAS | STU | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG04228 | hp2 | a0001 | c0007 | t0001 | g0154 | SAS | STU | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | CHB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18747 | hp1 | a0001 | c0024 | t0001 | g0094 | EAS | CHB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18906 | hp1 | a0001 | c0007 | t0004 | g0034 | AFR | YRI | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18906 | hp2 | a0001 | c0005 | t0004 | g0042 | AFR | YRI | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18946 | hp2 | a0001 | c0008 | t0001 | g0004 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18947 | hp2 | a0003 | c0022 | t0001 | g0181 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0174 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18959 | hp1 | a0001 | c0008 | t0001 | g0120 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18959 | hp2 | a0001 | c0003 | t0001 | g0314 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18964 | hp1 | a0001 | c0014 | t0001 | g0025 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18969 | hp1 | a0001 | c0003 | t0001 | g0329 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0272 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18970 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0269 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0334 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18983 | hp1 | a0001 | c0008 | t0001 | g0109 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18994 | hp1 | a0004 | c0019 | t0001 | g0203 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18994 | hp2 | a0001 | c0003 | t0001 | g0242 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19007 | hp1 | a0001 | c0008 | t0001 | g0068 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0179 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19012 | hp1 | a0001 | c0003 | t0001 | g0213 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19030 | hp1 | a0001 | c0021 | t0001 | g0252 | AFR | LWK | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19030 | hp2 | a0001 | c0006 | t0001 | g0142 | AFR | LWK | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19043 | hp1 | a0001 | c0007 | t0001 | g0145 | AFR | LWK | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | LWK | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19059 | hp2 | a0001 | c0003 | t0001 | g0059 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19063 | hp2 | a0005 | c0015 | t0001 | g0081 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19068 | hp1 | a0001 | c0003 | t0001 | g0304 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19074 | hp2 | a0001 | c0014 | t0001 | g0026 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19076 | hp2 | a0001 | c0003 | t0001 | g0237 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19084 | hp1 | a0001 | c0023 | t0001 | g0288 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19088 | hp2 | a0001 | c0009 | t0001 | g0170 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0317 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | YRI | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA19240 | hp2 | a0001 | c0007 | t0001 | g0149 | AFR | YRI | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | ASW | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ASW | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0236 | EUR | TSI | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | GIH | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | GIH | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02109 | hp2 | a0001 | c0003 | t0002 | g0020 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0276 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02486 | hp2 | a0001 | c0007 | t0001 | g0141 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03471 | hp1 | a0001 | c0004 | t0002 | g0337 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | MSL | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG06807 | hp1 | a0001 | c0004 | t0002 | g0346 | AFR | USA | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| HG06807 | hp2 | a0001 | c0006 | t0003 | g0144 | AFR | USA | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | USA | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | USA | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | LWK | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0265 | AFR | LWK | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| homoSapiens | chm13v2 | a0001 | c0005 | t0001 | g0331 | REF | REF | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| homoSapiens | grch38p0 | a0001 | c0005 | t0001 | g0190 | REF | REF | PRKCG_chr19_53877197_53912652 | PRKCG | chr19 | 53877197 | 53912652 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:53903084 | C | A | 1 | a0004 | 1 | NA18994.hp1 | stop_gained | HIGH | c.1587C>A | p.Tyr529* | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 15/18 | 1885/3149 | 1587/2094 | 529/697 | chr19 | 53903084 | |||
| chr19:53906360 | A | G | 1 | a0003 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.1808A>G | p.Asp603Gly | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 17/18 | 2106/3149 | 1808/2094 | 603/697 | chr19 | 53906360 | |||
| chr19:53906753 | C | T | 1 | a0005 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.1952C>T | p.Ala651Val | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 18/18 | 2250/3149 | 1952/2094 | 651/697 | chr19 | 53906753 | |||
| chr19:53906860 | A | G | 1 | a0002 | 2 | HG02615.hp2 HG03209.hp2 |
missense_variant | MODERATE | c.2059A>G | p.Ser687Gly | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 18/18 | 2357/3149 | 2059/2094 | 687/697 | chr19 | 53906860 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:53882566 | C | T | 22 | a0001c0001 a0001c0002 a0001c0003 others(19): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
synonymous_variant | LOW | c.72C>T | p.Ala24Ala | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 1/18 | 370/3149 | 72/2094 | 24/697 | chr19 | 53882566 | |||
| chr19:53884165 | C | T | 2 | a0001c0004 a0001c0011 |
19 | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(16): Show |
synonymous_variant | LOW | c.207C>T | p.Cys69Cys | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/18 | 505/3149 | 207/2094 | 69/697 | chr19 | 53884165 | |||
| chr19:53884243 | C | T | 4 | a0001c0006 a0001c0007 a0001c0025 others(1): Show |
16 | HG01943.hp1 HG02486.hp2 HG02622.hp1 others(13): Show |
splice_region_variant&synonymous_variant | LOW | c.285C>T | p.Asp95Asp | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/18 | 583/3149 | 285/2094 | 95/697 | chr19 | 53884243 | |||
| chr19:53889649 | C | T | 1 | a0001c0024 | 1 | NA18747.hp1 | synonymous_variant | LOW | c.297C>T | p.Asn99Asn | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 4/18 | 595/3149 | 297/2094 | 99/697 | chr19 | 53889649 | |||
| chr19:53889986 | G | T | 1 | a0001c0014 | 2 | NA18964.hp1 NA19074.hp2 |
synonymous_variant | LOW | c.498G>T | p.Arg166Arg | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/18 | 796/3149 | 498/2094 | 166/697 | chr19 | 53889986 | |||
| chr19:53891711 | T | C | 7 | a0001c0002 a0001c0008 a0001c0012 others(4): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
synonymous_variant | LOW | c.567T>C | p.Asn189Asn | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 6/18 | 865/3149 | 567/2094 | 189/697 | chr19 | 53891711 | |||
| chr19:53891768 | G | A | 1 | a0001c0025 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.624G>A | p.Thr208Thr | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 6/18 | 922/3149 | 624/2094 | 208/697 | chr19 | 53891768 | |||
| chr19:53892572 | C | T | 1 | a0001c0023 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.750C>T | p.Thr250Thr | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/18 | 1048/3149 | 750/2094 | 250/697 | chr19 | 53892572 | |||
| chr19:53892632 | C | T | 1 | a0001c0017 | 1 | HG01070.hp2 | synonymous_variant | LOW | c.810C>T | p.Pro270Pro | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/18 | 1108/3149 | 810/2094 | 270/697 | chr19 | 53892632 | |||
| chr19:53893027 | T | C | 1 | a0001c0018 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.861T>C | p.Asn287Asn | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 8/18 | 1159/3149 | 861/2094 | 287/697 | chr19 | 53893027 | |||
| chr19:53900671 | T | C | 5 | a0001c0003 a0001c0006 a0001c0011 others(2): Show |
45 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(42): Show |
synonymous_variant | LOW | c.1497T>C | p.Phe499Phe | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/18 | 1795/3149 | 1497/2094 | 499/697 | chr19 | 53900671 | |||
| chr19:53903138 | G | A | 1 | a0001c0020 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.1641G>A | p.Glu547Glu | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 15/18 | 1939/3149 | 1641/2094 | 547/697 | chr19 | 53903138 | |||
| chr19:53904700 | C | T | 2 | a0001c0010 a0001c0016 |
4 | HG02895.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.1722C>T | p.Tyr574Tyr | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/18 | 2020/3149 | 1722/2094 | 574/697 | chr19 | 53904700 | |||
| chr19:53906346 | G | A | 1 | a0001c0021 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1794G>A | p.Leu598Leu | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 17/18 | 2092/3149 | 1794/2094 | 598/697 | chr19 | 53906346 | |||
| chr19:53906742 | C | T | 3 | a0001c0008 a0001c0009 a0004c0019 |
8 | HG00423.hp2 HG00544.hp2 NA18946.hp2 others(5): Show |
synonymous_variant | LOW | c.1941C>T | p.Phe647Phe | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 18/18 | 2239/3149 | 1941/2094 | 647/697 | chr19 | 53906742 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:53882302 | TGGCGGAG others(8): Show |
T | 1 | a0001c0001t0007 | 1 | HG01981.hp1 | 5_prime_UTR_variant | MODIFIER | c.-192_-178delGGCGGA others(9): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 1/18 | 178 | chr19 | 53882302 | ||||||
| chr19:53906941 | C | T | 1 | a0001c0005t0006 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*46C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 18/18 | 46 | chr19 | 53906941 | ||||||
| chr19:53906950 | G | GC | 6 | a0001c0002t0002 a0001c0003t0002 a0001c0004t0002 others(3): Show |
18 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*59dupC | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 18/18 | 60 | INFO_REALIGN_3_PRIME | chr19 | 53906950 | |||||
| chr19:53907094 | C | T | 4 | a0001c0001t0005 a0001c0003t0005 a0001c0025t0005 others(1): Show |
4 | HG02886.hp1 HG03195.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*199C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 18/18 | 199 | chr19 | 53907094 | ||||||
| chr19:53907323 | C | G | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0003t0005 others(3): Show |
19 | HG01943.hp1 HG02004.hp1 HG02145.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*428C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 18/18 | 428 | chr19 | 53907323 | ||||||
| chr19:53907491 | C | T | 4 | a0001c0001t0004 a0001c0005t0004 a0001c0005t0006 others(1): Show |
11 | HG01109.hp2 HG02896.hp2 HG02897.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*596C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 18/18 | 596 | chr19 | 53907491 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:53882697 | A | C | 1 | a0001c0002t0002g0349 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.170+33A>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 1/17 | chr19 | 53882697 | |||||||
| chr19:53882951 | G | A | 1 | a0001c0002t0001g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.171-212G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 1/17 | chr19 | 53882951 | |||||||
| chr19:53882971 | G | T | 14 | a0001c0004t0001g0336 a0001c0004t0001g0340 a0001c0004t0001g0341 others(11): Show |
14 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.171-192G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 1/17 | chr19 | 53882971 | |||||||
| chr19:53883102 | G | C | 1 | a0001c0001t0001g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.171-61G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 1/17 | chr19 | 53883102 | |||||||
| chr19:53883208 | A | G | 1 | a0001c0003t0001g0334 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.202+14A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 2/17 | chr19 | 53883208 | |||||||
| chr19:53883209 | C | A | 1 | a0001c0003t0001g0334 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.202+15C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 2/17 | chr19 | 53883209 | |||||||
| chr19:53883211 | G | C | 1 | a0001c0003t0001g0334 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.202+17G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 2/17 | chr19 | 53883211 | |||||||
| chr19:53883625 | G | C | 1 | a0001c0002t0001g0014 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.202+431G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 2/17 | chr19 | 53883625 | |||||||
| chr19:53883720 | C | A | 1 | a0001c0002t0001g0015 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.203-441C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 2/17 | chr19 | 53883720 | |||||||
| chr19:53883782 | C | G | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | NA18945.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.203-379C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 2/17 | chr19 | 53883782 | |||||||
| chr19:53883837 | G | C | 7 | a0001c0001t0003g0021 a0001c0002t0002g0349 a0001c0003t0002g0020 others(4): Show |
7 | HG01070.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.203-324G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 2/17 | chr19 | 53883837 | |||||||
| chr19:53883922 | T | C | 1 | a0001c0016t0001g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.203-239T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 2/17 | chr19 | 53883922 | |||||||
| chr19:53884009 | T | G | 1 | a0001c0001t0001g0022 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.203-152T>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 2/17 | chr19 | 53884009 | |||||||
| chr19:53884144 | A | G | 2 | a0001c0003t0001g0329 a0001c0003t0001g0330 |
2 | HG00609.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.203-17A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 2/17 | chr19 | 53884144 | |||||||
| chr19:53884288 | G | A | 4 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0014t0001g0025 others(1): Show |
4 | HG02148.hp2 HG02273.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+45G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53884288 | |||||||
| chr19:53884465 | C | A | 4 | a0001c0002t0002g0349 a0001c0017t0001g0019 a0002c0013t0002g0017 others(1): Show |
4 | HG01070.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+222C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53884465 | |||||||
| chr19:53884517 | G | T | 1 | a0001c0001t0003g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.285+274G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53884517 | |||||||
| chr19:53884636 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.285+393G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53884636 | |||||||
| chr19:53884684 | G | T | 2 | a0001c0001t0001g0327 a0001c0001t0001g0328 |
2 | HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.285+441G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53884684 | |||||||
| chr19:53885141 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.285+898T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885141 | |||||||
| chr19:53885225 | T | A | 158 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0100 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.285+982T>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885225 | |||||||
| chr19:53885251 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.285+1008C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885251 | |||||||
| chr19:53885252 | G | A | 2 | a0001c0002t0001g0030 a0001c0002t0001g0031 |
2 | HG03017.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.285+1009G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885252 | |||||||
| chr19:53885290 | G | A | 1 | a0001c0006t0003g0032 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.285+1047G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885290 | |||||||
| chr19:53885311 | T | C | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+1068T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885311 | |||||||
| chr19:53885314 | C | T | 19 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0336 others(16): Show |
19 | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.285+1071C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885314 | |||||||
| chr19:53885482 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.285+1239G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885482 | |||||||
| chr19:53885519 | C | T | 2 | a0001c0003t0002g0020 a0001c0005t0001g0325 |
2 | HG00738.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.285+1276C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885519 | |||||||
| chr19:53885520 | G | A | 2 | a0001c0007t0004g0034 a0001c0007t0004g0035 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.285+1277G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885520 | |||||||
| chr19:53885524 | C | A | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+1281C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885524 | |||||||
| chr19:53885596 | A | T | 1 | a0001c0007t0001g0154 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.285+1353A>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885596 | |||||||
| chr19:53885744 | C | G | 1 | a0001c0002t0001g0153 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.285+1501C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885744 | |||||||
| chr19:53885772 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.285+1529A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885772 | |||||||
| chr19:53885899 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0321 a0001c0001t0001g0322 others(1): Show |
4 | HG02071.hp2 HG02132.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+1656C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885899 | |||||||
| chr19:53885914 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0160 |
3 | HG01256.hp2 HG01258.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.285+1671T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885914 | |||||||
| chr19:53885919 | AT | A | 20 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0003g0021 others(17): Show |
20 | HG01109.hp2 HG02004.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.285+1687delT | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53885919 | ||||||
| chr19:53885927 | T | G | 1 | a0001c0003t0001g0161 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.285+1684T>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885927 | |||||||
| chr19:53885938 | G | A | 2 | a0001c0010t0002g0036 a0001c0010t0002g0037 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.285+1695G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885938 | |||||||
| chr19:53885991 | G | A | 1 | a0001c0026t0005g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.285+1748G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53885991 | |||||||
| chr19:53886063 | GA | G | 138 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0100 others(135): Show |
139 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.285+1833delA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53886063 | ||||||
| chr19:53886076 | A | G | 1 | a0001c0002t0001g0152 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.285+1833A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886076 | |||||||
| chr19:53886077 | G | A | 1 | a0001c0002t0001g0152 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.285+1834G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886077 | |||||||
| chr19:53886078 | A | T | 1 | a0001c0002t0001g0152 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.285+1835A>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886078 | |||||||
| chr19:53886115 | G | A | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+1872G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886115 | |||||||
| chr19:53886225 | C | G | 16 | a0001c0006t0001g0142 a0001c0006t0003g0032 a0001c0006t0003g0143 others(13): Show |
16 | HG01943.hp1 HG02486.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.285+1982C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886225 | |||||||
| chr19:53886226 | T | C | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+1983T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886226 | |||||||
| chr19:53886228 | C | T | 19 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0336 others(16): Show |
19 | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.285+1985C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886228 | |||||||
| chr19:53886347 | A | G | 20 | a0001c0003t0002g0020 a0001c0004t0001g0155 a0001c0004t0001g0156 others(17): Show |
20 | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+2104A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886347 | |||||||
| chr19:53886356 | G | A | 18 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0003g0021 others(15): Show |
18 | HG01109.hp2 HG02004.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.285+2113G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886356 | |||||||
| chr19:53886573 | A | T | 1 | a0001c0004t0002g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.285+2330A>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886573 | |||||||
| chr19:53886577 | A | C | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+2334A>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886577 | |||||||
| chr19:53886587 | T | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA18954.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.285+2344T>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886587 | |||||||
| chr19:53886650 | G | A | 8 | a0001c0005t0001g0043 a0001c0005t0004g0038 a0001c0005t0004g0041 others(5): Show |
8 | HG01109.hp2 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.285+2407G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886650 | |||||||
| chr19:53886691 | C | T | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+2448C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886691 | |||||||
| chr19:53886747 | A | G | 37 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0003g0021 others(34): Show |
37 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.285+2504A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886747 | |||||||
| chr19:53886763 | T | C | 8 | a0001c0005t0001g0043 a0001c0005t0004g0038 a0001c0005t0004g0041 others(5): Show |
8 | HG01109.hp2 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+2520T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886763 | |||||||
| chr19:53886867 | T | C | 160 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0100 others(157): Show |
161 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.285+2624T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53886867 | |||||||
| chr19:53887013 | A | G | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286-2625A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887013 | |||||||
| chr19:53887060 | G | A | 100 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0007g0127 others(97): Show |
101 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.286-2578G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887060 | |||||||
| chr19:53887060 | G | T | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286-2578G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887060 | |||||||
| chr19:53887220 | A | G | 6 | a0001c0005t0001g0043 a0001c0005t0004g0038 a0001c0005t0004g0041 others(3): Show |
6 | HG01109.hp2 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-2418A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887220 | |||||||
| chr19:53887295 | C | T | 16 | a0001c0006t0001g0142 a0001c0006t0003g0032 a0001c0006t0003g0143 others(13): Show |
16 | HG01943.hp1 HG02486.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.286-2343C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887295 | |||||||
| chr19:53887326 | C | T | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286-2312C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887326 | |||||||
| chr19:53887358 | G | A | 4 | a0001c0005t0004g0038 a0001c0005t0004g0041 a0001c0005t0006g0039 others(1): Show |
4 | HG01109.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-2280G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887358 | |||||||
| chr19:53887428 | C | T | 1 | a0001c0001t0001g0320 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.286-2210C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887428 | |||||||
| chr19:53887491 | C | A | 3 | a0001c0002t0001g0054 a0001c0012t0001g0056 a0001c0012t0002g0055 |
3 | HG01891.hp1 HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.286-2147C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887491 | |||||||
| chr19:53887497 | C | CA | 11 | a0001c0001t0001g0027 a0001c0001t0001g0166 a0001c0001t0001g0168 others(8): Show |
11 | HG00423.hp2 HG02055.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.286-2103dupA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CA | C | 55 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0163 others(52): Show |
56 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.286-2103delA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CAA | C | 35 | a0001c0001t0001g0009 a0001c0001t0001g0245 a0001c0001t0001g0246 others(32): Show |
36 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.286-2104_286-2103d others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CAAA | C | 46 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0277 others(43): Show |
48 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.286-2105_286-2103d others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CAAAA | C | 50 | a0001c0001t0001g0044 a0001c0001t0001g0309 a0001c0001t0001g0310 others(47): Show |
54 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.286-2106_286-2103d others(6): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CAAAAA | C | 52 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0003g0316 others(49): Show |
52 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.286-2107_286-2103d others(7): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CAAAAAA | C | 11 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0002t0001g0133 others(8): Show |
11 | HG01928.hp2 HG01952.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.286-2108_286-2103d others(8): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CAAAAAAA | C | 19 | a0001c0001t0001g0047 a0001c0001t0003g0021 a0001c0001t0003g0048 others(16): Show |
19 | HG00741.hp2 HG01175.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.286-2109_286-2103d others(9): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CAAAAAAA others(1): Show |
C | 22 | a0001c0004t0001g0340 a0001c0004t0001g0341 a0001c0004t0001g0342 others(19): Show |
22 | HG01109.hp1 HG01243.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.286-2110_286-2103d others(10): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CAAAAAAA others(3): Show |
C | 2 | a0001c0002t0001g0138 a0001c0002t0001g0139 |
2 | NA18985.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.286-2112_286-2103d others(12): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0001g0140 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.286-2113_286-2103d others(13): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0160 |
3 | HG01256.hp2 HG01258.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.286-2118_286-2103d others(18): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CAAAAAAA others(10): Show |
C | 2 | a0001c0025t0005g0151 a0001c0026t0005g0053 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.286-2119_286-2103d others(19): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887497 | CAAAAAAA others(11): Show |
C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0318 a0001c0001t0001g0319 |
4 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-2120_286-2103d others(20): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887497 | ||||||
| chr19:53887551 | C | G | 1 | a0001c0002t0001g0015 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-2087C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887551 | |||||||
| chr19:53887606 | G | A | 1 | a0001c0003t0001g0174 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.286-2032G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887606 | |||||||
| chr19:53887627 | C | A | 42 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0003g0021 others(39): Show |
42 | HG00741.hp2 HG01070.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.286-2011C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887627 | |||||||
| chr19:53887697 | G | T | 16 | a0001c0006t0001g0142 a0001c0006t0003g0032 a0001c0006t0003g0143 others(13): Show |
16 | HG01943.hp1 HG02486.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.286-1941G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887697 | |||||||
| chr19:53887722 | C | T | 1 | a0001c0002t0001g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.286-1916C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887722 | |||||||
| chr19:53887829 | C | CA | 18 | a0001c0001t0001g0166 a0001c0001t0001g0175 a0001c0001t0001g0204 others(15): Show |
18 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.286-1788dupA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887829 | ||||||
| chr19:53887829 | CA | C | 30 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0271 others(27): Show |
30 | HG01070.hp2 HG01109.hp2 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.286-1788delA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887829 | ||||||
| chr19:53887829 | CAA | C | 20 | a0001c0001t0003g0021 a0001c0002t0001g0054 a0001c0003t0002g0020 others(17): Show |
20 | HG01891.hp1 HG01891.hp2 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.286-1789_286-1788d others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53887829 | ||||||
| chr19:53887926 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.286-1712G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887926 | |||||||
| chr19:53887985 | A | G | 16 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0003g0045 others(13): Show |
16 | HG01109.hp2 HG02004.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.286-1653A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53887985 | |||||||
| chr19:53888050 | C | T | 17 | a0001c0003t0002g0020 a0001c0006t0001g0142 a0001c0006t0003g0032 others(14): Show |
17 | HG01943.hp1 HG02109.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.286-1588C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53888050 | |||||||
| chr19:53888126 | C | T | 2 | a0001c0001t0001g0305 a0001c0001t0001g0313 |
2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.286-1512C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53888126 | |||||||
| chr19:53888279 | T | C | 3 | a0001c0002t0001g0054 a0001c0012t0001g0056 a0001c0012t0002g0055 |
3 | HG01891.hp1 HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.286-1359T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53888279 | |||||||
| chr19:53888336 | T | G | 3 | a0001c0002t0001g0054 a0001c0012t0001g0056 a0001c0012t0002g0055 |
3 | HG01891.hp1 HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.286-1302T>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53888336 | |||||||
| chr19:53888379 | G | A | 164 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0100 others(161): Show |
165 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.286-1259G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53888379 | |||||||
| chr19:53888383 | T | C | 165 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0100 others(162): Show |
166 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.286-1255T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53888383 | |||||||
| chr19:53888428 | T | A | 164 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0100 others(161): Show |
165 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.286-1210T>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53888428 | |||||||
| chr19:53888626 | A | G | 2 | a0001c0003t0005g0205 a0001c0016t0001g0016 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.286-1012A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53888626 | |||||||
| chr19:53888872 | A | C | 1 | a0001c0002t0001g0131 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.286-766A>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53888872 | |||||||
| chr19:53888908 | T | C | 1 | a0001c0016t0001g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.286-730T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53888908 | |||||||
| chr19:53888949 | TTTG | T | 3 | a0001c0002t0001g0054 a0001c0012t0001g0056 a0001c0012t0002g0055 |
3 | HG01891.hp1 HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.286-671_286-669del others(3): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53888949 | ||||||
| chr19:53888974 | A | T | 10 | a0001c0001t0001g0312 a0001c0003t0001g0001 a0001c0003t0001g0002 others(7): Show |
15 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.286-664A>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53888974 | |||||||
| chr19:53888993 | T | C | 26 | a0001c0001t0001g0044 a0001c0004t0001g0155 a0001c0004t0001g0156 others(23): Show |
26 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.286-645T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53888993 | |||||||
| chr19:53889005 | T | C | 62 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0003g0021 others(59): Show |
62 | HG00741.hp2 HG01070.hp2 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.286-633T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53889005 | |||||||
| chr19:53889062 | C | T | 26 | a0001c0001t0001g0044 a0001c0004t0001g0155 a0001c0004t0001g0156 others(23): Show |
26 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.286-576C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53889062 | |||||||
| chr19:53889101 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.286-537C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53889101 | |||||||
| chr19:53889205 | C | G | 27 | a0001c0001t0001g0044 a0001c0003t0002g0020 a0001c0004t0001g0155 others(24): Show |
27 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.286-433C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53889205 | |||||||
| chr19:53889327 | G | A | 37 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0002t0001g0054 others(34): Show |
37 | HG00741.hp2 HG01070.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.286-311G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53889327 | |||||||
| chr19:53889351 | A | G | 1 | a0001c0002t0001g0089 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.286-287A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53889351 | |||||||
| chr19:53889424 | G | GT | 51 | a0001c0001t0001g0044 a0001c0001t0003g0021 a0001c0001t0003g0045 others(48): Show |
51 | HG00741.hp1 HG00741.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.286-203dupT | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr19 | 53889424 | ||||||
| chr19:53889494 | C | G | 29 | a0001c0001t0001g0044 a0001c0003t0002g0020 a0001c0004t0001g0155 others(26): Show |
29 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.286-144C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53889494 | |||||||
| chr19:53889572 | A | C | 28 | a0001c0001t0001g0044 a0001c0003t0002g0020 a0001c0004t0001g0155 others(25): Show |
28 | HG00741.hp2 HG01109.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.286-66A>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53889572 | |||||||
| chr19:53889626 | C | A | 1 | a0001c0002t0001g0091 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.286-12C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 3/17 | chr19 | 53889626 | |||||||
| chr19:53889804 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.397+55G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 4/17 | chr19 | 53889804 | |||||||
| chr19:53889820 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.398-66G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 4/17 | chr19 | 53889820 | |||||||
| chr19:53889826 | G | C | 1 | a0001c0001t0001g0206 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.398-60G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 4/17 | chr19 | 53889826 | |||||||
| chr19:53889857 | G | C | 1 | a0001c0024t0001g0094 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.398-29G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 4/17 | chr19 | 53889857 | |||||||
| chr19:53890046 | G | A | 22 | a0001c0001t0003g0021 a0001c0001t0003g0046 a0001c0001t0003g0048 others(19): Show |
22 | HG01943.hp1 HG02004.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.529+29G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890046 | |||||||
| chr19:53890160 | C | A | 4 | a0001c0002t0002g0349 a0001c0017t0001g0019 a0002c0013t0002g0017 others(1): Show |
4 | HG01070.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+143C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890160 | |||||||
| chr19:53890249 | T | G | 1 | a0001c0002t0001g0133 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.529+232T>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890249 | |||||||
| chr19:53890275 | G | A | 2 | a0001c0002t0001g0095 a0001c0002t0001g0096 |
2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.529+258G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890275 | |||||||
| chr19:53890318 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.529+301G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890318 | |||||||
| chr19:53890472 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.529+455G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890472 | |||||||
| chr19:53890490 | C | T | 49 | a0001c0001t0001g0044 a0001c0001t0003g0021 a0001c0001t0003g0045 others(46): Show |
49 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.529+473C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890490 | |||||||
| chr19:53890551 | G | A | 27 | a0001c0001t0001g0044 a0001c0002t0001g0054 a0001c0004t0001g0336 others(24): Show |
27 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.529+534G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890551 | |||||||
| chr19:53890552 | C | T | 1 | a0001c0002t0001g0054 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.529+535C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890552 | |||||||
| chr19:53890581 | A | G | 22 | a0001c0001t0003g0021 a0001c0001t0003g0045 a0001c0001t0003g0046 others(19): Show |
22 | HG01943.hp1 HG02004.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.529+564A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890581 | |||||||
| chr19:53890605 | G | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0002t0001g0243 others(3): Show |
6 | HG01346.hp2 HG01975.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.529+588G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890605 | |||||||
| chr19:53890646 | A | G | 4 | a0001c0002t0001g0088 a0001c0002t0001g0128 a0001c0002t0001g0129 others(1): Show |
4 | NA18950.hp1 NA18982.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+629A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890646 | |||||||
| chr19:53890691 | C | T | 3 | a0001c0011t0001g0157 a0001c0011t0001g0158 a0001c0011t0001g0159 |
3 | HG03491.hp2 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.529+674C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890691 | |||||||
| chr19:53890712 | G | C | 6 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0003g0048 others(3): Show |
6 | HG02004.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.529+695G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890712 | |||||||
| chr19:53890745 | C | A | 1 | a0001c0004t0002g0339 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.529+728C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890745 | |||||||
| chr19:53890748 | AT | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0177 others(10): Show |
14 | HG00423.hp2 HG00609.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.529+752delT | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr19 | 53890748 | ||||||
| chr19:53890748 | ATT | A | 97 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0002t0001g0003 others(94): Show |
98 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.529+751_529+752del others(2): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr19 | 53890748 | ||||||
| chr19:53890748 | ATTT | A | 47 | a0001c0001t0001g0044 a0001c0002t0001g0097 a0001c0002t0001g0098 others(44): Show |
47 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.529+750_529+752del others(3): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr19 | 53890748 | ||||||
| chr19:53890748 | ATTTT | A | 8 | a0001c0001t0003g0021 a0001c0001t0003g0045 a0001c0001t0003g0046 others(5): Show |
8 | HG02004.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.529+749_529+752del others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr19 | 53890748 | ||||||
| chr19:53890813 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0318 a0001c0001t0001g0319 |
4 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+796A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890813 | |||||||
| chr19:53890917 | C | A | 49 | a0001c0001t0001g0044 a0001c0001t0003g0021 a0001c0001t0003g0045 others(46): Show |
49 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.530-757C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53890917 | |||||||
| chr19:53891047 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0160 others(13): Show |
18 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.530-627G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53891047 | |||||||
| chr19:53891099 | G | A | 43 | a0001c0001t0001g0044 a0001c0001t0003g0021 a0001c0003t0002g0020 others(40): Show |
43 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.530-575G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53891099 | |||||||
| chr19:53891210 | C | G | 22 | a0001c0001t0003g0021 a0001c0001t0003g0045 a0001c0001t0003g0046 others(19): Show |
22 | HG01943.hp1 HG02004.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.530-464C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53891210 | |||||||
| chr19:53891265 | A | C | 2 | a0001c0001t0001g0241 a0001c0001t0001g0268 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.530-409A>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53891265 | |||||||
| chr19:53891278 | C | CT | 29 | a0001c0001t0001g0164 a0001c0001t0001g0238 a0001c0001t0001g0239 others(26): Show |
29 | HG01070.hp2 HG01109.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.530-380dupT | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr19 | 53891278 | ||||||
| chr19:53891278 | CT | C | 7 | a0001c0001t0001g0160 a0001c0001t0001g0177 a0001c0001t0001g0210 others(4): Show |
7 | HG01256.hp2 HG01517.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.530-380delT | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr19 | 53891278 | ||||||
| chr19:53891339 | T | C | 1 | a0002c0013t0002g0017 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.530-335T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53891339 | |||||||
| chr19:53891432 | ACGC | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0318 a0001c0001t0001g0319 |
4 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-240_530-238del others(3): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr19 | 53891432 | ||||||
| chr19:53891443 | A | AT | 154 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0101 others(151): Show |
155 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.530-216dupT | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr19 | 53891443 | ||||||
| chr19:53891562 | A | G | 2 | a0001c0002t0001g0054 a0001c0002t0001g0096 |
2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.530-112A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 5/17 | chr19 | 53891562 | |||||||
| chr19:53891844 | G | T | 122 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0002t0001g0003 others(119): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.686+14G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 6/17 | chr19 | 53891844 | |||||||
| chr19:53891993 | G | A | 1 | a0001c0002t0001g0165 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.686+163G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 6/17 | chr19 | 53891993 | |||||||
| chr19:53892047 | T | G | 1 | a0001c0010t0002g0211 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.686+217T>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 6/17 | chr19 | 53892047 | |||||||
| chr19:53892110 | C | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0047 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.686+280C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 6/17 | chr19 | 53892110 | |||||||
| chr19:53892362 | G | C | 201 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(198): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.687-147G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 6/17 | chr19 | 53892362 | |||||||
| chr19:53892749 | TGC | T | 4 | a0001c0001t0003g0048 a0001c0001t0003g0050 a0001c0001t0003g0051 others(1): Show |
4 | HG02257.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.821+109_821+110del others(2): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr19 | 53892749 | ||||||
| chr19:53892752 | G | A | 4 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0003g0049 others(1): Show |
4 | HG02004.hp1 HG02145.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.821+109G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892752 | |||||||
| chr19:53892752 | G | GCA | 22 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0164 others(19): Show |
23 | HG00323.hp1 HG00673.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.821+137_821+138dup others(2): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr19 | 53892752 | ||||||
| chr19:53892752 | GCA | G | 6 | a0001c0001t0001g0311 a0001c0001t0001g0315 a0001c0002t0001g0060 others(3): Show |
6 | HG01981.hp2 HG02698.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.821+137_821+138del others(2): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr19 | 53892752 | ||||||
| chr19:53892754 | A | G | 150 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0101 others(147): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.821+111A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892754 | |||||||
| chr19:53892756 | A | G | 3 | a0001c0001t0001g0047 a0001c0001t0003g0021 a0001c0002t0001g0060 |
3 | HG01981.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.821+113A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892756 | |||||||
| chr19:53892758 | A | G | 1 | a0001c0002t0001g0031 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.821+115A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892758 | |||||||
| chr19:53892774 | A | G | 1 | a0001c0007t0001g0154 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.821+131A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892774 | |||||||
| chr19:53892776 | A | G | 2 | a0001c0002t0001g0086 a0001c0002t0001g0132 |
2 | HG00099.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.821+133A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892776 | |||||||
| chr19:53892778 | A | G | 191 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(188): Show |
199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.821+135A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892778 | |||||||
| chr19:53892780 | ACG | A | 4 | a0001c0001t0001g0263 a0001c0002t0001g0086 a0001c0002t0001g0132 others(1): Show |
4 | HG00099.hp1 HG00733.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.821+139_821+140del others(2): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr19 | 53892780 | ||||||
| chr19:53892782 | G | A | 199 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(196): Show |
207 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.821+139G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892782 | |||||||
| chr19:53892788 | A | G | 195 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(192): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.821+145A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892788 | |||||||
| chr19:53892792 | G | A | 194 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0101 others(191): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.821+149G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892792 | |||||||
| chr19:53892792 | G | GCACA | 7 | a0001c0001t0001g0259 a0001c0002t0001g0060 a0001c0002t0001g0065 others(4): Show |
7 | HG01361.hp2 HG01981.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.821+153_821+156dup others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr19 | 53892792 | ||||||
| chr19:53892793 | C | A | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.821+150C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892793 | |||||||
| chr19:53892891 | C | T | 2 | a0001c0010t0002g0036 a0001c0010t0002g0037 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.822-97C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892891 | |||||||
| chr19:53892954 | C | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0173 a0001c0001t0001g0195 others(3): Show |
6 | HG02055.hp2 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.822-34C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892954 | |||||||
| chr19:53892955 | G | A | 1 | a0001c0002t0001g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.822-33G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 7/17 | chr19 | 53892955 | |||||||
| chr19:53893485 | A | G | 7 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0003g0048 others(4): Show |
7 | HG02004.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.939+94A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53893485 | |||||||
| chr19:53893617 | T | C | 1 | a0001c0007t0001g0154 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.939+226T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53893617 | |||||||
| chr19:53893645 | C | A | 1 | a0001c0002t0001g0031 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.939+254C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53893645 | |||||||
| chr19:53893678 | TG | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0318 a0001c0001t0001g0319 |
4 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+292delG | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53893678 | ||||||
| chr19:53893736 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.939+345A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53893736 | |||||||
| chr19:53893744 | T | A | 23 | a0001c0001t0001g0011 a0001c0001t0001g0273 a0001c0001t0001g0281 others(20): Show |
24 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.939+353T>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53893744 | |||||||
| chr19:53893756 | A | ATTTATTT others(5): Show |
26 | a0001c0001t0001g0101 a0001c0001t0001g0193 a0001c0001t0001g0194 others(23): Show |
26 | HG00408.hp1 HG00673.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.939+385_939+396dup others(12): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53893756 | ||||||
| chr19:53893756 | A | ATTTATTT others(11): Show |
3 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0140 |
3 | NA18985.hp1 NA19084.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.939+379_939+396dup others(18): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53893756 | ||||||
| chr19:53893756 | ATTTATT | A | 15 | a0001c0004t0001g0336 a0001c0004t0001g0340 a0001c0004t0001g0341 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.939+391_939+396del others(6): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53893756 | ||||||
| chr19:53893756 | ATTTATTT others(5): Show |
A | 1 | a0001c0001t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.939+385_939+396del others(12): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53893756 | ||||||
| chr19:53893793 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.939+402G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53893793 | |||||||
| chr19:53893824 | C | G | 165 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0101 others(162): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.939+433C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53893824 | |||||||
| chr19:53893897 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.939+506G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53893897 | |||||||
| chr19:53893954 | G | T | 17 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0010 others(14): Show |
22 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.939+563G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53893954 | |||||||
| chr19:53893987 | A | C | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.939+596A>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53893987 | |||||||
| chr19:53893999 | C | T | 7 | a0001c0004t0001g0340 a0001c0004t0002g0337 a0001c0004t0002g0338 others(4): Show |
7 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.939+608C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53893999 | |||||||
| chr19:53894052 | C | T | 1 | a0001c0001t0005g0270 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.939+661C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894052 | |||||||
| chr19:53894100 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.939+709G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894100 | |||||||
| chr19:53894103 | A | T | 1 | a0001c0001t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.939+712A>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894103 | |||||||
| chr19:53894210 | C | T | 9 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0003g0048 others(6): Show |
9 | HG02004.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.939+819C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894210 | |||||||
| chr19:53894233 | T | A | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.939+842T>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894233 | |||||||
| chr19:53894287 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.939+896G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894287 | |||||||
| chr19:53894386 | C | T | 8 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0003g0048 others(5): Show |
8 | HG02004.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+995C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894386 | |||||||
| chr19:53894400 | C | G | 179 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0101 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.939+1009C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894400 | |||||||
| chr19:53894446 | TTTTC | T | 50 | a0001c0001t0001g0011 a0001c0001t0001g0273 a0001c0001t0001g0281 others(47): Show |
56 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.939+1075_939+1078d others(6): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53894446 | ||||||
| chr19:53894497 | T | A | 1 | a0001c0001t0001g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.939+1106T>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894497 | |||||||
| chr19:53894600 | C | T | 1 | a0001c0005t0004g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.939+1209C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894600 | |||||||
| chr19:53894657 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.939+1266G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894657 | |||||||
| chr19:53894680 | G | A | 1 | a0001c0004t0002g0348 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.939+1289G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894680 | |||||||
| chr19:53894706 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.939+1315C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894706 | |||||||
| chr19:53894724 | C | A | 2 | a0001c0002t0001g0067 a0001c0002t0001g0106 |
2 | NA18612.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.939+1333C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894724 | |||||||
| chr19:53894728 | G | T | 60 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0273 others(57): Show |
67 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.939+1337G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894728 | |||||||
| chr19:53894752 | G | A | 1 | a0001c0002t0001g0077 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.939+1361G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894752 | |||||||
| chr19:53894754 | C | G | 6 | a0001c0002t0001g0093 a0001c0002t0001g0198 a0001c0002t0001g0199 others(3): Show |
6 | HG01074.hp1 HG01106.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.939+1363C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894754 | |||||||
| chr19:53894924 | C | T | 1 | a0001c0002t0001g0054 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.939+1533C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894924 | |||||||
| chr19:53894986 | G | A | 45 | a0001c0001t0001g0273 a0001c0001t0001g0281 a0001c0001t0001g0324 others(42): Show |
50 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.939+1595G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53894986 | |||||||
| chr19:53895019 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.939+1628C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53895019 | |||||||
| chr19:53895158 | C | A | 1 | a0001c0012t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.939+1767C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53895158 | |||||||
| chr19:53895234 | C | T | 2 | a0001c0010t0002g0036 a0001c0010t0002g0037 |
2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.939+1843C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53895234 | |||||||
| chr19:53895256 | G | C | 42 | a0001c0001t0001g0273 a0001c0001t0001g0281 a0001c0001t0001g0324 others(39): Show |
47 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.939+1865G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53895256 | |||||||
| chr19:53895304 | G | A | 2 | a0001c0010t0002g0211 a0001c0016t0001g0016 |
2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.939+1913G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53895304 | |||||||
| chr19:53895487 | C | CA | 25 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0182 others(22): Show |
27 | HG00597.hp2 HG00621.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.939+2117dupA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53895487 | ||||||
| chr19:53895487 | CA | C | 60 | a0001c0001t0001g0044 a0001c0001t0001g0177 a0001c0001t0001g0273 others(57): Show |
66 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.939+2117delA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53895487 | ||||||
| chr19:53895539 | GCAA | G | 14 | a0001c0004t0001g0336 a0001c0004t0001g0341 a0001c0004t0001g0342 others(11): Show |
14 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.939+2154_939+2156d others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53895539 | ||||||
| chr19:53895673 | G | A | 6 | a0001c0002t0001g0097 a0001c0002t0001g0107 a0001c0002t0001g0243 others(3): Show |
6 | HG02486.hp1 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.939+2282G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53895673 | |||||||
| chr19:53895691 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.940-2268G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53895691 | |||||||
| chr19:53895782 | G | A | 2 | a0001c0001t0001g0311 a0001c0001t0001g0315 |
2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.940-2177G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53895782 | |||||||
| chr19:53895887 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.940-2072G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53895887 | |||||||
| chr19:53895958 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.940-2001G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53895958 | |||||||
| chr19:53896121 | T | C | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.940-1838T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53896121 | |||||||
| chr19:53896305 | A | G | 4 | a0001c0010t0002g0036 a0001c0010t0002g0037 a0001c0010t0002g0211 others(1): Show |
4 | HG02895.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-1654A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53896305 | |||||||
| chr19:53896376 | G | GATT | 4 | a0001c0001t0001g0245 a0001c0001t0001g0309 a0001c0001t0004g0233 others(1): Show |
4 | HG02280.hp2 HG02698.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.940-1538_940-1536d others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53896376 | ||||||
| chr19:53896376 | GATT | G | 105 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0027 others(102): Show |
105 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.940-1538_940-1536d others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53896376 | ||||||
| chr19:53896376 | GATTATT | G | 75 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0101 others(72): Show |
76 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.940-1541_940-1536d others(8): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53896376 | ||||||
| chr19:53896376 | GATTATTA others(2): Show |
G | 86 | a0001c0001t0001g0177 a0001c0001t0001g0183 a0001c0001t0001g0184 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.940-1544_940-1536d others(11): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53896376 | ||||||
| chr19:53896376 | GATTATTA others(5): Show |
G | 6 | a0001c0001t0001g0047 a0001c0001t0001g0280 a0001c0001t0001g0287 others(3): Show |
6 | HG02080.hp1 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-1547_940-1536d others(14): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53896376 | ||||||
| chr19:53896376 | GATTATTA others(8): Show |
G | 30 | a0001c0001t0005g0270 a0001c0002t0001g0098 a0001c0003t0001g0001 others(27): Show |
35 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.940-1550_940-1536d others(17): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53896376 | ||||||
| chr19:53896376 | GATTATTA others(11): Show |
G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0218 a0001c0001t0001g0318 others(1): Show |
5 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.940-1553_940-1536d others(20): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53896376 | ||||||
| chr19:53896376 | GATTATTA others(14): Show |
G | 1 | a0001c0002t0001g0104 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.940-1556_940-1536d others(23): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53896376 | ||||||
| chr19:53896542 | C | A | 1 | a0001c0004t0002g0344 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.940-1417C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53896542 | |||||||
| chr19:53896627 | C | T | 1 | a0001c0002t0001g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.940-1332C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53896627 | |||||||
| chr19:53896671 | C | T | 43 | a0001c0001t0001g0011 a0001c0001t0001g0318 a0001c0001t0001g0319 others(40): Show |
49 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.940-1288C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53896671 | |||||||
| chr19:53897020 | G | C | 4 | a0001c0010t0002g0036 a0001c0010t0002g0037 a0001c0010t0002g0211 others(1): Show |
4 | HG02895.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-939G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53897020 | |||||||
| chr19:53897030 | C | T | 1 | a0001c0026t0005g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.940-929C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53897030 | |||||||
| chr19:53897288 | C | T | 3 | a0001c0002t0001g0054 a0001c0012t0001g0056 a0001c0012t0002g0055 |
3 | HG01891.hp1 HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.940-671C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53897288 | |||||||
| chr19:53897356 | C | A | 1 | a0001c0001t0001g0287 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.940-603C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53897356 | |||||||
| chr19:53897357 | C | T | 3 | a0001c0002t0001g0054 a0001c0012t0001g0056 a0001c0012t0002g0055 |
3 | HG01891.hp1 HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.940-602C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53897357 | |||||||
| chr19:53897741 | GA | G | 12 | a0001c0001t0001g0044 a0001c0001t0004g0008 a0001c0001t0004g0212 others(9): Show |
13 | HG01109.hp2 HG02109.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.940-211delA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53897741 | ||||||
| chr19:53897768 | TAATA | T | 7 | a0001c0006t0001g0142 a0001c0006t0003g0032 a0001c0006t0003g0143 others(4): Show |
7 | HG01943.hp1 HG02622.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.940-184_940-181del others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr19 | 53897768 | ||||||
| chr19:53897779 | C | T | 2 | a0001c0010t0002g0211 a0001c0016t0001g0016 |
2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.940-180C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 9/17 | chr19 | 53897779 | |||||||
| chr19:53898240 | C | T | 2 | a0001c0002t0001g0062 a0001c0002t0001g0074 |
2 | HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1092+129C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 10/17 | chr19 | 53898240 | |||||||
| chr19:53898348 | G | C | 4 | a0001c0002t0001g0062 a0001c0002t0001g0074 a0001c0002t0001g0105 others(1): Show |
4 | HG01346.hp1 HG01433.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1093-92G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 10/17 | chr19 | 53898348 | |||||||
| chr19:53898391 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1093-49A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 10/17 | chr19 | 53898391 | |||||||
| chr19:53898654 | T | G | 55 | a0001c0001t0001g0044 a0001c0001t0003g0021 a0001c0001t0004g0008 others(52): Show |
61 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1281+26T>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898654 | |||||||
| chr19:53898763 | T | G | 52 | a0001c0001t0001g0044 a0001c0001t0003g0021 a0001c0001t0004g0008 others(49): Show |
58 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1281+135T>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898763 | |||||||
| chr19:53898782 | C | CG | 32 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0188 others(29): Show |
33 | HG00609.hp2 HG00673.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1281+163dupG | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr19 | 53898782 | ||||||
| chr19:53898782 | C | CGG | 57 | a0001c0001t0001g0009 a0001c0001t0001g0044 a0001c0001t0001g0047 others(54): Show |
58 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1281+162_1281+163d others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr19 | 53898782 | ||||||
| chr19:53898782 | C | CGGG | 85 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(82): Show |
88 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1281+161_1281+163d others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr19 | 53898782 | ||||||
| chr19:53898782 | C | CGGGG | 75 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(72): Show |
76 | HG00544.hp2 HG00735.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1281+160_1281+163d others(6): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr19 | 53898782 | ||||||
| chr19:53898782 | C | CGGGGG | 32 | a0001c0001t0001g0222 a0001c0001t0001g0281 a0001c0001t0001g0286 others(29): Show |
32 | HG01243.hp2 HG01346.hp1 HG01993.hp1 others(29): Show |
intron_variant | MODIFIER | c.1281+159_1281+163d others(7): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr19 | 53898782 | ||||||
| chr19:53898789 | GGGT | G | 29 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0010 others(26): Show |
34 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1281+162_1281+164d others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898789 | |||||||
| chr19:53898791 | GTCCTTGG others(77): Show |
G | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1281+164_1281+247d others(86): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898791 | |||||||
| chr19:53898799 | G | T | 1 | a0001c0001t0001g0027 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1281+171G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898799 | |||||||
| chr19:53898819 | G | T | 12 | a0001c0001t0001g0044 a0001c0001t0004g0008 a0001c0001t0004g0212 others(9): Show |
13 | HG01109.hp2 HG02109.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1281+191G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898819 | |||||||
| chr19:53898864 | A | T | 42 | a0001c0001t0003g0021 a0001c0002t0001g0165 a0001c0003t0001g0001 others(39): Show |
47 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1281+236A>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898864 | |||||||
| chr19:53898880 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1281+252C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898880 | |||||||
| chr19:53898880 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1281+252C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898880 | |||||||
| chr19:53898881 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1281+253T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898881 | |||||||
| chr19:53898883 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1281+255C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898883 | |||||||
| chr19:53898885 | C | G | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1281+257C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898885 | |||||||
| chr19:53898887 | G | GA | 45 | a0001c0001t0003g0021 a0001c0002t0002g0349 a0001c0003t0001g0001 others(42): Show |
50 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1281+259_1281+260i others(3): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898887 | |||||||
| chr19:53898893 | T | C | 1 | a0001c0002t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1281+265T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898893 | |||||||
| chr19:53898901 | T | C | 1 | a0001c0004t0001g0342 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1281+273T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898901 | |||||||
| chr19:53898908 | A | T | 1 | a0001c0004t0001g0342 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1281+280A>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898908 | |||||||
| chr19:53898912 | A | C | 1 | a0001c0004t0001g0342 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1281+284A>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898912 | |||||||
| chr19:53898914 | C | CGGGGGCG others(82): Show |
41 | a0001c0001t0003g0021 a0001c0003t0001g0001 a0001c0003t0001g0002 others(38): Show |
46 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1281+302_1281+303i others(91): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr19 | 53898914 | ||||||
| chr19:53898974 | G | C | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1281+346G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898974 | |||||||
| chr19:53898976 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1281+348G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53898976 | |||||||
| chr19:53899097 | A | G | 15 | a0001c0004t0001g0336 a0001c0004t0001g0341 a0001c0004t0001g0342 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1281+469A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899097 | |||||||
| chr19:53899109 | C | T | 4 | a0001c0001t0001g0286 a0001c0002t0001g0070 a0001c0002t0001g0089 others(1): Show |
4 | HG02083.hp2 HG03831.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281+481C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899109 | |||||||
| chr19:53899147 | T | A | 4 | a0001c0010t0002g0036 a0001c0010t0002g0037 a0001c0010t0002g0211 others(1): Show |
4 | HG02895.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+519T>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899147 | |||||||
| chr19:53899174 | A | T | 15 | a0001c0004t0001g0336 a0001c0004t0001g0341 a0001c0004t0001g0342 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1281+546A>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899174 | |||||||
| chr19:53899179 | C | T | 2 | a0001c0003t0001g0284 a0001c0003t0001g0317 |
2 | NA18970.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1281+551C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899179 | |||||||
| chr19:53899203 | G | T | 2 | a0001c0010t0002g0211 a0001c0016t0001g0016 |
2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1281+575G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899203 | |||||||
| chr19:53899234 | G | A | 29 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0010 others(26): Show |
34 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1281+606G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899234 | |||||||
| chr19:53899293 | G | C | 15 | a0001c0004t0001g0336 a0001c0004t0001g0341 a0001c0004t0001g0342 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1281+665G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899293 | |||||||
| chr19:53899478 | G | A | 1 | a0001c0003t0005g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1282-755G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899478 | |||||||
| chr19:53899591 | C | CT | 38 | a0001c0001t0003g0021 a0001c0003t0001g0001 a0001c0003t0001g0002 others(35): Show |
43 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1282-629dupT | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr19 | 53899591 | ||||||
| chr19:53899591 | CT | C | 10 | a0001c0001t0001g0047 a0001c0001t0001g0160 a0001c0001t0001g0278 others(7): Show |
10 | HG01256.hp2 HG01975.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1282-629delT | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr19 | 53899591 | ||||||
| chr19:53899618 | C | T | 1 | a0001c0002t0001g0297 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1282-615C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899618 | |||||||
| chr19:53899647 | C | T | 8 | a0001c0002t0002g0349 a0001c0010t0002g0036 a0001c0010t0002g0037 others(5): Show |
8 | HG01070.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1282-586C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899647 | |||||||
| chr19:53899822 | G | A | 12 | a0001c0001t0001g0044 a0001c0001t0004g0008 a0001c0001t0004g0212 others(9): Show |
13 | HG01109.hp2 HG02109.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1282-411G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899822 | |||||||
| chr19:53899833 | C | T | 12 | a0001c0001t0001g0044 a0001c0001t0004g0008 a0001c0001t0004g0212 others(9): Show |
13 | HG01109.hp2 HG02109.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1282-400C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899833 | |||||||
| chr19:53899836 | T | C | 12 | a0001c0001t0001g0044 a0001c0001t0004g0008 a0001c0001t0004g0212 others(9): Show |
13 | HG01109.hp2 HG02109.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1282-397T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899836 | |||||||
| chr19:53899839 | G | A | 12 | a0001c0001t0001g0044 a0001c0001t0004g0008 a0001c0001t0004g0212 others(9): Show |
13 | HG01109.hp2 HG02109.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1282-394G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899839 | |||||||
| chr19:53899855 | G | A | 86 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(83): Show |
93 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1282-378G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 11/17 | chr19 | 53899855 | |||||||
| chr19:53900372 | G | T | 1 | a0001c0006t0003g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1374-47G>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 12/17 | chr19 | 53900372 | |||||||
| chr19:53900399 | C | G | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1374-20C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 12/17 | chr19 | 53900399 | |||||||
| chr19:53900547 | T | C | 40 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0010 others(37): Show |
45 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1437-64T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 13/17 | chr19 | 53900547 | |||||||
| chr19:53900780 | T | C | 4 | a0001c0001t0001g0100 a0001c0001t0001g0222 a0001c0001t0001g0255 others(1): Show |
4 | NA18974.hp1 NA19056.hp1 NA19059.hp1 others(1): Show |
intron_variant | MODIFIER | c.1575+31T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53900780 | |||||||
| chr19:53900882 | T | G | 52 | a0001c0001t0001g0044 a0001c0001t0004g0008 a0001c0001t0004g0212 others(49): Show |
58 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1575+133T>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53900882 | |||||||
| chr19:53900883 | C | T | 1 | a0001c0004t0001g0155 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1575+134C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53900883 | |||||||
| chr19:53900992 | G | C | 4 | a0001c0002t0002g0349 a0001c0017t0001g0019 a0002c0013t0002g0017 others(1): Show |
4 | HG01070.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1575+243G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53900992 | |||||||
| chr19:53901008 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0188 a0001c0007t0001g0149 |
3 | NA18939.hp2 NA18945.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1575+259C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901008 | |||||||
| chr19:53901009 | G | A | 7 | a0001c0004t0002g0337 a0001c0004t0002g0338 a0001c0004t0002g0343 others(4): Show |
7 | HG01243.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1575+260G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901009 | |||||||
| chr19:53901060 | C | T | 2 | a0001c0002t0001g0108 a0001c0002t0001g0116 |
2 | HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1575+311C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901060 | |||||||
| chr19:53901090 | C | G | 12 | a0001c0001t0001g0044 a0001c0001t0004g0008 a0001c0001t0004g0212 others(9): Show |
13 | HG01109.hp2 HG02109.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1575+341C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901090 | |||||||
| chr19:53901172 | T | C | 2 | a0001c0001t0001g0273 a0001c0001t0001g0281 |
2 | HG02738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1575+423T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901172 | |||||||
| chr19:53901215 | G | C | 52 | a0001c0001t0001g0044 a0001c0001t0004g0008 a0001c0001t0004g0212 others(49): Show |
58 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1575+466G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901215 | |||||||
| chr19:53901220 | T | A | 1 | a0001c0001t0001g0027 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1575+471T>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901220 | |||||||
| chr19:53901222 | T | G | 288 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(285): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1575+473T>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901222 | |||||||
| chr19:53901324 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1575+575A>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901324 | |||||||
| chr19:53901476 | G | A | 1 | a0001c0003t0001g0283 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1575+727G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901476 | |||||||
| chr19:53901551 | C | CA | 56 | a0001c0001t0001g0227 a0001c0001t0001g0240 a0001c0001t0001g0249 others(53): Show |
61 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1575+822dupA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53901551 | ||||||
| chr19:53901551 | C | CAA | 11 | a0001c0003t0001g0307 a0001c0003t0002g0020 a0001c0004t0001g0336 others(8): Show |
11 | HG00741.hp1 HG01109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1575+821_1575+822d others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53901551 | ||||||
| chr19:53901551 | CA | C | 17 | a0001c0001t0001g0013 a0001c0001t0004g0008 a0001c0001t0005g0270 others(14): Show |
18 | HG01070.hp2 HG01109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1575+822delA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53901551 | ||||||
| chr19:53901616 | C | T | 40 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0010 others(37): Show |
45 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1575+867C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901616 | |||||||
| chr19:53901622 | C | T | 1 | a0001c0002t0001g0121 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1575+873C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901622 | |||||||
| chr19:53901682 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1575+933T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901682 | |||||||
| chr19:53901786 | G | C | 2 | a0001c0014t0001g0025 a0001c0014t0001g0026 |
2 | NA18964.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1575+1037G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901786 | |||||||
| chr19:53901849 | C | CA | 10 | a0001c0001t0001g0207 a0001c0001t0001g0256 a0001c0001t0001g0309 others(7): Show |
10 | HG01361.hp1 HG01433.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1575+1117dupA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53901849 | ||||||
| chr19:53901849 | C | CAA | 9 | a0001c0002t0002g0349 a0001c0005t0006g0040 a0001c0010t0002g0036 others(6): Show |
9 | HG01070.hp2 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1575+1116_1575+111 others(6): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53901849 | ||||||
| chr19:53901849 | C | CAAA | 11 | a0001c0001t0001g0044 a0001c0001t0004g0008 a0001c0001t0004g0212 others(8): Show |
12 | HG01109.hp2 HG02109.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1575+1115_1575+111 others(7): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53901849 | ||||||
| chr19:53901849 | CA | C | 43 | a0001c0001t0001g0100 a0001c0001t0001g0163 a0001c0001t0001g0177 others(40): Show |
48 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1575+1117delA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53901849 | ||||||
| chr19:53901862 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1575+1113A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901862 | |||||||
| chr19:53901863 | A | G | 7 | a0001c0001t0001g0047 a0001c0001t0003g0045 a0001c0001t0003g0046 others(4): Show |
7 | HG02004.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1575+1114A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53901863 | |||||||
| chr19:53902043 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1576-1030T>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53902043 | |||||||
| chr19:53902236 | AAACCCCG others(122): Show |
A | 1 | a0004c0019t0001g0203 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1576-835_1576-707d others(2): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53902236 | ||||||
| chr19:53902242 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0318 a0001c0001t0001g0319 |
4 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1576-831C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53902242 | |||||||
| chr19:53902420 | G | A | 1 | a0001c0002t0001g0064 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1576-653G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53902420 | |||||||
| chr19:53902539 | A | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG03688.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1576-534A>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53902539 | |||||||
| chr19:53902580 | A | G | 4 | a0001c0002t0002g0349 a0001c0017t0001g0019 a0002c0013t0002g0017 others(1): Show |
4 | HG01070.hp2 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1576-493A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53902580 | |||||||
| chr19:53902713 | A | C | 12 | a0001c0001t0001g0044 a0001c0001t0004g0008 a0001c0001t0004g0212 others(9): Show |
13 | HG01109.hp2 HG02109.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1576-360A>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53902713 | |||||||
| chr19:53902820 | G | A | 1 | a0001c0017t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1576-253G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53902820 | |||||||
| chr19:53902827 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1576-246G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53902827 | |||||||
| chr19:53902842 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1576-231G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53902842 | |||||||
| chr19:53902890 | C | CA | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
89 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1576-157dupA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53902890 | ||||||
| chr19:53902890 | C | CAA | 13 | a0001c0001t0001g0207 a0001c0001t0001g0267 a0001c0001t0001g0271 others(10): Show |
13 | HG01175.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1576-158_1576-157d others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53902890 | ||||||
| chr19:53902890 | C | CAAA | 6 | a0001c0001t0001g0222 a0001c0001t0001g0255 a0001c0001t0001g0310 others(3): Show |
6 | HG03453.hp2 HG03540.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.1576-159_1576-157d others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53902890 | ||||||
| chr19:53902890 | C | CAAAAAAA others(3): Show |
4 | a0001c0004t0002g0335 a0001c0004t0002g0337 a0001c0004t0002g0346 others(1): Show |
4 | HG03209.hp1 HG03471.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1576-166_1576-157d others(12): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53902890 | ||||||
| chr19:53902890 | C | CAAAAAAA others(4): Show |
7 | a0001c0004t0001g0341 a0001c0004t0002g0338 a0001c0004t0002g0343 others(4): Show |
7 | HG01243.hp2 HG02145.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1576-167_1576-157d others(13): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53902890 | ||||||
| chr19:53902890 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0011 | 2 | HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1576-168_1576-157d others(14): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53902890 | ||||||
| chr19:53902890 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0318 a0001c0001t0001g0319 |
2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1576-169_1576-157d others(15): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53902890 | ||||||
| chr19:53902890 | C | CAAAAAAA others(8): Show |
1 | a0001c0004t0001g0342 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1576-171_1576-157d others(17): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53902890 | ||||||
| chr19:53902890 | CA | C | 47 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0216 others(44): Show |
52 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1576-157delA | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53902890 | ||||||
| chr19:53902890 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0001g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1576-168_1576-157d others(14): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr19 | 53902890 | ||||||
| chr19:53902912 | A | C | 34 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0010 others(31): Show |
39 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1576-161A>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53902912 | |||||||
| chr19:53902937 | T | C | 42 | a0001c0001t0003g0021 a0001c0003t0001g0001 a0001c0003t0001g0002 others(39): Show |
47 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1576-136T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53902937 | |||||||
| chr19:53902957 | G | C | 6 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0003g0048 others(3): Show |
6 | HG02004.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1576-116G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 14/17 | chr19 | 53902957 | |||||||
| chr19:53903174 | G | C | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1656+21G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 15/17 | chr19 | 53903174 | |||||||
| chr19:53903222 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1656+69A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 15/17 | chr19 | 53903222 | |||||||
| chr19:53903344 | A | T | 10 | a0001c0003t0005g0205 a0001c0006t0001g0142 a0001c0006t0003g0032 others(7): Show |
10 | HG01943.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1656+191A>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 15/17 | chr19 | 53903344 | |||||||
| chr19:53903555 | C | CAACTAAA others(43): Show |
1 | a0001c0002t0001g0064 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1656+403_1656+452d others(52): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr19 | 53903555 | ||||||
| chr19:53903851 | T | C | 1 | a0001c0002t0001g0116 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1656+698T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 15/17 | chr19 | 53903851 | |||||||
| chr19:53904062 | A | T | 15 | a0001c0004t0001g0336 a0001c0004t0001g0341 a0001c0004t0001g0342 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1657-573A>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 15/17 | chr19 | 53904062 | |||||||
| chr19:53904284 | A | C | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1657-351A>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 15/17 | chr19 | 53904284 | |||||||
| chr19:53904356 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0318 a0001c0001t0001g0319 others(4): Show |
8 | HG01070.hp2 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1657-279T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 15/17 | chr19 | 53904356 | |||||||
| chr19:53904553 | C | T | 3 | a0001c0001t0003g0046 a0001c0001t0003g0048 a0001c0001t0003g0049 |
3 | HG02004.hp1 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1657-82C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 15/17 | chr19 | 53904553 | |||||||
| chr19:53904560 | G | A | 1 | a0001c0002t0001g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1657-75G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 15/17 | chr19 | 53904560 | |||||||
| chr19:53904781 | A | AT | 25 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0003g0045 others(22): Show |
26 | HG01109.hp2 HG01175.hp2 HG02004.hp1 others(23): Show |
intron_variant | MODIFIER | c.1764+39_1764+40ins others(1): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53904781 | |||||||
| chr19:53904918 | G | C | 1 | a0001c0003t0001g0317 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1764+176G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53904918 | |||||||
| chr19:53904961 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1764+219C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53904961 | |||||||
| chr19:53904971 | C | T | 1 | a0001c0002t0001g0128 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1764+229C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53904971 | |||||||
| chr19:53905085 | C | A | 3 | a0001c0002t0001g0088 a0001c0002t0001g0128 a0001c0002t0001g0130 |
3 | NA18950.hp1 NA18993.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1764+343C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905085 | |||||||
| chr19:53905136 | A | G | 1 | a0001c0002t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1764+394A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905136 | |||||||
| chr19:53905187 | G | A | 2 | a0001c0001t0001g0101 a0001c0002t0001g0083 |
2 | HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1764+445G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905187 | |||||||
| chr19:53905293 | G | C | 1 | a0001c0001t0001g0281 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1764+551G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905293 | |||||||
| chr19:53905339 | C | A | 1 | a0001c0006t0003g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1764+597C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905339 | |||||||
| chr19:53905347 | C | A | 1 | a0001c0007t0001g0141 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1764+605C>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905347 | |||||||
| chr19:53905382 | T | TAC | 11 | a0001c0001t0001g0274 a0001c0001t0003g0021 a0001c0001t0003g0046 others(8): Show |
11 | HG00621.hp1 HG01106.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.1764+647_1764+648d others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53905382 | ||||||
| chr19:53905390 | C | CAT | 58 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0173 others(55): Show |
63 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1764+648_1764+649i others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905390 | |||||||
| chr19:53905391 | G | A | 1 | a0001c0002t0001g0089 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1764+649G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905391 | |||||||
| chr19:53905413 | T | C | 1 | a0001c0003t0001g0179 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1764+671T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905413 | |||||||
| chr19:53905436 | T | C | 1 | a0004c0019t0001g0203 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1764+694T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905436 | |||||||
| chr19:53905548 | C | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0173 a0001c0001t0001g0195 others(2): Show |
5 | HG02055.hp2 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1765-769C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905548 | |||||||
| chr19:53905581 | T | G | 1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1765-736T>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905581 | |||||||
| chr19:53905671 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0172 |
2 | NA18944.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1765-646A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905671 | |||||||
| chr19:53905683 | C | T | 1 | a0004c0019t0001g0203 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1765-634C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905683 | |||||||
| chr19:53905685 | T | C | 1 | a0004c0019t0001g0203 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1765-632T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905685 | |||||||
| chr19:53905721 | ACTCTCCC others(39): Show |
A | 2 | a0001c0001t0001g0305 a0001c0001t0001g0313 |
2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1765-580_1765-535d others(48): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53905721 | ||||||
| chr19:53905761 | C | T | 9 | a0001c0001t0001g0044 a0001c0001t0001g0267 a0001c0002t0002g0349 others(6): Show |
9 | HG00597.hp1 HG01175.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1765-556C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905761 | |||||||
| chr19:53905761 | CG | C | 3 | a0001c0001t0001g0171 a0001c0001t0001g0228 a0001c0001t0001g0332 |
3 | NA18939.hp1 NA18945.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1765-555delG | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905761 | |||||||
| chr19:53905872 | A | ATTTCATC others(89): Show |
1 | a0004c0019t0001g0203 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1765-383_1765-382i others(98): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53905872 | ||||||
| chr19:53905893 | A | G | 1 | a0001c0006t0003g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1765-424A>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905893 | |||||||
| chr19:53905914 | G | GTC | 73 | a0001c0001t0001g0100 a0001c0001t0001g0177 a0001c0001t0001g0182 others(70): Show |
74 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.1765-384_1765-383d others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53905914 | ||||||
| chr19:53905914 | G | GTCTC | 23 | a0001c0001t0001g0257 a0001c0001t0001g0310 a0001c0002t0001g0091 others(20): Show |
28 | HG00423.hp1 HG00544.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1765-386_1765-383d others(6): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53905914 | ||||||
| chr19:53905914 | GTCTC | G | 6 | a0001c0001t0001g0186 a0001c0001t0001g0209 a0001c0001t0001g0239 others(3): Show |
6 | HG00609.hp2 HG00621.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1765-386_1765-383d others(6): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53905914 | ||||||
| chr19:53905935 | A | T | 2 | a0001c0002t0001g0087 a0001c0003t0002g0020 |
2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1765-382A>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53905935 | |||||||
| chr19:53906010 | G | A | 4 | a0001c0006t0003g0032 a0001c0006t0003g0144 a0001c0006t0003g0146 others(1): Show |
4 | HG01943.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1765-307G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906010 | |||||||
| chr19:53906013 | CTCTG | C | 34 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0173 others(31): Show |
35 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1765-296_1765-293d others(6): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906013 | ||||||
| chr19:53906021 | G | C | 9 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0004t0002g0337 others(6): Show |
9 | HG01943.hp1 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1765-296G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906021 | |||||||
| chr19:53906022 | T | C | 9 | a0001c0001t0003g0048 a0001c0001t0003g0049 a0001c0004t0002g0337 others(6): Show |
9 | HG01943.hp1 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1765-295T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906022 | |||||||
| chr19:53906024 | TC | T | 4 | a0001c0006t0003g0032 a0001c0006t0003g0144 a0001c0006t0003g0146 others(1): Show |
4 | HG01943.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1765-290delC | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906024 | ||||||
| chr19:53906025 | C | CCTCCTCC others(8): Show |
3 | a0001c0004t0002g0337 a0001c0004t0002g0344 a0001c0010t0002g0211 |
3 | HG03471.hp1 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1765-291_1765-290i others(17): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906025 | ||||||
| chr19:53906028 | TCCTCCTC others(6): Show |
T | 1 | a0001c0010t0002g0037 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1765-274_1765-262d others(15): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906028 | ||||||
| chr19:53906030 | C | T | 3 | a0001c0004t0002g0337 a0001c0004t0002g0344 a0001c0010t0002g0211 |
3 | HG03471.hp1 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1765-287C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906030 | |||||||
| chr19:53906031 | TCCTCCTC others(3): Show |
T | 3 | a0001c0001t0001g0286 a0001c0002t0001g0087 a0001c0010t0002g0036 |
3 | HG02083.hp2 HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1765-274_1765-265d others(12): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906031 | ||||||
| chr19:53906040 | T | C | 49 | a0001c0001t0001g0009 a0001c0001t0001g0193 a0001c0001t0001g0194 others(46): Show |
51 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1765-277T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906040 | |||||||
| chr19:53906040 | TC | T | 33 | a0001c0001t0001g0257 a0001c0001t0001g0310 a0001c0001t0003g0048 others(30): Show |
38 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1765-274delC | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906040 | ||||||
| chr19:53906041 | C | CCCT | 8 | a0001c0001t0001g0006 a0001c0001t0001g0253 a0001c0001t0001g0263 others(5): Show |
8 | HG00280.hp2 HG00621.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1765-233_1765-231d others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906041 | ||||||
| chr19:53906041 | C | CCCTCCTC others(8): Show |
2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA18966.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1765-245_1765-231d others(17): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906041 | ||||||
| chr19:53906041 | C | CCT | 43 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0001t0001g0183 others(40): Show |
43 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1765-275_1765-274i others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906041 | ||||||
| chr19:53906041 | C | CCTCCT | 8 | a0001c0001t0003g0021 a0001c0002t0001g0033 a0001c0002t0001g0064 others(5): Show |
8 | HG01358.hp1 HG02074.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1765-275_1765-274i others(7): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906041 | ||||||
| chr19:53906041 | C | CCTCCTCC others(4): Show |
1 | a0001c0002t0001g0121 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1765-275_1765-274i others(13): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906041 | ||||||
| chr19:53906041 | C | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0193 a0001c0001t0001g0194 others(46): Show |
51 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1765-276C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906041 | |||||||
| chr19:53906041 | CCCT | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0028 others(15): Show |
18 | HG00408.hp2 HG00741.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1765-233_1765-231d others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906041 | ||||||
| chr19:53906041 | CCCTCCT | C | 8 | a0001c0001t0001g0189 a0001c0001t0001g0210 a0001c0001t0001g0229 others(5): Show |
8 | HG01257.hp1 HG01358.hp2 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.1765-236_1765-231d others(8): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906041 | ||||||
| chr19:53906041 | CCCTCCTC others(8): Show |
C | 1 | a0001c0001t0001g0309 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1765-245_1765-231d others(17): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906041 | ||||||
| chr19:53906048 | CCTCCTCC others(47): Show |
C | 4 | a0001c0003t0001g0059 a0001c0003t0001g0272 a0001c0003t0001g0282 others(1): Show |
4 | HG02155.hp2 NA18969.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1765-266_1765-213d others(56): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906048 | ||||||
| chr19:53906049 | C | T | 9 | a0001c0004t0002g0335 a0001c0004t0002g0338 a0001c0004t0002g0339 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1765-268C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906049 | |||||||
| chr19:53906054 | CCTCCTCC others(38): Show |
C | 1 | a0001c0003t0001g0010 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1765-260_1765-216d others(47): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906054 | ||||||
| chr19:53906054 | CCTCCTCC others(41): Show |
C | 20 | a0001c0001t0001g0257 a0001c0001t0001g0310 a0001c0002t0001g0091 others(17): Show |
24 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1765-260_1765-213d others(50): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906054 | ||||||
| chr19:53906055 | C | G | 1 | a0001c0021t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1765-262C>G | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906055 | |||||||
| chr19:53906056 | T | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG02055.hp2 HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1765-261T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906056 | |||||||
| chr19:53906059 | T | TC | 9 | a0001c0004t0002g0335 a0001c0004t0002g0338 a0001c0004t0002g0339 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1765-256dupC | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906059 | ||||||
| chr19:53906061 | C | T | 1 | a0001c0001t0003g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1765-256C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906061 | |||||||
| chr19:53906063 | C | CCTTCTTC others(8): Show |
1 | a0001c0002t0001g0236 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1765-252_1765-251i others(17): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906063 | ||||||
| chr19:53906063 | C | T | 1 | a0001c0001t0003g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1765-254C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906063 | |||||||
| chr19:53906064 | C | T | 2 | a0001c0001t0003g0048 a0001c0001t0003g0049 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1765-253C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906064 | |||||||
| chr19:53906066 | C | T | 2 | a0001c0001t0003g0021 a0001c0002t0001g0236 |
2 | NA19043.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1765-251C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906066 | |||||||
| chr19:53906067 | C | T | 2 | a0001c0001t0003g0048 a0001c0001t0003g0049 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1765-250C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906067 | |||||||
| chr19:53906069 | C | CCTTCTTC others(8): Show |
1 | a0001c0004t0001g0342 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1765-246_1765-245i others(17): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906069 | ||||||
| chr19:53906069 | C | CCTTCTTC others(14): Show |
1 | a0001c0002t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1765-246_1765-245i others(23): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906069 | ||||||
| chr19:53906069 | C | CCTTCTTC others(26): Show |
1 | a0001c0002t0001g0200 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1765-246_1765-245i others(35): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906069 | ||||||
| chr19:53906069 | C | T | 4 | a0001c0001t0003g0021 a0001c0002t0001g0236 a0001c0004t0001g0341 others(1): Show |
4 | HG02809.hp2 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1765-248C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906069 | |||||||
| chr19:53906070 | C | T | 1 | a0001c0001t0003g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1765-247C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906070 | |||||||
| chr19:53906072 | C | CCTTCTTC others(5): Show |
1 | a0001c0003t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1765-243_1765-242i others(14): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906072 | ||||||
| chr19:53906072 | C | T | 9 | a0001c0001t0001g0271 a0001c0001t0003g0021 a0001c0002t0001g0200 others(6): Show |
9 | HG01952.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1765-245C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906072 | |||||||
| chr19:53906075 | C | CCTTCTTC others(29): Show |
1 | a0001c0005t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1765-240_1765-239i others(38): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906075 | ||||||
| chr19:53906075 | C | CCTTCTTC others(53): Show |
1 | a0001c0001t0001g0319 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1765-240_1765-239i others(62): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906075 | ||||||
| chr19:53906075 | C | T | 21 | a0001c0001t0001g0100 a0001c0001t0001g0271 a0001c0001t0003g0021 others(18): Show |
21 | HG00738.hp2 HG01358.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.1765-242C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906075 | |||||||
| chr19:53906078 | C | CCTT | 6 | a0001c0001t0001g0217 a0001c0001t0001g0313 a0001c0002t0001g0024 others(3): Show |
6 | HG00597.hp2 HG02027.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1765-237_1765-236i others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906078 | ||||||
| chr19:53906078 | C | CCTTCTT | 3 | a0001c0002t0001g0077 a0001c0002t0001g0122 a0001c0002t0001g0296 |
3 | HG00099.hp2 NA19070.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1765-237_1765-236i others(8): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906078 | ||||||
| chr19:53906078 | C | CCTTCTTC others(32): Show |
1 | a0001c0001t0001g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1765-237_1765-236i others(41): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906078 | ||||||
| chr19:53906078 | C | CCTTCTTC others(38): Show |
2 | a0001c0001t0001g0011 a0001c0012t0001g0056 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1765-237_1765-236i others(47): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906078 | ||||||
| chr19:53906078 | C | CCTTCTTC others(41): Show |
1 | a0001c0001t0001g0318 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1765-237_1765-236i others(50): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906078 | ||||||
| chr19:53906078 | C | CCTTCTTC others(50): Show |
1 | a0001c0001t0001g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1765-237_1765-236i others(59): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906078 | ||||||
| chr19:53906078 | C | CCTTCTTC others(53): Show |
1 | a0001c0001t0001g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1765-237_1765-236i others(62): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906078 | ||||||
| chr19:53906078 | C | CCTTCTTC others(56): Show |
1 | a0001c0001t0001g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1765-237_1765-236i others(65): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906078 | ||||||
| chr19:53906078 | C | CCTTCTTC others(8): Show |
1 | a0001c0002t0001g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1765-237_1765-236i others(17): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906078 | ||||||
| chr19:53906078 | C | T | 30 | a0001c0001t0001g0100 a0001c0001t0001g0271 a0001c0001t0001g0319 others(27): Show |
30 | HG00738.hp2 HG01358.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.1765-239C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906078 | |||||||
| chr19:53906079 | C | CTTCTTCT others(3): Show |
1 | a0001c0006t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1765-237_1765-236i others(12): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906079 | ||||||
| chr19:53906081 | C | CCTT | 5 | a0001c0001t0001g0238 a0001c0001t0001g0311 a0001c0001t0001g0315 others(2): Show |
5 | HG02698.hp2 HG03942.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1765-234_1765-233i others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTT | 5 | a0001c0001t0001g0240 a0001c0002t0001g0072 a0001c0002t0001g0082 others(2): Show |
5 | HG00673.hp2 HG01099.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765-234_1765-233i others(8): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(2): Show |
7 | a0001c0001t0001g0324 a0001c0002t0001g0090 a0001c0002t0001g0243 others(4): Show |
7 | HG02486.hp1 HG02965.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1765-234_1765-233i others(11): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(5): Show |
3 | a0001c0001t0001g0182 a0001c0002t0001g0114 a0001c0002t0001g0131 |
3 | HG01975.hp1 NA18947.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1765-234_1765-233i others(14): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(11): Show |
1 | a0001c0003t0005g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1765-234_1765-233i others(20): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(14): Show |
1 | a0001c0001t0005g0270 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1765-234_1765-233i others(23): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(17): Show |
1 | a0001c0001t0003g0046 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1765-234_1765-233i others(26): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(26): Show |
1 | a0001c0001t0003g0050 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1765-234_1765-233i others(35): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(29): Show |
1 | a0001c0001t0003g0051 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1765-234_1765-233i others(38): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(35): Show |
2 | a0001c0006t0003g0032 a0001c0006t0003g0144 |
2 | HG01943.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1765-234_1765-233i others(44): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(41): Show |
1 | a0001c0006t0003g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1765-234_1765-233i others(50): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(47): Show |
1 | a0001c0006t0003g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1765-234_1765-233i others(56): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(68): Show |
1 | a0001c0001t0003g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1765-234_1765-233i others(77): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(8): Show |
1 | a0001c0001t0001g0207 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1765-234_1765-233i others(17): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(14): Show |
1 | a0001c0002t0001g0111 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1765-234_1765-233i others(23): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(29): Show |
1 | a0001c0002t0001g0198 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1765-234_1765-233i others(38): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(32): Show |
1 | a0001c0007t0004g0034 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1765-234_1765-233i others(41): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | CCTTCTTC others(47): Show |
1 | a0001c0002t0001g0054 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1765-234_1765-233i others(56): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906081 | ||||||
| chr19:53906081 | C | T | 60 | a0001c0001t0001g0011 a0001c0001t0001g0100 a0001c0001t0001g0101 others(57): Show |
61 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1765-236C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906081 | |||||||
| chr19:53906084 | C | CCTCCTCC others(26): Show |
1 | a0001c0007t0001g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(35): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(41): Show |
1 | a0001c0012t0002g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(50): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(35): Show |
1 | a0001c0004t0002g0345 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(44): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(38): Show |
1 | a0001c0004t0002g0338 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(47): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(62): Show |
1 | a0001c0007t0004g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(71): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(32): Show |
1 | a0001c0004t0002g0347 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(41): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(35): Show |
1 | a0001c0004t0002g0346 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(44): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(38): Show |
1 | a0001c0004t0002g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(47): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(50): Show |
1 | a0001c0004t0002g0339 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(59): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(17): Show |
1 | a0001c0016t0001g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(26): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(38): Show |
1 | a0001c0001t0004g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(47): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(23): Show |
2 | a0001c0001t0001g0267 a0001c0007t0001g0154 |
2 | HG04228.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1765-231_1765-230i others(32): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(32): Show |
1 | a0001c0004t0002g0335 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(41): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(35): Show |
3 | a0001c0001t0004g0212 a0001c0004t0002g0348 a0002c0013t0002g0017 |
3 | HG02145.hp2 HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1765-231_1765-230i others(44): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(38): Show |
1 | a0001c0002t0001g0298 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(47): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(17): Show |
1 | a0001c0001t0001g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(26): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(29): Show |
1 | a0002c0013t0002g0018 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(38): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(38): Show |
1 | a0001c0002t0001g0292 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(47): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(44): Show |
1 | a0001c0005t0004g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(53): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(56): Show |
1 | a0001c0001t0004g0233 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(65): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(8): Show |
1 | a0001c0002t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(17): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(14): Show |
3 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0192 |
3 | HG02109.hp1 HG02723.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1765-231_1765-230i others(23): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(53): Show |
1 | a0001c0001t0003g0316 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(62): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(17): Show |
2 | a0001c0002t0001g0099 a0001c0002t0001g0119 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1765-231_1765-230i others(26): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(20): Show |
1 | a0001c0003t0001g0303 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(29): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(23): Show |
1 | a0001c0004t0001g0156 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(32): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(26): Show |
1 | a0001c0002t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(35): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(29): Show |
1 | a0001c0005t0004g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(38): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(53): Show |
1 | a0001c0002t0001g0264 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(62): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(5): Show |
1 | a0001c0002t0001g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(14): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(11): Show |
1 | a0001c0004t0002g0337 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(20): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(35): Show |
1 | a0001c0006t0003g0143 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(44): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(17): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0277 a0001c0007t0001g0141 |
3 | HG01346.hp2 HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1765-231_1765-230i others(26): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(20): Show |
2 | a0001c0005t0006g0039 a0001c0005t0006g0040 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1765-231_1765-230i others(29): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(23): Show |
2 | a0001c0001t0001g0259 a0001c0001t0004g0008 |
2 | HG01361.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1765-231_1765-230i others(32): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTCC others(44): Show |
1 | a0001c0002t0001g0093 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(53): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(2): Show |
4 | a0001c0001t0001g0175 a0001c0001t0001g0328 a0001c0002t0001g0003 others(1): Show |
4 | HG00733.hp1 HG01099.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1765-231_1765-230i others(11): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(5): Show |
1 | a0001c0002t0001g0014 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(14): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(8): Show |
1 | a0001c0001t0001g0327 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(17): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(20): Show |
1 | a0001c0025t0005g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(29): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(23): Show |
1 | a0001c0006t0003g0148 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(32): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(38): Show |
1 | a0001c0001t0001g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(47): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(47): Show |
1 | a0001c0001t0003g0308 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(56): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(53): Show |
1 | a0001c0001t0001g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(62): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(11): Show |
1 | a0001c0001t0001g0321 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(20): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(29): Show |
1 | a0001c0002t0001g0295 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1765-231_1765-230i others(38): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(38): Show |
1 | a0001c0005t0004g0041 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(47): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(44): Show |
1 | a0001c0002t0001g0234 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(53): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTCCTTC others(50): Show |
1 | a0001c0002t0001g0015 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1765-231_1765-230i others(59): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTT | 20 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0223 others(17): Show |
20 | HG00423.hp2 HG00544.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.1765-199_1765-197d others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTTCTT | 3 | a0001c0001t0001g0326 a0001c0002t0001g0135 a0001c0002t0002g0349 |
3 | HG01952.hp2 HG02258.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1765-202_1765-197d others(8): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTTCTTC others(2): Show |
11 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0177 others(8): Show |
11 | HG00099.hp1 HG00673.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1765-205_1765-197d others(11): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTTCTTC others(5): Show |
5 | a0001c0001t0001g0191 a0001c0002t0001g0075 a0001c0003t0001g0179 others(2): Show |
5 | HG01070.hp2 HG02602.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1765-208_1765-197d others(14): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTTCTTC others(20): Show |
1 | a0001c0026t0005g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1765-220_1765-219i others(29): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTTCTTC others(8): Show |
4 | a0001c0001t0001g0281 a0001c0002t0001g0030 a0001c0004t0002g0344 others(1): Show |
4 | HG03017.hp2 HG03540.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1765-211_1765-197d others(17): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTTCTTC others(14): Show |
1 | a0001c0002t0001g0060 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1765-217_1765-197d others(23): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTTCTTC others(17): Show |
1 | a0001c0002t0001g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1765-220_1765-197d others(26): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTTCTTC others(23): Show |
1 | a0001c0002t0001g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1765-226_1765-197d others(32): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTTCTTC others(26): Show |
2 | a0001c0002t0001g0116 a0001c0002t0001g0297 |
2 | HG01069.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1765-229_1765-197d others(35): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | CCTTCTTC others(47): Show |
1 | a0001c0002t0001g0235 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1765-197_1765-196i others(56): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906084 | C | T | 111 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0100 others(108): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1765-233C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906084 | |||||||
| chr19:53906084 | CCTT | C | 7 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0209 others(4): Show |
7 | HG00609.hp2 HG01169.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1765-199_1765-197d others(5): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906084 | ||||||
| chr19:53906087 | T | C | 8 | a0001c0001t0001g0250 a0001c0001t0001g0274 a0001c0001t0001g0300 others(5): Show |
8 | HG00621.hp1 HG00642.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1765-230T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906087 | |||||||
| chr19:53906090 | T | C | 1 | a0001c0021t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1765-227T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906090 | |||||||
| chr19:53906093 | T | C | 1 | a0001c0021t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1765-224T>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906093 | |||||||
| chr19:53906107 | T | TTCTTCTT others(4): Show |
1 | a0001c0002t0001g0138 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1765-208_1765-198d others(13): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906107 | ||||||
| chr19:53906124 | T | TTC | 24 | a0001c0001t0001g0257 a0001c0001t0001g0310 a0001c0002t0001g0087 others(21): Show |
29 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1765-180_1765-179d others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906124 | ||||||
| chr19:53906124 | T | TTCTC | 127 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0044 others(124): Show |
129 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1765-182_1765-179d others(6): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906124 | ||||||
| chr19:53906196 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1765-121C>T | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906196 | |||||||
| chr19:53906258 | G | A | 26 | a0001c0001t0001g0257 a0001c0001t0001g0310 a0001c0001t0001g0322 others(23): Show |
31 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1765-59G>A | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | chr19 | 53906258 | |||||||
| chr19:53906274 | CTCTG | C | 5 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0219 others(2): Show |
5 | HG00408.hp2 NA18960.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765-37_1765-34del others(4): Show |
PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr19 | 53906274 | ||||||
| chr19:53906529 | G | C | 84 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0177 others(81): Show |
84 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1905+72G>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 17/17 | chr19 | 53906529 | |||||||
| chr19:53906624 | A | C | 1 | a0001c0003t0001g0317 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1906-83A>C | PRKCG | ENSG00000126583.12 | transcript | ENST00000263431.4 | protein_coding | 17/17 | chr19 | 53906624 |