Item | Value |
---|---|
geneid | 57479 |
ensemblid | ENSG00000126464.15 |
hgncid | 29217 |
symbol | PRR12 |
name | proline rich 12 |
refseq_nuc | NM_020719.3 |
refseq_prot | NP_065770.1 |
ensembl_nuc | ENST00000418929.7 |
ensembl_prot | ENSP00000394510.1 |
mane_status | MANE Select |
chr | chr19 |
start | 49591182 |
end | 49626439 |
strand | + |
ver | v1.2 |
region | chr19:49591182-49626439 |
region5000 | chr19:49586182-49631439 |
regionname0 | PRR12_chr19_49591182_49626439 |
regionname5000 | PRR12_chr19_49586182_49631439 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2036 | 279 | 76 | 54 | 98 | 12 | 37 | 65 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0002 | 0/0 | 2036 | 12 | 3 | 4 | 0 | 0 | 5 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0003 | 0/0 | 935 | 9 | 2 | 4 | 3 | 0 | 0 | 3 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(930): Show |
chr19 | 49586182 | 49631439 |
a0004 | 0/0 | 2036 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0005 | 0/0 | 2036 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0006 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0007 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0008 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0009 | 0/0 | 2036 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0010 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0011 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0012 | 0/0 | 2036 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0013 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0014 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0015 | 0/0 | 2036 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0016 | 0/0 | 2036 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0017 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0018 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0019 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0020 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0021 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0022 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
a0023 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | MDRNY others(2031): Show |
chr19 | 49586182 | 49631439 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 6108 | 147 | 27 | 32 | 58 | 8 | 21 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0002 | 0/0 | 6108 | 57 | 23 | 10 | 24 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0003 | 0/1 | 6108 | 32 | 8 | 4 | 8 | 3 | 8 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0006 | 0/0 | 6108 | 4 | 3 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0007 | 0/0 | 6108 | 4 | 0 | 1 | 0 | 0 | 3 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0008 | 0/0 | 6108 | 4 | 0 | 0 | 4 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0009 | 0/0 | 6108 | 3 | 3 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0012 | 0/0 | 6108 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0014 | 0/0 | 6108 | 2 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0016 | 0/0 | 6108 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0017 | 0/0 | 6108 | 2 | 1 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0018 | 0/0 | 6108 | 2 | 0 | 1 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0019 | 0/0 | 6108 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0020 | 0/0 | 6108 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0021 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0024 | 0/0 | 6108 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0029 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0031 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0037 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0043 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0044 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0045 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0047 | 0/0 | 6108 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0048 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0049 | 0/0 | 6108 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0051 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0052 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0001c0054 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0002c0004 | 0/0 | 6108 | 8 | 1 | 3 | 0 | 0 | 4 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0002c0015 | 0/0 | 6108 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0002c0034 | 0/0 | 6108 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0002c0035 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0003c0005 | 0/0 | 6109 | 7 | 1 | 3 | 3 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6104): Show |
chr19 | 49586182 | 49631439 | ||
a0003c0011 | 0/0 | 6109 | 2 | 1 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6104): Show |
chr19 | 49586182 | 49631439 | ||
a0004c0010 | 0/0 | 6108 | 2 | 0 | 2 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0005c0013 | 0/0 | 6108 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0006c0040 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0007c0025 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0008c0023 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0009c0041 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0010c0030 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0011c0026 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0012c0027 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0013c0053 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0014c0033 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0015c0050 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0016c0032 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0017c0042 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0018c0038 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0019c0039 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0020c0028 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0021c0046 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0022c0036 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 | ||
a0023c0022 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | ATGGA others(6103): Show |
chr19 | 49586182 | 49631439 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 7416 | 139 | 27 | 30 | 56 | 8 | 17 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0001t0003 | 0/0 | 7417 | 6 | 0 | 2 | 2 | 0 | 2 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7412): Show |
chr19 | 49586182 | 49631439 |
a0001c0001t0009 | 0/0 | 7416 | 2 | 0 | 0 | 0 | 0 | 2 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0002t0001 | 0/0 | 7416 | 26 | 15 | 2 | 9 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0002t0002 | 0/0 | 7412 | 21 | 0 | 8 | 13 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7407): Show |
chr19 | 49586182 | 49631439 |
a0001c0002t0003 | 0/0 | 7417 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7412): Show |
chr19 | 49586182 | 49631439 |
a0001c0002t0005 | 0/0 | 7412 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7407): Show |
chr19 | 49586182 | 49631439 |
a0001c0002t0006 | 0/0 | 7416 | 3 | 3 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0002t0008 | 0/0 | 7416 | 3 | 3 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0002t0013 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0003t0001 | 0/1 | 7416 | 30 | 7 | 4 | 8 | 3 | 7 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0003t0002 | 0/0 | 7412 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7407): Show |
chr19 | 49586182 | 49631439 |
a0001c0003t0011 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0006t0001 | 0/0 | 7416 | 3 | 2 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0006t0003 | 0/0 | 7417 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7412): Show |
chr19 | 49586182 | 49631439 |
a0001c0007t0001 | 0/0 | 7416 | 4 | 0 | 1 | 0 | 0 | 3 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0008t0001 | 0/0 | 7416 | 4 | 0 | 0 | 4 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0009t0002 | 0/0 | 7412 | 3 | 3 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7407): Show |
chr19 | 49586182 | 49631439 |
a0001c0012t0001 | 0/0 | 7416 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0014t0001 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0014t0003 | 0/0 | 7417 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7412): Show |
chr19 | 49586182 | 49631439 |
a0001c0016t0001 | 0/0 | 7416 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0017t0001 | 0/0 | 7416 | 2 | 1 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0018t0001 | 0/0 | 7416 | 2 | 0 | 1 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0019t0001 | 0/0 | 7416 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0020t0002 | 0/0 | 7412 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7407): Show |
chr19 | 49586182 | 49631439 |
a0001c0021t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0024t0003 | 0/0 | 7417 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7412): Show |
chr19 | 49586182 | 49631439 |
a0001c0029t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0031t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0037t0001 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0043t0012 | 0/0 | 7390 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7385): Show |
chr19 | 49586182 | 49631439 |
a0001c0044t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0045t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0047t0010 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0048t0001 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0049t0001 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0051t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0052t0001 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0001c0054t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0002c0004t0004 | 0/0 | 7413 | 5 | 0 | 1 | 0 | 0 | 4 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7408): Show |
chr19 | 49586182 | 49631439 |
a0002c0004t0007 | 0/0 | 7416 | 3 | 1 | 2 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0002c0015t0001 | 0/0 | 7416 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0002c0034t0001 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0002c0035t0004 | 0/0 | 7413 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7408): Show |
chr19 | 49586182 | 49631439 |
a0003c0005t0001 | 0/0 | 7417 | 7 | 1 | 3 | 3 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7412): Show |
chr19 | 49586182 | 49631439 |
a0003c0011t0001 | 0/0 | 7417 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7412): Show |
chr19 | 49586182 | 49631439 |
a0003c0011t0002 | 0/0 | 7413 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7408): Show |
chr19 | 49586182 | 49631439 |
a0004c0010t0001 | 0/0 | 7416 | 2 | 0 | 2 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0005c0013t0005 | 0/0 | 7412 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7407): Show |
chr19 | 49586182 | 49631439 |
a0006c0040t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0007c0025t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0008c0023t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0009c0041t0001 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0010c0030t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0011c0026t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0012c0027t0001 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0013c0053t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0014c0033t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0015c0050t0001 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0016c0032t0004 | 0/0 | 7413 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7408): Show |
chr19 | 49586182 | 49631439 |
a0017c0042t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0018c0038t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0019c0039t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0020c0028t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0021c0046t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0022c0036t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
a0023c0022t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | CCCCC others(7411): Show |
chr19 | 49586182 | 49631439 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0009g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0008g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0013g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0015 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0011g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0006t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0006t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0006t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0006t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0007t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0007t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0007t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0008t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0008t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0008t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0008t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0009t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0009t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0009t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0012t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0012t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0014t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0014t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0016t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0016t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0017t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0017t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0018t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0018t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0019t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0019t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0020t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0020t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0021t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0024t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0029t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0031t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0037t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0043t0012g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0044t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0045t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0047t0010g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0048t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0049t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0051t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0052t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0054t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0007g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0007g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0015t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0015t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0034t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0035t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0011t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0011t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0004c0010t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0004c0010t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0005c0013t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0005c0013t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0006c0040t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0007c0025t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0008c0023t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0009c0041t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0010c0030t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0011c0026t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0012c0027t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0013c0053t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0014c0033t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0015c0050t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0016c0032t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0017c0042t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0018c0038t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0019c0039t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0020c0028t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0021c0046t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0022c0036t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0023c0022t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | GBR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0004 | EUR | GBR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | FIN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0019 | EUR | FIN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00408 | hp2 | a0001 | c0044 | t0001 | g0206 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0125 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00438 | hp2 | a0006 | c0040 | t0001 | g0185 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00544 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00597 | hp2 | a0001 | c0054 | t0001 | g0213 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0095 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00735 | hp1 | a0001 | c0017 | t0001 | g0257 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00735 | hp2 | a0003 | c0005 | t0001 | g0265 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0059 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01070 | hp1 | a0002 | c0004 | t0007 | g0029 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01071 | hp1 | a0002 | c0004 | t0007 | g0028 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01081 | hp1 | a0001 | c0018 | t0001 | g0184 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01099 | hp1 | a0001 | c0014 | t0001 | g0128 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01099 | hp2 | a0003 | c0005 | t0001 | g0283 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01106 | hp2 | a0001 | c0007 | t0001 | g0002 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0097 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01168 | hp2 | a0004 | c0010 | t0001 | g0123 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01169 | hp1 | a0001 | c0003 | t0001 | g0102 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01169 | hp2 | a0004 | c0010 | t0001 | g0124 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01175 | hp1 | a0003 | c0005 | t0001 | g0220 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01175 | hp2 | a0002 | c0004 | t0004 | g0038 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01192 | hp2 | a0002 | c0034 | t0001 | g0030 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01261 | hp1 | a0001 | c0024 | t0003 | g0079 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01346 | hp2 | a0001 | c0006 | t0001 | g0026 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01358 | hp2 | a0001 | c0047 | t0010 | g0293 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0073 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | IBS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01515 | hp2 | a0001 | c0018 | t0001 | g0182 | EUR | IBS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | IBS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01884 | hp1 | a0001 | c0002 | t0008 | g0118 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0072 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0042 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0112 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01993 | hp1 | a0003 | c0011 | t0002 | g0065 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02004 | hp1 | a0001 | c0049 | t0001 | g0271 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02040 | hp1 | a0001 | c0008 | t0001 | g0223 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0166 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0127 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02132 | hp1 | a0001 | c0003 | t0001 | g0126 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02132 | hp2 | a0001 | c0008 | t0001 | g0011 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02135 | hp1 | a0001 | c0002 | t0003 | g0057 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02145 | hp1 | a0002 | c0015 | t0001 | g0032 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0093 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CDX | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | CDX | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CDX | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02257 | hp2 | a0001 | c0002 | t0006 | g0088 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02258 | hp2 | a0001 | c0020 | t0002 | g0141 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0071 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02451 | hp1 | a0001 | c0016 | t0001 | g0137 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02572 | hp1 | a0001 | c0012 | t0001 | g0120 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02602 | hp2 | a0009 | c0041 | t0001 | g0174 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02615 | hp1 | a0001 | c0002 | t0006 | g0130 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02630 | hp2 | a0010 | c0030 | t0001 | g0116 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02698 | hp1 | a0001 | c0007 | t0001 | g0221 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02723 | hp2 | a0002 | c0015 | t0001 | g0031 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02735 | hp1 | a0001 | c0048 | t0001 | g0011 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02735 | hp2 | a0001 | c0001 | t0009 | g0013 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0262 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02738 | hp2 | a0001 | c0007 | t0001 | g0188 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02809 | hp1 | a0005 | c0013 | t0005 | g0083 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02809 | hp2 | a0001 | c0002 | t0008 | g0117 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02818 | hp1 | a0001 | c0002 | t0005 | g0081 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02818 | hp2 | a0001 | c0006 | t0001 | g0025 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02895 | hp1 | a0001 | c0019 | t0001 | g0169 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02895 | hp2 | a0011 | c0026 | t0001 | g0077 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0092 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02896 | hp2 | a0001 | c0009 | t0002 | g0138 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02897 | hp1 | a0001 | c0009 | t0002 | g0140 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02897 | hp2 | a0001 | c0019 | t0001 | g0170 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02922 | hp2 | a0005 | c0013 | t0005 | g0084 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0100 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02970 | hp2 | a0001 | c0002 | t0005 | g0082 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03017 | hp1 | a0012 | c0027 | t0001 | g0122 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03041 | hp2 | a0001 | c0012 | t0001 | g0089 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03130 | hp2 | a0001 | c0003 | t0002 | g0143 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0101 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0111 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03225 | hp1 | a0001 | c0020 | t0002 | g0142 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03225 | hp2 | a0013 | c0053 | t0001 | g0244 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03239 | hp1 | a0001 | c0003 | t0001 | g0018 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03453 | hp1 | a0001 | c0017 | t0001 | g0260 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03453 | hp2 | a0014 | c0033 | t0001 | g0022 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03486 | hp1 | a0001 | c0006 | t0001 | g0024 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03490 | hp1 | a0015 | c0050 | t0001 | g0288 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03516 | hp1 | a0003 | c0005 | t0001 | g0012 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03516 | hp2 | a0001 | c0031 | t0001 | g0090 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03540 | hp1 | a0001 | c0002 | t0006 | g0131 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03654 | hp1 | a0002 | c0004 | t0004 | g0036 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0110 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03688 | hp1 | a0001 | c0043 | t0012 | g0017 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03704 | hp1 | a0001 | c0001 | t0009 | g0013 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03704 | hp2 | a0002 | c0035 | t0004 | g0035 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03710 | hp1 | a0002 | c0004 | t0004 | g0033 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03831 | hp2 | a0016 | c0032 | t0004 | g0039 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03834 | hp1 | a0001 | c0052 | t0001 | g0233 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03927 | hp1 | a0001 | c0037 | t0001 | g0186 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03927 | hp2 | a0002 | c0004 | t0004 | g0037 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0096 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0108 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04115 | hp2 | a0001 | c0007 | t0001 | g0002 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04184 | hp2 | a0001 | c0014 | t0003 | g0129 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0107 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04199 | hp2 | a0002 | c0004 | t0004 | g0034 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0103 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0105 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18906 | hp1 | a0003 | c0011 | t0001 | g0003 | AFR | YRI | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0099 | AFR | YRI | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18948 | hp1 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18948 | hp2 | a0017 | c0042 | t0001 | g0228 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18951 | hp2 | a0018 | c0038 | t0001 | g0279 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18957 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18959 | hp2 | a0001 | c0051 | t0001 | g0275 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18967 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18967 | hp2 | a0001 | c0008 | t0001 | g0219 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18977 | hp1 | a0019 | c0039 | t0001 | g0168 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18979 | hp1 | a0003 | c0005 | t0001 | g0272 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18982 | hp2 | a0003 | c0005 | t0001 | g0278 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18986 | hp2 | a0001 | c0008 | t0001 | g0165 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18992 | hp1 | a0001 | c0029 | t0001 | g0091 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18998 | hp2 | a0001 | c0002 | t0013 | g0056 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19004 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | LWK | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19030 | hp2 | a0001 | c0021 | t0001 | g0043 | AFR | LWK | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19043 | hp1 | a0002 | c0004 | t0007 | g0027 | AFR | LWK | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | LWK | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19065 | hp1 | a0003 | c0005 | t0001 | g0202 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19065 | hp2 | a0020 | c0028 | t0001 | g0104 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19088 | hp2 | a0021 | c0046 | t0001 | g0249 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19089 | hp1 | a0022 | c0036 | t0001 | g0189 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19089 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19240 | hp1 | a0001 | c0016 | t0001 | g0136 | AFR | YRI | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20129 | hp1 | a0001 | c0009 | t0002 | g0139 | AFR | ASW | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0098 | AFR | ASW | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | TSI | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0106 | EUR | TSI | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20905 | hp1 | a0001 | c0003 | t0011 | g0113 | SAS | GIH | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | GIH | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02109 | hp1 | a0001 | c0002 | t0008 | g0119 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02109 | hp2 | a0007 | c0025 | t0001 | g0020 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02486 | hp1 | a0001 | c0006 | t0003 | g0023 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02486 | hp2 | a0008 | c0023 | t0001 | g0080 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02559 | hp2 | a0001 | c0045 | t0001 | g0230 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0121 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | USA | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | USA | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20300 | hp1 | a0023 | c0022 | t0001 | g0016 | AFR | USA | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | USA | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0015 | REF | REF | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0227 | REF | REF | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49594570 | G | A | 1 | a0022 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.316G>A | p.Ala106Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 3/14 | 789/7416 | 316/6111 | 106/2036 | chr19 | 49594570 | |||
chr19:49595011 | C | A | 1 | a0004 | 2 | HG01168.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.676C>A | p.Pro226Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 1149/7416 | 676/6111 | 226/2036 | chr19 | 49595011 | |||
chr19:49595011 | C | T | 1 | a0013 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.676C>T | p.Pro226Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 1149/7416 | 676/6111 | 226/2036 | chr19 | 49595011 | |||
chr19:49596308 | C | T | 1 | a0010 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1973C>T | p.Ala658Val | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2446/7416 | 1973/6111 | 658/2036 | chr19 | 49596308 | |||
chr19:49596376 | G | A | 1 | a0018 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.2041G>A | p.Gly681Arg | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2514/7416 | 2041/6111 | 681/2036 | chr19 | 49596376 | |||
chr19:49596781 | G | A | 1 | a0006 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.2446G>A | p.Ala816Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2919/7416 | 2446/6111 | 816/2036 | chr19 | 49596781 | |||
chr19:49596852 | A | AC | 1 | a0003 | 9 | HG00735.hp2 HG01099.hp2 HG01175.hp1 others(6): Show |
frameshift_variant | HIGH | c.2522dupC | p.Pro842fs | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2996/7416 | 2523/6111 | 841/2036 | INFO_REALIGN_3_PRIME | chr19 | 49596852 | ||
chr19:49596935 | G | A | 1 | a0009 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.2600G>A | p.Arg867His | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3073/7416 | 2600/6111 | 867/2036 | chr19 | 49596935 | |||
chr19:49597016 | C | A | 1 | a0017 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.2681C>A | p.Pro894His | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3154/7416 | 2681/6111 | 894/2036 | chr19 | 49597016 | |||
chr19:49597168 | A | G | 1 | a0015 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.2833A>G | p.Ser945Gly | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3306/7416 | 2833/6111 | 945/2036 | chr19 | 49597168 | |||
chr19:49597261 | G | C | 1 | a0023 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.2926G>C | p.Ala976Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3399/7416 | 2926/6111 | 976/2036 | chr19 | 49597261 | |||
chr19:49597283 | G | C | 1 | a0016 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.2948G>C | p.Gly983Ala | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3421/7416 | 2948/6111 | 983/2036 | chr19 | 49597283 | |||
chr19:49597327 | G | T | 1 | a0005 | 2 | HG02809.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.2992G>T | p.Ala998Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3465/7416 | 2992/6111 | 998/2036 | chr19 | 49597327 | |||
chr19:49597510 | C | T | 1 | a0011 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.3175C>T | p.Leu1059Phe | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3648/7416 | 3175/6111 | 1059/2036 | chr19 | 49597510 | |||
chr19:49597880 | C | T | 1 | a0020 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.3545C>T | p.Pro1182Leu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 4018/7416 | 3545/6111 | 1182/2036 | chr19 | 49597880 | |||
chr19:49599351 | G | T | 1 | a0023 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.3758G>T | p.Ser1253Ile | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/14 | 4231/7416 | 3758/6111 | 1253/2036 | chr19 | 49599351 | |||
chr19:49599594 | A | G | 1 | a0021 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.4001A>G | p.His1334Arg | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/14 | 4474/7416 | 4001/6111 | 1334/2036 | chr19 | 49599594 | |||
chr19:49599927 | A | G | 1 | a0012 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.4334A>G | p.Asn1445Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/14 | 4807/7416 | 4334/6111 | 1445/2036 | chr19 | 49599927 | |||
chr19:49601554 | A | C | 1 | a0014 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.4409A>C | p.Gln1470Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 4882/7416 | 4409/6111 | 1470/2036 | chr19 | 49601554 | |||
chr19:49601568 | C | A | 1 | a0004 | 2 | HG01168.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.4423C>A | p.Pro1475Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 4896/7416 | 4423/6111 | 1475/2036 | chr19 | 49601568 | |||
chr19:49601590 | T | C | 1 | a0019 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.4445T>C | p.Leu1482Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 4918/7416 | 4445/6111 | 1482/2036 | chr19 | 49601590 | |||
chr19:49601611 | T | C | 1 | a0008 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.4466T>C | p.Val1489Ala | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 4939/7416 | 4466/6111 | 1489/2036 | chr19 | 49601611 | |||
chr19:49601620 | C | T | 1 | a0007 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.4475C>T | p.Thr1492Met | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 4948/7416 | 4475/6111 | 1492/2036 | chr19 | 49601620 | |||
chr19:49601683 | C | A | 1 | a0019 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.4538C>A | p.Pro1513Gln | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 5011/7416 | 4538/6111 | 1513/2036 | chr19 | 49601683 | |||
chr19:49601691 | C | A | 2 | a0002 a0016 |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
missense_variant | MODERATE | c.4546C>A | p.Pro1516Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 5019/7416 | 4546/6111 | 1516/2036 | chr19 | 49601691 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49594527 | T | C | 25 | a0001c0002 a0001c0003 a0001c0006 others(22): Show |
127 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
synonymous_variant | LOW | c.273T>C | p.Leu91Leu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 3/14 | 746/7416 | 273/6111 | 91/2036 | chr19 | 49594527 | |||
chr19:49594554 | C | T | 1 | a0001c0054 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.300C>T | p.Pro100Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 3/14 | 773/7416 | 300/6111 | 100/2036 | chr19 | 49594554 | |||
chr19:49594569 | C | T | 1 | a0002c0035 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.315C>T | p.Ser105Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 3/14 | 788/7416 | 315/6111 | 105/2036 | chr19 | 49594569 | |||
chr19:49594815 | C | T | 1 | a0001c0008 | 4 | HG02040.hp1 HG02132.hp2 NA18967.hp2 others(1): Show |
synonymous_variant | LOW | c.480C>T | p.Arg160Arg | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 953/7416 | 480/6111 | 160/2036 | chr19 | 49594815 | |||
chr19:49595091 | C | T | 1 | a0001c0052 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.756C>T | p.Ser252Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 1229/7416 | 756/6111 | 252/2036 | chr19 | 49595091 | |||
chr19:49595112 | G | A | 1 | a0001c0037 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.777G>A | p.Glu259Glu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 1250/7416 | 777/6111 | 259/2036 | chr19 | 49595112 | |||
chr19:49595166 | G | A | 17 | a0001c0002 a0001c0003 a0001c0012 others(14): Show |
107 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(104): Show |
synonymous_variant | LOW | c.831G>A | p.Pro277Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 1304/7416 | 831/6111 | 277/2036 | chr19 | 49595166 | |||
chr19:49595335 | C | T | 2 | a0001c0009 a0001c0020 |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.1000C>T | p.Leu334Leu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 1473/7416 | 1000/6111 | 334/2036 | chr19 | 49595335 | |||
chr19:49596000 | C | T | 1 | a0001c0031 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1665C>T | p.Gly555Gly | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2138/7416 | 1665/6111 | 555/2036 | chr19 | 49596000 | |||
chr19:49596075 | C | T | 1 | a0001c0051 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.1740C>T | p.Val580Val | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2213/7416 | 1740/6111 | 580/2036 | chr19 | 49596075 | |||
chr19:49596102 | C | T | 1 | a0002c0034 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.1767C>T | p.Tyr589Tyr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2240/7416 | 1767/6111 | 589/2036 | chr19 | 49596102 | |||
chr19:49596144 | G | A | 1 | a0001c0016 | 2 | HG02451.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.1809G>A | p.Pro603Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2282/7416 | 1809/6111 | 603/2036 | chr19 | 49596144 | |||
chr19:49596165 | C | T | 8 | a0001c0003 a0001c0019 a0001c0029 others(5): Show |
40 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(37): Show |
synonymous_variant | LOW | c.1830C>T | p.Ala610Ala | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2303/7416 | 1830/6111 | 610/2036 | chr19 | 49596165 | |||
chr19:49596234 | G | A | 1 | a0001c0021 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1899G>A | p.Ala633Ala | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2372/7416 | 1899/6111 | 633/2036 | chr19 | 49596234 | |||
chr19:49596312 | C | T | 1 | a0001c0018 | 2 | HG01081.hp1 HG01515.hp2 |
synonymous_variant | LOW | c.1977C>T | p.Asp659Asp | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2450/7416 | 1977/6111 | 659/2036 | chr19 | 49596312 | |||
chr19:49596399 | C | T | 1 | a0001c0029 | 1 | NA18992.hp1 | synonymous_variant | LOW | c.2064C>T | p.Tyr688Tyr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2537/7416 | 2064/6111 | 688/2036 | chr19 | 49596399 | |||
chr19:49596447 | C | T | 1 | a0011c0026 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.2112C>T | p.Ile704Ile | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2585/7416 | 2112/6111 | 704/2036 | chr19 | 49596447 | |||
chr19:49596540 | T | G | 1 | a0019c0039 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.2205T>G | p.Gly735Gly | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2678/7416 | 2205/6111 | 735/2036 | chr19 | 49596540 | |||
chr19:49597038 | A | G | 27 | a0001c0002 a0001c0003 a0001c0006 others(24): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
synonymous_variant | LOW | c.2703A>G | p.Pro901Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3176/7416 | 2703/6111 | 901/2036 | chr19 | 49597038 | |||
chr19:49597147 | T | C | 2 | a0001c0009 a0001c0020 |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.2812T>C | p.Leu938Leu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3285/7416 | 2812/6111 | 938/2036 | chr19 | 49597147 | |||
chr19:49597215 | C | T | 1 | a0001c0049 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.2880C>T | p.Asp960Asp | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3353/7416 | 2880/6111 | 960/2036 | chr19 | 49597215 | |||
chr19:49597227 | G | A | 7 | a0001c0006 a0002c0004 a0002c0015 others(4): Show |
18 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(15): Show |
synonymous_variant | LOW | c.2892G>A | p.Lys964Lys | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3365/7416 | 2892/6111 | 964/2036 | chr19 | 49597227 | |||
chr19:49597407 | C | T | 1 | a0001c0009 | 3 | HG02896.hp2 HG02897.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.3072C>T | p.Ala1024Ala | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3545/7416 | 3072/6111 | 1024/2036 | chr19 | 49597407 | |||
chr19:49597419 | C | T | 1 | a0001c0048 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.3084C>T | p.Gly1028Gly | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3557/7416 | 3084/6111 | 1028/2036 | chr19 | 49597419 | |||
chr19:49597563 | C | T | 1 | a0001c0047 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.3228C>T | p.Ser1076Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3701/7416 | 3228/6111 | 1076/2036 | chr19 | 49597563 | |||
chr19:49597617 | G | A | 2 | a0001c0007 a0009c0041 |
5 | HG01106.hp2 HG02602.hp2 HG02698.hp1 others(2): Show |
synonymous_variant | LOW | c.3282G>A | p.Leu1094Leu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3755/7416 | 3282/6111 | 1094/2036 | chr19 | 49597617 | |||
chr19:49597635 | G | A | 1 | a0001c0017 | 2 | HG00735.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.3300G>A | p.Glu1100Glu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3773/7416 | 3300/6111 | 1100/2036 | chr19 | 49597635 | |||
chr19:49599394 | T | C | 3 | a0001c0009 a0001c0016 a0001c0020 |
7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
synonymous_variant | LOW | c.3801T>C | p.Ile1267Ile | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/14 | 4274/7416 | 3801/6111 | 1267/2036 | chr19 | 49599394 | |||
chr19:49599418 | G | A | 1 | a0001c0016 | 2 | HG02451.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.3825G>A | p.Pro1275Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/14 | 4298/7416 | 3825/6111 | 1275/2036 | chr19 | 49599418 | |||
chr19:49599847 | C | A | 1 | a0001c0016 | 2 | HG02451.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.4254C>A | p.Thr1418Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/14 | 4727/7416 | 4254/6111 | 1418/2036 | chr19 | 49599847 | |||
chr19:49601678 | G | A | 3 | a0001c0009 a0001c0016 a0001c0020 |
7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
synonymous_variant | LOW | c.4533G>A | p.Ser1511Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 5006/7416 | 4533/6111 | 1511/2036 | chr19 | 49601678 | |||
chr19:49601684 | A | C | 1 | a0019c0039 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.4539A>C | p.Pro1513Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 5012/7416 | 4539/6111 | 1513/2036 | chr19 | 49601684 | |||
chr19:49601747 | T | C | 3 | a0001c0009 a0001c0016 a0001c0020 |
7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
synonymous_variant | LOW | c.4602T>C | p.Ser1534Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 5075/7416 | 4602/6111 | 1534/2036 | chr19 | 49601747 | |||
chr19:49601807 | G | A | 1 | a0001c0043 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.4662G>A | p.Thr1554Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 5135/7416 | 4662/6111 | 1554/2036 | chr19 | 49601807 | |||
chr19:49615870 | G | A | 1 | a0001c0020 | 2 | HG02258.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.5148G>A | p.Glu1716Glu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/14 | 5621/7416 | 5148/6111 | 1716/2036 | chr19 | 49615870 | |||
chr19:49615966 | A | G | 2 | a0001c0009 a0001c0020 |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.5244A>G | p.Thr1748Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/14 | 5717/7416 | 5244/6111 | 1748/2036 | chr19 | 49615966 | |||
chr19:49616047 | A | G | 2 | a0001c0009 a0001c0020 |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.5325A>G | p.Gln1775Gln | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/14 | 5798/7416 | 5325/6111 | 1775/2036 | chr19 | 49616047 | |||
chr19:49616104 | C | T | 1 | a0001c0045 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.5382C>T | p.Pro1794Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/14 | 5855/7416 | 5382/6111 | 1794/2036 | chr19 | 49616104 | |||
chr19:49616212 | C | T | 1 | a0001c0024 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.5490C>T | p.Ser1830Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/14 | 5963/7416 | 5490/6111 | 1830/2036 | chr19 | 49616212 | |||
chr19:49621541 | C | T | 5 | a0001c0009 a0001c0020 a0002c0004 others(2): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
synonymous_variant | LOW | c.5640C>T | p.Pro1880Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/14 | 6113/7416 | 5640/6111 | 1880/2036 | chr19 | 49621541 | |||
chr19:49621599 | C | T | 1 | a0001c0044 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.5698C>T | p.Leu1900Leu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/14 | 6171/7416 | 5698/6111 | 1900/2036 | chr19 | 49621599 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49591240 | AGGC | A | 3 | a0002c0004t0004 a0002c0035t0004 a0016c0032t0004 |
7 | HG01175.hp2 HG03654.hp1 HG03704.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-398_-396delGCG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/14 | 396 | INFO_REALIGN_3_PRIME | chr19 | 49591240 | |||||
chr19:49591326 | G | GC | 5 | a0001c0001t0003 a0001c0002t0003 a0001c0006t0003 others(2): Show |
10 | HG01192.hp1 HG01261.hp1 HG01934.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-322dupC | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/14 | 321 | INFO_REALIGN_3_PRIME | chr19 | 49591326 | |||||
chr19:49591328 | C | T | 1 | a0001c0002t0013 | 1 | NA18998.hp2 | 5_prime_UTR_variant | MODIFIER | c.-327C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/14 | 327 | chr19 | 49591328 | ||||||
chr19:49591527 | AAAAG | A | 2 | a0001c0002t0005 a0005c0013t0005 |
4 | HG02809.hp1 HG02818.hp1 HG02922.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-126_-123delAAGA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/14 | 123 | INFO_REALIGN_3_PRIME | chr19 | 49591527 | |||||
chr19:49591540 | A | C | 1 | a0001c0002t0008 | 3 | HG01884.hp1 HG02109.hp1 HG02809.hp2 |
5_prime_UTR_variant | MODIFIER | c.-115A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/14 | 115 | chr19 | 49591540 | ||||||
chr19:49591601 | CCCCT | C | 5 | a0001c0002t0002 a0001c0003t0002 a0001c0009t0002 others(2): Show |
28 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-34_-31delTCCC | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/14 | 31 | INFO_REALIGN_3_PRIME | chr19 | 49591601 | |||||
chr19:49625648 | C | T | 4 | a0002c0004t0004 a0002c0004t0007 a0002c0035t0004 others(1): Show |
10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*41C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 14/14 | 41 | chr19 | 49625648 | ||||||
chr19:49625766 | C | T | 1 | a0001c0002t0006 | 3 | HG02257.hp2 HG02615.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*159C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 14/14 | 159 | chr19 | 49625766 | ||||||
chr19:49625895 | ACCCCCCC others(19): Show |
A | 1 | a0001c0043t0012 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294_*319delCCTCCA others(20): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 14/14 | 294 | INFO_REALIGN_3_PRIME | chr19 | 49625895 | |||||
chr19:49626013 | C | G | 1 | a0001c0003t0011 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*406C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 14/14 | 406 | chr19 | 49626013 | ||||||
chr19:49626317 | C | T | 1 | a0001c0001t0009 | 2 | HG02735.hp2 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*710C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 14/14 | 710 | chr19 | 49626317 | ||||||
chr19:49626426 | C | T | 1 | a0001c0047t0010 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 14/14 | 819 | chr19 | 49626426 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49591754 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.86+14G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49591754 | |||||||
chr19:49591790 | AGCCGG | A | 130 | a0001c0002t0001g0003 a0001c0002t0001g0021 a0001c0002t0001g0040 others(127): Show |
131 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.86+74_86+78delGGGC others(1): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 49591790 | ||||||
chr19:49591790 | AGCCGGGC others(3): Show |
A | 7 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0270 others(4): Show |
7 | HG00735.hp1 HG02258.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.86+69_86+78delGGGC others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 49591790 | ||||||
chr19:49591794 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0172 a0001c0001t0003g0225 others(1): Show |
4 | HG02135.hp2 NA18959.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+54G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49591794 | |||||||
chr19:49592062 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.86+322C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592062 | |||||||
chr19:49592113 | G | T | 9 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 others(6): Show |
9 | HG01928.hp2 HG01981.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.86+373G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592113 | |||||||
chr19:49592270 | T | TTG | 17 | a0001c0001t0001g0282 a0001c0001t0001g0284 a0001c0001t0001g0285 others(14): Show |
18 | HG00280.hp1 HG00738.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.86+540_86+541dupGT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 49592270 | ||||||
chr19:49592319 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.86+579A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592319 | |||||||
chr19:49592406 | C | T | 1 | a0001c0002t0001g0281 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.86+666C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592406 | |||||||
chr19:49592454 | T | C | 1 | a0023c0022t0001g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.86+714T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592454 | |||||||
chr19:49592569 | C | A | 1 | a0001c0043t0012g0017 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.87-758C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592569 | |||||||
chr19:49592704 | T | C | 152 | a0001c0001t0001g0005 a0001c0001t0001g0144 a0001c0001t0001g0145 others(149): Show |
154 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.87-623T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592704 | |||||||
chr19:49592727 | A | G | 1 | a0001c0002t0001g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.87-600A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592727 | |||||||
chr19:49592858 | C | A | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.87-469C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592858 | |||||||
chr19:49592887 | T | C | 124 | a0001c0002t0001g0003 a0001c0002t0001g0021 a0001c0002t0001g0040 others(121): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.87-440T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592887 | |||||||
chr19:49592970 | G | C | 1 | a0001c0008t0001g0165 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.87-357G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592970 | |||||||
chr19:49592971 | C | T | 1 | a0001c0008t0001g0165 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.87-356C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592971 | |||||||
chr19:49592972 | T | G | 1 | a0001c0008t0001g0165 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.87-355T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592972 | |||||||
chr19:49593036 | C | T | 3 | a0001c0002t0001g0133 a0001c0002t0001g0134 a0001c0002t0001g0135 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.87-291C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49593036 | |||||||
chr19:49593164 | C | G | 124 | a0001c0002t0001g0003 a0001c0002t0001g0021 a0001c0002t0001g0040 others(121): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.87-163C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49593164 | |||||||
chr19:49593602 | G | C | 133 | a0001c0002t0001g0003 a0001c0002t0001g0021 a0001c0002t0001g0040 others(130): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.199+163G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49593602 | |||||||
chr19:49593840 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.199+401C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49593840 | |||||||
chr19:49594170 | G | A | 2 | a0001c0003t0001g0018 a0001c0003t0001g0019 |
2 | HG00280.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.200-284G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49594170 | |||||||
chr19:49594268 | T | C | 1 | a0007c0025t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.200-186T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49594268 | |||||||
chr19:49594290 | A | G | 127 | a0001c0001t0001g0306 a0001c0002t0001g0003 a0001c0002t0001g0021 others(124): Show |
128 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.200-164A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49594290 | |||||||
chr19:49594340 | C | T | 1 | a0001c0002t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.200-114C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49594340 | |||||||
chr19:49594350 | C | T | 61 | a0001c0002t0001g0003 a0001c0002t0001g0078 a0001c0002t0001g0085 others(58): Show |
62 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.200-104C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49594350 | |||||||
chr19:49594648 | T | G | 1 | a0001c0002t0001g0021 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.361+33T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 3/13 | chr19 | 49594648 | |||||||
chr19:49594675 | G | C | 132 | a0001c0002t0001g0003 a0001c0002t0001g0021 a0001c0002t0001g0040 others(129): Show |
133 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.362-22G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 3/13 | chr19 | 49594675 | |||||||
chr19:49598031 | C | T | 7 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3678+18C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598031 | |||||||
chr19:49598075 | CT | C | 25 | a0001c0001t0001g0167 a0001c0006t0001g0024 a0001c0006t0001g0025 others(22): Show |
25 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.3678+78delT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 49598075 | ||||||
chr19:49598096 | C | CA | 18 | a0001c0006t0001g0024 a0001c0006t0001g0025 a0001c0006t0001g0026 others(15): Show |
18 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.3678+84dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 49598096 | ||||||
chr19:49598113 | G | T | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG01070.hp2 HG01255.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.3678+100G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598113 | |||||||
chr19:49598114 | T | C | 1 | a0014c0033t0001g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3678+101T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598114 | |||||||
chr19:49598117 | A | C | 3 | a0001c0001t0001g0277 a0003c0005t0001g0278 a0018c0038t0001g0279 |
3 | NA18951.hp2 NA18982.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.3678+104A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598117 | |||||||
chr19:49598145 | T | C | 7 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3678+132T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598145 | |||||||
chr19:49598164 | C | T | 13 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.3678+151C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598164 | |||||||
chr19:49598174 | C | T | 13 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.3678+161C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598174 | |||||||
chr19:49598240 | GT | G | 8 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(5): Show |
8 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3678+234delT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 49598240 | ||||||
chr19:49598242 | T | G | 13 | a0001c0002t0001g0003 a0001c0002t0001g0078 a0001c0002t0001g0085 others(10): Show |
13 | HG00733.hp2 HG01261.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3678+229T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598242 | |||||||
chr19:49598285 | A | G | 18 | a0001c0006t0001g0024 a0001c0006t0001g0025 a0001c0006t0001g0026 others(15): Show |
18 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.3678+272A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598285 | |||||||
chr19:49598365 | C | T | 2 | a0001c0002t0006g0130 a0001c0002t0006g0131 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3678+352C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598365 | |||||||
chr19:49598456 | T | C | 134 | a0001c0001t0001g0144 a0001c0002t0001g0003 a0001c0002t0001g0021 others(131): Show |
135 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.3678+443T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598456 | |||||||
chr19:49598459 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3678+446A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598459 | |||||||
chr19:49598480 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3678+467G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598480 | |||||||
chr19:49598545 | C | G | 3 | a0001c0003t0001g0125 a0001c0003t0001g0126 a0001c0003t0001g0127 |
3 | HG00438.hp1 HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.3678+532C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598545 | |||||||
chr19:49598618 | G | C | 1 | a0001c0002t0001g0040 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3678+605G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598618 | |||||||
chr19:49598801 | A | G | 3 | a0004c0010t0001g0123 a0004c0010t0001g0124 a0012c0027t0001g0122 |
3 | HG01168.hp2 HG01169.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.3679-471A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598801 | |||||||
chr19:49598941 | C | G | 1 | a0001c0051t0001g0275 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3679-331C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598941 | |||||||
chr19:49599032 | C | T | 17 | a0001c0002t0001g0003 a0001c0002t0001g0078 a0001c0002t0001g0085 others(14): Show |
17 | HG00733.hp2 HG01261.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3679-240C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49599032 | |||||||
chr19:49599067 | AG | A | 134 | a0001c0001t0001g0144 a0001c0002t0001g0003 a0001c0002t0001g0021 others(131): Show |
135 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.3679-203delG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 49599067 | ||||||
chr19:49599088 | C | T | 7 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3679-184C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49599088 | |||||||
chr19:49599140 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3679-132G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49599140 | |||||||
chr19:49599185 | G | A | 1 | a0001c0002t0001g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3679-87G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49599185 | |||||||
chr19:49599195 | A | G | 1 | a0001c0002t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3679-77A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49599195 | |||||||
chr19:49599995 | G | A | 134 | a0001c0001t0001g0144 a0001c0002t0001g0003 a0001c0002t0001g0021 others(131): Show |
135 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.4345+57G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49599995 | |||||||
chr19:49600048 | T | G | 2 | a0001c0016t0001g0136 a0001c0016t0001g0137 |
2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4345+110T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600048 | |||||||
chr19:49600104 | G | C | 1 | a0001c0001t0001g0172 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.4345+166G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600104 | |||||||
chr19:49600109 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4345+171A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600109 | |||||||
chr19:49600121 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4345+183T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600121 | |||||||
chr19:49600480 | C | CA | 13 | a0001c0001t0001g0175 a0001c0001t0001g0277 a0001c0001t0001g0298 others(10): Show |
13 | HG00140.hp1 HG01928.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.4345+557dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 49600480 | ||||||
chr19:49600480 | C | CAA | 11 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.4345+556_4345+557d others(4): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 49600480 | ||||||
chr19:49600694 | G | A | 1 | a0001c0002t0002g0042 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4345+756G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600694 | |||||||
chr19:49600729 | A | G | 2 | a0001c0001t0001g0273 a0003c0005t0001g0272 |
2 | NA18971.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.4346-762A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600729 | |||||||
chr19:49600795 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4346-696G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600795 | |||||||
chr19:49600947 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4346-544A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600947 | |||||||
chr19:49601087 | T | A | 1 | a0019c0039t0001g0168 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4346-404T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49601087 | |||||||
chr19:49601144 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4346-347G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49601144 | |||||||
chr19:49601221 | A | T | 1 | a0019c0039t0001g0168 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4346-270A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49601221 | |||||||
chr19:49601305 | TCTC | T | 7 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4346-183_4346-181d others(5): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 49601305 | ||||||
chr19:49601431 | A | G | 1 | a0001c0049t0001g0271 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4346-60A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49601431 | |||||||
chr19:49601449 | ATGATGAA others(13): Show |
A | 1 | a0001c0012t0001g0120 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4346-36_4346-17del others(20): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 49601449 | ||||||
chr19:49601982 | C | T | 143 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0263 others(140): Show |
144 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.4773+64C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49601982 | |||||||
chr19:49602120 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4773+202A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602120 | |||||||
chr19:49602150 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.4773+232T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602150 | |||||||
chr19:49602158 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4773+240C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602158 | |||||||
chr19:49602164 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4773+246T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602164 | |||||||
chr19:49602198 | C | G | 7 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4773+280C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602198 | |||||||
chr19:49602236 | G | A | 1 | a0001c0031t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4773+318G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602236 | |||||||
chr19:49602241 | A | T | 1 | a0019c0039t0001g0168 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4773+323A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602241 | |||||||
chr19:49602484 | T | C | 1 | a0001c0049t0001g0271 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4773+566T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602484 | |||||||
chr19:49602508 | A | G | 1 | a0001c0002t0006g0088 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4773+590A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602508 | |||||||
chr19:49602554 | A | G | 1 | a0007c0025t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4773+636A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602554 | |||||||
chr19:49602584 | C | T | 6 | a0001c0006t0001g0024 a0001c0006t0001g0025 a0001c0006t0001g0026 others(3): Show |
6 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4773+666C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602584 | |||||||
chr19:49602647 | G | A | 1 | a0001c0002t0001g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4773+729G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602647 | |||||||
chr19:49602713 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4773+795G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602713 | |||||||
chr19:49602772 | G | A | 13 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+854G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602772 | |||||||
chr19:49602951 | C | G | 128 | a0001c0001t0001g0144 a0001c0001t0001g0258 a0001c0001t0001g0259 others(125): Show |
129 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.4773+1033C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602951 | |||||||
chr19:49602965 | C | A | 5 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0270 others(2): Show |
5 | HG00735.hp1 HG02258.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+1047C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602965 | |||||||
chr19:49603051 | T | C | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+1133T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603051 | |||||||
chr19:49603159 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4773+1241T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603159 | |||||||
chr19:49603276 | GTCAGCCC others(8): Show |
G | 1 | a0001c0002t0006g0088 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4773+1359_4773+137 others(19): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603276 | |||||||
chr19:49603282 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA18950.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.4773+1364C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603282 | |||||||
chr19:49603363 | C | T | 5 | a0001c0006t0001g0024 a0001c0006t0001g0025 a0001c0006t0001g0026 others(2): Show |
5 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4773+1445C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603363 | |||||||
chr19:49603384 | C | T | 1 | a0001c0002t0006g0088 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4773+1466C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603384 | |||||||
chr19:49603410 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4773+1492G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603410 | |||||||
chr19:49603467 | G | C | 1 | a0001c0021t0001g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4773+1549G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603467 | |||||||
chr19:49603504 | A | G | 1 | a0001c0002t0001g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4773+1586A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603504 | |||||||
chr19:49603562 | C | T | 1 | a0011c0026t0001g0077 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4773+1644C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603562 | |||||||
chr19:49603627 | G | C | 1 | a0001c0002t0002g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4773+1709G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603627 | |||||||
chr19:49603649 | G | T | 128 | a0001c0001t0001g0144 a0001c0001t0001g0258 a0001c0001t0001g0259 others(125): Show |
129 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.4773+1731G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603649 | |||||||
chr19:49603734 | T | C | 1 | a0001c0024t0003g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4773+1816T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603734 | |||||||
chr19:49603753 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4773+1835G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603753 | |||||||
chr19:49603782 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4773+1864T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603782 | |||||||
chr19:49603801 | A | T | 7 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4773+1883A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603801 | |||||||
chr19:49603810 | A | G | 28 | a0001c0002t0001g0040 a0001c0002t0001g0075 a0001c0002t0001g0133 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.4773+1892A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603810 | |||||||
chr19:49603824 | T | G | 28 | a0001c0002t0001g0040 a0001c0002t0001g0075 a0001c0002t0001g0133 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.4773+1906T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603824 | |||||||
chr19:49603881 | C | T | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+1963C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603881 | |||||||
chr19:49603913 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4773+1995C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603913 | |||||||
chr19:49603916 | G | A | 13 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+1998G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603916 | |||||||
chr19:49604003 | T | C | 38 | a0001c0001t0001g0295 a0001c0003t0001g0004 a0001c0003t0001g0018 others(35): Show |
39 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.4773+2085T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604003 | |||||||
chr19:49604189 | A | G | 2 | a0001c0002t0003g0057 a0001c0002t0013g0056 |
2 | HG02135.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.4773+2271A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604189 | |||||||
chr19:49604296 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4773+2378A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604296 | |||||||
chr19:49604345 | A | C | 1 | a0023c0022t0001g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4773+2427A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604345 | |||||||
chr19:49604353 | G | A | 13 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+2435G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604353 | |||||||
chr19:49604363 | CA | C | 9 | a0001c0001t0001g0146 a0001c0001t0001g0167 a0001c0001t0001g0253 others(6): Show |
9 | HG01496.hp1 HG01993.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.4773+2461delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49604363 | ||||||
chr19:49604384 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4773+2466A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604384 | |||||||
chr19:49604503 | G | C | 147 | a0001c0001t0001g0144 a0001c0001t0001g0258 a0001c0001t0001g0259 others(144): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.4773+2585G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604503 | |||||||
chr19:49604585 | G | A | 13 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+2667G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604585 | |||||||
chr19:49604977 | G | A | 2 | a0002c0004t0007g0028 a0002c0004t0007g0029 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.4773+3059G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604977 | |||||||
chr19:49605462 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.4773+3544A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605462 | |||||||
chr19:49605482 | G | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | NA18969.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.4773+3564G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605482 | |||||||
chr19:49605558 | A | G | 7 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4773+3640A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605558 | |||||||
chr19:49605618 | C | T | 28 | a0001c0002t0001g0040 a0001c0002t0001g0075 a0001c0002t0001g0133 others(25): Show |
28 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.4773+3700C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605618 | |||||||
chr19:49605726 | G | A | 13 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+3808G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605726 | |||||||
chr19:49605733 | C | T | 2 | a0001c0016t0001g0136 a0001c0016t0001g0137 |
2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4773+3815C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605733 | |||||||
chr19:49605777 | C | T | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+3859C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605777 | |||||||
chr19:49605841 | G | T | 6 | a0001c0006t0001g0024 a0001c0006t0001g0025 a0001c0006t0001g0026 others(3): Show |
6 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4773+3923G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605841 | |||||||
chr19:49605973 | C | T | 13 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+4055C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605973 | |||||||
chr19:49606004 | T | G | 5 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG02451.hp1 HG02723.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+4086T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606004 | |||||||
chr19:49606034 | CT | C | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+4118delT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49606034 | ||||||
chr19:49606155 | C | T | 17 | a0001c0002t0001g0003 a0001c0002t0001g0078 a0001c0002t0001g0085 others(14): Show |
17 | HG00733.hp2 HG01261.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4773+4237C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606155 | |||||||
chr19:49606198 | C | G | 1 | a0001c0002t0001g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4773+4280C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606198 | |||||||
chr19:49606315 | C | CT | 9 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0002t0006g0088 others(6): Show |
9 | HG02257.hp2 HG02258.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.4773+4411dupT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49606315 | ||||||
chr19:49606315 | CT | C | 82 | a0001c0001t0001g0144 a0001c0001t0001g0181 a0001c0001t0001g0258 others(79): Show |
83 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.4773+4411delT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49606315 | ||||||
chr19:49606323 | T | G | 1 | a0001c0002t0002g0058 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4773+4405T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606323 | |||||||
chr19:49606508 | TGGTCAGG others(3): Show |
T | 1 | a0001c0001t0001g0277 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4773+4592_4773+460 others(14): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49606508 | ||||||
chr19:49606645 | C | CT | 13 | a0001c0001t0001g0164 a0001c0001t0001g0250 a0001c0001t0001g0277 others(10): Show |
13 | HG01255.hp1 HG01261.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+4746dupT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49606645 | ||||||
chr19:49606645 | CT | C | 10 | a0001c0001t0001g0183 a0001c0001t0001g0282 a0001c0002t0001g0133 others(7): Show |
10 | HG01069.hp1 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.4773+4746delT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49606645 | ||||||
chr19:49606855 | C | T | 1 | a0007c0025t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4773+4937C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606855 | |||||||
chr19:49606872 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4773+4954C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606872 | |||||||
chr19:49606895 | A | T | 2 | a0001c0020t0002g0141 a0001c0020t0002g0142 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4773+4977A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606895 | |||||||
chr19:49606920 | A | G | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+5002A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606920 | |||||||
chr19:49606953 | C | A | 13 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+5035C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606953 | |||||||
chr19:49607060 | G | A | 1 | a0002c0034t0001g0030 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4773+5142G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607060 | |||||||
chr19:49607121 | C | G | 1 | a0001c0001t0001g0305 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4773+5203C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607121 | |||||||
chr19:49607255 | G | T | 1 | a0002c0004t0004g0038 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4773+5337G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607255 | |||||||
chr19:49607333 | G | A | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+5415G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607333 | |||||||
chr19:49607356 | C | CAT | 12 | a0001c0002t0001g0003 a0001c0002t0001g0078 a0001c0002t0001g0085 others(9): Show |
12 | HG00733.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.4773+5438_4773+543 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607356 | |||||||
chr19:49607360 | T | C | 12 | a0001c0002t0001g0003 a0001c0002t0001g0078 a0001c0002t0001g0085 others(9): Show |
12 | HG00733.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.4773+5442T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607360 | |||||||
chr19:49607361 | G | GCA | 29 | a0001c0001t0001g0155 a0001c0001t0001g0258 a0001c0001t0001g0259 others(26): Show |
29 | HG00735.hp1 HG00735.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.4773+5462_4773+546 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | ||||||
chr19:49607361 | G | GCACACA | 4 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.4773+5458_4773+546 others(10): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | ||||||
chr19:49607361 | G | GCGCACAC others(9): Show |
3 | a0002c0004t0007g0027 a0002c0015t0001g0031 a0002c0015t0001g0032 |
3 | HG02145.hp1 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4773+5444_4773+544 others(20): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | ||||||
chr19:49607361 | G | GCGCACAC others(13): Show |
2 | a0002c0004t0007g0028 a0002c0004t0007g0029 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.4773+5444_4773+544 others(24): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | ||||||
chr19:49607361 | G | GCGCACAC others(15): Show |
1 | a0002c0034t0001g0030 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4773+5444_4773+544 others(26): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | ||||||
chr19:49607361 | G | GCGCGCAC others(7): Show |
1 | a0002c0035t0004g0035 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4773+5444_4773+544 others(18): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | ||||||
chr19:49607361 | G | GCGCGCAC others(9): Show |
2 | a0002c0004t0004g0034 a0002c0004t0004g0037 |
2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.4773+5444_4773+544 others(20): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | ||||||
chr19:49607361 | G | GCGCGCAC others(11): Show |
2 | a0002c0004t0004g0033 a0016c0032t0004g0039 |
2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.4773+5444_4773+544 others(22): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | ||||||
chr19:49607361 | G | GCGCGCAC others(13): Show |
1 | a0002c0004t0004g0038 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4773+5444_4773+544 others(24): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | ||||||
chr19:49607361 | G | GCGCGCGC others(13): Show |
1 | a0002c0004t0004g0036 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4773+5444_4773+544 others(24): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | ||||||
chr19:49607363 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.4773+5445A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607363 | |||||||
chr19:49607372 | C | T | 1 | a0001c0002t0002g0076 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4773+5454C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607372 | |||||||
chr19:49607382 | G | C | 6 | a0001c0002t0001g0003 a0001c0002t0001g0085 a0001c0002t0001g0086 others(3): Show |
6 | HG01261.hp1 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4773+5464G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607382 | |||||||
chr19:49607531 | C | T | 2 | a0002c0004t0004g0036 a0016c0032t0004g0039 |
2 | HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.4773+5613C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607531 | |||||||
chr19:49607532 | G | A | 1 | a0001c0002t0002g0061 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4773+5614G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607532 | |||||||
chr19:49607532 | G | GC | 21 | a0001c0001t0001g0146 a0001c0001t0001g0172 a0001c0001t0001g0187 others(18): Show |
21 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.4773+5621dupC | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607532 | ||||||
chr19:49607657 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4773+5739G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607657 | |||||||
chr19:49607658 | A | T | 1 | a0001c0001t0001g0305 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4773+5740A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607658 | |||||||
chr19:49607666 | G | C | 148 | a0001c0001t0001g0144 a0001c0001t0001g0258 a0001c0001t0001g0259 others(145): Show |
149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.4773+5748G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607666 | |||||||
chr19:49607699 | C | A | 2 | a0001c0002t0006g0130 a0001c0002t0006g0131 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4773+5781C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607699 | |||||||
chr19:49607796 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4773+5878G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607796 | |||||||
chr19:49607880 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0183 others(6): Show |
11 | HG01934.hp2 HG02056.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.4773+5962G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607880 | |||||||
chr19:49607880 | G | C | 128 | a0001c0001t0001g0144 a0001c0001t0001g0258 a0001c0001t0001g0259 others(125): Show |
129 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.4773+5962G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607880 | |||||||
chr19:49608005 | G | C | 5 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0270 others(2): Show |
5 | HG00735.hp1 HG02258.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+6087G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608005 | |||||||
chr19:49608051 | T | A | 2 | a0001c0002t0006g0130 a0001c0002t0006g0131 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4773+6133T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608051 | |||||||
chr19:49608198 | C | T | 1 | a0021c0046t0001g0249 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4773+6280C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608198 | |||||||
chr19:49608334 | T | G | 128 | a0001c0001t0001g0144 a0001c0001t0001g0258 a0001c0001t0001g0259 others(125): Show |
129 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.4774-6199T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608334 | |||||||
chr19:49608344 | T | A | 1 | a0002c0004t0004g0037 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4774-6189T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608344 | |||||||
chr19:49608345 | A | T | 23 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(20): Show |
23 | HG01070.hp2 HG01109.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.4774-6188A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608345 | |||||||
chr19:49608346 | A | T | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-6187A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608346 | |||||||
chr19:49608405 | C | T | 5 | a0001c0001t0001g0295 a0001c0003t0001g0095 a0001c0003t0001g0114 others(2): Show |
5 | HG00544.hp1 HG00642.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.4774-6128C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608405 | |||||||
chr19:49608444 | C | T | 1 | a0002c0004t0004g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4774-6089C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608444 | |||||||
chr19:49608503 | G | A | 2 | a0001c0002t0005g0081 a0001c0002t0005g0082 |
2 | HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4774-6030G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608503 | |||||||
chr19:49608510 | A | G | 13 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4774-6023A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608510 | |||||||
chr19:49608590 | C | T | 1 | a0023c0022t0001g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4774-5943C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608590 | |||||||
chr19:49608659 | G | A | 1 | a0002c0004t0007g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4774-5874G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608659 | |||||||
chr19:49608751 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4774-5782A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608751 | |||||||
chr19:49608841 | C | CA | 17 | a0001c0002t0001g0021 a0001c0002t0001g0045 a0001c0002t0001g0046 others(14): Show |
17 | HG01433.hp1 HG02055.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.4774-5681dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49608841 | ||||||
chr19:49608853 | C | A | 1 | a0001c0001t0001g0305 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4774-5680C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608853 | |||||||
chr19:49608854 | A | C | 1 | a0001c0001t0001g0305 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4774-5679A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608854 | |||||||
chr19:49608883 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0243 a0001c0001t0001g0245 others(2): Show |
5 | HG02886.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.4774-5650A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608883 | |||||||
chr19:49608900 | C | T | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-5633C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608900 | |||||||
chr19:49609114 | C | A | 2 | a0001c0016t0001g0136 a0001c0016t0001g0137 |
2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4774-5419C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609114 | |||||||
chr19:49609133 | G | A | 13 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4774-5400G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609133 | |||||||
chr19:49609134 | C | T | 4 | a0001c0001t0001g0175 a0001c0001t0001g0242 a0001c0018t0001g0182 others(1): Show |
4 | HG00140.hp1 HG01081.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.4774-5399C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609134 | |||||||
chr19:49609329 | G | T | 1 | a0001c0001t0001g0305 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4774-5204G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609329 | |||||||
chr19:49609346 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4774-5187A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609346 | |||||||
chr19:49609408 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4774-5125C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609408 | |||||||
chr19:49609469 | C | T | 1 | a0002c0004t0004g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4774-5064C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609469 | |||||||
chr19:49609472 | G | T | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-5061G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609472 | |||||||
chr19:49609556 | A | G | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-4977A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609556 | |||||||
chr19:49609592 | C | A | 17 | a0001c0002t0001g0003 a0001c0002t0001g0078 a0001c0002t0001g0085 others(14): Show |
17 | HG00733.hp2 HG01261.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4774-4941C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609592 | |||||||
chr19:49609598 | C | T | 2 | a0001c0002t0001g0052 a0001c0002t0001g0053 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4774-4935C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609598 | |||||||
chr19:49609598 | CA | C | 141 | a0001c0001t0001g0144 a0001c0001t0001g0193 a0001c0001t0001g0240 others(138): Show |
142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.4774-4915delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49609598 | ||||||
chr19:49609598 | CAA | C | 8 | a0001c0001t0001g0269 a0001c0002t0001g0054 a0001c0002t0001g0075 others(5): Show |
8 | HG01069.hp2 HG01070.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.4774-4916_4774-491 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49609598 | ||||||
chr19:49609599 | A | C | 2 | a0001c0002t0001g0052 a0001c0002t0001g0053 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4774-4934A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609599 | |||||||
chr19:49609633 | A | G | 1 | a0001c0003t0001g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4774-4900A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609633 | |||||||
chr19:49609718 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4774-4815G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609718 | |||||||
chr19:49609766 | G | T | 1 | a0001c0001t0001g0305 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4774-4767G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609766 | |||||||
chr19:49609852 | G | A | 2 | a0001c0020t0002g0141 a0001c0020t0002g0142 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4774-4681G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609852 | |||||||
chr19:49609942 | C | T | 1 | a0001c0003t0001g0110 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4774-4591C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609942 | |||||||
chr19:49609979 | CT | C | 31 | a0001c0001t0001g0305 a0001c0002t0001g0040 a0001c0002t0001g0075 others(28): Show |
31 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.4774-4542delT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49609979 | ||||||
chr19:49610119 | C | T | 44 | a0001c0001t0001g0144 a0001c0001t0001g0295 a0001c0002t0008g0117 others(41): Show |
45 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.4774-4414C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610119 | |||||||
chr19:49610131 | C | T | 9 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
9 | HG01070.hp2 HG01255.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4774-4402C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610131 | |||||||
chr19:49610186 | G | A | 1 | a0001c0003t0001g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4774-4347G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610186 | |||||||
chr19:49610203 | G | A | 13 | a0001c0002t0001g0003 a0001c0002t0001g0078 a0001c0002t0001g0085 others(10): Show |
13 | HG00733.hp2 HG01261.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.4774-4330G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610203 | |||||||
chr19:49610298 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4774-4235T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610298 | |||||||
chr19:49610341 | G | A | 13 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(10): Show |
13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4774-4192G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610341 | |||||||
chr19:49610546 | A | ATTTTTTT others(2): Show |
14 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0156 others(11): Show |
14 | HG01070.hp2 HG01167.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.4774-3981_4774-397 others(13): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49610546 | ||||||
chr19:49610546 | A | ATTTTTTT others(3): Show |
73 | a0001c0001t0001g0144 a0001c0001t0001g0155 a0001c0001t0001g0160 others(70): Show |
74 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.4774-3982_4774-397 others(14): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49610546 | ||||||
chr19:49610546 | A | ATTTTTTT others(4): Show |
42 | a0001c0001t0003g0262 a0001c0002t0001g0040 a0001c0002t0001g0055 others(39): Show |
42 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.4774-3983_4774-397 others(15): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49610546 | ||||||
chr19:49610546 | A | ATTTTTTT others(5): Show |
25 | a0001c0002t0001g0003 a0001c0002t0001g0078 a0001c0002t0001g0086 others(22): Show |
25 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.4774-3984_4774-397 others(16): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49610546 | ||||||
chr19:49610546 | A | ATTTTTTT others(6): Show |
6 | a0001c0002t0001g0087 a0001c0002t0001g0121 a0001c0002t0001g0132 others(3): Show |
6 | HG01175.hp2 HG01261.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.4774-3985_4774-397 others(17): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49610546 | ||||||
chr19:49610629 | G | A | 6 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(3): Show |
6 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.4774-3904G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610629 | |||||||
chr19:49610658 | C | T | 1 | a0001c0003t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4774-3875C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610658 | |||||||
chr19:49610661 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4774-3872C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610661 | |||||||
chr19:49610702 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4774-3831C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610702 | |||||||
chr19:49610725 | A | T | 1 | a0001c0003t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4774-3808A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610725 | |||||||
chr19:49610789 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4774-3744C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610789 | |||||||
chr19:49610790 | G | A | 14 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(11): Show |
14 | HG01070.hp2 HG01255.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.4774-3743G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610790 | |||||||
chr19:49610949 | A | G | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-3584A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610949 | |||||||
chr19:49611015 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4774-3518G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611015 | |||||||
chr19:49611083 | C | T | 1 | a0012c0027t0001g0122 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4774-3450C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611083 | |||||||
chr19:49611093 | C | T | 108 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(105): Show |
109 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.4774-3440C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611093 | |||||||
chr19:49611163 | A | G | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-3370A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611163 | |||||||
chr19:49611384 | C | T | 19 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0002t0001g0021 others(16): Show |
19 | HG01109.hp1 HG01192.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.4774-3149C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611384 | |||||||
chr19:49611632 | AAAAAAAA others(283): Show |
A | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2891_4774-260 others(4): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49611632 | ||||||
chr19:49611748 | C | T | 2 | a0001c0016t0001g0136 a0001c0016t0001g0137 |
2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4774-2785C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611748 | |||||||
chr19:49611765 | T | A | 1 | a0001c0001t0001g0277 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4774-2768T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611765 | |||||||
chr19:49611767 | C | A | 1 | a0001c0001t0001g0277 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4774-2766C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611767 | |||||||
chr19:49611774 | A | T | 147 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(144): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.4774-2759A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611774 | |||||||
chr19:49611779 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0274 |
2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4774-2754C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611779 | |||||||
chr19:49611796 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4774-2737G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611796 | |||||||
chr19:49611800 | G | A | 80 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(77): Show |
81 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.4774-2733G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611800 | |||||||
chr19:49611884 | C | T | 1 | a0001c0052t0001g0233 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4774-2649C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611884 | |||||||
chr19:49611889 | C | T | 12 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.4774-2644C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611889 | |||||||
chr19:49611902 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4774-2631G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611902 | |||||||
chr19:49611922 | CAAAAA | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0146 others(37): Show |
40 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.4774-2589_4774-258 others(9): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49611922 | ||||||
chr19:49611922 | CAAAAAA | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(254): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.4774-2590_4774-258 others(10): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49611922 | ||||||
chr19:49611922 | CAAAAAAA | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
9 | HG01243.hp2 HG01943.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.4774-2591_4774-258 others(11): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49611922 | ||||||
chr19:49611934 | A | C | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2599A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611934 | |||||||
chr19:49611942 | A | C | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2591A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611942 | |||||||
chr19:49611955 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0274 |
2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4774-2578G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611955 | |||||||
chr19:49611999 | C | G | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2534C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611999 | |||||||
chr19:49612041 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0190 a0001c0001t0001g0193 |
4 | HG02056.hp2 HG02071.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.4774-2492G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612041 | |||||||
chr19:49612056 | C | A | 2 | a0001c0016t0001g0136 a0001c0016t0001g0137 |
2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4774-2477C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612056 | |||||||
chr19:49612208 | G | A | 1 | a0001c0003t0001g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4774-2325G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612208 | |||||||
chr19:49612211 | AGAGCAAG others(5): Show |
A | 7 | a0001c0002t0001g0075 a0001c0002t0002g0041 a0001c0002t0002g0060 others(4): Show |
7 | HG01433.hp2 HG01928.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.4774-2320_4774-230 others(16): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49612211 | ||||||
chr19:49612225 | T | G | 7 | a0001c0002t0001g0075 a0001c0002t0002g0041 a0001c0002t0002g0060 others(4): Show |
7 | HG01433.hp2 HG01928.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.4774-2308T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612225 | |||||||
chr19:49612228 | C | CA | 19 | a0001c0001t0001g0193 a0001c0001t0001g0196 a0001c0001t0001g0247 others(16): Show |
19 | HG00438.hp2 HG00735.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.4774-2286dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49612228 | ||||||
chr19:49612228 | CA | C | 7 | a0001c0001t0001g0181 a0001c0001t0001g0236 a0001c0001t0001g0277 others(4): Show |
7 | HG01943.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4774-2286delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49612228 | ||||||
chr19:49612344 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0243 a0001c0001t0001g0245 others(2): Show |
5 | HG02886.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.4774-2189G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612344 | |||||||
chr19:49612355 | T | C | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2178T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612355 | |||||||
chr19:49612427 | G | A | 1 | a0001c0003t0001g0127 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4774-2106G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612427 | |||||||
chr19:49612480 | G | A | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2053G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612480 | |||||||
chr19:49612488 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4774-2045G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612488 | |||||||
chr19:49612505 | T | G | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2028T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612505 | |||||||
chr19:49612746 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4774-1787C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612746 | |||||||
chr19:49612812 | G | A | 9 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
9 | HG01070.hp2 HG01255.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4774-1721G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612812 | |||||||
chr19:49612876 | C | T | 2 | a0001c0016t0001g0136 a0001c0016t0001g0137 |
2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4774-1657C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612876 | |||||||
chr19:49612924 | A | G | 2 | a0004c0010t0001g0123 a0004c0010t0001g0124 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4774-1609A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612924 | |||||||
chr19:49612984 | T | G | 116 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(113): Show |
117 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.4774-1549T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612984 | |||||||
chr19:49613057 | A | C | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-1476A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49613057 | |||||||
chr19:49613145 | C | T | 1 | a0001c0043t0012g0017 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4774-1388C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49613145 | |||||||
chr19:49613284 | G | A | 12 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.4774-1249G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49613284 | |||||||
chr19:49613330 | C | CA | 13 | a0001c0001t0001g0248 a0001c0001t0001g0254 a0001c0001t0001g0258 others(10): Show |
13 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4774-1181dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49613330 | ||||||
chr19:49613330 | CA | C | 79 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0150 others(76): Show |
79 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.4774-1181delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49613330 | ||||||
chr19:49613661 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4774-872C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49613661 | |||||||
chr19:49614033 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4774-500C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49614033 | |||||||
chr19:49614299 | C | T | 1 | a0001c0052t0001g0233 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4774-234C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49614299 | |||||||
chr19:49614347 | C | T | 1 | a0001c0003t0001g0112 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.4774-186C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49614347 | |||||||
chr19:49614773 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4891-103G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 7/13 | chr19 | 49614773 | |||||||
chr19:49614804 | A | G | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4891-72A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 7/13 | chr19 | 49614804 | |||||||
chr19:49615060 | A | T | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5024+51A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615060 | |||||||
chr19:49615133 | G | C | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5024+124G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615133 | |||||||
chr19:49615154 | G | A | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5024+145G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615154 | |||||||
chr19:49615357 | C | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(272): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.5024+348C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615357 | |||||||
chr19:49615379 | CG | C | 12 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.5025-365delG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 49615379 | ||||||
chr19:49615434 | C | G | 133 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(130): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.5025-313C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615434 | |||||||
chr19:49615479 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0192 |
3 | NA18982.hp1 NA18983.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.5025-268C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615479 | |||||||
chr19:49615525 | A | T | 6 | a0001c0002t0001g0121 a0001c0009t0002g0138 a0001c0009t0002g0139 others(3): Show |
6 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.5025-222A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615525 | |||||||
chr19:49615525 | ACCCAGAG others(17): Show |
A | 12 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.5025-157_5025-134d others(26): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 49615525 | ||||||
chr19:49615590 | G | A | 17 | a0001c0002t0001g0133 a0001c0002t0001g0134 a0001c0002t0001g0135 others(14): Show |
17 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.5025-157G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615590 | |||||||
chr19:49615590 | G | GGTCAGAG others(67): Show |
5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5025-157_5025-156i others(76): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615590 | |||||||
chr19:49615590 | G | GTCAGAGT others(17): Show |
140 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0001g0150 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.5025-156_5025-133d others(26): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 49615590 | ||||||
chr19:49615683 | A | G | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5025-64A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615683 | |||||||
chr19:49616369 | CA | C | 133 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(130): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.5497+151delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616369 | |||||||
chr19:49616372 | TACAC | T | 133 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(130): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.5497+154_5497+157d others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616372 | |||||||
chr19:49616447 | C | T | 3 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0106 |
3 | HG00280.hp2 HG03239.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.5497+228C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616447 | |||||||
chr19:49616507 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5497+288G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616507 | |||||||
chr19:49616864 | C | T | 4 | a0001c0002t0001g0121 a0001c0002t0001g0132 a0001c0002t0006g0130 others(1): Show |
4 | HG02615.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5497+645C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616864 | |||||||
chr19:49616903 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5497+684C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616903 | |||||||
chr19:49616994 | G | A | 1 | a0001c0001t0003g0197 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5497+775G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616994 | |||||||
chr19:49617000 | T | C | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5497+781T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617000 | |||||||
chr19:49617006 | T | C | 2 | a0001c0002t0006g0130 a0001c0002t0006g0131 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5497+787T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617006 | |||||||
chr19:49617025 | C | T | 2 | a0001c0012t0001g0089 a0001c0012t0001g0120 |
2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.5497+806C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617025 | |||||||
chr19:49617130 | CA | C | 7 | a0001c0001t0001g0154 a0001c0001t0001g0226 a0001c0001t0001g0269 others(4): Show |
7 | HG01069.hp2 HG01099.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.5497+927delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49617130 | ||||||
chr19:49617155 | A | G | 1 | a0001c0003t0001g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5497+936A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617155 | |||||||
chr19:49617231 | A | C | 16 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0263 others(13): Show |
16 | HG00735.hp1 HG00735.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.5497+1012A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617231 | |||||||
chr19:49617346 | G | A | 29 | a0001c0001t0001g0237 a0001c0002t0001g0040 a0001c0002t0001g0075 others(26): Show |
29 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.5497+1127G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617346 | |||||||
chr19:49617369 | G | A | 7 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.5497+1150G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617369 | |||||||
chr19:49617492 | T | C | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5497+1273T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617492 | |||||||
chr19:49617714 | AG | A | 4 | a0001c0002t0001g0121 a0001c0002t0001g0132 a0001c0002t0006g0130 others(1): Show |
4 | HG02615.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5497+1499delG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49617714 | ||||||
chr19:49617727 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5497+1508T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617727 | |||||||
chr19:49617762 | A | C | 30 | a0001c0001t0001g0150 a0001c0001t0001g0237 a0001c0002t0001g0040 others(27): Show |
30 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.5497+1543A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617762 | |||||||
chr19:49617765 | C | T | 133 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(130): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.5497+1546C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617765 | |||||||
chr19:49617772 | G | C | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5497+1553G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617772 | |||||||
chr19:49617824 | G | A | 1 | a0001c0002t0001g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5497+1605G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617824 | |||||||
chr19:49617864 | G | A | 1 | a0001c0002t0008g0119 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5497+1645G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617864 | |||||||
chr19:49617954 | C | T | 16 | a0001c0001t0001g0164 a0001c0009t0002g0138 a0001c0009t0002g0139 others(13): Show |
16 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.5497+1735C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617954 | |||||||
chr19:49618017 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.5497+1798G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618017 | |||||||
chr19:49618058 | A | G | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5497+1839A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618058 | |||||||
chr19:49618092 | G | T | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5497+1873G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618092 | |||||||
chr19:49618155 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5497+1936C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618155 | |||||||
chr19:49618194 | G | T | 25 | a0001c0001t0001g0237 a0001c0002t0001g0040 a0001c0002t0001g0075 others(22): Show |
25 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.5497+1975G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618194 | |||||||
chr19:49618294 | T | C | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5498-2058T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618294 | |||||||
chr19:49618387 | T | C | 2 | a0001c0001t0001g0289 a0001c0001t0001g0297 |
2 | HG01258.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.5498-1965T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618387 | |||||||
chr19:49618410 | G | A | 1 | a0001c0016t0001g0136 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5498-1942G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618410 | |||||||
chr19:49618491 | G | A | 16 | a0001c0001t0001g0144 a0001c0002t0001g0021 a0001c0002t0001g0045 others(13): Show |
16 | HG01109.hp1 HG01433.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.5498-1861G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618491 | |||||||
chr19:49618713 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5498-1639C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618713 | |||||||
chr19:49618773 | G | T | 1 | a0001c0003t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5498-1579G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618773 | |||||||
chr19:49618821 | T | C | 150 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(147): Show |
151 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.5498-1531T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618821 | |||||||
chr19:49618965 | A | T | 3 | a0001c0002t0001g0078 a0001c0002t0006g0088 a0008c0023t0001g0080 |
3 | HG00733.hp2 HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.5498-1387A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618965 | |||||||
chr19:49619027 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.5498-1325C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619027 | |||||||
chr19:49619047 | A | G | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5498-1305A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619047 | |||||||
chr19:49619141 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5498-1211C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619141 | |||||||
chr19:49619174 | C | A | 3 | a0002c0004t0007g0027 a0002c0004t0007g0028 a0002c0004t0007g0029 |
3 | HG01070.hp1 HG01071.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.5498-1178C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619174 | |||||||
chr19:49619224 | G | GT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(119): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.5498-1103dupT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619224 | ||||||
chr19:49619224 | G | GTT | 43 | a0001c0001t0001g0150 a0001c0001t0001g0159 a0001c0001t0001g0215 others(40): Show |
43 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.5498-1104_5498-110 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619224 | ||||||
chr19:49619224 | G | GTTT | 14 | a0001c0001t0001g0144 a0001c0002t0001g0021 a0001c0002t0001g0046 others(11): Show |
14 | HG01109.hp1 HG01433.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.5498-1105_5498-110 others(7): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619224 | ||||||
chr19:49619224 | G | GTTTT | 9 | a0001c0002t0001g0045 a0001c0002t0001g0051 a0001c0002t0001g0053 others(6): Show |
9 | HG01346.hp2 HG02055.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.5498-1106_5498-110 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619224 | ||||||
chr19:49619224 | GTT | G | 12 | a0001c0009t0002g0138 a0001c0009t0002g0140 a0001c0020t0002g0141 others(9): Show |
12 | HG01070.hp1 HG01071.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.5498-1104_5498-110 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619224 | ||||||
chr19:49619224 | GTTTTTTT others(5): Show |
G | 1 | a0023c0022t0001g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5498-1114_5498-110 others(16): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619224 | ||||||
chr19:49619280 | A | G | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5498-1072A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619280 | |||||||
chr19:49619312 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5498-1040C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619312 | |||||||
chr19:49619501 | G | C | 150 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(147): Show |
151 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.5498-851G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619501 | |||||||
chr19:49619535 | C | CT | 81 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0152 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.5498-794dupT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619535 | ||||||
chr19:49619535 | C | CTT | 74 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(71): Show |
74 | HG00423.hp2 HG00642.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.5498-795_5498-794d others(4): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619535 | ||||||
chr19:49619535 | C | CTTT | 23 | a0001c0001t0001g0266 a0001c0002t0001g0050 a0001c0002t0001g0054 others(20): Show |
24 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.5498-796_5498-794d others(5): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619535 | ||||||
chr19:49619535 | CTT | C | 9 | a0001c0016t0001g0136 a0001c0016t0001g0137 a0002c0004t0004g0033 others(6): Show |
9 | HG02451.hp1 HG03654.hp1 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.5498-795_5498-794d others(4): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619535 | ||||||
chr19:49619563 | C | T | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5498-789C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619563 | |||||||
chr19:49619659 | A | C | 1 | a0016c0032t0004g0039 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5498-693A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619659 | |||||||
chr19:49619703 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.5498-649G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619703 | |||||||
chr19:49619715 | A | G | 2 | a0001c0001t0001g0291 a0003c0005t0001g0283 |
2 | HG01099.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.5498-637A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619715 | |||||||
chr19:49619769 | C | G | 1 | a0001c0003t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5498-583C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619769 | |||||||
chr19:49619770 | G | A | 1 | a0001c0003t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5498-582G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619770 | |||||||
chr19:49619771 | A | G | 1 | a0001c0003t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5498-581A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619771 | |||||||
chr19:49619781 | A | T | 1 | a0001c0003t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5498-571A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619781 | |||||||
chr19:49619792 | T | C | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5498-560T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619792 | |||||||
chr19:49619793 | C | T | 1 | a0001c0002t0001g0087 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5498-559C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619793 | |||||||
chr19:49619851 | C | CT | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(78): Show |
87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.5498-476dupT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619851 | ||||||
chr19:49619851 | C | CTT | 45 | a0001c0001t0001g0155 a0001c0001t0001g0252 a0001c0001t0001g0259 others(42): Show |
45 | HG00280.hp2 HG00544.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.5498-477_5498-476d others(4): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619851 | ||||||
chr19:49619851 | C | CTTT | 59 | a0001c0001t0001g0144 a0001c0001t0001g0258 a0001c0001t0001g0263 others(56): Show |
60 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.5498-478_5498-476d others(5): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619851 | ||||||
chr19:49619851 | C | CTTTT | 24 | a0001c0001t0001g0150 a0001c0001t0001g0237 a0001c0001t0003g0261 others(21): Show |
24 | HG00423.hp2 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.5498-479_5498-476d others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619851 | ||||||
chr19:49619851 | CTTTT | C | 9 | a0002c0004t0004g0033 a0002c0004t0004g0036 a0002c0004t0004g0037 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.5498-479_5498-476d others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619851 | ||||||
chr19:49619851 | CTTTTTTT others(6): Show |
C | 1 | a0001c0003t0001g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5498-488_5498-476d others(15): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619851 | ||||||
chr19:49619997 | C | T | 1 | a0002c0004t0004g0036 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5498-355C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619997 | |||||||
chr19:49620009 | C | T | 10 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5498-343C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49620009 | |||||||
chr19:49620055 | G | A | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5498-297G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49620055 | |||||||
chr19:49620055 | G | T | 1 | a0001c0001t0001g0296 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5498-297G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49620055 | |||||||
chr19:49620302 | G | A | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5498-50G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49620302 | |||||||
chr19:49620333 | C | T | 10 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5498-19C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49620333 | |||||||
chr19:49620499 | A | AG | 36 | a0001c0001t0001g0009 a0001c0001t0001g0144 a0001c0001t0001g0146 others(33): Show |
36 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.5623+32dupG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49620499 | ||||||
chr19:49620499 | A | G | 1 | a0001c0001t0003g0262 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5623+22A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49620499 | |||||||
chr19:49620502 | G | C | 7 | a0001c0001t0001g0181 a0001c0001t0001g0198 a0001c0001t0001g0229 others(4): Show |
7 | HG00544.hp2 NA18957.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.5623+25G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49620502 | |||||||
chr19:49620504 | G | T | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5623+27G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49620504 | |||||||
chr19:49620768 | A | AGGGCTGG others(30): Show |
25 | a0001c0001t0001g0237 a0001c0002t0001g0040 a0001c0002t0001g0075 others(22): Show |
25 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.5623+317_5623+353d others(39): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49620768 | ||||||
chr19:49620882 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.5623+405G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49620882 | |||||||
chr19:49620965 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5623+488G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49620965 | |||||||
chr19:49620982 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5623+505A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49620982 | |||||||
chr19:49621012 | G | A | 2 | a0001c0002t0006g0130 a0001c0002t0006g0131 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5624-513G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621012 | |||||||
chr19:49621020 | T | TGGGGGTC others(9): Show |
5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5624-501_5624-500i others(18): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621020 | ||||||
chr19:49621022 | GGGTCTGG others(6): Show |
G | 10 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5624-500_5624-488d others(15): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621022 | ||||||
chr19:49621040 | CTGAGGGA others(1): Show |
C | 10 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5624-484_5624-477d others(10): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621040 | |||||||
chr19:49621054 | G | C | 10 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5624-471G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621054 | |||||||
chr19:49621056 | T | TG | 10 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5624-465dupG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621056 | ||||||
chr19:49621061 | C | T | 10 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5624-464C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621061 | |||||||
chr19:49621090 | A | G | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-435A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621090 | |||||||
chr19:49621092 | T | TG | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-429dupG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621092 | ||||||
chr19:49621097 | C | T | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-428C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621097 | |||||||
chr19:49621128 | TGGGGGTC others(9): Show |
T | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-392_5624-377d others(18): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621128 | ||||||
chr19:49621149 | T | C | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-376T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621149 | |||||||
chr19:49621180 | T | TG | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-341dupG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621180 | ||||||
chr19:49621185 | C | T | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-340C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621185 | |||||||
chr19:49621194 | C | T | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-331C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621194 | |||||||
chr19:49621201 | T | A | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-324T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621201 | |||||||
chr19:49621205 | G | A | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-320G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621205 | |||||||
chr19:49621231 | T | C | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-294T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621231 | |||||||
chr19:49621238 | A | T | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-287A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621238 | |||||||
chr19:49621241 | G | A | 1 | a0007c0025t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5624-284G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621241 | |||||||
chr19:49621242 | A | G | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-283A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621242 | |||||||
chr19:49621249 | G | C | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-276G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621249 | |||||||
chr19:49621249 | GGGCTGGG others(30): Show |
G | 1 | a0001c0002t0001g0054 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5624-202_5624-166d others(39): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621249 | ||||||
chr19:49621406 | G | A | 116 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(113): Show |
117 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.5624-119G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621406 | |||||||
chr19:49621625 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG00544.hp2 | splice_region_variant&intron_variant | LOW | c.5721+3G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621625 | |||||||
chr19:49621670 | G | A | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5721+48G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621670 | |||||||
chr19:49621689 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0145 a0001c0001t0001g0147 others(5): Show |
9 | HG01243.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.5721+67C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621689 | |||||||
chr19:49621690 | G | C | 1 | a0001c0002t0005g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5721+68G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621690 | |||||||
chr19:49621872 | T | G | 15 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(12): Show |
15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5721+250T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621872 | |||||||
chr19:49621907 | C | T | 2 | a0001c0002t0001g0134 a0001c0002t0001g0135 |
2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.5721+285C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621907 | |||||||
chr19:49621935 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5721+313T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621935 | |||||||
chr19:49621960 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5721+338G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621960 | |||||||
chr19:49622033 | TCAGGGCT others(8): Show |
T | 2 | a0001c0002t0001g0054 a0002c0034t0001g0030 |
2 | HG01192.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.5721+415_5721+429d others(17): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622033 | ||||||
chr19:49622319 | G | A | 2 | a0001c0016t0001g0136 a0001c0016t0001g0137 |
2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5721+697G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622319 | |||||||
chr19:49622472 | G | C | 1 | a0001c0052t0001g0233 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5721+850G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622472 | |||||||
chr19:49622527 | G | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | NA18969.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.5721+905G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622527 | |||||||
chr19:49622555 | G | A | 1 | a0001c0024t0003g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5721+933G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622555 | |||||||
chr19:49622597 | G | GA | 150 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(147): Show |
151 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.5721+985dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622597 | ||||||
chr19:49622687 | C | T | 10 | a0002c0004t0004g0033 a0002c0004t0004g0034 a0002c0004t0004g0036 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5721+1065C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622687 | |||||||
chr19:49622760 | C | T | 2 | a0001c0016t0001g0136 a0001c0016t0001g0137 |
2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5721+1138C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622760 | |||||||
chr19:49622824 | G | A | 128 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(125): Show |
129 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.5721+1202G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622824 | |||||||
chr19:49622840 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0145 a0001c0001t0001g0147 others(5): Show |
9 | HG01243.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.5721+1218C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622840 | |||||||
chr19:49622846 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5721+1224C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622846 | |||||||
chr19:49622869 | G | A | 2 | a0001c0016t0001g0136 a0001c0016t0001g0137 |
2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5721+1247G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622869 | |||||||
chr19:49622891 | C | CA | 92 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0237 others(89): Show |
93 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.5721+1279dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622891 | ||||||
chr19:49622900 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.5721+1278A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622900 | |||||||
chr19:49622901 | AC | A | 5 | a0001c0002t0001g0087 a0001c0003t0001g0018 a0001c0003t0001g0100 others(2): Show |
5 | HG01261.hp1 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.5721+1280delC | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622901 | |||||||
chr19:49622902 | C | A | 145 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(142): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.5721+1280C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622902 | |||||||
chr19:49622906 | A | AAAC | 14 | a0001c0002t0001g0040 a0001c0002t0002g0041 a0001c0002t0002g0044 others(11): Show |
14 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.5721+1285_5721+128 others(7): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622906 | ||||||
chr19:49622906 | A | AAACATAT | 4 | a0001c0002t0002g0070 a0001c0002t0002g0071 a0001c0002t0013g0056 others(1): Show |
4 | HG02132.hp1 HG02273.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.5721+1285_5721+128 others(11): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622906 | ||||||
chr19:49622906 | A | AAACATAT others(2): Show |
4 | a0001c0001t0001g0144 a0001c0002t0001g0021 a0001c0002t0001g0048 others(1): Show |
4 | HG01109.hp1 HG02129.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.5721+1285_5721+128 others(13): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622906 | ||||||
chr19:49622906 | A | AAACATAT others(4): Show |
2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.5721+1285_5721+128 others(15): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622906 | ||||||
chr19:49622906 | A | AAACATAT others(6): Show |
2 | a0001c0002t0001g0049 a0001c0002t0003g0057 |
2 | HG02135.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.5721+1285_5721+128 others(17): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622906 | ||||||
chr19:49622906 | A | AAACATAT others(10): Show |
1 | a0001c0002t0001g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5721+1285_5721+128 others(21): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622906 | ||||||
chr19:49622907 | ACATAT | A | 3 | a0001c0002t0008g0117 a0001c0002t0008g0118 a0001c0002t0008g0119 |
3 | HG01884.hp1 HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.5721+1286_5721+129 others(9): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622907 | |||||||
chr19:49622908 | C | A | 8 | a0001c0002t0001g0087 a0001c0002t0002g0073 a0001c0003t0001g0018 others(5): Show |
8 | HG01261.hp1 HG01433.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.5721+1286C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622908 | |||||||
chr19:49622908 | C | CAT | 5 | a0001c0001t0001g0006 a0001c0001t0001g0179 a0001c0001t0001g0253 others(2): Show |
5 | HG00639.hp2 HG02071.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.5721+1306_5721+130 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622908 | ||||||
chr19:49622908 | C | CATAT | 3 | a0001c0001t0001g0007 a0001c0001t0001g0192 a0001c0001t0001g0247 |
4 | HG02056.hp1 NA18982.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.5721+1304_5721+130 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622908 | ||||||
chr19:49622908 | C | CATATATA others(3): Show |
1 | a0001c0002t0001g0050 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5721+1298_5721+130 others(14): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622908 | ||||||
chr19:49622908 | C | T | 29 | a0001c0001t0001g0144 a0001c0002t0001g0021 a0001c0002t0001g0040 others(26): Show |
29 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.5721+1286C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622908 | |||||||
chr19:49622908 | CAT | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
8 | HG01243.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.5721+1306_5721+130 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622908 | ||||||
chr19:49622908 | CATAT | C | 11 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
11 | HG01070.hp2 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.5721+1304_5721+130 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622908 | ||||||
chr19:49622910 | T | C | 8 | a0001c0002t0001g0087 a0001c0002t0002g0073 a0001c0003t0001g0018 others(5): Show |
8 | HG01261.hp1 HG01433.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.5721+1288T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622910 | |||||||
chr19:49622914 | T | C | 3 | a0001c0002t0008g0117 a0001c0002t0008g0118 a0001c0002t0008g0119 |
3 | HG01884.hp1 HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.5721+1292T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622914 | |||||||
chr19:49622922 | T | C | 2 | a0001c0001t0001g0267 a0001c0001t0003g0262 |
2 | HG01516.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.5721+1300T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622922 | |||||||
chr19:49622924 | T | G | 7 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0204 others(4): Show |
7 | HG00673.hp2 HG01175.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.5721+1302T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622924 | |||||||
chr19:49622924 | T | TAGAG | 3 | a0001c0001t0001g0236 a0001c0001t0001g0277 a0003c0005t0001g0278 |
3 | NA18982.hp2 NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.5721+1303_5721+130 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622924 | ||||||
chr19:49622926 | T | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
26 | HG00673.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.5721+1304T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622926 | |||||||
chr19:49622926 | T | TAG | 3 | a0001c0001t0001g0183 a0001c0001t0001g0191 a0001c0001t0001g0298 |
3 | HG01928.hp2 HG02155.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.5721+1305_5721+130 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622926 | ||||||
chr19:49622926 | TATAG | T | 9 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0167 others(6): Show |
9 | HG00597.hp1 HG01255.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.5721+1306_5721+130 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622926 | ||||||
chr19:49622926 | TATAGAG | T | 3 | a0001c0001t0001g0289 a0001c0001t0001g0292 a0001c0001t0001g0297 |
3 | HG01258.hp1 HG01496.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.5721+1306_5721+131 others(10): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622926 | ||||||
chr19:49622928 | T | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(53): Show |
59 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.5721+1306T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622928 | |||||||
chr19:49622928 | T | TAGAG | 4 | a0001c0001t0001g0209 a0001c0001t0001g0214 a0001c0001t0003g0014 others(1): Show |
4 | HG01934.hp2 HG02080.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.5721+1332_5721+133 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622928 | ||||||
chr19:49622928 | T | TATATATA others(9): Show |
1 | a0001c0002t0001g0281 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.5721+1307_5721+130 others(20): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622928 | ||||||
chr19:49622928 | T | TATATATA others(5): Show |
2 | a0001c0002t0001g0047 a0001c0002t0001g0051 |
2 | NA18971.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.5721+1307_5721+130 others(16): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622928 | ||||||
chr19:49622928 | TAG | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0152 a0001c0001t0001g0154 others(1): Show |
4 | HG00609.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.5721+1334_5721+133 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622928 | ||||||
chr19:49622928 | TAGAG | T | 4 | a0001c0001t0001g0190 a0001c0001t0001g0208 a0001c0001t0001g0218 others(1): Show |
4 | HG00099.hp1 HG01358.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.5721+1332_5721+133 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622928 | ||||||
chr19:49622928 | TAGAGAG | T | 12 | a0001c0001t0001g0282 a0001c0001t0001g0284 a0001c0001t0001g0285 others(9): Show |
13 | HG00280.hp1 HG00738.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.5721+1330_5721+133 others(10): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622928 | ||||||
chr19:49622930 | G | T | 148 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0144 others(145): Show |
150 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.5721+1308G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622930 | |||||||
chr19:49622932 | G | T | 111 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0152 others(108): Show |
112 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.5721+1310G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622932 | |||||||
chr19:49622934 | G | T | 83 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0179 others(80): Show |
84 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.5721+1312G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622934 | |||||||
chr19:49622936 | G | T | 51 | a0001c0001t0001g0150 a0001c0001t0001g0190 a0001c0001t0001g0252 others(48): Show |
51 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.5721+1314G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622936 | |||||||
chr19:49622938 | G | T | 24 | a0001c0001t0001g0190 a0001c0001t0001g0252 a0001c0001t0001g0266 others(21): Show |
24 | HG00438.hp1 HG00735.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.5721+1316G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622938 | |||||||
chr19:49622940 | G | T | 13 | a0001c0001t0001g0252 a0001c0002t0001g0075 a0001c0003t0001g0105 others(10): Show |
13 | HG00438.hp1 HG01943.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.5721+1318G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622940 | |||||||
chr19:49622940 | GAGAGAGA others(11): Show |
G | 1 | a0001c0003t0001g0019 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5721+1336_5721+135 others(22): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622940 | ||||||
chr19:49622942 | G | T | 3 | a0001c0001t0001g0252 a0001c0003t0001g0125 a0001c0003t0001g0126 |
3 | HG00438.hp1 HG02132.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.5721+1320G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622942 | |||||||
chr19:49622944 | G | A | 1 | a0001c0002t0002g0044 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.5721+1322G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622944 | |||||||
chr19:49622944 | GAGAGAGA others(7): Show |
G | 3 | a0001c0003t0001g0111 a0005c0013t0005g0083 a0005c0013t0005g0084 |
3 | HG02809.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.5721+1336_5721+134 others(18): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622944 | ||||||
chr19:49622946 | GAGAGAGA others(5): Show |
G | 11 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0270 others(8): Show |
11 | HG00733.hp2 HG00735.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.5721+1336_5721+134 others(16): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622946 | ||||||
chr19:49622948 | GAGAGAGA others(3): Show |
G | 7 | a0001c0002t0006g0130 a0001c0002t0006g0131 a0001c0003t0001g0100 others(4): Show |
7 | HG02615.hp1 HG02970.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.5721+1336_5721+134 others(14): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622948 | ||||||
chr19:49622950 | GAGAGAGA others(1): Show |
G | 25 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0266 others(22): Show |
25 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.5721+1336_5721+134 others(12): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622950 | ||||||
chr19:49622952 | GAGAGAA | G | 16 | a0001c0001t0001g0295 a0001c0002t0001g0087 a0001c0002t0001g0121 others(13): Show |
16 | HG00544.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.5721+1336_5721+134 others(10): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622952 | ||||||
chr19:49622954 | GAGAA | G | 21 | a0001c0001t0001g0155 a0001c0001t0001g0252 a0001c0002t0001g0054 others(18): Show |
22 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.5721+1336_5721+133 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622954 | ||||||
chr19:49622956 | G | A | 1 | a0002c0015t0001g0032 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5721+1334G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622956 | |||||||
chr19:49622956 | GAA | G | 12 | a0001c0001t0001g0150 a0001c0002t0001g0133 a0001c0002t0002g0166 others(9): Show |
12 | HG00642.hp1 HG01943.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.5721+1336_5721+133 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622956 | ||||||
chr19:49622958 | A | G | 55 | a0001c0001t0001g0144 a0001c0001t0001g0237 a0001c0002t0001g0021 others(52): Show |
55 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.5721+1336A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622958 | |||||||
chr19:49622974 | G | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0264 a0001c0001t0001g0284 |
3 | HG01106.hp1 HG02602.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.5721+1352G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622974 | |||||||
chr19:49623201 | A | G | 1 | a0002c0004t0004g0036 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5721+1579A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623201 | |||||||
chr19:49623265 | A | G | 3 | a0001c0016t0001g0136 a0001c0016t0001g0137 a0007c0025t0001g0020 |
3 | HG02109.hp2 HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5722-1579A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623265 | |||||||
chr19:49623278 | G | T | 1 | a0001c0003t0001g0092 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5722-1566G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623278 | |||||||
chr19:49623314 | T | C | 18 | a0001c0001t0001g0252 a0001c0003t0001g0004 a0001c0003t0001g0094 others(15): Show |
19 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.5722-1530T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623314 | |||||||
chr19:49623319 | C | T | 1 | a0001c0031t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5722-1525C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623319 | |||||||
chr19:49623328 | G | A | 1 | a0001c0044t0001g0206 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.5722-1516G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623328 | |||||||
chr19:49623423 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5722-1421A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623423 | |||||||
chr19:49623488 | C | T | 1 | a0003c0005t0001g0220 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.5722-1356C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623488 | |||||||
chr19:49623494 | T | C | 1 | a0001c0003t0001g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5722-1350T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623494 | |||||||
chr19:49623573 | A | G | 123 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(120): Show |
124 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.5722-1271A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623573 | |||||||
chr19:49623619 | G | A | 2 | a0001c0016t0001g0136 a0001c0016t0001g0137 |
2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5722-1225G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623619 | |||||||
chr19:49623631 | T | TA | 6 | a0001c0001t0001g0201 a0001c0001t0001g0251 a0001c0002t0002g0044 others(3): Show |
6 | HG01884.hp1 HG02155.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.5722-1197dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623631 | ||||||
chr19:49623631 | TA | T | 9 | a0001c0001t0001g0151 a0001c0001t0001g0204 a0001c0001t0001g0235 others(6): Show |
9 | HG00738.hp1 HG01081.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.5722-1197delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623631 | ||||||
chr19:49623729 | ATAGATGG others(59): Show |
A | 4 | a0001c0001t0001g0144 a0001c0002t0001g0045 a0001c0002t0001g0046 others(1): Show |
4 | HG01109.hp1 HG01433.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.5722-1095_5722-103 others(70): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623729 | ||||||
chr19:49623799 | A | ATGGTTAG others(125): Show |
12 | a0001c0002t0001g0003 a0001c0002t0001g0078 a0001c0002t0001g0085 others(9): Show |
12 | HG00733.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.5722-1016_5722-885 others(135): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623799 | ||||||
chr19:49623799 | ATGGTTAG others(59): Show |
A | 17 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(14): Show |
17 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.5722-950_5722-885d others(68): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623799 | ||||||
chr19:49623815 | T | C | 2 | a0001c0002t0001g0054 a0002c0034t0001g0030 |
2 | HG01192.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.5722-1029T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623815 | |||||||
chr19:49623832 | C | CTGGTTAG others(493): Show |
1 | a0007c0025t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5722-951_5722-950i others(502): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623832 | ||||||
chr19:49623898 | C | CTGGTTAG others(26): Show |
1 | a0001c0021t0001g0043 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5722-915_5722-883d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623898 | ||||||
chr19:49623934 | G | T | 5 | a0001c0006t0001g0024 a0001c0006t0001g0025 a0001c0006t0001g0026 others(2): Show |
5 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5722-910G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623934 | |||||||
chr19:49623947 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5722-897T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623947 | |||||||
chr19:49623957 | G | A | 1 | a0003c0005t0001g0202 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.5722-887G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623957 | |||||||
chr19:49623981 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.5722-863A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623981 | |||||||
chr19:49623995 | G | A | 140 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.5722-849G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623995 | |||||||
chr19:49624080 | A | G | 26 | a0001c0001t0001g0237 a0001c0002t0001g0040 a0001c0002t0001g0075 others(23): Show |
26 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.5722-764A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624080 | |||||||
chr19:49624136 | G | C | 1 | a0018c0038t0001g0279 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.5722-708G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624136 | |||||||
chr19:49624229 | GTAGGTGG others(26): Show |
G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0268 |
2 | HG02683.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.5722-595_5722-563d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624229 | ||||||
chr19:49624262 | A | ATAGGTGG others(26): Show |
1 | a0001c0001t0001g0250 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5722-565_5722-533d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624262 | ||||||
chr19:49624279 | GGCTGAGA others(26): Show |
G | 3 | a0001c0002t0001g0133 a0001c0002t0001g0134 a0001c0002t0001g0135 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5722-516_5722-484d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624279 | ||||||
chr19:49624312 | T | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(303): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.5722-532T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624312 | |||||||
chr19:49624317 | A | G | 3 | a0001c0002t0008g0117 a0001c0002t0008g0118 a0001c0002t0008g0119 |
3 | HG01884.hp1 HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.5722-527A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624317 | |||||||
chr19:49624328 | G | GTGGGTGG others(295): Show |
3 | a0001c0002t0008g0117 a0001c0002t0008g0118 a0001c0002t0008g0119 |
3 | HG01884.hp1 HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.5722-515_5722-514i others(304): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624328 | ||||||
chr19:49624328 | GTAGGTGG others(26): Show |
G | 1 | a0001c0001t0001g0229 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5722-499_5722-467d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624328 | ||||||
chr19:49624345 | T | G | 3 | a0001c0002t0001g0133 a0001c0002t0001g0134 a0001c0002t0001g0135 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5722-499T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624345 | |||||||
chr19:49624413 | C | T | 123 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(120): Show |
124 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.5722-431C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624413 | |||||||
chr19:49624416 | A | AGAATTCT others(26): Show |
1 | a0001c0001t0001g0294 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.5722-401_5722-400i others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624416 | ||||||
chr19:49624416 | A | AGAATTCT others(59): Show |
2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | NA18969.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.5722-400_5722-335d others(68): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624416 | ||||||
chr19:49624450 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5722-394A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624450 | |||||||
chr19:49624455 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5722-389T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624455 | |||||||
chr19:49624460 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5722-384G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624460 | |||||||
chr19:49624466 | G | GGTTAGGA others(26): Show |
1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5722-363_5722-362i others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624466 | ||||||
chr19:49624493 | G | A | 1 | a0001c0003t0001g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5722-351G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624493 | |||||||
chr19:49624497 | GTGGTTAG others(26): Show |
G | 3 | a0001c0003t0001g0092 a0001c0003t0001g0093 a0001c0003t0002g0143 |
3 | HG02145.hp2 HG02896.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.5722-329_5722-297d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624497 | ||||||
chr19:49624508 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5722-336G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624508 | |||||||
chr19:49624531 | T | C | 1 | a0023c0022t0001g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5722-313T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624531 | |||||||
chr19:49624559 | ATAGATGG others(26): Show |
A | 1 | a0001c0049t0001g0271 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.5722-247_5722-215d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624559 | ||||||
chr19:49624710 | C | G | 1 | a0001c0002t0008g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5722-134C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624710 | |||||||
chr19:49624795 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5722-49G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624795 | |||||||
chr19:49624814 | G | T | 17 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(14): Show |
17 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.5722-30G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624814 | |||||||
chr19:49624815 | C | T | 17 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(14): Show |
17 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.5722-29C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624815 | |||||||
chr19:49624820 | A | G | 15 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0002t0001g0021 others(12): Show |
15 | HG01109.hp1 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5722-24A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624820 | |||||||
chr19:49625086 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.5869-19C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 12/13 | chr19 | 49625086 | |||||||
chr19:49625265 | T | C | 17 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(14): Show |
17 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.5964+65T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 13/13 | chr19 | 49625265 | |||||||
chr19:49625286 | A | G | 140 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.5964+86A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 13/13 | chr19 | 49625286 | |||||||
chr19:49625393 | GCCCCAGC others(33): Show |
G | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5965-61_5965-22del others(40): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 49625393 | ||||||
chr19:49625441 | G | GC | 5 | a0001c0009t0002g0138 a0001c0009t0002g0139 a0001c0009t0002g0140 others(2): Show |
5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5965-18dupC | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 49625441 |