Item | Value |
---|---|
geneid | 729359 |
ensemblid | ENSG00000167676.5 |
hgncid | 29393 |
symbol | PLIN4 |
name | perilipin 4 |
refseq_nuc | NM_001367868.2 |
refseq_prot | NP_001354797.1 |
ensembl_nuc | ENST00000301286.5 |
ensembl_prot | ENSP00000301286.4 |
mane_status | MANE Select |
chr | chr19 |
start | 4502192 |
end | 4518486 |
strand | - |
ver | v1.2 |
region | chr19:4502192-4518486 |
region5000 | chr19:4497192-4523486 |
regionname0 | PLIN4_chr19_4502192_4518486 |
regionname5000 | PLIN4_chr19_4497192_4523486 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1437 | 277 | 27 | 55 | 149 | 13 | 33 | 107 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1432): Show |
chr19 | 4497192 | 4523486 |
a0002 | 0/0 | 1206 | 19 | 12 | 6 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1201): Show |
chr19 | 4497192 | 4523486 |
a0003 | 0/0 | 1371 | 12 | 4 | 5 | 2 | 0 | 1 | 2 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0004 | 0/0 | 1371 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0005 | 0/0 | 1371 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0006 | 0/0 | 1437 | 7 | 0 | 4 | 1 | 0 | 2 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1432): Show |
chr19 | 4497192 | 4523486 |
a0007 | 0/0 | 1437 | 7 | 0 | 3 | 1 | 2 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1432): Show |
chr19 | 4497192 | 4523486 |
a0008 | 0/0 | 1371 | 6 | 4 | 1 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0009 | 0/0 | 1371 | 5 | 0 | 1 | 3 | 0 | 1 | 2 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0010 | 0/0 | 1184 | 5 | 1 | 1 | 2 | 0 | 1 | 2 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1179): Show |
chr19 | 4497192 | 4523486 |
a0011 | 0/0 | 1206 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1201): Show |
chr19 | 4497192 | 4523486 |
a0012 | 0/0 | 1371 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0013 | 0/0 | 953 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(948): Show |
chr19 | 4497192 | 4523486 |
a0014 | 0/0 | 1272 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1267): Show |
chr19 | 4497192 | 4523486 |
a0015 | 0/0 | 1272 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1267): Show |
chr19 | 4497192 | 4523486 |
a0016 | 0/0 | 1470 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1465): Show |
chr19 | 4497192 | 4523486 |
a0017 | 0/0 | 1371 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0018 | 0/0 | 1404 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1399): Show |
chr19 | 4497192 | 4523486 |
a0019 | 0/0 | 1239 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1234): Show |
chr19 | 4497192 | 4523486 |
a0020 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1432): Show |
chr19 | 4497192 | 4523486 |
a0021 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1498): Show |
chr19 | 4497192 | 4523486 |
a0022 | 1/0 | 1371 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0023 | 0/0 | 1371 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0024 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1432): Show |
chr19 | 4497192 | 4523486 |
a0025 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1432): Show |
chr19 | 4497192 | 4523486 |
a0026 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1465): Show |
chr19 | 4497192 | 4523486 |
a0027 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1432): Show |
chr19 | 4497192 | 4523486 |
a0028 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0029 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0030 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0031 | 0/0 | 1118 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1113): Show |
chr19 | 4497192 | 4523486 |
a0032 | 0/0 | 1470 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1465): Show |
chr19 | 4497192 | 4523486 |
a0033 | 0/0 | 1074 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1069): Show |
chr19 | 4497192 | 4523486 |
a0034 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0035 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0036 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0037 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0038 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1135): Show |
chr19 | 4497192 | 4523486 |
a0039 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1432): Show |
chr19 | 4497192 | 4523486 |
a0040 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0041 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0042 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0043 | 0/0 | 1118 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1113): Show |
chr19 | 4497192 | 4523486 |
a0044 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0045 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0046 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1366): Show |
chr19 | 4497192 | 4523486 |
a0047 | 0/0 | 1206 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1201): Show |
chr19 | 4497192 | 4523486 |
a0048 | 0/1 | 1437 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | MSAPD others(1432): Show |
chr19 | 4497192 | 4523486 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4311 | 120 | 4 | 22 | 81 | 4 | 9 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0002 | 0/0 | 4311 | 57 | 4 | 16 | 31 | 3 | 3 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0003 | 0/0 | 4311 | 18 | 2 | 1 | 7 | 3 | 5 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0004 | 0/0 | 4311 | 16 | 1 | 6 | 3 | 1 | 5 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0006 | 0/0 | 4311 | 9 | 1 | 1 | 2 | 1 | 4 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0007 | 0/0 | 4311 | 9 | 0 | 0 | 5 | 0 | 4 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0011 | 0/0 | 4311 | 5 | 0 | 0 | 5 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0012 | 0/0 | 4311 | 5 | 0 | 0 | 5 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0013 | 0/0 | 4311 | 5 | 5 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0016 | 0/0 | 4311 | 4 | 0 | 1 | 3 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0017 | 0/0 | 4311 | 4 | 4 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0022 | 0/0 | 4311 | 3 | 0 | 0 | 3 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0025 | 0/0 | 4311 | 3 | 0 | 3 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0033 | 0/0 | 4311 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0040 | 0/0 | 4311 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0044 | 0/0 | 4311 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0063 | 0/0 | 4311 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0064 | 0/0 | 4311 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0065 | 0/0 | 4311 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0066 | 0/0 | 4311 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0068 | 0/0 | 4311 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0069 | 0/0 | 4311 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0070 | 0/0 | 4311 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0071 | 0/0 | 4311 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0072 | 0/0 | 4311 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0073 | 0/0 | 4311 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0078 | 0/0 | 4311 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0080 | 0/0 | 4311 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0088 | 0/0 | 4311 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0090 | 0/0 | 4311 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0001c0100 | 0/0 | 4311 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0002c0005 | 0/0 | 3618 | 9 | 9 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3613): Show |
chr19 | 4497192 | 4523486 | ||
a0002c0010 | 0/0 | 3618 | 6 | 0 | 6 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3613): Show |
chr19 | 4497192 | 4523486 | ||
a0002c0049 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3613): Show |
chr19 | 4497192 | 4523486 | ||
a0002c0050 | 0/0 | 3618 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3613): Show |
chr19 | 4497192 | 4523486 | ||
a0002c0054 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3613): Show |
chr19 | 4497192 | 4523486 | ||
a0002c0055 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3613): Show |
chr19 | 4497192 | 4523486 | ||
a0003c0008 | 0/0 | 4113 | 7 | 3 | 1 | 2 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0003c0023 | 0/0 | 4113 | 3 | 0 | 3 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0003c0067 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0003c0075 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0004c0009 | 0/0 | 4113 | 6 | 6 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0004c0026 | 0/0 | 4113 | 3 | 2 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0004c0041 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0005c0019 | 0/0 | 4113 | 4 | 4 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0005c0032 | 0/0 | 4113 | 2 | 1 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0005c0076 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0006c0037 | 0/0 | 4311 | 2 | 0 | 0 | 0 | 0 | 2 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0006c0092 | 0/0 | 4311 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0006c0093 | 0/0 | 4311 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0006c0094 | 0/0 | 4311 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0006c0095 | 0/0 | 4311 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0006c0096 | 0/0 | 4311 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0007c0018 | 0/0 | 4311 | 4 | 0 | 3 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0007c0036 | 0/0 | 4311 | 2 | 0 | 0 | 0 | 2 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0007c0086 | 0/0 | 4311 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0008c0027 | 0/0 | 4113 | 3 | 3 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0008c0034 | 0/0 | 4113 | 2 | 0 | 1 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0008c0079 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0009c0014 | 0/0 | 4113 | 5 | 0 | 1 | 3 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0010c0024 | 0/0 | 4312 | 3 | 1 | 0 | 2 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4307): Show |
chr19 | 4497192 | 4523486 | ||
a0010c0031 | 0/0 | 4312 | 2 | 0 | 1 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4307): Show |
chr19 | 4497192 | 4523486 | ||
a0011c0021 | 0/0 | 3618 | 3 | 3 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3613): Show |
chr19 | 4497192 | 4523486 | ||
a0011c0030 | 0/0 | 3618 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3613): Show |
chr19 | 4497192 | 4523486 | ||
a0012c0015 | 0/0 | 4113 | 4 | 0 | 0 | 4 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0013c0046 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3614): Show |
chr19 | 4497192 | 4523486 | ||
a0013c0048 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3614): Show |
chr19 | 4497192 | 4523486 | ||
a0013c0053 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3614): Show |
chr19 | 4497192 | 4523486 | ||
a0014c0020 | 0/0 | 3816 | 3 | 3 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3811): Show |
chr19 | 4497192 | 4523486 | ||
a0015c0029 | 0/0 | 3816 | 2 | 1 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3811): Show |
chr19 | 4497192 | 4523486 | ||
a0015c0047 | 0/0 | 3816 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3811): Show |
chr19 | 4497192 | 4523486 | ||
a0016c0043 | 0/0 | 4410 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4405): Show |
chr19 | 4497192 | 4523486 | ||
a0016c0084 | 0/0 | 4410 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4405): Show |
chr19 | 4497192 | 4523486 | ||
a0017c0039 | 0/0 | 4113 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0018c0038 | 0/0 | 4212 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4207): Show |
chr19 | 4497192 | 4523486 | ||
a0019c0077 | 0/0 | 3717 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3712): Show |
chr19 | 4497192 | 4523486 | ||
a0019c0081 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3712): Show |
chr19 | 4497192 | 4523486 | ||
a0020c0028 | 0/0 | 4311 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0021c0035 | 0/0 | 4509 | 2 | 0 | 0 | 2 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4504): Show |
chr19 | 4497192 | 4523486 | ||
a0022c0097 | 1/0 | 4113 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0023c0074 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0024c0091 | 0/0 | 4311 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0025c0099 | 0/0 | 4311 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0026c0083 | 0/0 | 4410 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4405): Show |
chr19 | 4497192 | 4523486 | ||
a0027c0059 | 0/0 | 4311 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0028c0057 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0029c0089 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0030c0045 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0031c0104 | 0/0 | 4114 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4109): Show |
chr19 | 4497192 | 4523486 | ||
a0032c0056 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4405): Show |
chr19 | 4497192 | 4523486 | ||
a0033c0052 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3217): Show |
chr19 | 4497192 | 4523486 | ||
a0034c0058 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0035c0042 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0036c0061 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0037c0060 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0038c0051 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3415): Show |
chr19 | 4497192 | 4523486 | ||
a0039c0098 | 0/0 | 4311 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 | ||
a0040c0105 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0041c0103 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0042c0101 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0043c0062 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4109): Show |
chr19 | 4497192 | 4523486 | ||
a0044c0087 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0045c0102 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0046c0106 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4108): Show |
chr19 | 4497192 | 4523486 | ||
a0047c0085 | 0/0 | 3618 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(3613): Show |
chr19 | 4497192 | 4523486 | ||
a0048c0082 | 0/1 | 4311 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | ATGTC others(4306): Show |
chr19 | 4497192 | 4523486 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0001t0002 | 0/0 | 6700 | 62 | 1 | 16 | 39 | 3 | 3 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0001t0003 | 0/0 | 6700 | 36 | 0 | 3 | 32 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0001t0004 | 0/0 | 6700 | 7 | 3 | 1 | 1 | 0 | 2 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0001t0005 | 0/0 | 6700 | 9 | 0 | 0 | 6 | 0 | 3 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0001t0010 | 0/0 | 6700 | 3 | 0 | 2 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0001t0021 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0001t0022 | 0/0 | 6700 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0002t0001 | 0/0 | 6700 | 50 | 3 | 16 | 26 | 2 | 3 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0002t0003 | 0/0 | 6700 | 4 | 0 | 0 | 4 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0002t0004 | 0/0 | 6700 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0002t0015 | 0/0 | 6700 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0002t0032 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0003t0003 | 0/0 | 6700 | 5 | 0 | 0 | 3 | 0 | 2 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0003t0004 | 0/0 | 6700 | 13 | 2 | 1 | 4 | 3 | 3 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0004t0001 | 0/0 | 6700 | 13 | 0 | 5 | 3 | 1 | 4 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0004t0004 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0004t0011 | 0/0 | 6700 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0004t0016 | 0/0 | 6700 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0006t0001 | 0/0 | 6700 | 8 | 1 | 1 | 2 | 1 | 3 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0006t0002 | 0/0 | 6700 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0007t0003 | 0/0 | 6700 | 3 | 0 | 0 | 3 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0007t0004 | 0/0 | 6700 | 6 | 0 | 0 | 2 | 0 | 4 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0011t0003 | 0/0 | 6700 | 5 | 0 | 0 | 5 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0012t0003 | 0/0 | 6700 | 5 | 0 | 0 | 5 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0013t0004 | 0/0 | 6700 | 4 | 4 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0013t0028 | 0/0 | 6700 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0016t0002 | 0/0 | 6700 | 2 | 0 | 0 | 2 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0016t0003 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0016t0004 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0017t0001 | 0/0 | 6700 | 4 | 4 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0022t0001 | 0/0 | 6700 | 3 | 0 | 0 | 3 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0025t0002 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0025t0003 | 0/0 | 6700 | 2 | 0 | 2 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0033t0004 | 0/0 | 6700 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0040t0004 | 0/0 | 6700 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0044t0011 | 0/0 | 6700 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0063t0002 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0064t0002 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0065t0004 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0066t0003 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0068t0001 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0069t0004 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0070t0001 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0071t0001 | 0/0 | 6700 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0072t0001 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0073t0001 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0078t0004 | 0/0 | 6700 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0080t0003 | 0/0 | 6700 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0088t0004 | 0/0 | 6700 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0090t0004 | 0/0 | 6700 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0001c0100t0003 | 0/0 | 6700 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0002c0005t0004 | 0/0 | 6007 | 9 | 9 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6002): Show |
chr19 | 4497192 | 4523486 |
a0002c0010t0001 | 0/0 | 6007 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6002): Show |
chr19 | 4497192 | 4523486 |
a0002c0010t0007 | 0/0 | 6011 | 3 | 0 | 3 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6006): Show |
chr19 | 4497192 | 4523486 |
a0002c0010t0014 | 0/0 | 6011 | 2 | 0 | 2 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6006): Show |
chr19 | 4497192 | 4523486 |
a0002c0049t0033 | 0/0 | 5995 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(5990): Show |
chr19 | 4497192 | 4523486 |
a0002c0050t0007 | 0/0 | 6011 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6006): Show |
chr19 | 4497192 | 4523486 |
a0002c0054t0001 | 0/0 | 6007 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6002): Show |
chr19 | 4497192 | 4523486 |
a0002c0055t0004 | 0/0 | 6007 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6002): Show |
chr19 | 4497192 | 4523486 |
a0003c0008t0001 | 0/0 | 6502 | 3 | 1 | 1 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0003c0008t0003 | 0/0 | 6502 | 3 | 1 | 0 | 1 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0003c0008t0025 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0003c0023t0001 | 0/0 | 6502 | 3 | 0 | 3 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0003c0067t0001 | 0/0 | 6502 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0003c0075t0004 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0004c0009t0001 | 0/0 | 6502 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0004c0009t0004 | 0/0 | 6502 | 3 | 3 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0004c0009t0023 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0004c0026t0001 | 0/0 | 6502 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0004c0026t0004 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0004c0026t0034 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0004c0041t0026 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0005c0019t0006 | 0/0 | 6502 | 4 | 4 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0005c0032t0006 | 0/0 | 6502 | 2 | 1 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0005c0076t0031 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0006c0037t0003 | 0/0 | 6700 | 2 | 0 | 0 | 0 | 0 | 2 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0006c0092t0004 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0006c0093t0001 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0006c0094t0004 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0006c0095t0004 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0006c0096t0004 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0007c0018t0001 | 0/0 | 6700 | 4 | 0 | 3 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0007c0036t0004 | 0/0 | 6700 | 2 | 0 | 0 | 0 | 2 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0007c0086t0003 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0008c0027t0009 | 0/0 | 6502 | 3 | 3 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0008c0034t0009 | 0/0 | 6502 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0008c0034t0029 | 0/0 | 6502 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0008c0079t0009 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0009c0014t0001 | 0/0 | 6502 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0009c0014t0003 | 0/0 | 6502 | 4 | 0 | 1 | 2 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0010c0024t0001 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6696): Show |
chr19 | 4497192 | 4523486 |
a0010c0024t0003 | 0/0 | 6701 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6696): Show |
chr19 | 4497192 | 4523486 |
a0010c0024t0015 | 0/0 | 6701 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6696): Show |
chr19 | 4497192 | 4523486 |
a0010c0031t0002 | 0/0 | 6701 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6696): Show |
chr19 | 4497192 | 4523486 |
a0010c0031t0003 | 0/0 | 6701 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6696): Show |
chr19 | 4497192 | 4523486 |
a0011c0021t0004 | 0/0 | 6007 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6002): Show |
chr19 | 4497192 | 4523486 |
a0011c0021t0008 | 0/0 | 6007 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6002): Show |
chr19 | 4497192 | 4523486 |
a0011c0030t0002 | 0/0 | 6007 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6002): Show |
chr19 | 4497192 | 4523486 |
a0012c0015t0002 | 0/0 | 6502 | 4 | 0 | 0 | 4 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0013c0046t0008 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6003): Show |
chr19 | 4497192 | 4523486 |
a0013c0048t0035 | 0/0 | 5996 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(5991): Show |
chr19 | 4497192 | 4523486 |
a0013c0053t0004 | 0/0 | 6008 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6003): Show |
chr19 | 4497192 | 4523486 |
a0014c0020t0008 | 0/0 | 6205 | 3 | 3 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6200): Show |
chr19 | 4497192 | 4523486 |
a0015c0029t0011 | 0/0 | 6205 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6200): Show |
chr19 | 4497192 | 4523486 |
a0015c0029t0024 | 0/0 | 6205 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6200): Show |
chr19 | 4497192 | 4523486 |
a0015c0047t0004 | 0/0 | 6205 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6200): Show |
chr19 | 4497192 | 4523486 |
a0016c0043t0001 | 0/0 | 6799 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6794): Show |
chr19 | 4497192 | 4523486 |
a0016c0084t0002 | 0/0 | 6799 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6794): Show |
chr19 | 4497192 | 4523486 |
a0017c0039t0001 | 0/0 | 6502 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0018c0038t0013 | 0/0 | 6601 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6596): Show |
chr19 | 4497192 | 4523486 |
a0019c0077t0001 | 0/0 | 6106 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6101): Show |
chr19 | 4497192 | 4523486 |
a0019c0081t0004 | 0/0 | 6106 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6101): Show |
chr19 | 4497192 | 4523486 |
a0020c0028t0004 | 0/0 | 6700 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0021c0035t0002 | 0/0 | 6898 | 2 | 0 | 0 | 2 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6893): Show |
chr19 | 4497192 | 4523486 |
a0022c0097t0003 | 1/0 | 6502 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0023c0074t0020 | 0/0 | 6502 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0024c0091t0001 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0025c0099t0002 | 0/0 | 6700 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0026c0083t0002 | 0/0 | 6799 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6794): Show |
chr19 | 4497192 | 4523486 |
a0027c0059t0001 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0028c0057t0018 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0029c0089t0017 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0030c0045t0004 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0031c0104t0001 | 0/0 | 6503 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6498): Show |
chr19 | 4497192 | 4523486 |
a0032c0056t0001 | 0/0 | 6799 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6794): Show |
chr19 | 4497192 | 4523486 |
a0033c0052t0027 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(5606): Show |
chr19 | 4497192 | 4523486 |
a0034c0058t0019 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0035c0042t0001 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0036c0061t0001 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0037c0060t0004 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0038c0051t0004 | 0/0 | 5809 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(5804): Show |
chr19 | 4497192 | 4523486 |
a0039c0098t0003 | 0/0 | 6700 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
a0040c0105t0030 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0041c0103t0012 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0042c0101t0004 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0043c0062t0002 | 0/0 | 6503 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6498): Show |
chr19 | 4497192 | 4523486 |
a0044c0087t0001 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0045c0102t0012 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0046c0106t0001 | 0/0 | 6502 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6497): Show |
chr19 | 4497192 | 4523486 |
a0047c0085t0007 | 0/0 | 6011 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6006): Show |
chr19 | 4497192 | 4523486 |
a0048c0082t0002 | 0/1 | 6700 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | AGCTG others(6695): Show |
chr19 | 4497192 | 4523486 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0001 | 0/0 | 20 | 0 | 6 | 9 | 3 | 2 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0004 | 0/0 | 8 | 0 | 2 | 5 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0002 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0010 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0004g0026 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0005g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0010g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0010g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0021g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0001t0022g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0003 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0011 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0017 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0003g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0015g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0002t0032g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0003g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0004g0018 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0003t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0004t0001g0006 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0004t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0004t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0004t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0004t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0004t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0004t0016g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0006t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0006t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0006t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0006t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0006t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0006t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0007t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0007t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0007t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0007t0004g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0007t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0007t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0007t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0011t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0011t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0011t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0011t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0011t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0012t0003g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0012t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0013t0004g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0013t0028g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0016t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0016t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0016t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0016t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0017t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0017t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0017t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0022t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0022t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0025t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0025t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0025t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0033t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0040t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0044t0011g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0063t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0064t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0065t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0066t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0068t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0069t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0070t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0071t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0072t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0073t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0078t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0080t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0088t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0090t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0001c0100t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0005t0004g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0005t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0005t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0005t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0010t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0010t0007g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0010t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0010t0007g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0010t0014g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0010t0014g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0049t0033g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0050t0007g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0054t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0002c0055t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0003c0008t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0003c0008t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0003c0008t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0003c0008t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0003c0008t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0003c0008t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0003c0008t0025g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0003c0023t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0003c0067t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0003c0075t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0004c0009t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0004c0009t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0004c0009t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0004c0009t0023g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0004c0026t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0004c0026t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0004c0026t0034g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0004c0041t0026g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0005c0019t0006g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0005c0019t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0005c0032t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0005c0032t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0005c0076t0031g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0006c0037t0003g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0006c0092t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0006c0093t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0006c0094t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0006c0095t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0006c0096t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0007c0018t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0007c0018t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0007c0018t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0007c0036t0004g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0007c0036t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0007c0086t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0008c0027t0009g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0008c0027t0009g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0008c0034t0009g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0008c0034t0029g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0008c0079t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0009c0014t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0009c0014t0003g0025 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0009c0014t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0010c0024t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0010c0024t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0010c0024t0015g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0010c0031t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0010c0031t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0011c0021t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0011c0021t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0011c0030t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0011c0030t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0012c0015t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0012c0015t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0012c0015t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0012c0015t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0013c0046t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0013c0048t0035g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0013c0053t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0014c0020t0008g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0015c0029t0011g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0015c0029t0024g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0015c0047t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0016c0043t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0016c0084t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0017c0039t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0017c0039t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0018c0038t0013g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0018c0038t0013g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0019c0077t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0019c0081t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0020c0028t0004g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0021c0035t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0021c0035t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0022c0097t0003g0258 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0023c0074t0020g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0024c0091t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0025c0099t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0026c0083t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0027c0059t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0028c0057t0018g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0029c0089t0017g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0030c0045t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0031c0104t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0032c0056t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0033c0052t0027g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0034c0058t0019g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0035c0042t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0036c0061t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0037c0060t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0038c0051t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0039c0098t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0040c0105t0030g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0041c0103t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0042c0101t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0043c0062t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0044c0087t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0045c0102t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0046c0106t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0047c0085t0007g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
a0048c0082t0002g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0078 | t0004 | g0142 | EUR | GBR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0154 | EUR | GBR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00140 | hp2 | a0001 | c0003 | t0004 | g0145 | EUR | GBR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00280 | hp1 | a0001 | c0006 | t0001 | g0034 | EUR | FIN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00280 | hp2 | a0001 | c0003 | t0004 | g0018 | EUR | FIN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00323 | hp1 | a0001 | c0001 | t0022 | g0152 | EUR | FIN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0219 | EUR | FIN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00438 | hp1 | a0001 | c0001 | t0010 | g0176 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00558 | hp1 | a0009 | c0014 | t0003 | g0025 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00609 | hp1 | a0001 | c0003 | t0004 | g0077 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00621 | hp2 | a0001 | c0006 | t0001 | g0155 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00639 | hp2 | a0008 | c0034 | t0009 | g0109 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00673 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00735 | hp1 | a0002 | c0010 | t0001 | g0088 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00735 | hp2 | a0023 | c0074 | t0020 | g0096 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00738 | hp1 | a0001 | c0004 | t0001 | g0039 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00741 | hp1 | a0001 | c0004 | t0004 | g0144 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01069 | hp1 | a0001 | c0064 | t0002 | g0170 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01069 | hp2 | a0001 | c0004 | t0001 | g0006 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01070 | hp2 | a0002 | c0010 | t0014 | g0089 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01071 | hp1 | a0001 | c0004 | t0001 | g0006 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01071 | hp2 | a0002 | c0010 | t0014 | g0090 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01074 | hp2 | a0002 | c0010 | t0007 | g0092 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01099 | hp2 | a0002 | c0010 | t0007 | g0091 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01109 | hp1 | a0005 | c0032 | t0006 | g0100 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01167 | hp1 | a0006 | c0094 | t0004 | g0251 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0214 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01175 | hp2 | a0002 | c0010 | t0007 | g0093 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01192 | hp1 | a0009 | c0014 | t0003 | g0025 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01192 | hp2 | a0010 | c0031 | t0002 | g0164 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01243 | hp1 | a0004 | c0026 | t0001 | g0104 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01255 | hp1 | a0001 | c0016 | t0004 | g0139 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01255 | hp2 | a0006 | c0096 | t0004 | g0243 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01256 | hp2 | a0001 | c0001 | t0010 | g0043 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01257 | hp2 | a0003 | c0023 | t0001 | g0020 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01258 | hp1 | a0001 | c0001 | t0010 | g0043 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01258 | hp2 | a0003 | c0023 | t0001 | g0020 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01261 | hp1 | a0001 | c0069 | t0004 | g0216 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01261 | hp2 | a0003 | c0023 | t0001 | g0020 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01346 | hp1 | a0001 | c0073 | t0001 | g0226 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01346 | hp2 | a0007 | c0018 | t0001 | g0050 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01358 | hp2 | a0001 | c0004 | t0001 | g0038 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01361 | hp1 | a0007 | c0018 | t0001 | g0237 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01433 | hp2 | a0001 | c0006 | t0001 | g0035 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01496 | hp1 | a0016 | c0043 | t0001 | g0076 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01496 | hp2 | a0007 | c0018 | t0001 | g0050 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01515 | hp1 | a0001 | c0004 | t0001 | g0038 | EUR | IBS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01515 | hp2 | a0007 | c0036 | t0004 | g0239 | EUR | IBS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01517 | hp1 | a0007 | c0036 | t0004 | g0240 | EUR | IBS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01884 | hp1 | a0017 | c0039 | t0001 | g0281 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01884 | hp2 | a0005 | c0019 | t0006 | g0016 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01891 | hp1 | a0013 | c0048 | t0035 | g0082 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01891 | hp2 | a0001 | c0013 | t0004 | g0014 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01934 | hp1 | a0001 | c0004 | t0001 | g0006 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01934 | hp2 | a0006 | c0092 | t0004 | g0250 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01943 | hp1 | a0001 | c0025 | t0003 | g0112 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01952 | hp2 | a0001 | c0066 | t0003 | g0197 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01975 | hp2 | a0024 | c0091 | t0001 | g0150 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01978 | hp2 | a0003 | c0067 | t0001 | g0130 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01993 | hp1 | a0001 | c0025 | t0003 | g0203 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02004 | hp1 | a0001 | c0025 | t0002 | g0204 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02004 | hp2 | a0025 | c0099 | t0002 | g0241 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02027 | hp1 | a0001 | c0016 | t0002 | g0225 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02055 | hp1 | a0013 | c0046 | t0008 | g0064 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02055 | hp2 | a0013 | c0053 | t0004 | g0086 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0173 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02071 | hp2 | a0007 | c0086 | t0003 | g0236 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02074 | hp1 | a0026 | c0083 | t0002 | g0148 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02080 | hp1 | a0001 | c0070 | t0001 | g0207 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02080 | hp2 | a0001 | c0007 | t0004 | g0192 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02083 | hp2 | a0027 | c0059 | t0001 | g0157 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02145 | hp1 | a0004 | c0026 | t0034 | g0105 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02145 | hp2 | a0003 | c0008 | t0025 | g0254 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02148 | hp2 | a0006 | c0093 | t0001 | g0242 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02155 | hp1 | a0001 | c0022 | t0001 | g0156 | EAS | CDX | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02155 | hp2 | a0001 | c0012 | t0003 | g0013 | EAS | CDX | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02165 | hp1 | a0001 | c0063 | t0002 | g0165 | EAS | CDX | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CDX | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02257 | hp1 | a0029 | c0089 | t0017 | g0263 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02257 | hp2 | a0002 | c0005 | t0004 | g0061 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02258 | hp1 | a0014 | c0020 | t0008 | g0015 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02258 | hp2 | a0010 | c0024 | t0015 | g0133 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0270 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02280 | hp2 | a0002 | c0005 | t0004 | g0005 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02293 | hp1 | a0003 | c0008 | t0001 | g0198 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02293 | hp2 | a0001 | c0072 | t0001 | g0138 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02300 | hp2 | a0001 | c0003 | t0004 | g0229 | AMR | PEL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02451 | hp1 | a0030 | c0045 | t0004 | g0280 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02451 | hp2 | a0001 | c0002 | t0015 | g0135 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02523 | hp1 | a0001 | c0011 | t0003 | g0189 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02523 | hp2 | a0001 | c0016 | t0003 | g0140 | EAS | KHV | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02572 | hp1 | a0011 | c0021 | t0004 | g0029 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02572 | hp2 | a0031 | c0104 | t0001 | g0074 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02602 | hp1 | a0001 | c0004 | t0001 | g0006 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02602 | hp2 | a0001 | c0004 | t0001 | g0039 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02615 | hp1 | a0004 | c0009 | t0023 | g0058 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02622 | hp1 | a0005 | c0019 | t0006 | g0016 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02622 | hp2 | a0001 | c0044 | t0011 | g0075 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02630 | hp1 | a0001 | c0017 | t0001 | g0102 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02630 | hp2 | a0002 | c0049 | t0033 | g0273 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02647 | hp1 | a0005 | c0076 | t0031 | g0278 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02647 | hp2 | a0011 | c0021 | t0004 | g0029 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02683 | hp1 | a0001 | c0007 | t0004 | g0022 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02683 | hp2 | a0001 | c0006 | t0001 | g0035 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02698 | hp1 | a0001 | c0003 | t0004 | g0018 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02717 | hp1 | a0001 | c0006 | t0001 | g0099 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02717 | hp2 | a0008 | c0079 | t0009 | g0106 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02723 | hp1 | a0002 | c0005 | t0004 | g0005 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02723 | hp2 | a0032 | c0056 | t0001 | g0094 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02738 | hp1 | a0009 | c0014 | t0003 | g0025 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02738 | hp2 | a0002 | c0050 | t0007 | g0084 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02809 | hp1 | a0008 | c0027 | t0009 | g0031 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02809 | hp2 | a0005 | c0019 | t0006 | g0016 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02818 | hp1 | a0033 | c0052 | t0027 | g0085 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02818 | hp2 | a0011 | c0030 | t0002 | g0068 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02886 | hp1 | a0034 | c0058 | t0019 | g0276 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02895 | hp1 | a0005 | c0019 | t0006 | g0070 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02895 | hp2 | a0001 | c0017 | t0001 | g0030 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02896 | hp1 | a0035 | c0042 | t0001 | g0060 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02896 | hp2 | a0001 | c0033 | t0004 | g0040 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02897 | hp1 | a0001 | c0017 | t0001 | g0030 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02897 | hp2 | a0001 | c0033 | t0004 | g0040 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02922 | hp1 | a0014 | c0020 | t0008 | g0015 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02922 | hp2 | a0015 | c0029 | t0011 | g0065 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02965 | hp2 | a0002 | c0005 | t0004 | g0005 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02970 | hp1 | a0003 | c0008 | t0003 | g0253 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02970 | hp2 | a0001 | c0013 | t0028 | g0261 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02976 | hp1 | a0036 | c0061 | t0001 | g0259 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02976 | hp2 | a0002 | c0005 | t0004 | g0005 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03041 | hp1 | a0008 | c0027 | t0009 | g0279 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03041 | hp2 | a0004 | c0026 | t0004 | g0103 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03098 | hp1 | a0037 | c0060 | t0004 | g0274 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03098 | hp2 | a0018 | c0038 | t0013 | g0266 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03130 | hp1 | a0019 | c0081 | t0004 | g0272 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03130 | hp2 | a0001 | c0004 | t0011 | g0107 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03139 | hp1 | a0002 | c0054 | t0001 | g0087 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03139 | hp2 | a0004 | c0009 | t0004 | g0028 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03195 | hp1 | a0011 | c0021 | t0008 | g0063 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03195 | hp2 | a0001 | c0003 | t0004 | g0115 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03209 | hp1 | a0018 | c0038 | t0013 | g0265 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03209 | hp2 | a0004 | c0009 | t0004 | g0028 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03225 | hp1 | a0011 | c0030 | t0002 | g0098 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03225 | hp2 | a0001 | c0013 | t0004 | g0014 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03239 | hp1 | a0001 | c0003 | t0004 | g0232 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03239 | hp2 | a0001 | c0071 | t0001 | g0136 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03453 | hp1 | a0001 | c0003 | t0004 | g0108 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03453 | hp2 | a0038 | c0051 | t0004 | g0066 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03486 | hp1 | a0004 | c0041 | t0026 | g0057 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03486 | hp2 | a0017 | c0039 | t0001 | g0282 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03490 | hp1 | a0007 | c0018 | t0001 | g0238 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03490 | hp2 | a0006 | c0037 | t0003 | g0053 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03492 | hp1 | a0006 | c0037 | t0003 | g0053 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03516 | hp1 | a0001 | c0040 | t0004 | g0056 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03516 | hp2 | a0020 | c0028 | t0004 | g0054 | AFR | ESN | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03540 | hp1 | a0002 | c0005 | t0004 | g0062 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03540 | hp2 | a0002 | c0005 | t0004 | g0067 | AFR | GWD | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03579 | hp1 | a0004 | c0009 | t0001 | g0027 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03579 | hp2 | a0001 | c0017 | t0001 | g0101 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0169 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03654 | hp2 | a0001 | c0006 | t0001 | g0128 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03669 | hp1 | a0001 | c0003 | t0003 | g0233 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03669 | hp2 | a0008 | c0034 | t0029 | g0110 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0026 | SAS | STU | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03688 | hp2 | a0001 | c0004 | t0001 | g0143 | SAS | STU | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0044 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03704 | hp2 | a0001 | c0080 | t0003 | g0147 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03710 | hp1 | a0001 | c0004 | t0001 | g0006 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03710 | hp2 | a0039 | c0098 | t0003 | g0252 | SAS | PJL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03831 | hp1 | a0001 | c0003 | t0003 | g0019 | SAS | BEB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | BEB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03834 | hp1 | a0001 | c0006 | t0001 | g0034 | SAS | BEB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0047 | SAS | BEB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0168 | SAS | BEB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03927 | hp2 | a0001 | c0003 | t0004 | g0230 | SAS | BEB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03942 | hp1 | a0001 | c0007 | t0004 | g0022 | SAS | BEB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03942 | hp2 | a0001 | c0006 | t0002 | g0186 | SAS | BEB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG04115 | hp1 | a0001 | c0007 | t0004 | g0022 | SAS | STU | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG04115 | hp2 | a0001 | c0004 | t0016 | g0055 | SAS | STU | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG04184 | hp1 | a0001 | c0100 | t0003 | g0151 | SAS | BEB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG04184 | hp2 | a0010 | c0031 | t0003 | g0163 | SAS | BEB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG04199 | hp1 | a0001 | c0001 | t0005 | g0179 | SAS | STU | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG04199 | hp2 | a0019 | c0077 | t0001 | g0141 | SAS | STU | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG04204 | hp2 | a0015 | c0029 | t0024 | g0083 | SAS | STU | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG04228 | hp1 | a0001 | c0007 | t0004 | g0193 | SAS | STU | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG04228 | hp2 | a0003 | c0008 | t0003 | g0132 | SAS | STU | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18522 | hp1 | a0008 | c0027 | t0009 | g0031 | AFR | YRI | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18522 | hp2 | a0020 | c0028 | t0004 | g0054 | AFR | YRI | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | CHB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18612 | hp2 | a0001 | c0012 | t0003 | g0227 | EAS | CHB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18747 | hp2 | a0001 | c0016 | t0002 | g0224 | EAS | CHB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18906 | hp1 | a0041 | c0103 | t0012 | g0073 | AFR | YRI | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18906 | hp2 | a0042 | c0101 | t0004 | g0071 | AFR | YRI | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18943 | hp1 | a0001 | c0003 | t0004 | g0153 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18944 | hp1 | a0001 | c0011 | t0003 | g0188 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18950 | hp1 | a0001 | c0002 | t0032 | g0212 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18950 | hp2 | a0001 | c0004 | t0001 | g0049 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18951 | hp2 | a0001 | c0022 | t0001 | g0041 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18952 | hp1 | a0001 | c0068 | t0001 | g0206 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18959 | hp1 | a0001 | c0012 | t0003 | g0013 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18959 | hp2 | a0001 | c0003 | t0004 | g0231 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18963 | hp1 | a0043 | c0062 | t0002 | g0158 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18969 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18974 | hp1 | a0001 | c0011 | t0003 | g0187 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18977 | hp1 | a0001 | c0022 | t0001 | g0041 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18982 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18983 | hp1 | a0009 | c0014 | t0003 | g0255 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18983 | hp2 | a0001 | c0007 | t0003 | g0195 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18988 | hp2 | a0001 | c0012 | t0003 | g0013 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18990 | hp2 | a0021 | c0035 | t0002 | g0234 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18993 | hp1 | a0012 | c0015 | t0002 | g0159 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18993 | hp2 | a0010 | c0024 | t0001 | g0201 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18997 | hp1 | a0012 | c0015 | t0002 | g0160 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18997 | hp2 | a0001 | c0012 | t0003 | g0013 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18998 | hp2 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18999 | hp1 | a0006 | c0095 | t0004 | g0257 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19000 | hp1 | a0001 | c0011 | t0003 | g0191 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19002 | hp1 | a0001 | c0011 | t0003 | g0190 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19002 | hp2 | a0001 | c0004 | t0001 | g0228 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19003 | hp1 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19005 | hp1 | a0001 | c0003 | t0003 | g0019 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19005 | hp2 | a0012 | c0015 | t0002 | g0161 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19009 | hp1 | a0001 | c0001 | t0021 | g0122 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19012 | hp2 | a0012 | c0015 | t0002 | g0162 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19030 | hp1 | a0001 | c0090 | t0004 | g0264 | AFR | LWK | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19030 | hp2 | a0044 | c0087 | t0001 | g0277 | AFR | LWK | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19043 | hp1 | a0002 | c0005 | t0004 | g0005 | AFR | LWK | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19043 | hp2 | a0001 | c0013 | t0004 | g0014 | AFR | LWK | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19055 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19057 | hp2 | a0003 | c0008 | t0001 | g0131 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19060 | hp2 | a0001 | c0002 | t0003 | g0218 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19066 | hp1 | a0009 | c0014 | t0001 | g0256 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19066 | hp2 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19074 | hp1 | a0001 | c0007 | t0003 | g0194 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19077 | hp1 | a0001 | c0006 | t0001 | g0129 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19077 | hp2 | a0001 | c0007 | t0003 | g0196 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19079 | hp1 | a0001 | c0007 | t0004 | g0269 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19079 | hp2 | a0016 | c0084 | t0002 | g0149 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19081 | hp1 | a0001 | c0065 | t0004 | g0177 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19081 | hp2 | a0001 | c0004 | t0001 | g0049 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19085 | hp1 | a0003 | c0008 | t0003 | g0200 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19088 | hp1 | a0001 | c0003 | t0003 | g0019 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19090 | hp1 | a0001 | c0003 | t0004 | g0078 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19090 | hp2 | a0010 | c0024 | t0003 | g0202 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | YRI | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA19240 | hp2 | a0045 | c0102 | t0012 | g0072 | AFR | YRI | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ASW | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA20129 | hp2 | a0003 | c0075 | t0004 | g0079 | AFR | ASW | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA20752 | hp1 | a0001 | c0003 | t0004 | g0018 | EUR | TSI | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA20752 | hp2 | a0047 | c0085 | t0007 | g0095 | EUR | TSI | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA20805 | hp2 | a0001 | c0002 | t0004 | g0211 | EUR | TSI | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | CLM | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02109 | hp1 | a0004 | c0009 | t0004 | g0059 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02109 | hp2 | a0028 | c0057 | t0018 | g0275 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02486 | hp1 | a0001 | c0013 | t0004 | g0014 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02486 | hp2 | a0002 | c0005 | t0004 | g0005 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02559 | hp1 | a0005 | c0032 | t0006 | g0069 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG02559 | hp2 | a0002 | c0055 | t0004 | g0080 | AFR | ACB | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03471 | hp1 | a0014 | c0020 | t0008 | g0015 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG03471 | hp2 | a0001 | c0088 | t0004 | g0262 | AFR | MSL | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG06807 | hp1 | a0004 | c0009 | t0001 | g0027 | AFR | USA | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
HG06807 | hp2 | a0040 | c0105 | t0030 | g0267 | AFR | USA | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18955 | hp1 | a0021 | c0035 | t0002 | g0235 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA18955 | hp2 | a0001 | c0003 | t0003 | g0146 | EAS | JPT | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA20300 | hp1 | a0046 | c0106 | t0001 | g0268 | AFR | USA | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | USA | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA21309 | hp1 | a0003 | c0008 | t0001 | g0199 | AFR | LWK | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
NA21309 | hp2 | a0015 | c0047 | t0004 | g0081 | AFR | LWK | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
homoSapiens | chm13v2 | a0048 | c0082 | t0002 | g0111 | REF | REF | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
homoSapiens | grch38p0 | a0022 | c0097 | t0003 | g0258 | REF | REF | PLIN4_chr19_4497192_4523486 | PLIN4 | chr19 | 4497192 | 4523486 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4504539 | G | A | 1 | a0001 | 1 | HG01069.hp1 | stop_gained | HIGH | c.4036C>T | p.Gln1346* | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 4155/6502 | 4036/4116 | 1346/1371 | chr19 | 4504539 | |||
chr19:4504590 | G | A | 1 | a0001 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.3985C>T | p.Arg1329Trp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 4104/6502 | 3985/4116 | 1329/1371 | chr19 | 4504590 | |||
chr19:4504658 | C | T | 1 | a0001 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.3917G>A | p.Arg1306Gln | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 4036/6502 | 3917/4116 | 1306/1371 | chr19 | 4504658 | |||
chr19:4504742 | C | T | 1 | a0037 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.3833G>A | p.Arg1278Gln | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 3952/6502 | 3833/4116 | 1278/1371 | chr19 | 4504742 | |||
chr19:4508893 | C | T | 3 | a0008 a0028 a0029 |
8 | HG00639.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
missense_variant | MODERATE | c.3577G>A | p.Val1193Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/8 | 3696/6502 | 3577/4116 | 1193/1371 | chr19 | 4508893 | |||
chr19:4510518 | G | A | 9 | a0001 a0002 a0004 others(6): Show |
24 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(21): Show |
missense_variant | MODERATE | c.3442C>T | p.Arg1148Cys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3561/6502 | 3442/4116 | 1148/1371 | chr19 | 4510518 | |||
chr19:4510548 | C | T | 15 | a0001 a0005 a0006 others(12): Show |
173 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(170): Show |
missense_variant | MODERATE | c.3412G>A | p.Ala1138Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3531/6502 | 3412/4116 | 1138/1371 | chr19 | 4510548 | |||
chr19:4510779 | C | CG | 4 | a0010 a0013 a0031 others(1): Show |
10 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
frameshift_variant | HIGH | c.3180dupC | p.Ala1061fs | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3299/6502 | 3180/4116 | 1060/1371 | chr19 | 4510779 | |||
chr19:4510838 | G | A | 2 | a0001 a0018 |
3 | HG01346.hp1 HG03098.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.3122C>T | p.Ala1041Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3241/6502 | 3122/4116 | 1041/1371 | chr19 | 4510838 | |||
chr19:4510862 | C | G | 1 | a0040 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.3098G>C | p.Gly1033Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3217/6502 | 3098/4116 | 1033/1371 | chr19 | 4510862 | |||
chr19:4510874 | G | A | 1 | a0001 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.3086C>T | p.Ala1029Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3205/6502 | 3086/4116 | 1029/1371 | chr19 | 4510874 | |||
chr19:4510926 | C | T | 5 | a0004 a0035 a0041 others(2): Show |
14 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
missense_variant | MODERATE | c.3034G>A | p.Val1012Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3153/6502 | 3034/4116 | 1012/1371 | chr19 | 4510926 | |||
chr19:4510931 | C | T | 1 | a0045 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.3029G>A | p.Gly1010Glu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3148/6502 | 3029/4116 | 1010/1371 | chr19 | 4510931 | |||
chr19:4511029 | TCCTTTGG others(191): Show |
T | 1 | a0038 | 1 | HG03453.hp2 | disruptive_inframe_deletion | MODERATE | c.2733_2930del | p.Thr912_Gly977del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3049/6502 | 2733/4116 | 911/1371 | chr19 | 4511029 | |||
chr19:4511114 | C | T | 1 | a0043 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.2846G>A | p.Gly949Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2965/6502 | 2846/4116 | 949/1371 | chr19 | 4511114 | |||
chr19:4511169 | C | T | 1 | a0008 | 6 | HG00639.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
missense_variant | MODERATE | c.2791G>A | p.Val931Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2910/6502 | 2791/4116 | 931/1371 | chr19 | 4511169 | |||
chr19:4511211 | C | CGCCGGTC others(389): Show |
1 | a0002 | 1 | HG02559.hp2 | conservative_inframe_insertion | MODERATE | c.2748_2749insATGGAC others(390): Show |
p.Gly916_Val917insMe others(394): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2867/6502 | 2748/4116 | 916/1371 | chr19 | 4511211 | |||
chr19:4511211 | C | CGCCGGTC others(389): Show |
3 | a0002 a0013 a0047 |
9 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
conservative_inframe_insertion | MODERATE | c.2748_2749insATGGAC others(390): Show |
p.Gly916_Val917insMe others(394): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2867/6502 | 2748/4116 | 916/1371 | chr19 | 4511211 | |||
chr19:4511211 | C | CGCCGGTC others(389): Show |
1 | a0018 | 2 | HG03098.hp2 HG03209.hp1 |
conservative_inframe_insertion | MODERATE | c.2748_2749insATGGAC others(390): Show |
p.Gly916_Val917insMe others(394): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2867/6502 | 2748/4116 | 916/1371 | chr19 | 4511211 | |||
chr19:4511211 | C | CGCCGGTC others(389): Show |
1 | a0040 | 1 | HG06807.hp2 | conservative_inframe_insertion | MODERATE | c.2748_2749insATGGAC others(390): Show |
p.Gly916_Val917insMe others(394): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2867/6502 | 2748/4116 | 916/1371 | chr19 | 4511211 | |||
chr19:4511239 | GTTCACAG others(389): Show |
G | 1 | a0033 | 1 | HG02818.hp1 | disruptive_inframe_deletion | MODERATE | c.2325_2720del | p.Lys775_Val906del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2839/6502 | 2325/4116 | 775/1371 | chr19 | 4511239 | |||
chr19:4511268 | C | T | 1 | a0001 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.2692G>A | p.Val898Met | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2811/6502 | 2692/4116 | 898/1371 | chr19 | 4511268 | |||
chr19:4511271 | C | T | 18 | a0001 a0002 a0005 others(15): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
missense_variant | MODERATE | c.2689G>A | p.Ala897Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2808/6502 | 2689/4116 | 897/1371 | chr19 | 4511271 | |||
chr19:4511316 | CCTGGACG others(191): Show |
C | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
conservative_inframe_deletion | MODERATE | c.2446_2643del | p.Met816_Gln881del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2762/6502 | 2446/4116 | 816/1371 | chr19 | 4511316 | |||
chr19:4511322 | CGGCCCCT others(389): Show |
C | 1 | a0019 | 1 | HG03130.hp1 | conservative_inframe_deletion | MODERATE | c.2242_2637del | p.Ile748_Ala879del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2756/6502 | 2242/4116 | 748/1371 | chr19 | 4511322 | |||
chr19:4511338 | T | A | 22 | a0001 a0002 a0004 others(19): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
missense_variant | MODERATE | c.2622A>T | p.Lys874Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2741/6502 | 2622/4116 | 874/1371 | chr19 | 4511338 | |||
chr19:4511338 | T | TTTCGCAG others(389): Show |
7 | a0002 a0003 a0013 others(4): Show |
8 | HG01891.hp1 HG02109.hp2 HG02630.hp2 others(5): Show |
disruptive_inframe_insertion | MODERATE | c.2621_2622insTGTGGC others(390): Show |
p.Ala873_Lys874insAs others(394): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2740/6502 | 2621/4116 | 874/1371 | chr19 | 4511338 | |||
chr19:4511338 | TTTCGCAG others(389): Show |
T | 3 | a0003 a0013 a0019 |
4 | HG01978.hp2 HG02055.hp1 HG04199.hp2 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.2226_2621del | p.Asn742_Ala873del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2740/6502 | 2226/4116 | 742/1371 | chr19 | 4511338 | |||
chr19:4511364 | C | A | 33 | a0001 a0002 a0003 others(30): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
missense_variant | MODERATE | c.2596G>T | p.Gly866Cys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2715/6502 | 2596/4116 | 866/1371 | chr19 | 4511364 | |||
chr19:4511367 | G | C | 33 | a0001 a0002 a0003 others(30): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
missense_variant | MODERATE | c.2593C>G | p.Leu865Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2712/6502 | 2593/4116 | 865/1371 | chr19 | 4511367 | |||
chr19:4511369 | G | A | 1 | a0020 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.2591C>T | p.Thr864Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2710/6502 | 2591/4116 | 864/1371 | chr19 | 4511369 | |||
chr19:4511373 | T | C | 33 | a0001 a0002 a0003 others(30): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
missense_variant | MODERATE | c.2587A>G | p.Asn863Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2706/6502 | 2587/4116 | 863/1371 | chr19 | 4511373 | |||
chr19:4511381 | C | T | 1 | a0001 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.2579G>A | p.Gly860Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2698/6502 | 2579/4116 | 860/1371 | chr19 | 4511381 | |||
chr19:4511387 | G | A | 33 | a0001 a0002 a0003 others(30): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
missense_variant | MODERATE | c.2573C>T | p.Ala858Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2692/6502 | 2573/4116 | 858/1371 | chr19 | 4511387 | |||
chr19:4511388 | C | G | 33 | a0001 a0002 a0003 others(30): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
missense_variant | MODERATE | c.2572G>C | p.Ala858Pro | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2691/6502 | 2572/4116 | 858/1371 | chr19 | 4511388 | |||
chr19:4511391 | T | C | 33 | a0001 a0002 a0003 others(30): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
missense_variant | MODERATE | c.2569A>G | p.Ile857Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2688/6502 | 2569/4116 | 857/1371 | chr19 | 4511391 | |||
chr19:4511393 | T | G | 33 | a0001 a0002 a0003 others(30): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
missense_variant | MODERATE | c.2567A>C | p.Asn856Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2686/6502 | 2567/4116 | 856/1371 | chr19 | 4511393 | |||
chr19:4511394 | T | C | 1 | a0001 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.2566A>G | p.Asn856Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2685/6502 | 2566/4116 | 856/1371 | chr19 | 4511394 | |||
chr19:4511397 | G | T | 33 | a0001 a0002 a0003 others(30): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
missense_variant | MODERATE | c.2563C>A | p.Gln855Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2682/6502 | 2563/4116 | 855/1371 | chr19 | 4511397 | |||
chr19:4511399 | G | C | 1 | a0020 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.2561C>G | p.Thr854Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2680/6502 | 2561/4116 | 854/1371 | chr19 | 4511399 | |||
chr19:4511404 | T | G | 33 | a0001 a0002 a0003 others(30): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
missense_variant | MODERATE | c.2556A>C | p.Lys852Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2675/6502 | 2556/4116 | 852/1371 | chr19 | 4511404 | |||
chr19:4511406 | T | C | 33 | a0001 a0002 a0003 others(30): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
missense_variant | MODERATE | c.2554A>G | p.Lys852Glu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2673/6502 | 2554/4116 | 852/1371 | chr19 | 4511406 | |||
chr19:4511409 | G | C | 33 | a0001 a0002 a0003 others(30): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
missense_variant | MODERATE | c.2551C>G | p.Leu851Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2670/6502 | 2551/4116 | 851/1371 | chr19 | 4511409 | |||
chr19:4511412 | C | T | 33 | a0001 a0002 a0003 others(30): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
missense_variant | MODERATE | c.2548G>A | p.Gly850Arg | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2667/6502 | 2548/4116 | 850/1371 | chr19 | 4511412 | |||
chr19:4511421 | C | T | 1 | a0001 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.2539G>A | p.Val847Met | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2658/6502 | 2539/4116 | 847/1371 | chr19 | 4511421 | |||
chr19:4511422 | A | AGTCCCTT others(92): Show |
1 | a0020 | 1 | NA18522.hp2 | disruptive_inframe_insertion | MODERATE | c.2537_2538insCGTCCA others(93): Show |
p.Ala846_Val847insVa others(97): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2656/6502 | 2537/4116 | 846/1371 | chr19 | 4511422 | |||
chr19:4511424 | C | T | 33 | a0001 a0002 a0003 others(30): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
missense_variant | MODERATE | c.2536G>A | p.Ala846Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2655/6502 | 2536/4116 | 846/1371 | chr19 | 4511424 | |||
chr19:4511441 | G | A | 39 | a0001 a0002 a0003 others(36): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
missense_variant | MODERATE | c.2519C>T | p.Ala840Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2638/6502 | 2519/4116 | 840/1371 | chr19 | 4511441 | |||
chr19:4511450 | G | A | 33 | a0001 a0002 a0003 others(30): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
missense_variant | MODERATE | c.2510C>T | p.Thr837Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2629/6502 | 2510/4116 | 837/1371 | chr19 | 4511450 | |||
chr19:4511454 | C | G | 33 | a0001 a0002 a0003 others(30): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
missense_variant | MODERATE | c.2506G>C | p.Val836Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2625/6502 | 2506/4116 | 836/1371 | chr19 | 4511454 | |||
chr19:4511459 | C | G | 33 | a0001 a0002 a0003 others(30): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
missense_variant | MODERATE | c.2501G>C | p.Ser834Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2620/6502 | 2501/4116 | 834/1371 | chr19 | 4511459 | |||
chr19:4511462 | C | G | 33 | a0001 a0002 a0003 others(30): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
missense_variant | MODERATE | c.2498G>C | p.Cys833Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2617/6502 | 2498/4116 | 833/1371 | chr19 | 4511462 | |||
chr19:4511463 | A | T | 33 | a0001 a0002 a0003 others(30): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
missense_variant | MODERATE | c.2497T>A | p.Cys833Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2616/6502 | 2497/4116 | 833/1371 | chr19 | 4511463 | |||
chr19:4511479 | A | ACCCGTTA others(92): Show |
1 | a0020 | 1 | NA18522.hp2 | disruptive_inframe_insertion | MODERATE | c.2480_2481insCACCAA others(93): Show |
p.Gly827_Thr828insTh others(97): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2599/6502 | 2480/4116 | 827/1371 | chr19 | 4511479 | |||
chr19:4511492 | G | A | 1 | a0044 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2468C>T | p.Thr823Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2587/6502 | 2468/4116 | 823/1371 | chr19 | 4511492 | |||
chr19:4511513 | A | G | 40 | a0001 a0002 a0003 others(37): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
missense_variant | MODERATE | c.2447T>C | p.Met816Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2566/6502 | 2447/4116 | 816/1371 | chr19 | 4511513 | |||
chr19:4511547 | C | T | 1 | a0001 | 5 | HG02486.hp1 HG02970.hp2 HG03516.hp1 others(2): Show |
missense_variant | MODERATE | c.2413G>A | p.Gly805Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2532/6502 | 2413/4116 | 805/1371 | chr19 | 4511547 | |||
chr19:4511568 | C | T | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
missense_variant | MODERATE | c.2392G>A | p.Ala798Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2511/6502 | 2392/4116 | 798/1371 | chr19 | 4511568 | |||
chr19:4511590 | A | AGTCTTGG others(290): Show |
7 | a0004 a0031 a0035 others(4): Show |
16 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(13): Show |
disruptive_inframe_insertion | MODERATE | c.2369_2370insCATGCT others(291): Show |
p.Thr790_Val791insMe others(295): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2488/6502 | 2369/4116 | 790/1371 | chr19 | 4511590 | |||
chr19:4511607 | T | C | 3 | a0003 a0012 a0043 |
7 | HG01257.hp2 HG01258.hp2 NA18963.hp1 others(4): Show |
missense_variant | MODERATE | c.2353A>G | p.Met785Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2472/6502 | 2353/4116 | 785/1371 | chr19 | 4511607 | |||
chr19:4511610 | C | T | 3 | a0002 a0012 a0043 |
6 | HG02559.hp2 NA18963.hp1 NA18993.hp1 others(3): Show |
missense_variant | MODERATE | c.2350G>A | p.Gly784Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2469/6502 | 2350/4116 | 784/1371 | chr19 | 4511610 | |||
chr19:4511610 | CGGTCTGG others(191): Show |
C | 1 | a0003 | 4 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(1): Show |
conservative_inframe_deletion | MODERATE | c.2152_2349del | p.Ser718_Thr783del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2468/6502 | 2152/4116 | 718/1371 | chr19 | 4511610 | |||
chr19:4511626 | T | TTTGGCCA others(290): Show |
2 | a0005 a0023 |
8 | HG00735.hp2 HG01109.hp1 HG01884.hp2 others(5): Show |
disruptive_inframe_insertion | MODERATE | c.2333_2334insGGGGAC others(291): Show |
p.Lys778_Gly779insGl others(295): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2452/6502 | 2333/4116 | 778/1371 | chr19 | 4511626 | |||
chr19:4511632 | C | G | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
missense_variant | MODERATE | c.2328G>C | p.Leu776Phe | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2447/6502 | 2328/4116 | 776/1371 | chr19 | 4511632 | |||
chr19:4511634 | A | C | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
missense_variant | MODERATE | c.2326T>G | p.Leu776Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2445/6502 | 2326/4116 | 776/1371 | chr19 | 4511634 | |||
chr19:4511635 | C | A | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
missense_variant | MODERATE | c.2325G>T | p.Lys775Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2444/6502 | 2325/4116 | 775/1371 | chr19 | 4511635 | |||
chr19:4511635 | C | G | 19 | a0001 a0006 a0007 others(16): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
missense_variant | MODERATE | c.2325G>C | p.Lys775Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2444/6502 | 2325/4116 | 775/1371 | chr19 | 4511635 | |||
chr19:4511635 | CTTCACAG others(785): Show |
G | 1 | a0003 | 1 | NA19057.hp2 | conservative_inframe_deletion | MODERATE | c.1534_2325del | p.Val512_Lys775del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2444/6502 | 1534/4116 | 512/1371 | chr19 | 4511635 | |||
chr19:4511648 | G | A | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
missense_variant | MODERATE | c.2312C>T | p.Thr771Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2431/6502 | 2312/4116 | 771/1371 | chr19 | 4511648 | |||
chr19:4511661 | A | T | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
missense_variant | MODERATE | c.2299T>A | p.Ser767Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2418/6502 | 2299/4116 | 767/1371 | chr19 | 4511661 | |||
chr19:4511667 | C | T | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
missense_variant | MODERATE | c.2293G>A | p.Ala765Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2412/6502 | 2293/4116 | 765/1371 | chr19 | 4511667 | |||
chr19:4511691 | A | T | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
missense_variant | MODERATE | c.2269T>A | p.Ser757Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2388/6502 | 2269/4116 | 757/1371 | chr19 | 4511691 | |||
chr19:4511697 | T | C | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
missense_variant | MODERATE | c.2263A>G | p.Thr755Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2382/6502 | 2263/4116 | 755/1371 | chr19 | 4511697 | |||
chr19:4511706 | G | C | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
missense_variant | MODERATE | c.2254C>G | p.Leu752Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2373/6502 | 2254/4116 | 752/1371 | chr19 | 4511706 | |||
chr19:4511711 | C | G | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
missense_variant | MODERATE | c.2249G>C | p.Gly750Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2368/6502 | 2249/4116 | 750/1371 | chr19 | 4511711 | |||
chr19:4511712 | C | T | 2 | a0012 a0043 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
missense_variant | MODERATE | c.2248G>A | p.Gly750Arg | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2367/6502 | 2248/4116 | 750/1371 | chr19 | 4511712 | |||
chr19:4511718 | T | C | 20 | a0001 a0006 a0007 others(17): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
missense_variant | MODERATE | c.2242A>G | p.Ile748Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2361/6502 | 2242/4116 | 748/1371 | chr19 | 4511718 | |||
chr19:4511725 | T | TTTGGCCA others(191): Show |
13 | a0001 a0006 a0007 others(10): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
disruptive_inframe_insertion | MODERATE | c.2234_2235insGGGGGC others(192): Show |
p.Lys745_Gly746insGl others(196): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2353/6502 | 2234/4116 | 745/1371 | chr19 | 4511725 | |||
chr19:4511725 | T | TTTGGCCA others(191): Show |
1 | a0014 | 3 | HG02258.hp1 HG02922.hp1 HG03471.hp1 |
disruptive_inframe_insertion | MODERATE | c.2234_2235insGGGGGC others(192): Show |
p.Lys745_Gly746insGl others(196): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2353/6502 | 2234/4116 | 745/1371 | chr19 | 4511725 | |||
chr19:4511734 | A | T | 2 | a0005 a0023 |
8 | HG00735.hp2 HG01109.hp1 HG01884.hp2 others(5): Show |
missense_variant | MODERATE | c.2226T>A | p.Asn742Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2345/6502 | 2226/4116 | 742/1371 | chr19 | 4511734 | |||
chr19:4511745 | C | T | 11 | a0004 a0011 a0017 others(8): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(23): Show |
missense_variant | MODERATE | c.2215G>A | p.Gly739Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2334/6502 | 2215/4116 | 739/1371 | chr19 | 4511745 | |||
chr19:4511896 | C | CGTGTCTA others(92): Show |
1 | a0018 | 2 | HG03098.hp2 HG03209.hp1 |
disruptive_inframe_insertion | MODERATE | c.2063_2064insAGCCAA others(93): Show |
p.Thr688_Ala689insAl others(97): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2182/6502 | 2063/4116 | 688/1371 | chr19 | 4511896 | |||
chr19:4511901 | C | T | 2 | a0028 a0034 |
2 | HG02109.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.2059G>A | p.Asp687Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2178/6502 | 2059/4116 | 687/1371 | chr19 | 4511901 | |||
chr19:4511910 | T | TCTGGACG others(191): Show |
1 | a0032 | 1 | HG02723.hp2 | conservative_inframe_insertion | MODERATE | c.2049_2050insGGGGGC others(192): Show |
p.Gln683_Thr684insGl others(196): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2168/6502 | 2049/4116 | 683/1371 | chr19 | 4511910 | |||
chr19:4511910 | TCTGGGCA others(389): Show |
T | 1 | a0019 | 2 | HG03130.hp1 HG04199.hp2 |
conservative_inframe_deletion | MODERATE | c.1654_2049del | p.Gly552_Gln683del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2168/6502 | 1654/4116 | 552/1371 | chr19 | 4511910 | |||
chr19:4511915 | G | A | 14 | a0001 a0003 a0006 others(11): Show |
180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
missense_variant | MODERATE | c.2045C>T | p.Ala682Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2164/6502 | 2045/4116 | 682/1371 | chr19 | 4511915 | |||
chr19:4511936 | A | G | 6 | a0003 a0011 a0017 others(3): Show |
11 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(8): Show |
missense_variant | MODERATE | c.2024T>C | p.Val675Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2143/6502 | 2024/4116 | 675/1371 | chr19 | 4511936 | |||
chr19:4511943 | T | C | 43 | a0001 a0002 a0003 others(40): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
missense_variant | MODERATE | c.2017A>G | p.Ser673Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2136/6502 | 2017/4116 | 673/1371 | chr19 | 4511943 | |||
chr19:4511961 | A | G | 5 | a0004 a0032 a0035 others(2): Show |
14 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
missense_variant | MODERATE | c.1999T>C | p.Phe667Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2118/6502 | 1999/4116 | 667/1371 | chr19 | 4511961 | |||
chr19:4512035 | A | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1925T>C | p.Val642Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2044/6502 | 1925/4116 | 642/1371 | chr19 | 4512035 | |||
chr19:4512042 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1918A>G | p.Ser640Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2037/6502 | 1918/4116 | 640/1371 | chr19 | 4512042 | |||
chr19:4512056 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1904A>G | p.Tyr635Cys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2023/6502 | 1904/4116 | 635/1371 | chr19 | 4512056 | |||
chr19:4512060 | T | C | 7 | a0004 a0018 a0023 others(4): Show |
9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
missense_variant | MODERATE | c.1900A>G | p.Ile634Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2019/6502 | 1900/4116 | 634/1371 | chr19 | 4512060 | |||
chr19:4512093 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1867A>G | p.Thr623Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1986/6502 | 1867/4116 | 623/1371 | chr19 | 4512093 | |||
chr19:4512100 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1860G>A | p.Met620Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1979/6502 | 1860/4116 | 620/1371 | chr19 | 4512100 | |||
chr19:4512102 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1858A>G | p.Met620Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1977/6502 | 1858/4116 | 620/1371 | chr19 | 4512102 | |||
chr19:4512107 | G | A | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1853C>T | p.Thr618Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1972/6502 | 1853/4116 | 618/1371 | chr19 | 4512107 | |||
chr19:4512114 | C | T | 5 | a0031 a0036 a0041 others(2): Show |
5 | HG02572.hp2 HG02976.hp1 NA18906.hp1 others(2): Show |
missense_variant | MODERATE | c.1846G>A | p.Val616Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1965/6502 | 1846/4116 | 616/1371 | chr19 | 4512114 | |||
chr19:4512117 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1843A>G | p.Thr615Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1962/6502 | 1843/4116 | 615/1371 | chr19 | 4512117 | |||
chr19:4512134 | A | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1826T>C | p.Val609Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1945/6502 | 1826/4116 | 609/1371 | chr19 | 4512134 | |||
chr19:4512143 | A | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1817T>C | p.Val606Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1936/6502 | 1817/4116 | 606/1371 | chr19 | 4512143 | |||
chr19:4512144 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1816G>A | p.Val606Met | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1935/6502 | 1816/4116 | 606/1371 | chr19 | 4512144 | |||
chr19:4512147 | G | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1813C>G | p.Leu605Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1932/6502 | 1813/4116 | 605/1371 | chr19 | 4512147 | |||
chr19:4512152 | G | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1808C>G | p.Thr603Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1927/6502 | 1808/4116 | 603/1371 | chr19 | 4512152 | |||
chr19:4512155 | G | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1805C>G | p.Thr602Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1924/6502 | 1805/4116 | 602/1371 | chr19 | 4512155 | |||
chr19:4512156 | T | A | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1804A>T | p.Thr602Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1923/6502 | 1804/4116 | 602/1371 | chr19 | 4512156 | |||
chr19:4512162 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1798A>G | p.Thr600Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1917/6502 | 1798/4116 | 600/1371 | chr19 | 4512162 | |||
chr19:4512171 | T | G | 1 | a0002 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1789A>C | p.Thr597Pro | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1908/6502 | 1789/4116 | 597/1371 | chr19 | 4512171 | |||
chr19:4512192 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1768G>A | p.Ala590Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1887/6502 | 1768/4116 | 590/1371 | chr19 | 4512192 | |||
chr19:4512201 | C | T | 2 | a0001 a0032 |
2 | HG02630.hp1 HG02723.hp2 |
missense_variant | MODERATE | c.1759G>A | p.Val587Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1878/6502 | 1759/4116 | 587/1371 | chr19 | 4512201 | |||
chr19:4512216 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1744G>A | p.Ala582Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1863/6502 | 1744/4116 | 582/1371 | chr19 | 4512216 | |||
chr19:4512228 | C | A | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1732G>T | p.Val578Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1851/6502 | 1732/4116 | 578/1371 | chr19 | 4512228 | |||
chr19:4512229 | A | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1731T>G | p.Asn577Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1850/6502 | 1731/4116 | 577/1371 | chr19 | 4512229 | |||
chr19:4512233 | G | A | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1727C>T | p.Ala576Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1846/6502 | 1727/4116 | 576/1371 | chr19 | 4512233 | |||
chr19:4512246 | G | A | 1 | a0002 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1714C>T | p.Leu572Phe | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1833/6502 | 1714/4116 | 572/1371 | chr19 | 4512246 | |||
chr19:4512252 | T | C | 1 | a0001 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.1708A>G | p.Thr570Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1827/6502 | 1708/4116 | 570/1371 | chr19 | 4512252 | |||
chr19:4512258 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1702A>G | p.Met568Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1821/6502 | 1702/4116 | 568/1371 | chr19 | 4512258 | |||
chr19:4512260 | G | A | 1 | a0011 | 5 | HG02572.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
missense_variant | MODERATE | c.1700C>T | p.Thr567Met | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1819/6502 | 1700/4116 | 567/1371 | chr19 | 4512260 | |||
chr19:4512261 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1699A>G | p.Thr567Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1818/6502 | 1699/4116 | 567/1371 | chr19 | 4512261 | |||
chr19:4512275 | A | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1685T>C | p.Ile562Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1804/6502 | 1685/4116 | 562/1371 | chr19 | 4512275 | |||
chr19:4512279 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1681G>C | p.Val561Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1800/6502 | 1681/4116 | 561/1371 | chr19 | 4512279 | |||
chr19:4512281 | A | T | 1 | a0001 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.1679T>A | p.Val560Glu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1798/6502 | 1679/4116 | 560/1371 | chr19 | 4512281 | |||
chr19:4512312 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1648G>A | p.Val550Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1767/6502 | 1648/4116 | 550/1371 | chr19 | 4512312 | |||
chr19:4512332 | A | G | 2 | a0019 a0032 |
3 | HG02723.hp2 HG03130.hp1 HG04199.hp2 |
missense_variant | MODERATE | c.1628T>C | p.Val543Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1747/6502 | 1628/4116 | 543/1371 | chr19 | 4512332 | |||
chr19:4512339 | T | C | 2 | a0019 a0032 |
3 | HG02723.hp2 HG03130.hp1 HG04199.hp2 |
missense_variant | MODERATE | c.1621A>G | p.Ser541Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1740/6502 | 1621/4116 | 541/1371 | chr19 | 4512339 | |||
chr19:4512360 | T | C | 1 | a0019 | 2 | HG03130.hp1 HG04199.hp2 |
missense_variant | MODERATE | c.1600A>G | p.Thr534Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1719/6502 | 1600/4116 | 534/1371 | chr19 | 4512360 | |||
chr19:4512399 | C | T | 1 | a0019 | 2 | HG03130.hp1 HG04199.hp2 |
missense_variant | MODERATE | c.1561G>A | p.Val521Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1680/6502 | 1561/4116 | 521/1371 | chr19 | 4512399 | |||
chr19:4512402 | C | T | 2 | a0026 a0032 |
2 | HG02074.hp1 HG02723.hp2 |
missense_variant | MODERATE | c.1558G>A | p.Gly520Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1677/6502 | 1558/4116 | 520/1371 | chr19 | 4512402 | |||
chr19:4512411 | C | T | 1 | a0027 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.1549G>A | p.Val517Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1668/6502 | 1549/4116 | 517/1371 | chr19 | 4512411 | |||
chr19:4512426 | C | A | 1 | a0019 | 2 | HG03130.hp1 HG04199.hp2 |
missense_variant | MODERATE | c.1534G>T | p.Val512Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1653/6502 | 1534/4116 | 512/1371 | chr19 | 4512426 | |||
chr19:4512440 | G | A | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1520C>T | p.Thr507Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1639/6502 | 1520/4116 | 507/1371 | chr19 | 4512440 | |||
chr19:4512453 | A | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1507T>A | p.Ser503Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1626/6502 | 1507/4116 | 503/1371 | chr19 | 4512453 | |||
chr19:4512459 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1501G>A | p.Ala501Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1620/6502 | 1501/4116 | 501/1371 | chr19 | 4512459 | |||
chr19:4512483 | A | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1477T>A | p.Ser493Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1596/6502 | 1477/4116 | 493/1371 | chr19 | 4512483 | |||
chr19:4512489 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1471A>G | p.Thr491Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1590/6502 | 1471/4116 | 491/1371 | chr19 | 4512489 | |||
chr19:4512498 | G | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1462C>G | p.Leu488Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1581/6502 | 1462/4116 | 488/1371 | chr19 | 4512498 | |||
chr19:4512503 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1457G>C | p.Gly486Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1576/6502 | 1457/4116 | 486/1371 | chr19 | 4512503 | |||
chr19:4512504 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1456G>A | p.Gly486Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1575/6502 | 1456/4116 | 486/1371 | chr19 | 4512504 | |||
chr19:4512509 | A | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1451T>C | p.Val484Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1570/6502 | 1451/4116 | 484/1371 | chr19 | 4512509 | |||
chr19:4512522 | C | T | 2 | a0028 a0034 |
2 | HG02109.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.1438G>A | p.Ala480Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1557/6502 | 1438/4116 | 480/1371 | chr19 | 4512522 | |||
chr19:4512530 | G | A | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1430C>T | p.Ala477Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1549/6502 | 1430/4116 | 477/1371 | chr19 | 4512530 | |||
chr19:4512537 | C | CGGTCACC others(92): Show |
1 | a0032 | 1 | HG02723.hp2 | conservative_inframe_insertion | MODERATE | c.1422_1423insAGTGCC others(93): Show |
p.Thr474_Gly475insSe others(97): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1541/6502 | 1422/4116 | 474/1371 | chr19 | 4512537 | |||
chr19:4512551 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1409G>A | p.Cys470Tyr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1528/6502 | 1409/4116 | 470/1371 | chr19 | 4512551 | |||
chr19:4512555 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1405G>A | p.Val469Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1524/6502 | 1405/4116 | 469/1371 | chr19 | 4512555 | |||
chr19:4512581 | A | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1379T>C | p.Ile460Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1498/6502 | 1379/4116 | 460/1371 | chr19 | 4512581 | |||
chr19:4512587 | GTGGTGTC others(488): Show |
G | 8 | a0002 a0011 a0013 others(5): Show |
36 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(33): Show |
disruptive_inframe_deletion | MODERATE | c.878_1372del | p.Ser293_Thr457del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1491/6502 | 878/4116 | 293/1371 | chr19 | 4512587 | |||
chr19:4512597 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1363G>A | p.Val455Met | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1482/6502 | 1363/4116 | 455/1371 | chr19 | 4512597 | |||
chr19:4512609 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1351A>G | p.Ile451Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1470/6502 | 1351/4116 | 451/1371 | chr19 | 4512609 | |||
chr19:4512617 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1343G>A | p.Arg448Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1462/6502 | 1343/4116 | 448/1371 | chr19 | 4512617 | |||
chr19:4512622 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1338G>C | p.Leu446Phe | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1457/6502 | 1338/4116 | 446/1371 | chr19 | 4512622 | |||
chr19:4512624 | A | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1336T>G | p.Leu446Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1455/6502 | 1336/4116 | 446/1371 | chr19 | 4512624 | |||
chr19:4512624 | AATTCATG others(389): Show |
A | 12 | a0001 a0004 a0005 others(9): Show |
42 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(39): Show |
conservative_inframe_deletion | MODERATE | c.940_1335del | p.Val314_Asn445del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1454/6502 | 940/4116 | 314/1371 | chr19 | 4512624 | |||
chr19:4512627 | T | G | 2 | a0005 a0018 |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
missense_variant | MODERATE | c.1333A>C | p.Asn445His | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1452/6502 | 1333/4116 | 445/1371 | chr19 | 4512627 | |||
chr19:4512630 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1330A>G | p.Met444Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1449/6502 | 1330/4116 | 444/1371 | chr19 | 4512630 | |||
chr19:4512638 | G | A | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1322C>T | p.Thr441Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1441/6502 | 1322/4116 | 441/1371 | chr19 | 4512638 | |||
chr19:4512639 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1321A>G | p.Thr441Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1440/6502 | 1321/4116 | 441/1371 | chr19 | 4512639 | |||
chr19:4512642 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1318G>C | p.Val440Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1437/6502 | 1318/4116 | 440/1371 | chr19 | 4512642 | |||
chr19:4512647 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1313G>C | p.Ser438Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1432/6502 | 1313/4116 | 438/1371 | chr19 | 4512647 | |||
chr19:4512650 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1310G>C | p.Cys437Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1429/6502 | 1310/4116 | 437/1371 | chr19 | 4512650 | |||
chr19:4512651 | A | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1309T>A | p.Cys437Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1428/6502 | 1309/4116 | 437/1371 | chr19 | 4512651 | |||
chr19:4512657 | T | C | 12 | a0001 a0003 a0006 others(9): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
missense_variant | MODERATE | c.1303A>G | p.Thr435Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1422/6502 | 1303/4116 | 435/1371 | chr19 | 4512657 | |||
chr19:4512674 | G | A | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1286C>T | p.Ala429Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1405/6502 | 1286/4116 | 429/1371 | chr19 | 4512674 | |||
chr19:4512675 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1285G>C | p.Ala429Pro | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1404/6502 | 1285/4116 | 429/1371 | chr19 | 4512675 | |||
chr19:4512676 | G | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1284C>G | p.Ile428Met | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1403/6502 | 1284/4116 | 428/1371 | chr19 | 4512676 | |||
chr19:4512678 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1282A>G | p.Ile428Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1401/6502 | 1282/4116 | 428/1371 | chr19 | 4512678 | |||
chr19:4512680 | T | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1280A>C | p.Asn427Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1399/6502 | 1280/4116 | 427/1371 | chr19 | 4512680 | |||
chr19:4512684 | G | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1276C>A | p.Gln426Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1395/6502 | 1276/4116 | 426/1371 | chr19 | 4512684 | |||
chr19:4512687 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1273A>G | p.Thr425Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1392/6502 | 1273/4116 | 425/1371 | chr19 | 4512687 | |||
chr19:4512693 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1267A>G | p.Asn423Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1386/6502 | 1267/4116 | 423/1371 | chr19 | 4512693 | |||
chr19:4512696 | G | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1264C>G | p.Leu422Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1383/6502 | 1264/4116 | 422/1371 | chr19 | 4512696 | |||
chr19:4512706 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1254G>C | p.Met418Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1373/6502 | 1254/4116 | 418/1371 | chr19 | 4512706 | |||
chr19:4512708 | T | C | 2 | a0032 a0036 |
2 | HG02723.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.1252A>G | p.Met418Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1371/6502 | 1252/4116 | 418/1371 | chr19 | 4512708 | |||
chr19:4512769 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1191G>A | p.Met397Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1310/6502 | 1191/4116 | 397/1371 | chr19 | 4512769 | |||
chr19:4512777 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1183A>G | p.Met395Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1302/6502 | 1183/4116 | 395/1371 | chr19 | 4512777 | |||
chr19:4512807 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1153A>G | p.Ile385Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1272/6502 | 1153/4116 | 385/1371 | chr19 | 4512807 | |||
chr19:4512812 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1148A>G | p.Glu383Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1267/6502 | 1148/4116 | 383/1371 | chr19 | 4512812 | |||
chr19:4512822 | A | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1138T>G | p.Leu380Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1257/6502 | 1138/4116 | 380/1371 | chr19 | 4512822 | |||
chr19:4512834 | C | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1126G>A | p.Gly376Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1245/6502 | 1126/4116 | 376/1371 | chr19 | 4512834 | |||
chr19:4512847 | GCAGACAG others(191): Show |
G | 9 | a0003 a0005 a0031 others(6): Show |
14 | HG01884.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
disruptive_inframe_deletion | MODERATE | c.915_1112del | p.Ser306_Cys371del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1231/6502 | 915/4116 | 305/1371 | chr19 | 4512847 | |||
chr19:4512858 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1102A>G | p.Asn368Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1221/6502 | 1102/4116 | 368/1371 | chr19 | 4512858 | |||
chr19:4512884 | GTGGTGTC others(92): Show |
G | 5 | a0001 a0007 a0010 others(2): Show |
42 | HG00423.hp2 HG00741.hp2 HG01074.hp1 others(39): Show |
disruptive_inframe_deletion | MODERATE | c.977_1075delGTAAGAC others(92): Show |
p.Ser326_Thr358del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1194/6502 | 977/4116 | 326/1371 | chr19 | 4512884 | |||
chr19:4512884 | GTGGTGTC others(191): Show |
G | 1 | a0007 | 1 | HG02071.hp2 | disruptive_inframe_deletion | MODERATE | c.878_1075del | p.Ser293_Thr358del | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1194/6502 | 878/4116 | 293/1371 | chr19 | 4512884 | |||
chr19:4512906 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1054A>G | p.Ile352Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1173/6502 | 1054/4116 | 352/1371 | chr19 | 4512906 | |||
chr19:4512927 | T | C | 2 | a0001 a0032 |
6 | HG02027.hp1 HG02155.hp2 HG02723.hp2 others(3): Show |
missense_variant | MODERATE | c.1033A>G | p.Met345Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1152/6502 | 1033/4116 | 345/1371 | chr19 | 4512927 | |||
chr19:4512934 | A | AGTCACCC others(290): Show |
1 | a0034 | 1 | HG02886.hp1 | disruptive_inframe_insertion | MODERATE | c.1025_1026insCAGTGC others(291): Show |
p.Thr342_Gly343insSe others(295): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1144/6502 | 1025/4116 | 342/1371 | chr19 | 4512934 | |||
chr19:4512939 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1021G>C | p.Val341Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1140/6502 | 1021/4116 | 341/1371 | chr19 | 4512939 | |||
chr19:4512941 | C | A | 1 | a0001 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.1019G>T | p.Gly340Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1138/6502 | 1019/4116 | 340/1371 | chr19 | 4512941 | |||
chr19:4512944 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1016G>C | p.Ser339Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1135/6502 | 1016/4116 | 339/1371 | chr19 | 4512944 | |||
chr19:4512947 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1013G>C | p.Cys338Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1132/6502 | 1013/4116 | 338/1371 | chr19 | 4512947 | |||
chr19:4512953 | G | T | 2 | a0001 a0006 |
6 | HG00558.hp2 HG02129.hp1 NA18943.hp2 others(3): Show |
missense_variant | MODERATE | c.1007C>A | p.Thr336Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1126/6502 | 1007/4116 | 336/1371 | chr19 | 4512953 | |||
chr19:4512954 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1006A>G | p.Thr336Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1125/6502 | 1006/4116 | 336/1371 | chr19 | 4512954 | |||
chr19:4512978 | T | A | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.982A>T | p.Thr328Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1101/6502 | 982/4116 | 328/1371 | chr19 | 4512978 | |||
chr19:4512982 | A | T | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.978T>A | p.Ser326Arg | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1097/6502 | 978/4116 | 326/1371 | chr19 | 4512982 | |||
chr19:4512983 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.977G>C | p.Ser326Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1096/6502 | 977/4116 | 326/1371 | chr19 | 4512983 | |||
chr19:4512993 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.967G>C | p.Val323Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1086/6502 | 967/4116 | 323/1371 | chr19 | 4512993 | |||
chr19:4512998 | G | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.962C>G | p.Thr321Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1081/6502 | 962/4116 | 321/1371 | chr19 | 4512998 | |||
chr19:4512999 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.961A>G | p.Thr321Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1080/6502 | 961/4116 | 321/1371 | chr19 | 4512999 | |||
chr19:4513005 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.955A>G | p.Ile319Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1074/6502 | 955/4116 | 319/1371 | chr19 | 4513005 | |||
chr19:4513008 | T | C | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.952A>G | p.Thr318Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1071/6502 | 952/4116 | 318/1371 | chr19 | 4513008 | |||
chr19:4513025 | A | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.935T>C | p.Met312Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1054/6502 | 935/4116 | 312/1371 | chr19 | 4513025 | |||
chr19:4513026 | T | C | 13 | a0001 a0004 a0005 others(10): Show |
43 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(40): Show |
missense_variant | MODERATE | c.934A>G | p.Met312Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1053/6502 | 934/4116 | 312/1371 | chr19 | 4513026 | |||
chr19:4513032 | C | T | 1 | a0026 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.928G>A | p.Gly310Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1047/6502 | 928/4116 | 310/1371 | chr19 | 4513032 | |||
chr19:4513076 | G | A | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.884C>T | p.Thr295Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1003/6502 | 884/4116 | 295/1371 | chr19 | 4513076 | |||
chr19:4513082 | C | G | 1 | a0032 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.878G>C | p.Ser293Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 997/6502 | 878/4116 | 293/1371 | chr19 | 4513082 | |||
chr19:4513131 | C | T | 41 | a0001 a0002 a0003 others(38): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
missense_variant | MODERATE | c.829G>A | p.Gly277Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 948/6502 | 829/4116 | 277/1371 | chr19 | 4513131 | |||
chr19:4513132 | A | AGTCACCC others(191): Show |
1 | a0021 | 2 | NA18955.hp1 NA18990.hp2 |
disruptive_inframe_insertion | MODERATE | c.827_828insCAGTGCCA others(190): Show |
p.Thr276_Gly277insSe others(196): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 946/6502 | 827/4116 | 276/1371 | chr19 | 4513132 | |||
chr19:4513132 | A | AGTCACCC others(92): Show |
2 | a0016 a0026 |
3 | HG01496.hp1 HG02074.hp1 NA19079.hp2 |
disruptive_inframe_insertion | MODERATE | c.827_828insCAGTGCCA others(91): Show |
p.Thr276_Gly277insSe others(97): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 946/6502 | 827/4116 | 276/1371 | chr19 | 4513132 | |||
chr19:4513136 | A | G | 2 | a0040 a0046 |
2 | HG06807.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.824T>C | p.Val275Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 943/6502 | 824/4116 | 275/1371 | chr19 | 4513136 | |||
chr19:4513185 | T | C | 1 | a0039 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.775A>G | p.Thr259Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 894/6502 | 775/4116 | 259/1371 | chr19 | 4513185 | |||
chr19:4513198 | C | A | 1 | a0044 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.762G>T | p.Gln254His | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 881/6502 | 762/4116 | 254/1371 | chr19 | 4513198 | |||
chr19:4513401 | C | T | 2 | a0020 a0030 |
3 | HG02451.hp1 HG03516.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.559G>A | p.Val187Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 678/6502 | 559/4116 | 187/1371 | chr19 | 4513401 | |||
chr19:4513478 | G | A | 1 | a0024 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.482C>T | p.Ser161Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 601/6502 | 482/4116 | 161/1371 | chr19 | 4513478 | |||
chr19:4513547 | A | G | 43 | a0001 a0002 a0003 others(40): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
missense_variant | MODERATE | c.413T>C | p.Val138Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 532/6502 | 413/4116 | 138/1371 | chr19 | 4513547 | |||
chr19:4513562 | G | A | 1 | a0025 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.398C>T | p.Thr133Met | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 517/6502 | 398/4116 | 133/1371 | chr19 | 4513562 | |||
chr19:4516658 | T | C | 4 | a0031 a0041 a0042 others(1): Show |
4 | HG02572.hp2 NA18906.hp1 NA18906.hp2 others(1): Show |
missense_variant | MODERATE | c.217A>G | p.Thr73Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/8 | 336/6502 | 217/4116 | 73/1371 | chr19 | 4516658 | |||
chr19:4517637 | T | C | 2 | a0040 a0046 |
2 | HG06807.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.113A>G | p.Asn38Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/8 | 232/6502 | 113/4116 | 38/1371 | chr19 | 4517637 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4504462 | C | T | 2 | a0001c0069 a0007c0018 |
5 | HG01261.hp1 HG01346.hp2 HG01361.hp1 others(2): Show |
synonymous_variant | LOW | c.4113G>A | p.Gln1371Gln | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 4232/6502 | 4113/4116 | 1371/1371 | chr19 | 4504462 | |||
chr19:4508822 | G | A | 1 | a0001c0065 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.3648C>T | p.His1216His | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/8 | 3767/6502 | 3648/4116 | 1216/1371 | chr19 | 4508822 | |||
chr19:4508933 | A | G | 103 | a0001c0001 a0001c0002 a0001c0003 others(100): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
synonymous_variant | LOW | c.3537T>C | p.Pro1179Pro | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/8 | 3656/6502 | 3537/4116 | 1179/1371 | chr19 | 4508933 | |||
chr19:4508948 | C | T | 7 | a0008c0027 a0008c0034 a0008c0079 others(4): Show |
10 | HG00639.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
synonymous_variant | LOW | c.3522G>A | p.Leu1174Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/8 | 3641/6502 | 3522/4116 | 1174/1371 | chr19 | 4508948 | |||
chr19:4510465 | G | C | 1 | a0037c0060 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.3495C>G | p.Pro1165Pro | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3614/6502 | 3495/4116 | 1165/1371 | chr19 | 4510465 | |||
chr19:4510603 | G | A | 3 | a0001c0011 a0001c0072 a0007c0086 |
7 | HG02071.hp2 HG02293.hp2 HG02523.hp1 others(4): Show |
synonymous_variant | LOW | c.3357C>T | p.Asp1119Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3476/6502 | 3357/4116 | 1119/1371 | chr19 | 4510603 | |||
chr19:4510672 | C | T | 1 | a0001c0063 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.3288G>A | p.Pro1096Pro | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3407/6502 | 3288/4116 | 1096/1371 | chr19 | 4510672 | |||
chr19:4510711 | G | A | 14 | a0001c0003 a0001c0007 a0001c0016 others(11): Show |
45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
synonymous_variant | LOW | c.3249C>T | p.Ser1083Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3368/6502 | 3249/4116 | 1083/1371 | chr19 | 4510711 | |||
chr19:4510954 | G | A | 4 | a0001c0080 a0001c0100 a0006c0037 others(1): Show |
5 | HG03490.hp2 HG03492.hp1 HG03704.hp2 others(2): Show |
synonymous_variant | LOW | c.3006C>T | p.Thr1002Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3125/6502 | 3006/4116 | 1002/1371 | chr19 | 4510954 | |||
chr19:4511026 | G | A | 2 | a0008c0027 a0008c0034 |
5 | HG00639.hp2 HG02809.hp1 HG03041.hp1 others(2): Show |
synonymous_variant | LOW | c.2934C>T | p.Thr978Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 3053/6502 | 2934/4116 | 978/1371 | chr19 | 4511026 | |||
chr19:4511128 | C | G | 64 | a0001c0001 a0001c0003 a0001c0006 others(61): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
synonymous_variant | LOW | c.2832G>C | p.Gly944Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2951/6502 | 2832/4116 | 944/1371 | chr19 | 4511128 | |||
chr19:4511170 | G | A | 1 | a0040c0105 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.2790C>T | p.Thr930Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2909/6502 | 2790/4116 | 930/1371 | chr19 | 4511170 | |||
chr19:4511266 | C | T | 45 | a0001c0001 a0001c0003 a0001c0006 others(42): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
synonymous_variant | LOW | c.2694G>A | p.Val898Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2813/6502 | 2694/4116 | 898/1371 | chr19 | 4511266 | |||
chr19:4511269 | G | A | 19 | a0001c0004 a0001c0033 a0001c0044 others(16): Show |
32 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(29): Show |
synonymous_variant | LOW | c.2691C>T | p.Ala897Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2810/6502 | 2691/4116 | 897/1371 | chr19 | 4511269 | |||
chr19:4511272 | A | G | 44 | a0001c0001 a0001c0003 a0001c0006 others(41): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
synonymous_variant | LOW | c.2688T>C | p.Asp896Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2807/6502 | 2688/4116 | 896/1371 | chr19 | 4511272 | |||
chr19:4511329 | T | C | 37 | a0001c0001 a0001c0003 a0001c0006 others(34): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
synonymous_variant | LOW | c.2631A>G | p.Lys877Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2750/6502 | 2631/4116 | 877/1371 | chr19 | 4511329 | |||
chr19:4511341 | C | T | 1 | a0001c0002 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.2619G>A | p.Ala873Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2738/6502 | 2619/4116 | 873/1371 | chr19 | 4511341 | |||
chr19:4511353 | C | G | 6 | a0002c0010 a0002c0050 a0002c0054 others(3): Show |
11 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
synonymous_variant | LOW | c.2607G>C | p.Val869Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2726/6502 | 2607/4116 | 869/1371 | chr19 | 4511353 | |||
chr19:4511365 | A | G | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
synonymous_variant | LOW | c.2595T>C | p.Leu865Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2714/6502 | 2595/4116 | 865/1371 | chr19 | 4511365 | |||
chr19:4511377 | T | G | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
synonymous_variant | LOW | c.2583A>C | p.Thr861Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2702/6502 | 2583/4116 | 861/1371 | chr19 | 4511377 | |||
chr19:4511383 | T | A | 42 | a0001c0001 a0001c0003 a0001c0006 others(39): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
synonymous_variant | LOW | c.2577A>T | p.Thr859Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2696/6502 | 2577/4116 | 859/1371 | chr19 | 4511383 | |||
chr19:4511383 | T | C | 44 | a0001c0002 a0001c0004 a0001c0006 others(41): Show |
157 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(154): Show |
synonymous_variant | LOW | c.2577A>G | p.Thr859Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2696/6502 | 2577/4116 | 859/1371 | chr19 | 4511383 | |||
chr19:4511395 | T | C | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
synonymous_variant | LOW | c.2565A>G | p.Gln855Gln | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2684/6502 | 2565/4116 | 855/1371 | chr19 | 4511395 | |||
chr19:4511401 | C | G | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
synonymous_variant | LOW | c.2559G>C | p.Thr853Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2678/6502 | 2559/4116 | 853/1371 | chr19 | 4511401 | |||
chr19:4511410 | C | A | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.2550G>T | p.Gly850Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2669/6502 | 2550/4116 | 850/1371 | chr19 | 4511410 | |||
chr19:4511410 | C | G | 1 | a0020c0028 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.2550G>C | p.Gly850Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2669/6502 | 2550/4116 | 850/1371 | chr19 | 4511410 | |||
chr19:4511413 | A | G | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
synonymous_variant | LOW | c.2547T>C | p.Thr849Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2666/6502 | 2547/4116 | 849/1371 | chr19 | 4511413 | |||
chr19:4511416 | T | C | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
synonymous_variant | LOW | c.2544A>G | p.Gln848Gln | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2663/6502 | 2544/4116 | 848/1371 | chr19 | 4511416 | |||
chr19:4511419 | C | G | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
synonymous_variant | LOW | c.2541G>C | p.Val847Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2660/6502 | 2541/4116 | 847/1371 | chr19 | 4511419 | |||
chr19:4511422 | A | G | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.2538T>C | p.Ala846Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2657/6502 | 2538/4116 | 846/1371 | chr19 | 4511422 | |||
chr19:4511425 | A | C | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
synonymous_variant | LOW | c.2535T>G | p.Gly845Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2654/6502 | 2535/4116 | 845/1371 | chr19 | 4511425 | |||
chr19:4511428 | C | T | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.2532G>A | p.Lys844Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2651/6502 | 2532/4116 | 844/1371 | chr19 | 4511428 | |||
chr19:4511434 | C | G | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.2526G>C | p.Val842Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2645/6502 | 2526/4116 | 842/1371 | chr19 | 4511434 | |||
chr19:4511437 | G | A | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
synonymous_variant | LOW | c.2523C>T | p.Asn841Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2642/6502 | 2523/4116 | 841/1371 | chr19 | 4511437 | |||
chr19:4511443 | A | T | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.2517T>A | p.Ala839Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2636/6502 | 2517/4116 | 839/1371 | chr19 | 4511443 | |||
chr19:4511446 | A | C | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.2514T>G | p.Gly838Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2633/6502 | 2514/4116 | 838/1371 | chr19 | 4511446 | |||
chr19:4511449 | G | C | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.2511C>G | p.Thr837Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2630/6502 | 2511/4116 | 837/1371 | chr19 | 4511449 | |||
chr19:4511452 | G | A | 12 | a0001c0003 a0001c0007 a0001c0016 others(9): Show |
43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): Show |
synonymous_variant | LOW | c.2508C>T | p.Val836Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2627/6502 | 2508/4116 | 836/1371 | chr19 | 4511452 | |||
chr19:4511452 | G | C | 1 | a0020c0028 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.2508C>G | p.Val836Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2627/6502 | 2508/4116 | 836/1371 | chr19 | 4511452 | |||
chr19:4511461 | G | A | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.2499C>T | p.Cys833Cys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2618/6502 | 2499/4116 | 833/1371 | chr19 | 4511461 | |||
chr19:4511467 | A | G | 2 | a0002c0005 a0020c0028 |
2 | HG03540.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.2493T>C | p.Thr831Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2612/6502 | 2493/4116 | 831/1371 | chr19 | 4511467 | |||
chr19:4511467 | A | T | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.2493T>A | p.Thr831Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2612/6502 | 2493/4116 | 831/1371 | chr19 | 4511467 | |||
chr19:4511479 | A | G | 81 | a0001c0001 a0001c0002 a0001c0003 others(78): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.2481T>C | p.Gly827Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2600/6502 | 2481/4116 | 827/1371 | chr19 | 4511479 | |||
chr19:4511482 | G | A | 5 | a0004c0009 a0004c0026 a0004c0041 others(2): Show |
12 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
synonymous_variant | LOW | c.2478C>T | p.Thr826Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2597/6502 | 2478/4116 | 826/1371 | chr19 | 4511482 | |||
chr19:4511527 | C | T | 2 | a0001c0002 a0010c0024 |
3 | HG02258.hp2 HG02451.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.2433G>A | p.Lys811Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2552/6502 | 2433/4116 | 811/1371 | chr19 | 4511527 | |||
chr19:4511536 | A | G | 1 | a0018c0038 | 2 | HG03098.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.2424T>C | p.Asn808Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2543/6502 | 2424/4116 | 808/1371 | chr19 | 4511536 | |||
chr19:4511563 | C | G | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2397G>C | p.Val799Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2516/6502 | 2397/4116 | 799/1371 | chr19 | 4511563 | |||
chr19:4511566 | A | G | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2394T>C | p.Ala798Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2513/6502 | 2394/4116 | 798/1371 | chr19 | 4511566 | |||
chr19:4511569 | A | G | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2391T>C | p.Asp797Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2510/6502 | 2391/4116 | 797/1371 | chr19 | 4511569 | |||
chr19:4511586 | A | G | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2374T>C | p.Leu792Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2493/6502 | 2374/4116 | 792/1371 | chr19 | 4511586 | |||
chr19:4511587 | C | G | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2373G>C | p.Val791Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2492/6502 | 2373/4116 | 791/1371 | chr19 | 4511587 | |||
chr19:4511608 | G | A | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2352C>T | p.Gly784Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2471/6502 | 2352/4116 | 784/1371 | chr19 | 4511608 | |||
chr19:4511620 | A | G | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2340T>C | p.Thr780Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2459/6502 | 2340/4116 | 780/1371 | chr19 | 4511620 | |||
chr19:4511641 | A | T | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2319T>A | p.Ala773Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2438/6502 | 2319/4116 | 773/1371 | chr19 | 4511641 | |||
chr19:4511647 | T | C | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2313A>G | p.Thr771Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2432/6502 | 2313/4116 | 771/1371 | chr19 | 4511647 | |||
chr19:4511659 | G | A | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2301C>T | p.Ser767Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2420/6502 | 2301/4116 | 767/1371 | chr19 | 4511659 | |||
chr19:4511662 | C | G | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2298G>C | p.Val766Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2417/6502 | 2298/4116 | 766/1371 | chr19 | 4511662 | |||
chr19:4511665 | A | G | 4 | a0002c0005 a0029c0089 a0038c0051 others(1): Show |
12 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
synonymous_variant | LOW | c.2295T>C | p.Ala765Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2414/6502 | 2295/4116 | 765/1371 | chr19 | 4511665 | |||
chr19:4511665 | A | T | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2295T>A | p.Ala765Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2414/6502 | 2295/4116 | 765/1371 | chr19 | 4511665 | |||
chr19:4511668 | A | G | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2292T>C | p.Asp764Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2411/6502 | 2292/4116 | 764/1371 | chr19 | 4511668 | |||
chr19:4511671 | T | C | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2289A>G | p.Lys763Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2408/6502 | 2289/4116 | 763/1371 | chr19 | 4511671 | |||
chr19:4511674 | A | G | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2286T>C | p.Thr762Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2405/6502 | 2286/4116 | 762/1371 | chr19 | 4511674 | |||
chr19:4511680 | A | G | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2280T>C | p.Thr760Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2399/6502 | 2280/4116 | 760/1371 | chr19 | 4511680 | |||
chr19:4511685 | G | A | 4 | a0031c0104 a0036c0061 a0041c0103 others(1): Show |
4 | HG02572.hp2 HG02976.hp1 NA18906.hp1 others(1): Show |
synonymous_variant | LOW | c.2275C>T | p.Leu759Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2394/6502 | 2275/4116 | 759/1371 | chr19 | 4511685 | |||
chr19:4511686 | G | C | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2274C>G | p.Val758Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2393/6502 | 2274/4116 | 758/1371 | chr19 | 4511686 | |||
chr19:4511689 | A | G | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2271T>C | p.Ser757Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2390/6502 | 2271/4116 | 757/1371 | chr19 | 4511689 | |||
chr19:4511695 | T | G | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2265A>C | p.Thr755Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2384/6502 | 2265/4116 | 755/1371 | chr19 | 4511695 | |||
chr19:4511698 | A | C | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2262T>G | p.Thr754Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2381/6502 | 2262/4116 | 754/1371 | chr19 | 4511698 | |||
chr19:4511704 | C | T | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2256G>A | p.Leu752Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2375/6502 | 2256/4116 | 752/1371 | chr19 | 4511704 | |||
chr19:4511707 | G | A | 2 | a0012c0015 a0043c0062 |
5 | NA18963.hp1 NA18993.hp1 NA18997.hp1 others(2): Show |
synonymous_variant | LOW | c.2253C>T | p.Gly751Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2372/6502 | 2253/4116 | 751/1371 | chr19 | 4511707 | |||
chr19:4511713 | T | C | 72 | a0001c0001 a0001c0002 a0001c0003 others(69): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
synonymous_variant | LOW | c.2247A>G | p.Gln749Gln | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2366/6502 | 2247/4116 | 749/1371 | chr19 | 4511713 | |||
chr19:4511725 | T | C | 3 | a0012c0015 a0019c0081 a0043c0062 |
6 | HG03130.hp1 NA18963.hp1 NA18993.hp1 others(3): Show |
synonymous_variant | LOW | c.2235A>G | p.Lys745Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2354/6502 | 2235/4116 | 745/1371 | chr19 | 4511725 | |||
chr19:4511779 | A | C | 3 | a0003c0067 a0013c0046 a0019c0077 |
3 | HG01978.hp2 HG02055.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.2181T>G | p.Thr727Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2300/6502 | 2181/4116 | 727/1371 | chr19 | 4511779 | |||
chr19:4511818 | A | G | 14 | a0002c0050 a0003c0067 a0004c0041 others(11): Show |
22 | HG00735.hp2 HG01109.hp1 HG01884.hp1 others(19): Show |
synonymous_variant | LOW | c.2142T>C | p.Thr714Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2261/6502 | 2142/4116 | 714/1371 | chr19 | 4511818 | |||
chr19:4511848 | G | A | 1 | a0019c0081 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.2112C>T | p.Leu704Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2231/6502 | 2112/4116 | 704/1371 | chr19 | 4511848 | |||
chr19:4511878 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.2082C>T | p.Thr694Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2201/6502 | 2082/4116 | 694/1371 | chr19 | 4511878 | |||
chr19:4511896 | C | T | 41 | a0001c0001 a0001c0006 a0001c0007 others(38): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
synonymous_variant | LOW | c.2064G>A | p.Thr688Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2183/6502 | 2064/4116 | 688/1371 | chr19 | 4511896 | |||
chr19:4511908 | T | C | 16 | a0002c0005 a0002c0010 a0002c0050 others(13): Show |
31 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(28): Show |
synonymous_variant | LOW | c.2052A>G | p.Thr684Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2171/6502 | 2052/4116 | 684/1371 | chr19 | 4511908 | |||
chr19:4511917 | A | G | 55 | a0001c0001 a0001c0006 a0001c0007 others(52): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
synonymous_variant | LOW | c.2043T>C | p.Ala681Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2162/6502 | 2043/4116 | 681/1371 | chr19 | 4511917 | |||
chr19:4511932 | A | G | 1 | a0018c0038 | 2 | HG03098.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.2028T>C | p.Asn676Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2147/6502 | 2028/4116 | 676/1371 | chr19 | 4511932 | |||
chr19:4511947 | C | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.2013G>C | p.Val671Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2132/6502 | 2013/4116 | 671/1371 | chr19 | 4511947 | |||
chr19:4511980 | C | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1980G>A | p.Ala660Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2099/6502 | 1980/4116 | 660/1371 | chr19 | 4511980 | |||
chr19:4511995 | C | T | 3 | a0005c0019 a0005c0032 a0005c0076 |
6 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
synonymous_variant | LOW | c.1965G>A | p.Thr655Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2084/6502 | 1965/4116 | 655/1371 | chr19 | 4511995 | |||
chr19:4512019 | C | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1941G>T | p.Gly647Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2060/6502 | 1941/4116 | 647/1371 | chr19 | 4512019 | |||
chr19:4512037 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1923C>T | p.Ala641Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2042/6502 | 1923/4116 | 641/1371 | chr19 | 4512037 | |||
chr19:4512061 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1899C>T | p.Thr633Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2018/6502 | 1899/4116 | 633/1371 | chr19 | 4512061 | |||
chr19:4512079 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1881A>G | p.Leu627Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 2000/6502 | 1881/4116 | 627/1371 | chr19 | 4512079 | |||
chr19:4512082 | G | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1878C>G | p.Val626Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1997/6502 | 1878/4116 | 626/1371 | chr19 | 4512082 | |||
chr19:4512085 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1875T>C | p.Thr625Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1994/6502 | 1875/4116 | 625/1371 | chr19 | 4512085 | |||
chr19:4512088 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1872A>G | p.Lys624Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1991/6502 | 1872/4116 | 624/1371 | chr19 | 4512088 | |||
chr19:4512094 | G | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1866C>G | p.Thr622Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1985/6502 | 1866/4116 | 622/1371 | chr19 | 4512094 | |||
chr19:4512103 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1857C>T | p.Gly619Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1976/6502 | 1857/4116 | 619/1371 | chr19 | 4512103 | |||
chr19:4512106 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1854A>G | p.Thr618Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1973/6502 | 1854/4116 | 618/1371 | chr19 | 4512106 | |||
chr19:4512115 | G | A | 1 | a0002c0005 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1845C>T | p.Thr615Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1964/6502 | 1845/4116 | 615/1371 | chr19 | 4512115 | |||
chr19:4512121 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1839A>G | p.Lys613Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1958/6502 | 1839/4116 | 613/1371 | chr19 | 4512121 | |||
chr19:4512127 | G | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1833C>G | p.Val611Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1952/6502 | 1833/4116 | 611/1371 | chr19 | 4512127 | |||
chr19:4512136 | T | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1824A>T | p.Ala608Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1943/6502 | 1824/4116 | 608/1371 | chr19 | 4512136 | |||
chr19:4512139 | C | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1821G>T | p.Gly607Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1940/6502 | 1821/4116 | 607/1371 | chr19 | 4512139 | |||
chr19:4512142 | C | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1818G>C | p.Val606Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1937/6502 | 1818/4116 | 606/1371 | chr19 | 4512142 | |||
chr19:4512145 | G | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1815C>G | p.Leu605Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1934/6502 | 1815/4116 | 605/1371 | chr19 | 4512145 | |||
chr19:4512154 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1806T>C | p.Thr602Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1925/6502 | 1806/4116 | 602/1371 | chr19 | 4512154 | |||
chr19:4512157 | C | G | 3 | a0002c0005 a0011c0021 a0011c0030 |
6 | HG02572.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
synonymous_variant | LOW | c.1803G>C | p.Val601Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1922/6502 | 1803/4116 | 601/1371 | chr19 | 4512157 | |||
chr19:4512160 | T | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1800A>T | p.Thr600Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1919/6502 | 1800/4116 | 600/1371 | chr19 | 4512160 | |||
chr19:4512163 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1797C>T | p.Asp599Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1916/6502 | 1797/4116 | 599/1371 | chr19 | 4512163 | |||
chr19:4512166 | C | T | 6 | a0031c0104 a0036c0061 a0037c0060 others(3): Show |
6 | HG02572.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
synonymous_variant | LOW | c.1794G>A | p.Lys598Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1913/6502 | 1794/4116 | 598/1371 | chr19 | 4512166 | |||
chr19:4512172 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1788C>T | p.Gly596Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1907/6502 | 1788/4116 | 596/1371 | chr19 | 4512172 | |||
chr19:4512175 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1785C>T | p.Thr595Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1904/6502 | 1785/4116 | 595/1371 | chr19 | 4512175 | |||
chr19:4512178 | C | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1782G>A | p.Leu594Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1901/6502 | 1782/4116 | 594/1371 | chr19 | 4512178 | |||
chr19:4512180 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1780C>T | p.Leu594Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1899/6502 | 1780/4116 | 594/1371 | chr19 | 4512180 | |||
chr19:4512184 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1776C>T | p.Thr592Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1895/6502 | 1776/4116 | 592/1371 | chr19 | 4512184 | |||
chr19:4512193 | T | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1767A>C | p.Thr589Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1886/6502 | 1767/4116 | 589/1371 | chr19 | 4512193 | |||
chr19:4512199 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1761A>G | p.Val587Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1880/6502 | 1761/4116 | 587/1371 | chr19 | 4512199 | |||
chr19:4512202 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1758T>C | p.Gly586Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1877/6502 | 1758/4116 | 586/1371 | chr19 | 4512202 | |||
chr19:4512205 | T | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1755A>C | p.Thr585Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1874/6502 | 1755/4116 | 585/1371 | chr19 | 4512205 | |||
chr19:4512214 | A | G | 1 | a0030c0045 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1746T>C | p.Ala582Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1865/6502 | 1746/4116 | 582/1371 | chr19 | 4512214 | |||
chr19:4512220 | C | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1740G>A | p.Lys580Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1859/6502 | 1740/4116 | 580/1371 | chr19 | 4512220 | |||
chr19:4512235 | T | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1725A>T | p.Ala575Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1844/6502 | 1725/4116 | 575/1371 | chr19 | 4512235 | |||
chr19:4512241 | C | T | 7 | a0031c0104 a0032c0056 a0034c0058 others(4): Show |
7 | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
synonymous_variant | LOW | c.1719G>A | p.Thr573Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1838/6502 | 1719/4116 | 573/1371 | chr19 | 4512241 | |||
chr19:4512259 | C | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1701G>T | p.Thr567Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1820/6502 | 1701/4116 | 567/1371 | chr19 | 4512259 | |||
chr19:4512262 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1698C>T | p.Asp566Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1817/6502 | 1698/4116 | 566/1371 | chr19 | 4512262 | |||
chr19:4512268 | T | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1692A>T | p.Thr564Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1811/6502 | 1692/4116 | 564/1371 | chr19 | 4512268 | |||
chr19:4512271 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1689T>C | p.Gly563Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1808/6502 | 1689/4116 | 563/1371 | chr19 | 4512271 | |||
chr19:4512274 | T | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1686A>T | p.Ile562Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1805/6502 | 1686/4116 | 562/1371 | chr19 | 4512274 | |||
chr19:4512277 | G | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1683C>G | p.Val561Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1802/6502 | 1683/4116 | 561/1371 | chr19 | 4512277 | |||
chr19:4512280 | C | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1680G>C | p.Val560Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1799/6502 | 1680/4116 | 560/1371 | chr19 | 4512280 | |||
chr19:4512289 | G | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1671C>A | p.Thr557Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1790/6502 | 1671/4116 | 557/1371 | chr19 | 4512289 | |||
chr19:4512292 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1668C>T | p.Thr556Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1787/6502 | 1668/4116 | 556/1371 | chr19 | 4512292 | |||
chr19:4512307 | C | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1653G>A | p.Gln551Gln | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1772/6502 | 1653/4116 | 551/1371 | chr19 | 4512307 | |||
chr19:4512319 | T | C | 2 | a0019c0077 a0019c0081 |
2 | HG03130.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.1641A>G | p.Lys547Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1760/6502 | 1641/4116 | 547/1371 | chr19 | 4512319 | |||
chr19:4512328 | G | A | 3 | a0019c0077 a0019c0081 a0032c0056 |
3 | HG02723.hp2 HG03130.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.1632C>T | p.Asn544Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1751/6502 | 1632/4116 | 544/1371 | chr19 | 4512328 | |||
chr19:4512355 | G | C | 2 | a0019c0077 a0019c0081 |
2 | HG03130.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.1605C>G | p.Val535Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1724/6502 | 1605/4116 | 535/1371 | chr19 | 4512355 | |||
chr19:4512358 | G | A | 2 | a0019c0077 a0019c0081 |
2 | HG03130.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.1602C>T | p.Thr534Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1721/6502 | 1602/4116 | 534/1371 | chr19 | 4512358 | |||
chr19:4512361 | G | A | 2 | a0019c0077 a0019c0081 |
2 | HG03130.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.1599C>T | p.Asp533Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1718/6502 | 1599/4116 | 533/1371 | chr19 | 4512361 | |||
chr19:4512370 | G | A | 3 | a0019c0077 a0019c0081 a0032c0056 |
3 | HG02723.hp2 HG03130.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.1590C>T | p.Gly530Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1709/6502 | 1590/4116 | 530/1371 | chr19 | 4512370 | |||
chr19:4512373 | G | A | 3 | a0019c0077 a0019c0081 a0032c0056 |
3 | HG02723.hp2 HG03130.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.1587C>T | p.Thr529Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1706/6502 | 1587/4116 | 529/1371 | chr19 | 4512373 | |||
chr19:4512378 | G | A | 2 | a0019c0077 a0019c0081 |
2 | HG03130.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.1582C>T | p.Leu528Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1701/6502 | 1582/4116 | 528/1371 | chr19 | 4512378 | |||
chr19:4512379 | G | C | 2 | a0019c0077 a0019c0081 |
2 | HG03130.hp1 HG04199.hp2 |
synonymous_variant | LOW | c.1581C>G | p.Val527Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1700/6502 | 1581/4116 | 527/1371 | chr19 | 4512379 | |||
chr19:4512397 | T | C | 20 | a0001c0033 a0001c0090 a0002c0005 others(17): Show |
37 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(34): Show |
synonymous_variant | LOW | c.1563A>G | p.Val521Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1682/6502 | 1563/4116 | 521/1371 | chr19 | 4512397 | |||
chr19:4512400 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1560C>T | p.Gly520Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1679/6502 | 1560/4116 | 520/1371 | chr19 | 4512400 | |||
chr19:4512412 | G | A | 5 | a0002c0055 a0005c0076 a0019c0077 others(2): Show |
5 | HG02559.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
synonymous_variant | LOW | c.1548C>T | p.Thr516Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1667/6502 | 1548/4116 | 516/1371 | chr19 | 4512412 | |||
chr19:4512424 | C | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1536G>C | p.Val512Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1655/6502 | 1536/4116 | 512/1371 | chr19 | 4512424 | |||
chr19:4512427 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1533C>T | p.Asn511Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1652/6502 | 1533/4116 | 511/1371 | chr19 | 4512427 | |||
chr19:4512433 | A | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1527T>A | p.Ala509Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1646/6502 | 1527/4116 | 509/1371 | chr19 | 4512433 | |||
chr19:4512439 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1521A>G | p.Thr507Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1640/6502 | 1521/4116 | 507/1371 | chr19 | 4512439 | |||
chr19:4512451 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1509C>T | p.Ser503Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1628/6502 | 1509/4116 | 503/1371 | chr19 | 4512451 | |||
chr19:4512454 | C | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1506G>C | p.Val502Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1625/6502 | 1506/4116 | 502/1371 | chr19 | 4512454 | |||
chr19:4512457 | A | G | 1 | a0013c0046 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1503T>C | p.Ala501Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1622/6502 | 1503/4116 | 501/1371 | chr19 | 4512457 | |||
chr19:4512457 | A | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1503T>A | p.Ala501Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1622/6502 | 1503/4116 | 501/1371 | chr19 | 4512457 | |||
chr19:4512460 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1500T>C | p.Asp500Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1619/6502 | 1500/4116 | 500/1371 | chr19 | 4512460 | |||
chr19:4512463 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1497A>G | p.Lys499Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1616/6502 | 1497/4116 | 499/1371 | chr19 | 4512463 | |||
chr19:4512466 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1494T>C | p.Thr498Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1613/6502 | 1494/4116 | 498/1371 | chr19 | 4512466 | |||
chr19:4512472 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1488T>C | p.Thr496Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1607/6502 | 1488/4116 | 496/1371 | chr19 | 4512472 | |||
chr19:4512478 | G | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1482C>G | p.Val494Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1601/6502 | 1482/4116 | 494/1371 | chr19 | 4512478 | |||
chr19:4512481 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1479T>C | p.Ser493Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1598/6502 | 1479/4116 | 493/1371 | chr19 | 4512481 | |||
chr19:4512487 | T | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1473A>C | p.Thr491Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1592/6502 | 1473/4116 | 491/1371 | chr19 | 4512487 | |||
chr19:4512490 | A | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1470T>G | p.Thr490Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1589/6502 | 1470/4116 | 490/1371 | chr19 | 4512490 | |||
chr19:4512496 | C | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1464G>A | p.Leu488Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1583/6502 | 1464/4116 | 488/1371 | chr19 | 4512496 | |||
chr19:4512499 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1461C>T | p.Gly487Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1580/6502 | 1461/4116 | 487/1371 | chr19 | 4512499 | |||
chr19:4512502 | G | C | 43 | a0001c0003 a0001c0004 a0001c0012 others(40): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
synonymous_variant | LOW | c.1458C>G | p.Gly486Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1577/6502 | 1458/4116 | 486/1371 | chr19 | 4512502 | |||
chr19:4512511 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1449C>T | p.Ala483Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1568/6502 | 1449/4116 | 483/1371 | chr19 | 4512511 | |||
chr19:4512529 | C | T | 1 | a0001c0022 | 3 | HG02155.hp1 NA18951.hp2 NA18977.hp1 |
synonymous_variant | LOW | c.1431G>A | p.Ala477Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1550/6502 | 1431/4116 | 477/1371 | chr19 | 4512529 | |||
chr19:4512541 | G | C | 3 | a0008c0034 a0011c0021 a0011c0030 |
7 | HG00639.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
synonymous_variant | LOW | c.1419C>G | p.Val473Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1538/6502 | 1419/4116 | 473/1371 | chr19 | 4512541 | |||
chr19:4512556 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1404T>C | p.Thr468Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1523/6502 | 1404/4116 | 468/1371 | chr19 | 4512556 | |||
chr19:4512571 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1389T>C | p.Thr463Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1508/6502 | 1389/4116 | 463/1371 | chr19 | 4512571 | |||
chr19:4512577 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1383T>C | p.Val461Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1502/6502 | 1383/4116 | 461/1371 | chr19 | 4512577 | |||
chr19:4512580 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1380C>T | p.Ile460Ile | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1499/6502 | 1380/4116 | 460/1371 | chr19 | 4512580 | |||
chr19:4512583 | C | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1377G>A | p.Lys459Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1496/6502 | 1377/4116 | 459/1371 | chr19 | 4512583 | |||
chr19:4512613 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1347A>G | p.Gly449Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1466/6502 | 1347/4116 | 449/1371 | chr19 | 4512613 | |||
chr19:4512625 | A | G | 14 | a0003c0075 a0005c0019 a0005c0032 others(11): Show |
18 | HG01884.hp2 HG02109.hp2 HG02559.hp1 others(15): Show |
synonymous_variant | LOW | c.1335T>C | p.Asn445Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1454/6502 | 1335/4116 | 445/1371 | chr19 | 4512625 | |||
chr19:4512631 | G | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1329C>A | p.Ala443Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1448/6502 | 1329/4116 | 443/1371 | chr19 | 4512631 | |||
chr19:4512634 | A | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1326T>G | p.Gly442Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1445/6502 | 1326/4116 | 442/1371 | chr19 | 4512634 | |||
chr19:4512637 | A | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1323T>G | p.Thr441Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1442/6502 | 1323/4116 | 441/1371 | chr19 | 4512637 | |||
chr19:4512640 | C | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1320G>C | p.Val440Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1439/6502 | 1320/4116 | 440/1371 | chr19 | 4512640 | |||
chr19:4512649 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1311C>T | p.Cys437Cys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1430/6502 | 1311/4116 | 437/1371 | chr19 | 4512649 | |||
chr19:4512652 | G | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1308C>G | p.Val436Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1427/6502 | 1308/4116 | 436/1371 | chr19 | 4512652 | |||
chr19:4512655 | G | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1305C>A | p.Thr435Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1424/6502 | 1305/4116 | 435/1371 | chr19 | 4512655 | |||
chr19:4512664 | T | G | 2 | a0001c0007 a0032c0056 |
5 | HG02683.hp1 HG02723.hp2 HG03942.hp1 others(2): Show |
synonymous_variant | LOW | c.1296A>C | p.Thr432Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1415/6502 | 1296/4116 | 432/1371 | chr19 | 4512664 | |||
chr19:4512667 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1293T>C | p.Gly431Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1412/6502 | 1293/4116 | 431/1371 | chr19 | 4512667 | |||
chr19:4512670 | T | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1290A>C | p.Thr430Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1409/6502 | 1290/4116 | 430/1371 | chr19 | 4512670 | |||
chr19:4512673 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1287A>G | p.Ala429Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1406/6502 | 1287/4116 | 429/1371 | chr19 | 4512673 | |||
chr19:4512679 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1281T>C | p.Asn427Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1400/6502 | 1281/4116 | 427/1371 | chr19 | 4512679 | |||
chr19:4512682 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1278A>G | p.Gln426Gln | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1397/6502 | 1278/4116 | 426/1371 | chr19 | 4512682 | |||
chr19:4512694 | C | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1266G>A | p.Leu422Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1385/6502 | 1266/4116 | 422/1371 | chr19 | 4512694 | |||
chr19:4512697 | C | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1263G>T | p.Gly421Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1382/6502 | 1263/4116 | 421/1371 | chr19 | 4512697 | |||
chr19:4512700 | A | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1260T>A | p.Thr420Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1379/6502 | 1260/4116 | 420/1371 | chr19 | 4512700 | |||
chr19:4512703 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1257A>G | p.Gln419Gln | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1376/6502 | 1257/4116 | 419/1371 | chr19 | 4512703 | |||
chr19:4512709 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1251C>T | p.Ala417Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1370/6502 | 1251/4116 | 417/1371 | chr19 | 4512709 | |||
chr19:4512736 | T | C | 8 | a0001c0001 a0001c0003 a0001c0004 others(5): Show |
24 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(21): Show |
synonymous_variant | LOW | c.1224A>G | p.Thr408Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1343/6502 | 1224/4116 | 408/1371 | chr19 | 4512736 | |||
chr19:4512763 | C | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1197G>A | p.Thr399Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1316/6502 | 1197/4116 | 399/1371 | chr19 | 4512763 | |||
chr19:4512784 | G | C | 1 | a0005c0032 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1176C>G | p.Thr392Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1295/6502 | 1176/4116 | 392/1371 | chr19 | 4512784 | |||
chr19:4512790 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1170T>C | p.Asp390Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1289/6502 | 1170/4116 | 390/1371 | chr19 | 4512790 | |||
chr19:4512829 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1131C>T | p.Ala377Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1250/6502 | 1131/4116 | 377/1371 | chr19 | 4512829 | |||
chr19:4512853 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1107T>C | p.Thr369Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1226/6502 | 1107/4116 | 369/1371 | chr19 | 4512853 | |||
chr19:4512868 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1092T>C | p.Thr364Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1211/6502 | 1092/4116 | 364/1371 | chr19 | 4512868 | |||
chr19:4512910 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1050A>G | p.Gly350Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1169/6502 | 1050/4116 | 350/1371 | chr19 | 4512910 | |||
chr19:4512922 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1038T>C | p.Asn346Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1157/6502 | 1038/4116 | 346/1371 | chr19 | 4512922 | |||
chr19:4512928 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1032C>T | p.Ala344Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1151/6502 | 1032/4116 | 344/1371 | chr19 | 4512928 | |||
chr19:4512931 | A | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1029T>G | p.Gly343Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1148/6502 | 1029/4116 | 343/1371 | chr19 | 4512931 | |||
chr19:4512934 | A | G | 1 | a0001c0016 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.1026T>C | p.Thr342Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1145/6502 | 1026/4116 | 342/1371 | chr19 | 4512934 | |||
chr19:4512934 | A | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1026T>A | p.Thr342Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1145/6502 | 1026/4116 | 342/1371 | chr19 | 4512934 | |||
chr19:4512937 | C | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1023G>C | p.Val341Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1142/6502 | 1023/4116 | 341/1371 | chr19 | 4512937 | |||
chr19:4512946 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1014T>C | p.Cys338Cys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1133/6502 | 1014/4116 | 338/1371 | chr19 | 4512946 | |||
chr19:4512949 | G | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1011C>G | p.Val337Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1130/6502 | 1011/4116 | 337/1371 | chr19 | 4512949 | |||
chr19:4512952 | G | A | 2 | a0001c0001 a0032c0056 |
2 | HG02723.hp2 HG04204.hp1 |
synonymous_variant | LOW | c.1008C>T | p.Thr336Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1127/6502 | 1008/4116 | 336/1371 | chr19 | 4512952 | |||
chr19:4512955 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1005C>T | p.Asp335Asp | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1124/6502 | 1005/4116 | 335/1371 | chr19 | 4512955 | |||
chr19:4512958 | C | T | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1002G>A | p.Lys334Lys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1121/6502 | 1002/4116 | 334/1371 | chr19 | 4512958 | |||
chr19:4512961 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.999C>T | p.Thr333Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1118/6502 | 999/4116 | 333/1371 | chr19 | 4512961 | |||
chr19:4512964 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.996T>C | p.Gly332Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1115/6502 | 996/4116 | 332/1371 | chr19 | 4512964 | |||
chr19:4512967 | T | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.993A>T | p.Thr331Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1112/6502 | 993/4116 | 331/1371 | chr19 | 4512967 | |||
chr19:4512970 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.990A>G | p.Leu330Leu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1109/6502 | 990/4116 | 330/1371 | chr19 | 4512970 | |||
chr19:4512985 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.975C>T | p.Thr325Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1094/6502 | 975/4116 | 325/1371 | chr19 | 4512985 | |||
chr19:4512997 | G | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.963C>G | p.Thr321Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1082/6502 | 963/4116 | 321/1371 | chr19 | 4512997 | |||
chr19:4513009 | T | C | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.951A>G | p.Gly317Gly | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1070/6502 | 951/4116 | 317/1371 | chr19 | 4513009 | |||
chr19:4513021 | A | G | 23 | a0001c0003 a0001c0004 a0001c0006 others(20): Show |
42 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(39): Show |
synonymous_variant | LOW | c.939T>C | p.Asn313Asn | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1058/6502 | 939/4116 | 313/1371 | chr19 | 4513021 | |||
chr19:4513027 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.933C>T | p.Ala311Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1052/6502 | 933/4116 | 311/1371 | chr19 | 4513027 | |||
chr19:4513033 | A | G | 3 | a0001c0001 a0026c0083 a0032c0056 |
4 | HG02074.hp1 HG02723.hp2 NA18952.hp2 others(1): Show |
synonymous_variant | LOW | c.927T>C | p.Thr309Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1046/6502 | 927/4116 | 309/1371 | chr19 | 4513033 | |||
chr19:4513036 | C | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.924G>C | p.Val308Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1043/6502 | 924/4116 | 308/1371 | chr19 | 4513036 | |||
chr19:4513045 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.915T>C | p.Cys305Cys | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1034/6502 | 915/4116 | 305/1371 | chr19 | 4513045 | |||
chr19:4513051 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.909C>T | p.Thr303Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1028/6502 | 909/4116 | 303/1371 | chr19 | 4513051 | |||
chr19:4513060 | G | A | 3 | a0001c0006 a0001c0017 a0023c0074 |
5 | HG00735.hp2 HG02717.hp1 HG02895.hp2 others(2): Show |
synonymous_variant | LOW | c.900C>T | p.Thr300Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1019/6502 | 900/4116 | 300/1371 | chr19 | 4513060 | |||
chr19:4513066 | T | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.894A>T | p.Thr298Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1013/6502 | 894/4116 | 298/1371 | chr19 | 4513066 | |||
chr19:4513072 | G | A | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.888C>T | p.Val296Val | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1007/6502 | 888/4116 | 296/1371 | chr19 | 4513072 | |||
chr19:4513075 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.885T>C | p.Thr295Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 1004/6502 | 885/4116 | 295/1371 | chr19 | 4513075 | |||
chr19:4513081 | A | G | 1 | a0032c0056 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.879T>C | p.Ser293Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 998/6502 | 879/4116 | 293/1371 | chr19 | 4513081 | |||
chr19:4513132 | A | G | 97 | a0001c0001 a0001c0002 a0001c0003 others(94): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
synonymous_variant | LOW | c.828T>C | p.Thr276Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 947/6502 | 828/4116 | 276/1371 | chr19 | 4513132 | |||
chr19:4513264 | G | A | 7 | a0001c0013 a0001c0088 a0001c0090 others(4): Show |
15 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(12): Show |
synonymous_variant | LOW | c.696C>T | p.Thr232Thr | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 815/6502 | 696/4116 | 232/1371 | chr19 | 4513264 | |||
chr19:4513624 | G | A | 1 | a0001c0100 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.336C>T | p.Ser112Ser | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/8 | 455/6502 | 336/4116 | 112/1371 | chr19 | 4513624 | |||
chr19:4517576 | C | T | 1 | a0001c0044 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.174G>A | p.Glu58Glu | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/8 | 293/6502 | 174/4116 | 58/1371 | chr19 | 4517576 | |||
chr19:4517606 | G | A | 1 | a0018c0038 | 2 | HG03098.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.144C>T | p.Ala48Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/8 | 263/6502 | 144/4116 | 48/1371 | chr19 | 4517606 | |||
chr19:4517621 | C | T | 1 | a0016c0043 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.129G>A | p.Ala43Ala | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/8 | 248/6502 | 129/4116 | 43/1371 | chr19 | 4517621 | |||
chr19:4518237 | G | A | 1 | a0017c0039 | 2 | HG01884.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.36C>T | p.Pro12Pro | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 2/8 | 155/6502 | 36/4116 | 12/1371 | chr19 | 4518237 | |||
chr19:4518237 | G | T | 4 | a0001c0040 a0004c0009 a0004c0041 others(1): Show |
9 | HG02109.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
synonymous_variant | LOW | c.36C>A | p.Pro12Pro | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 2/8 | 155/6502 | 36/4116 | 12/1371 | chr19 | 4518237 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4502219 | T | C | 1 | a0004c0009t0023 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2240A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 2240 | chr19 | 4502219 | ||||||
chr19:4502237 | G | C | 1 | a0015c0029t0024 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2222C>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 2222 | chr19 | 4502237 | ||||||
chr19:4502270 | C | T | 52 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0022 others(49): Show |
141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2189G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 2189 | chr19 | 4502270 | ||||||
chr19:4502275 | G | T | 120 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(117): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*2184C>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 2184 | chr19 | 4502275 | ||||||
chr19:4502306 | G | T | 1 | a0002c0010t0014 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2153C>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 2153 | chr19 | 4502306 | ||||||
chr19:4502328 | G | GAGAA | 4 | a0002c0010t0007 a0002c0010t0014 a0002c0050t0007 others(1): Show |
7 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2127_*2130dupTTCT | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 2130 | chr19 | 4502328 | ||||||
chr19:4502351 | G | C | 1 | a0003c0008t0025 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2108C>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 2108 | chr19 | 4502351 | ||||||
chr19:4502525 | C | A | 1 | a0004c0041t0026 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1934G>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1934 | chr19 | 4502525 | ||||||
chr19:4502553 | C | T | 2 | a0002c0049t0033 a0013c0048t0035 |
2 | HG01891.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1906G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1906 | chr19 | 4502553 | ||||||
chr19:4502557 | G | T | 1 | a0001c0001t0022 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1902C>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1902 | chr19 | 4502557 | ||||||
chr19:4502608 | G | A | 3 | a0011c0021t0008 a0013c0046t0008 a0014c0020t0008 |
5 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1851C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1851 | chr19 | 4502608 | ||||||
chr19:4502611 | G | C | 1 | a0008c0034t0029 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1848C>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1848 | chr19 | 4502611 | ||||||
chr19:4502618 | G | A | 2 | a0001c0002t0015 a0010c0024t0015 |
2 | HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1841C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1841 | chr19 | 4502618 | ||||||
chr19:4502693 | C | T | 1 | a0001c0001t0021 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1766G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1766 | chr19 | 4502693 | ||||||
chr19:4502801 | G | A | 11 | a0001c0004t0011 a0001c0044t0011 a0008c0027t0009 others(8): Show |
13 | HG00639.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1658C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1658 | chr19 | 4502801 | ||||||
chr19:4503002 | C | T | 1 | a0018c0038t0013 | 2 | HG03098.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1457G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1457 | chr19 | 4503002 | ||||||
chr19:4503093 | G | A | 1 | a0040c0105t0030 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1366C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1366 | chr19 | 4503093 | ||||||
chr19:4503132 | G | A | 1 | a0001c0013t0028 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1327C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1327 | chr19 | 4503132 | ||||||
chr19:4503157 | C | T | 18 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 others(15): Show |
95 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1302G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1302 | chr19 | 4503157 | ||||||
chr19:4503158 | G | A | 5 | a0008c0027t0009 a0008c0034t0009 a0008c0034t0029 others(2): Show |
7 | HG00639.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1301C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1301 | chr19 | 4503158 | ||||||
chr19:4503230 | A | G | 2 | a0041c0103t0012 a0045c0102t0012 |
2 | NA18906.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1229T>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1229 | chr19 | 4503230 | ||||||
chr19:4503260 | G | A | 11 | a0001c0004t0011 a0001c0044t0011 a0008c0027t0009 others(8): Show |
13 | HG00639.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1199C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 1199 | chr19 | 4503260 | ||||||
chr19:4503514 | G | A | 3 | a0005c0019t0006 a0005c0032t0006 a0005c0076t0031 |
7 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*945C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 945 | chr19 | 4503514 | ||||||
chr19:4503597 | C | T | 1 | a0023c0074t0020 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*862G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 862 | chr19 | 4503597 | ||||||
chr19:4503999 | G | A | 1 | a0001c0002t0032 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*460C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 460 | chr19 | 4503999 | ||||||
chr19:4504128 | C | T | 1 | a0034c0058t0019 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*331G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 331 | chr19 | 4504128 | ||||||
chr19:4504274 | GCGTGGGG others(5): Show |
G | 2 | a0002c0049t0033 a0013c0048t0035 |
2 | HG01891.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*173_*184delAGCCAC others(6): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 173 | chr19 | 4504274 | ||||||
chr19:4504384 | G | A | 1 | a0004c0026t0034 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*75C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 75 | chr19 | 4504384 | ||||||
chr19:4504426 | G | A | 1 | a0013c0048t0035 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*33C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 33 | chr19 | 4504426 | ||||||
chr19:4504427 | C | T | 2 | a0028c0057t0018 a0029c0089t0017 |
2 | HG02109.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*32G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 8/8 | 32 | chr19 | 4504427 | ||||||
chr19:4518475 | C | T | 1 | a0001c0004t0016 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-108G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 1/8 | 203 | chr19 | 4518475 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4504800 | C | T | 1 | a0001c0073t0001g0226 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3790-15G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 7/7 | chr19 | 4504800 | |||||||
chr19:4505070 | C | T | 6 | a0008c0027t0009g0031 a0008c0027t0009g0279 a0008c0034t0009g0109 others(3): Show |
7 | HG00639.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3703-123G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505070 | |||||||
chr19:4505094 | G | A | 2 | a0001c0001t0010g0176 a0026c0083t0002g0148 |
2 | HG00438.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.3703-147C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505094 | |||||||
chr19:4505098 | T | C | 10 | a0002c0010t0001g0088 a0002c0010t0007g0091 a0002c0010t0007g0092 others(7): Show |
10 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3703-151A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505098 | |||||||
chr19:4505137 | A | T | 4 | a0008c0027t0009g0031 a0008c0027t0009g0279 a0008c0079t0009g0106 others(1): Show |
5 | HG02717.hp2 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3703-190T>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505137 | |||||||
chr19:4505177 | C | T | 1 | a0001c0001t0003g0182 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3703-230G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505177 | |||||||
chr19:4505344 | C | T | 102 | a0001c0001t0001g0260 a0001c0002t0001g0003 a0001c0002t0001g0011 others(99): Show |
143 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.3703-397G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505344 | |||||||
chr19:4505400 | G | A | 4 | a0001c0001t0002g0009 a0001c0001t0002g0119 a0001c0001t0002g0180 others(1): Show |
7 | HG02129.hp1 NA18943.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.3703-453C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505400 | |||||||
chr19:4505433 | G | A | 103 | a0001c0001t0001g0260 a0001c0001t0004g0175 a0001c0002t0001g0003 others(100): Show |
144 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.3703-486C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505433 | |||||||
chr19:4505518 | C | T | 1 | a0001c0001t0002g0126 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3703-571G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505518 | |||||||
chr19:4505528 | G | A | 8 | a0001c0001t0004g0175 a0001c0007t0003g0195 a0001c0017t0001g0101 others(5): Show |
10 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3703-581C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505528 | |||||||
chr19:4505539 | G | A | 1 | a0017c0039t0001g0281 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3703-592C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505539 | |||||||
chr19:4505557 | T | C | 2 | a0012c0015t0002g0160 a0012c0015t0002g0162 |
2 | NA18997.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3703-610A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505557 | |||||||
chr19:4505582 | G | A | 33 | a0001c0003t0003g0019 a0001c0003t0003g0146 a0001c0003t0003g0233 others(30): Show |
40 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.3703-635C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505582 | |||||||
chr19:4505632 | G | T | 1 | a0001c0002t0001g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3703-685C>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505632 | |||||||
chr19:4505709 | C | T | 1 | a0037c0060t0004g0274 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3703-762G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505709 | |||||||
chr19:4505807 | G | C | 1 | a0003c0008t0003g0132 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3703-860C>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505807 | |||||||
chr19:4505930 | G | A | 1 | a0008c0034t0029g0110 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3703-983C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505930 | |||||||
chr19:4505938 | T | TG | 108 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0008 others(105): Show |
180 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.3703-992dupC | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505938 | |||||||
chr19:4505975 | G | A | 2 | a0002c0049t0033g0273 a0013c0048t0035g0082 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3703-1028C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4505975 | |||||||
chr19:4506160 | C | T | 1 | a0001c0001t0005g0174 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3703-1213G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506160 | |||||||
chr19:4506182 | G | T | 1 | a0001c0022t0001g0156 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3703-1235C>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506182 | |||||||
chr19:4506233 | C | T | 1 | a0029c0089t0017g0263 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3703-1286G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506233 | |||||||
chr19:4506283 | C | T | 1 | a0027c0059t0001g0157 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3703-1336G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506283 | |||||||
chr19:4506284 | A | G | 108 | a0001c0001t0001g0260 a0001c0001t0005g0173 a0001c0002t0001g0003 others(105): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.3703-1337T>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506284 | |||||||
chr19:4506293 | C | G | 1 | a0001c0001t0002g0172 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3703-1346G>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506293 | |||||||
chr19:4506322 | C | G | 4 | a0001c0001t0003g0178 a0001c0001t0003g0249 a0001c0001t0004g0171 others(1): Show |
4 | NA18940.hp2 NA19065.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.3703-1375G>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506322 | |||||||
chr19:4506323 | G | A | 1 | a0002c0010t0001g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3703-1376C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506323 | |||||||
chr19:4506357 | T | G | 1 | a0033c0052t0027g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3703-1410A>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506357 | |||||||
chr19:4506420 | C | T | 1 | a0003c0008t0001g0131 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3703-1473G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506420 | |||||||
chr19:4506477 | C | T | 4 | a0001c0001t0002g0121 a0001c0001t0002g0125 a0001c0001t0021g0122 others(1): Show |
4 | NA19009.hp1 NA19055.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.3703-1530G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506477 | |||||||
chr19:4506478 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3703-1531C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506478 | |||||||
chr19:4506525 | G | A | 3 | a0001c0001t0002g0181 a0028c0057t0018g0275 a0029c0089t0017g0263 |
3 | HG01123.hp1 HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3703-1578C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506525 | |||||||
chr19:4506537 | C | T | 42 | a0001c0002t0001g0003 a0001c0002t0001g0011 a0001c0002t0001g0032 others(39): Show |
62 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.3703-1590G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506537 | |||||||
chr19:4506848 | C | T | 1 | a0001c0002t0001g0047 | 2 | HG03834.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.3703-1901G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506848 | |||||||
chr19:4506859 | C | T | 1 | a0001c0001t0004g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3702+1909G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506859 | |||||||
chr19:4506903 | A | G | 34 | a0001c0001t0003g0184 a0001c0003t0003g0019 a0001c0003t0003g0146 others(31): Show |
41 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.3702+1865T>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506903 | |||||||
chr19:4506952 | C | T | 1 | a0001c0001t0002g0247 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3702+1816G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506952 | |||||||
chr19:4506987 | T | C | 2 | a0007c0036t0004g0239 a0007c0036t0004g0240 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3702+1781A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4506987 | |||||||
chr19:4507164 | G | A | 11 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0121 others(8): Show |
15 | NA18969.hp1 NA18970.hp1 NA18977.hp2 others(12): Show |
intron_variant | MODIFIER | c.3702+1604C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4507164 | |||||||
chr19:4507215 | C | A | 1 | a0001c0001t0003g0182 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3702+1553G>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4507215 | |||||||
chr19:4507475 | G | A | 1 | a0002c0005t0004g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3702+1293C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4507475 | |||||||
chr19:4507514 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3702+1254G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4507514 | |||||||
chr19:4507651 | T | C | 6 | a0001c0017t0001g0101 a0011c0021t0008g0063 a0013c0046t0008g0064 others(3): Show |
8 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3702+1117A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4507651 | |||||||
chr19:4507704 | T | C | 227 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0004 others(224): Show |
341 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.3702+1064A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4507704 | |||||||
chr19:4507849 | A | C | 9 | a0008c0027t0009g0031 a0008c0027t0009g0279 a0008c0034t0009g0109 others(6): Show |
10 | HG00639.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3702+919T>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4507849 | |||||||
chr19:4507853 | C | G | 7 | a0008c0027t0009g0031 a0008c0027t0009g0279 a0008c0034t0009g0109 others(4): Show |
8 | HG00639.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3702+915G>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4507853 | |||||||
chr19:4507915 | G | C | 1 | a0034c0058t0019g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3702+853C>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4507915 | |||||||
chr19:4507976 | C | T | 1 | a0001c0001t0002g0127 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3702+792G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4507976 | |||||||
chr19:4508030 | G | A | 4 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0001c0002t0001g0213 others(1): Show |
4 | HG02129.hp2 NA18947.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.3702+738C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4508030 | |||||||
chr19:4508075 | G | A | 11 | a0002c0010t0001g0088 a0002c0010t0007g0091 a0002c0010t0007g0092 others(8): Show |
11 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.3702+693C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4508075 | |||||||
chr19:4508089 | C | T | 1 | a0002c0055t0004g0080 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3702+679G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4508089 | |||||||
chr19:4508140 | T | A | 2 | a0018c0038t0013g0265 a0018c0038t0013g0266 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3702+628A>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4508140 | |||||||
chr19:4508206 | C | A | 1 | a0001c0003t0004g0230 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3702+562G>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4508206 | |||||||
chr19:4508216 | T | A | 8 | a0008c0027t0009g0031 a0008c0027t0009g0279 a0008c0034t0009g0109 others(5): Show |
9 | HG00639.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.3702+552A>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4508216 | |||||||
chr19:4508266 | T | A | 1 | a0004c0026t0001g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3702+502A>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4508266 | |||||||
chr19:4508296 | G | A | 1 | a0034c0058t0019g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3702+472C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4508296 | |||||||
chr19:4508672 | C | T | 2 | a0001c0001t0005g0118 a0001c0001t0005g0120 |
2 | NA18969.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.3702+96G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4508672 | |||||||
chr19:4508681 | C | T | 1 | a0034c0058t0019g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3702+87G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4508681 | |||||||
chr19:4508718 | G | A | 5 | a0005c0019t0006g0016 a0005c0019t0006g0070 a0005c0032t0006g0069 others(2): Show |
7 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3702+50C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4508718 | |||||||
chr19:4508761 | C | T | 1 | a0017c0039t0001g0281 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.3702+7G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 6/7 | chr19 | 4508761 | |||||||
chr19:4508974 | C | T | 1 | a0001c0003t0003g0233 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3515-19G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4508974 | |||||||
chr19:4509047 | C | T | 33 | a0001c0003t0003g0019 a0001c0003t0003g0146 a0001c0003t0003g0233 others(30): Show |
40 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.3515-92G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509047 | |||||||
chr19:4509092 | G | A | 1 | a0002c0010t0001g0088 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3515-137C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509092 | |||||||
chr19:4509125 | C | T | 3 | a0002c0049t0033g0273 a0013c0048t0035g0082 a0037c0060t0004g0274 |
3 | HG01891.hp1 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3515-170G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509125 | |||||||
chr19:4509171 | C | T | 19 | a0001c0013t0004g0014 a0001c0013t0028g0261 a0001c0033t0004g0040 others(16): Show |
26 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.3515-216G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509171 | |||||||
chr19:4509183 | T | C | 2 | a0001c0003t0004g0145 a0036c0061t0001g0259 |
2 | HG00140.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3515-228A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509183 | |||||||
chr19:4509205 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3515-250C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509205 | |||||||
chr19:4509267 | A | C | 48 | a0001c0003t0003g0019 a0001c0003t0003g0146 a0001c0003t0003g0233 others(45): Show |
57 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.3515-312T>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509267 | |||||||
chr19:4509268 | G | A | 33 | a0001c0003t0003g0019 a0001c0003t0003g0146 a0001c0003t0003g0233 others(30): Show |
40 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.3515-313C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509268 | |||||||
chr19:4509310 | C | CAAAAA | 10 | a0001c0002t0001g0134 a0001c0013t0004g0014 a0001c0013t0028g0261 others(7): Show |
15 | HG01081.hp1 HG01891.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.3515-360_3515-356d others(7): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAA | 17 | a0001c0002t0001g0003 a0001c0002t0001g0032 a0001c0002t0001g0205 others(14): Show |
35 | HG00621.hp1 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.3515-361_3515-356d others(8): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA | 5 | a0001c0001t0003g0042 a0001c0002t0001g0220 a0001c0011t0003g0187 others(2): Show |
6 | HG02083.hp2 HG06807.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.3515-362_3515-356d others(9): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(1): Show |
10 | a0003c0075t0004g0079 a0008c0027t0009g0031 a0008c0027t0009g0279 others(7): Show |
11 | HG00639.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3515-363_3515-356d others(10): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(3): Show |
7 | a0001c0002t0001g0209 a0002c0005t0004g0005 a0002c0005t0004g0061 others(4): Show |
13 | HG02129.hp2 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.3515-365_3515-356d others(12): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(4): Show |
2 | a0002c0005t0004g0067 a0010c0024t0001g0201 |
2 | HG03540.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.3515-366_3515-356d others(13): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0003g0167 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3515-369_3515-356d others(16): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(10): Show |
1 | a0003c0008t0001g0131 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3515-356_3515-355i others(19): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(13): Show |
1 | a0018c0038t0013g0265 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3515-356_3515-355i others(22): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(14): Show |
4 | a0004c0009t0001g0027 a0004c0009t0004g0028 a0018c0038t0013g0266 others(1): Show |
6 | HG02896.hp1 HG03098.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.3515-356_3515-355i others(23): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(15): Show |
19 | a0001c0001t0002g0021 a0001c0001t0002g0113 a0001c0001t0002g0119 others(16): Show |
22 | HG00673.hp2 HG00735.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.3515-356_3515-355i others(24): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(16): Show |
75 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0009 others(72): Show |
133 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.3515-356_3515-355i others(25): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(17): Show |
52 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0024 others(49): Show |
75 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.3515-356_3515-355i others(26): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(18): Show |
17 | a0001c0001t0002g0183 a0001c0001t0003g0045 a0001c0001t0003g0052 others(14): Show |
19 | HG01074.hp2 HG01361.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.3515-356_3515-355i others(27): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(19): Show |
7 | a0001c0001t0002g0127 a0001c0001t0003g0184 a0001c0002t0001g0217 others(4): Show |
7 | HG00408.hp1 HG01261.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.3515-356_3515-355i others(28): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(20): Show |
5 | a0002c0010t0007g0093 a0003c0008t0001g0199 a0007c0018t0001g0238 others(2): Show |
5 | HG01175.hp2 HG01884.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3515-356_3515-355i others(29): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(21): Show |
1 | a0001c0002t0003g0218 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3515-356_3515-355i others(30): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509310 | C | CAAAAAAA others(23): Show |
1 | a0001c0001t0003g0046 | 2 | NA18966.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.3515-356_3515-355i others(32): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509310 | |||||||
chr19:4509312 | A | AAAAAAAA others(16): Show |
1 | a0023c0074t0020g0096 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3515-358_3515-357i others(25): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509312 | |||||||
chr19:4509316 | A | AAAAAAAA others(42): Show |
1 | a0001c0003t0004g0078 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3515-362_3515-361i others(51): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509316 | |||||||
chr19:4509316 | A | AAAAAAAA others(37): Show |
1 | a0006c0096t0004g0243 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3515-362_3515-361i others(46): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509316 | |||||||
chr19:4509316 | A | AAAAAAAA others(41): Show |
13 | a0001c0003t0003g0146 a0001c0003t0004g0077 a0001c0003t0004g0108 others(10): Show |
15 | HG00609.hp1 HG01517.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.3515-362_3515-361i others(50): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509316 | |||||||
chr19:4509316 | A | AAAAAAAA others(40): Show |
19 | a0001c0003t0003g0019 a0001c0003t0003g0233 a0001c0003t0004g0018 others(16): Show |
25 | HG00099.hp1 HG00280.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.3515-362_3515-361i others(49): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509316 | |||||||
chr19:4509316 | A | AAAAAAAC others(40): Show |
1 | a0001c0016t0003g0140 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3515-362_3515-361i others(49): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509316 | |||||||
chr19:4509316 | A | AAAACAAA others(40): Show |
1 | a0001c0003t0004g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3515-362_3515-361i others(49): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509316 | |||||||
chr19:4509320 | A | AAACAAAA others(40): Show |
1 | a0001c0003t0004g0145 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3515-366_3515-365i others(49): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509320 | |||||||
chr19:4509347 | T | C | 2 | a0003c0008t0003g0200 a0009c0014t0003g0255 |
2 | NA18983.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.3515-392A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509347 | |||||||
chr19:4509362 | A | G | 2 | a0028c0057t0018g0275 a0029c0089t0017g0263 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3515-407T>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509362 | |||||||
chr19:4509366 | C | T | 11 | a0002c0010t0001g0088 a0002c0010t0007g0091 a0002c0010t0007g0092 others(8): Show |
11 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.3515-411G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509366 | |||||||
chr19:4509379 | G | A | 1 | a0001c0002t0001g0222 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3515-424C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509379 | |||||||
chr19:4509457 | A | C | 105 | a0001c0002t0001g0003 a0001c0002t0001g0011 a0001c0002t0001g0012 others(102): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.3515-502T>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509457 | |||||||
chr19:4509493 | C | T | 2 | a0001c0001t0003g0117 a0010c0031t0003g0163 |
2 | HG04184.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.3515-538G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509493 | |||||||
chr19:4509497 | C | T | 2 | a0003c0075t0004g0079 a0030c0045t0004g0280 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3515-542G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509497 | |||||||
chr19:4509561 | G | C | 1 | a0034c0058t0019g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3515-606C>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509561 | |||||||
chr19:4509679 | C | A | 1 | a0019c0081t0004g0272 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3515-724G>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509679 | |||||||
chr19:4509753 | A | G | 5 | a0001c0001t0003g0007 a0001c0001t0003g0042 a0001c0001t0003g0116 others(2): Show |
10 | HG01081.hp2 HG01952.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.3514+693T>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509753 | |||||||
chr19:4509869 | G | A | 1 | a0009c0014t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3514+577C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4509869 | |||||||
chr19:4510006 | G | A | 1 | a0008c0027t0009g0279 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3514+440C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510006 | |||||||
chr19:4510023 | C | T | 157 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0004 others(154): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.3514+423G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510023 | |||||||
chr19:4510060 | A | AT | 127 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0004 others(124): Show |
206 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.3514+385dupA | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510060 | |||||||
chr19:4510064 | T | TA | 10 | a0001c0003t0003g0019 a0001c0003t0003g0146 a0001c0003t0003g0233 others(7): Show |
13 | HG02523.hp2 HG03490.hp2 HG03492.hp1 others(10): Show |
intron_variant | MODIFIER | c.3514+381_3514+382i others(3): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510064 | |||||||
chr19:4510065 | T | A | 10 | a0001c0003t0003g0019 a0001c0003t0003g0146 a0001c0003t0003g0233 others(7): Show |
13 | HG02523.hp2 HG03490.hp2 HG03492.hp1 others(10): Show |
intron_variant | MODIFIER | c.3514+381A>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510065 | |||||||
chr19:4510065 | T | TA | 25 | a0001c0003t0004g0018 a0001c0003t0004g0077 a0001c0003t0004g0078 others(22): Show |
29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.3514+380dupT | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510065 | |||||||
chr19:4510066 | A | T | 222 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0004 others(219): Show |
340 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.3514+380T>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510066 | |||||||
chr19:4510067 | A | T | 120 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0004 others(117): Show |
198 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.3514+379T>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510067 | |||||||
chr19:4510068 | A | T | 1 | a0001c0001t0003g0166 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3514+378T>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510068 | |||||||
chr19:4510141 | C | T | 13 | a0002c0005t0004g0005 a0002c0005t0004g0061 a0002c0005t0004g0062 others(10): Show |
19 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3514+305G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510141 | |||||||
chr19:4510142 | G | A | 10 | a0001c0003t0003g0019 a0001c0003t0003g0146 a0001c0003t0003g0233 others(7): Show |
13 | HG02523.hp2 HG03490.hp2 HG03492.hp1 others(10): Show |
intron_variant | MODIFIER | c.3514+304C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510142 | |||||||
chr19:4510234 | T | C | 121 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0004 others(118): Show |
200 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.3514+212A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510234 | |||||||
chr19:4510238 | C | T | 2 | a0041c0103t0012g0073 a0045c0102t0012g0072 |
2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3514+208G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510238 | |||||||
chr19:4510245 | A | C | 2 | a0018c0038t0013g0265 a0018c0038t0013g0266 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3514+201T>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510245 | |||||||
chr19:4510306 | C | T | 10 | a0002c0005t0004g0005 a0002c0005t0004g0061 a0002c0005t0004g0062 others(7): Show |
16 | HG02257.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.3514+140G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510306 | |||||||
chr19:4510354 | C | T | 5 | a0008c0027t0009g0031 a0008c0027t0009g0279 a0008c0034t0009g0109 others(2): Show |
6 | HG00639.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3514+92G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510354 | |||||||
chr19:4510361 | G | A | 2 | a0001c0004t0011g0107 a0015c0029t0011g0065 |
2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3514+85C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510361 | |||||||
chr19:4510365 | C | CA | 20 | a0001c0002t0001g0220 a0001c0002t0001g0221 a0001c0002t0001g0222 others(17): Show |
26 | HG01433.hp1 HG02257.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.3514+80dupT | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510365 | |||||||
chr19:4510376 | AC | A | 3 | a0001c0002t0001g0223 a0001c0006t0001g0034 a0001c0006t0001g0035 |
5 | HG00280.hp1 HG01433.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.3514+69delG | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510376 | |||||||
chr19:4510377 | C | A | 115 | a0001c0002t0001g0003 a0001c0002t0001g0011 a0001c0002t0001g0012 others(112): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.3514+69G>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510377 | |||||||
chr19:4510400 | C | A | 1 | a0013c0046t0008g0064 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3514+46G>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 5/7 | chr19 | 4510400 | |||||||
chr19:4513882 | A | G | 1 | a0001c0003t0004g0115 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.259-181T>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4513882 | |||||||
chr19:4514119 | G | A | 2 | a0001c0001t0002g0051 a0001c0001t0022g0152 |
3 | HG00323.hp1 HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.259-418C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514119 | |||||||
chr19:4514123 | C | T | 267 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0004 others(264): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.259-422G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514123 | |||||||
chr19:4514178 | G | A | 1 | a0001c0003t0004g0153 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.259-477C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514178 | |||||||
chr19:4514259 | C | T | 2 | a0018c0038t0013g0265 a0018c0038t0013g0266 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.259-558G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514259 | |||||||
chr19:4514457 | G | A | 19 | a0001c0013t0004g0014 a0001c0013t0028g0261 a0001c0088t0004g0262 others(16): Show |
23 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.259-756C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514457 | |||||||
chr19:4514644 | A | G | 3 | a0006c0092t0004g0250 a0006c0094t0004g0251 a0039c0098t0003g0252 |
3 | HG01167.hp1 HG01934.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.259-943T>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514644 | |||||||
chr19:4514682 | C | T | 5 | a0002c0049t0033g0273 a0005c0019t0006g0016 a0005c0019t0006g0070 others(2): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.259-981G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514682 | |||||||
chr19:4514715 | G | A | 1 | a0001c0002t0001g0244 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.259-1014C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514715 | |||||||
chr19:4514728 | AAAT | A | 5 | a0002c0049t0033g0273 a0005c0019t0006g0016 a0005c0019t0006g0070 others(2): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.259-1030_259-1028d others(5): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514728 | |||||||
chr19:4514823 | G | A | 1 | a0001c0001t0005g0245 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.259-1122C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514823 | |||||||
chr19:4514840 | G | A | 5 | a0002c0049t0033g0273 a0005c0019t0006g0016 a0005c0019t0006g0070 others(2): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.259-1139C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514840 | |||||||
chr19:4514880 | T | TAA | 9 | a0001c0013t0004g0014 a0001c0013t0028g0261 a0001c0088t0004g0262 others(6): Show |
13 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.259-1181_259-1180d others(4): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514880 | |||||||
chr19:4514898 | G | A | 7 | a0001c0013t0004g0014 a0001c0013t0028g0261 a0001c0088t0004g0262 others(4): Show |
11 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.259-1197C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514898 | |||||||
chr19:4514903 | C | T | 12 | a0002c0049t0033g0273 a0005c0019t0006g0016 a0005c0019t0006g0070 others(9): Show |
14 | HG01884.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.259-1202G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514903 | |||||||
chr19:4514996 | C | T | 9 | a0002c0049t0033g0273 a0005c0019t0006g0016 a0005c0019t0006g0070 others(6): Show |
11 | HG01884.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.259-1295G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4514996 | |||||||
chr19:4515157 | C | G | 2 | a0001c0006t0001g0155 a0001c0007t0004g0269 |
2 | HG00621.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.259-1456G>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515157 | |||||||
chr19:4515180 | TA | T | 24 | a0001c0013t0004g0014 a0001c0013t0028g0261 a0001c0088t0004g0262 others(21): Show |
30 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.258+1436delT | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515180 | |||||||
chr19:4515195 | A | C | 9 | a0002c0049t0033g0273 a0005c0019t0006g0016 a0005c0019t0006g0070 others(6): Show |
11 | HG01884.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+1422T>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515195 | |||||||
chr19:4515267 | T | G | 10 | a0002c0005t0004g0005 a0002c0005t0004g0061 a0002c0005t0004g0062 others(7): Show |
18 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.258+1350A>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515267 | |||||||
chr19:4515355 | C | T | 1 | a0001c0002t0001g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.258+1262G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515355 | |||||||
chr19:4515422 | C | T | 9 | a0002c0049t0033g0273 a0005c0019t0006g0016 a0005c0019t0006g0070 others(6): Show |
11 | HG01884.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+1195G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515422 | |||||||
chr19:4515459 | A | G | 1 | a0006c0037t0003g0053 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.258+1158T>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515459 | |||||||
chr19:4515510 | C | T | 1 | a0001c0003t0004g0153 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.258+1107G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515510 | |||||||
chr19:4515527 | C | T | 54 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0119 others(51): Show |
75 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.258+1090G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515527 | |||||||
chr19:4515559 | G | A | 7 | a0001c0013t0004g0014 a0001c0013t0028g0261 a0001c0088t0004g0262 others(4): Show |
11 | HG01891.hp2 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.258+1058C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515559 | |||||||
chr19:4515707 | C | T | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG01106.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.258+910G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515707 | |||||||
chr19:4515709 | C | T | 1 | a0001c0002t0001g0246 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.258+908G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515709 | |||||||
chr19:4515710 | G | A | 3 | a0005c0019t0006g0016 a0005c0019t0006g0070 a0005c0032t0006g0069 |
5 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+907C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515710 | |||||||
chr19:4515853 | T | C | 2 | a0003c0075t0004g0079 a0023c0074t0020g0096 |
2 | HG00735.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.258+764A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515853 | |||||||
chr19:4515879 | C | T | 1 | a0001c0025t0003g0112 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.258+738G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515879 | |||||||
chr19:4515997 | A | C | 1 | a0001c0002t0001g0032 | 2 | HG01074.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.258+620T>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4515997 | |||||||
chr19:4516008 | C | CT | 14 | a0002c0005t0004g0005 a0002c0005t0004g0061 a0002c0005t0004g0062 others(11): Show |
22 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.258+608dupA | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4516008 | |||||||
chr19:4516023 | C | T | 9 | a0002c0049t0033g0273 a0005c0019t0006g0016 a0005c0019t0006g0070 others(6): Show |
11 | HG01884.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+594G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4516023 | |||||||
chr19:4516084 | GGTGAA | G | 25 | a0001c0013t0004g0014 a0001c0013t0028g0261 a0001c0088t0004g0262 others(22): Show |
31 | HG00735.hp2 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.258+528_258+532del others(5): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4516084 | |||||||
chr19:4516194 | C | T | 9 | a0002c0049t0033g0273 a0005c0019t0006g0016 a0005c0019t0006g0070 others(6): Show |
11 | HG01884.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+423G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4516194 | |||||||
chr19:4516226 | A | G | 79 | a0001c0003t0004g0108 a0001c0004t0011g0107 a0001c0006t0001g0099 others(76): Show |
97 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.258+391T>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4516226 | |||||||
chr19:4516312 | C | T | 3 | a0005c0076t0031g0278 a0008c0027t0009g0279 a0044c0087t0001g0277 |
3 | HG02647.hp1 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.258+305G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4516312 | |||||||
chr19:4516480 | CAGCAGCC others(35): Show |
C | 2 | a0018c0038t0013g0265 a0018c0038t0013g0266 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.258+95_258+136delC others(41): Show |
PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4516480 | |||||||
chr19:4516493 | G | C | 2 | a0003c0075t0004g0079 a0023c0074t0020g0096 |
2 | HG00735.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.258+124C>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4516493 | |||||||
chr19:4516552 | T | C | 2 | a0005c0076t0031g0278 a0008c0027t0009g0279 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.258+65A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4516552 | |||||||
chr19:4516582 | T | C | 4 | a0001c0001t0002g0024 a0001c0001t0002g0247 a0001c0001t0003g0052 others(1): Show |
7 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+35A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4516582 | |||||||
chr19:4516593 | A | C | 1 | a0001c0001t0002g0097 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.258+24T>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 4/7 | chr19 | 4516593 | |||||||
chr19:4516696 | G | A | 3 | a0005c0076t0031g0278 a0008c0027t0009g0279 a0044c0087t0001g0277 |
3 | HG02647.hp1 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.197-18C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4516696 | |||||||
chr19:4516855 | C | T | 3 | a0005c0076t0031g0278 a0008c0027t0009g0279 a0044c0087t0001g0277 |
3 | HG02647.hp1 HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.197-177G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4516855 | |||||||
chr19:4516882 | G | A | 1 | a0001c0002t0001g0248 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.197-204C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4516882 | |||||||
chr19:4516884 | G | A | 14 | a0002c0005t0004g0005 a0002c0005t0004g0061 a0002c0005t0004g0062 others(11): Show |
22 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-206C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4516884 | |||||||
chr19:4516886 | C | T | 1 | a0003c0075t0004g0079 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-208G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4516886 | |||||||
chr19:4516970 | A | G | 55 | a0001c0013t0004g0014 a0001c0013t0028g0261 a0001c0088t0004g0262 others(52): Show |
69 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.197-292T>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4516970 | |||||||
chr19:4517021 | G | C | 4 | a0005c0076t0031g0278 a0008c0027t0009g0279 a0030c0045t0004g0280 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-343C>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4517021 | |||||||
chr19:4517156 | C | T | 9 | a0002c0049t0033g0273 a0005c0019t0006g0016 a0005c0019t0006g0070 others(6): Show |
11 | HG01884.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+398G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4517156 | |||||||
chr19:4517172 | G | T | 1 | a0002c0005t0004g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.196+382C>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4517172 | |||||||
chr19:4517199 | G | C | 1 | a0001c0001t0003g0249 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.196+355C>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4517199 | |||||||
chr19:4517200 | C | T | 1 | a0001c0001t0003g0249 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.196+354G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4517200 | |||||||
chr19:4517201 | T | G | 1 | a0001c0001t0003g0249 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.196+353A>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4517201 | |||||||
chr19:4517322 | TG | T | 269 | a0001c0001t0001g0260 a0001c0001t0002g0001 a0001c0001t0002g0004 others(266): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.196+231delC | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4517322 | |||||||
chr19:4517381 | C | T | 2 | a0001c0003t0004g0077 a0001c0003t0004g0078 |
2 | HG00609.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.196+173G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4517381 | |||||||
chr19:4517395 | A | G | 8 | a0001c0013t0004g0014 a0001c0013t0028g0261 a0001c0088t0004g0262 others(5): Show |
12 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.196+159T>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4517395 | |||||||
chr19:4517415 | G | A | 1 | a0036c0061t0001g0259 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196+139C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4517415 | |||||||
chr19:4517497 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.196+57A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4517497 | |||||||
chr19:4517511 | T | C | 8 | a0001c0013t0004g0014 a0001c0013t0028g0261 a0001c0088t0004g0262 others(5): Show |
12 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.196+43A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 3/7 | chr19 | 4517511 | |||||||
chr19:4517711 | G | A | 1 | a0001c0007t0004g0269 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.52-13C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 2/7 | chr19 | 4517711 | |||||||
chr19:4517714 | G | A | 4 | a0001c0001t0002g0271 a0001c0001t0004g0026 a0001c0001t0004g0270 others(1): Show |
6 | HG00642.hp2 HG02280.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.52-16C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 2/7 | chr19 | 4517714 | |||||||
chr19:4517722 | A | G | 1 | a0002c0005t0004g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.52-24T>C | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 2/7 | chr19 | 4517722 | |||||||
chr19:4517787 | C | T | 7 | a0001c0040t0004g0056 a0004c0009t0001g0027 a0004c0009t0004g0028 others(4): Show |
9 | HG02109.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-89G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 2/7 | chr19 | 4517787 | |||||||
chr19:4517887 | T | C | 11 | a0002c0049t0033g0273 a0005c0019t0006g0016 a0005c0019t0006g0070 others(8): Show |
13 | HG01884.hp2 HG02109.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.52-189A>G | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 2/7 | chr19 | 4517887 | |||||||
chr19:4517983 | G | A | 4 | a0005c0076t0031g0278 a0008c0027t0009g0279 a0030c0045t0004g0280 others(1): Show |
4 | HG02451.hp1 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+239C>T | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 2/7 | chr19 | 4517983 | |||||||
chr19:4518123 | C | T | 1 | a0001c0044t0011g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.51+99G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 2/7 | chr19 | 4518123 | |||||||
chr19:4518213 | C | T | 18 | a0002c0005t0004g0005 a0002c0005t0004g0061 a0002c0005t0004g0062 others(15): Show |
28 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.51+9G>A | PLIN4 | ENSG00000167676.5 | transcript | ENST00000301286.5 | protein_coding | 2/7 | chr19 | 4518213 |