| geneid | 126206 |
|---|---|
| ensemblid | ENSG00000171487.16 |
| hgncid | 21269 |
| symbol | NLRP5 |
| name | NLR family pyrin domain containing 5 |
| refseq_nuc | NM_153447.4 |
| refseq_prot | NP_703148.4 |
| ensembl_nuc | ENST00000390649.8 |
| ensembl_prot | ENSP00000375063.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 55999726 |
| end | 56061810 |
| strand | + |
| ver | v1.2 |
| region | chr19:55999726-56061810 |
| region5000 | chr19:55994726-56066810 |
| regionname0 | NLRP5_chr19_55999726_56061810 |
| regionname5000 | NLRP5_chr19_55994726_56066810 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1200 | 141 | 21 | 50 | 42 | 6 | 21 | 30 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002 | 0/0 | 1200 | 36 | 3 | 9 | 19 | 2 | 3 | 12 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003 | 0/0 | 1200 | 30 | 17 | 3 | 5 | 1 | 4 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004 | 0/0 | 1200 | 27 | 15 | 3 | 7 | 2 | 0 | 6 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005 | 1/0 | 1200 | 25 | 2 | 0 | 20 | 0 | 2 | 16 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0006 | 0/0 | 1200 | 23 | 1 | 0 | 22 | 0 | 0 | 21 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007 | 0/0 | 1200 | 21 | 7 | 4 | 8 | 0 | 2 | 7 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0008 | 0/0 | 1200 | 12 | 2 | 3 | 4 | 2 | 1 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0009 | 0/0 | 1200 | 11 | 6 | 0 | 5 | 0 | 0 | 3 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0010 | 0/0 | 1200 | 9 | 1 | 0 | 6 | 2 | 0 | 6 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0011 | 0/0 | 1200 | 7 | 0 | 0 | 6 | 0 | 1 | 4 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0012 | 0/0 | 1200 | 7 | 0 | 0 | 3 | 1 | 3 | 3 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0013 | 0/0 | 1200 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0014 | 0/0 | 1200 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0015 | 0/0 | 1200 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0016 | 0/0 | 1181 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0017 | 0/0 | 1200 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0018 | 0/0 | 1200 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0019 | 0/0 | 1200 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0020 | 0/0 | 1200 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0021 | 0/0 | 1200 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0022 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0023 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0024 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0025 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0026 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0027 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0028 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0029 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0030 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0031 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0032 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0033 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0034 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0035 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0036 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0037 | 0/0 | 1200 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0038 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0039 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0040 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0041 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0042 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0043 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0044 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0045 | 0/0 | 1181 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3603 | 34 | 4 | 15 | 9 | 0 | 6 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0002 | 0/0 | 3603 | 29 | 2 | 13 | 8 | 0 | 6 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0003 | 0/0 | 3603 | 20 | 0 | 6 | 8 | 1 | 5 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0004 | 0/0 | 3603 | 18 | 0 | 4 | 12 | 2 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0005 | 0/0 | 3603 | 13 | 1 | 0 | 12 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0006 | 0/0 | 3603 | 12 | 0 | 0 | 11 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0007 | 0/0 | 3603 | 10 | 5 | 1 | 2 | 2 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0008 | 0/0 | 3603 | 10 | 8 | 0 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0009 | 0/0 | 3603 | 10 | 1 | 1 | 8 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0010 | 0/0 | 3603 | 8 | 2 | 2 | 3 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0011 | 0/0 | 3603 | 8 | 0 | 0 | 8 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0012 | 0/0 | 3603 | 8 | 0 | 1 | 5 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0013 | 0/0 | 3603 | 7 | 5 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0014 | 0/0 | 3603 | 6 | 0 | 5 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0015 | 0/0 | 3603 | 6 | 0 | 2 | 2 | 1 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0016 | 0/0 | 3603 | 6 | 0 | 0 | 5 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0017 | 0/0 | 3603 | 5 | 2 | 2 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0018 | 0/0 | 3603 | 5 | 0 | 0 | 2 | 1 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0019 | 0/0 | 3603 | 5 | 5 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0020 | 0/0 | 3603 | 5 | 2 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0021 | 0/0 | 3603 | 5 | 1 | 0 | 4 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0022 | 0/0 | 3603 | 5 | 1 | 2 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0023 | 0/0 | 3603 | 4 | 4 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0024 | 0/0 | 3603 | 4 | 0 | 2 | 1 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0025 | 0/0 | 3603 | 4 | 0 | 0 | 3 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0026 | 0/0 | 3603 | 4 | 0 | 0 | 4 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0027 | 0/0 | 3603 | 3 | 1 | 0 | 1 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0028 | 0/0 | 3603 | 3 | 0 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0029 | 1/0 | 3603 | 3 | 1 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0030 | 0/0 | 3603 | 3 | 0 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0031 | 0/0 | 3603 | 3 | 0 | 2 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0032 | 0/0 | 3603 | 3 | 1 | 2 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0033 | 0/0 | 3603 | 3 | 0 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0034 | 0/0 | 3603 | 3 | 0 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0035 | 0/0 | 3603 | 3 | 3 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0036 | 0/0 | 3603 | 2 | 0 | 0 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0037 | 0/0 | 3603 | 2 | 0 | 0 | 0 | 2 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0038 | 0/0 | 3603 | 2 | 0 | 0 | 1 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0039 | 0/0 | 3603 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0040 | 0/0 | 3603 | 2 | 2 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0041 | 0/0 | 3603 | 2 | 1 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0042 | 0/0 | 3603 | 2 | 2 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0043 | 0/0 | 3603 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0044 | 0/0 | 3603 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0045 | 0/0 | 3603 | 2 | 1 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0046 | 0/0 | 3603 | 2 | 0 | 2 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0047 | 0/0 | 3603 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0048 | 0/0 | 3603 | 2 | 0 | 0 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0049 | 0/0 | 3603 | 2 | 1 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0050 | 0/0 | 3603 | 2 | 1 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0051 | 0/0 | 3603 | 2 | 2 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0052 | 0/0 | 3603 | 2 | 0 | 1 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0053 | 0/0 | 3603 | 2 | 2 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0054 | 0/0 | 3603 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0055 | 0/0 | 3603 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0056 | 0/0 | 3603 | 2 | 0 | 1 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0057 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0058 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0059 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0060 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0061 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0062 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0063 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0064 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0065 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0066 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0067 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0068 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0069 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0070 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0071 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0072 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0073 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0074 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0075 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0076 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0077 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0078 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0079 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0080 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0081 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0082 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0083 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0084 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0085 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0086 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0087 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0088 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0089 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0090 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0091 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0092 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0093 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0094 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0095 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0096 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0097 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0098 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0099 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0100 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0101 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0102 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0103 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0104 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0105 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0106 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0107 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0108 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0109 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0110 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0111 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0112 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0113 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0114 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0115 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0116 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0117 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0118 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0119 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0120 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0121 | 0/1 | 3603 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0122 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0123 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0124 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0125 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0126 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0127 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0128 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0129 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0130 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0131 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| c0132 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 283 | 300 | 77 | 64 | 108 | 14 | 35 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| t0002 | 0/0 | 283 | 89 | 5 | 10 | 60 | 4 | 10 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| t0003 | 0/0 | 283 | 6 | 6 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| t0004 | 0/0 | 283 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0290 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0361 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0389 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0390 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3603 | 34 | 4 | 15 | 9 | 0 | 6 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0002 | 0/0 | 3603 | 29 | 2 | 13 | 8 | 0 | 6 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0003 | 0/0 | 3603 | 20 | 0 | 6 | 8 | 1 | 5 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0009 | 0/0 | 3603 | 10 | 1 | 1 | 8 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0014 | 0/0 | 3603 | 6 | 0 | 5 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0015 | 0/0 | 3603 | 6 | 0 | 2 | 2 | 1 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0019 | 0/0 | 3603 | 5 | 5 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0022 | 0/0 | 3603 | 5 | 1 | 2 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0023 | 0/0 | 3603 | 4 | 4 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0030 | 0/0 | 3603 | 3 | 0 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0042 | 0/0 | 3603 | 2 | 2 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0046 | 0/0 | 3603 | 2 | 0 | 2 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0052 | 0/0 | 3603 | 2 | 0 | 1 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0056 | 0/0 | 3603 | 2 | 0 | 1 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0068 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0082 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0084 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0085 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0086 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0092 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0115 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0121 | 0/1 | 3603 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0123 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0124 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0132 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0004 | 0/0 | 3603 | 18 | 0 | 4 | 12 | 2 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0012 | 0/0 | 3603 | 8 | 0 | 1 | 5 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0031 | 0/0 | 3603 | 3 | 0 | 2 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0041 | 0/0 | 3603 | 2 | 1 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0079 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0087 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0112 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0116 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0127 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0008 | 0/0 | 3603 | 10 | 8 | 0 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0024 | 0/0 | 3603 | 4 | 0 | 2 | 1 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0040 | 0/0 | 3603 | 2 | 2 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0043 | 0/0 | 3603 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0045 | 0/0 | 3603 | 2 | 1 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0051 | 0/0 | 3603 | 2 | 2 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0075 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0076 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0077 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0111 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0114 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0118 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0122 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0126 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0007 | 0/0 | 3603 | 10 | 5 | 1 | 2 | 2 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0020 | 0/0 | 3603 | 5 | 2 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0035 | 0/0 | 3603 | 3 | 3 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0050 | 0/0 | 3603 | 2 | 1 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0053 | 0/0 | 3603 | 2 | 2 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0055 | 0/0 | 3603 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0070 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0080 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0125 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0006 | 0/0 | 3603 | 12 | 0 | 0 | 11 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0025 | 0/0 | 3603 | 4 | 0 | 0 | 3 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0029 | 1/0 | 3603 | 3 | 1 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0034 | 0/0 | 3603 | 3 | 0 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0083 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0095 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0113 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0006c0005 | 0/0 | 3603 | 13 | 1 | 0 | 12 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0006c0011 | 0/0 | 3603 | 8 | 0 | 0 | 8 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0006c0081 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0006c0128 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0010 | 0/0 | 3603 | 8 | 2 | 2 | 3 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0021 | 0/0 | 3603 | 5 | 1 | 0 | 4 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0032 | 0/0 | 3603 | 3 | 1 | 2 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0071 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0072 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0073 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0108 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0110 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0008c0017 | 0/0 | 3603 | 5 | 2 | 2 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0008c0028 | 0/0 | 3603 | 3 | 0 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0008c0037 | 0/0 | 3603 | 2 | 0 | 0 | 0 | 2 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0008c0104 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0008c0105 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0009c0013 | 0/0 | 3603 | 7 | 5 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0009c0054 | 0/0 | 3603 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0009c0090 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0009c0094 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0010c0016 | 0/0 | 3603 | 6 | 0 | 0 | 5 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0010c0027 | 0/0 | 3603 | 3 | 1 | 0 | 1 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0011c0033 | 0/0 | 3603 | 3 | 0 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0011c0038 | 0/0 | 3603 | 2 | 0 | 0 | 1 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0011c0039 | 0/0 | 3603 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0012c0018 | 0/0 | 3603 | 5 | 0 | 0 | 2 | 1 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0012c0065 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0012c0106 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0013c0026 | 0/0 | 3603 | 4 | 0 | 0 | 4 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0014c0064 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0014c0100 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0014c0102 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0015c0044 | 0/0 | 3603 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0015c0117 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0016c0097 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0016c0129 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0016c0130 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0017c0063 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0017c0099 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0018c0036 | 0/0 | 3603 | 2 | 0 | 0 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0019c0047 | 0/0 | 3603 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0020c0049 | 0/0 | 3603 | 2 | 1 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0021c0048 | 0/0 | 3603 | 2 | 0 | 0 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0022c0096 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0023c0057 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0024c0058 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0025c0089 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0026c0059 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0027c0060 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0028c0093 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0029c0103 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0030c0098 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0031c0101 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0032c0062 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0033c0061 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0034c0066 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0035c0067 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0036c0088 | 0/0 | 3603 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0037c0091 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0038c0120 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0039c0078 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0040c0074 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0041c0109 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0042c0069 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0043c0119 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0044c0107 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0045c0131 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3885 | 34 | 4 | 15 | 9 | 0 | 6 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0002t0001 | 0/0 | 3885 | 29 | 2 | 13 | 8 | 0 | 6 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0003t0001 | 0/0 | 3885 | 20 | 0 | 6 | 8 | 1 | 5 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0009t0001 | 0/0 | 3885 | 10 | 1 | 1 | 8 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0014t0001 | 0/0 | 3885 | 6 | 0 | 5 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0015t0001 | 0/0 | 3885 | 6 | 0 | 2 | 2 | 1 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0019t0001 | 0/0 | 3885 | 5 | 5 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0022t0001 | 0/0 | 3885 | 5 | 1 | 2 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0023t0001 | 0/0 | 3885 | 4 | 4 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0030t0001 | 0/0 | 3885 | 3 | 0 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0042t0001 | 0/0 | 3885 | 2 | 2 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0046t0001 | 0/0 | 3885 | 2 | 0 | 2 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0052t0001 | 0/0 | 3885 | 2 | 0 | 1 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0056t0001 | 0/0 | 3885 | 2 | 0 | 1 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0068t0001 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0082t0001 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0084t0001 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0085t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0086t0001 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0092t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0115t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0121t0001 | 0/1 | 3885 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0123t0001 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0124t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0001c0132t0001 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0004t0002 | 0/0 | 3885 | 18 | 0 | 4 | 12 | 2 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0012t0002 | 0/0 | 3885 | 8 | 0 | 1 | 5 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0031t0002 | 0/0 | 3885 | 3 | 0 | 2 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0041t0002 | 0/0 | 3885 | 2 | 1 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0079t0002 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0087t0002 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0112t0002 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0116t0002 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0002c0127t0002 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0008t0001 | 0/0 | 3885 | 9 | 7 | 0 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0008t0003 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0024t0001 | 0/0 | 3885 | 4 | 0 | 2 | 1 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0040t0001 | 0/0 | 3885 | 2 | 2 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0043t0001 | 0/0 | 3885 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0045t0001 | 0/0 | 3885 | 2 | 1 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0051t0001 | 0/0 | 3885 | 2 | 2 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0075t0001 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0076t0002 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0077t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0111t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0114t0002 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0118t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0122t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0003c0126t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0007t0001 | 0/0 | 3885 | 8 | 3 | 1 | 2 | 2 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0007t0003 | 0/0 | 3885 | 2 | 2 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0020t0001 | 0/0 | 3885 | 4 | 1 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0020t0003 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0035t0001 | 0/0 | 3885 | 3 | 3 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0050t0001 | 0/0 | 3885 | 2 | 1 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0053t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0053t0003 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0055t0001 | 0/0 | 3885 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0070t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0080t0001 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0004c0125t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0006t0001 | 0/0 | 3885 | 12 | 0 | 0 | 11 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0025t0001 | 0/0 | 3885 | 4 | 0 | 0 | 3 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0029t0001 | 1/0 | 3885 | 3 | 1 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0034t0001 | 0/0 | 3885 | 3 | 0 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0083t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0095t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0005c0113t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0006c0005t0002 | 0/0 | 3885 | 13 | 1 | 0 | 12 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0006c0011t0002 | 0/0 | 3885 | 8 | 0 | 0 | 8 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0006c0081t0002 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0006c0128t0002 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0010t0001 | 0/0 | 3885 | 8 | 2 | 2 | 3 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0021t0001 | 0/0 | 3885 | 5 | 1 | 0 | 4 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0032t0001 | 0/0 | 3885 | 3 | 1 | 2 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0071t0001 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0072t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0073t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0108t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0007c0110t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0008c0017t0001 | 0/0 | 3885 | 5 | 2 | 2 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0008c0028t0001 | 0/0 | 3885 | 3 | 0 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0008c0037t0001 | 0/0 | 3885 | 2 | 0 | 0 | 0 | 2 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0008c0104t0001 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0008c0105t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0009c0013t0001 | 0/0 | 3885 | 7 | 5 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0009c0054t0001 | 0/0 | 3885 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0009c0090t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0009c0094t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0010c0016t0001 | 0/0 | 3885 | 6 | 0 | 0 | 5 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0010c0027t0001 | 0/0 | 3885 | 3 | 1 | 0 | 1 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0011c0033t0001 | 0/0 | 3885 | 3 | 0 | 0 | 3 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0011c0038t0001 | 0/0 | 3885 | 2 | 0 | 0 | 1 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0011c0039t0001 | 0/0 | 3885 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0012c0018t0002 | 0/0 | 3885 | 5 | 0 | 0 | 2 | 1 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0012c0065t0002 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0012c0106t0002 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0013c0026t0002 | 0/0 | 3885 | 4 | 0 | 0 | 4 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0014c0064t0002 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0014c0100t0002 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0014c0102t0002 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0015c0044t0002 | 0/0 | 3885 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0015c0117t0002 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0016c0097t0001 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0016c0129t0001 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0016c0130t0003 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0017c0063t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0017c0099t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0018c0036t0002 | 0/0 | 3885 | 2 | 0 | 0 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0019c0047t0002 | 0/0 | 3885 | 2 | 0 | 0 | 2 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0020c0049t0001 | 0/0 | 3885 | 2 | 1 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0021c0048t0002 | 0/0 | 3885 | 2 | 0 | 0 | 0 | 0 | 2 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0022c0096t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0023c0057t0004 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0024c0058t0002 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0025c0089t0002 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0026c0059t0001 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0027c0060t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0028c0093t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0029c0103t0001 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0030c0098t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0031c0101t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0032c0062t0001 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0033c0061t0001 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0034c0066t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0035c0067t0002 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0036c0088t0001 | 0/0 | 3885 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0037c0091t0001 | 0/0 | 3885 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0038c0120t0002 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0039c0078t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0040c0074t0002 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0041c0109t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0042c0069t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0043c0119t0001 | 0/0 | 3885 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0044c0107t0001 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| a0045c0131t0001 | 0/0 | 3828 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | copy fasta | chr19 | 55994726 | 56066810 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0001t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0002t0001g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0003t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0009t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0009t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0009t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0009t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0009t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0009t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0009t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0009t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0009t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0009t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0014t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0014t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0014t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0014t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0014t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0014t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0015t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0015t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0015t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0015t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0015t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0015t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0019t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0019t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0019t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0019t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0019t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0022t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0022t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0022t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0022t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0022t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0023t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0023t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0023t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0023t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0030t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0030t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0030t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0042t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0042t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0046t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0046t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0052t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0052t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0056t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0056t0001g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0068t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0082t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0084t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0085t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0086t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0092t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0115t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0121t0001g0290 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0123t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0124t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0001c0132t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0004t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0012t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0012t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0012t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0012t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0012t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0012t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0012t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0012t0002g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0031t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0031t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0031t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0041t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0041t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0079t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0087t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0112t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0116t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0002c0127t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0008t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0008t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0008t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0008t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0008t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0008t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0008t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0008t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0008t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0008t0003g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0024t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0024t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0024t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0024t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0040t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0040t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0043t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0043t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0045t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0045t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0051t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0051t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0075t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0076t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0077t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0111t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0114t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0118t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0122t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0003c0126t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0007t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0007t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0007t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0007t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0007t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0007t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0007t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0007t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0007t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0007t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0020t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0020t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0020t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0020t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0020t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0035t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0035t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0035t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0050t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0050t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0053t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0053t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0055t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0055t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0070t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0080t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0004c0125t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0006t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0006t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0006t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0006t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0006t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0006t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0006t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0006t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0006t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0006t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0006t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0025t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0025t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0025t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0025t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0029t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0029t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0029t0001g0361 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0034t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0034t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0034t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0083t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0095t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0005c0113t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0005t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0011t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0011t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0011t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0011t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0011t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0011t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0011t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0011t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0081t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0006c0128t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0010t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0010t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0010t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0010t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0010t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0010t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0010t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0010t0001g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0021t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0021t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0021t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0021t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0021t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0032t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0032t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0032t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0071t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0072t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0073t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0108t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0007c0110t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0008c0017t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0008c0017t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0008c0017t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0008c0017t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0008c0017t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0008c0028t0001g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0008c0028t0001g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0008c0028t0001g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0008c0037t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0008c0037t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0008c0104t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0008c0105t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0009c0013t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0009c0013t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0009c0013t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0009c0013t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0009c0013t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0009c0013t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0009c0013t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0009c0054t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0009c0054t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0009c0090t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0009c0094t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0010c0016t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0010c0016t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0010c0016t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0010c0016t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0010c0016t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0010c0016t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0010c0027t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0010c0027t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0010c0027t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0011c0033t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0011c0033t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0011c0033t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0011c0038t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0011c0038t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0011c0039t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0011c0039t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0012c0018t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0012c0018t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0012c0018t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0012c0018t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0012c0018t0002g0389 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0012c0065t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0012c0106t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0013c0026t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0013c0026t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0013c0026t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0013c0026t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0014c0064t0002g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0014c0100t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0014c0102t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0015c0044t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0015c0044t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0015c0117t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0016c0097t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0016c0129t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0016c0130t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0017c0063t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0017c0099t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0018c0036t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0018c0036t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0019c0047t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0019c0047t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0020c0049t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0020c0049t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0021c0048t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0021c0048t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0022c0096t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0023c0057t0004g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0024c0058t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0025c0089t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0026c0059t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0027c0060t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0028c0093t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0029c0103t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0030c0098t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0031c0101t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0032c0062t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0033c0061t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0034c0066t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0035c0067t0002g0390 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0036c0088t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0037c0091t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0038c0120t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0039c0078t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0040c0074t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0041c0109t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0042c0069t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0043c0119t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0044c0107t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| a0045c0131t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0015 | t0001 | g0046 | EUR | GBR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0182 | EUR | GBR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00140 | hp1 | a0010 | c0016 | t0001 | g0294 | EUR | GBR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00140 | hp2 | a0035 | c0067 | t0002 | g0390 | EUR | GBR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00280 | hp1 | a0003 | c0024 | t0001 | g0025 | EUR | FIN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00280 | hp2 | a0004 | c0007 | t0001 | g0136 | EUR | FIN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00323 | hp1 | a0001 | c0068 | t0001 | g0008 | EUR | FIN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00323 | hp2 | a0001 | c0014 | t0001 | g0206 | EUR | FIN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00423 | hp1 | a0002 | c0004 | t0002 | g0237 | EAS | CHS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00423 | hp2 | a0008 | c0105 | t0001 | g0372 | EAS | CHS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00438 | hp1 | a0002 | c0004 | t0002 | g0125 | EAS | CHS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00438 | hp2 | a0005 | c0006 | t0001 | g0159 | EAS | CHS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00544 | hp1 | a0003 | c0043 | t0001 | g0195 | EAS | CHS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0162 | EAS | CHS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00597 | hp1 | a0003 | c0043 | t0001 | g0123 | EAS | CHS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00597 | hp2 | a0002 | c0012 | t0002 | g0003 | EAS | CHS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00609 | hp1 | a0002 | c0004 | t0002 | g0124 | EAS | CHS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00609 | hp2 | a0013 | c0026 | t0002 | g0228 | EAS | CHS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00639 | hp1 | a0002 | c0112 | t0002 | g0271 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00673 | hp1 | a0009 | c0054 | t0001 | g0326 | EAS | CHS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00673 | hp2 | a0043 | c0119 | t0001 | g0272 | EAS | CHS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00733 | hp1 | a0004 | c0007 | t0001 | g0139 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00733 | hp2 | a0001 | c0086 | t0001 | g0018 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00735 | hp2 | a0001 | c0014 | t0001 | g0171 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01069 | hp1 | a0008 | c0017 | t0001 | g0173 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01069 | hp2 | a0001 | c0014 | t0001 | g0022 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01070 | hp1 | a0001 | c0014 | t0001 | g0048 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01070 | hp2 | a0008 | c0017 | t0001 | g0227 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01074 | hp2 | a0001 | c0014 | t0001 | g0362 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0388 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01081 | hp2 | a0002 | c0004 | t0002 | g0059 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01099 | hp1 | a0004 | c0080 | t0001 | g0019 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01109 | hp1 | a0003 | c0076 | t0002 | g0250 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01109 | hp2 | a0002 | c0079 | t0002 | g0089 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0386 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0387 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01175 | hp1 | a0002 | c0012 | t0002 | g0031 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01175 | hp2 | a0002 | c0031 | t0002 | g0058 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01192 | hp1 | a0001 | c0014 | t0001 | g0120 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01192 | hp2 | a0037 | c0091 | t0001 | g0167 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01243 | hp1 | a0020 | c0049 | t0001 | g0028 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01243 | hp2 | a0004 | c0050 | t0001 | g0329 | AMR | PUR | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01255 | hp1 | a0001 | c0052 | t0001 | g0023 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01255 | hp2 | a0001 | c0046 | t0001 | g0261 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01256 | hp1 | a0003 | c0024 | t0001 | g0070 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01257 | hp1 | a0007 | c0010 | t0001 | g0172 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01257 | hp2 | a0001 | c0022 | t0001 | g0273 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01258 | hp2 | a0001 | c0022 | t0001 | g0274 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01261 | hp2 | a0001 | c0046 | t0001 | g0262 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01346 | hp1 | a0007 | c0032 | t0001 | g0327 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0263 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01433 | hp2 | a0003 | c0024 | t0001 | g0052 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01515 | hp1 | a0036 | c0088 | t0001 | g0016 | EUR | IBS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01515 | hp2 | a0008 | c0037 | t0001 | g0009 | EUR | IBS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01516 | hp1 | a0002 | c0004 | t0002 | g0180 | EUR | IBS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01516 | hp2 | a0001 | c0082 | t0001 | g0168 | EUR | IBS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01517 | hp1 | a0002 | c0004 | t0002 | g0181 | EUR | IBS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01517 | hp2 | a0008 | c0037 | t0001 | g0004 | EUR | IBS | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01884 | hp1 | a0007 | c0110 | t0001 | g0349 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01884 | hp2 | a0001 | c0019 | t0001 | g0122 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01891 | hp1 | a0002 | c0127 | t0002 | g0306 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01891 | hp2 | a0010 | c0027 | t0001 | g0170 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01928 | hp1 | a0001 | c0015 | t0001 | g0081 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0257 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01943 | hp2 | a0001 | c0009 | t0001 | g0333 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01952 | hp1 | a0002 | c0004 | t0002 | g0259 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0141 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01975 | hp1 | a0002 | c0004 | t0002 | g0202 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01975 | hp2 | a0001 | c0056 | t0001 | g0384 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0075 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01981 | hp1 | a0008 | c0104 | t0001 | g0374 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02004 | hp1 | a0007 | c0032 | t0001 | g0017 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0255 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02015 | hp1 | a0011 | c0039 | t0001 | g0092 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02015 | hp2 | a0004 | c0020 | t0001 | g0285 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02027 | hp1 | a0003 | c0122 | t0001 | g0276 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02027 | hp2 | a0001 | c0009 | t0001 | g0286 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02040 | hp1 | a0011 | c0033 | t0001 | g0340 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02056 | hp1 | a0001 | c0015 | t0001 | g0106 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02056 | hp2 | a0001 | c0015 | t0001 | g0002 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02071 | hp1 | a0008 | c0028 | t0001 | g0395 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02071 | hp2 | a0005 | c0006 | t0001 | g0238 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02074 | hp1 | a0002 | c0004 | t0002 | g0183 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02074 | hp2 | a0009 | c0054 | t0001 | g0297 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02080 | hp2 | a0013 | c0026 | t0002 | g0143 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02083 | hp1 | a0007 | c0021 | t0001 | g0302 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02129 | hp1 | a0003 | c0024 | t0001 | g0239 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02129 | hp2 | a0005 | c0006 | t0001 | g0127 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02132 | hp1 | a0027 | c0060 | t0001 | g0156 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02132 | hp2 | a0001 | c0030 | t0001 | g0343 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02135 | hp1 | a0002 | c0004 | t0002 | g0204 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02135 | hp2 | a0001 | c0022 | t0001 | g0289 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02145 | hp1 | a0028 | c0093 | t0001 | g0269 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02145 | hp2 | a0042 | c0069 | t0001 | g0365 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02148 | hp1 | a0002 | c0004 | t0002 | g0234 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02155 | hp1 | a0015 | c0044 | t0002 | g0153 | EAS | CDX | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | CDX | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02165 | hp1 | a0001 | c0030 | t0001 | g0187 | EAS | CDX | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02165 | hp2 | a0006 | c0011 | t0002 | g0225 | EAS | CDX | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02257 | hp1 | a0004 | c0007 | t0001 | g0307 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02257 | hp2 | a0003 | c0008 | t0003 | g0381 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02258 | hp1 | a0001 | c0042 | t0001 | g0021 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02273 | hp2 | a0001 | c0015 | t0001 | g0084 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0258 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02293 | hp2 | a0001 | c0123 | t0001 | g0342 | AMR | PEL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02451 | hp1 | a0039 | c0078 | t0001 | g0313 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0363 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02523 | hp1 | a0005 | c0006 | t0001 | g0101 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02523 | hp2 | a0002 | c0012 | t0002 | g0240 | EAS | KHV | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02572 | hp1 | a0003 | c0051 | t0001 | g0252 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02572 | hp2 | a0004 | c0035 | t0001 | g0097 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02615 | hp1 | a0001 | c0023 | t0001 | g0314 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02615 | hp2 | a0030 | c0098 | t0001 | g0354 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02622 | hp1 | a0001 | c0023 | t0001 | g0248 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02630 | hp1 | a0009 | c0013 | t0001 | g0351 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02630 | hp2 | a0004 | c0053 | t0001 | g0088 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02647 | hp1 | a0004 | c0020 | t0003 | g0098 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0378 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02683 | hp1 | a0026 | c0059 | t0001 | g0060 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02698 | hp1 | a0002 | c0012 | t0002 | g0055 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02698 | hp2 | a0001 | c0052 | t0001 | g0026 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02717 | hp1 | a0009 | c0013 | t0001 | g0061 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02717 | hp2 | a0003 | c0045 | t0001 | g0090 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02723 | hp1 | a0001 | c0022 | t0001 | g0356 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02723 | hp2 | a0001 | c0023 | t0001 | g0249 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02735 | hp1 | a0001 | c0084 | t0001 | g0053 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02735 | hp2 | a0012 | c0018 | t0002 | g0175 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02809 | hp1 | a0007 | c0073 | t0001 | g0218 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02809 | hp2 | a0016 | c0130 | t0003 | g0316 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02818 | hp1 | a0004 | c0035 | t0001 | g0094 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02818 | hp2 | a0009 | c0013 | t0001 | g0350 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02886 | hp1 | a0004 | c0035 | t0001 | g0095 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02886 | hp2 | a0003 | c0008 | t0001 | g0311 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02896 | hp1 | a0003 | c0040 | t0001 | g0165 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02896 | hp2 | a0002 | c0041 | t0002 | g0358 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02897 | hp1 | a0003 | c0040 | t0001 | g0177 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02897 | hp2 | a0044 | c0107 | t0001 | g0344 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02922 | hp1 | a0007 | c0108 | t0001 | g0275 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02922 | hp2 | a0001 | c0019 | t0001 | g0066 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02965 | hp2 | a0004 | c0125 | t0001 | g0013 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02970 | hp1 | a0007 | c0032 | t0001 | g0254 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02970 | hp2 | a0004 | c0053 | t0003 | g0317 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02976 | hp1 | a0001 | c0019 | t0001 | g0065 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02976 | hp2 | a0006 | c0005 | t0002 | g0355 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03017 | hp1 | a0007 | c0071 | t0001 | g0178 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03041 | hp1 | a0003 | c0008 | t0001 | g0246 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03041 | hp2 | a0004 | c0020 | t0001 | g0096 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03130 | hp1 | a0045 | c0131 | t0001 | g0315 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03130 | hp2 | a0004 | c0050 | t0001 | g0328 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03139 | hp1 | a0003 | c0114 | t0002 | g0347 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03139 | hp2 | a0001 | c0019 | t0001 | g0359 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03195 | hp1 | a0004 | c0070 | t0001 | g0069 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03195 | hp2 | a0007 | c0010 | t0001 | g0391 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03209 | hp2 | a0003 | c0008 | t0001 | g0245 | AFR | MSL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03225 | hp1 | a0031 | c0101 | t0001 | g0346 | AFR | MSL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03225 | hp2 | a0004 | c0007 | t0001 | g0325 | AFR | MSL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03239 | hp1 | a0032 | c0062 | t0001 | g0080 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03239 | hp2 | a0007 | c0010 | t0001 | g0224 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03453 | hp1 | a0007 | c0021 | t0001 | g0348 | AFR | MSL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03453 | hp2 | a0041 | c0109 | t0001 | g0345 | AFR | MSL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03486 | hp1 | a0003 | c0008 | t0001 | g0247 | AFR | MSL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03486 | hp2 | a0016 | c0097 | t0001 | g0107 | AFR | MSL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03490 | hp1 | a0002 | c0012 | t0002 | g0057 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03490 | hp2 | a0021 | c0048 | t0002 | g0193 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03492 | hp1 | a0021 | c0048 | t0002 | g0198 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03516 | hp1 | a0001 | c0042 | t0001 | g0377 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03516 | hp2 | a0007 | c0010 | t0001 | g0385 | AFR | ESN | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03540 | hp1 | a0009 | c0013 | t0001 | g0062 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03540 | hp2 | a0003 | c0008 | t0001 | g0312 | AFR | GWD | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03579 | hp1 | a0016 | c0129 | t0001 | g0100 | AFR | MSL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03579 | hp2 | a0009 | c0090 | t0001 | g0131 | AFR | MSL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03654 | hp2 | a0003 | c0008 | t0001 | g0265 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03669 | hp1 | a0018 | c0036 | t0002 | g0035 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0155 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03688 | hp1 | a0012 | c0018 | t0002 | g0033 | SAS | STU | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03688 | hp2 | a0003 | c0075 | t0001 | g0213 | SAS | STU | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03704 | hp1 | a0023 | c0057 | t0004 | g0360 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03704 | hp2 | a0029 | c0103 | t0001 | g0373 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03710 | hp2 | a0018 | c0036 | t0002 | g0034 | SAS | PJL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03834 | hp1 | a0005 | c0006 | t0001 | g0056 | SAS | BEB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03834 | hp2 | a0033 | c0061 | t0001 | g0256 | SAS | BEB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03927 | hp1 | a0008 | c0017 | t0001 | g0154 | SAS | BEB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0320 | SAS | BEB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03942 | hp1 | a0005 | c0025 | t0001 | g0078 | SAS | BEB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03942 | hp2 | a0012 | c0065 | t0002 | g0005 | SAS | BEB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0260 | SAS | STU | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0111 | SAS | STU | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG04184 | hp1 | a0001 | c0015 | t0001 | g0045 | SAS | BEB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG04184 | hp2 | a0001 | c0056 | t0001 | g0382 | SAS | BEB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG04199 | hp1 | a0003 | c0008 | t0001 | g0119 | SAS | STU | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | STU | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0079 | SAS | STU | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG04228 | hp1 | a0002 | c0041 | t0002 | g0232 | SAS | STU | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0380 | SAS | STU | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18747 | hp1 | a0008 | c0028 | t0001 | g0394 | EAS | CHB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | CHB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18906 | hp1 | a0001 | c0092 | t0001 | g0211 | AFR | YRI | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18906 | hp2 | a0004 | c0007 | t0003 | g0164 | AFR | YRI | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18939 | hp2 | a0002 | c0004 | t0002 | g0176 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18940 | hp1 | a0038 | c0120 | t0002 | g0278 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18940 | hp2 | a0010 | c0016 | t0001 | g0364 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18941 | hp1 | a0002 | c0012 | t0002 | g0014 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18941 | hp2 | a0010 | c0016 | t0001 | g0292 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18942 | hp1 | a0002 | c0012 | t0002 | g0383 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18942 | hp2 | a0034 | c0066 | t0001 | g0219 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18944 | hp1 | a0013 | c0026 | t0002 | g0114 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18944 | hp2 | a0005 | c0006 | t0001 | g0226 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18945 | hp2 | a0040 | c0074 | t0002 | g0322 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18946 | hp1 | a0002 | c0031 | t0002 | g0071 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18946 | hp2 | a0006 | c0011 | t0002 | g0191 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18947 | hp1 | a0012 | c0106 | t0002 | g0371 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18947 | hp2 | a0001 | c0009 | t0001 | g0293 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18948 | hp1 | a0006 | c0005 | t0002 | g0288 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18950 | hp1 | a0006 | c0011 | t0002 | g0129 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18950 | hp2 | a0007 | c0021 | t0001 | g0303 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18951 | hp1 | a0006 | c0011 | t0002 | g0205 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18952 | hp1 | a0007 | c0010 | t0001 | g0321 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18952 | hp2 | a0015 | c0044 | t0002 | g0188 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18954 | hp1 | a0006 | c0005 | t0002 | g0308 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18954 | hp2 | a0005 | c0025 | t0001 | g0222 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18957 | hp1 | a0006 | c0005 | t0002 | g0280 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18957 | hp2 | a0024 | c0058 | t0002 | g0169 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18959 | hp1 | a0006 | c0011 | t0002 | g0109 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18959 | hp2 | a0005 | c0006 | t0001 | g0113 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18960 | hp1 | a0001 | c0009 | t0001 | g0283 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18960 | hp2 | a0011 | c0033 | t0001 | g0376 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18961 | hp1 | a0002 | c0004 | t0002 | g0128 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18961 | hp2 | a0005 | c0006 | t0001 | g0163 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18962 | hp1 | a0019 | c0047 | t0002 | g0179 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0251 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18964 | hp1 | a0009 | c0013 | t0001 | g0126 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18964 | hp2 | a0011 | c0033 | t0001 | g0370 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18967 | hp2 | a0001 | c0022 | t0001 | g0267 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18969 | hp1 | a0007 | c0021 | t0001 | g0305 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18969 | hp2 | a0001 | c0009 | t0001 | g0341 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18970 | hp1 | a0006 | c0011 | t0002 | g0102 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18970 | hp2 | a0004 | c0007 | t0001 | g0149 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18971 | hp1 | a0005 | c0095 | t0001 | g0209 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18972 | hp1 | a0014 | c0102 | t0002 | g0287 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18972 | hp2 | a0002 | c0012 | t0002 | g0223 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18973 | hp1 | a0006 | c0081 | t0002 | g0221 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18978 | hp1 | a0006 | c0005 | t0002 | g0270 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18978 | hp2 | a0012 | c0018 | t0002 | g0142 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18979 | hp2 | a0010 | c0027 | t0001 | g0319 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18980 | hp1 | a0017 | c0099 | t0001 | g0367 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18980 | hp2 | a0002 | c0004 | t0002 | g0220 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18983 | hp1 | a0004 | c0020 | t0001 | g0105 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18983 | hp2 | a0019 | c0047 | t0002 | g0192 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18984 | hp2 | a0006 | c0005 | t0002 | g0304 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18986 | hp1 | a0008 | c0028 | t0001 | g0396 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18986 | hp2 | a0017 | c0063 | t0001 | g0116 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18988 | hp1 | a0010 | c0016 | t0001 | g0375 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18988 | hp2 | a0010 | c0016 | t0001 | g0324 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18989 | hp2 | a0013 | c0026 | t0002 | g0229 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18990 | hp1 | a0007 | c0021 | t0001 | g0279 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18990 | hp2 | a0001 | c0009 | t0001 | g0332 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18994 | hp1 | a0006 | c0011 | t0002 | g0186 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18994 | hp2 | a0004 | c0055 | t0001 | g0323 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0393 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18995 | hp2 | a0005 | c0025 | t0001 | g0150 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18998 | hp1 | a0005 | c0083 | t0001 | g0121 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18998 | hp2 | a0006 | c0128 | t0002 | g0339 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18999 | hp1 | a0006 | c0005 | t0002 | g0298 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18999 | hp2 | a0011 | c0038 | t0001 | g0006 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19003 | hp1 | a0005 | c0006 | t0001 | g0231 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19003 | hp2 | a0011 | c0039 | t0001 | g0093 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19004 | hp1 | a0010 | c0016 | t0001 | g0366 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19007 | hp1 | a0001 | c0085 | t0001 | g0236 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19007 | hp2 | a0001 | c0009 | t0001 | g0282 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19009 | hp1 | a0006 | c0005 | t0002 | g0295 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19011 | hp1 | a0014 | c0100 | t0002 | g0368 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19012 | hp1 | a0003 | c0111 | t0001 | g0291 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19012 | hp2 | a0006 | c0005 | t0002 | g0300 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19043 | hp1 | a0001 | c0115 | t0001 | g0040 | AFR | LWK | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19043 | hp2 | a0008 | c0017 | t0001 | g0103 | AFR | LWK | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19054 | hp1 | a0001 | c0030 | t0001 | g0318 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19054 | hp2 | a0006 | c0005 | t0002 | g0369 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19055 | hp1 | a0004 | c0020 | t0001 | g0268 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19055 | hp2 | a0006 | c0005 | t0002 | g0284 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19056 | hp1 | a0005 | c0034 | t0001 | g0337 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19060 | hp1 | a0006 | c0005 | t0002 | g0299 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19060 | hp2 | a0005 | c0029 | t0001 | g0085 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19062 | hp1 | a0009 | c0094 | t0001 | g0208 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19062 | hp2 | a0005 | c0025 | t0001 | g0132 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19064 | hp1 | a0006 | c0005 | t0002 | g0296 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19064 | hp2 | a0006 | c0011 | t0002 | g0037 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19065 | hp2 | a0005 | c0034 | t0001 | g0334 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19067 | hp1 | a0002 | c0004 | t0002 | g0194 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19067 | hp2 | a0012 | c0018 | t0002 | g0152 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19068 | hp1 | a0007 | c0010 | t0001 | g0235 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19068 | hp2 | a0005 | c0006 | t0001 | g0189 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19074 | hp1 | a0001 | c0009 | t0001 | g0281 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19074 | hp2 | a0002 | c0004 | t0002 | g0166 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19077 | hp1 | a0015 | c0117 | t0002 | g0336 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19079 | hp1 | a0004 | c0007 | t0001 | g0197 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19079 | hp2 | a0004 | c0055 | t0001 | g0301 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19081 | hp1 | a0002 | c0004 | t0002 | g0184 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19081 | hp2 | a0001 | c0009 | t0001 | g0277 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19082 | hp1 | a0001 | c0124 | t0001 | g0331 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19082 | hp2 | a0005 | c0006 | t0001 | g0104 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19083 | hp1 | a0014 | c0064 | t0002 | g0392 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19083 | hp2 | a0025 | c0089 | t0002 | g0243 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19084 | hp1 | a0007 | c0072 | t0001 | g0233 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19084 | hp2 | a0007 | c0010 | t0001 | g0036 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19085 | hp1 | a0005 | c0006 | t0001 | g0144 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19085 | hp2 | a0002 | c0116 | t0002 | g0330 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19088 | hp1 | a0002 | c0004 | t0002 | g0196 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19088 | hp2 | a0005 | c0034 | t0001 | g0338 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19240 | hp1 | a0004 | c0007 | t0001 | g0051 | AFR | YRI | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA19240 | hp2 | a0001 | c0023 | t0001 | g0244 | AFR | YRI | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA20129 | hp1 | a0001 | c0009 | t0001 | g0335 | AFR | ASW | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA20129 | hp2 | a0008 | c0017 | t0001 | g0146 | AFR | ASW | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA20752 | hp1 | a0001 | c0132 | t0001 | g0242 | EUR | TSI | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA20752 | hp2 | a0012 | c0018 | t0002 | g0389 | EUR | TSI | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA20805 | hp1 | a0004 | c0007 | t0001 | g0212 | EUR | TSI | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA20805 | hp2 | a0010 | c0027 | t0001 | g0185 | EUR | TSI | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA20905 | hp1 | a0011 | c0038 | t0001 | g0157 | SAS | GIH | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA20905 | hp2 | a0003 | c0045 | t0001 | g0266 | SAS | GIH | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01123 | hp1 | a0007 | c0010 | t0001 | g0214 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG01123 | hp2 | a0002 | c0031 | t0002 | g0064 | AMR | CLM | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02109 | hp1 | a0003 | c0077 | t0001 | g0379 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02109 | hp2 | a0003 | c0008 | t0001 | g0310 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02486 | hp1 | a0004 | c0007 | t0003 | g0210 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02486 | hp2 | a0003 | c0051 | t0001 | g0020 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02559 | hp1 | a0005 | c0029 | t0001 | g0015 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG02559 | hp2 | a0003 | c0118 | t0001 | g0357 | AFR | ACB | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03471 | hp1 | a0005 | c0113 | t0001 | g0099 | AFR | MSL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG03471 | hp2 | a0022 | c0096 | t0001 | g0030 | AFR | MSL | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG06807 | hp1 | a0003 | c0008 | t0001 | g0309 | AFR | USA | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| HG06807 | hp2 | a0009 | c0013 | t0001 | g0352 | AFR | USA | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18955 | hp1 | a0009 | c0013 | t0001 | g0147 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA20300 | hp1 | a0001 | c0019 | t0001 | g0118 | AFR | USA | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA20300 | hp2 | a0002 | c0087 | t0002 | g0024 | AFR | USA | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA21309 | hp1 | a0020 | c0049 | t0001 | g0029 | AFR | LWK | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| NA21309 | hp2 | a0003 | c0126 | t0001 | g0012 | AFR | LWK | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0121 | t0001 | g0290 | REF | REF | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| homoSapiens_grch38 | hp1 | a0005 | c0029 | t0001 | g0361 | REF | REF | NLRP5_chr19_55994726_56066810 | NLRP5 | chr19 | 55994726 | 56066810 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:56019729
|
CAGTAATT others(1026): Show |
C | 2 | a0016a0045 | 4 | HG02809.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.622+438_679+437del | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 56019729 | |||||
| chr19:56020420
|
C | T | 1 | a0022 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.668C>T | p.Thr223Ile | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/15 | 668/3885 | 668/3603 | 223/1200 | chr19 | 56020420 | ||
| chr19:56027072
|
G | A | 1 | a0023 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.839G>A | p.Arg280His | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 839/3885 | 839/3603 | 280/1200 | chr19 | 56027072 | ||
| chr19:56027147
|
A | G | 1 | a0013 | 4 | HG00609.hp2 HG02080.hp2 NA18944.hp1 others(1): Show |
missense_variant | MODERATE | c.914A>G | p.Gln305Arg | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 914/3885 | 914/3603 | 305/1200 | chr19 | 56027147 | ||
| chr19:56027179
|
G | A | 1 | a0024 | 1 | NA18957.hp2 | missense_variant | MODERATE | c.946G>A | p.Val316Ile | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 946/3885 | 946/3603 | 316/1200 | chr19 | 56027179 | ||
| chr19:56027280
|
G | T | 1 | a0025 | 1 | NA19083.hp2 | missense_variant | MODERATE | c.1047G>T | p.Glu349Asp | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1047/3885 | 1047/3603 | 349/1200 | chr19 | 56027280 | ||
| chr19:56027291
|
G | A | 1 | a0026 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1058G>A | p.Arg353Gln | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1058/3885 | 1058/3603 | 353/1200 | chr19 | 56027291 | ||
| chr19:56027425
|
G | A | 1 | a0027 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.1192G>A | p.Val398Ile | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1192/3885 | 1192/3603 | 398/1200 | chr19 | 56027425 | ||
| chr19:56027554
|
C | T | 1 | a0028 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1321C>T | p.Leu441Phe | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1321/3885 | 1321/3603 | 441/1200 | chr19 | 56027554 | ||
| chr19:56027610
|
G | C | 12 | a0008a0010a0011others(9): Show | 47 | HG00140.hp1 HG00423.hp2 HG01069.hp1 others(44): Show |
missense_variant | MODERATE | c.1377G>C | p.Met459Ile | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1377/3885 | 1377/3603 | 459/1200 | chr19 | 56027610 | ||
| chr19:56027647
|
G | A | 2 | a0018a0033 | 3 | HG03669.hp1 HG03710.hp2 HG03834.hp2 |
missense_variant | MODERATE | c.1414G>A | p.Ala472Thr | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1414/3885 | 1414/3603 | 472/1200 | chr19 | 56027647 | ||
| chr19:56027696
|
G | A | 1 | a0034 | 1 | NA18942.hp2 | missense_variant | MODERATE | c.1463G>A | p.Gly488Glu | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1463/3885 | 1463/3603 | 488/1200 | chr19 | 56027696 | ||
| chr19:56027788
|
T | C | 1 | a0044 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.1555T>C | p.Cys519Arg | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1555/3885 | 1555/3603 | 519/1200 | chr19 | 56027788 | ||
| chr19:56027918
|
G | A | 1 | a0035 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1685G>A | p.Arg562His | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1685/3885 | 1685/3603 | 562/1200 | chr19 | 56027918 | ||
| chr19:56027986
|
C | A | 1 | a0025 | 1 | NA19083.hp2 | missense_variant | MODERATE | c.1753C>A | p.Leu585Ile | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1753/3885 | 1753/3603 | 585/1200 | chr19 | 56027986 | ||
| chr19:56032616
|
G | T | 1 | a0036 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2282G>T | p.Arg761Leu | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/15 | 2282/3885 | 2282/3603 | 761/1200 | chr19 | 56032616 | ||
| chr19:56032631
|
T | C | 1 | a0032 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.2297T>C | p.Ile766Thr | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/15 | 2297/3885 | 2297/3603 | 766/1200 | chr19 | 56032631 | ||
| chr19:56032678
|
C | T | 1 | a0021 | 2 | HG03490.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.2344C>T | p.His782Tyr | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/15 | 2344/3885 | 2344/3603 | 782/1200 | chr19 | 56032678 | ||
| chr19:56032708
|
A | C | 1 | a0043 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.2374A>C | p.Ile792Leu | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/15 | 2374/3885 | 2374/3603 | 792/1200 | chr19 | 56032708 | ||
| chr19:56033603
|
C | T | 1 | a0019 | 2 | NA18962.hp1 NA18983.hp2 |
missense_variant | MODERATE | c.2509C>T | p.Arg837Cys | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/15 | 2509/3885 | 2509/3603 | 837/1200 | chr19 | 56033603 | ||
| chr19:56038144
|
T | C | 21 | a0004a0006a0007others(18): Show | 114 | HG00140.hp1 HG00280.hp2 HG00673.hp1 others(111): Show |
missense_variant | MODERATE | c.2735T>C | p.Met912Thr | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/15 | 2735/3885 | 2735/3603 | 912/1200 | chr19 | 56038144 | ||
| chr19:56040932
|
T | G | 1 | a0042 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.2797T>G | p.Cys933Gly | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/15 | 2797/3885 | 2797/3603 | 933/1200 | chr19 | 56040932 | ||
| chr19:56041030
|
C | G | 1 | a0040 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.2895C>G | p.Asn965Lys | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/15 | 2895/3885 | 2895/3603 | 965/1200 | chr19 | 56041030 | ||
| chr19:56050468
|
C | T | 1 | a0020 | 2 | HG01243.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.3008C>T | p.Ala1003Val | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/15 | 3008/3885 | 3008/3603 | 1003/1200 | chr19 | 56050468 | ||
| chr19:56050554
|
A | G | 1 | a0039 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.3094A>G | p.Met1032Val | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/15 | 3094/3885 | 3094/3603 | 1032/1200 | chr19 | 56050554 | ||
| chr19:56050587
|
G | A | 1 | a0038 | 1 | NA18940.hp1 | missense_variant&splice_region_variant | MODERATE | c.3127G>A | p.Glu1043Lys | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/15 | 3127/3885 | 3127/3603 | 1043/1200 | chr19 | 56050587 | ||
| chr19:56053747
|
G | A | 1 | a0037 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.3238G>A | p.Gly1080Ser | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/15 | 3238/3885 | 3238/3603 | 1080/1200 | chr19 | 56053747 | ||
| chr19:56053798
|
G | A | 35 | a0001a0002a0003others(32): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
missense_variant | MODERATE | c.3289G>A | p.Ala1097Thr | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/15 | 3289/3885 | 3289/3603 | 1097/1200 | chr19 | 56053798 | ||
| chr19:56058263
|
C | G | 14 | a0002a0006a0012others(11): Show | 87 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
missense_variant | MODERATE | c.3323C>G | p.Ser1108Cys | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/15 | 3323/3885 | 3323/3603 | 1108/1200 | chr19 | 56058263 | ||
| chr19:56058343
|
A | G | 1 | a0044 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.3403A>G | p.Ser1135Gly | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/15 | 3403/3885 | 3403/3603 | 1135/1200 | chr19 | 56058343 | ||
| chr19:56061466
|
G | A | 26 | a0002a0003a0004others(23): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
missense_variant | MODERATE | c.3541G>A | p.Val1181Ile | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 15/15 | 3541/3885 | 3541/3603 | 1181/1200 | chr19 | 56061466 | ||
| chr19:56061509
|
G | A | 14 | a0002a0006a0012others(11): Show | 87 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
missense_variant | MODERATE | c.3584G>A | p.Arg1195Gln | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 15/15 | 3584/3885 | 3584/3603 | 1195/1200 | chr19 | 56061509 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:56003965
|
C | T | 2 | a0001c0056a0001c0132 | 3 | HG01975.hp2 HG04184.hp2 NA20752.hp1 |
synonymous_variant | LOW | c.312C>T | p.Ala104Ala | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/15 | 312/3885 | 312/3603 | 104/1200 | chr19 | 56003965 | ||
| chr19:56003968
|
C | T | 45 | a0001c0009a0001c0022a0001c0115others(42): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
synonymous_variant | LOW | c.315C>T | p.Asn105Asn | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/15 | 315/3885 | 315/3603 | 105/1200 | chr19 | 56003968 | ||
| chr19:56027049
|
A | C | 3 | a0005c0095a0006c0128a0009c0094 | 3 | NA18971.hp1 NA18998.hp2 NA19062.hp1 |
synonymous_variant | LOW | c.816A>C | p.Ser272Ser | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 816/3885 | 816/3603 | 272/1200 | chr19 | 56027049 | ||
| chr19:56027154
|
A | G | 9 | a0001c0019a0001c0092a0002c0127others(6): Show | 16 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
synonymous_variant | LOW | c.921A>G | p.Gly307Gly | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 921/3885 | 921/3603 | 307/1200 | chr19 | 56027154 | ||
| chr19:56027466
|
C | T | 8 | a0001c0052a0001c0086a0002c0087others(5): Show | 13 | HG00733.hp2 HG01243.hp2 HG01255.hp1 others(10): Show |
synonymous_variant | LOW | c.1233C>T | p.Asp411Asp | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1233/3885 | 1233/3603 | 411/1200 | chr19 | 56027466 | ||
| chr19:56027469
|
G | T | 1 | a0025c0089 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.1236G>T | p.Val412Val | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1236/3885 | 1236/3603 | 412/1200 | chr19 | 56027469 | ||
| chr19:56027739
|
C | T | 2 | a0001c0085a0012c0065 | 2 | HG03942.hp2 NA19007.hp1 |
synonymous_variant | LOW | c.1506C>T | p.His502His | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1506/3885 | 1506/3603 | 502/1200 | chr19 | 56027739 | ||
| chr19:56027874
|
C | T | 45 | a0001c0002a0001c0015a0001c0082others(42): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
synonymous_variant | LOW | c.1641C>T | p.Asp547Asp | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/15 | 1641/3885 | 1641/3603 | 547/1200 | chr19 | 56027874 | ||
| chr19:56032719
|
G | A | 1 | a0003c0040 | 2 | HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.2385G>A | p.Glu795Glu | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/15 | 2385/3885 | 2385/3603 | 795/1200 | chr19 | 56032719 | ||
| chr19:56038082
|
G | A | 1 | a0001c0068 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.2673G>A | p.Thr891Thr | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/15 | 2673/3885 | 2673/3603 | 891/1200 | chr19 | 56038082 | ||
| chr19:56038166
|
A | G | 55 | a0001c0046a0001c0084a0002c0079others(52): Show | 123 | HG00140.hp1 HG00280.hp2 HG00673.hp1 others(120): Show |
synonymous_variant | LOW | c.2757A>G | p.Arg919Arg | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/15 | 2757/3885 | 2757/3603 | 919/1200 | chr19 | 56038166 | ||
| chr19:56041090
|
G | T | 30 | a0001c0003a0001c0009a0001c0015others(27): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
splice_region_variant&synonymous_variant | LOW | c.2955G>T | p.Leu985Leu | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/15 | 2955/3885 | 2955/3603 | 985/1200 | chr19 | 56041090 | ||
| chr19:56050448
|
C | T | 2 | a0001c0092a0001c0115 | 2 | NA18906.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.2988C>T | p.Gly996Gly | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/15 | 2988/3885 | 2988/3603 | 996/1200 | chr19 | 56050448 | ||
| chr19:56053746
|
C | T | 2 | a0001c0023a0003c0077 | 5 | HG02109.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
synonymous_variant | LOW | c.3237C>T | p.Asp1079Asp | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/15 | 3237/3885 | 3237/3603 | 1079/1200 | chr19 | 56053746 | ||
| chr19:56053761
|
G | A | 14 | a0001c0014a0001c0030a0001c0056others(11): Show | 23 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(20): Show |
synonymous_variant | LOW | c.3252G>A | p.Ala1084Ala | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/15 | 3252/3885 | 3252/3603 | 1084/1200 | chr19 | 56053761 | ||
| chr19:56053761
|
G | T | 1 | a0014c0102 | 1 | NA18972.hp1 | synonymous_variant | LOW | c.3252G>T | p.Ala1084Ala | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/15 | 3252/3885 | 3252/3603 | 1084/1200 | chr19 | 56053761 | ||
| chr19:56053788
|
C | T | 5 | a0001c0042a0003c0076a0003c0114others(2): Show | 6 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
synonymous_variant | LOW | c.3279C>T | p.Asn1093Asn | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/15 | 3279/3885 | 3279/3603 | 1093/1200 | chr19 | 56053788 | ||
| chr19:56061447
|
G | A | 1 | a0041c0109 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.3522G>A | p.Val1174Val | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 15/15 | 3522/3885 | 3522/3603 | 1174/1200 | chr19 | 56061447 | ||
| chr19:56061465
|
A | G | 1 | a0007c0072 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.3540A>G | p.Arg1180Arg | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 15/15 | 3540/3885 | 3540/3603 | 1180/1200 | chr19 | 56061465 | ||
| chr19:56061477
|
C | T | 1 | a0001c0086 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.3552C>T | p.Asp1184Asp | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 15/15 | 3552/3885 | 3552/3603 | 1184/1200 | chr19 | 56061477 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:56061594
|
G | C | 1 | a0023c0057t0004 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 15/15 | 66 | chr19 | 56061594 | |||||
| chr19:56061601
|
A | T | 5 | a0003c0008t0003a0004c0007t0003a0004c0020t0003others(2): Show | 6 | HG02257.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*73A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 15/15 | 73 | chr19 | 56061601 | |||||
| chr19:56061728
|
T | A | 32 | a0002c0004t0002a0002c0012t0002a0002c0031t0002others(29): Show | 89 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*200T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 15/15 | 200 | chr19 | 56061728 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:55999851
|
G | A | 87 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(84): Show | 87 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.62+64G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 55999851 | ||||||
| chr19:55999867
|
C | T | 61 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(58): Show | 61 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.62+80C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 55999867 | ||||||
| chr19:55999988
|
C | CATGACAG others(34): Show |
4 | a0001c0001t0001g0091a0001c0002t0001g0032a0011c0039t0001g0092others(1): Show | 4 | HG02015.hp1 HG03017.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.62+230_62+270dupCC others(39): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 55999988 | |||||
| chr19:55999988
|
C | CATGACAG others(75): Show |
147 | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0130others(144): Show | 147 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.62+230_62+311dupCC others(80): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 55999988 | |||||
| chr19:55999988
|
C | CATGACAG others(116): Show |
1 | a0006c0011t0002g0102 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.62+311_62+312insCC others(121): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 55999988 | |||||
| chr19:55999988
|
C | CATGACAG others(198): Show |
1 | a0005c0006t0001g0101 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.62+311_62+312insCC others(203): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 55999988 | |||||
| chr19:56000017
|
C | CCCACTCT others(157): Show |
3 | a0002c0079t0002g0089a0003c0045t0001g0090a0004c0053t0001g0088 | 3 | HG01109.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.62+270_62+271insCC others(162): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56000017 | |||||
| chr19:56000017
|
CCCACTCT others(34): Show |
C | 8 | a0004c0020t0001g0096a0004c0020t0003g0098a0004c0035t0001g0094others(5): Show | 8 | HG02572.hp2 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.62+303_62+343delTG others(39): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56000017 | |||||
| chr19:56000044
|
G | GGGACTGC others(157): Show |
8 | a0001c0003t0001g0255a0001c0003t0001g0257a0001c0003t0001g0258others(5): Show | 8 | HG01934.hp2 HG01952.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.62+344_62+345insAC others(162): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56000044 | |||||
| chr19:56000058
|
T | C | 3 | a0002c0079t0002g0089a0003c0045t0001g0090a0004c0053t0001g0088 | 3 | HG01109.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.62+271T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000058 | ||||||
| chr19:56000058
|
T | TCCACTCT others(34): Show |
3 | a0001c0003t0001g0001a0005c0006t0001g0104a0008c0017t0001g0103 | 3 | HG04199.hp2 NA19043.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.62+311_62+312insCC others(39): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56000058 | |||||
| chr19:56000112
|
A | G | 1 | a0001c0003t0001g0251 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.62+325A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000112 | ||||||
| chr19:56000130
|
CGGCCACC others(34): Show |
C | 1 | a0007c0010t0001g0391 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.62+356_62+396delAC others(39): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56000130 | |||||
| chr19:56000131
|
G | T | 2 | a0002c0012t0002g0031a0003c0076t0002g0250 | 2 | HG01109.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.62+344G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000131 | ||||||
| chr19:56000132
|
G | A | 3 | a0001c0001t0001g0253a0003c0051t0001g0252a0007c0032t0001g0254 | 3 | HG00741.hp1 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.62+345G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000132 | ||||||
| chr19:56000149
|
C | T | 1 | a0003c0076t0002g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.62+362C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000149 | ||||||
| chr19:56000177
|
C | T | 1 | a0035c0067t0002g0390 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.62+390C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000177 | ||||||
| chr19:56000207
|
G | A | 47 | a0001c0001t0001g0264a0001c0003t0001g0260a0001c0003t0001g0263others(44): Show | 47 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.62+420G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000207 | ||||||
| chr19:56000310
|
C | T | 4 | a0001c0001t0001g0386a0001c0001t0001g0387a0001c0001t0001g0388others(1): Show | 4 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.62+523C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000310 | ||||||
| chr19:56000356
|
C | T | 7 | a0001c0023t0001g0244a0001c0023t0001g0248a0001c0023t0001g0249others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.62+569C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000356 | ||||||
| chr19:56000361
|
GT | G | 278 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(275): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.62+583delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56000361 | |||||
| chr19:56000362
|
T | A | 1 | a0001c0015t0001g0106 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.62+575T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000362 | ||||||
| chr19:56000401
|
G | C | 1 | a0001c0015t0001g0106 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.62+614G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000401 | ||||||
| chr19:56000509
|
C | A | 13 | a0001c0001t0001g0353a0001c0115t0001g0040a0003c0114t0002g0347others(10): Show | 13 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.62+722C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000509 | ||||||
| chr19:56000511
|
C | T | 1 | a0001c0052t0001g0026 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.62+724C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000511 | ||||||
| chr19:56000513
|
C | T | 80 | a0001c0001t0001g0253a0001c0002t0001g0241a0001c0009t0001g0277others(77): Show | 80 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.62+726C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000513 | ||||||
| chr19:56000566
|
G | A | 43 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(40): Show | 43 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.62+779G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000566 | ||||||
| chr19:56000600
|
A | G | 263 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0091others(260): Show | 263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.62+813A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000600 | ||||||
| chr19:56000659
|
C | A | 8 | a0001c0022t0001g0356a0001c0115t0001g0040a0003c0114t0002g0347others(5): Show | 8 | HG01884.hp1 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.62+872C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000659 | ||||||
| chr19:56000682
|
T | C | 1 | a0001c0022t0001g0267 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.62+895T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000682 | ||||||
| chr19:56000744
|
A | G | 87 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(84): Show | 87 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.62+957A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000744 | ||||||
| chr19:56000804
|
G | C | 53 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0253others(50): Show | 53 | HG00280.hp1 HG00673.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.62+1017G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000804 | ||||||
| chr19:56000813
|
C | T | 2 | a0001c0002t0001g0086a0001c0002t0001g0087 | 2 | NA18967.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.62+1026C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000813 | ||||||
| chr19:56000883
|
G | A | 1 | a0001c0023t0001g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.62+1096G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000883 | ||||||
| chr19:56000921
|
G | C | 6 | a0004c0020t0001g0096a0004c0020t0003g0098a0004c0035t0001g0094others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.62+1134G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000921 | ||||||
| chr19:56000936
|
G | A | 1 | a0001c0052t0001g0026 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.62+1149G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56000936 | ||||||
| chr19:56001076
|
C | T | 1 | a0008c0028t0001g0396 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.62+1289C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001076 | ||||||
| chr19:56001088
|
A | G | 1 | a0005c0006t0001g0238 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.62+1301A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001088 | ||||||
| chr19:56001090
|
G | A | 1 | a0006c0011t0002g0109 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.62+1303G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001090 | ||||||
| chr19:56001159
|
C | CT | 16 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(13): Show | 16 | HG01943.hp2 HG02040.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.62+1387dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56001159 | |||||
| chr19:56001159
|
CT | C | 111 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(108): Show | 111 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.62+1387delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56001159 | |||||
| chr19:56001159
|
CTT | C | 176 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(173): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.62+1386_62+1387del others(2): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56001159 | |||||
| chr19:56001165
|
T | C | 1 | a0004c0020t0001g0268 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.62+1378T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001165 | ||||||
| chr19:56001175
|
A | T | 1 | a0002c0127t0002g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.62+1388A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001175 | ||||||
| chr19:56001187
|
C | T | 42 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(39): Show | 42 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.62+1400C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001187 | ||||||
| chr19:56001193
|
T | C | 264 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(261): Show | 264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.62+1406T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001193 | ||||||
| chr19:56001202
|
G | T | 172 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(169): Show | 172 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.62+1415G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001202 | ||||||
| chr19:56001324
|
T | TA | 12 | a0001c0002t0001g0010a0001c0002t0001g0043a0001c0002t0001g0044others(9): Show | 12 | HG01070.hp2 HG01106.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+1548dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56001324 | |||||
| chr19:56001324
|
T | TAA | 123 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(120): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.62+1547_62+1548dup others(2): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56001324 | |||||
| chr19:56001324
|
T | TAAA | 29 | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0130others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.62+1546_62+1548dup others(3): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56001324 | |||||
| chr19:56001332
|
A | C | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.62+1545A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001332 | ||||||
| chr19:56001334
|
AAC | A | 71 | a0001c0001t0001g0253a0001c0009t0001g0277a0001c0009t0001g0281others(68): Show | 71 | HG00140.hp1 HG00280.hp1 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.62+1549_62+1550del others(2): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56001334 | |||||
| chr19:56001335
|
AC | A | 29 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0009t0001g0332others(26): Show | 29 | HG00639.hp1 HG00673.hp1 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.62+1549delC | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001335 | ||||||
| chr19:56001336
|
C | A | 284 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0047others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.62+1549C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001336 | ||||||
| chr19:56001340
|
C | A | 168 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(165): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.62+1553C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001340 | ||||||
| chr19:56001347
|
C | A | 1 | a0001c0015t0001g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.62+1560C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001347 | ||||||
| chr19:56001436
|
A | T | 251 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(248): Show | 251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.62+1649A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001436 | ||||||
| chr19:56001437
|
C | G | 251 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(248): Show | 251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.62+1650C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001437 | ||||||
| chr19:56001438
|
TCTCCTAA others(9): Show |
T | 251 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(248): Show | 251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.62+1652_62+1667del others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001438 | ||||||
| chr19:56001459
|
T | A | 1 | a0003c0076t0002g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.62+1672T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001459 | ||||||
| chr19:56001719
|
A | G | 63 | a0001c0001t0001g0253a0001c0009t0001g0277a0001c0009t0001g0281others(60): Show | 63 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.62+1932A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001719 | ||||||
| chr19:56001786
|
T | C | 14 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(11): Show | 14 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.63-1930T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001786 | ||||||
| chr19:56001882
|
A | G | 19 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(16): Show | 19 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.63-1834A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001882 | ||||||
| chr19:56001901
|
TG | T | 15 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(12): Show | 15 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-1809delG | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56001901 | |||||
| chr19:56001907
|
G | A | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.63-1809G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001907 | ||||||
| chr19:56001910
|
A | C | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.63-1806A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001910 | ||||||
| chr19:56001911
|
G | C | 15 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(12): Show | 15 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-1805G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001911 | ||||||
| chr19:56001912
|
G | A | 15 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(12): Show | 15 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.63-1804G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001912 | ||||||
| chr19:56001924
|
A | C | 1 | a0005c0029t0001g0085 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.63-1792A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001924 | ||||||
| chr19:56001943
|
G | C | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-1773G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001943 | ||||||
| chr19:56001950
|
C | T | 16 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(13): Show | 16 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.63-1766C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001950 | ||||||
| chr19:56001964
|
C | T | 16 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(13): Show | 16 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.63-1752C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56001964 | ||||||
| chr19:56002018
|
C | A | 2 | a0001c0015t0001g0045a0001c0015t0001g0046 | 2 | HG00099.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.63-1698C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002018 | ||||||
| chr19:56002019
|
C | T | 16 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(13): Show | 16 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.63-1697C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002019 | ||||||
| chr19:56002033
|
T | C | 16 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(13): Show | 16 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.63-1683T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002033 | ||||||
| chr19:56002035
|
C | T | 16 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(13): Show | 16 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.63-1681C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002035 | ||||||
| chr19:56002041
|
A | G | 16 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(13): Show | 16 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.63-1675A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002041 | ||||||
| chr19:56002105
|
G | A | 14 | a0003c0126t0001g0012a0006c0005t0002g0308a0006c0005t0002g0369others(11): Show | 14 | HG00423.hp2 HG01981.hp1 HG03704.hp2 others(11): Show |
intron_variant | MODIFIER | c.63-1611G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002105 | ||||||
| chr19:56002109
|
A | G | 22 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(19): Show | 22 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.63-1607A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002109 | ||||||
| chr19:56002199
|
A | G | 21 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(18): Show | 21 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.63-1517A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002199 | ||||||
| chr19:56002253
|
C | T | 21 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(18): Show | 21 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.63-1463C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002253 | ||||||
| chr19:56002262
|
T | A | 22 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(19): Show | 22 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.63-1454T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002262 | ||||||
| chr19:56002269
|
T | C | 22 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(19): Show | 22 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.63-1447T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002269 | ||||||
| chr19:56002290
|
A | G | 32 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(29): Show | 32 | HG00673.hp1 HG01884.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.63-1426A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002290 | ||||||
| chr19:56002382
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.63-1334G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002382 | ||||||
| chr19:56002452
|
A | T | 48 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(45): Show | 48 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.63-1264A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002452 | ||||||
| chr19:56002504
|
A | G | 48 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(45): Show | 48 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.63-1212A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002504 | ||||||
| chr19:56002507
|
C | A | 48 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(45): Show | 48 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.63-1209C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002507 | ||||||
| chr19:56002512
|
C | A | 48 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(45): Show | 48 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.63-1204C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002512 | ||||||
| chr19:56002539
|
C | T | 34 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(31): Show | 34 | HG00673.hp1 HG01884.hp1 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.63-1177C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002539 | ||||||
| chr19:56002606
|
C | T | 4 | a0001c0001t0001g0253a0003c0051t0001g0252a0007c0032t0001g0254others(1): Show | 4 | HG00741.hp1 HG02572.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-1110C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002606 | ||||||
| chr19:56002607
|
G | A | 46 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(43): Show | 46 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.63-1109G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002607 | ||||||
| chr19:56002609
|
T | TC | 61 | a0001c0001t0001g0047a0001c0002t0001g0043a0001c0002t0001g0086others(58): Show | 61 | HG00423.hp2 HG00597.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63-1101dupC | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56002609 | |||||
| chr19:56002622
|
A | C | 46 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(43): Show | 46 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.63-1094A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002622 | ||||||
| chr19:56002674
|
A | T | 48 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(45): Show | 48 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.63-1042A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002674 | ||||||
| chr19:56002686
|
A | G | 2 | a0001c0022t0001g0356a0003c0118t0001g0357 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.63-1030A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002686 | ||||||
| chr19:56002698
|
G | A | 15 | a0003c0126t0001g0012a0006c0005t0002g0308a0006c0005t0002g0369others(12): Show | 15 | HG00423.hp2 HG01981.hp1 HG02897.hp2 others(12): Show |
intron_variant | MODIFIER | c.63-1018G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002698 | ||||||
| chr19:56002711
|
C | T | 48 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(45): Show | 48 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.63-1005C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002711 | ||||||
| chr19:56002712
|
A | G | 48 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(45): Show | 48 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.63-1004A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002712 | ||||||
| chr19:56002719
|
G | C | 42 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(39): Show | 42 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.63-997G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002719 | ||||||
| chr19:56002719
|
G | T | 6 | a0004c0020t0001g0096a0004c0020t0003g0098a0004c0035t0001g0094others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.63-997G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002719 | ||||||
| chr19:56002721
|
C | T | 48 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(45): Show | 48 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.63-995C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002721 | ||||||
| chr19:56002734
|
C | G | 1 | a0007c0010t0001g0224 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.63-982C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002734 | ||||||
| chr19:56002734
|
C | T | 1 | a0001c0001t0001g0353 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.63-982C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002734 | ||||||
| chr19:56002740
|
T | A | 3 | a0016c0129t0001g0100a0016c0130t0003g0316a0045c0131t0001g0315 | 3 | HG02809.hp2 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.63-976T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002740 | ||||||
| chr19:56002752
|
G | T | 48 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(45): Show | 48 | HG00423.hp2 HG00673.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.63-964G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002752 | ||||||
| chr19:56002914
|
C | T | 91 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.63-802C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002914 | ||||||
| chr19:56002924
|
T | A | 3 | a0001c0022t0001g0273a0001c0022t0001g0274a0007c0108t0001g0275 | 3 | HG01257.hp2 HG01258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.63-792T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56002924 | ||||||
| chr19:56003012
|
C | T | 91 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.63-704C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003012 | ||||||
| chr19:56003026
|
G | A | 91 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.63-690G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003026 | ||||||
| chr19:56003047
|
G | T | 91 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.63-669G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003047 | ||||||
| chr19:56003108
|
A | C | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-608A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003108 | ||||||
| chr19:56003116
|
T | A | 91 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.63-600T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003116 | ||||||
| chr19:56003121
|
A | G | 91 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.63-595A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003121 | ||||||
| chr19:56003161
|
T | TTTTG | 91 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.63-551_63-548dupGT others(2): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56003161 | |||||
| chr19:56003176
|
T | C | 98 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(95): Show | 98 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.63-540T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003176 | ||||||
| chr19:56003183
|
T | G | 91 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.63-533T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003183 | ||||||
| chr19:56003211
|
A | G | 97 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(94): Show | 97 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.63-505A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003211 | ||||||
| chr19:56003218
|
C | A | 181 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(178): Show | 181 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.63-498C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003218 | ||||||
| chr19:56003220
|
T | C | 91 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.63-496T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003220 | ||||||
| chr19:56003408
|
T | C | 90 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.63-308T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003408 | ||||||
| chr19:56003434
|
G | A | 91 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.63-282G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003434 | ||||||
| chr19:56003449
|
T | C | 90 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.63-267T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003449 | ||||||
| chr19:56003450
|
G | A | 1 | a0045c0131t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.63-266G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003450 | ||||||
| chr19:56003491
|
A | G | 91 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.63-225A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003491 | ||||||
| chr19:56003507
|
C | T | 91 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.63-209C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003507 | ||||||
| chr19:56003521
|
C | A | 3 | a0001c0001t0001g0253a0003c0051t0001g0252a0007c0032t0001g0254 | 3 | HG00741.hp1 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.63-195C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 1/14 | chr19 | 56003521 | ||||||
| chr19:56004101
|
C | T | 6 | a0002c0004t0002g0220a0002c0012t0002g0223a0005c0025t0001g0132others(3): Show | 6 | NA18942.hp2 NA18954.hp2 NA18972.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.442+6C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004101 | ||||||
| chr19:56004151
|
C | T | 3 | a0016c0129t0001g0100a0016c0130t0003g0316a0045c0131t0001g0315 | 3 | HG02809.hp2 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.442+56C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004151 | ||||||
| chr19:56004227
|
C | T | 53 | a0001c0001t0001g0253a0001c0009t0001g0277a0001c0009t0001g0281others(50): Show | 53 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.442+132C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004227 | ||||||
| chr19:56004228
|
T | C | 86 | a0001c0001t0001g0253a0001c0009t0001g0277a0001c0009t0001g0281others(83): Show | 86 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.442+133T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004228 | ||||||
| chr19:56004308
|
C | T | 2 | a0007c0073t0001g0218a0009c0090t0001g0131 | 2 | HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.442+213C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004308 | ||||||
| chr19:56004350
|
G | A | 10 | a0001c0001t0001g0253a0002c0041t0002g0358a0003c0008t0001g0309others(7): Show | 10 | HG00741.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.442+255G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004350 | ||||||
| chr19:56004378
|
C | T | 3 | a0001c0001t0001g0217a0001c0002t0001g0082a0012c0018t0002g0389 | 3 | HG01496.hp2 NA19056.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.442+283C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004378 | ||||||
| chr19:56004406
|
G | A | 2 | a0006c0005t0002g0355a0030c0098t0001g0354 | 2 | HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.442+311G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004406 | ||||||
| chr19:56004491
|
A | G | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442+396A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004491 | ||||||
| chr19:56004509
|
G | A | 18 | a0001c0001t0001g0253a0001c0001t0001g0264a0001c0002t0001g0108others(15): Show | 18 | HG00741.hp1 HG01255.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.442+414G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004509 | ||||||
| chr19:56004566
|
G | A | 1 | a0001c0003t0001g0111 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.442+471G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004566 | ||||||
| chr19:56004624
|
T | C | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+529T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004624 | ||||||
| chr19:56004642
|
C | T | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+547C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004642 | ||||||
| chr19:56004649
|
C | T | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+554C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004649 | ||||||
| chr19:56004830
|
T | C | 34 | a0001c0001t0001g0253a0001c0001t0001g0264a0001c0002t0001g0108others(31): Show | 34 | HG00423.hp2 HG00741.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.442+735T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004830 | ||||||
| chr19:56004921
|
C | T | 14 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(11): Show | 14 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.442+826C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004921 | ||||||
| chr19:56004922
|
G | A | 1 | a0001c0014t0001g0048 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.442+827G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004922 | ||||||
| chr19:56004955
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0049 | 2 | HG00735.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.442+860G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56004955 | ||||||
| chr19:56005010
|
C | T | 43 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(40): Show | 43 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.442+915C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005010 | ||||||
| chr19:56005048
|
T | C | 34 | a0001c0001t0001g0253a0001c0001t0001g0264a0001c0002t0001g0108others(31): Show | 34 | HG00423.hp2 HG00741.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.442+953T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005048 | ||||||
| chr19:56005052
|
C | T | 14 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(11): Show | 14 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.442+957C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005052 | ||||||
| chr19:56005062
|
C | T | 8 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(5): Show | 8 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.442+967C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005062 | ||||||
| chr19:56005093
|
C | CA | 8 | a0001c0022t0001g0356a0001c0115t0001g0040a0003c0114t0002g0347others(5): Show | 8 | HG01884.hp1 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.442+1013dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005093 | |||||
| chr19:56005093
|
C | CAA | 13 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(10): Show | 13 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.442+1012_442+1013d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005093 | |||||
| chr19:56005093
|
C | CAAA | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+1011_442+1013d others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005093 | |||||
| chr19:56005093
|
CA | C | 96 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.442+1013delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005093 | |||||
| chr19:56005093
|
CAAA | C | 9 | a0003c0126t0001g0012a0006c0005t0002g0369a0008c0104t0001g0374others(6): Show | 9 | HG00423.hp2 HG01981.hp1 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.442+1011_442+1013d others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005093 | |||||
| chr19:56005105
|
A | T | 3 | a0004c0050t0001g0329a0007c0010t0001g0321a0040c0074t0002g0322 | 3 | HG01243.hp2 NA18945.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.442+1010A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005105 | ||||||
| chr19:56005106
|
AAAT | A | 9 | a0001c0001t0001g0253a0001c0046t0001g0261a0001c0046t0001g0262others(6): Show | 9 | HG00741.hp1 HG01255.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.442+1013_442+1015d others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005106 | |||||
| chr19:56005107
|
A | AT | 4 | a0003c0045t0001g0266a0004c0020t0001g0096a0004c0020t0003g0098others(1): Show | 4 | HG02647.hp1 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+1012_442+1013i others(3): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005107 | ||||||
| chr19:56005107
|
A | T | 43 | a0001c0001t0001g0130a0001c0001t0001g0215a0001c0001t0001g0216others(40): Show | 43 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.442+1012A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005107 | ||||||
| chr19:56005107
|
AAT | A | 59 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.442+1030_442+1031d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005107 | |||||
| chr19:56005108
|
AT | A | 144 | a0001c0001t0001g0027a0001c0001t0001g0091a0001c0001t0001g0110others(141): Show | 144 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.442+1014delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005108 | ||||||
| chr19:56005108
|
ATAT | A | 5 | a0002c0041t0002g0358a0003c0008t0003g0381a0003c0024t0001g0070others(2): Show | 5 | HG01256.hp1 HG02257.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.442+1014_442+1016d others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005108 | ||||||
| chr19:56005109
|
T | A | 14 | a0001c0001t0001g0117a0001c0003t0001g0162a0001c0009t0001g0277others(11): Show | 14 | HG00544.hp2 HG01884.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.442+1014T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005109 | ||||||
| chr19:56005111
|
T | A | 86 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0133others(83): Show | 86 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.442+1016T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005111 | ||||||
| chr19:56005113
|
T | A | 4 | a0001c0003t0001g0145a0003c0122t0001g0276a0005c0006t0001g0144others(1): Show | 4 | HG01243.hp1 HG02027.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+1018T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005113 | ||||||
| chr19:56005148
|
T | C | 3 | a0001c0001t0001g0253a0003c0051t0001g0252a0007c0032t0001g0254 | 3 | HG00741.hp1 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.442+1053T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005148 | ||||||
| chr19:56005148
|
TACAC | T | 8 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(5): Show | 8 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.442+1059_442+1062d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005148 | |||||
| chr19:56005150
|
CACACACA others(53): Show |
C | 1 | a0001c0001t0001g0133 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.442+1096_442+1155d others(62): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005150 | |||||
| chr19:56005169
|
A | T | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+1074A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005169 | ||||||
| chr19:56005173
|
T | A | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+1078T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005173 | ||||||
| chr19:56005180
|
T | C | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+1085T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005180 | ||||||
| chr19:56005186
|
C | CAT | 28 | a0001c0001t0001g0253a0001c0001t0001g0264a0001c0002t0001g0108others(25): Show | 28 | HG00423.hp2 HG00741.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.442+1094_442+1095d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005186 | |||||
| chr19:56005186
|
C | T | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+1091C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005186 | ||||||
| chr19:56005206
|
CACAT | C | 11 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(8): Show | 11 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.442+1115_442+1118d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005206 | |||||
| chr19:56005208
|
CAT | C | 6 | a0006c0005t0002g0308a0006c0005t0002g0369a0008c0105t0001g0372others(3): Show | 6 | HG00423.hp2 NA18947.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+1115_442+1116d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005208 | |||||
| chr19:56005210
|
T | TAC | 42 | a0001c0001t0001g0253a0001c0001t0001g0264a0001c0002t0001g0108others(39): Show | 42 | HG00673.hp1 HG00741.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.442+1121_442+1122d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005210 | |||||
| chr19:56005210
|
TAC | T | 43 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(40): Show | 43 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.442+1121_442+1122d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005210 | |||||
| chr19:56005218
|
T | C | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+1123T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005218 | ||||||
| chr19:56005246
|
CAT | C | 27 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(24): Show | 27 | HG00673.hp1 HG01255.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.442+1158_442+1159d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005246 | |||||
| chr19:56005249
|
ATATATT | A | 18 | a0001c0001t0001g0253a0002c0041t0002g0358a0003c0051t0001g0252others(15): Show | 18 | HG00423.hp2 HG00741.hp1 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.442+1160_442+1165d others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005249 | |||||
| chr19:56005250
|
T | C | 1 | a0002c0004t0002g0220 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.442+1155T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005250 | ||||||
| chr19:56005251
|
ATATT | A | 4 | a0001c0002t0001g0050a0001c0002t0001g0083a0003c0126t0001g0012others(1): Show | 4 | HG01928.hp2 HG02273.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+1160_442+1163d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005251 | |||||
| chr19:56005256
|
T | A | 1 | a0029c0103t0001g0373 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.442+1161T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005256 | ||||||
| chr19:56005272
|
CAT | C | 8 | a0001c0001t0001g0047a0001c0001t0001g0049a0004c0020t0001g0096others(5): Show | 8 | HG00735.hp1 HG00738.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.442+1181_442+1182d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005272 | |||||
| chr19:56005284
|
T | C | 1 | a0001c0115t0001g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442+1189T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005284 | ||||||
| chr19:56005305
|
ATATT | A | 7 | a0001c0003t0001g0162a0004c0020t0001g0096a0004c0020t0003g0098others(4): Show | 7 | HG00544.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.442+1214_442+1217d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005305 | |||||
| chr19:56005332
|
TATACAC | T | 3 | a0001c0019t0001g0122a0014c0100t0002g0368a0017c0099t0001g0367 | 3 | HG01884.hp2 NA18980.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.442+1253_442+1258d others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005332 | |||||
| chr19:56005346
|
TACAC | T | 24 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(21): Show | 24 | HG00423.hp2 HG01255.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.442+1253_442+1256d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005346 | |||||
| chr19:56005350
|
CAT | C | 5 | a0001c0001t0001g0130a0001c0001t0001g0215a0001c0001t0001g0216others(2): Show | 5 | HG03491.hp2 HG03492.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.442+1260_442+1261d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005350 | |||||
| chr19:56005354
|
T | C | 4 | a0001c0001t0001g0253a0002c0041t0002g0358a0003c0051t0001g0252others(1): Show | 4 | HG00741.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+1259T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005354 | ||||||
| chr19:56005354
|
TA | T | 18 | a0001c0022t0001g0356a0003c0118t0001g0357a0003c0126t0001g0012others(15): Show | 18 | HG00423.hp2 HG01981.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.442+1260delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005354 | ||||||
| chr19:56005355
|
A | ACATATAT | 3 | a0001c0001t0001g0253a0003c0051t0001g0252a0007c0032t0001g0254 | 3 | HG00741.hp1 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.442+1260_442+1261i others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005355 | ||||||
| chr19:56005355
|
A | AT | 28 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(25): Show | 28 | HG00673.hp1 HG01884.hp1 HG01943.hp2 others(25): Show |
intron_variant | MODIFIER | c.442+1265dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005355 | |||||
| chr19:56005355
|
A | G | 2 | a0007c0010t0001g0391a0042c0069t0001g0365 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.442+1260A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005355 | ||||||
| chr19:56005360
|
TA | T | 17 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(14): Show | 17 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.442+1266delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005360 | ||||||
| chr19:56005362
|
T | C | 1 | a0010c0027t0001g0319 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.442+1267T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005362 | ||||||
| chr19:56005366
|
C | T | 17 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(14): Show | 17 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.442+1271C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005366 | ||||||
| chr19:56005370
|
CAT | C | 6 | a0004c0020t0001g0096a0004c0020t0003g0098a0004c0035t0001g0094others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+1282_442+1283d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005370 | |||||
| chr19:56005372
|
T | C | 9 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(6): Show | 9 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.442+1277T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005372 | ||||||
| chr19:56005386
|
TACATATA others(5): Show |
T | 1 | a0001c0001t0001g0207 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.442+1303_442+1314d others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005386 | |||||
| chr19:56005392
|
TAC | T | 9 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.442+1305_442+1306d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005392 | |||||
| chr19:56005400
|
CAT | C | 3 | a0002c0116t0002g0330a0006c0011t0002g0102a0007c0021t0001g0279 | 3 | NA18970.hp1 NA18990.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.442+1309_442+1310d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005400 | |||||
| chr19:56005423
|
A | G | 3 | a0016c0129t0001g0100a0016c0130t0003g0316a0045c0131t0001g0315 | 3 | HG02809.hp2 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.442+1328A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005423 | ||||||
| chr19:56005458
|
T | TAC | 42 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(39): Show | 42 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.442+1373_442+1374d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005458 | |||||
| chr19:56005458
|
TAC | T | 8 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(5): Show | 8 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.442+1373_442+1374d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005458 | |||||
| chr19:56005468
|
C | CATTTATA others(38): Show |
20 | a0001c0001t0001g0253a0002c0041t0002g0358a0003c0051t0001g0252others(17): Show | 20 | HG00423.hp2 HG00741.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.442+1375_442+1376i others(47): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005468 | |||||
| chr19:56005470
|
T | C | 1 | a0007c0021t0001g0302 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.442+1375T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005470 | ||||||
| chr19:56005473
|
T | A | 1 | a0007c0021t0001g0302 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.442+1378T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005473 | ||||||
| chr19:56005475
|
A | T | 1 | a0007c0021t0001g0302 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.442+1380A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005475 | ||||||
| chr19:56005476
|
TACAC | T | 18 | a0001c0001t0001g0353a0001c0019t0001g0359a0001c0022t0001g0356others(15): Show | 18 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.442+1390_442+1393d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005476 | |||||
| chr19:56005478
|
C | T | 1 | a0007c0021t0001g0302 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.442+1383C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005478 | ||||||
| chr19:56005504
|
G | A | 14 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(11): Show | 14 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.442+1409G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005504 | ||||||
| chr19:56005504
|
G | GTA | 13 | a0006c0005t0002g0308a0006c0005t0002g0369a0008c0104t0001g0374others(10): Show | 13 | HG00423.hp2 HG01981.hp1 HG03704.hp2 others(10): Show |
intron_variant | MODIFIER | c.442+1410_442+1411d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005504 | |||||
| chr19:56005505
|
T | TAC | 27 | a0001c0001t0001g0253a0001c0001t0001g0264a0001c0002t0001g0108others(24): Show | 27 | HG00673.hp1 HG00741.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.442+1414_442+1415d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005505 | |||||
| chr19:56005505
|
T | TACACACA others(48): Show |
1 | a0001c0003t0001g0263 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.442+1415_442+1416i others(57): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005505 | |||||
| chr19:56005505
|
T | TACACACA others(46): Show |
6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+1415_442+1416i others(55): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005505 | |||||
| chr19:56005521
|
TACAC | T | 46 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(43): Show | 46 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.442+1433_442+1436d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005521 | |||||
| chr19:56005523
|
C | CACACACA others(44): Show |
1 | a0001c0014t0001g0206 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.442+1488_442+1538d others(53): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005523 | |||||
| chr19:56005524
|
ACACACAC others(1): Show |
A | 10 | a0001c0022t0001g0356a0001c0115t0001g0040a0003c0114t0002g0347others(7): Show | 10 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.442+1440_442+1447d others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005524 | |||||
| chr19:56005532
|
G | A | 23 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(20): Show | 23 | HG00423.hp2 HG01255.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.442+1437G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005532 | ||||||
| chr19:56005574
|
T | TAC | 25 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(22): Show | 25 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.442+1486_442+1487d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005574 | |||||
| chr19:56005574
|
T | TACAC | 142 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(139): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.442+1484_442+1487d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005574 | |||||
| chr19:56005576
|
CACACACG others(42): Show |
C | 13 | a0001c0009t0001g0332a0001c0009t0001g0333a0001c0009t0001g0335others(10): Show | 13 | HG00673.hp1 HG01943.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.442+1488_442+1536d others(51): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005576 | |||||
| chr19:56005581
|
ACG | A | 7 | a0001c0002t0001g0363a0001c0002t0001g0378a0001c0042t0001g0377others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.442+1488_442+1489d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005581 | |||||
| chr19:56005625
|
TAC | T | 4 | a0001c0001t0001g0253a0003c0051t0001g0252a0007c0032t0001g0254others(1): Show | 4 | HG00741.hp1 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+1547_442+1548d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005625 | |||||
| chr19:56005638
|
A | ACG | 4 | a0004c0055t0001g0301a0006c0005t0002g0300a0010c0016t0001g0366others(1): Show | 4 | NA18988.hp1 NA19004.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+1544_442+1545i others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005638 | |||||
| chr19:56005638
|
A | G | 7 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(4): Show | 7 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.442+1543A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005638 | ||||||
| chr19:56005640
|
A | ACG | 39 | a0001c0009t0001g0277a0001c0009t0001g0281a0001c0009t0001g0282others(36): Show | 39 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.442+1546_442+1547i others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005640 | |||||
| chr19:56005640
|
A | G | 7 | a0004c0055t0001g0301a0006c0005t0002g0300a0009c0013t0001g0350others(4): Show | 7 | HG02630.hp1 HG02818.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.442+1545A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005640 | ||||||
| chr19:56005642
|
A | ACACGCAG others(54): Show |
5 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0046t0001g0261others(2): Show | 5 | HG01255.hp2 HG01346.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+1548_442+1549i others(63): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005642 | |||||
| chr19:56005642
|
A | ACACGCAG others(56): Show |
2 | a0001c0003t0001g0260a0001c0046t0001g0262 | 2 | HG01261.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.442+1548_442+1549i others(65): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005642 | |||||
| chr19:56005642
|
A | ACG | 27 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0127t0002g0306others(24): Show | 27 | HG00423.hp2 HG01884.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.442+1553_442+1554d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005642 | |||||
| chr19:56005642
|
A | ACGCG | 7 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(4): Show | 7 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.442+1551_442+1554d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005642 | |||||
| chr19:56005642
|
A | G | 65 | a0001c0001t0001g0253a0001c0001t0001g0353a0001c0003t0001g0263others(62): Show | 65 | HG00140.hp1 HG00639.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.442+1547A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005642 | ||||||
| chr19:56005643
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.442+1548C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005643 | ||||||
| chr19:56005647
|
C | CGT | 6 | a0004c0020t0001g0096a0004c0020t0003g0098a0004c0035t0001g0094others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+1553_442+1554i others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56005647 | |||||
| chr19:56005714
|
A | G | 1 | a0028c0093t0001g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.442+1619A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005714 | ||||||
| chr19:56005744
|
G | A | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+1649G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005744 | ||||||
| chr19:56005755
|
G | C | 3 | a0001c0092t0001g0211a0004c0007t0003g0164a0004c0007t0003g0210 | 3 | HG02486.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.442+1660G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005755 | ||||||
| chr19:56005824
|
A | C | 8 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(5): Show | 8 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.442+1729A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005824 | ||||||
| chr19:56005992
|
C | T | 3 | a0018c0036t0002g0034a0018c0036t0002g0035a0033c0061t0001g0256 | 3 | HG03669.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.442+1897C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56005992 | ||||||
| chr19:56006014
|
C | T | 80 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(77): Show | 80 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.442+1919C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006014 | ||||||
| chr19:56006023
|
G | A | 189 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(186): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.442+1928G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006023 | ||||||
| chr19:56006189
|
A | G | 16 | a0003c0126t0001g0012a0004c0125t0001g0013a0006c0005t0002g0308others(13): Show | 16 | HG00423.hp2 HG01981.hp1 HG02897.hp2 others(13): Show |
intron_variant | MODIFIER | c.442+2094A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006189 | ||||||
| chr19:56006217
|
T | C | 6 | a0004c0020t0001g0096a0004c0020t0003g0098a0004c0035t0001g0094others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+2122T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006217 | ||||||
| chr19:56006296
|
T | G | 2 | a0016c0130t0003g0316a0045c0131t0001g0315 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.442+2201T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006296 | ||||||
| chr19:56006399
|
A | G | 6 | a0006c0005t0002g0295a0006c0005t0002g0296a0006c0005t0002g0298others(3): Show | 6 | HG00673.hp2 HG02074.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+2304A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006399 | ||||||
| chr19:56006406
|
C | A | 3 | a0001c0009t0001g0281a0001c0009t0001g0282a0006c0005t0002g0280 | 3 | NA18957.hp1 NA19007.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.442+2311C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006406 | ||||||
| chr19:56006427
|
T | A | 10 | a0001c0001t0001g0353a0001c0019t0001g0359a0003c0008t0001g0245others(7): Show | 10 | HG01256.hp1 HG01433.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.442+2332T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006427 | ||||||
| chr19:56006427
|
TA | T | 107 | a0001c0001t0001g0253a0001c0001t0001g0264a0001c0002t0001g0108others(104): Show | 107 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.442+2342delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56006427 | |||||
| chr19:56006428
|
A | T | 180 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(177): Show | 180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.442+2333A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006428 | ||||||
| chr19:56006429
|
A | T | 97 | a0001c0001t0001g0253a0001c0001t0001g0264a0001c0002t0001g0108others(94): Show | 97 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.442+2334A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006429 | ||||||
| chr19:56006430
|
A | T | 3 | a0001c0001t0001g0253a0003c0051t0001g0252a0007c0032t0001g0254 | 3 | HG00741.hp1 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.442+2335A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006430 | ||||||
| chr19:56006633
|
G | T | 3 | a0001c0001t0001g0253a0003c0051t0001g0252a0007c0032t0001g0254 | 3 | HG00741.hp1 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.443-2155G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006633 | ||||||
| chr19:56006656
|
C | T | 2 | a0016c0130t0003g0316a0045c0131t0001g0315 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.443-2132C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006656 | ||||||
| chr19:56006657
|
G | A | 3 | a0001c0001t0001g0386a0001c0001t0001g0387a0001c0001t0001g0388 | 3 | HG01081.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.443-2131G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006657 | ||||||
| chr19:56006696
|
C | T | 1 | a0038c0120t0002g0278 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.443-2092C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006696 | ||||||
| chr19:56006725
|
C | A | 178 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(175): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.443-2063C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006725 | ||||||
| chr19:56006726
|
C | A | 178 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(175): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.443-2062C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006726 | ||||||
| chr19:56006726
|
C | T | 15 | a0001c0001t0001g0160a0001c0003t0001g0161a0001c0009t0001g0283others(12): Show | 15 | HG01943.hp2 HG02040.hp1 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.443-2062C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006726 | ||||||
| chr19:56006778
|
C | T | 357 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(354): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.443-2010C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006778 | ||||||
| chr19:56006800
|
C | T | 1 | a0004c0007t0001g0139 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.443-1988C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006800 | ||||||
| chr19:56006816
|
C | T | 2 | a0008c0028t0001g0394a0008c0028t0001g0395 | 2 | HG02071.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.443-1972C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006816 | ||||||
| chr19:56006817
|
G | A | 1 | a0001c0003t0001g0112 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.443-1971G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006817 | ||||||
| chr19:56006833
|
G | A | 1 | a0004c0125t0001g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.443-1955G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006833 | ||||||
| chr19:56006840
|
T | C | 1 | a0004c0007t0003g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.443-1948T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006840 | ||||||
| chr19:56006874
|
A | G | 2 | a0003c0024t0001g0052a0003c0024t0001g0070 | 2 | HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.443-1914A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006874 | ||||||
| chr19:56006888
|
C | T | 123 | a0001c0001t0001g0117a0001c0001t0001g0130a0001c0001t0001g0160others(120): Show | 123 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.443-1900C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006888 | ||||||
| chr19:56006900
|
TGGCTAAT others(1182): Show |
T | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-1859_443-671de others(1): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56006900 | |||||
| chr19:56006929
|
A | C | 1 | a0001c0002t0001g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.443-1859A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006929 | ||||||
| chr19:56006930
|
G | A | 124 | a0001c0001t0001g0117a0001c0001t0001g0130a0001c0001t0001g0160others(121): Show | 124 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.443-1858G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006930 | ||||||
| chr19:56006936
|
T | C | 4 | a0003c0008t0003g0381a0003c0077t0001g0379a0007c0010t0001g0391others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.443-1852T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006936 | ||||||
| chr19:56006938
|
A | C | 1 | a0001c0002t0001g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.443-1850A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006938 | ||||||
| chr19:56006941
|
T | A | 6 | a0001c0002t0001g0067a0001c0009t0001g0286a0004c0020t0001g0285others(3): Show | 6 | HG02015.hp2 HG02027.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-1847T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006941 | ||||||
| chr19:56006941
|
T | G | 4 | a0002c0004t0002g0183a0007c0010t0001g0235a0007c0010t0001g0321others(1): Show | 4 | HG02074.hp1 NA18945.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-1847T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006941 | ||||||
| chr19:56006947
|
G | T | 82 | a0001c0001t0001g0117a0001c0001t0001g0130a0001c0001t0001g0174others(79): Show | 82 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.443-1841G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006947 | ||||||
| chr19:56006950
|
A | G | 111 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(108): Show | 111 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.443-1838A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006950 | ||||||
| chr19:56006968
|
C | T | 133 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.443-1820C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006968 | ||||||
| chr19:56006969
|
G | A | 3 | a0003c0076t0002g0250a0003c0114t0002g0347a0007c0021t0001g0348 | 3 | HG01109.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.443-1819G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006969 | ||||||
| chr19:56006986
|
A | G | 1 | a0003c0126t0001g0012 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.443-1802A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006986 | ||||||
| chr19:56006990
|
T | C | 1 | a0003c0126t0001g0012 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.443-1798T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006990 | ||||||
| chr19:56006992
|
G | A | 1 | a0003c0126t0001g0012 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.443-1796G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56006992 | ||||||
| chr19:56007030
|
T | C | 353 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(350): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.443-1758T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007030 | ||||||
| chr19:56007034
|
T | C | 7 | a0001c0023t0001g0314a0004c0020t0001g0096a0004c0020t0003g0098others(4): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-1754T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007034 | ||||||
| chr19:56007122
|
A | G | 3 | a0003c0076t0002g0250a0003c0114t0002g0347a0007c0021t0001g0348 | 3 | HG01109.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.443-1666A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007122 | ||||||
| chr19:56007134
|
G | T | 1 | a0010c0016t0001g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.443-1654G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007134 | ||||||
| chr19:56007137
|
C | T | 7 | a0001c0023t0001g0314a0004c0020t0001g0096a0004c0020t0003g0098others(4): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-1651C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007137 | ||||||
| chr19:56007293
|
G | A | 4 | a0004c0020t0001g0285a0004c0055t0001g0301a0006c0005t0002g0284others(1): Show | 4 | HG02015.hp2 NA19012.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.443-1495G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007293 | ||||||
| chr19:56007359
|
C | CT | 109 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(106): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.443-1417dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007359 | |||||
| chr19:56007359
|
C | CTTT | 186 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.443-1419_443-1417d others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007359 | |||||
| chr19:56007385
|
C | A | 85 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0130others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.443-1403C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007385 | ||||||
| chr19:56007425
|
C | T | 85 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0130others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.443-1363C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007425 | ||||||
| chr19:56007461
|
G | C | 12 | a0006c0005t0002g0369a0008c0104t0001g0374a0008c0105t0001g0372others(9): Show | 12 | HG00423.hp2 HG01981.hp1 HG03704.hp2 others(9): Show |
intron_variant | MODIFIER | c.443-1327G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007461 | ||||||
| chr19:56007475
|
G | A | 1 | a0003c0043t0001g0123 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.443-1313G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007475 | ||||||
| chr19:56007513
|
A | G | 7 | a0001c0023t0001g0314a0004c0020t0001g0096a0004c0020t0003g0098others(4): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-1275A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007513 | ||||||
| chr19:56007522
|
G | C | 1 | a0003c0051t0001g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.443-1266G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007522 | ||||||
| chr19:56007531
|
A | G | 4 | a0001c0019t0001g0122a0001c0115t0001g0040a0007c0110t0001g0349others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.443-1257A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007531 | ||||||
| chr19:56007594
|
C | CT | 18 | a0001c0001t0001g0160a0001c0003t0001g0161a0001c0009t0001g0283others(15): Show | 18 | HG01943.hp2 HG02040.hp1 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.443-1193dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007594 | |||||
| chr19:56007596
|
A | T | 1 | a0005c0034t0001g0337 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.443-1192A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007596 | ||||||
| chr19:56007693
|
C | A | 103 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(100): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.443-1095C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007693 | ||||||
| chr19:56007694
|
C | G | 80 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0130others(77): Show | 80 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.443-1094C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007694 | ||||||
| chr19:56007751
|
A | AGAG | 8 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.443-1036_443-1035i others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007751 | |||||
| chr19:56007869
|
T | TTG | 5 | a0002c0041t0002g0358a0003c0118t0001g0357a0005c0006t0001g0163others(2): Show | 5 | HG00140.hp2 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-900_443-899dup others(2): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007869 | |||||
| chr19:56007869
|
T | TTGTGTG | 3 | a0001c0001t0001g0253a0003c0051t0001g0252a0007c0032t0001g0254 | 3 | HG00741.hp1 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.443-904_443-899dup others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007869 | |||||
| chr19:56007869
|
T | TTGTGTGT others(3): Show |
4 | a0001c0115t0001g0040a0007c0110t0001g0349a0030c0098t0001g0354others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.443-908_443-899dup others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007869 | |||||
| chr19:56007869
|
T | TTGTGTGT others(7): Show |
1 | a0001c0022t0001g0356 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.443-912_443-899dup others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007869 | |||||
| chr19:56007869
|
TTG | T | 20 | a0001c0001t0001g0160a0001c0003t0001g0161a0001c0009t0001g0283others(17): Show | 20 | HG01891.hp1 HG01943.hp2 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.443-900_443-899del others(2): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007869 | |||||
| chr19:56007869
|
TTGTGTGT others(29): Show |
T | 7 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0263others(4): Show | 7 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.443-898_443-863del others(36): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007869 | |||||
| chr19:56007870
|
TGTGTGTG others(27): Show |
T | 1 | a0001c0003t0001g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.443-898_443-865del others(34): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007870 | |||||
| chr19:56007874
|
TGTGTGTG others(23): Show |
T | 1 | a0007c0032t0001g0327 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.443-898_443-869del others(30): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007874 | |||||
| chr19:56007888
|
T | C | 14 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0174others(11): Show | 14 | HG00735.hp2 HG01069.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.443-900T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007888 | ||||||
| chr19:56007888
|
TGC | T | 9 | a0001c0023t0001g0314a0003c0076t0002g0250a0004c0020t0001g0096others(6): Show | 9 | HG01109.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.443-896_443-895del others(2): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007888 | |||||
| chr19:56007888
|
TGCGC | T | 5 | a0001c0002t0001g0363a0001c0002t0001g0378a0003c0114t0002g0347others(2): Show | 5 | HG02451.hp2 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-898_443-895del others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007888 | |||||
| chr19:56007890
|
C | T | 98 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.443-898C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007890 | ||||||
| chr19:56007891
|
G | A | 1 | a0001c0056t0001g0382 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.443-897G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007891 | ||||||
| chr19:56007892
|
C | T | 95 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.443-896C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007892 | ||||||
| chr19:56007894
|
T | C | 142 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.443-894T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007894 | ||||||
| chr19:56007894
|
T | TGTGCGCG others(5): Show |
4 | a0001c0002t0001g0151a0004c0007t0001g0149a0005c0025t0001g0150others(1): Show | 4 | HG02083.hp2 NA18970.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.443-893_443-892ins others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007894 | |||||
| chr19:56007895
|
G | A | 60 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.443-893G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007895 | ||||||
| chr19:56007896
|
C | T | 107 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.443-892C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007896 | ||||||
| chr19:56007896
|
CGCGCGTG others(13): Show |
C | 53 | a0001c0001t0001g0027a0001c0001t0001g0091a0001c0001t0001g0174others(50): Show | 53 | HG00639.hp1 HG00673.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.443-890_443-871del others(20): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007896 | |||||
| chr19:56007897
|
G | A | 29 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0002t0001g0050others(26): Show | 29 | HG01109.hp1 HG01123.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.443-891G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007897 | ||||||
| chr19:56007898
|
C | T | 5 | a0001c0002t0001g0151a0004c0007t0001g0149a0005c0025t0001g0150others(2): Show | 5 | HG02083.hp2 NA18970.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-890C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007898 | ||||||
| chr19:56007898
|
CGCGTGCG others(11): Show |
C | 60 | a0001c0001t0001g0117a0001c0001t0001g0130a0001c0001t0001g0190others(57): Show | 60 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.443-888_443-871del others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007898 | |||||
| chr19:56007898
|
CGCGTGCG others(13): Show |
C | 3 | a0001c0014t0001g0206a0003c0075t0001g0213a0007c0010t0001g0214 | 3 | HG00323.hp2 HG01123.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.443-888_443-869del others(20): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007898 | |||||
| chr19:56007899
|
G | A | 8 | a0003c0008t0003g0381a0003c0077t0001g0379a0007c0010t0001g0391others(5): Show | 8 | HG00423.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-889G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007899 | ||||||
| chr19:56007900
|
C | CGTGTGCG others(7): Show |
1 | a0001c0002t0001g0148 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.443-885_443-884ins others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007900 | |||||
| chr19:56007900
|
C | CGTGTGCG others(11): Show |
1 | a0009c0013t0001g0147 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.443-885_443-884ins others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007900 | |||||
| chr19:56007900
|
C | T | 2 | a0006c0005t0002g0369a0016c0129t0001g0100 | 2 | HG03579.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.443-888C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007900 | ||||||
| chr19:56007900
|
CGTGCGTG others(7): Show |
C | 1 | a0002c0004t0002g0204 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.443-884_443-871del others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007900 | |||||
| chr19:56007900
|
CGTGCGTG others(9): Show |
C | 2 | a0001c0003t0001g0111a0006c0011t0002g0186 | 2 | HG04115.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.443-884_443-869del others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007900 | |||||
| chr19:56007900
|
CGTGCGTG others(10): Show |
C | 1 | a0025c0089t0002g0243 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.443-887_443-871del others(17): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007900 | ||||||
| chr19:56007900
|
CGTGCGTG others(11): Show |
C | 2 | a0001c0030t0001g0187a0001c0030t0001g0343 | 2 | HG02132.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.443-884_443-867del others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007900 | |||||
| chr19:56007902
|
T | C | 87 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.443-886T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007902 | ||||||
| chr19:56007904
|
C | CGT | 8 | a0001c0001t0001g0353a0001c0002t0001g0320a0001c0015t0001g0084others(5): Show | 8 | HG00673.hp1 HG01515.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-855_443-854dup others(2): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007904 | |||||
| chr19:56007904
|
C | CGTGT | 73 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(70): Show | 73 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.443-857_443-854dup others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007904 | |||||
| chr19:56007904
|
C | CGTGTGT | 13 | a0001c0001t0001g0230a0001c0003t0001g0140a0001c0023t0001g0244others(10): Show | 13 | HG01109.hp2 HG01175.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.443-859_443-854dup others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007904 | |||||
| chr19:56007904
|
C | CGTGTGTG others(1): Show |
5 | a0001c0003t0001g0251a0001c0019t0001g0118a0001c0023t0001g0248others(2): Show | 5 | HG02622.hp1 HG02723.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.443-861_443-854dup others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007904 | |||||
| chr19:56007904
|
C | CGTGTGTG others(3): Show |
1 | a0003c0126t0001g0012 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.443-863_443-854dup others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007904 | |||||
| chr19:56007904
|
C | T | 6 | a0001c0002t0001g0148a0001c0002t0001g0151a0004c0007t0001g0149others(3): Show | 6 | HG02083.hp2 HG02155.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-884C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007904 | ||||||
| chr19:56007904
|
CGTGT | C | 20 | a0001c0001t0001g0160a0001c0003t0001g0161a0001c0009t0001g0283others(17): Show | 20 | HG01891.hp1 HG01943.hp2 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.443-857_443-854del others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007904 | |||||
| chr19:56007904
|
CGTGTGT | C | 9 | a0003c0008t0003g0381a0003c0077t0001g0379a0007c0010t0001g0391others(6): Show | 9 | HG00423.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.443-859_443-854del others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007904 | |||||
| chr19:56007904
|
CGTGTGTG others(1): Show |
C | 28 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0002t0001g0050others(25): Show | 28 | HG01109.hp1 HG01123.hp2 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.443-861_443-854del others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007904 | |||||
| chr19:56007904
|
CGTGTGTG others(3): Show |
C | 60 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.443-863_443-854del others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007904 | |||||
| chr19:56007904
|
CGTGTGTG others(7): Show |
C | 3 | a0001c0002t0001g0363a0001c0002t0001g0378a0001c0056t0001g0382 | 3 | HG02451.hp2 HG02647.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.443-867_443-854del others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007904 | |||||
| chr19:56007905
|
G | A | 1 | a0006c0005t0002g0369 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.443-883G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007905 | ||||||
| chr19:56007906
|
T | C | 2 | a0006c0005t0002g0369a0016c0129t0001g0100 | 2 | HG03579.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.443-882T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007906 | ||||||
| chr19:56007908
|
T | C | 1 | a0006c0005t0002g0369 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.443-880T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007908 | ||||||
| chr19:56007910
|
T | C | 2 | a0006c0005t0002g0369a0016c0129t0001g0100 | 2 | HG03579.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.443-878T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007910 | ||||||
| chr19:56007910
|
T | TGGGCACA others(79): Show |
1 | a0016c0130t0003g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.443-877_443-876ins others(86): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007910 | |||||
| chr19:56007910
|
T | TGGGCACA others(77): Show |
1 | a0001c0022t0001g0356 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.443-877_443-876ins others(84): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007910 | |||||
| chr19:56007910
|
T | TGGGCACA others(79): Show |
2 | a0030c0098t0001g0354a0045c0131t0001g0315 | 2 | HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.443-877_443-876ins others(86): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007910 | |||||
| chr19:56007910
|
T | TGGGCACA others(79): Show |
3 | a0001c0115t0001g0040a0007c0110t0001g0349a0041c0109t0001g0345 | 3 | HG01884.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.443-877_443-876ins others(86): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007910 | |||||
| chr19:56007910
|
T | TGGGCACA others(81): Show |
1 | a0002c0041t0002g0358 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.443-877_443-876ins others(88): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007910 | |||||
| chr19:56007910
|
T | TGGGCACA others(83): Show |
1 | a0003c0051t0001g0252 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.443-877_443-876ins others(90): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007910 | |||||
| chr19:56007910
|
T | TGGGCACA others(85): Show |
1 | a0001c0001t0001g0253 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.443-877_443-876ins others(92): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007910 | |||||
| chr19:56007910
|
T | TGGGCACA others(85): Show |
1 | a0007c0032t0001g0254 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.443-877_443-876ins others(92): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56007910 | |||||
| chr19:56007912
|
T | C | 20 | a0001c0001t0001g0253a0001c0022t0001g0356a0001c0115t0001g0040others(17): Show | 20 | HG00423.hp2 HG00741.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.443-876T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007912 | ||||||
| chr19:56007914
|
T | C | 47 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0253others(44): Show | 47 | HG00423.hp2 HG00741.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.443-874T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007914 | ||||||
| chr19:56007916
|
T | C | 1 | a0001c0022t0001g0356 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.443-872T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007916 | ||||||
| chr19:56007918
|
T | C | 107 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.443-870T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007918 | ||||||
| chr19:56007929
|
G | A | 2 | a0016c0130t0003g0316a0045c0131t0001g0315 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.443-859G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007929 | ||||||
| chr19:56007934
|
T | TGTGTG | 3 | a0001c0015t0001g0002a0004c0080t0001g0019a0008c0017t0001g0154 | 3 | HG01099.hp1 HG02056.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.443-854_443-853ins others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007934 | ||||||
| chr19:56007943
|
G | A | 96 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.443-845G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007943 | ||||||
| chr19:56007968
|
GGCTGTCG others(3): Show |
G | 100 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.443-819_443-810del others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007968 | ||||||
| chr19:56007981
|
T | C | 100 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.443-807T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007981 | ||||||
| chr19:56007989
|
C | T | 88 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0130others(85): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.443-799C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007989 | ||||||
| chr19:56007994
|
T | C | 88 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0130others(85): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.443-794T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007994 | ||||||
| chr19:56007997
|
C | T | 2 | a0016c0130t0003g0316a0045c0131t0001g0315 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.443-791C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56007997 | ||||||
| chr19:56008010
|
A | G | 188 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.443-778A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008010 | ||||||
| chr19:56008028
|
G | A | 197 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.443-760G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008028 | ||||||
| chr19:56008029
|
T | A | 90 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.443-759T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008029 | ||||||
| chr19:56008029
|
T | C | 107 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0130others(104): Show | 107 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.443-759T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008029 | ||||||
| chr19:56008032
|
C | G | 90 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.443-756C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008032 | ||||||
| chr19:56008077
|
C | T | 90 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0130others(87): Show | 90 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.443-711C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008077 | ||||||
| chr19:56008085
|
C | T | 305 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.443-703C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008085 | ||||||
| chr19:56008089
|
C | T | 188 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.443-699C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008089 | ||||||
| chr19:56008105
|
T | A | 8 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(5): Show | 8 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-683T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008105 | ||||||
| chr19:56008114
|
G | A | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.443-674G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008114 | ||||||
| chr19:56008130
|
A | G | 2 | a0001c0002t0001g0363a0001c0002t0001g0378 | 2 | HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.443-658A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008130 | ||||||
| chr19:56008138
|
C | A | 18 | a0001c0001t0001g0160a0001c0003t0001g0161a0001c0009t0001g0283others(15): Show | 18 | HG01943.hp2 HG02040.hp1 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.443-650C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008138 | ||||||
| chr19:56008149
|
C | G | 1 | a0002c0041t0002g0358 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.443-639C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008149 | ||||||
| chr19:56008180
|
A | G | 188 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.443-608A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008180 | ||||||
| chr19:56008187
|
T | C | 188 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.443-601T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008187 | ||||||
| chr19:56008219
|
C | T | 88 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0130others(85): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.443-569C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008219 | ||||||
| chr19:56008220
|
G | A | 13 | a0001c0002t0001g0042a0001c0002t0001g0044a0001c0002t0001g0072others(10): Show | 13 | HG00738.hp2 HG01074.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.443-568G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008220 | ||||||
| chr19:56008224
|
G | T | 2 | a0007c0072t0001g0233a0010c0016t0001g0292 | 2 | NA18941.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.443-564G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008224 | ||||||
| chr19:56008227
|
C | A | 3 | a0001c0002t0001g0041a0001c0002t0001g0054a0001c0084t0001g0053 | 3 | HG00741.hp2 HG01099.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.443-561C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008227 | ||||||
| chr19:56008290
|
A | C | 8 | a0001c0001t0001g0110a0001c0001t0001g0133a0001c0001t0001g0134others(5): Show | 8 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.443-498A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008290 | ||||||
| chr19:56008290
|
A | G | 12 | a0006c0005t0002g0369a0008c0104t0001g0374a0008c0105t0001g0372others(9): Show | 12 | HG00423.hp2 HG01981.hp1 HG03704.hp2 others(9): Show |
intron_variant | MODIFIER | c.443-498A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008290 | ||||||
| chr19:56008316
|
A | G | 2 | a0004c0050t0001g0328a0004c0050t0001g0329 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.443-472A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008316 | ||||||
| chr19:56008329
|
G | A | 159 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(156): Show | 159 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.443-459G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008329 | ||||||
| chr19:56008429
|
C | G | 1 | a0001c0002t0001g0108 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.443-359C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008429 | ||||||
| chr19:56008436
|
G | A | 87 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0130others(84): Show | 87 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.443-352G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008436 | ||||||
| chr19:56008447
|
G | A | 8 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(5): Show | 8 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-341G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008447 | ||||||
| chr19:56008492
|
G | C | 103 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.443-296G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008492 | ||||||
| chr19:56008519
|
C | T | 191 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0049others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.443-269C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008519 | ||||||
| chr19:56008581
|
C | T | 88 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0130others(85): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.443-207C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008581 | ||||||
| chr19:56008631
|
T | C | 114 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.443-157T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008631 | ||||||
| chr19:56008697
|
C | T | 11 | a0001c0001t0001g0253a0001c0022t0001g0356a0001c0115t0001g0040others(8): Show | 11 | HG00741.hp1 HG01884.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.443-91C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008697 | ||||||
| chr19:56008704
|
T | A | 1 | a0036c0088t0001g0016 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.443-84T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008704 | ||||||
| chr19:56008725
|
C | T | 103 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.443-63C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008725 | ||||||
| chr19:56008759
|
G | A | 4 | a0001c0001t0001g0253a0002c0041t0002g0358a0003c0051t0001g0252others(1): Show | 4 | HG00741.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.443-29G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008759 | ||||||
| chr19:56008763
|
G | A | 103 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.443-25G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008763 | ||||||
| chr19:56008784
|
C | G | 103 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
splice_region_variant&intron_variant | LOW | c.443-4C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 2/14 | chr19 | 56008784 | ||||||
| chr19:56008989
|
C | T | 42 | a0001c0001t0001g0091a0001c0009t0001g0277a0001c0009t0001g0281others(39): Show | 42 | HG00639.hp1 HG00673.hp2 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.508+136C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56008989 | ||||||
| chr19:56009090
|
G | T | 1 | a0004c0007t0001g0212 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.508+237G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009090 | ||||||
| chr19:56009104
|
T | C | 103 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.508+251T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009104 | ||||||
| chr19:56009114
|
A | G | 101 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(98): Show | 101 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.508+261A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009114 | ||||||
| chr19:56009165
|
G | C | 367 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(364): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.508+312G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009165 | ||||||
| chr19:56009175
|
C | T | 8 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(5): Show | 8 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.508+322C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009175 | ||||||
| chr19:56009232
|
T | A | 3 | a0001c0001t0001g0253a0003c0051t0001g0252a0007c0032t0001g0254 | 3 | HG00741.hp1 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.508+379T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009232 | ||||||
| chr19:56009267
|
T | A | 103 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.508+414T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009267 | ||||||
| chr19:56009289
|
G | A | 102 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.508+436G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009289 | ||||||
| chr19:56009297
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.508+444A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009297 | ||||||
| chr19:56009326
|
C | A | 1 | a0001c0030t0001g0318 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.508+473C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009326 | ||||||
| chr19:56009339
|
C | CAA | 18 | a0001c0002t0001g0054a0001c0002t0001g0076a0001c0002t0001g0077others(15): Show | 18 | HG00741.hp2 HG01070.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.508+505_508+506dup others(2): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAA | 75 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.508+504_508+506dup others(3): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA | 59 | a0001c0001t0001g0027a0001c0001t0001g0130a0001c0001t0001g0174others(56): Show | 59 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.508+500_508+506dup others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(1): Show |
26 | a0001c0001t0001g0117a0001c0001t0001g0203a0001c0001t0001g0217others(23): Show | 26 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.508+499_508+506dup others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(2): Show |
10 | a0001c0001t0001g0353a0003c0008t0001g0245a0003c0008t0001g0246others(7): Show | 10 | HG02015.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.508+498_508+506dup others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(3): Show |
48 | a0001c0001t0001g0007a0001c0001t0001g0230a0001c0001t0001g0387others(45): Show | 48 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.508+497_508+506dup others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(4): Show |
34 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0386others(31): Show | 34 | HG00597.hp2 HG00609.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.508+496_508+506dup others(11): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(5): Show |
13 | a0001c0015t0001g0002a0001c0019t0001g0118a0001c0019t0001g0122others(10): Show | 13 | HG01884.hp2 HG02056.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.508+495_508+506dup others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(6): Show |
2 | a0007c0010t0001g0385a0037c0091t0001g0167 | 2 | HG01192.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.508+494_508+506dup others(13): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(9): Show |
2 | a0004c0053t0003g0317a0009c0054t0001g0297 | 2 | HG02074.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.508+491_508+506dup others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(10): Show |
9 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0022t0001g0267others(6): Show | 9 | HG00639.hp1 HG01261.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+490_508+506dup others(17): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(11): Show |
19 | a0001c0001t0001g0091a0001c0003t0001g0263a0001c0009t0001g0277others(16): Show | 19 | HG00673.hp2 HG01255.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.508+489_508+506dup others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(12): Show |
12 | a0001c0003t0001g0260a0004c0020t0001g0268a0004c0055t0001g0323others(9): Show | 12 | HG02083.hp1 HG04115.hp1 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.508+488_508+506dup others(19): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(13): Show |
12 | a0001c0003t0001g0161a0001c0009t0001g0333a0001c0009t0001g0335others(9): Show | 12 | HG01943.hp2 HG02027.hp1 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.508+487_508+506dup others(20): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(14): Show |
6 | a0001c0009t0001g0283a0001c0009t0001g0332a0005c0034t0001g0338others(3): Show | 6 | HG02040.hp1 NA18940.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.508+506_508+507ins others(21): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
C | CAAAAAAA others(15): Show |
3 | a0001c0001t0001g0160a0001c0124t0001g0331a0002c0004t0002g0184 | 3 | NA18971.hp2 NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.508+506_508+507ins others(22): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009339
|
CA | C | 12 | a0001c0002t0001g0393a0001c0022t0001g0356a0001c0115t0001g0040others(9): Show | 12 | HG01884.hp1 HG02071.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.508+506delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009339 | |||||
| chr19:56009358
|
A | AAAAAAAA others(11): Show |
1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.508+506_508+507ins others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56009358 | |||||
| chr19:56009360
|
G | A | 1 | a0009c0054t0001g0297 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.508+507G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009360 | ||||||
| chr19:56009407
|
G | A | 104 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.508+554G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009407 | ||||||
| chr19:56009478
|
T | C | 104 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.508+625T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009478 | ||||||
| chr19:56009481
|
A | G | 104 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.508+628A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009481 | ||||||
| chr19:56009586
|
A | G | 105 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.508+733A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009586 | ||||||
| chr19:56009615
|
T | C | 107 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.508+762T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009615 | ||||||
| chr19:56009656
|
A | C | 368 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(365): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.508+803A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009656 | ||||||
| chr19:56009713
|
C | T | 7 | a0001c0023t0001g0314a0004c0020t0001g0096a0004c0020t0003g0098others(4): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.508+860C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009713 | ||||||
| chr19:56009714
|
T | G | 116 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.508+861T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009714 | ||||||
| chr19:56009731
|
T | C | 115 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.508+878T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009731 | ||||||
| chr19:56009735
|
A | T | 1 | a0001c0092t0001g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.508+882A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009735 | ||||||
| chr19:56009821
|
C | A | 73 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.508+968C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009821 | ||||||
| chr19:56009839
|
T | G | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.508+986T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009839 | ||||||
| chr19:56009862
|
A | G | 1 | a0002c0127t0002g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.508+1009A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009862 | ||||||
| chr19:56009886
|
A | G | 115 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.508+1033A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009886 | ||||||
| chr19:56009950
|
C | T | 2 | a0006c0005t0002g0299a0006c0011t0002g0129 | 2 | NA18950.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.508+1097C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56009950 | ||||||
| chr19:56010015
|
A | G | 116 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.508+1162A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010015 | ||||||
| chr19:56010091
|
G | A | 3 | a0003c0051t0001g0020a0007c0032t0001g0017a0007c0032t0001g0327 | 3 | HG01346.hp1 HG02004.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.508+1238G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010091 | ||||||
| chr19:56010170
|
T | G | 370 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(367): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.508+1317T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010170 | ||||||
| chr19:56010178
|
C | T | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1325C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010178 | ||||||
| chr19:56010193
|
CT | C | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1343delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010193 | |||||
| chr19:56010199
|
T | C | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1346T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010199 | ||||||
| chr19:56010247
|
C | T | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1394C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010247 | ||||||
| chr19:56010250
|
G | T | 21 | a0001c0001t0001g0253a0003c0008t0003g0381a0003c0051t0001g0252others(18): Show | 21 | HG00423.hp2 HG00741.hp1 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.508+1397G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010250 | ||||||
| chr19:56010374
|
A | G | 239 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(236): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.508+1521A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010374 | ||||||
| chr19:56010395
|
C | G | 1 | a0001c0009t0001g0286 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.508+1542C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010395 | ||||||
| chr19:56010418
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.508+1565C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010418 | ||||||
| chr19:56010470
|
C | T | 8 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(5): Show | 8 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.508+1617C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010470 | ||||||
| chr19:56010471
|
G | A | 1 | a0027c0060t0001g0156 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.508+1618G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010471 | ||||||
| chr19:56010482
|
C | T | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1629C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010482 | ||||||
| chr19:56010507
|
G | A | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1654G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010507 | ||||||
| chr19:56010511
|
G | A | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.508+1658G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010511 | ||||||
| chr19:56010535
|
G | A | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1682G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010535 | ||||||
| chr19:56010542
|
C | T | 1 | a0002c0004t0002g0128 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.508+1689C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010542 | ||||||
| chr19:56010549
|
A | G | 1 | a0002c0127t0002g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.508+1696A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010549 | ||||||
| chr19:56010556
|
C | G | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1703C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010556 | ||||||
| chr19:56010576
|
G | C | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1723G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010576 | ||||||
| chr19:56010593
|
G | GA | 90 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.508+1750dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010593 | |||||
| chr19:56010593
|
G | GAA | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1749_508+1750d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010593 | |||||
| chr19:56010594
|
A | G | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+1741A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010594 | ||||||
| chr19:56010597
|
A | G | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+1744A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010597 | ||||||
| chr19:56010614
|
G | A | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1761G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010614 | ||||||
| chr19:56010630
|
G | A | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.508+1777G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010630 | ||||||
| chr19:56010684
|
T | C | 2 | a0016c0130t0003g0316a0045c0131t0001g0315 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.508+1831T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010684 | ||||||
| chr19:56010740
|
C | CAAAAAAA others(19): Show |
1 | a0005c0113t0001g0099 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.508+1887_508+1888i others(28): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010740 | ||||||
| chr19:56010740
|
C | CAAAAAAA others(20): Show |
1 | a0004c0020t0003g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.508+1887_508+1888i others(29): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010740 | ||||||
| chr19:56010741
|
T | A | 2 | a0004c0020t0003g0098a0005c0113t0001g0099 | 2 | HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.508+1888T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010741 | ||||||
| chr19:56010742
|
C | A | 2 | a0004c0020t0003g0098a0005c0113t0001g0099 | 2 | HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.508+1889C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010742 | ||||||
| chr19:56010742
|
C | CAAA | 9 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(6): Show | 9 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1900_508+1902d others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(3): Show |
1 | a0004c0055t0001g0301 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.508+1893_508+1902d others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(6): Show |
2 | a0001c0003t0001g0140a0005c0025t0001g0150 | 2 | NA18995.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.508+1890_508+1902d others(15): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(9): Show |
1 | a0009c0090t0001g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.508+1902_508+1903i others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(12): Show |
2 | a0004c0050t0001g0328a0004c0050t0001g0329 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.508+1902_508+1903i others(21): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(13): Show |
9 | a0001c0052t0001g0026a0001c0086t0001g0018a0002c0004t0002g0202others(6): Show | 9 | HG00280.hp1 HG00733.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.508+1902_508+1903i others(22): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(14): Show |
28 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(25): Show | 28 | HG00140.hp2 HG01069.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.508+1902_508+1903i others(23): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(15): Show |
54 | a0001c0001t0001g0117a0001c0001t0001g0203a0001c0001t0001g0207others(51): Show | 54 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.508+1902_508+1903i others(24): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(16): Show |
60 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0091others(57): Show | 60 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.508+1902_508+1903i others(25): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(17): Show |
43 | a0001c0001t0001g0038a0001c0001t0001g0174a0001c0002t0001g0158others(40): Show | 43 | HG00323.hp1 HG00609.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.508+1902_508+1903i others(26): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(18): Show |
16 | a0001c0003t0001g0011a0001c0009t0001g0332a0001c0009t0001g0333others(13): Show | 16 | HG00639.hp1 HG01884.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.508+1902_508+1903i others(27): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(19): Show |
16 | a0001c0001t0001g0007a0001c0001t0001g0386a0001c0001t0001g0387others(13): Show | 16 | HG00597.hp2 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.508+1902_508+1903i others(28): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(20): Show |
3 | a0001c0002t0001g0148a0001c0002t0001g0151a0002c0012t0002g0031 | 3 | HG01175.hp1 HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.508+1902_508+1903i others(29): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CAAAAAAA others(25): Show |
1 | a0001c0009t0001g0293 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.508+1902_508+1903i others(34): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010742 | |||||
| chr19:56010742
|
C | CCAAAAAA others(7): Show |
1 | a0003c0008t0001g0312 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.508+1889_508+1890i others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010742 | ||||||
| chr19:56010742
|
C | CCAAAAAA others(10): Show |
1 | a0006c0005t0002g0355 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.508+1889_508+1890i others(19): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010742 | ||||||
| chr19:56010742
|
C | CCAAAAAA others(11): Show |
3 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311 | 3 | HG02109.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.508+1889_508+1890i others(20): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010742 | ||||||
| chr19:56010742
|
C | CCAAAAAA others(12): Show |
1 | a0039c0078t0001g0313 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.508+1889_508+1890i others(21): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010742 | ||||||
| chr19:56010742
|
C | CCAAAAAA others(18): Show |
3 | a0001c0023t0001g0314a0004c0035t0001g0094a0004c0035t0001g0095 | 3 | HG02615.hp1 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.508+1889_508+1890i others(27): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010742 | ||||||
| chr19:56010742
|
C | CCAAAAAA others(19): Show |
2 | a0003c0114t0002g0347a0004c0035t0001g0097 | 2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.508+1889_508+1890i others(28): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010742 | ||||||
| chr19:56010742
|
C | CCAAAAAA others(20): Show |
2 | a0003c0076t0002g0250a0007c0021t0001g0348 | 2 | HG01109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.508+1889_508+1890i others(29): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010742 | ||||||
| chr19:56010742
|
C | CCAAAAAA others(21): Show |
1 | a0004c0020t0001g0096 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.508+1889_508+1890i others(30): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010742 | ||||||
| chr19:56010742
|
C | CCCAAAAA others(29): Show |
1 | a0002c0079t0002g0089 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.508+1889_508+1890i others(38): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010742 | ||||||
| chr19:56010755
|
A | AAAAAAAA others(4): Show |
3 | a0002c0127t0002g0306a0016c0130t0003g0316a0045c0131t0001g0315 | 3 | HG01891.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.508+1902_508+1903i others(13): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010755 | ||||||
| chr19:56010755
|
A | AAAAAAAA others(3): Show |
6 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(3): Show | 6 | HG01884.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.508+1902_508+1903i others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010755 | ||||||
| chr19:56010755
|
A | AAAAAAAT | 10 | a0001c0001t0001g0068a0001c0001t0001g0253a0001c0042t0001g0377others(7): Show | 10 | HG00741.hp1 HG02572.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.508+1902_508+1903i others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010755 | ||||||
| chr19:56010755
|
A | AAAAAAT | 85 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.508+1902_508+1903i others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010755 | ||||||
| chr19:56010770
|
A | G | 1 | a0002c0127t0002g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.508+1917A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010770 | ||||||
| chr19:56010782
|
A | G | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1929A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010782 | ||||||
| chr19:56010789
|
GT | G | 98 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.508+1946delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010789 | |||||
| chr19:56010799
|
T | A | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+1946T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010799 | ||||||
| chr19:56010799
|
T | TA | 8 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(5): Show | 8 | HG01255.hp2 HG01261.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.508+1947dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56010799 | |||||
| chr19:56010812
|
A | G | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.508+1959A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010812 | ||||||
| chr19:56010825
|
C | A | 102 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.508+1972C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010825 | ||||||
| chr19:56010889
|
T | C | 1 | a0001c0019t0001g0359 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.508+2036T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010889 | ||||||
| chr19:56010935
|
C | T | 1 | a0001c0003t0001g0380 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.508+2082C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010935 | ||||||
| chr19:56010980
|
G | C | 102 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.508+2127G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56010980 | ||||||
| chr19:56011026
|
C | A | 1 | a0006c0005t0002g0355 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.508+2173C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011026 | ||||||
| chr19:56011027
|
G | A | 1 | a0028c0093t0001g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.508+2174G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011027 | ||||||
| chr19:56011076
|
CA | C | 16 | a0001c0001t0001g0160a0001c0003t0001g0161a0001c0009t0001g0283others(13): Show | 16 | HG01943.hp2 HG02040.hp1 HG02293.hp2 others(13): Show |
intron_variant | MODIFIER | c.508+2224delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011076 | ||||||
| chr19:56011096
|
T | C | 1 | a0027c0060t0001g0156 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.508+2243T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011096 | ||||||
| chr19:56011111
|
T | C | 102 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.508+2258T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011111 | ||||||
| chr19:56011115
|
T | C | 1 | a0002c0127t0002g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.508+2262T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011115 | ||||||
| chr19:56011158
|
A | AAAAAAAA others(5): Show |
1 | a0045c0131t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.508+2306_508+2307i others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56011158 | |||||
| chr19:56011158
|
A | AAAAAATA others(5): Show |
1 | a0016c0130t0003g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.508+2306_508+2307i others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56011158 | |||||
| chr19:56011158
|
A | AAAAATAT others(4): Show |
1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.508+2306_508+2307i others(13): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56011158 | |||||
| chr19:56011158
|
A | AAAAATAT others(6): Show |
2 | a0001c0115t0001g0040a0007c0110t0001g0349 | 2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.508+2306_508+2307i others(15): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56011158 | |||||
| chr19:56011158
|
A | AAATATAT others(8): Show |
1 | a0041c0109t0001g0345 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.508+2306_508+2307i others(17): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56011158 | |||||
| chr19:56011158
|
A | AATATATA others(3): Show |
2 | a0002c0041t0002g0358a0030c0098t0001g0354 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.508+2314_508+2315i others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56011158 | |||||
| chr19:56011158
|
A | AATATATA others(5): Show |
1 | a0001c0022t0001g0356 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.508+2314_508+2315i others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56011158 | |||||
| chr19:56011162
|
T | C | 1 | a0004c0007t0001g0212 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.508+2309T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011162 | ||||||
| chr19:56011166
|
T | C | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.508+2313T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011166 | ||||||
| chr19:56011166
|
T | TATATATA others(3): Show |
1 | a0008c0104t0001g0374 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.508+2314_508+2315i others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56011166 | |||||
| chr19:56011166
|
T | TATATATA others(3): Show |
89 | a0001c0001t0001g0047a0001c0001t0001g0068a0001c0001t0001g0110others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.508+2314_508+2315i others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56011166 | |||||
| chr19:56011166
|
T | TATATATA others(5): Show |
2 | a0001c0001t0001g0049a0001c0015t0001g0046 | 2 | HG00099.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.508+2314_508+2315i others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56011166 | |||||
| chr19:56011178
|
T | C | 370 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(367): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.508+2325T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011178 | ||||||
| chr19:56011231
|
A | G | 14 | a0001c0014t0001g0022a0001c0052t0001g0023a0001c0052t0001g0026others(11): Show | 14 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.508+2378A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011231 | ||||||
| chr19:56011250
|
T | A | 1 | a0001c0022t0001g0356 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.508+2397T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011250 | ||||||
| chr19:56011256
|
G | T | 1 | a0020c0049t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.508+2403G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011256 | ||||||
| chr19:56011340
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG03491.hp2 HG03492.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.508+2487G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011340 | ||||||
| chr19:56011396
|
T | A | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+2543T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011396 | ||||||
| chr19:56011451
|
T | G | 1 | a0002c0041t0002g0358 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.508+2598T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011451 | ||||||
| chr19:56011461
|
C | G | 102 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.508+2608C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011461 | ||||||
| chr19:56011463
|
A | G | 5 | a0003c0040t0001g0165a0003c0040t0001g0177a0008c0017t0001g0103others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+2610A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011463 | ||||||
| chr19:56011472
|
T | C | 102 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.508+2619T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011472 | ||||||
| chr19:56011519
|
A | G | 1 | a0004c0053t0003g0317 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.508+2666A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011519 | ||||||
| chr19:56011545
|
C | T | 102 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.508+2692C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011545 | ||||||
| chr19:56011557
|
C | T | 93 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.508+2704C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011557 | ||||||
| chr19:56011558
|
G | A | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.508+2705G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011558 | ||||||
| chr19:56011568
|
C | T | 93 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.508+2715C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011568 | ||||||
| chr19:56011602
|
A | G | 352 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(349): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.508+2749A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011602 | ||||||
| chr19:56011627
|
A | AT | 9 | a0001c0022t0001g0356a0001c0030t0001g0343a0001c0115t0001g0040others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+2784dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56011627 | |||||
| chr19:56011691
|
C | CT | 54 | a0001c0001t0001g0091a0001c0001t0001g0117a0001c0001t0001g0160others(51): Show | 54 | HG00639.hp1 HG00673.hp2 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.508+2850dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56011691 | |||||
| chr19:56011776
|
C | T | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.508+2923C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011776 | ||||||
| chr19:56011836
|
C | T | 102 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.508+2983C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011836 | ||||||
| chr19:56011838
|
C | T | 102 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.508+2985C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011838 | ||||||
| chr19:56011840
|
C | T | 79 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0130others(76): Show | 79 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.508+2987C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011840 | ||||||
| chr19:56011847
|
G | A | 2 | a0007c0010t0001g0172a0007c0071t0001g0178 | 2 | HG01257.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.508+2994G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011847 | ||||||
| chr19:56011878
|
G | A | 1 | a0001c0002t0001g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.508+3025G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011878 | ||||||
| chr19:56011883
|
A | G | 102 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.508+3030A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011883 | ||||||
| chr19:56011955
|
C | G | 89 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.508+3102C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56011955 | ||||||
| chr19:56012009
|
A | G | 1 | a0006c0005t0002g0355 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.508+3156A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012009 | ||||||
| chr19:56012038
|
A | G | 89 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.508+3185A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012038 | ||||||
| chr19:56012126
|
T | G | 1 | a0001c0002t0001g0054 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.508+3273T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012126 | ||||||
| chr19:56012306
|
G | A | 9 | a0001c0022t0001g0356a0001c0115t0001g0040a0002c0041t0002g0358others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.509-3436G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012306 | ||||||
| chr19:56012340
|
G | A | 13 | a0006c0005t0002g0369a0008c0104t0001g0374a0008c0105t0001g0372others(10): Show | 13 | HG00423.hp2 HG01981.hp1 HG03704.hp2 others(10): Show |
intron_variant | MODIFIER | c.509-3402G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012340 | ||||||
| chr19:56012448
|
C | CT | 31 | a0001c0022t0001g0267a0001c0023t0001g0314a0001c0115t0001g0040others(28): Show | 31 | HG00423.hp2 HG01109.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.509-3277dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56012448 | |||||
| chr19:56012448
|
CT | C | 244 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.509-3277delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56012448 | |||||
| chr19:56012448
|
CTT | C | 14 | a0001c0001t0001g0068a0001c0002t0001g0043a0001c0002t0001g0063others(11): Show | 14 | HG01123.hp2 HG01243.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.509-3278_509-3277d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56012448 | |||||
| chr19:56012477
|
G | A | 1 | a0002c0127t0002g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.509-3265G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012477 | ||||||
| chr19:56012492
|
A | G | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.509-3250A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012492 | ||||||
| chr19:56012576
|
CA | C | 69 | a0001c0001t0001g0117a0001c0001t0001g0160a0001c0001t0001g0253others(66): Show | 69 | HG00423.hp2 HG00609.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.509-3151delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56012576 | |||||
| chr19:56012576
|
CAA | C | 293 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.509-3152_509-3151d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56012576 | |||||
| chr19:56012602
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.509-3140G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012602 | ||||||
| chr19:56012635
|
A | T | 84 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.509-3107A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012635 | ||||||
| chr19:56012647
|
TTTGGAAC others(19): Show |
T | 84 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.509-3068_509-3043d others(28): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56012647 | |||||
| chr19:56012651
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.509-3091G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012651 | ||||||
| chr19:56012654
|
C | T | 5 | a0001c0023t0001g0314a0004c0020t0001g0096a0004c0035t0001g0094others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-3088C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012654 | ||||||
| chr19:56012705
|
C | A | 2 | a0008c0037t0001g0004a0008c0037t0001g0009 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.509-3037C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012705 | ||||||
| chr19:56012707
|
T | C | 1 | a0002c0041t0002g0358 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.509-3035T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012707 | ||||||
| chr19:56012851
|
G | A | 4 | a0002c0041t0002g0358a0002c0127t0002g0306a0016c0130t0003g0316others(1): Show | 4 | HG01891.hp1 HG02809.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-2891G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012851 | ||||||
| chr19:56012900
|
C | CT | 15 | a0006c0005t0002g0369a0008c0104t0001g0374a0008c0105t0001g0372others(12): Show | 15 | HG00423.hp2 HG01981.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.509-2836dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56012900 | |||||
| chr19:56012999
|
C | T | 84 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.509-2743C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56012999 | ||||||
| chr19:56013041
|
C | T | 1 | a0024c0058t0002g0169 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.509-2701C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013041 | ||||||
| chr19:56013054
|
C | T | 15 | a0001c0001t0001g0160a0001c0003t0001g0161a0001c0009t0001g0283others(12): Show | 15 | HG01943.hp2 HG02293.hp2 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.509-2688C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013054 | ||||||
| chr19:56013099
|
G | A | 1 | a0001c0085t0001g0236 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.509-2643G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013099 | ||||||
| chr19:56013214
|
A | C | 5 | a0001c0023t0001g0314a0004c0020t0001g0096a0004c0035t0001g0094others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-2528A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013214 | ||||||
| chr19:56013222
|
G | A | 16 | a0006c0005t0002g0369a0008c0104t0001g0374a0008c0105t0001g0372others(13): Show | 16 | HG00423.hp2 HG01981.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.509-2520G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013222 | ||||||
| chr19:56013234
|
T | C | 310 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(307): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.509-2508T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013234 | ||||||
| chr19:56013335
|
G | C | 15 | a0001c0001t0001g0160a0001c0003t0001g0161a0001c0009t0001g0283others(12): Show | 15 | HG01943.hp2 HG02293.hp2 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.509-2407G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013335 | ||||||
| chr19:56013438
|
C | T | 1 | a0001c0082t0001g0168 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.509-2304C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013438 | ||||||
| chr19:56013484
|
G | A | 6 | a0001c0001t0001g0353a0003c0008t0003g0381a0005c0029t0001g0015others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.509-2258G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013484 | ||||||
| chr19:56013515
|
T | A | 7 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(4): Show | 7 | HG00280.hp2 HG01255.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.509-2227T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013515 | ||||||
| chr19:56013584
|
A | T | 73 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.509-2158A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013584 | ||||||
| chr19:56013595
|
G | GT | 4 | a0001c0001t0001g0264a0001c0003t0001g0263a0003c0045t0001g0266others(1): Show | 4 | HG00280.hp2 HG01346.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-2147_509-2146i others(3): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013595 | ||||||
| chr19:56013596
|
G | GGTTTTTT | 36 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(33): Show | 36 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.509-2146_509-2145i others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013596 | ||||||
| chr19:56013596
|
G | GGTTTTTT others(1): Show |
18 | a0001c0001t0001g0135a0001c0002t0001g0032a0001c0002t0001g0042others(15): Show | 18 | HG00741.hp2 HG01243.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.509-2146_509-2145i others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013596 | ||||||
| chr19:56013596
|
G | GGTTTTTT others(2): Show |
7 | a0001c0002t0001g0044a0001c0002t0001g0063a0001c0002t0001g0079others(4): Show | 7 | HG00733.hp1 HG01106.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.509-2146_509-2145i others(11): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013596 | ||||||
| chr19:56013596
|
G | GGTTTTTT others(3): Show |
2 | a0001c0002t0001g0043a0012c0018t0002g0033 | 2 | HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.509-2146_509-2145i others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013596 | ||||||
| chr19:56013596
|
G | GT | 20 | a0001c0001t0001g0027a0001c0001t0001g0117a0001c0001t0001g0174others(17): Show | 20 | HG00597.hp1 HG01106.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.509-2125dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTT | 8 | a0001c0009t0001g0281a0001c0019t0001g0118a0001c0019t0001g0122others(5): Show | 8 | HG01192.hp2 HG01884.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.509-2127_509-2125d others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTT | 31 | a0001c0001t0001g0007a0001c0001t0001g0207a0001c0001t0001g0230others(28): Show | 31 | HG00140.hp2 HG00280.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.509-2129_509-2125d others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTT | 14 | a0001c0003t0001g0140a0001c0003t0001g0155a0001c0003t0001g0162others(11): Show | 14 | HG00323.hp1 HG00544.hp2 HG03669.hp2 others(11): Show |
intron_variant | MODIFIER | c.509-2130_509-2125d others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT | 12 | a0001c0001t0001g0253a0010c0016t0001g0366a0011c0033t0001g0376others(9): Show | 12 | HG00741.hp1 HG02015.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.509-2131_509-2125d others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(5): Show |
2 | a0002c0079t0002g0089a0003c0045t0001g0090 | 2 | HG01109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.509-2137_509-2136i others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(3): Show |
6 | a0001c0023t0001g0314a0004c0020t0001g0096a0004c0035t0001g0095others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.509-2134_509-2125d others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(4): Show |
4 | a0001c0092t0001g0211a0003c0076t0002g0250a0003c0114t0002g0347others(1): Show | 4 | HG01109.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-2135_509-2125d others(13): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(5): Show |
2 | a0007c0110t0001g0349a0030c0098t0001g0354 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.509-2136_509-2125d others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(6): Show |
1 | a0018c0036t0002g0034 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.509-2137_509-2125d others(15): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(7): Show |
1 | a0018c0036t0002g0035 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.509-2138_509-2125d others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(8): Show |
4 | a0001c0002t0001g0320a0009c0013t0001g0350a0033c0061t0001g0256others(1): Show | 4 | HG02818.hp2 HG03834.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-2139_509-2125d others(17): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(9): Show |
1 | a0007c0010t0001g0321 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.509-2140_509-2125d others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(10): Show |
3 | a0002c0004t0002g0183a0003c0008t0003g0381a0009c0013t0001g0351 | 3 | HG02074.hp1 HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.509-2141_509-2125d others(19): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(11): Show |
7 | a0001c0001t0001g0386a0001c0002t0001g0010a0005c0029t0001g0015others(4): Show | 7 | HG00673.hp2 HG01167.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.509-2142_509-2125d others(20): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(12): Show |
20 | a0001c0001t0001g0091a0001c0001t0001g0353a0001c0001t0001g0387others(17): Show | 20 | HG00597.hp2 HG01081.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.509-2143_509-2125d others(21): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(13): Show |
28 | a0001c0002t0001g0148a0001c0002t0001g0393a0001c0015t0001g0002others(25): Show | 28 | HG01175.hp1 HG01346.hp1 HG01515.hp1 others(25): Show |
intron_variant | MODIFIER | c.509-2144_509-2125d others(22): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(14): Show |
18 | a0001c0022t0001g0267a0001c0022t0001g0273a0001c0022t0001g0289others(15): Show | 18 | HG00733.hp2 HG01099.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.509-2145_509-2125d others(23): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(15): Show |
6 | a0001c0022t0001g0274a0001c0023t0001g0249a0001c0121t0001g0290others(3): Show | 6 | HG01258.hp2 HG02723.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.509-2125_509-2124i others(24): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(16): Show |
3 | a0001c0023t0001g0244a0001c0023t0001g0248a0006c0005t0002g0300 | 3 | HG02622.hp1 NA19012.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.509-2125_509-2124i others(25): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(17): Show |
4 | a0001c0009t0001g0286a0003c0077t0001g0379a0003c0122t0001g0276others(1): Show | 4 | HG02027.hp1 HG02027.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-2125_509-2124i others(26): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(18): Show |
6 | a0004c0050t0001g0329a0004c0053t0003g0317a0006c0005t0002g0284others(3): Show | 6 | HG01243.hp2 HG02970.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.509-2125_509-2124i others(27): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(19): Show |
1 | a0003c0008t0001g0311 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.509-2125_509-2124i others(28): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(20): Show |
1 | a0003c0008t0001g0245 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.509-2125_509-2124i others(29): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | GTTTTTTT others(22): Show |
1 | a0004c0020t0001g0285 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.509-2125_509-2124i others(31): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013596
|
G | T | 8 | a0001c0001t0001g0264a0001c0002t0001g0108a0001c0003t0001g0260others(5): Show | 8 | HG00280.hp2 HG01255.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.509-2146G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013596 | ||||||
| chr19:56013596
|
GTTTTTT | G | 14 | a0001c0001t0001g0160a0001c0009t0001g0283a0001c0009t0001g0332others(11): Show | 14 | HG01943.hp2 NA18939.hp2 NA18940.hp2 others(11): Show |
intron_variant | MODIFIER | c.509-2130_509-2125d others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56013596 | |||||
| chr19:56013601
|
T | G | 1 | a0010c0016t0001g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.509-2141T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013601 | ||||||
| chr19:56013602
|
T | G | 1 | a0004c0007t0001g0212 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.509-2140T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013602 | ||||||
| chr19:56013629
|
C | T | 80 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.509-2113C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013629 | ||||||
| chr19:56013642
|
G | T | 1 | a0005c0006t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.509-2100G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013642 | ||||||
| chr19:56013651
|
G | A | 14 | a0001c0001t0001g0160a0001c0009t0001g0283a0001c0009t0001g0332others(11): Show | 14 | HG01943.hp2 HG02293.hp2 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.509-2091G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013651 | ||||||
| chr19:56013676
|
T | C | 192 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(189): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.509-2066T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013676 | ||||||
| chr19:56013831
|
T | C | 1 | a0007c0073t0001g0218 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.509-1911T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013831 | ||||||
| chr19:56013902
|
A | C | 1 | a0001c0014t0001g0362 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.509-1840A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013902 | ||||||
| chr19:56013920
|
T | C | 8 | a0001c0092t0001g0211a0002c0079t0002g0089a0003c0045t0001g0090others(5): Show | 8 | HG01109.hp1 HG01109.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.509-1822T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56013920 | ||||||
| chr19:56014002
|
T | C | 1 | a0009c0013t0001g0351 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.509-1740T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014002 | ||||||
| chr19:56014019
|
G | A | 1 | a0001c0042t0001g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.509-1723G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014019 | ||||||
| chr19:56014033
|
G | C | 25 | a0002c0041t0002g0358a0008c0104t0001g0374a0008c0105t0001g0372others(22): Show | 25 | HG00423.hp2 HG01981.hp1 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.509-1709G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014033 | ||||||
| chr19:56014114
|
C | T | 24 | a0002c0041t0002g0358a0002c0127t0002g0306a0003c0008t0001g0309others(21): Show | 24 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.509-1628C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014114 | ||||||
| chr19:56014176
|
A | G | 3 | a0001c0115t0001g0040a0007c0110t0001g0349a0041c0109t0001g0345 | 3 | HG01884.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.509-1566A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014176 | ||||||
| chr19:56014177
|
T | A | 1 | a0001c0002t0001g0072 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.509-1565T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014177 | ||||||
| chr19:56014207
|
T | C | 25 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(22): Show | 25 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.509-1535T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014207 | ||||||
| chr19:56014219
|
C | G | 7 | a0001c0001t0001g0264a0001c0003t0001g0260a0001c0003t0001g0263others(4): Show | 7 | HG00280.hp2 HG01255.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.509-1523C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014219 | ||||||
| chr19:56014248
|
A | G | 37 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(34): Show | 37 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.509-1494A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014248 | ||||||
| chr19:56014336
|
C | T | 1 | a0002c0127t0002g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.509-1406C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014336 | ||||||
| chr19:56014337
|
A | G | 37 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(34): Show | 37 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.509-1405A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014337 | ||||||
| chr19:56014353
|
T | G | 37 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(34): Show | 37 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.509-1389T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014353 | ||||||
| chr19:56014389
|
G | A | 1 | a0001c0009t0001g0286 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.509-1353G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014389 | ||||||
| chr19:56014468
|
C | A | 6 | a0002c0127t0002g0306a0003c0008t0001g0309a0003c0008t0001g0310others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.509-1274C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014468 | ||||||
| chr19:56014469
|
G | A | 5 | a0001c0002t0001g0041a0001c0002t0001g0054a0001c0084t0001g0053others(2): Show | 5 | HG00741.hp2 HG01099.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-1273G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014469 | ||||||
| chr19:56014478
|
C | CA | 20 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0003t0001g0251others(17): Show | 20 | HG01943.hp2 HG02293.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.509-1246dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56014478 | |||||
| chr19:56014478
|
CA | C | 131 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(128): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.509-1246delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56014478 | |||||
| chr19:56014478
|
CAA | C | 60 | a0001c0001t0001g0353a0001c0002t0001g0010a0001c0002t0001g0067others(57): Show | 60 | HG00423.hp2 HG01109.hp1 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.509-1247_509-1246d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56014478 | |||||
| chr19:56014478
|
CAAA | C | 32 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(29): Show | 32 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.509-1248_509-1246d others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56014478 | |||||
| chr19:56014608
|
T | C | 1 | a0002c0041t0002g0358 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.509-1134T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014608 | ||||||
| chr19:56014639
|
T | C | 31 | a0001c0002t0001g0320a0002c0041t0002g0358a0008c0104t0001g0374others(28): Show | 31 | HG00423.hp2 HG01981.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.509-1103T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014639 | ||||||
| chr19:56014809
|
C | T | 37 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(34): Show | 37 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.509-933C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014809 | ||||||
| chr19:56014815
|
T | A | 1 | a0001c0002t0001g0087 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.509-927T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014815 | ||||||
| chr19:56014829
|
T | C | 1 | a0002c0127t0002g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.509-913T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014829 | ||||||
| chr19:56014938
|
G | A | 37 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(34): Show | 37 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.509-804G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56014938 | ||||||
| chr19:56015090
|
C | T | 7 | a0001c0001t0001g0264a0001c0003t0001g0260a0001c0003t0001g0263others(4): Show | 7 | HG00280.hp2 HG01255.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.509-652C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56015090 | ||||||
| chr19:56015191
|
C | T | 37 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(34): Show | 37 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.509-551C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56015191 | ||||||
| chr19:56015196
|
T | G | 1 | a0001c0002t0001g0087 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.509-546T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56015196 | ||||||
| chr19:56015238
|
T | G | 31 | a0001c0002t0001g0320a0002c0041t0002g0358a0008c0104t0001g0374others(28): Show | 31 | HG00423.hp2 HG01981.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.509-504T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56015238 | ||||||
| chr19:56015274
|
A | C | 37 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(34): Show | 37 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.509-468A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56015274 | ||||||
| chr19:56015471
|
G | C | 37 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(34): Show | 37 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.509-271G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56015471 | ||||||
| chr19:56015501
|
CATTTT | C | 3 | a0011c0033t0001g0370a0012c0018t0002g0175a0012c0106t0002g0371 | 3 | HG02735.hp2 NA18947.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.509-235_509-231del others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | 56015501 | |||||
| chr19:56015547
|
G | A | 37 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(34): Show | 37 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.509-195G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 3/14 | chr19 | 56015547 | ||||||
| chr19:56015813
|
T | TC | 37 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(34): Show | 37 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+16dupC | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 56015813 | |||||
| chr19:56015849
|
TGA | T | 3 | a0003c0076t0002g0250a0003c0114t0002g0347a0007c0021t0001g0348 | 3 | HG01109.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.565+56_565+57delGA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 56015849 | |||||
| chr19:56015883
|
A | G | 1 | a0001c0030t0001g0318 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.565+85A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56015883 | ||||||
| chr19:56015931
|
C | T | 10 | a0001c0092t0001g0211a0002c0079t0002g0089a0003c0045t0001g0090others(7): Show | 10 | HG01109.hp1 HG01109.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+133C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56015931 | ||||||
| chr19:56015947
|
C | T | 33 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(30): Show | 33 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(30): Show |
intron_variant | MODIFIER | c.565+149C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56015947 | ||||||
| chr19:56015979
|
C | T | 33 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(30): Show | 33 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(30): Show |
intron_variant | MODIFIER | c.565+181C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56015979 | ||||||
| chr19:56016070
|
G | A | 33 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0127t0002g0306others(30): Show | 33 | HG00423.hp2 HG01891.hp1 HG01981.hp1 others(30): Show |
intron_variant | MODIFIER | c.565+272G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016070 | ||||||
| chr19:56016075
|
T | A | 2 | a0003c0040t0001g0165a0003c0040t0001g0177 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565+277T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016075 | ||||||
| chr19:56016131
|
T | C | 2 | a0007c0010t0001g0391a0042c0069t0001g0365 | 2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.565+333T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016131 | ||||||
| chr19:56016166
|
A | C | 29 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0079t0002g0089others(26): Show | 29 | HG00423.hp2 HG01109.hp2 HG01981.hp1 others(26): Show |
intron_variant | MODIFIER | c.565+368A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016166 | ||||||
| chr19:56016172
|
A | C | 30 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(27): Show | 30 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.565+374A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016172 | ||||||
| chr19:56016182
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.565+384C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016182 | ||||||
| chr19:56016210
|
G | A | 35 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0079t0002g0089others(32): Show | 35 | HG00423.hp2 HG01109.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.565+412G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016210 | ||||||
| chr19:56016218
|
A | G | 3 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311 | 3 | HG02109.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.565+420A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016218 | ||||||
| chr19:56016223
|
A | G | 35 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0079t0002g0089others(32): Show | 35 | HG00423.hp2 HG01109.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.565+425A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016223 | ||||||
| chr19:56016297
|
G | A | 35 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0079t0002g0089others(32): Show | 35 | HG00423.hp2 HG01109.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.565+499G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016297 | ||||||
| chr19:56016310
|
C | A | 35 | a0001c0002t0001g0320a0002c0041t0002g0358a0002c0079t0002g0089others(32): Show | 35 | HG00423.hp2 HG01109.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.565+512C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016310 | ||||||
| chr19:56016361
|
C | T | 3 | a0018c0036t0002g0034a0018c0036t0002g0035a0033c0061t0001g0256 | 3 | HG03669.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.565+563C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016361 | ||||||
| chr19:56016450
|
G | A | 1 | a0012c0018t0002g0389 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.565+652G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016450 | ||||||
| chr19:56016466
|
T | G | 32 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(29): Show | 32 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.565+668T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016466 | ||||||
| chr19:56016472
|
T | C | 1 | a0001c0002t0001g0087 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.565+674T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016472 | ||||||
| chr19:56016480
|
T | C | 142 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(139): Show | 142 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.565+682T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016480 | ||||||
| chr19:56016488
|
T | G | 3 | a0018c0036t0002g0034a0018c0036t0002g0035a0033c0061t0001g0256 | 3 | HG03669.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.565+690T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016488 | ||||||
| chr19:56016507
|
T | C | 1 | a0016c0097t0001g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.565+709T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016507 | ||||||
| chr19:56016514
|
T | G | 1 | a0006c0005t0002g0355 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.565+716T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016514 | ||||||
| chr19:56016518
|
C | G | 1 | a0039c0078t0001g0313 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.565+720C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016518 | ||||||
| chr19:56016550
|
C | G | 1 | a0001c0030t0001g0318 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.565+752C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016550 | ||||||
| chr19:56016639
|
T | C | 213 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(210): Show | 213 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.565+841T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016639 | ||||||
| chr19:56016680
|
A | T | 214 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(211): Show | 214 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.565+882A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016680 | ||||||
| chr19:56016752
|
A | G | 12 | a0001c0052t0001g0023a0001c0052t0001g0026a0001c0086t0001g0018others(9): Show | 12 | HG00733.hp2 HG01099.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.565+954A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016752 | ||||||
| chr19:56016780
|
T | C | 38 | a0001c0001t0001g0264a0001c0002t0001g0320a0001c0003t0001g0260others(35): Show | 38 | HG00280.hp2 HG00423.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.565+982T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016780 | ||||||
| chr19:56016787
|
T | C | 11 | a0001c0001t0001g0353a0001c0023t0001g0314a0003c0008t0003g0381others(8): Show | 11 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.565+989T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016787 | ||||||
| chr19:56016821
|
A | T | 6 | a0002c0127t0002g0306a0003c0008t0001g0309a0003c0008t0001g0310others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+1023A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016821 | ||||||
| chr19:56016865
|
G | A | 1 | a0009c0094t0001g0208 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.565+1067G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016865 | ||||||
| chr19:56016958
|
G | A | 3 | a0005c0034t0001g0338a0005c0083t0001g0121a0009c0013t0001g0147 | 3 | NA18955.hp1 NA18998.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.565+1160G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016958 | ||||||
| chr19:56016970
|
A | G | 1 | a0007c0010t0001g0224 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.565+1172A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56016970 | ||||||
| chr19:56017012
|
T | A | 1 | a0041c0109t0001g0345 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.565+1214T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017012 | ||||||
| chr19:56017030
|
G | A | 14 | a0001c0092t0001g0211a0002c0127t0002g0306a0003c0008t0001g0309others(11): Show | 14 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.565+1232G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017030 | ||||||
| chr19:56017093
|
C | T | 3 | a0005c0034t0001g0338a0005c0083t0001g0121a0009c0013t0001g0147 | 3 | NA18955.hp1 NA18998.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.565+1295C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017093 | ||||||
| chr19:56017097
|
G | A | 9 | a0001c0092t0001g0211a0002c0127t0002g0306a0003c0076t0002g0250others(6): Show | 9 | HG01109.hp1 HG01891.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+1299G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017097 | ||||||
| chr19:56017098
|
C | T | 9 | a0001c0092t0001g0211a0002c0127t0002g0306a0003c0076t0002g0250others(6): Show | 9 | HG01109.hp1 HG01891.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+1300C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017098 | ||||||
| chr19:56017103
|
G | A | 9 | a0001c0092t0001g0211a0002c0127t0002g0306a0003c0076t0002g0250others(6): Show | 9 | HG01109.hp1 HG01891.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.565+1305G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017103 | ||||||
| chr19:56017161
|
C | T | 2 | a0007c0110t0001g0349a0041c0109t0001g0345 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.565+1363C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017161 | ||||||
| chr19:56017225
|
T | C | 14 | a0001c0092t0001g0211a0002c0127t0002g0306a0003c0008t0001g0309others(11): Show | 14 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.565+1427T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017225 | ||||||
| chr19:56017338
|
ACTAAC | A | 6 | a0002c0127t0002g0306a0003c0008t0001g0309a0003c0008t0001g0310others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+1542_565+1546d others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 56017338 | |||||
| chr19:56017347
|
A | C | 6 | a0002c0127t0002g0306a0003c0008t0001g0309a0003c0008t0001g0310others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+1549A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017347 | ||||||
| chr19:56017380
|
GTTATA | G | 128 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(125): Show | 128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.565+1590_565+1594d others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 56017380 | |||||
| chr19:56017465
|
T | C | 6 | a0002c0127t0002g0306a0003c0008t0001g0309a0003c0008t0001g0310others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+1667T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017465 | ||||||
| chr19:56017477
|
T | A | 1 | a0001c0003t0001g0161 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.565+1679T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017477 | ||||||
| chr19:56017527
|
G | A | 10 | a0002c0127t0002g0306a0003c0008t0001g0309a0003c0008t0001g0310others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+1729G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017527 | ||||||
| chr19:56017565
|
A | G | 6 | a0002c0127t0002g0306a0003c0008t0001g0309a0003c0008t0001g0310others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.565+1767A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017565 | ||||||
| chr19:56017598
|
T | C | 1 | a0012c0106t0002g0371 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.566-1744T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017598 | ||||||
| chr19:56017643
|
T | C | 10 | a0002c0127t0002g0306a0003c0008t0001g0309a0003c0008t0001g0310others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-1699T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017643 | ||||||
| chr19:56017671
|
G | A | 10 | a0002c0127t0002g0306a0003c0008t0001g0309a0003c0008t0001g0310others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-1671G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017671 | ||||||
| chr19:56017677
|
A | G | 1 | a0033c0061t0001g0256 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.566-1665A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017677 | ||||||
| chr19:56017772
|
G | A | 6 | a0002c0127t0002g0306a0003c0008t0001g0309a0003c0008t0001g0310others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-1570G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017772 | ||||||
| chr19:56017790
|
G | A | 10 | a0002c0127t0002g0306a0003c0008t0001g0309a0003c0008t0001g0310others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-1552G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017790 | ||||||
| chr19:56017808
|
C | G | 4 | a0001c0022t0001g0356a0001c0046t0001g0261a0001c0046t0001g0262others(1): Show | 4 | HG01255.hp2 HG01261.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-1534C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017808 | ||||||
| chr19:56017832
|
G | A | 2 | a0002c0079t0002g0089a0003c0045t0001g0090 | 2 | HG01109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.566-1510G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017832 | ||||||
| chr19:56017868
|
C | T | 1 | a0026c0059t0001g0060 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.566-1474C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017868 | ||||||
| chr19:56017939
|
T | G | 10 | a0002c0127t0002g0306a0003c0008t0001g0309a0003c0008t0001g0310others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.566-1403T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017939 | ||||||
| chr19:56017955
|
T | A | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-1387T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017955 | ||||||
| chr19:56017975
|
A | T | 238 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(235): Show | 238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.566-1367A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56017975 | ||||||
| chr19:56018020
|
T | G | 1 | a0001c0030t0001g0318 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.566-1322T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018020 | ||||||
| chr19:56018027
|
C | A | 2 | a0008c0037t0001g0004a0008c0037t0001g0009 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.566-1315C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018027 | ||||||
| chr19:56018082
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.566-1260G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018082 | ||||||
| chr19:56018165
|
C | T | 108 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(105): Show | 108 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.566-1177C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018165 | ||||||
| chr19:56018193
|
C | T | 4 | a0016c0097t0001g0107a0016c0129t0001g0100a0016c0130t0003g0316others(1): Show | 4 | HG02809.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.566-1149C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018193 | ||||||
| chr19:56018304
|
G | A | 19 | a0003c0040t0001g0165a0003c0040t0001g0177a0008c0017t0001g0103others(16): Show | 19 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.566-1038G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018304 | ||||||
| chr19:56018347
|
C | T | 1 | a0030c0098t0001g0354 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.566-995C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018347 | ||||||
| chr19:56018386
|
G | C | 3 | a0005c0034t0001g0338a0005c0083t0001g0121a0009c0013t0001g0147 | 3 | NA18955.hp1 NA18998.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.566-956G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018386 | ||||||
| chr19:56018435
|
C | T | 4 | a0016c0097t0001g0107a0016c0129t0001g0100a0016c0130t0003g0316others(1): Show | 4 | HG02809.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.566-907C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018435 | ||||||
| chr19:56018482
|
C | A | 4 | a0016c0097t0001g0107a0016c0129t0001g0100a0016c0130t0003g0316others(1): Show | 4 | HG02809.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.566-860C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018482 | ||||||
| chr19:56018639
|
A | G | 6 | a0001c0001t0001g0353a0003c0008t0003g0381a0005c0029t0001g0015others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-703A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018639 | ||||||
| chr19:56018830
|
A | C | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-512A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018830 | ||||||
| chr19:56018839
|
T | A | 6 | a0001c0092t0001g0211a0002c0127t0002g0306a0003c0076t0002g0250others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-503T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018839 | ||||||
| chr19:56018941
|
G | A | 4 | a0016c0097t0001g0107a0016c0129t0001g0100a0016c0130t0003g0316others(1): Show | 4 | HG02809.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.566-401G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018941 | ||||||
| chr19:56018983
|
A | C | 6 | a0001c0001t0001g0353a0003c0008t0003g0381a0005c0029t0001g0015others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.566-359A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018983 | ||||||
| chr19:56018993
|
A | C | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-349A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56018993 | ||||||
| chr19:56019029
|
C | CT | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-312dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 56019029 | |||||
| chr19:56019050
|
C | T | 1 | a0001c0014t0001g0362 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.566-292C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56019050 | ||||||
| chr19:56019124
|
G | T | 1 | a0009c0013t0001g0352 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.566-218G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56019124 | ||||||
| chr19:56019177
|
G | T | 78 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(75): Show | 78 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.566-165G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56019177 | ||||||
| chr19:56019187
|
C | G | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-155C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56019187 | ||||||
| chr19:56019188
|
C | T | 9 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.566-154C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56019188 | ||||||
| chr19:56019298
|
A | G | 89 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(86): Show | 89 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.566-44A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 4/14 | chr19 | 56019298 | ||||||
| chr19:56019491
|
T | C | 1 | a0001c0009t0001g0335 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.622+93T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019491 | ||||||
| chr19:56019506
|
C | T | 1 | a0013c0026t0002g0143 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.622+108C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019506 | ||||||
| chr19:56019508
|
T | A | 4 | a0016c0097t0001g0107a0016c0129t0001g0100a0016c0130t0003g0316others(1): Show | 4 | HG02809.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+110T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019508 | ||||||
| chr19:56019508
|
T | TTCTCATT others(1029): Show |
1 | a0001c0003t0001g0145 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.623-42_623-41insAA others(1034): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56019508 | |||||
| chr19:56019588
|
G | A | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.622+190G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019588 | ||||||
| chr19:56019664
|
C | A | 3 | a0005c0034t0001g0338a0005c0083t0001g0121a0009c0013t0001g0147 | 3 | NA18955.hp1 NA18998.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.622+266C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019664 | ||||||
| chr19:56019711
|
G | T | 4 | a0016c0097t0001g0107a0016c0129t0001g0100a0016c0130t0003g0316others(1): Show | 4 | HG02809.hp2 HG03130.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+313G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019711 | ||||||
| chr19:56019729
|
C | T | 3 | a0001c0001t0001g0207a0003c0051t0001g0252a0007c0032t0001g0254 | 3 | HG02040.hp2 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.622+331C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019729 | ||||||
| chr19:56019836
|
A | G | 8 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.622+438A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019836 | ||||||
| chr19:56019841
|
A | AT | 97 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(94): Show | 97 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.622+456dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56019841 | |||||
| chr19:56019841
|
AT | A | 6 | a0001c0003t0001g0260a0001c0009t0001g0341a0005c0006t0001g0113others(3): Show | 6 | HG04115.hp1 NA18946.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.622+456delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56019841 | |||||
| chr19:56019867
|
C | T | 13 | a0001c0019t0001g0065a0001c0019t0001g0066a0001c0042t0001g0021others(10): Show | 13 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.622+469C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019867 | ||||||
| chr19:56019897
|
C | T | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.623-478C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019897 | ||||||
| chr19:56019900
|
G | T | 1 | a0028c0093t0001g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.623-475G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019900 | ||||||
| chr19:56019906
|
A | G | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-469A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019906 | ||||||
| chr19:56019940
|
G | A | 1 | a0005c0029t0001g0085 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.623-435G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019940 | ||||||
| chr19:56019966
|
A | G | 1 | a0032c0062t0001g0080 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.623-409A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56019966 | ||||||
| chr19:56020071
|
G | A | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.623-304G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56020071 | ||||||
| chr19:56020170
|
G | T | 19 | a0003c0040t0001g0165a0003c0040t0001g0177a0008c0017t0001g0103others(16): Show | 19 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.623-205G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56020170 | ||||||
| chr19:56020251
|
G | A | 1 | a0009c0013t0001g0061 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.623-124G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56020251 | ||||||
| chr19:56020259
|
T | C | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.623-116T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56020259 | ||||||
| chr19:56020283
|
T | C | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.623-92T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56020283 | ||||||
| chr19:56020288
|
A | G | 2 | a0008c0028t0001g0394a0008c0028t0001g0395 | 2 | HG02071.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.623-87A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56020288 | ||||||
| chr19:56020334
|
G | A | 13 | a0001c0022t0001g0356a0001c0023t0001g0244a0001c0023t0001g0248others(10): Show | 13 | HG00639.hp1 HG01255.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.623-41G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56020334 | ||||||
| chr19:56020345
|
AC | A | 3 | a0005c0034t0001g0338a0005c0083t0001g0121a0009c0013t0001g0147 | 3 | NA18955.hp1 NA18998.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.623-29delC | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | chr19 | 56020345 | ||||||
| chr19:56020363
|
A | ATTC | 19 | a0003c0040t0001g0165a0003c0040t0001g0177a0008c0017t0001g0103others(16): Show | 19 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.623-9_623-7dupCTT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56020363 | |||||
| chr19:56020547
|
T | A | 2 | a0001c0023t0001g0244a0007c0010t0001g0385 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.679+116T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56020547 | ||||||
| chr19:56020608
|
G | T | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.679+177G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56020608 | ||||||
| chr19:56020718
|
CAT | C | 32 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(29): Show | 32 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.679+290_679+291del others(2): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56020718 | |||||
| chr19:56020744
|
G | T | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.679+313G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56020744 | ||||||
| chr19:56020762
|
T | C | 105 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(102): Show | 105 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.679+331T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56020762 | ||||||
| chr19:56020771
|
T | C | 12 | a0001c0001t0001g0353a0001c0023t0001g0314a0003c0008t0003g0381others(9): Show | 12 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.679+340T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56020771 | ||||||
| chr19:56020807
|
A | G | 1 | a0035c0067t0002g0390 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.679+376A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56020807 | ||||||
| chr19:56020874
|
A | AT | 13 | a0001c0002t0001g0042a0001c0002t0001g0087a0001c0002t0001g0158others(10): Show | 13 | HG01109.hp1 HG01255.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.679+460dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56020874 | |||||
| chr19:56020874
|
AT | A | 47 | a0001c0001t0001g0264a0001c0001t0001g0353a0001c0002t0001g0010others(44): Show | 47 | HG00597.hp2 HG01109.hp2 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.679+460delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56020874 | |||||
| chr19:56020874
|
ATT | A | 35 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(32): Show | 35 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.679+459_679+460del others(2): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56020874 | |||||
| chr19:56020923
|
T | G | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG01192.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+492T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56020923 | ||||||
| chr19:56020937
|
T | G | 31 | a0001c0002t0001g0010a0001c0002t0001g0108a0001c0002t0001g0148others(28): Show | 31 | HG00597.hp2 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.679+506T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56020937 | ||||||
| chr19:56020943
|
G | A | 28 | a0001c0002t0001g0010a0001c0002t0001g0108a0001c0002t0001g0148others(25): Show | 28 | HG00597.hp2 HG01175.hp1 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.679+512G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56020943 | ||||||
| chr19:56020996
|
C | T | 1 | a0001c0003t0001g0111 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.679+565C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56020996 | ||||||
| chr19:56020998
|
C | T | 1 | a0006c0005t0002g0288 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.679+567C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56020998 | ||||||
| chr19:56021043
|
T | G | 9 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.679+612T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021043 | ||||||
| chr19:56021105
|
C | T | 1 | a0001c0123t0001g0342 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.679+674C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021105 | ||||||
| chr19:56021211
|
A | G | 3 | a0005c0034t0001g0338a0005c0083t0001g0121a0009c0013t0001g0147 | 3 | NA18955.hp1 NA18998.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.679+780A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021211 | ||||||
| chr19:56021217
|
T | C | 44 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(41): Show | 44 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.679+786T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021217 | ||||||
| chr19:56021286
|
C | T | 1 | a0016c0130t0003g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.679+855C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021286 | ||||||
| chr19:56021401
|
C | T | 9 | a0001c0022t0001g0356a0001c0046t0001g0261a0001c0046t0001g0262others(6): Show | 9 | HG01255.hp2 HG01261.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.679+970C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021401 | ||||||
| chr19:56021428
|
C | T | 19 | a0003c0040t0001g0165a0003c0040t0001g0177a0008c0017t0001g0103others(16): Show | 19 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.679+997C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021428 | ||||||
| chr19:56021541
|
G | T | 5 | a0002c0127t0002g0306a0003c0076t0002g0250a0003c0114t0002g0347others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.679+1110G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021541 | ||||||
| chr19:56021611
|
G | C | 1 | a0003c0126t0001g0012 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.679+1180G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021611 | ||||||
| chr19:56021673
|
T | C | 9 | a0001c0022t0001g0356a0001c0046t0001g0261a0001c0046t0001g0262others(6): Show | 9 | HG01255.hp2 HG01261.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.679+1242T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021673 | ||||||
| chr19:56021691
|
G | T | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.679+1260G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021691 | ||||||
| chr19:56021759
|
A | G | 19 | a0003c0040t0001g0165a0003c0040t0001g0177a0008c0017t0001g0103others(16): Show | 19 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.679+1328A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021759 | ||||||
| chr19:56021838
|
T | C | 1 | a0002c0112t0002g0271 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.679+1407T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021838 | ||||||
| chr19:56021840
|
A | C | 1 | a0002c0004t0002g0183 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.679+1409A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021840 | ||||||
| chr19:56021874
|
A | C | 1 | a0010c0027t0001g0319 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.679+1443A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021874 | ||||||
| chr19:56021983
|
G | A | 2 | a0001c0001t0001g0217a0001c0003t0001g0161 | 2 | NA18939.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.679+1552G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021983 | ||||||
| chr19:56021988
|
A | G | 11 | a0001c0019t0001g0065a0001c0019t0001g0066a0001c0092t0001g0211others(8): Show | 11 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.679+1557A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56021988 | ||||||
| chr19:56022062
|
A | G | 8 | a0001c0023t0001g0244a0001c0023t0001g0248a0001c0023t0001g0249others(5): Show | 8 | HG02109.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.679+1631A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022062 | ||||||
| chr19:56022100
|
G | A | 1 | a0006c0011t0002g0129 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.679+1669G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022100 | ||||||
| chr19:56022185
|
C | T | 2 | a0004c0007t0001g0051a0004c0020t0001g0096 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.679+1754C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022185 | ||||||
| chr19:56022375
|
C | T | 18 | a0001c0019t0001g0065a0001c0019t0001g0066a0001c0092t0001g0211others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.679+1944C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022375 | ||||||
| chr19:56022397
|
G | A | 1 | a0003c0045t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.679+1966G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022397 | ||||||
| chr19:56022406
|
AG | A | 124 | a0001c0001t0001g0253a0001c0001t0001g0353a0001c0001t0001g0386others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.679+1977delG | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56022406 | |||||
| chr19:56022408
|
G | C | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.679+1977G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022408 | ||||||
| chr19:56022409
|
A | C | 124 | a0001c0001t0001g0253a0001c0001t0001g0353a0001c0001t0001g0386others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.679+1978A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022409 | ||||||
| chr19:56022409
|
A | G | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.679+1978A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022409 | ||||||
| chr19:56022473
|
C | T | 110 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(107): Show | 110 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.679+2042C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022473 | ||||||
| chr19:56022511
|
G | A | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.679+2080G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022511 | ||||||
| chr19:56022520
|
C | T | 270 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(267): Show | 270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.679+2089C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022520 | ||||||
| chr19:56022621
|
A | T | 1 | a0002c0041t0002g0358 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.679+2190A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022621 | ||||||
| chr19:56022662
|
T | TC | 8 | a0001c0001t0001g0353a0003c0008t0003g0381a0005c0029t0001g0015others(5): Show | 8 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.679+2232dupC | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56022662 | |||||
| chr19:56022740
|
T | G | 6 | a0001c0001t0001g0091a0001c0009t0001g0277a0006c0005t0002g0369others(3): Show | 6 | NA18945.hp2 NA18948.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+2309T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022740 | ||||||
| chr19:56022811
|
G | A | 7 | a0002c0116t0002g0330a0003c0051t0001g0252a0003c0076t0002g0250others(4): Show | 7 | HG01109.hp1 HG02572.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.679+2380G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022811 | ||||||
| chr19:56022868
|
G | A | 3 | a0001c0023t0001g0248a0001c0023t0001g0249a0001c0023t0001g0314 | 3 | HG02615.hp1 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.679+2437G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022868 | ||||||
| chr19:56022975
|
C | T | 1 | a0001c0068t0001g0008 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.679+2544C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56022975 | ||||||
| chr19:56023003
|
G | A | 1 | a0005c0029t0001g0085 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.679+2572G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023003 | ||||||
| chr19:56023082
|
G | T | 33 | a0001c0002t0001g0320a0001c0019t0001g0065a0001c0019t0001g0066others(30): Show | 33 | HG01192.hp2 HG01884.hp2 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.679+2651G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023082 | ||||||
| chr19:56023128
|
C | T | 1 | a0005c0006t0001g0226 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.679+2697C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023128 | ||||||
| chr19:56023153
|
G | A | 1 | a0003c0008t0001g0245 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.679+2722G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023153 | ||||||
| chr19:56023158
|
G | A | 244 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(241): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.679+2727G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023158 | ||||||
| chr19:56023187
|
G | GGT | 3 | a0003c0076t0002g0250a0003c0114t0002g0347a0007c0021t0001g0348 | 3 | HG01109.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.679+2759_679+2760d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56023187 | |||||
| chr19:56023236
|
T | C | 2 | a0001c0092t0001g0211a0002c0127t0002g0306 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.679+2805T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023236 | ||||||
| chr19:56023308
|
C | T | 11 | a0001c0023t0001g0244a0001c0023t0001g0248a0001c0023t0001g0249others(8): Show | 11 | HG02109.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.679+2877C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023308 | ||||||
| chr19:56023368
|
C | T | 2 | a0004c0050t0001g0328a0004c0050t0001g0329 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.679+2937C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023368 | ||||||
| chr19:56023405
|
C | T | 3 | a0001c0115t0001g0040a0007c0110t0001g0349a0041c0109t0001g0345 | 3 | HG01884.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.679+2974C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023405 | ||||||
| chr19:56023455
|
G | A | 1 | a0001c0002t0001g0077 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.679+3024G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023455 | ||||||
| chr19:56023687
|
C | T | 3 | a0001c0115t0001g0040a0007c0110t0001g0349a0041c0109t0001g0345 | 3 | HG01884.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.680-3226C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023687 | ||||||
| chr19:56023701
|
C | T | 28 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(25): Show | 28 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.680-3212C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023701 | ||||||
| chr19:56023923
|
G | A | 22 | a0001c0022t0001g0356a0001c0046t0001g0261a0001c0046t0001g0262others(19): Show | 22 | HG01255.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.680-2990G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023923 | ||||||
| chr19:56023968
|
G | A | 1 | a0002c0004t0002g0204 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.680-2945G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023968 | ||||||
| chr19:56023997
|
G | A | 22 | a0001c0022t0001g0356a0001c0046t0001g0261a0001c0046t0001g0262others(19): Show | 22 | HG01255.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.680-2916G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56023997 | ||||||
| chr19:56024133
|
T | C | 3 | a0001c0030t0001g0187a0001c0030t0001g0318a0001c0030t0001g0343 | 3 | HG02132.hp2 HG02165.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.680-2780T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024133 | ||||||
| chr19:56024214
|
T | A | 5 | a0008c0028t0001g0394a0008c0028t0001g0395a0008c0028t0001g0396others(2): Show | 5 | HG02071.hp1 NA18747.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.680-2699T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024214 | ||||||
| chr19:56024340
|
T | TA | 22 | a0001c0001t0001g0007a0001c0003t0001g0011a0001c0019t0001g0065others(19): Show | 22 | HG01109.hp2 HG01192.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.680-2557dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024340 | |||||
| chr19:56024340
|
TA | T | 9 | a0001c0001t0001g0353a0001c0014t0001g0048a0001c0014t0001g0206others(6): Show | 9 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.680-2557delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024340 | |||||
| chr19:56024356
|
AG | A | 9 | a0001c0022t0001g0356a0001c0046t0001g0261a0001c0046t0001g0262others(6): Show | 9 | HG01255.hp2 HG01261.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.680-2556delG | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024356 | ||||||
| chr19:56024362
|
A | AAT | 4 | a0001c0023t0001g0244a0001c0046t0001g0261a0001c0046t0001g0262others(1): Show | 4 | HG01255.hp2 HG01261.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-2540_680-2539d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024362 | |||||
| chr19:56024362
|
AAT | A | 5 | a0001c0092t0001g0211a0002c0127t0002g0306a0004c0035t0001g0094others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-2540_680-2539d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024362 | |||||
| chr19:56024369
|
A | G | 210 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.680-2544A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024369 | ||||||
| chr19:56024377
|
G | GTA | 50 | a0001c0002t0001g0320a0001c0115t0001g0040a0002c0079t0002g0089others(47): Show | 50 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.680-2529_680-2528d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024377 | |||||
| chr19:56024402
|
G | A | 44 | a0001c0002t0001g0320a0003c0076t0002g0250a0003c0114t0002g0347others(41): Show | 44 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.680-2511G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024402 | ||||||
| chr19:56024403
|
T | C | 44 | a0001c0002t0001g0320a0003c0076t0002g0250a0003c0114t0002g0347others(41): Show | 44 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.680-2510T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024403 | ||||||
| chr19:56024421
|
T | TG | 106 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(103): Show | 106 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.680-2492_680-2491i others(3): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024421 | ||||||
| chr19:56024424
|
T | C | 5 | a0004c0070t0001g0069a0016c0097t0001g0107a0016c0129t0001g0100others(2): Show | 5 | HG02809.hp2 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-2489T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024424 | ||||||
| chr19:56024428
|
T | C | 2 | a0003c0051t0001g0252a0007c0032t0001g0254 | 2 | HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.680-2485T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024428 | ||||||
| chr19:56024429
|
AC | A | 14 | a0001c0022t0001g0356a0001c0046t0001g0261a0001c0046t0001g0262others(11): Show | 14 | HG01255.hp2 HG01261.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.680-2483delC | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024429 | ||||||
| chr19:56024434
|
TATAC | T | 5 | a0001c0092t0001g0211a0002c0127t0002g0306a0004c0035t0001g0094others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-2475_680-2472d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024434 | |||||
| chr19:56024445
|
T | G | 14 | a0001c0022t0001g0356a0001c0046t0001g0261a0001c0046t0001g0262others(11): Show | 14 | HG01255.hp2 HG01261.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.680-2468T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024445 | ||||||
| chr19:56024454
|
C | T | 27 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.680-2459C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024454 | ||||||
| chr19:56024455
|
G | T | 5 | a0001c0092t0001g0211a0002c0127t0002g0306a0004c0035t0001g0094others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-2458G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024455 | ||||||
| chr19:56024455
|
GTACA | G | 8 | a0001c0001t0001g0353a0003c0008t0003g0381a0005c0029t0001g0015others(5): Show | 8 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.680-2451_680-2448d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024455 | |||||
| chr19:56024480
|
C | T | 8 | a0001c0001t0001g0353a0003c0008t0003g0381a0005c0029t0001g0015others(5): Show | 8 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.680-2433C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024480 | ||||||
| chr19:56024513
|
GTGTATGT others(9): Show |
G | 53 | a0001c0002t0001g0320a0001c0022t0001g0356a0001c0046t0001g0261others(50): Show | 53 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.680-2399_680-2384d others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024513 | ||||||
| chr19:56024514
|
T | C | 263 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.680-2399T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024514 | ||||||
| chr19:56024521
|
A | ATATG | 112 | a0001c0001t0001g0353a0001c0002t0001g0010a0001c0002t0001g0032others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.680-2388_680-2385d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024521 | |||||
| chr19:56024528
|
TAC | T | 114 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.680-2383_680-2382d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024528 | |||||
| chr19:56024529
|
A | G | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2384A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024529 | ||||||
| chr19:56024530
|
C | T | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2383C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024530 | ||||||
| chr19:56024531
|
A | G | 167 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.680-2382A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024531 | ||||||
| chr19:56024535
|
G | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.680-2378G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024535 | ||||||
| chr19:56024536
|
T | C | 114 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(111): Show | 114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.680-2377T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024536 | ||||||
| chr19:56024537
|
A | G | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2376A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024537 | ||||||
| chr19:56024541
|
G | A | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2372G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024541 | ||||||
| chr19:56024551
|
G | A | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2362G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024551 | ||||||
| chr19:56024553
|
G | A | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2360G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024553 | ||||||
| chr19:56024561
|
G | A | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2352G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024561 | ||||||
| chr19:56024562
|
T | C | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2351T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024562 | ||||||
| chr19:56024566
|
T | C | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2347T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024566 | ||||||
| chr19:56024568
|
T | C | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2345T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024568 | ||||||
| chr19:56024573
|
A | G | 8 | a0001c0115t0001g0040a0003c0118t0001g0357a0004c0007t0003g0164others(5): Show | 8 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-2340A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024573 | ||||||
| chr19:56024574
|
T | C | 3 | a0001c0086t0001g0018a0002c0087t0002g0024a0044c0107t0001g0344 | 3 | HG00733.hp2 HG02897.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.680-2339T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024574 | ||||||
| chr19:56024576
|
T | C | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2337T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024576 | ||||||
| chr19:56024578
|
T | C | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2335T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024578 | ||||||
| chr19:56024580
|
T | C | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2333T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024580 | ||||||
| chr19:56024582
|
C | CAT | 5 | a0002c0004t0002g0196a0005c0006t0001g0189a0006c0011t0002g0191others(2): Show | 5 | NA18946.hp2 NA18962.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.680-2329_680-2328d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024582 | |||||
| chr19:56024584
|
T | C | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-2329T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024584 | ||||||
| chr19:56024584
|
T | TAC | 10 | a0001c0002t0001g0082a0001c0092t0001g0211a0002c0012t0002g0057others(7): Show | 10 | HG00140.hp1 HG01109.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.680-2311_680-2310d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024584 | |||||
| chr19:56024584
|
T | TACAC | 29 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(26): Show | 29 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.680-2313_680-2310d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024584 | |||||
| chr19:56024584
|
T | TACACAC | 48 | a0001c0002t0001g0320a0001c0014t0001g0048a0001c0022t0001g0356others(45): Show | 48 | HG01069.hp1 HG01070.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.680-2315_680-2310d others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024584 | |||||
| chr19:56024584
|
T | TACACACA others(1): Show |
3 | a0008c0105t0001g0372a0010c0016t0001g0366a0017c0063t0001g0116 | 3 | HG00423.hp2 NA18986.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.680-2317_680-2310d others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024584 | |||||
| chr19:56024586
|
C | T | 110 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.680-2327C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024586 | ||||||
| chr19:56024684
|
G | A | 1 | a0001c0019t0001g0122 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.680-2229G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024684 | ||||||
| chr19:56024714
|
C | T | 5 | a0001c0092t0001g0211a0002c0127t0002g0306a0004c0035t0001g0094others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-2199C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024714 | ||||||
| chr19:56024757
|
C | CAA | 9 | a0001c0022t0001g0356a0001c0046t0001g0261a0001c0046t0001g0262others(6): Show | 9 | HG01255.hp2 HG01261.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.680-2145_680-2144d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024757 | |||||
| chr19:56024757
|
CA | C | 8 | a0001c0115t0001g0040a0003c0118t0001g0357a0004c0007t0003g0164others(5): Show | 8 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-2144delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56024757 | |||||
| chr19:56024824
|
C | T | 3 | a0001c0042t0001g0021a0001c0042t0001g0377a0004c0007t0001g0307 | 3 | HG02257.hp1 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.680-2089C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024824 | ||||||
| chr19:56024942
|
CAT | C | 14 | a0001c0022t0001g0356a0001c0046t0001g0261a0001c0046t0001g0262others(11): Show | 14 | HG01255.hp2 HG01261.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.680-1970_680-1969d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56024942 | ||||||
| chr19:56025004
|
C | T | 34 | a0001c0001t0001g0091a0001c0009t0001g0277a0001c0009t0001g0286others(31): Show | 34 | HG00673.hp1 HG00673.hp2 HG02027.hp1 others(31): Show |
intron_variant | MODIFIER | c.680-1909C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025004 | ||||||
| chr19:56025050
|
G | GCTT | 317 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.680-1862_680-1860d others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56025050 | |||||
| chr19:56025055
|
T | G | 1 | a0028c0093t0001g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.680-1858T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025055 | ||||||
| chr19:56025152
|
C | G | 1 | a0001c0023t0001g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.680-1761C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025152 | ||||||
| chr19:56025262
|
C | T | 1 | a0006c0011t0002g0191 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.680-1651C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025262 | ||||||
| chr19:56025293
|
C | T | 10 | a0001c0023t0001g0244a0001c0023t0001g0248a0001c0023t0001g0249others(7): Show | 10 | HG02109.hp1 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.680-1620C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025293 | ||||||
| chr19:56025334
|
G | A | 3 | a0001c0002t0001g0082a0002c0012t0002g0057a0010c0016t0001g0294 | 3 | HG00140.hp1 HG01496.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.680-1579G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025334 | ||||||
| chr19:56025386
|
T | TTC | 5 | a0001c0092t0001g0211a0002c0127t0002g0306a0004c0035t0001g0094others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-1509_680-1508d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56025386 | |||||
| chr19:56025386
|
T | TTCTC | 29 | a0003c0076t0002g0250a0003c0114t0002g0347a0007c0021t0001g0348others(26): Show | 29 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.680-1511_680-1508d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56025386 | |||||
| chr19:56025386
|
T | TTCTCTC | 15 | a0010c0016t0001g0292a0010c0016t0001g0324a0010c0016t0001g0364others(12): Show | 15 | HG02040.hp1 HG03239.hp1 HG03669.hp1 others(12): Show |
intron_variant | MODIFIER | c.680-1513_680-1508d others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56025386 | |||||
| chr19:56025386
|
T | TTCTCTCT others(7): Show |
1 | a0018c0036t0002g0034 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.680-1521_680-1508d others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56025386 | |||||
| chr19:56025386
|
T | TTCTCTCT others(9): Show |
4 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-1523_680-1508d others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56025386 | |||||
| chr19:56025386
|
T | TTCTCTCT others(15): Show |
1 | a0039c0078t0001g0313 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.680-1508_680-1507i others(24): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56025386 | |||||
| chr19:56025386
|
T | TTCTCTCT others(17): Show |
1 | a0001c0046t0001g0261 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.680-1508_680-1507i others(26): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56025386 | |||||
| chr19:56025386
|
T | TTCTCTCT others(19): Show |
1 | a0001c0046t0001g0262 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.680-1508_680-1507i others(28): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56025386 | |||||
| chr19:56025386
|
T | TTCTCTCT others(25): Show |
1 | a0003c0045t0001g0266 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.680-1508_680-1507i others(34): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56025386 | |||||
| chr19:56025436
|
C | T | 192 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.680-1477C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025436 | ||||||
| chr19:56025445
|
G | A | 8 | a0001c0115t0001g0040a0003c0118t0001g0357a0004c0007t0003g0164others(5): Show | 8 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-1468G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025445 | ||||||
| chr19:56025472
|
C | A | 1 | a0004c0035t0001g0095 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.680-1441C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025472 | ||||||
| chr19:56025479
|
C | T | 1 | a0023c0057t0004g0360 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.680-1434C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025479 | ||||||
| chr19:56025573
|
C | CT | 312 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.680-1331dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56025573 | |||||
| chr19:56025573
|
CT | C | 7 | a0002c0004t0002g0124a0002c0004t0002g0125a0002c0004t0002g0194others(4): Show | 7 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.680-1331delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56025573 | |||||
| chr19:56025600
|
C | T | 8 | a0001c0115t0001g0040a0003c0118t0001g0357a0004c0007t0003g0164others(5): Show | 8 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-1313C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025600 | ||||||
| chr19:56025601
|
G | A | 1 | a0040c0074t0002g0322 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.680-1312G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025601 | ||||||
| chr19:56025640
|
G | A | 1 | a0002c0012t0002g0031 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.680-1273G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025640 | ||||||
| chr19:56025705
|
C | A | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-1208C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025705 | ||||||
| chr19:56025747
|
G | A | 2 | a0001c0092t0001g0211a0002c0127t0002g0306 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.680-1166G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025747 | ||||||
| chr19:56025803
|
C | G | 37 | a0001c0001t0001g0091a0001c0009t0001g0277a0001c0009t0001g0286others(34): Show | 37 | HG00673.hp1 HG00673.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.680-1110C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025803 | ||||||
| chr19:56025819
|
A | C | 3 | a0003c0076t0002g0250a0003c0114t0002g0347a0007c0021t0001g0348 | 3 | HG01109.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.680-1094A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025819 | ||||||
| chr19:56025852
|
C | T | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.680-1061C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025852 | ||||||
| chr19:56025939
|
G | C | 1 | a0002c0012t0002g0055 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.680-974G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025939 | ||||||
| chr19:56025960
|
A | G | 2 | a0011c0033t0001g0340a0012c0065t0002g0005 | 2 | HG02040.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.680-953A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025960 | ||||||
| chr19:56025972
|
T | C | 2 | a0004c0050t0001g0328a0004c0050t0001g0329 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.680-941T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56025972 | ||||||
| chr19:56026008
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.680-905G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026008 | ||||||
| chr19:56026066
|
C | T | 1 | a0006c0005t0002g0355 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.680-847C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026066 | ||||||
| chr19:56026079
|
T | C | 1 | a0001c0082t0001g0168 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.680-834T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026079 | ||||||
| chr19:56026084
|
A | C | 102 | a0001c0001t0001g0386a0001c0001t0001g0387a0001c0001t0001g0388others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.680-829A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026084 | ||||||
| chr19:56026162
|
A | G | 27 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.680-751A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026162 | ||||||
| chr19:56026196
|
C | T | 5 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(2): Show | 5 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.680-717C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026196 | ||||||
| chr19:56026255
|
G | A | 1 | a0006c0005t0002g0298 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.680-658G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026255 | ||||||
| chr19:56026276
|
C | G | 212 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.680-637C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026276 | ||||||
| chr19:56026463
|
C | G | 395 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(392): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.680-450C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026463 | ||||||
| chr19:56026464
|
G | C | 395 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(392): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.680-449G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026464 | ||||||
| chr19:56026527
|
C | CA | 115 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.680-364dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56026527 | |||||
| chr19:56026527
|
C | CAA | 28 | a0001c0022t0001g0356a0001c0052t0001g0023a0001c0052t0001g0026others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.680-365_680-364dup others(2): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56026527 | |||||
| chr19:56026527
|
C | CAAA | 16 | a0001c0001t0001g0386a0001c0001t0001g0387a0001c0001t0001g0388others(13): Show | 16 | HG00280.hp1 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.680-366_680-364dup others(3): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56026527 | |||||
| chr19:56026527
|
C | CAAAA | 69 | a0001c0002t0001g0010a0001c0002t0001g0032a0001c0002t0001g0041others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.680-367_680-364dup others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56026527 | |||||
| chr19:56026527
|
CA | C | 10 | a0001c0001t0001g0215a0001c0009t0001g0333a0002c0004t0002g0202others(7): Show | 10 | HG01943.hp2 HG01975.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.680-364delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56026527 | |||||
| chr19:56026527
|
CAAAAAA | C | 8 | a0001c0001t0001g0353a0003c0008t0003g0381a0005c0029t0001g0015others(5): Show | 8 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.680-369_680-364del others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56026527 | |||||
| chr19:56026577
|
ATTTATT | A | 5 | a0004c0070t0001g0069a0016c0097t0001g0107a0016c0129t0001g0100others(2): Show | 5 | HG02809.hp2 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-321_680-316del others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | 56026577 | |||||
| chr19:56026603
|
A | G | 314 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(311): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.680-310A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026603 | ||||||
| chr19:56026671
|
C | T | 212 | a0001c0001t0001g0007a0001c0001t0001g0091a0001c0001t0001g0160others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.680-242C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026671 | ||||||
| chr19:56026807
|
C | G | 5 | a0001c0092t0001g0211a0002c0127t0002g0306a0004c0035t0001g0094others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-106C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026807 | ||||||
| chr19:56026837
|
C | A | 317 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.680-76C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 6/14 | chr19 | 56026837 | ||||||
| chr19:56028559
|
C | G | 2 | a0006c0005t0002g0270a0009c0054t0001g0297 | 2 | HG02074.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.2276+50C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56028559 | ||||||
| chr19:56028696
|
G | A | 10 | a0004c0007t0003g0164a0004c0007t0003g0210a0004c0020t0003g0098others(7): Show | 10 | HG02486.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2276+187G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56028696 | ||||||
| chr19:56028849
|
C | G | 3 | a0001c0115t0001g0040a0003c0118t0001g0357a0041c0109t0001g0345 | 3 | HG02559.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2276+340C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56028849 | ||||||
| chr19:56028890
|
G | A | 1 | a0006c0011t0002g0191 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2276+381G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56028890 | ||||||
| chr19:56028974
|
A | G | 117 | a0001c0002t0001g0010a0001c0002t0001g0032a0001c0002t0001g0041others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.2276+465A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56028974 | ||||||
| chr19:56029051
|
A | C | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2276+542A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56029051 | ||||||
| chr19:56029057
|
C | G | 1 | a0017c0063t0001g0116 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2276+548C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56029057 | ||||||
| chr19:56029074
|
G | A | 3 | a0001c0022t0001g0356a0002c0041t0002g0358a0012c0018t0002g0033 | 3 | HG02723.hp1 HG02896.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2276+565G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56029074 | ||||||
| chr19:56029215
|
GGTGA | G | 10 | a0004c0007t0003g0164a0004c0007t0003g0210a0004c0020t0003g0098others(7): Show | 10 | HG02486.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2276+712_2276+715d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56029215 | |||||
| chr19:56029226
|
CTG | C | 69 | a0001c0002t0001g0010a0001c0002t0001g0032a0001c0002t0001g0041others(66): Show | 69 | HG00099.hp1 HG00597.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.2276+720_2276+721d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56029226 | |||||
| chr19:56029370
|
G | A | 1 | a0023c0057t0004g0360 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2276+861G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56029370 | ||||||
| chr19:56029481
|
A | G | 1 | a0004c0007t0003g0210 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2276+972A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56029481 | ||||||
| chr19:56029656
|
C | T | 1 | a0002c0012t0002g0003 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2276+1147C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56029656 | ||||||
| chr19:56029664
|
G | A | 1 | a0001c0015t0001g0106 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2276+1155G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56029664 | ||||||
| chr19:56029778
|
T | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(25): Show | 28 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.2276+1269T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56029778 | ||||||
| chr19:56029898
|
T | C | 1 | a0003c0024t0001g0025 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2276+1389T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56029898 | ||||||
| chr19:56029952
|
C | A | 93 | a0001c0002t0001g0010a0001c0002t0001g0032a0001c0002t0001g0041others(90): Show | 93 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.2276+1443C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56029952 | ||||||
| chr19:56029991
|
G | A | 9 | a0001c0001t0001g0353a0003c0008t0003g0381a0005c0029t0001g0015others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2276+1482G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56029991 | ||||||
| chr19:56030054
|
C | CAAAAAAT others(1): Show |
27 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0049others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.2276+1552_2276+155 others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030054 | |||||
| chr19:56030097
|
C | T | 1 | a0007c0110t0001g0349 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2276+1588C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030097 | ||||||
| chr19:56030212
|
A | T | 1 | a0001c0001t0001g0091 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2276+1703A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030212 | ||||||
| chr19:56030229
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0174 | 2 | HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.2276+1720G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030229 | ||||||
| chr19:56030280
|
G | A | 1 | a0007c0110t0001g0349 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2276+1771G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030280 | ||||||
| chr19:56030296
|
G | A | 35 | a0001c0001t0001g0091a0001c0009t0001g0286a0001c0009t0001g0293others(32): Show | 35 | HG00673.hp1 HG00673.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.2276+1787G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030296 | ||||||
| chr19:56030319
|
A | G | 1 | a0006c0005t0002g0300 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2276+1810A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030319 | ||||||
| chr19:56030378
|
A | G | 2 | a0005c0025t0001g0132a0005c0025t0001g0222 | 2 | NA18954.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2276+1869A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030378 | ||||||
| chr19:56030382
|
T | A | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2276+1873T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030382 | ||||||
| chr19:56030443
|
A | G | 1 | a0041c0109t0001g0345 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2276+1934A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030443 | ||||||
| chr19:56030517
|
G | A | 6 | a0001c0001t0001g0353a0003c0008t0003g0381a0005c0029t0001g0015others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2276+2008G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030517 | ||||||
| chr19:56030526
|
G | T | 21 | a0001c0009t0001g0277a0008c0017t0001g0103a0008c0017t0001g0146others(18): Show | 21 | HG00423.hp2 HG01069.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.2276+2017G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030526 | ||||||
| chr19:56030527
|
C | G | 2 | a0011c0033t0001g0340a0012c0065t0002g0005 | 2 | HG02040.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2276+2018C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030527 | ||||||
| chr19:56030555
|
G | C | 3 | a0006c0005t0002g0298a0006c0005t0002g0299a0006c0011t0002g0129 | 3 | NA18950.hp1 NA18999.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2276+2046G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030555 | ||||||
| chr19:56030560
|
G | T | 2 | a0001c0022t0001g0356a0002c0041t0002g0358 | 2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2276+2051G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030560 | ||||||
| chr19:56030567
|
C | G | 1 | a0001c0086t0001g0018 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2277-2044C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030567 | ||||||
| chr19:56030600
|
G | A | 3 | a0001c0092t0001g0211a0002c0127t0002g0306a0044c0107t0001g0344 | 3 | HG01891.hp1 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2277-2011G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030600 | ||||||
| chr19:56030702
|
C | A | 1 | a0024c0058t0002g0169 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2277-1909C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030702 | ||||||
| chr19:56030711
|
C | CTTTTT | 9 | a0001c0002t0001g0158a0001c0015t0001g0046a0001c0022t0001g0273others(6): Show | 9 | HG00099.hp1 HG01257.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.2277-1898_2277-189 others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030711 | |||||
| chr19:56030711
|
C | CTTTTTT | 53 | a0001c0001t0001g0091a0001c0002t0001g0010a0001c0002t0001g0032others(50): Show | 53 | HG00597.hp2 HG00733.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.2277-1898_2277-189 others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030711 | |||||
| chr19:56030711
|
C | CTTTTTTT | 6 | a0001c0002t0001g0076a0001c0124t0001g0331a0002c0012t0002g0031others(3): Show | 6 | HG01175.hp1 HG01981.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.2277-1898_2277-189 others(11): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030711 | |||||
| chr19:56030711
|
C | CTTTTTTT others(11): Show |
1 | a0001c0009t0001g0293 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2277-1898_2277-189 others(22): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030711 | |||||
| chr19:56030714
|
C | CTTCTTCT others(11): Show |
1 | a0022c0096t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2277-1895_2277-189 others(22): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTCTTTT | 22 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.2277-1895_2277-189 others(11): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTCTTTT others(1): Show |
6 | a0001c0001t0001g0007a0001c0001t0001g0190a0001c0003t0001g0011others(3): Show | 6 | HG01169.hp1 NA18946.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.2277-1895_2277-189 others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTCTTTT others(2): Show |
58 | a0001c0001t0001g0160a0001c0001t0001g0199a0001c0001t0001g0217others(55): Show | 58 | HG00099.hp2 HG00609.hp2 HG01346.hp2 others(55): Show |
intron_variant | MODIFIER | c.2277-1895_2277-189 others(13): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTCTTTT others(3): Show |
7 | a0002c0004t0002g0059a0003c0024t0001g0025a0005c0006t0001g0056others(4): Show | 7 | HG00140.hp2 HG00280.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.2277-1895_2277-189 others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTCTTTT others(4): Show |
3 | a0004c0007t0001g0051a0004c0020t0001g0096a0006c0005t0002g0355 | 3 | HG02976.hp2 HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2277-1895_2277-189 others(15): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTCTTTT others(14): Show |
1 | a0004c0007t0003g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2277-1895_2277-189 others(25): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTCTTTT others(15): Show |
2 | a0004c0007t0003g0210a0030c0098t0001g0354 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2277-1895_2277-189 others(26): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTCTTTT others(16): Show |
2 | a0004c0020t0003g0098a0005c0113t0001g0099 | 2 | HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2277-1895_2277-189 others(27): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(3): Show |
59 | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0001g0203others(56): Show | 59 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.2277-1888_2277-187 others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(4): Show |
17 | a0001c0001t0001g0174a0001c0001t0001g0200a0002c0004t0002g0128others(14): Show | 17 | HG00423.hp1 HG00544.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.2277-1889_2277-187 others(15): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(5): Show |
31 | a0001c0001t0001g0230a0001c0003t0001g0001a0001c0009t0001g0277others(28): Show | 31 | HG00423.hp2 HG01070.hp2 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.2277-1890_2277-187 others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(6): Show |
8 | a0003c0008t0001g0119a0003c0045t0001g0090a0003c0126t0001g0012others(5): Show | 8 | HG02717.hp2 HG02735.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.2277-1891_2277-187 others(17): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(7): Show |
2 | a0011c0038t0001g0006a0018c0036t0002g0035 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2277-1892_2277-187 others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(8): Show |
10 | a0004c0053t0001g0088a0006c0005t0002g0270a0006c0005t0002g0288others(7): Show | 10 | HG01515.hp2 HG01517.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2277-1893_2277-187 others(19): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(9): Show |
17 | a0001c0009t0001g0286a0001c0046t0001g0261a0004c0020t0001g0268others(14): Show | 17 | HG00673.hp2 HG01099.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.2277-1894_2277-187 others(20): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(10): Show |
27 | a0001c0046t0001g0262a0003c0114t0002g0347a0004c0020t0001g0105others(24): Show | 27 | HG00673.hp1 HG01261.hp2 HG02074.hp2 others(24): Show |
intron_variant | MODIFIER | c.2277-1895_2277-187 others(21): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(11): Show |
10 | a0001c0052t0001g0023a0003c0051t0001g0252a0003c0076t0002g0250others(7): Show | 10 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.2277-1896_2277-187 others(22): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(12): Show |
8 | a0002c0079t0002g0089a0003c0008t0003g0381a0003c0051t0001g0020others(5): Show | 8 | HG01109.hp2 HG01243.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.2277-1879_2277-187 others(23): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(13): Show |
6 | a0001c0001t0001g0353a0001c0002t0001g0363a0004c0070t0001g0069others(3): Show | 6 | HG01346.hp1 HG02004.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2277-1879_2277-187 others(24): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(14): Show |
3 | a0003c0008t0001g0312a0009c0013t0001g0351a0016c0097t0001g0107 | 3 | HG02630.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2277-1879_2277-187 others(25): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(15): Show |
2 | a0001c0002t0001g0378a0016c0129t0001g0100 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2277-1879_2277-187 others(26): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(16): Show |
1 | a0001c0115t0001g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2277-1879_2277-187 others(27): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(17): Show |
2 | a0003c0008t0001g0310a0003c0008t0001g0311 | 2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2277-1879_2277-187 others(28): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | CTTTTTTT others(18): Show |
1 | a0003c0008t0001g0309 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2277-1879_2277-187 others(29): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56030714 | |||||
| chr19:56030714
|
C | T | 71 | a0001c0001t0001g0091a0001c0002t0001g0010a0001c0002t0001g0032others(68): Show | 71 | HG00099.hp1 HG00597.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.2277-1897C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030714 | ||||||
| chr19:56030772
|
T | C | 1 | a0010c0027t0001g0170 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2277-1839T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030772 | ||||||
| chr19:56030774
|
G | A | 3 | a0001c0030t0001g0187a0001c0030t0001g0318a0001c0030t0001g0343 | 3 | HG02132.hp2 HG02165.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.2277-1837G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030774 | ||||||
| chr19:56030822
|
C | T | 1 | a0014c0100t0002g0368 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2277-1789C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030822 | ||||||
| chr19:56030831
|
C | T | 2 | a0001c0115t0001g0040a0041c0109t0001g0345 | 2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2277-1780C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030831 | ||||||
| chr19:56030875
|
G | A | 1 | a0006c0005t0002g0298 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2277-1736G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030875 | ||||||
| chr19:56030960
|
T | C | 239 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.2277-1651T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56030960 | ||||||
| chr19:56031067
|
AACGTGGG others(17): Show |
A | 73 | a0001c0001t0001g0091a0001c0001t0001g0386a0001c0001t0001g0387others(70): Show | 73 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.2277-1528_2277-150 others(28): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56031067 | |||||
| chr19:56031137
|
G | A | 1 | a0004c0020t0003g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2277-1474G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56031137 | ||||||
| chr19:56031192
|
G | A | 2 | a0001c0003t0001g0141a0006c0011t0002g0129 | 2 | HG01952.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.2277-1419G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56031192 | ||||||
| chr19:56031252
|
T | A | 1 | a0005c0006t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2277-1359T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56031252 | ||||||
| chr19:56031426
|
T | C | 247 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(244): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.2277-1185T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56031426 | ||||||
| chr19:56031486
|
C | T | 1 | a0003c0122t0001g0276 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2277-1125C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56031486 | ||||||
| chr19:56031627
|
C | CA | 79 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0049others(76): Show | 79 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.2277-965dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56031627 | |||||
| chr19:56031627
|
C | CAA | 7 | a0001c0001t0001g0039a0003c0051t0001g0020a0007c0010t0001g0036others(4): Show | 7 | HG01346.hp1 HG02083.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2277-966_2277-965d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56031627 | |||||
| chr19:56031627
|
CA | C | 179 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0174others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.2277-965delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56031627 | |||||
| chr19:56031711
|
A | G | 31 | a0001c0002t0001g0363a0001c0002t0001g0378a0003c0008t0001g0309others(28): Show | 31 | HG00140.hp1 HG01099.hp1 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.2277-900A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56031711 | ||||||
| chr19:56031758
|
C | T | 2 | a0004c0070t0001g0069a0016c0097t0001g0107 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2277-853C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56031758 | ||||||
| chr19:56031779
|
C | G | 1 | a0001c0014t0001g0206 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2277-832C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56031779 | ||||||
| chr19:56031951
|
T | C | 218 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(215): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.2277-660T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56031951 | ||||||
| chr19:56031955
|
A | G | 33 | a0001c0001t0001g0353a0001c0019t0001g0065a0001c0019t0001g0066others(30): Show | 33 | HG01192.hp2 HG01255.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.2277-656A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56031955 | ||||||
| chr19:56032032
|
C | T | 3 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311 | 3 | HG02109.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2277-579C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032032 | ||||||
| chr19:56032053
|
G | A | 1 | a0007c0073t0001g0218 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2277-558G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032053 | ||||||
| chr19:56032070
|
G | A | 1 | a0001c0014t0001g0120 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2277-541G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032070 | ||||||
| chr19:56032116
|
G | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0174others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.2277-495G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032116 | ||||||
| chr19:56032259
|
C | T | 1 | a0004c0007t0001g0139 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2277-352C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032259 | ||||||
| chr19:56032264
|
G | C | 1 | a0003c0118t0001g0357 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2277-347G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032264 | ||||||
| chr19:56032302
|
G | A | 1 | a0014c0100t0002g0368 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2277-309G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032302 | ||||||
| chr19:56032302
|
G | C | 2 | a0002c0079t0002g0089a0002c0127t0002g0306 | 2 | HG01109.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.2277-309G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032302 | ||||||
| chr19:56032310
|
G | A | 3 | a0001c0092t0001g0211a0003c0076t0002g0250a0003c0114t0002g0347 | 3 | HG01109.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2277-301G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032310 | ||||||
| chr19:56032326
|
C | T | 1 | a0022c0096t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2277-285C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032326 | ||||||
| chr19:56032344
|
C | CA | 74 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(71): Show | 74 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.2277-251dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56032344 | |||||
| chr19:56032344
|
C | CAA | 6 | a0004c0070t0001g0069a0009c0090t0001g0131a0016c0097t0001g0107others(3): Show | 6 | HG02145.hp1 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2277-252_2277-251d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56032344 | |||||
| chr19:56032344
|
CA | C | 7 | a0001c0046t0001g0261a0001c0046t0001g0262a0001c0124t0001g0331others(4): Show | 7 | HG01255.hp2 HG01261.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2277-251delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | 56032344 | |||||
| chr19:56032367
|
A | T | 2 | a0010c0016t0001g0324a0010c0016t0001g0366 | 2 | NA18988.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2277-244A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032367 | ||||||
| chr19:56032444
|
C | A | 83 | a0001c0001t0001g0007a0001c0001t0001g0353a0001c0003t0001g0011others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.2277-167C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032444 | ||||||
| chr19:56032528
|
G | A | 2 | a0001c0002t0001g0148a0001c0002t0001g0151 | 2 | HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2277-83G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 7/14 | chr19 | 56032528 | ||||||
| chr19:56032793
|
C | T | 2 | a0002c0079t0002g0089a0002c0127t0002g0306 | 2 | HG01109.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.2447+12C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/14 | chr19 | 56032793 | ||||||
| chr19:56032811
|
C | T | 14 | a0004c0007t0001g0051a0004c0007t0001g0307a0004c0020t0001g0096others(11): Show | 14 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.2447+30C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/14 | chr19 | 56032811 | ||||||
| chr19:56032819
|
A | G | 1 | a0041c0109t0001g0345 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2447+38A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/14 | chr19 | 56032819 | ||||||
| chr19:56032824
|
G | A | 1 | a0006c0011t0002g0225 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2447+43G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/14 | chr19 | 56032824 | ||||||
| chr19:56033012
|
G | A | 29 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(26): Show | 29 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.2447+231G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/14 | chr19 | 56033012 | ||||||
| chr19:56033243
|
T | G | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2448-299T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/14 | chr19 | 56033243 | ||||||
| chr19:56033261
|
CA | C | 6 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2448-272delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | 56033261 | |||||
| chr19:56033318
|
C | T | 1 | a0010c0016t0001g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2448-224C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/14 | chr19 | 56033318 | ||||||
| chr19:56033444
|
G | C | 1 | a0041c0109t0001g0345 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2448-98G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/14 | chr19 | 56033444 | ||||||
| chr19:56033508
|
C | T | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2448-34C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 8/14 | chr19 | 56033508 | ||||||
| chr19:56033770
|
T | A | 2 | a0003c0076t0002g0250a0003c0114t0002g0347 | 2 | HG01109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2615+61T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56033770 | ||||||
| chr19:56033785
|
A | G | 7 | a0004c0070t0001g0069a0009c0090t0001g0131a0016c0097t0001g0107others(4): Show | 7 | HG02145.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2615+76A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56033785 | ||||||
| chr19:56033918
|
T | G | 54 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(51): Show | 54 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.2615+209T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56033918 | ||||||
| chr19:56033919
|
A | T | 6 | a0004c0007t0003g0164a0004c0007t0003g0210a0004c0020t0003g0098others(3): Show | 6 | HG02486.hp1 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2615+210A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56033919 | ||||||
| chr19:56033966
|
C | T | 3 | a0004c0020t0001g0285a0006c0011t0002g0109a0009c0013t0001g0147 | 3 | HG02015.hp2 NA18955.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.2615+257C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56033966 | ||||||
| chr19:56034001
|
C | A | 16 | a0001c0115t0001g0040a0003c0118t0001g0357a0004c0007t0003g0164others(13): Show | 16 | HG02486.hp1 HG02559.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.2615+292C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034001 | ||||||
| chr19:56034040
|
G | A | 6 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2615+331G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034040 | ||||||
| chr19:56034049
|
C | T | 8 | a0001c0014t0001g0048a0001c0014t0001g0120a0001c0014t0001g0206others(5): Show | 8 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.2615+340C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034049 | ||||||
| chr19:56034100
|
C | T | 5 | a0004c0070t0001g0069a0009c0090t0001g0131a0016c0097t0001g0107others(2): Show | 5 | HG02145.hp1 HG03195.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2615+391C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034100 | ||||||
| chr19:56034127
|
G | A | 2 | a0018c0036t0002g0034a0018c0036t0002g0035 | 2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2615+418G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034127 | ||||||
| chr19:56034234
|
C | G | 7 | a0004c0070t0001g0069a0009c0090t0001g0131a0016c0097t0001g0107others(4): Show | 7 | HG02145.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2615+525C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034234 | ||||||
| chr19:56034247
|
G | A | 3 | a0001c0046t0001g0261a0001c0046t0001g0262a0003c0045t0001g0266 | 3 | HG01255.hp2 HG01261.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2615+538G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034247 | ||||||
| chr19:56034257
|
C | G | 38 | a0001c0115t0001g0040a0004c0007t0001g0149a0004c0007t0003g0164others(35): Show | 38 | HG01884.hp1 HG02015.hp2 HG02145.hp1 others(35): Show |
intron_variant | MODIFIER | c.2615+548C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034257 | ||||||
| chr19:56034281
|
G | A | 2 | a0011c0039t0001g0092a0011c0039t0001g0093 | 2 | HG02015.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2615+572G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034281 | ||||||
| chr19:56034341
|
G | A | 23 | a0001c0001t0001g0353a0001c0019t0001g0065a0001c0019t0001g0066others(20): Show | 23 | HG01109.hp1 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.2615+632G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034341 | ||||||
| chr19:56034370
|
G | A | 1 | a0001c0092t0001g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2615+661G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034370 | ||||||
| chr19:56034372
|
G | A | 145 | a0001c0001t0001g0007a0001c0001t0001g0201a0001c0001t0001g0217others(142): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.2615+663G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034372 | ||||||
| chr19:56034455
|
A | G | 53 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(50): Show | 53 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2615+746A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034455 | ||||||
| chr19:56034552
|
C | T | 8 | a0001c0001t0001g0190a0001c0002t0001g0054a0001c0052t0001g0026others(5): Show | 8 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.2615+843C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034552 | ||||||
| chr19:56034598
|
G | C | 281 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0049others(278): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.2615+889G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034598 | ||||||
| chr19:56034625
|
T | C | 1 | a0007c0073t0001g0218 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2615+916T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034625 | ||||||
| chr19:56034633
|
T | C | 1 | a0041c0109t0001g0345 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2615+924T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034633 | ||||||
| chr19:56034663
|
G | A | 18 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(15): Show | 18 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.2615+954G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034663 | ||||||
| chr19:56034675
|
C | T | 6 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2615+966C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034675 | ||||||
| chr19:56034679
|
G | A | 8 | a0002c0012t0002g0223a0002c0012t0002g0240a0005c0025t0001g0132others(5): Show | 8 | HG02523.hp2 HG02735.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.2615+970G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034679 | ||||||
| chr19:56034685
|
A | G | 40 | a0001c0019t0001g0118a0001c0019t0001g0122a0001c0115t0001g0040others(37): Show | 40 | HG01884.hp1 HG01884.hp2 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.2615+976A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034685 | ||||||
| chr19:56034731
|
G | A | 145 | a0001c0001t0001g0007a0001c0001t0001g0201a0001c0001t0001g0217others(142): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.2615+1022G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034731 | ||||||
| chr19:56034758
|
G | C | 7 | a0004c0070t0001g0069a0009c0090t0001g0131a0016c0097t0001g0107others(4): Show | 7 | HG02145.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2615+1049G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034758 | ||||||
| chr19:56034759
|
A | G | 7 | a0004c0070t0001g0069a0009c0090t0001g0131a0016c0097t0001g0107others(4): Show | 7 | HG02145.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2615+1050A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034759 | ||||||
| chr19:56034762
|
A | T | 7 | a0004c0070t0001g0069a0009c0090t0001g0131a0016c0097t0001g0107others(4): Show | 7 | HG02145.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2615+1053A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034762 | ||||||
| chr19:56034817
|
CGTTG | C | 145 | a0001c0001t0001g0007a0001c0001t0001g0201a0001c0001t0001g0217others(142): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.2615+1127_2615+113 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56034817 | |||||
| chr19:56034840
|
C | T | 7 | a0004c0070t0001g0069a0009c0090t0001g0131a0016c0097t0001g0107others(4): Show | 7 | HG02145.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2615+1131C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56034840 | ||||||
| chr19:56035071
|
TGG | T | 7 | a0004c0070t0001g0069a0009c0090t0001g0131a0016c0097t0001g0107others(4): Show | 7 | HG02145.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2615+1364_2615+136 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56035071 | |||||
| chr19:56035130
|
G | T | 1 | a0041c0109t0001g0345 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2615+1421G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56035130 | ||||||
| chr19:56035221
|
A | AC | 10 | a0004c0007t0001g0149a0004c0020t0001g0285a0006c0011t0002g0109others(7): Show | 10 | HG02015.hp2 NA18940.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.2615+1513dupC | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56035221 | |||||
| chr19:56035400
|
G | A | 10 | a0001c0046t0001g0261a0001c0046t0001g0262a0003c0045t0001g0266others(7): Show | 10 | HG01243.hp2 HG01255.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.2615+1691G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56035400 | ||||||
| chr19:56035567
|
G | A | 2 | a0031c0101t0001g0346a0045c0131t0001g0315 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2615+1858G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56035567 | ||||||
| chr19:56035675
|
C | T | 1 | a0016c0130t0003g0316 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2615+1966C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56035675 | ||||||
| chr19:56035821
|
T | C | 11 | a0004c0007t0001g0149a0004c0020t0001g0285a0004c0055t0001g0301others(8): Show | 11 | HG02015.hp2 NA18940.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.2615+2112T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56035821 | ||||||
| chr19:56035848
|
A | G | 2 | a0003c0076t0002g0250a0003c0114t0002g0347 | 2 | HG01109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2615+2139A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56035848 | ||||||
| chr19:56035873
|
C | T | 2 | a0001c0022t0001g0273a0001c0022t0001g0274 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2616-2152C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56035873 | ||||||
| chr19:56035945
|
G | A | 1 | a0010c0027t0001g0319 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2616-2080G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56035945 | ||||||
| chr19:56036018
|
C | T | 7 | a0001c0001t0001g0027a0001c0001t0001g0174a0001c0002t0001g0041others(4): Show | 7 | HG01099.hp2 HG01106.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.2616-2007C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036018 | ||||||
| chr19:56036058
|
C | CT | 27 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0137others(24): Show | 27 | HG00639.hp2 HG00738.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.2616-1945dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTT | 27 | a0002c0079t0002g0089a0003c0008t0001g0309a0003c0008t0001g0310others(24): Show | 27 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.2616-1946_2616-194 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTT | 62 | a0001c0001t0001g0007a0001c0003t0001g0011a0001c0003t0001g0112others(59): Show | 62 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.2616-1947_2616-194 others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTT | 66 | a0001c0001t0001g0160a0001c0001t0001g0217a0001c0003t0001g0001others(63): Show | 66 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.2616-1948_2616-194 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTT | 25 | a0001c0003t0001g0111a0001c0003t0001g0140a0001c0003t0001g0258others(22): Show | 25 | HG01123.hp2 HG01516.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.2616-1949_2616-194 others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(3): Show |
3 | a0004c0007t0003g0210a0004c0020t0003g0098a0009c0013t0001g0062 | 3 | HG02486.hp1 HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2616-1954_2616-194 others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(4): Show |
5 | a0001c0115t0001g0040a0004c0070t0001g0069a0009c0013t0001g0061others(2): Show | 5 | HG02717.hp1 HG03195.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2616-1955_2616-194 others(15): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(5): Show |
2 | a0016c0097t0001g0107a0016c0130t0003g0316 | 2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2616-1956_2616-194 others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(8): Show |
1 | a0036c0088t0001g0016 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2616-1959_2616-194 others(19): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(9): Show |
2 | a0004c0050t0001g0328a0004c0125t0001g0013 | 2 | HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2616-1960_2616-194 others(20): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(10): Show |
6 | a0004c0007t0001g0307a0004c0020t0001g0096a0004c0050t0001g0329others(3): Show | 6 | HG01243.hp2 HG01346.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.2616-1961_2616-194 others(21): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(11): Show |
1 | a0004c0007t0001g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2616-1962_2616-194 others(22): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(12): Show |
4 | a0004c0035t0001g0095a0004c0035t0001g0097a0004c0053t0001g0088others(1): Show | 4 | HG02145.hp1 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2616-1963_2616-194 others(23): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(13): Show |
1 | a0004c0035t0001g0094 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2616-1964_2616-194 others(24): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(14): Show |
1 | a0003c0118t0001g0357 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2616-1965_2616-194 others(25): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(475): Show |
1 | a0039c0078t0001g0313 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2616-1945_2616-194 others(486): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(476): Show |
2 | a0003c0008t0001g0311a0003c0008t0001g0312 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2616-1945_2616-194 others(487): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
C | CTTTTTTT others(477): Show |
2 | a0001c0002t0001g0363a0001c0002t0001g0378 | 2 | HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2616-1945_2616-194 others(488): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036058
|
CTTTTTTT others(4): Show |
C | 1 | a0007c0021t0001g0305 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2616-1955_2616-194 others(15): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036058 | |||||
| chr19:56036213
|
G | A | 4 | a0001c0001t0001g0230a0003c0008t0001g0119a0003c0008t0001g0265others(1): Show | 4 | HG03654.hp2 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.2616-1812G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036213 | ||||||
| chr19:56036220
|
C | T | 80 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(77): Show | 80 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.2616-1805C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036220 | ||||||
| chr19:56036229
|
AATTTTTT others(3): Show |
A | 2 | a0031c0101t0001g0346a0045c0131t0001g0315 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2616-1787_2616-177 others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036229 | |||||
| chr19:56036246
|
T | A | 2 | a0003c0051t0001g0252a0007c0021t0001g0348 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2616-1779T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036246 | ||||||
| chr19:56036252
|
A | G | 4 | a0004c0070t0001g0069a0009c0090t0001g0131a0016c0097t0001g0107others(1): Show | 4 | HG03195.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2616-1773A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036252 | ||||||
| chr19:56036270
|
G | T | 2 | a0031c0101t0001g0346a0045c0131t0001g0315 | 2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2616-1755G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036270 | ||||||
| chr19:56036323
|
T | C | 1 | a0003c0008t0001g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2616-1702T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036323 | ||||||
| chr19:56036366
|
T | C | 260 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0049others(257): Show | 260 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.2616-1659T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036366 | ||||||
| chr19:56036432
|
G | A | 1 | a0001c0115t0001g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2616-1593G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036432 | ||||||
| chr19:56036464
|
T | C | 11 | a0004c0007t0001g0149a0004c0020t0001g0285a0004c0055t0001g0301others(8): Show | 11 | HG02015.hp2 NA18940.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.2616-1561T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036464 | ||||||
| chr19:56036472
|
C | T | 3 | a0001c0046t0001g0261a0001c0046t0001g0262a0003c0045t0001g0266 | 3 | HG01255.hp2 HG01261.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2616-1553C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036472 | ||||||
| chr19:56036537
|
G | A | 5 | a0001c0003t0001g0075a0001c0009t0001g0283a0001c0009t0001g0333others(2): Show | 5 | HG01928.hp1 HG01943.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.2616-1488G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036537 | ||||||
| chr19:56036551
|
C | T | 3 | a0001c0001t0001g0264a0001c0022t0001g0273a0001c0022t0001g0274 | 3 | HG01257.hp2 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.2616-1474C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036551 | ||||||
| chr19:56036611
|
C | T | 7 | a0004c0007t0001g0051a0004c0020t0001g0096a0004c0035t0001g0094others(4): Show | 7 | HG02572.hp2 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2616-1414C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036611 | ||||||
| chr19:56036649
|
A | G | 31 | a0001c0001t0001g0091a0001c0001t0001g0200a0001c0001t0001g0203others(28): Show | 31 | HG00597.hp2 HG00738.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.2616-1376A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036649 | ||||||
| chr19:56036725
|
G | T | 158 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0049others(155): Show | 158 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.2616-1300G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036725 | ||||||
| chr19:56036754
|
C | T | 3 | a0001c0046t0001g0261a0001c0046t0001g0262a0003c0045t0001g0266 | 3 | HG01255.hp2 HG01261.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2616-1271C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036754 | ||||||
| chr19:56036755
|
A | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0049others(251): Show | 254 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.2616-1270A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036755 | ||||||
| chr19:56036782
|
C | G | 14 | a0004c0007t0001g0051a0004c0007t0001g0307a0004c0020t0001g0096others(11): Show | 14 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.2616-1243C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036782 | ||||||
| chr19:56036821
|
A | G | 14 | a0004c0007t0003g0164a0004c0007t0003g0210a0004c0020t0003g0098others(11): Show | 14 | HG02486.hp1 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.2616-1204A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036821 | ||||||
| chr19:56036888
|
CAG | C | 4 | a0002c0079t0002g0089a0002c0127t0002g0306a0003c0045t0001g0090others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2616-1134_2616-113 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56036888 | |||||
| chr19:56036928
|
G | A | 2 | a0008c0028t0001g0394a0008c0028t0001g0395 | 2 | HG02071.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2616-1097G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036928 | ||||||
| chr19:56036991
|
A | G | 3 | a0007c0010t0001g0321a0014c0064t0002g0392a0040c0074t0002g0322 | 3 | NA18945.hp2 NA18952.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2616-1034A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56036991 | ||||||
| chr19:56037009
|
T | C | 215 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0049others(212): Show | 215 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.2616-1016T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037009 | ||||||
| chr19:56037015
|
C | T | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2616-1010C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037015 | ||||||
| chr19:56037026
|
C | T | 159 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0049others(156): Show | 159 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.2616-999C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037026 | ||||||
| chr19:56037027
|
G | A | 2 | a0002c0079t0002g0089a0002c0127t0002g0306 | 2 | HG01109.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.2616-998G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037027 | ||||||
| chr19:56037131
|
C | T | 4 | a0001c0001t0001g0230a0003c0008t0001g0119a0003c0008t0001g0265others(1): Show | 4 | HG03654.hp2 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.2616-894C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037131 | ||||||
| chr19:56037205
|
C | G | 1 | a0001c0042t0001g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2616-820C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037205 | ||||||
| chr19:56037241
|
C | T | 2 | a0003c0024t0001g0239a0003c0122t0001g0276 | 2 | HG02027.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2616-784C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037241 | ||||||
| chr19:56037298
|
C | A | 3 | a0009c0013t0001g0350a0009c0013t0001g0351a0009c0013t0001g0352 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2616-727C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037298 | ||||||
| chr19:56037298
|
C | T | 1 | a0031c0101t0001g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2616-727C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037298 | ||||||
| chr19:56037404
|
G | A | 29 | a0004c0007t0001g0197a0004c0020t0001g0268a0004c0020t0001g0285others(26): Show | 29 | HG00673.hp1 HG02015.hp2 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.2616-621G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037404 | ||||||
| chr19:56037424
|
A | G | 1 | a0011c0038t0001g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2616-601A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037424 | ||||||
| chr19:56037433
|
T | C | 34 | a0001c0002t0001g0363a0001c0002t0001g0378a0003c0008t0001g0309others(31): Show | 34 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.2616-592T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037433 | ||||||
| chr19:56037522
|
G | A | 4 | a0002c0079t0002g0089a0002c0127t0002g0306a0003c0045t0001g0090others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2616-503G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037522 | ||||||
| chr19:56037650
|
G | A | 1 | a0003c0118t0001g0357 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2616-375G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037650 | ||||||
| chr19:56037693
|
C | CA | 10 | a0001c0001t0001g0199a0001c0022t0001g0267a0006c0005t0002g0270others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.2616-311dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56037693 | |||||
| chr19:56037693
|
CA | C | 185 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0049others(182): Show | 185 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.2616-311delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56037693 | |||||
| chr19:56037693
|
CAA | C | 22 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.2616-312_2616-311d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56037693 | |||||
| chr19:56037693
|
CAAAAAAA others(3): Show |
C | 1 | a0007c0073t0001g0218 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2616-320_2616-311d others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56037693 | |||||
| chr19:56037714
|
A | AAAAAAAG | 22 | a0001c0002t0001g0363a0001c0002t0001g0378a0003c0008t0001g0309others(19): Show | 22 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.2616-311_2616-310i others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037714 | ||||||
| chr19:56037714
|
A | AG | 4 | a0004c0070t0001g0069a0009c0090t0001g0131a0016c0097t0001g0107others(1): Show | 4 | HG03195.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2616-311_2616-310i others(3): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037714 | ||||||
| chr19:56037714
|
A | C | 17 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0134others(14): Show | 17 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.2616-311A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037714 | ||||||
| chr19:56037720
|
G | C | 1 | a0030c0098t0001g0354 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2616-305G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037720 | ||||||
| chr19:56037830
|
A | AGTAGGAA others(117): Show |
1 | a0001c0022t0001g0289 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2616-195_2616-194i others(126): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037830 | ||||||
| chr19:56037920
|
C | T | 1 | a0001c0115t0001g0040 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2616-105C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037920 | ||||||
| chr19:56037929
|
G | A | 6 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2616-96G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56037929 | ||||||
| chr19:56038001
|
G | A | 3 | a0007c0010t0001g0391a0007c0032t0001g0254a0042c0069t0001g0365 | 3 | HG02145.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2616-24G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 9/14 | chr19 | 56038001 | ||||||
| chr19:56038209
|
C | T | 1 | a0012c0018t0002g0152 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2786+14C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038209 | ||||||
| chr19:56038211
|
T | C | 1 | a0012c0018t0002g0152 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2786+16T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038211 | ||||||
| chr19:56038212
|
T | A | 1 | a0012c0018t0002g0152 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2786+17T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038212 | ||||||
| chr19:56038213
|
T | C | 1 | a0012c0018t0002g0152 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2786+18T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038213 | ||||||
| chr19:56038214
|
C | T | 1 | a0012c0018t0002g0152 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2786+19C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038214 | ||||||
| chr19:56038417
|
G | A | 1 | a0001c0002t0001g0043 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2786+222G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038417 | ||||||
| chr19:56038490
|
G | C | 1 | a0045c0131t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2786+295G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038490 | ||||||
| chr19:56038556
|
T | G | 6 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2786+361T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038556 | ||||||
| chr19:56038577
|
C | T | 19 | a0004c0007t0001g0136a0004c0007t0001g0139a0004c0007t0001g0212others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2786+382C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038577 | ||||||
| chr19:56038753
|
A | T | 38 | a0003c0118t0001g0357a0004c0007t0001g0051a0004c0007t0001g0149others(35): Show | 38 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.2786+558A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038753 | ||||||
| chr19:56038762
|
C | G | 26 | a0002c0079t0002g0089a0002c0127t0002g0306a0003c0045t0001g0090others(23): Show | 26 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.2786+567C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038762 | ||||||
| chr19:56038762
|
C | T | 3 | a0009c0013t0001g0350a0009c0013t0001g0351a0009c0013t0001g0352 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2786+567C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038762 | ||||||
| chr19:56038772
|
C | T | 31 | a0004c0007t0001g0051a0004c0007t0001g0149a0004c0007t0001g0307others(28): Show | 31 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.2786+577C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038772 | ||||||
| chr19:56038868
|
G | A | 38 | a0004c0007t0001g0051a0004c0007t0001g0136a0004c0007t0001g0139others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.2786+673G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038868 | ||||||
| chr19:56038995
|
G | A | 2 | a0028c0093t0001g0269a0041c0109t0001g0345 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2786+800G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56038995 | ||||||
| chr19:56039012
|
C | T | 2 | a0001c0002t0001g0148a0001c0002t0001g0151 | 2 | HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2786+817C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039012 | ||||||
| chr19:56039046
|
C | G | 6 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2786+851C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039046 | ||||||
| chr19:56039136
|
T | TG | 101 | a0002c0079t0002g0089a0002c0127t0002g0306a0003c0045t0001g0090others(98): Show | 101 | HG00140.hp1 HG00280.hp2 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.2786+942dupG | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 56039136 | |||||
| chr19:56039202
|
G | C | 3 | a0009c0013t0001g0350a0009c0013t0001g0351a0009c0013t0001g0352 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2786+1007G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039202 | ||||||
| chr19:56039203
|
G | T | 1 | a0001c0015t0001g0106 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2786+1008G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039203 | ||||||
| chr19:56039214
|
G | A | 3 | a0001c0023t0001g0248a0001c0023t0001g0249a0001c0023t0001g0314 | 3 | HG02615.hp1 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2786+1019G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039214 | ||||||
| chr19:56039359
|
A | C | 1 | a0022c0096t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2786+1164A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039359 | ||||||
| chr19:56039385
|
G | C | 10 | a0004c0007t0003g0164a0004c0007t0003g0210a0004c0020t0003g0098others(7): Show | 10 | HG01243.hp1 HG02486.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2786+1190G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039385 | ||||||
| chr19:56039472
|
C | G | 42 | a0004c0007t0001g0197a0004c0020t0001g0268a0006c0005t0002g0270others(39): Show | 42 | HG00673.hp1 HG01257.hp1 HG02074.hp2 others(39): Show |
intron_variant | MODIFIER | c.2786+1277C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039472 | ||||||
| chr19:56039479
|
C | G | 2 | a0028c0093t0001g0269a0041c0109t0001g0345 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2786+1284C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039479 | ||||||
| chr19:56039546
|
G | A | 15 | a0004c0007t0001g0051a0004c0007t0001g0307a0004c0020t0001g0096others(12): Show | 15 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.2786+1351G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039546 | ||||||
| chr19:56039567
|
C | A | 104 | a0002c0079t0002g0089a0002c0127t0002g0306a0003c0045t0001g0090others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00673.hp1 others(101): Show |
intron_variant | MODIFIER | c.2787-1355C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039567 | ||||||
| chr19:56039568
|
T | C | 3 | a0009c0013t0001g0350a0009c0013t0001g0351a0009c0013t0001g0352 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2787-1354T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039568 | ||||||
| chr19:56039604
|
C | T | 4 | a0001c0046t0001g0261a0001c0046t0001g0262a0001c0084t0001g0053others(1): Show | 4 | HG01255.hp2 HG01261.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.2787-1318C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039604 | ||||||
| chr19:56039650
|
C | T | 1 | a0001c0009t0001g0282 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2787-1272C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039650 | ||||||
| chr19:56039651
|
G | A | 16 | a0004c0007t0001g0051a0004c0007t0001g0307a0004c0007t0001g0325others(13): Show | 16 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.2787-1271G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039651 | ||||||
| chr19:56039659
|
C | T | 20 | a0004c0007t0001g0136a0004c0007t0001g0139a0004c0007t0001g0212others(17): Show | 20 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.2787-1263C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039659 | ||||||
| chr19:56039688
|
G | C | 1 | a0001c0009t0001g0282 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2787-1234G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039688 | ||||||
| chr19:56039736
|
A | T | 2 | a0003c0045t0001g0090a0003c0126t0001g0012 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2787-1186A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039736 | ||||||
| chr19:56039839
|
G | A | 3 | a0002c0004t0002g0124a0002c0004t0002g0125a0002c0004t0002g0204 | 3 | HG00438.hp1 HG00609.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.2787-1083G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039839 | ||||||
| chr19:56039849
|
G | A | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2787-1073G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039849 | ||||||
| chr19:56039850
|
G | C | 1 | a0005c0034t0001g0337 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2787-1072G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039850 | ||||||
| chr19:56039871
|
G | A | 6 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2787-1051G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039871 | ||||||
| chr19:56039903
|
A | T | 1 | a0003c0008t0001g0247 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2787-1019A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039903 | ||||||
| chr19:56039907
|
T | C | 9 | a0004c0007t0003g0164a0004c0007t0003g0210a0004c0020t0003g0098others(6): Show | 9 | HG01243.hp1 HG02486.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2787-1015T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039907 | ||||||
| chr19:56039972
|
T | C | 11 | a0004c0007t0001g0149a0004c0020t0001g0285a0004c0055t0001g0301others(8): Show | 11 | HG02015.hp2 NA18940.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.2787-950T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039972 | ||||||
| chr19:56039974
|
G | C | 1 | a0007c0073t0001g0218 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2787-948G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56039974 | ||||||
| chr19:56040043
|
C | T | 3 | a0009c0013t0001g0350a0009c0013t0001g0351a0009c0013t0001g0352 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2787-879C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040043 | ||||||
| chr19:56040062
|
T | C | 2 | a0006c0011t0002g0109a0009c0013t0001g0147 | 2 | NA18955.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.2787-860T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040062 | ||||||
| chr19:56040111
|
C | T | 4 | a0001c0001t0001g0386a0001c0001t0001g0387a0001c0001t0001g0388others(1): Show | 4 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2787-811C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040111 | ||||||
| chr19:56040166
|
C | T | 2 | a0003c0118t0001g0357a0016c0129t0001g0100 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2787-756C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040166 | ||||||
| chr19:56040213
|
C | T | 18 | a0004c0007t0001g0136a0004c0007t0001g0139a0004c0007t0001g0212others(15): Show | 18 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.2787-709C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040213 | ||||||
| chr19:56040242
|
C | T | 20 | a0004c0007t0001g0136a0004c0007t0001g0139a0004c0007t0001g0212others(17): Show | 20 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.2787-680C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040242 | ||||||
| chr19:56040340
|
G | T | 1 | a0003c0043t0001g0195 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2787-582G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040340 | ||||||
| chr19:56040407
|
T | G | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2787-515T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040407 | ||||||
| chr19:56040439
|
A | G | 12 | a0001c0003t0001g0140a0001c0003t0001g0161a0001c0003t0001g0251others(9): Show | 12 | HG01934.hp2 HG01952.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.2787-483A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040439 | ||||||
| chr19:56040455
|
C | G | 1 | a0015c0044t0002g0188 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2787-467C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040455 | ||||||
| chr19:56040474
|
C | T | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2787-448C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040474 | ||||||
| chr19:56040510
|
T | C | 2 | a0003c0075t0001g0213a0032c0062t0001g0080 | 2 | HG03239.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2787-412T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040510 | ||||||
| chr19:56040553
|
C | T | 2 | a0021c0048t0002g0193a0021c0048t0002g0198 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2787-369C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040553 | ||||||
| chr19:56040554
|
G | A | 20 | a0004c0007t0001g0136a0004c0007t0001g0139a0004c0007t0001g0212others(17): Show | 20 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.2787-368G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040554 | ||||||
| chr19:56040566
|
CAAAT | C | 3 | a0009c0013t0001g0350a0009c0013t0001g0351a0009c0013t0001g0352 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2787-348_2787-345d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | 56040566 | |||||
| chr19:56040636
|
A | G | 1 | a0001c0003t0001g0251 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2787-286A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040636 | ||||||
| chr19:56040678
|
C | T | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2787-244C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040678 | ||||||
| chr19:56040720
|
A | G | 23 | a0004c0007t0001g0136a0004c0007t0001g0139a0004c0007t0001g0212others(20): Show | 23 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.2787-202A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040720 | ||||||
| chr19:56040824
|
A | G | 46 | a0004c0007t0001g0197a0004c0020t0001g0268a0004c0070t0001g0069others(43): Show | 46 | HG00673.hp1 HG01257.hp1 HG02074.hp2 others(43): Show |
intron_variant | MODIFIER | c.2787-98A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040824 | ||||||
| chr19:56040836
|
C | T | 1 | a0004c0007t0003g0210 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2787-86C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040836 | ||||||
| chr19:56040849
|
C | T | 4 | a0001c0046t0001g0261a0001c0046t0001g0262a0001c0084t0001g0053others(1): Show | 4 | HG01255.hp2 HG01261.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.2787-73C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040849 | ||||||
| chr19:56040864
|
A | G | 306 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0047others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.2787-58A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 10/14 | chr19 | 56040864 | ||||||
| chr19:56041181
|
G | T | 1 | a0001c0002t0001g0074 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2957+89G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56041181 | ||||||
| chr19:56041536
|
C | T | 19 | a0004c0007t0001g0136a0004c0007t0001g0139a0004c0007t0001g0212others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2957+444C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56041536 | ||||||
| chr19:56041549
|
C | T | 3 | a0007c0010t0001g0391a0007c0032t0001g0254a0042c0069t0001g0365 | 3 | HG02145.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2957+457C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56041549 | ||||||
| chr19:56041550
|
G | A | 1 | a0018c0036t0002g0035 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2957+458G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56041550 | ||||||
| chr19:56041675
|
C | T | 1 | a0001c0068t0001g0008 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2957+583C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56041675 | ||||||
| chr19:56041676
|
G | A | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2957+584G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56041676 | ||||||
| chr19:56041686
|
A | G | 108 | a0002c0079t0002g0089a0002c0127t0002g0306a0003c0045t0001g0090others(105): Show | 108 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(105): Show |
intron_variant | MODIFIER | c.2957+594A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56041686 | ||||||
| chr19:56041729
|
T | C | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2957+637T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56041729 | ||||||
| chr19:56041793
|
C | A | 1 | a0006c0011t0002g0129 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2957+701C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56041793 | ||||||
| chr19:56041875
|
C | T | 1 | a0031c0101t0001g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2957+783C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56041875 | ||||||
| chr19:56041913
|
T | C | 83 | a0002c0079t0002g0089a0002c0127t0002g0306a0003c0045t0001g0090others(80): Show | 83 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.2957+821T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56041913 | ||||||
| chr19:56041914
|
G | A | 1 | a0031c0101t0001g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2957+822G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56041914 | ||||||
| chr19:56042041
|
G | A | 1 | a0031c0101t0001g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2957+949G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042041 | ||||||
| chr19:56042080
|
C | T | 1 | a0003c0118t0001g0357 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2957+988C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042080 | ||||||
| chr19:56042101
|
T | C | 3 | a0009c0013t0001g0350a0009c0013t0001g0351a0009c0013t0001g0352 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2957+1009T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042101 | ||||||
| chr19:56042120
|
A | C | 2 | a0004c0007t0001g0197a0009c0013t0001g0126 | 2 | NA18964.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2957+1028A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042120 | ||||||
| chr19:56042120
|
A | G | 91 | a0002c0079t0002g0089a0002c0127t0002g0306a0003c0045t0001g0090others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.2957+1028A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042120 | ||||||
| chr19:56042131
|
G | C | 18 | a0001c0002t0001g0363a0001c0002t0001g0378a0003c0008t0001g0309others(15): Show | 18 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2957+1039G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042131 | ||||||
| chr19:56042149
|
C | T | 18 | a0004c0007t0001g0136a0004c0007t0001g0139a0004c0007t0001g0212others(15): Show | 18 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.2957+1057C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042149 | ||||||
| chr19:56042270
|
TACAG | T | 9 | a0004c0007t0003g0164a0004c0007t0003g0210a0004c0020t0003g0098others(6): Show | 9 | HG01243.hp1 HG02486.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2957+1182_2957+118 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56042270 | |||||
| chr19:56042324
|
C | A | 4 | a0004c0070t0001g0069a0009c0090t0001g0131a0016c0097t0001g0107others(1): Show | 4 | HG03195.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2957+1232C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042324 | ||||||
| chr19:56042404
|
C | T | 2 | a0003c0075t0001g0213a0032c0062t0001g0080 | 2 | HG03239.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2957+1312C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042404 | ||||||
| chr19:56042405
|
G | A | 1 | a0002c0012t0002g0383 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2957+1313G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042405 | ||||||
| chr19:56042436
|
C | T | 4 | a0001c0001t0001g0134a0002c0112t0002g0271a0008c0017t0001g0173others(1): Show | 4 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.2957+1344C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042436 | ||||||
| chr19:56042456
|
C | A | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2957+1364C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042456 | ||||||
| chr19:56042500
|
C | T | 174 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0047others(171): Show | 174 | HG00280.hp1 HG00597.hp2 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.2957+1408C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042500 | ||||||
| chr19:56042508
|
C | T | 173 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0047others(170): Show | 173 | HG00280.hp1 HG00597.hp2 HG00639.hp1 others(170): Show |
intron_variant | MODIFIER | c.2957+1416C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042508 | ||||||
| chr19:56042515
|
C | G | 1 | a0010c0027t0001g0170 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2957+1423C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042515 | ||||||
| chr19:56042546
|
A | G | 100 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(97): Show | 100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.2957+1454A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042546 | ||||||
| chr19:56042595
|
T | TGCCTCG | 100 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(97): Show | 100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.2957+1508_2957+150 others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56042595 | |||||
| chr19:56042604
|
G | A | 100 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(97): Show | 100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.2957+1512G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042604 | ||||||
| chr19:56042629
|
C | T | 6 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2957+1537C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042629 | ||||||
| chr19:56042668
|
G | A | 1 | a0001c0003t0001g0162 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2957+1576G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042668 | ||||||
| chr19:56042765
|
C | A | 1 | a0002c0012t0002g0223 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2957+1673C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042765 | ||||||
| chr19:56042777
|
A | C | 40 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(37): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.2957+1685A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042777 | ||||||
| chr19:56042784
|
T | C | 46 | a0001c0068t0001g0008a0004c0007t0001g0197a0004c0020t0001g0268others(43): Show | 46 | HG00323.hp1 HG01257.hp1 HG02074.hp2 others(43): Show |
intron_variant | MODIFIER | c.2957+1692T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042784 | ||||||
| chr19:56042862
|
T | G | 1 | a0005c0006t0001g0226 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2957+1770T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042862 | ||||||
| chr19:56042885
|
T | C | 1 | a0007c0010t0001g0224 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2957+1793T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042885 | ||||||
| chr19:56042934
|
CT | C | 46 | a0001c0068t0001g0008a0004c0007t0001g0197a0004c0020t0001g0268others(43): Show | 46 | HG00323.hp1 HG01257.hp1 HG02074.hp2 others(43): Show |
intron_variant | MODIFIER | c.2957+1847delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56042934 | |||||
| chr19:56042954
|
T | G | 2 | a0001c0001t0001g0190a0001c0052t0001g0026 | 2 | HG01169.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2957+1862T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56042954 | ||||||
| chr19:56042969
|
A | ATG | 5 | a0001c0046t0001g0261a0001c0046t0001g0262a0001c0084t0001g0053others(2): Show | 5 | HG01255.hp2 HG01261.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.2957+1893_2957+189 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56042969 | |||||
| chr19:56042969
|
ATG | A | 99 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(96): Show | 99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.2957+1893_2957+189 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56042969 | |||||
| chr19:56043066
|
T | C | 10 | a0004c0007t0001g0149a0004c0020t0001g0285a0004c0055t0001g0301others(7): Show | 10 | HG02015.hp2 NA18940.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.2957+1974T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043066 | ||||||
| chr19:56043088
|
G | C | 41 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(38): Show | 41 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.2957+1996G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043088 | ||||||
| chr19:56043176
|
C | G | 1 | a0045c0131t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2957+2084C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043176 | ||||||
| chr19:56043431
|
A | C | 15 | a0001c0009t0001g0281a0001c0046t0001g0261a0001c0046t0001g0262others(12): Show | 15 | HG01109.hp1 HG01255.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.2957+2339A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043431 | ||||||
| chr19:56043536
|
G | GCTGA | 100 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.2957+2446_2957+244 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043536 | |||||
| chr19:56043537
|
CTATTCTT others(4): Show |
C | 1 | a0031c0101t0001g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2957+2447_2957+245 others(15): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043537 | |||||
| chr19:56043537
|
CTATTCTT others(5): Show |
C | 2 | a0004c0007t0001g0307a0004c0125t0001g0013 | 2 | HG02257.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2957+2447_2957+245 others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043537 | |||||
| chr19:56043537
|
CTATTCTT others(6): Show |
C | 13 | a0004c0007t0001g0051a0004c0020t0001g0096a0004c0035t0001g0094others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.2957+2447_2957+245 others(17): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043537 | |||||
| chr19:56043538
|
T | TG | 3 | a0004c0020t0001g0285a0009c0013t0001g0147a0010c0016t0001g0292 | 3 | HG02015.hp2 NA18941.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.2957+2446_2957+244 others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043538 | ||||||
| chr19:56043539
|
A | G | 1 | a0003c0043t0001g0195 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2957+2447A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043539 | ||||||
| chr19:56043540
|
T | A | 1 | a0003c0043t0001g0195 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2957+2448T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043540 | ||||||
| chr19:56043540
|
T | C | 3 | a0004c0020t0001g0285a0009c0013t0001g0147a0010c0016t0001g0292 | 3 | HG02015.hp2 NA18941.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.2957+2448T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043540 | ||||||
| chr19:56043541
|
T | C | 1 | a0003c0043t0001g0195 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2957+2449T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043541 | ||||||
| chr19:56043542
|
C | A | 3 | a0004c0020t0001g0285a0009c0013t0001g0147a0010c0016t0001g0292 | 3 | HG02015.hp2 NA18941.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.2957+2450C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043542 | ||||||
| chr19:56043542
|
C | CT | 47 | a0001c0001t0001g0134a0001c0001t0001g0199a0001c0003t0001g0011others(44): Show | 47 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.2957+2491dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
C | CTT | 29 | a0001c0003t0001g0001a0001c0003t0001g0115a0001c0003t0001g0251others(26): Show | 29 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.2957+2490_2957+249 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
C | CTTT | 16 | a0001c0001t0001g0353a0001c0003t0001g0155a0001c0019t0001g0122others(13): Show | 16 | HG01192.hp2 HG01884.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2957+2489_2957+249 others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
C | CTTTT | 7 | a0001c0019t0001g0118a0001c0023t0001g0244a0001c0042t0001g0377others(4): Show | 7 | HG03041.hp1 HG03239.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2957+2488_2957+249 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
C | T | 2 | a0003c0043t0001g0195a0012c0018t0002g0033 | 2 | HG00544.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2957+2450C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043542 | ||||||
| chr19:56043542
|
CT | C | 6 | a0001c0009t0001g0277a0002c0041t0002g0232a0005c0025t0001g0132others(3): Show | 6 | HG03490.hp2 HG03492.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.2957+2491delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTT | C | 11 | a0001c0001t0001g0049a0001c0015t0001g0002a0001c0052t0001g0023others(8): Show | 11 | HG00738.hp1 HG01255.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.2957+2490_2957+249 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTT | C | 11 | a0001c0001t0001g0230a0003c0008t0001g0119a0003c0008t0001g0265others(8): Show | 11 | HG02683.hp1 HG02717.hp2 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.2957+2489_2957+249 others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTT | C | 11 | a0001c0009t0001g0286a0001c0068t0001g0008a0002c0004t0002g0259others(8): Show | 11 | HG00323.hp1 HG01952.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.2957+2488_2957+249 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTT | C | 19 | a0001c0009t0001g0293a0002c0004t0002g0176a0002c0127t0002g0306others(16): Show | 19 | HG01109.hp1 HG01891.hp1 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.2957+2487_2957+249 others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTT | C | 11 | a0001c0022t0001g0356a0002c0041t0002g0358a0002c0079t0002g0089others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2957+2486_2957+249 others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT | C | 10 | a0001c0001t0001g0068a0001c0056t0001g0382a0002c0004t0002g0166others(7): Show | 10 | HG01257.hp1 HG02965.hp1 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.2957+2485_2957+249 others(11): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(1): Show |
C | 11 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0014t0001g0022others(8): Show | 11 | HG00735.hp2 HG01069.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.2957+2484_2957+249 others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(2): Show |
C | 10 | a0004c0007t0001g0136a0004c0020t0001g0105a0008c0037t0001g0009others(7): Show | 10 | HG00280.hp2 HG01515.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2957+2483_2957+249 others(13): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(3): Show |
C | 15 | a0001c0002t0001g0378a0001c0014t0001g0048a0001c0014t0001g0120others(12): Show | 15 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.2957+2482_2957+249 others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(4): Show |
C | 7 | a0001c0002t0001g0363a0003c0008t0001g0312a0003c0051t0001g0252others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2957+2481_2957+249 others(15): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(5): Show |
C | 3 | a0003c0045t0001g0266a0006c0005t0002g0270a0038c0120t0002g0278 | 3 | NA18940.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2957+2480_2957+249 others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(6): Show |
C | 6 | a0003c0118t0001g0357a0004c0007t0001g0149a0006c0005t0002g0295others(3): Show | 6 | HG02559.hp2 NA18957.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2957+2479_2957+249 others(17): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(7): Show |
C | 1 | a0004c0007t0003g0210 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2957+2478_2957+249 others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(8): Show |
C | 9 | a0001c0003t0001g0162a0002c0004t0002g0128a0002c0116t0002g0330others(6): Show | 9 | HG00544.hp2 HG02257.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2957+2477_2957+249 others(19): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(10): Show |
C | 4 | a0001c0092t0001g0211a0004c0007t0001g0325a0041c0109t0001g0345others(1): Show | 4 | HG02897.hp2 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2957+2475_2957+249 others(21): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(11): Show |
C | 4 | a0001c0115t0001g0040a0003c0008t0001g0309a0003c0008t0001g0310others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2957+2474_2957+249 others(22): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(12): Show |
C | 1 | a0007c0073t0001g0218 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2957+2473_2957+249 others(23): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(13): Show |
C | 2 | a0002c0004t0002g0237a0005c0006t0001g0159 | 2 | HG00423.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.2957+2472_2957+249 others(24): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(16): Show |
C | 1 | a0007c0072t0001g0233 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2957+2469_2957+249 others(27): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(26): Show |
C | 1 | a0002c0012t0002g0223 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2957+2459_2957+249 others(37): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043542
|
CTTTTTTT others(27): Show |
C | 92 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.2957+2458_2957+249 others(38): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56043542 | |||||
| chr19:56043543
|
T | A | 1 | a0003c0043t0001g0195 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2957+2451T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043543 | ||||||
| chr19:56043545
|
T | C | 8 | a0004c0020t0001g0285a0004c0055t0001g0301a0006c0011t0002g0109others(5): Show | 8 | HG02015.hp2 NA18940.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.2957+2453T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043545 | ||||||
| chr19:56043546
|
T | C | 4 | a0003c0043t0001g0195a0004c0020t0001g0285a0009c0013t0001g0147others(1): Show | 4 | HG00544.hp1 HG02015.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.2957+2454T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043546 | ||||||
| chr19:56043547
|
T | C | 1 | a0003c0043t0001g0195 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2957+2455T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043547 | ||||||
| chr19:56043550
|
T | G | 1 | a0031c0101t0001g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2957+2458T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043550 | ||||||
| chr19:56043551
|
T | A | 1 | a0031c0101t0001g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2957+2459T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043551 | ||||||
| chr19:56043551
|
T | G | 2 | a0004c0007t0001g0307a0004c0125t0001g0013 | 2 | HG02257.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2957+2459T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043551 | ||||||
| chr19:56043552
|
T | A | 2 | a0004c0007t0001g0307a0004c0125t0001g0013 | 2 | HG02257.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2957+2460T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043552 | ||||||
| chr19:56043552
|
T | C | 1 | a0031c0101t0001g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2957+2460T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043552 | ||||||
| chr19:56043552
|
T | G | 13 | a0004c0007t0001g0051a0004c0020t0001g0096a0004c0035t0001g0094others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.2957+2460T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043552 | ||||||
| chr19:56043553
|
T | A | 13 | a0004c0007t0001g0051a0004c0020t0001g0096a0004c0035t0001g0094others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.2957+2461T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043553 | ||||||
| chr19:56043553
|
T | C | 2 | a0004c0007t0001g0307a0004c0125t0001g0013 | 2 | HG02257.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2957+2461T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043553 | ||||||
| chr19:56043554
|
T | A | 1 | a0031c0101t0001g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2957+2462T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043554 | ||||||
| chr19:56043554
|
T | C | 13 | a0004c0007t0001g0051a0004c0020t0001g0096a0004c0035t0001g0094others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.2957+2462T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043554 | ||||||
| chr19:56043555
|
T | A | 2 | a0004c0007t0001g0307a0004c0125t0001g0013 | 2 | HG02257.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2957+2463T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043555 | ||||||
| chr19:56043556
|
T | A | 13 | a0004c0007t0001g0051a0004c0020t0001g0096a0004c0035t0001g0094others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.2957+2464T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043556 | ||||||
| chr19:56043557
|
T | C | 1 | a0031c0101t0001g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2957+2465T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043557 | ||||||
| chr19:56043558
|
T | C | 3 | a0004c0007t0001g0307a0004c0125t0001g0013a0031c0101t0001g0346 | 3 | HG02257.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2957+2466T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043558 | ||||||
| chr19:56043559
|
T | C | 15 | a0004c0007t0001g0051a0004c0007t0001g0307a0004c0020t0001g0096others(12): Show | 15 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.2957+2467T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043559 | ||||||
| chr19:56043560
|
T | C | 13 | a0004c0007t0001g0051a0004c0020t0001g0096a0004c0035t0001g0094others(10): Show | 13 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.2957+2468T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043560 | ||||||
| chr19:56043628
|
T | C | 1 | a0006c0005t0002g0304 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2957+2536T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043628 | ||||||
| chr19:56043651
|
T | C | 71 | a0001c0001t0001g0230a0001c0002t0001g0363a0001c0002t0001g0378others(68): Show | 71 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2957+2559T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043651 | ||||||
| chr19:56043661
|
G | A | 1 | a0001c0009t0001g0281 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2957+2569G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043661 | ||||||
| chr19:56043666
|
T | C | 11 | a0002c0079t0002g0089a0002c0127t0002g0306a0003c0008t0003g0381others(8): Show | 11 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2957+2574T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043666 | ||||||
| chr19:56043690
|
C | T | 10 | a0002c0079t0002g0089a0002c0127t0002g0306a0003c0008t0003g0381others(7): Show | 10 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.2957+2598C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043690 | ||||||
| chr19:56043691
|
G | A | 11 | a0001c0001t0001g0353a0001c0092t0001g0211a0001c0115t0001g0040others(8): Show | 11 | HG02145.hp2 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2957+2599G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043691 | ||||||
| chr19:56043717
|
C | T | 1 | a0009c0013t0001g0352 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2957+2625C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043717 | ||||||
| chr19:56043722
|
A | G | 10 | a0001c0002t0001g0032a0001c0002t0001g0043a0001c0002t0001g0050others(7): Show | 10 | HG01928.hp2 HG01934.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.2957+2630A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043722 | ||||||
| chr19:56043733
|
C | T | 15 | a0001c0001t0001g0049a0001c0001t0001g0190a0001c0002t0001g0054others(12): Show | 15 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.2957+2641C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043733 | ||||||
| chr19:56043734
|
G | A | 9 | a0002c0031t0002g0071a0005c0006t0001g0163a0005c0034t0001g0338others(6): Show | 9 | HG00423.hp2 HG02015.hp1 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.2957+2642G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043734 | ||||||
| chr19:56043739
|
A | G | 7 | a0001c0001t0001g0353a0001c0092t0001g0211a0001c0115t0001g0040others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2957+2647A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043739 | ||||||
| chr19:56043768
|
A | G | 4 | a0001c0003t0001g0263a0001c0009t0001g0281a0001c0009t0001g0282others(1): Show | 4 | HG01433.hp1 NA19007.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2957+2676A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043768 | ||||||
| chr19:56043776
|
A | G | 1 | a0009c0054t0001g0326 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2957+2684A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043776 | ||||||
| chr19:56043779
|
A | G | 4 | a0001c0002t0001g0041a0001c0046t0001g0261a0001c0046t0001g0262others(1): Show | 4 | HG01099.hp2 HG01255.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2957+2687A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043779 | ||||||
| chr19:56043780
|
C | T | 4 | a0001c0002t0001g0041a0001c0046t0001g0261a0001c0046t0001g0262others(1): Show | 4 | HG01099.hp2 HG01255.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2957+2688C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043780 | ||||||
| chr19:56043781
|
G | A | 27 | a0001c0001t0001g0230a0001c0002t0001g0378a0003c0008t0001g0119others(24): Show | 27 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.2957+2689G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043781 | ||||||
| chr19:56043818
|
T | C | 31 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(28): Show | 31 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.2957+2726T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043818 | ||||||
| chr19:56043819
|
T | C | 50 | a0001c0001t0001g0049a0001c0003t0001g0182a0001c0042t0001g0021others(47): Show | 50 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.2957+2727T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043819 | ||||||
| chr19:56043820
|
G | A | 1 | a0001c0015t0001g0084 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2957+2728G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043820 | ||||||
| chr19:56043824
|
T | G | 81 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0049others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.2957+2732T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043824 | ||||||
| chr19:56043854
|
G | A | 1 | a0001c0042t0001g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2957+2762G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043854 | ||||||
| chr19:56043856
|
CG | C | 15 | a0001c0001t0001g0049a0001c0003t0001g0111a0001c0003t0001g0182others(12): Show | 15 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.2957+2765delG | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043856 | ||||||
| chr19:56043859
|
G | A | 1 | a0005c0006t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2957+2767G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043859 | ||||||
| chr19:56043863
|
C | T | 129 | a0001c0001t0001g0027a0001c0001t0001g0047a0001c0001t0001g0091others(126): Show | 129 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.2957+2771C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043863 | ||||||
| chr19:56043867
|
A | G | 23 | a0001c0001t0001g0049a0001c0001t0001g0386a0001c0001t0001g0387others(20): Show | 23 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.2957+2775A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043867 | ||||||
| chr19:56043908
|
T | C | 2 | a0001c0002t0001g0032a0001c0002t0001g0079 | 2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2957+2816T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043908 | ||||||
| chr19:56043927
|
C | T | 43 | a0001c0001t0001g0049a0001c0022t0001g0356a0001c0052t0001g0023others(40): Show | 43 | HG00544.hp1 HG00738.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.2957+2835C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56043927 | ||||||
| chr19:56044003
|
C | T | 2 | a0001c0022t0001g0273a0001c0022t0001g0274 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2957+2911C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044003 | ||||||
| chr19:56044004
|
G | A | 55 | a0001c0001t0001g0049a0001c0002t0001g0363a0001c0002t0001g0378others(52): Show | 55 | HG00738.hp1 HG01243.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2957+2912G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044004 | ||||||
| chr19:56044009
|
G | GT | 82 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(79): Show | 82 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2957+2922dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56044009 | |||||
| chr19:56044015
|
C | T | 1 | a0008c0104t0001g0374 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2957+2923C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044015 | ||||||
| chr19:56044067
|
C | CT | 136 | a0001c0001t0001g0049a0001c0001t0001g0230a0001c0001t0001g0353others(133): Show | 136 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.2957+2988dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56044067 | |||||
| chr19:56044067
|
C | CTT | 22 | a0001c0052t0001g0023a0003c0051t0001g0020a0004c0007t0001g0051others(19): Show | 22 | HG01243.hp2 HG01255.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.2957+2987_2957+298 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56044067 | |||||
| chr19:56044178
|
C | G | 6 | a0004c0070t0001g0069a0009c0013t0001g0350a0009c0013t0001g0351others(3): Show | 6 | HG02630.hp1 HG02818.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2957+3086C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044178 | ||||||
| chr19:56044212
|
C | T | 63 | a0001c0002t0001g0148a0001c0002t0001g0151a0001c0002t0001g0393others(60): Show | 63 | HG00597.hp2 HG01109.hp1 HG01109.hp2 others(60): Show |
intron_variant | MODIFIER | c.2957+3120C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044212 | ||||||
| chr19:56044253
|
G | A | 1 | a0001c0002t0001g0041 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2957+3161G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044253 | ||||||
| chr19:56044293
|
A | G | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2957+3201A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044293 | ||||||
| chr19:56044322
|
G | A | 9 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(6): Show | 9 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2957+3230G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044322 | ||||||
| chr19:56044413
|
C | T | 1 | a0031c0101t0001g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2957+3321C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044413 | ||||||
| chr19:56044414
|
G | A | 1 | a0001c0014t0001g0206 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2957+3322G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044414 | ||||||
| chr19:56044426
|
C | T | 2 | a0004c0070t0001g0069a0016c0129t0001g0100 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2957+3334C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044426 | ||||||
| chr19:56044553
|
C | G | 151 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.2957+3461C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044553 | ||||||
| chr19:56044590
|
C | T | 15 | a0003c0051t0001g0020a0004c0007t0001g0051a0004c0007t0001g0307others(12): Show | 15 | HG01243.hp2 HG01346.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.2957+3498C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044590 | ||||||
| chr19:56044637
|
G | A | 23 | a0003c0043t0001g0195a0003c0051t0001g0020a0004c0007t0001g0051others(20): Show | 23 | HG00544.hp1 HG01243.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.2957+3545G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044637 | ||||||
| chr19:56044646
|
T | G | 3 | a0001c0022t0001g0356a0002c0041t0002g0358a0003c0118t0001g0357 | 3 | HG02559.hp2 HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2957+3554T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044646 | ||||||
| chr19:56044688
|
T | C | 267 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(264): Show | 267 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.2957+3596T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044688 | ||||||
| chr19:56044696
|
C | CT | 13 | a0004c0020t0001g0268a0005c0006t0001g0056a0005c0025t0001g0078others(10): Show | 13 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(10): Show |
intron_variant | MODIFIER | c.2957+3611dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56044696 | |||||
| chr19:56044700
|
T | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(119): Show | 122 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.2957+3608T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044700 | ||||||
| chr19:56044710
|
A | G | 6 | a0001c0042t0001g0021a0001c0042t0001g0377a0003c0076t0002g0250others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2957+3618A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044710 | ||||||
| chr19:56044772
|
G | A | 3 | a0007c0032t0001g0017a0007c0032t0001g0327a0028c0093t0001g0269 | 3 | HG01346.hp1 HG02004.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2957+3680G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044772 | ||||||
| chr19:56044773
|
T | C | 4 | a0001c0022t0001g0356a0002c0041t0002g0358a0003c0118t0001g0357others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2957+3681T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044773 | ||||||
| chr19:56044903
|
C | T | 16 | a0002c0004t0002g0166a0002c0004t0002g0176a0002c0004t0002g0184others(13): Show | 16 | HG03942.hp2 NA18939.hp2 NA18946.hp2 others(13): Show |
intron_variant | MODIFIER | c.2957+3811C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044903 | ||||||
| chr19:56044939
|
T | C | 41 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(38): Show | 41 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.2957+3847T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56044939 | ||||||
| chr19:56045031
|
T | A | 4 | a0009c0013t0001g0061a0009c0013t0001g0062a0020c0049t0001g0028others(1): Show | 4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2957+3939T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045031 | ||||||
| chr19:56045033
|
T | C | 6 | a0003c0008t0003g0381a0004c0007t0003g0164a0004c0007t0003g0210others(3): Show | 6 | HG02257.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2957+3941T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045033 | ||||||
| chr19:56045194
|
A | G | 1 | a0004c0055t0001g0323 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2957+4102A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045194 | ||||||
| chr19:56045205
|
G | A | 1 | a0045c0131t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2957+4113G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045205 | ||||||
| chr19:56045312
|
C | A | 130 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(127): Show | 130 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.2957+4220C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045312 | ||||||
| chr19:56045335
|
C | A | 132 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(129): Show | 132 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.2957+4243C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045335 | ||||||
| chr19:56045384
|
C | T | 41 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(38): Show | 41 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.2957+4292C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045384 | ||||||
| chr19:56045402
|
G | C | 92 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(89): Show | 92 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.2957+4310G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045402 | ||||||
| chr19:56045463
|
T | G | 41 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(38): Show | 41 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.2957+4371T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045463 | ||||||
| chr19:56045502
|
A | G | 11 | a0003c0008t0003g0381a0004c0007t0003g0164a0004c0007t0003g0210others(8): Show | 11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2957+4410A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045502 | ||||||
| chr19:56045554
|
C | T | 29 | a0001c0001t0001g0230a0001c0002t0001g0363a0001c0002t0001g0378others(26): Show | 29 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.2957+4462C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045554 | ||||||
| chr19:56045592
|
C | T | 1 | a0008c0017t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2957+4500C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045592 | ||||||
| chr19:56045735
|
C | T | 33 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(30): Show | 33 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.2957+4643C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045735 | ||||||
| chr19:56045780
|
A | G | 92 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(89): Show | 92 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.2958-4638A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045780 | ||||||
| chr19:56045842
|
G | A | 12 | a0005c0006t0001g0056a0005c0025t0001g0078a0008c0017t0001g0103others(9): Show | 12 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(9): Show |
intron_variant | MODIFIER | c.2958-4576G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045842 | ||||||
| chr19:56045859
|
T | C | 1 | a0001c0092t0001g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2958-4559T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045859 | ||||||
| chr19:56045882
|
G | A | 33 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(30): Show | 33 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.2958-4536G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045882 | ||||||
| chr19:56045973
|
C | T | 1 | a0007c0108t0001g0275 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2958-4445C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56045973 | ||||||
| chr19:56046102
|
G | T | 1 | a0045c0131t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2958-4316G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046102 | ||||||
| chr19:56046138
|
A | G | 4 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2958-4280A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046138 | ||||||
| chr19:56046150
|
G | A | 33 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(30): Show | 33 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.2958-4268G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046150 | ||||||
| chr19:56046212
|
G | A | 7 | a0001c0002t0001g0378a0003c0008t0001g0309a0003c0008t0001g0310others(4): Show | 7 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2958-4206G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046212 | ||||||
| chr19:56046231
|
C | A | 1 | a0010c0027t0001g0319 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2958-4187C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046231 | ||||||
| chr19:56046302
|
C | T | 1 | a0016c0097t0001g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2958-4116C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046302 | ||||||
| chr19:56046344
|
C | T | 196 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(193): Show | 196 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.2958-4074C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046344 | ||||||
| chr19:56046369
|
A | G | 1 | a0001c0003t0001g0380 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2958-4049A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046369 | ||||||
| chr19:56046398
|
T | C | 3 | a0001c0030t0001g0187a0001c0030t0001g0318a0001c0030t0001g0343 | 3 | HG02132.hp2 HG02165.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.2958-4020T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046398 | ||||||
| chr19:56046399
|
C | CGT | 7 | a0001c0030t0001g0187a0001c0030t0001g0318a0001c0030t0001g0343others(4): Show | 7 | HG00140.hp2 HG01081.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.2958-3996_2958-399 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046399
|
C | CGTGT | 27 | a0001c0001t0001g0230a0001c0002t0001g0363a0001c0002t0001g0378others(24): Show | 27 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.2958-3998_2958-399 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046399
|
C | CGTGTGTG others(3): Show |
1 | a0001c0023t0001g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2958-4004_2958-399 others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046399
|
C | CGTGTGTG others(5): Show |
22 | a0001c0001t0001g0353a0001c0009t0001g0283a0001c0019t0001g0065others(19): Show | 22 | HG01069.hp1 HG01070.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2958-4006_2958-399 others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046399
|
C | CGTGTGTG others(7): Show |
56 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0039others(53): Show | 56 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.2958-4008_2958-399 others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046399
|
C | CGTGTGTG others(9): Show |
8 | a0001c0001t0001g0027a0001c0001t0001g0135a0001c0001t0001g0137others(5): Show | 8 | HG01167.hp2 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2958-4010_2958-399 others(20): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046399
|
C | CGTGTGTG others(11): Show |
6 | a0001c0001t0001g0110a0001c0009t0001g0286a0001c0022t0001g0356others(3): Show | 6 | HG00639.hp2 HG02015.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.2958-4012_2958-399 others(22): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046399
|
C | CGTGTGTG others(13): Show |
1 | a0006c0005t0002g0355 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2958-4014_2958-399 others(24): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046399
|
C | CGTGTGTG others(15): Show |
2 | a0004c0020t0001g0268a0010c0016t0001g0375 | 2 | NA18988.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.2958-4016_2958-399 others(26): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046399
|
C | CGTGTGTG others(17): Show |
2 | a0010c0016t0001g0292a0010c0016t0001g0364 | 2 | NA18940.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.2958-4018_2958-399 others(28): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046399
|
C | CGTGTGTG others(19): Show |
1 | a0003c0043t0001g0195 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2958-3995_2958-399 others(30): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046399
|
CGT | C | 93 | a0001c0003t0001g0011a0001c0015t0001g0002a0001c0042t0001g0021others(90): Show | 93 | HG00597.hp2 HG01109.hp1 HG01109.hp2 others(90): Show |
intron_variant | MODIFIER | c.2958-3996_2958-399 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046399
|
CGTGTGTG others(7): Show |
C | 4 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2958-4008_2958-399 others(18): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046399 | |||||
| chr19:56046410
|
G | GTGTGTGT others(33): Show |
1 | a0001c0001t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2958-3995_2958-399 others(44): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046410 | |||||
| chr19:56046410
|
G | GTGTGTGT others(25): Show |
2 | a0001c0086t0001g0018a0002c0087t0002g0024 | 2 | HG00733.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2958-3995_2958-399 others(36): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046410 | |||||
| chr19:56046432
|
C | T | 268 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(265): Show | 268 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.2958-3986C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046432 | ||||||
| chr19:56046494
|
C | T | 2 | a0044c0107t0001g0344a0045c0131t0001g0315 | 2 | HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2958-3924C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046494 | ||||||
| chr19:56046523
|
C | T | 1 | a0001c0015t0001g0106 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2958-3895C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046523 | ||||||
| chr19:56046540
|
C | G | 13 | a0003c0051t0001g0020a0004c0007t0001g0051a0004c0007t0001g0307others(10): Show | 13 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2958-3878C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046540 | ||||||
| chr19:56046546
|
GT | G | 30 | a0001c0001t0001g0230a0001c0002t0001g0363a0001c0002t0001g0378others(27): Show | 30 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.2958-3862delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046546 | |||||
| chr19:56046564
|
G | A | 1 | a0006c0005t0002g0355 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2958-3854G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046564 | ||||||
| chr19:56046580
|
G | A | 3 | a0005c0113t0001g0099a0030c0098t0001g0354a0041c0109t0001g0345 | 3 | HG02615.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2958-3838G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046580 | ||||||
| chr19:56046626
|
T | C | 2 | a0001c0002t0001g0108a0008c0017t0001g0154 | 2 | HG03491.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2958-3792T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046626 | ||||||
| chr19:56046645
|
A | G | 15 | a0005c0006t0001g0056a0005c0025t0001g0078a0005c0113t0001g0099others(12): Show | 15 | HG01243.hp1 HG02615.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.2958-3773A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046645 | ||||||
| chr19:56046689
|
C | T | 4 | a0001c0022t0001g0356a0002c0041t0002g0358a0003c0118t0001g0357others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2958-3729C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046689 | ||||||
| chr19:56046707
|
A | AT | 19 | a0001c0001t0001g0027a0003c0008t0003g0381a0004c0007t0003g0164others(16): Show | 19 | HG01167.hp2 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2958-3701dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56046707 | |||||
| chr19:56046735
|
G | A | 6 | a0001c0003t0001g0115a0001c0003t0001g0140a0001c0003t0001g0161others(3): Show | 6 | HG02080.hp1 NA18939.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.2958-3683G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046735 | ||||||
| chr19:56046746
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2958-3672G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046746 | ||||||
| chr19:56046776
|
C | G | 13 | a0003c0051t0001g0020a0004c0007t0001g0051a0004c0007t0001g0307others(10): Show | 13 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2958-3642C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046776 | ||||||
| chr19:56046833
|
C | T | 7 | a0001c0002t0001g0378a0003c0008t0001g0309a0003c0008t0001g0310others(4): Show | 7 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2958-3585C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046833 | ||||||
| chr19:56046865
|
G | A | 92 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(89): Show | 92 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.2958-3553G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046865 | ||||||
| chr19:56046872
|
C | T | 1 | a0037c0091t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2958-3546C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046872 | ||||||
| chr19:56046886
|
C | A | 1 | a0009c0094t0001g0208 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2958-3532C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56046886 | ||||||
| chr19:56047068
|
T | TA | 349 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(346): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2958-3350_2958-334 others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047068 | ||||||
| chr19:56047077
|
A | G | 341 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.2958-3341A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047077 | ||||||
| chr19:56047082
|
A | G | 7 | a0001c0002t0001g0378a0003c0008t0001g0309a0003c0008t0001g0310others(4): Show | 7 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2958-3336A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047082 | ||||||
| chr19:56047156
|
A | G | 1 | a0001c0002t0001g0363 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2958-3262A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047156 | ||||||
| chr19:56047265
|
T | A | 1 | a0001c0019t0001g0359 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2958-3153T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047265 | ||||||
| chr19:56047364
|
G | A | 1 | a0003c0024t0001g0025 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2958-3054G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047364 | ||||||
| chr19:56047441
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2958-2977G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047441 | ||||||
| chr19:56047471
|
A | ATTGAT | 341 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.2958-2945_2958-294 others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56047471 | |||||
| chr19:56047502
|
C | A | 1 | a0001c0002t0001g0363 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2958-2916C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047502 | ||||||
| chr19:56047733
|
C | T | 174 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(171): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2958-2685C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047733 | ||||||
| chr19:56047852
|
T | C | 2 | a0008c0017t0001g0103a0008c0017t0001g0146 | 2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2958-2566T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047852 | ||||||
| chr19:56047901
|
C | T | 90 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(87): Show | 90 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(87): Show |
intron_variant | MODIFIER | c.2958-2517C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047901 | ||||||
| chr19:56047903
|
C | G | 163 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(160): Show | 163 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2958-2515C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047903 | ||||||
| chr19:56047912
|
G | C | 4 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2958-2506G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047912 | ||||||
| chr19:56047968
|
A | G | 27 | a0001c0001t0001g0230a0001c0002t0001g0363a0001c0002t0001g0378others(24): Show | 27 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.2958-2450A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56047968 | ||||||
| chr19:56048004
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2958-2414C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048004 | ||||||
| chr19:56048013
|
T | G | 1 | a0007c0071t0001g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2958-2405T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048013 | ||||||
| chr19:56048084
|
T | C | 162 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(159): Show | 162 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2958-2334T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048084 | ||||||
| chr19:56048141
|
ATGGT | A | 4 | a0001c0001t0001g0207a0001c0002t0001g0241a0001c0003t0001g0251others(1): Show | 4 | HG02040.hp2 NA18951.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2958-2268_2958-226 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56048141 | |||||
| chr19:56048192
|
C | T | 88 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(85): Show | 88 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.2958-2226C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048192 | ||||||
| chr19:56048351
|
G | C | 1 | a0007c0021t0001g0348 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2958-2067G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048351 | ||||||
| chr19:56048385
|
A | C | 1 | a0003c0118t0001g0357 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2958-2033A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048385 | ||||||
| chr19:56048422
|
G | C | 1 | a0037c0091t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2958-1996G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048422 | ||||||
| chr19:56048439
|
TTGTC | T | 4 | a0001c0022t0001g0356a0002c0041t0002g0358a0003c0118t0001g0357others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2958-1972_2958-196 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56048439 | |||||
| chr19:56048534
|
A | AGCT | 174 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(171): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2958-1884_2958-188 others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048534 | ||||||
| chr19:56048535
|
C | G | 174 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(171): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2958-1883C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048535 | ||||||
| chr19:56048538
|
A | G | 174 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(171): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2958-1880A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048538 | ||||||
| chr19:56048539
|
C | A | 174 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(171): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2958-1879C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048539 | ||||||
| chr19:56048540
|
A | T | 174 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(171): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2958-1878A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048540 | ||||||
| chr19:56048548
|
CA | C | 174 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(171): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2958-1867delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56048548 | |||||
| chr19:56048592
|
A | T | 6 | a0003c0008t0003g0381a0004c0007t0003g0164a0004c0007t0003g0210others(3): Show | 6 | HG02257.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2958-1826A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048592 | ||||||
| chr19:56048638
|
A | C | 163 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(160): Show | 163 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2958-1780A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048638 | ||||||
| chr19:56048830
|
C | CT | 7 | a0001c0001t0001g0353a0001c0019t0001g0065a0001c0019t0001g0066others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2958-1582dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56048830 | |||||
| chr19:56048904
|
A | G | 2 | a0004c0035t0001g0094a0004c0035t0001g0095 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2958-1514A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048904 | ||||||
| chr19:56048977
|
T | TA | 4 | a0001c0001t0001g0091a0001c0003t0001g0112a0001c0019t0001g0065others(1): Show | 4 | HG02976.hp1 NA18948.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.2958-1439dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56048977 | |||||
| chr19:56048977
|
T | TAA | 68 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(65): Show | 68 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.2958-1440_2958-143 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56048977 | |||||
| chr19:56048977
|
T | TTA | 20 | a0001c0001t0001g0130a0001c0001t0001g0215a0001c0001t0001g0216others(17): Show | 20 | HG00544.hp1 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.2958-1441_2958-144 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048977 | ||||||
| chr19:56048978
|
A | T | 55 | a0001c0001t0001g0230a0001c0002t0001g0363a0001c0002t0001g0378others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2958-1440A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048978 | ||||||
| chr19:56048979
|
A | AAAT | 4 | a0001c0002t0001g0043a0001c0002t0001g0320a0001c0009t0001g0286others(1): Show | 4 | HG02027.hp2 HG02559.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.2958-1439_2958-143 others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048979 | ||||||
| chr19:56048979
|
A | AATT | 4 | a0010c0016t0001g0364a0010c0027t0001g0185a0044c0107t0001g0344others(1): Show | 4 | HG02897.hp2 HG03130.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.2958-1439_2958-143 others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048979 | ||||||
| chr19:56048979
|
A | AATTT | 22 | a0001c0001t0001g0230a0001c0002t0001g0363a0003c0008t0001g0119others(19): Show | 22 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.2958-1439_2958-143 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048979 | ||||||
| chr19:56048979
|
A | AATTTT | 13 | a0001c0002t0001g0378a0003c0051t0001g0020a0004c0007t0001g0051others(10): Show | 13 | HG01099.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2958-1439_2958-143 others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048979 | ||||||
| chr19:56048979
|
A | AATTTTT | 4 | a0004c0007t0001g0325a0004c0035t0001g0097a0004c0053t0001g0088others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2958-1439_2958-143 others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048979 | ||||||
| chr19:56048979
|
A | ATTT | 19 | a0001c0014t0001g0022a0001c0014t0001g0120a0001c0014t0001g0171others(16): Show | 19 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2958-1421_2958-141 others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56048979 | |||||
| chr19:56048979
|
A | T | 8 | a0002c0012t0002g0223a0003c0043t0001g0195a0004c0007t0001g0149others(5): Show | 8 | HG00544.hp1 HG02015.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.2958-1439A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048979 | ||||||
| chr19:56048979
|
AT | A | 64 | a0001c0001t0001g0160a0001c0092t0001g0211a0001c0115t0001g0040others(61): Show | 64 | HG00438.hp2 HG00673.hp1 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.2958-1419delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56048979 | |||||
| chr19:56048979
|
ATT | A | 150 | a0001c0001t0001g0190a0001c0001t0001g0199a0001c0001t0001g0200others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.2958-1420_2958-141 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56048979 | |||||
| chr19:56048980
|
T | A | 11 | a0001c0001t0001g0091a0001c0003t0001g0112a0001c0019t0001g0065others(8): Show | 11 | HG02257.hp2 HG02486.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2958-1438T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048980 | ||||||
| chr19:56048981
|
T | A | 5 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(2): Show | 5 | HG01192.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2958-1437T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56048981 | ||||||
| chr19:56049133
|
C | A | 6 | a0003c0051t0001g0020a0004c0007t0001g0307a0004c0050t0001g0328others(3): Show | 6 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2958-1285C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049133 | ||||||
| chr19:56049166
|
A | ATATT | 59 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0047others(56): Show | 59 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.2958-1225_2958-122 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56049166 | |||||
| chr19:56049166
|
A | ATATTTAT others(1): Show |
9 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0137others(6): Show | 9 | HG00733.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2958-1229_2958-122 others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56049166 | |||||
| chr19:56049166
|
A | ATATTTAT others(5): Show |
9 | a0002c0041t0002g0358a0003c0043t0001g0195a0004c0007t0001g0149others(6): Show | 9 | HG00544.hp1 HG02015.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2958-1233_2958-122 others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56049166 | |||||
| chr19:56049166
|
ATATT | A | 214 | a0001c0001t0001g0190a0001c0001t0001g0199a0001c0001t0001g0200others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.2958-1225_2958-122 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56049166 | |||||
| chr19:56049166
|
ATATTTAT others(5): Show |
A | 14 | a0003c0051t0001g0020a0004c0007t0001g0051a0004c0007t0001g0307others(11): Show | 14 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2958-1233_2958-122 others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56049166 | |||||
| chr19:56049201
|
C | T | 29 | a0001c0001t0001g0230a0001c0002t0001g0363a0001c0002t0001g0378others(26): Show | 29 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.2958-1217C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049201 | ||||||
| chr19:56049220
|
C | T | 162 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(159): Show | 162 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2958-1198C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049220 | ||||||
| chr19:56049305
|
G | A | 2 | a0001c0086t0001g0018a0002c0087t0002g0024 | 2 | HG00733.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2958-1113G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049305 | ||||||
| chr19:56049320
|
C | T | 1 | a0012c0065t0002g0005 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2958-1098C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049320 | ||||||
| chr19:56049336
|
C | T | 174 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(171): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2958-1082C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049336 | ||||||
| chr19:56049369
|
T | C | 162 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(159): Show | 162 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2958-1049T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049369 | ||||||
| chr19:56049518
|
C | G | 3 | a0007c0010t0001g0214a0008c0017t0001g0173a0008c0017t0001g0227 | 3 | HG01069.hp1 HG01070.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.2958-900C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049518 | ||||||
| chr19:56049554
|
C | T | 1 | a0007c0021t0001g0348 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2958-864C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049554 | ||||||
| chr19:56049556
|
C | A | 12 | a0003c0051t0001g0020a0004c0007t0001g0051a0004c0007t0001g0307others(9): Show | 12 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2958-862C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049556 | ||||||
| chr19:56049667
|
A | G | 162 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(159): Show | 162 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2958-751A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049667 | ||||||
| chr19:56049685
|
C | G | 6 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0137others(3): Show | 6 | HG00733.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2958-733C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049685 | ||||||
| chr19:56049750
|
G | A | 1 | a0001c0015t0001g0106 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2958-668G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049750 | ||||||
| chr19:56049773
|
C | T | 22 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(19): Show | 22 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.2958-645C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049773 | ||||||
| chr19:56049831
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2958-587A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049831 | ||||||
| chr19:56049902
|
G | T | 12 | a0003c0008t0003g0381a0004c0007t0003g0164a0004c0007t0003g0210others(9): Show | 12 | HG01192.hp2 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2958-516G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049902 | ||||||
| chr19:56049957
|
C | T | 8 | a0003c0043t0001g0195a0004c0007t0001g0149a0004c0020t0001g0268others(5): Show | 8 | HG00544.hp1 HG02015.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.2958-461C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049957 | ||||||
| chr19:56049975
|
G | A | 140 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(137): Show | 140 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.2958-443G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56049975 | ||||||
| chr19:56050008
|
G | A | 140 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(137): Show | 140 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.2958-410G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56050008 | ||||||
| chr19:56050034
|
C | T | 29 | a0001c0001t0001g0230a0001c0002t0001g0363a0001c0002t0001g0378others(26): Show | 29 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.2958-384C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56050034 | ||||||
| chr19:56050097
|
T | C | 12 | a0003c0051t0001g0020a0004c0007t0001g0051a0004c0007t0001g0307others(9): Show | 12 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2958-321T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56050097 | ||||||
| chr19:56050098
|
C | T | 1 | a0014c0102t0002g0287 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2958-320C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56050098 | ||||||
| chr19:56050153
|
G | A | 1 | a0016c0097t0001g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2958-265G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56050153 | ||||||
| chr19:56050276
|
C | CA | 134 | a0001c0001t0001g0160a0001c0001t0001g0190a0001c0001t0001g0199others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2958-130dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56050276 | |||||
| chr19:56050288
|
A | AAG | 104 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(101): Show | 104 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.2958-130_2958-129i others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56050288 | ||||||
| chr19:56050289
|
G | A | 107 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(104): Show | 107 | HG00423.hp2 HG00544.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.2958-129G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56050289 | ||||||
| chr19:56050383
|
A | G | 339 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(336): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.2958-35A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 11/14 | chr19 | 56050383 | ||||||
| chr19:56050606
|
G | A | 1 | a0007c0110t0001g0349 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3128+18G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56050606 | ||||||
| chr19:56050680
|
A | G | 1 | a0045c0131t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3128+92A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56050680 | ||||||
| chr19:56050739
|
A | G | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3128+151A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56050739 | ||||||
| chr19:56050740
|
G | A | 22 | a0001c0002t0001g0363a0001c0002t0001g0378a0003c0008t0001g0309others(19): Show | 22 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.3128+152G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56050740 | ||||||
| chr19:56050799
|
A | G | 140 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(137): Show | 140 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.3128+211A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56050799 | ||||||
| chr19:56050839
|
T | C | 12 | a0003c0051t0001g0020a0004c0007t0001g0051a0004c0007t0001g0307others(9): Show | 12 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3128+251T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56050839 | ||||||
| chr19:56051035
|
G | A | 1 | a0037c0091t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3128+447G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051035 | ||||||
| chr19:56051192
|
TTTTG | T | 16 | a0003c0051t0001g0020a0004c0007t0001g0051a0004c0007t0001g0307others(13): Show | 16 | HG01243.hp2 HG01515.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3128+616_3128+619d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 56051192 | |||||
| chr19:56051208
|
A | G | 2 | a0021c0048t0002g0193a0021c0048t0002g0198 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3128+620A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051208 | ||||||
| chr19:56051291
|
T | C | 297 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.3128+703T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051291 | ||||||
| chr19:56051296
|
G | A | 96 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(93): Show | 96 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.3128+708G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051296 | ||||||
| chr19:56051350
|
T | G | 202 | a0001c0001t0001g0160a0001c0001t0001g0190a0001c0001t0001g0199others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.3128+762T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051350 | ||||||
| chr19:56051353
|
C | A | 3 | a0005c0113t0001g0099a0030c0098t0001g0354a0041c0109t0001g0345 | 3 | HG02615.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3128+765C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051353 | ||||||
| chr19:56051354
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3128+766G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051354 | ||||||
| chr19:56051395
|
G | A | 190 | a0001c0001t0001g0160a0001c0001t0001g0190a0001c0001t0001g0199others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.3128+807G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051395 | ||||||
| chr19:56051440
|
A | G | 234 | a0001c0001t0001g0160a0001c0001t0001g0190a0001c0001t0001g0199others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.3128+852A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051440 | ||||||
| chr19:56051570
|
AC | A | 235 | a0001c0001t0001g0160a0001c0001t0001g0190a0001c0001t0001g0199others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.3128+989delC | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 56051570 | |||||
| chr19:56051676
|
A | C | 96 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(93): Show | 96 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.3128+1088A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051676 | ||||||
| chr19:56051800
|
C | A | 4 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3128+1212C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051800 | ||||||
| chr19:56051834
|
A | G | 105 | a0001c0001t0001g0160a0001c0001t0001g0190a0001c0001t0001g0199others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.3128+1246A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051834 | ||||||
| chr19:56051999
|
A | G | 27 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(24): Show | 27 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.3128+1411A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56051999 | ||||||
| chr19:56052019
|
A | T | 6 | a0001c0042t0001g0021a0001c0042t0001g0377a0003c0076t0002g0250others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3128+1431A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052019 | ||||||
| chr19:56052023
|
G | A | 12 | a0003c0051t0001g0020a0004c0007t0001g0051a0004c0007t0001g0307others(9): Show | 12 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3128+1435G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052023 | ||||||
| chr19:56052058
|
G | A | 2 | a0004c0050t0001g0328a0004c0050t0001g0329 | 2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3128+1470G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052058 | ||||||
| chr19:56052072
|
A | T | 22 | a0001c0002t0001g0363a0001c0002t0001g0378a0003c0008t0001g0309others(19): Show | 22 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.3128+1484A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052072 | ||||||
| chr19:56052101
|
C | T | 1 | a0008c0017t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3128+1513C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052101 | ||||||
| chr19:56052102
|
G | A | 2 | a0001c0003t0001g0140a0008c0028t0001g0396 | 2 | NA18986.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.3128+1514G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052102 | ||||||
| chr19:56052168
|
TTTTG | T | 8 | a0001c0002t0001g0032a0001c0002t0001g0043a0001c0002t0001g0050others(5): Show | 8 | HG01928.hp2 HG01934.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.3129-1462_3129-145 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 56052168 | |||||
| chr19:56052235
|
GGTTTT | G | 60 | a0001c0003t0001g0011a0001c0015t0001g0002a0001c0124t0001g0331others(57): Show | 60 | HG00597.hp2 HG01109.hp2 HG01175.hp1 others(57): Show |
intron_variant | MODIFIER | c.3129-1387_3129-138 others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 56052235 | |||||
| chr19:56052246
|
GTTTTGTT others(5): Show |
G | 22 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(19): Show | 22 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.3129-1377_3129-136 others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 56052246 | |||||
| chr19:56052284
|
T | C | 1 | a0037c0091t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3129-1354T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052284 | ||||||
| chr19:56052331
|
C | T | 2 | a0004c0070t0001g0069a0016c0129t0001g0100 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3129-1307C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052331 | ||||||
| chr19:56052373
|
A | G | 342 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(339): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.3129-1265A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052373 | ||||||
| chr19:56052422
|
C | A | 19 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(16): Show | 19 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.3129-1216C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052422 | ||||||
| chr19:56052501
|
C | T | 37 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(34): Show | 37 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.3129-1137C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052501 | ||||||
| chr19:56052524
|
C | T | 12 | a0003c0051t0001g0020a0004c0007t0001g0051a0004c0007t0001g0307others(9): Show | 12 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3129-1114C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052524 | ||||||
| chr19:56052583
|
A | G | 1 | a0045c0131t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3129-1055A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052583 | ||||||
| chr19:56052615
|
A | G | 44 | a0001c0002t0001g0363a0001c0002t0001g0378a0001c0022t0001g0356others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.3129-1023A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052615 | ||||||
| chr19:56052679
|
G | A | 2 | a0001c0092t0001g0211a0001c0115t0001g0040 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3129-959G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052679 | ||||||
| chr19:56052735
|
C | T | 6 | a0001c0002t0001g0148a0001c0002t0001g0151a0001c0002t0001g0393others(3): Show | 6 | HG01255.hp2 HG01261.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.3129-903C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052735 | ||||||
| chr19:56052866
|
C | G | 1 | a0001c0002t0001g0073 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3129-772C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052866 | ||||||
| chr19:56052878
|
C | T | 141 | a0001c0001t0001g0160a0001c0001t0001g0190a0001c0001t0001g0199others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.3129-760C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052878 | ||||||
| chr19:56052889
|
T | A | 1 | a0034c0066t0001g0219 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3129-749T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56052889 | ||||||
| chr19:56053088
|
C | A | 25 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(22): Show | 25 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.3129-550C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053088 | ||||||
| chr19:56053122
|
G | A | 1 | a0004c0080t0001g0019 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3129-516G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053122 | ||||||
| chr19:56053189
|
A | G | 1 | a0016c0097t0001g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3129-449A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053189 | ||||||
| chr19:56053265
|
C | T | 60 | a0001c0003t0001g0011a0001c0015t0001g0002a0001c0124t0001g0331others(57): Show | 60 | HG00597.hp2 HG01109.hp2 HG01175.hp1 others(57): Show |
intron_variant | MODIFIER | c.3129-373C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053265 | ||||||
| chr19:56053266
|
G | A | 22 | a0001c0042t0001g0021a0001c0042t0001g0377a0001c0092t0001g0211others(19): Show | 22 | HG01109.hp1 HG01243.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.3129-372G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053266 | ||||||
| chr19:56053288
|
G | C | 60 | a0001c0003t0001g0011a0001c0015t0001g0002a0001c0124t0001g0331others(57): Show | 60 | HG00597.hp2 HG01109.hp2 HG01175.hp1 others(57): Show |
intron_variant | MODIFIER | c.3129-350G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053288 | ||||||
| chr19:56053309
|
T | C | 2 | a0003c0024t0001g0239a0003c0122t0001g0276 | 2 | HG02027.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.3129-329T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053309 | ||||||
| chr19:56053338
|
G | C | 2 | a0021c0048t0002g0193a0021c0048t0002g0198 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3129-300G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053338 | ||||||
| chr19:56053372
|
G | A | 1 | a0007c0010t0001g0224 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3129-266G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053372 | ||||||
| chr19:56053396
|
C | CA | 143 | a0001c0001t0001g0160a0001c0001t0001g0190a0001c0001t0001g0199others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.3129-234dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 56053396 | |||||
| chr19:56053426
|
C | T | 1 | a0012c0018t0002g0152 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3129-212C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053426 | ||||||
| chr19:56053452
|
G | A | 62 | a0001c0003t0001g0011a0001c0015t0001g0002a0001c0124t0001g0331others(59): Show | 62 | HG00597.hp2 HG01109.hp2 HG01175.hp1 others(59): Show |
intron_variant | MODIFIER | c.3129-186G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053452 | ||||||
| chr19:56053487
|
A | G | 1 | a0003c0008t0001g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3129-151A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053487 | ||||||
| chr19:56053490
|
A | T | 1 | a0002c0012t0002g0003 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3129-148A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053490 | ||||||
| chr19:56053550
|
G | C | 91 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(88): Show | 91 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.3129-88G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053550 | ||||||
| chr19:56053583
|
G | A | 22 | a0001c0002t0001g0363a0001c0002t0001g0378a0003c0008t0001g0309others(19): Show | 22 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.3129-55G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053583 | ||||||
| chr19:56053606
|
G | A | 60 | a0001c0003t0001g0011a0001c0015t0001g0002a0001c0124t0001g0331others(57): Show | 60 | HG00597.hp2 HG01109.hp2 HG01175.hp1 others(57): Show |
intron_variant | MODIFIER | c.3129-32G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 12/14 | chr19 | 56053606 | ||||||
| chr19:56053833
|
C | T | 3 | a0001c0002t0001g0363a0008c0017t0001g0103a0008c0017t0001g0146 | 3 | HG02451.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3299+25C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56053833 | ||||||
| chr19:56053849
|
G | A | 2 | a0001c0092t0001g0211a0001c0115t0001g0040 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3299+41G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56053849 | ||||||
| chr19:56053867
|
A | T | 154 | a0001c0001t0001g0160a0001c0001t0001g0190a0001c0001t0001g0199others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.3299+59A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56053867 | ||||||
| chr19:56053924
|
G | C | 1 | a0001c0015t0001g0084 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3299+116G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56053924 | ||||||
| chr19:56053946
|
A | G | 22 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(19): Show | 22 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.3299+138A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56053946 | ||||||
| chr19:56053947
|
C | T | 4 | a0009c0013t0001g0350a0009c0013t0001g0351a0009c0013t0001g0352others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3299+139C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56053947 | ||||||
| chr19:56053969
|
C | T | 22 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(19): Show | 22 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.3299+161C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56053969 | ||||||
| chr19:56053992
|
C | T | 1 | a0001c0085t0001g0236 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3299+184C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56053992 | ||||||
| chr19:56053993
|
G | A | 1 | a0003c0077t0001g0379 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3299+185G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56053993 | ||||||
| chr19:56054044
|
A | G | 2 | a0008c0037t0001g0004a0008c0037t0001g0009 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.3299+236A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054044 | ||||||
| chr19:56054090
|
C | T | 26 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(23): Show | 26 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.3299+282C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054090 | ||||||
| chr19:56054115
|
T | TTG | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068 | 3 | HG02258.hp2 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3299+311_3299+312d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054115 | |||||
| chr19:56054150
|
G | A | 1 | a0016c0097t0001g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3299+342G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054150 | ||||||
| chr19:56054259
|
G | A | 252 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.3299+451G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054259 | ||||||
| chr19:56054270
|
T | C | 2 | a0016c0097t0001g0107a0037c0091t0001g0167 | 2 | HG01192.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3299+462T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054270 | ||||||
| chr19:56054289
|
G | A | 4 | a0001c0014t0001g0120a0004c0080t0001g0019a0010c0027t0001g0170others(1): Show | 4 | HG01099.hp1 HG01192.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.3299+481G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054289 | ||||||
| chr19:56054304
|
C | T | 4 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3299+496C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054304 | ||||||
| chr19:56054305
|
A | G | 273 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.3299+497A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054305 | ||||||
| chr19:56054386
|
T | C | 7 | a0004c0070t0001g0069a0009c0013t0001g0350a0009c0013t0001g0351others(4): Show | 7 | HG02630.hp1 HG02818.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.3299+578T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054386 | ||||||
| chr19:56054417
|
G | T | 5 | a0001c0042t0001g0021a0001c0042t0001g0377a0003c0076t0002g0250others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.3299+609G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054417 | ||||||
| chr19:56054511
|
C | G | 64 | a0001c0003t0001g0011a0001c0015t0001g0002a0001c0022t0001g0356others(61): Show | 64 | HG00438.hp2 HG00597.hp2 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.3299+703C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054511 | ||||||
| chr19:56054530
|
C | T | 1 | a0003c0024t0001g0239 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3299+722C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054530 | ||||||
| chr19:56054531
|
T | G | 1 | a0003c0024t0001g0239 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3299+723T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054531 | ||||||
| chr19:56054558
|
A | G | 10 | a0003c0043t0001g0123a0003c0043t0001g0195a0003c0111t0001g0291others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.3299+750A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054558 | ||||||
| chr19:56054566
|
T | TG | 3 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254 | 3 | HG02970.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3299+759dupG | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054566 | |||||
| chr19:56054567
|
G | GA | 14 | a0005c0006t0001g0104a0005c0006t0001g0163a0005c0034t0001g0338others(11): Show | 14 | HG00673.hp1 HG02630.hp1 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.3299+776dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054567 | |||||
| chr19:56054567
|
GA | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(44): Show | 47 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.3299+776delA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054567 | |||||
| chr19:56054567
|
GAA | G | 114 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.3299+775_3299+776d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054567 | |||||
| chr19:56054567
|
GAAA | G | 105 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3299+774_3299+776d others(5): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054567 | |||||
| chr19:56054567
|
GAAAA | G | 67 | a0001c0003t0001g0011a0001c0015t0001g0002a0001c0022t0001g0356others(64): Show | 67 | HG00438.hp2 HG00597.hp2 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.3299+773_3299+776d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054567 | |||||
| chr19:56054666
|
G | T | 11 | a0001c0001t0001g0353a0001c0019t0001g0065a0001c0019t0001g0066others(8): Show | 11 | HG01884.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.3299+858G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054666 | ||||||
| chr19:56054672
|
A | C | 4 | a0002c0012t0002g0014a0006c0005t0002g0308a0006c0005t0002g0369others(1): Show | 4 | NA18941.hp1 NA18954.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.3299+864A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054672 | ||||||
| chr19:56054699
|
C | G | 1 | a0001c0003t0001g0141 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3299+891C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054699 | ||||||
| chr19:56054703
|
C | T | 1 | a0028c0093t0001g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3299+895C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054703 | ||||||
| chr19:56054714
|
A | G | 60 | a0001c0003t0001g0011a0001c0015t0001g0002a0001c0022t0001g0356others(57): Show | 60 | HG00438.hp2 HG00597.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.3299+906A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054714 | ||||||
| chr19:56054752
|
A | G | 32 | a0001c0002t0001g0363a0003c0008t0001g0245a0003c0008t0001g0246others(29): Show | 32 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.3299+944A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054752 | ||||||
| chr19:56054761
|
G | C | 3 | a0001c0002t0001g0378a0007c0021t0001g0348a0007c0073t0001g0218 | 3 | HG02647.hp2 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3299+953G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054761 | ||||||
| chr19:56054765
|
C | T | 67 | a0001c0003t0001g0011a0001c0015t0001g0002a0001c0124t0001g0331others(64): Show | 67 | HG00438.hp2 HG00597.hp2 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.3299+957C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054765 | ||||||
| chr19:56054847
|
C | G | 1 | a0037c0091t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3299+1039C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054847 | ||||||
| chr19:56054980
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3299+1172G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56054980 | ||||||
| chr19:56054992
|
C | CT | 14 | a0005c0006t0001g0163a0005c0006t0001g0238a0005c0025t0001g0150others(11): Show | 14 | HG02071.hp2 HG02145.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.3299+1209dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054992 | |||||
| chr19:56054992
|
CT | C | 59 | a0001c0001t0001g0038a0001c0001t0001g0091a0001c0002t0001g0043others(56): Show | 59 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.3299+1209delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054992 | |||||
| chr19:56054992
|
CTT | C | 190 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0068others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.3299+1208_3299+120 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054992 | |||||
| chr19:56054992
|
CTTT | C | 6 | a0001c0003t0001g0011a0001c0056t0001g0382a0002c0004t0002g0166others(3): Show | 6 | HG01256.hp1 HG04184.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.3299+1207_3299+120 others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054992 | |||||
| chr19:56054992
|
CTTTT | C | 27 | a0001c0001t0001g0230a0001c0014t0001g0022a0001c0014t0001g0048others(24): Show | 27 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.3299+1206_3299+120 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054992 | |||||
| chr19:56054992
|
CTTTTT | C | 16 | a0001c0002t0001g0378a0001c0056t0001g0384a0003c0008t0001g0119others(13): Show | 16 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.3299+1205_3299+120 others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054992 | |||||
| chr19:56054992
|
CTTTTTT | C | 28 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(25): Show | 28 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.3299+1204_3299+120 others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56054992 | |||||
| chr19:56055019
|
A | G | 1 | a0007c0010t0001g0385 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3299+1211A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055019 | ||||||
| chr19:56055091
|
C | A | 1 | a0009c0013t0001g0126 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3299+1283C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055091 | ||||||
| chr19:56055189
|
A | G | 12 | a0001c0001t0001g0160a0001c0001t0001g0199a0001c0002t0001g0042others(9): Show | 12 | HG01261.hp1 HG01928.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.3299+1381A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055189 | ||||||
| chr19:56055194
|
G | A | 2 | a0001c0002t0001g0378a0007c0073t0001g0218 | 2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3299+1386G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055194 | ||||||
| chr19:56055219
|
T | A | 4 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3299+1411T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055219 | ||||||
| chr19:56055284
|
G | A | 6 | a0003c0008t0001g0309a0003c0008t0001g0310a0003c0008t0001g0311others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3299+1476G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055284 | ||||||
| chr19:56055352
|
C | G | 1 | a0001c0002t0001g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3299+1544C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055352 | ||||||
| chr19:56055363
|
A | G | 20 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(17): Show | 20 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.3299+1555A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055363 | ||||||
| chr19:56055375
|
G | A | 101 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(98): Show | 101 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.3299+1567G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055375 | ||||||
| chr19:56055423
|
A | G | 9 | a0003c0043t0001g0123a0003c0043t0001g0195a0003c0111t0001g0291others(6): Show | 9 | HG00544.hp1 HG00597.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.3299+1615A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055423 | ||||||
| chr19:56055492
|
C | T | 2 | a0007c0032t0001g0017a0007c0032t0001g0327 | 2 | HG01346.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.3299+1684C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055492 | ||||||
| chr19:56055531
|
CTCTG | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0217others(1): Show | 4 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3299+1727_3299+173 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055531 | |||||
| chr19:56055533
|
C | CTTTT | 4 | a0001c0001t0001g0216a0001c0001t0001g0387a0001c0002t0001g0108others(1): Show | 4 | HG01070.hp2 HG01169.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.3299+1726_3299+172 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055533 | |||||
| chr19:56055533
|
C | CTTTTT | 13 | a0001c0001t0001g0049a0001c0001t0001g0110a0001c0001t0001g0117others(10): Show | 13 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.3299+1726_3299+172 others(9): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055533 | |||||
| chr19:56055533
|
C | CTTTTTTT | 6 | a0001c0001t0001g0047a0001c0001t0001g0174a0001c0001t0001g0264others(3): Show | 6 | HG00735.hp1 HG01106.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3299+1726_3299+172 others(11): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055533 | |||||
| chr19:56055533
|
CTG | C | 4 | a0001c0001t0001g0091a0001c0009t0001g0286a0002c0012t0002g0240others(1): Show | 4 | HG02027.hp2 HG02523.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.3299+1727_3299+172 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055533 | |||||
| chr19:56055533
|
CTGTCTTT | C | 9 | a0003c0008t0001g0119a0003c0008t0001g0265a0003c0045t0001g0266others(6): Show | 9 | HG02145.hp2 HG02970.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.3299+1727_3299+173 others(11): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055533 | |||||
| chr19:56055533
|
CTGTCTTT others(4): Show |
C | 1 | a0001c0124t0001g0331 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.3299+1727_3299+173 others(15): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055533 | |||||
| chr19:56055533
|
CTGTCTTT others(5): Show |
C | 1 | a0001c0003t0001g0011 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3299+1727_3299+173 others(16): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055533 | |||||
| chr19:56055534
|
TGTC | T | 44 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0039others(41): Show | 44 | HG00423.hp2 HG00544.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.3299+1727_3299+172 others(7): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055534 | ||||||
| chr19:56055535
|
G | C | 2 | a0007c0010t0001g0235a0015c0044t0002g0188 | 2 | NA18952.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3299+1727G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055535 | ||||||
| chr19:56055535
|
G | T | 27 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(24): Show | 27 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.3299+1727G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055535 | ||||||
| chr19:56055537
|
C | CT | 99 | a0001c0001t0001g0190a0001c0001t0001g0199a0001c0001t0001g0200others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.3299+1755dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055537 | |||||
| chr19:56055537
|
C | CTT | 21 | a0001c0002t0001g0041a0001c0002t0001g0393a0001c0003t0001g0111others(18): Show | 21 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.3299+1754_3299+175 others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055537 | |||||
| chr19:56055537
|
C | CTTTTTTT others(1): Show |
13 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0171others(10): Show | 13 | HG00323.hp2 HG00735.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.3299+1748_3299+175 others(12): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055537 | |||||
| chr19:56055537
|
C | CTTTTTTT others(2): Show |
9 | a0001c0014t0001g0120a0001c0014t0001g0362a0001c0030t0001g0318others(6): Show | 9 | HG00323.hp1 HG01074.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.3299+1747_3299+175 others(13): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055537 | |||||
| chr19:56055537
|
C | CTTTTTTT others(3): Show |
4 | a0003c0008t0003g0381a0004c0053t0003g0317a0007c0071t0001g0178others(1): Show | 4 | HG02257.hp2 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3299+1746_3299+175 others(14): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055537 | |||||
| chr19:56055537
|
C | T | 27 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(24): Show | 27 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.3299+1729C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055537 | ||||||
| chr19:56055537
|
CT | C | 23 | a0001c0002t0001g0363a0001c0022t0001g0356a0001c0042t0001g0021others(20): Show | 23 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.3299+1755delT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055537 | |||||
| chr19:56055537
|
CTTTTTT | C | 6 | a0002c0004t0002g0196a0003c0076t0002g0250a0006c0005t0002g0369others(3): Show | 6 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.3299+1750_3299+175 others(10): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055537 | |||||
| chr19:56055537
|
CTTTTTTT | C | 52 | a0001c0015t0001g0002a0002c0004t0002g0166a0002c0004t0002g0176others(49): Show | 52 | HG00438.hp2 HG00597.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.3299+1749_3299+175 others(11): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56055537 | |||||
| chr19:56055538
|
T | C | 44 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0039others(41): Show | 44 | HG00423.hp2 HG00544.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.3299+1730T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055538 | ||||||
| chr19:56055539
|
T | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0217others(1): Show | 4 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3299+1731T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055539 | ||||||
| chr19:56055564
|
A | G | 1 | a0005c0025t0001g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3299+1756A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055564 | ||||||
| chr19:56055568
|
T | C | 1 | a0005c0025t0001g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3299+1760T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055568 | ||||||
| chr19:56055569
|
A | G | 1 | a0005c0025t0001g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3299+1761A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055569 | ||||||
| chr19:56055571
|
A | G | 19 | a0001c0014t0001g0022a0001c0014t0001g0048a0001c0014t0001g0120others(16): Show | 19 | HG00323.hp1 HG00323.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.3299+1763A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055571 | ||||||
| chr19:56055573
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3299+1765T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055573 | ||||||
| chr19:56055582
|
G | A | 1 | a0044c0107t0001g0344 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3299+1774G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055582 | ||||||
| chr19:56055585
|
C | A | 1 | a0011c0038t0001g0006 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3299+1777C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055585 | ||||||
| chr19:56055600
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0174a0001c0001t0001g0215others(1): Show | 4 | HG01106.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3299+1792C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055600 | ||||||
| chr19:56055603
|
T | C | 4 | a0009c0013t0001g0350a0009c0013t0001g0351a0009c0013t0001g0352others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3299+1795T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055603 | ||||||
| chr19:56055655
|
C | T | 26 | a0003c0008t0001g0245a0003c0008t0001g0246a0003c0008t0001g0247others(23): Show | 26 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.3299+1847C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055655 | ||||||
| chr19:56055671
|
A | G | 99 | a0001c0001t0001g0160a0001c0001t0001g0190a0001c0001t0001g0199others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.3299+1863A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055671 | ||||||
| chr19:56055690
|
T | C | 38 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.3299+1882T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055690 | ||||||
| chr19:56055691
|
G | C | 1 | a0006c0011t0002g0191 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3299+1883G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055691 | ||||||
| chr19:56055694
|
C | T | 1 | a0037c0091t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3299+1886C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055694 | ||||||
| chr19:56055702
|
C | T | 68 | a0001c0002t0001g0032a0001c0002t0001g0079a0001c0003t0001g0011others(65): Show | 68 | HG00438.hp2 HG00597.hp2 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.3299+1894C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055702 | ||||||
| chr19:56055707
|
G | A | 67 | a0001c0002t0001g0032a0001c0002t0001g0079a0001c0003t0001g0011others(64): Show | 67 | HG00438.hp2 HG00597.hp2 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.3299+1899G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055707 | ||||||
| chr19:56055733
|
G | C | 3 | a0001c0042t0001g0021a0001c0042t0001g0377a0001c0085t0001g0236 | 3 | HG02258.hp1 HG03516.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.3299+1925G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055733 | ||||||
| chr19:56055735
|
C | T | 3 | a0001c0042t0001g0021a0001c0042t0001g0377a0001c0085t0001g0236 | 3 | HG02258.hp1 HG03516.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.3299+1927C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055735 | ||||||
| chr19:56055736
|
G | A | 17 | a0004c0007t0001g0136a0004c0007t0001g0139a0004c0007t0001g0149others(14): Show | 17 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.3299+1928G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055736 | ||||||
| chr19:56055747
|
G | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0001t0001g0215others(1): Show | 4 | HG01943.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3299+1939G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055747 | ||||||
| chr19:56055759
|
A | C | 1 | a0002c0012t0002g0003 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3299+1951A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055759 | ||||||
| chr19:56055761
|
G | A | 1 | a0005c0006t0001g0056 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3299+1953G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055761 | ||||||
| chr19:56055762
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3299+1954G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055762 | ||||||
| chr19:56055767
|
A | G | 24 | a0001c0001t0001g0133a0001c0001t0001g0137a0001c0001t0001g0138others(21): Show | 24 | HG00099.hp1 HG01256.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.3299+1959A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055767 | ||||||
| chr19:56055780
|
C | G | 1 | a0033c0061t0001g0256 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3299+1972C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055780 | ||||||
| chr19:56055781
|
A | G | 20 | a0001c0002t0001g0158a0001c0002t0001g0378a0001c0015t0001g0046others(17): Show | 20 | HG00099.hp1 HG00140.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.3299+1973A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055781 | ||||||
| chr19:56055787
|
T | C | 16 | a0001c0002t0001g0158a0001c0002t0001g0378a0002c0012t0002g0223others(13): Show | 16 | HG02027.hp1 HG02129.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.3299+1979T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055787 | ||||||
| chr19:56055788
|
G | A | 2 | a0003c0045t0001g0090a0003c0126t0001g0012 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3299+1980G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055788 | ||||||
| chr19:56055791
|
C | T | 8 | a0003c0051t0001g0020a0004c0007t0001g0307a0004c0035t0001g0094others(5): Show | 8 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3299+1983C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055791 | ||||||
| chr19:56055792
|
G | A | 6 | a0003c0045t0001g0090a0003c0126t0001g0012a0007c0010t0001g0385others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3299+1984G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055792 | ||||||
| chr19:56055796
|
T | C | 11 | a0001c0002t0001g0378a0003c0045t0001g0090a0003c0126t0001g0012others(8): Show | 11 | HG01069.hp1 HG01070.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.3299+1988T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055796 | ||||||
| chr19:56055797
|
G | A | 2 | a0001c0002t0001g0378a0007c0073t0001g0218 | 2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3299+1989G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055797 | ||||||
| chr19:56055808
|
G | C | 2 | a0001c0001t0001g0091a0007c0010t0001g0036 | 2 | NA18948.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.3299+2000G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055808 | ||||||
| chr19:56055816
|
A | G | 4 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3299+2008A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055816 | ||||||
| chr19:56055825
|
A | G | 2 | a0003c0118t0001g0357a0010c0027t0001g0319 | 2 | HG02559.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.3299+2017A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055825 | ||||||
| chr19:56055827
|
A | G | 2 | a0003c0118t0001g0357a0010c0027t0001g0319 | 2 | HG02559.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.3299+2019A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055827 | ||||||
| chr19:56055835
|
G | A | 2 | a0001c0001t0001g0190a0001c0052t0001g0026 | 2 | HG01169.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3299+2027G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055835 | ||||||
| chr19:56055866
|
C | T | 64 | a0001c0003t0001g0011a0001c0019t0001g0065a0001c0124t0001g0331others(61): Show | 64 | HG00438.hp2 HG00597.hp2 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.3299+2058C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055866 | ||||||
| chr19:56055888
|
T | C | 2 | a0003c0045t0001g0090a0003c0126t0001g0012 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3299+2080T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055888 | ||||||
| chr19:56055894
|
G | C | 4 | a0002c0012t0002g0014a0006c0005t0002g0308a0006c0005t0002g0369others(1): Show | 4 | NA18941.hp1 NA18954.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.3299+2086G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055894 | ||||||
| chr19:56055944
|
C | T | 22 | a0001c0002t0001g0363a0001c0014t0001g0022a0001c0014t0001g0048others(19): Show | 22 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.3299+2136C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055944 | ||||||
| chr19:56055976
|
G | C | 1 | a0034c0066t0001g0219 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3299+2168G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56055976 | ||||||
| chr19:56056000
|
G | C | 34 | a0003c0008t0001g0245a0003c0008t0001g0246a0003c0008t0001g0247others(31): Show | 34 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.3299+2192G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056000 | ||||||
| chr19:56056029
|
G | A | 1 | a0001c0084t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3300-2211G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056029 | ||||||
| chr19:56056280
|
G | A | 1 | a0002c0116t0002g0330 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3300-1960G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056280 | ||||||
| chr19:56056307
|
C | T | 57 | a0001c0002t0001g0363a0001c0014t0001g0022a0001c0014t0001g0048others(54): Show | 57 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.3300-1933C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056307 | ||||||
| chr19:56056326
|
G | C | 3 | a0003c0076t0002g0250a0003c0114t0002g0347a0016c0097t0001g0107 | 3 | HG01109.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3300-1914G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056326 | ||||||
| chr19:56056355
|
C | A | 1 | a0002c0004t0002g0259 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3300-1885C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056355 | ||||||
| chr19:56056377
|
G | C | 96 | a0001c0002t0001g0063a0002c0004t0002g0059a0002c0004t0002g0124others(93): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.3300-1863G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056377 | ||||||
| chr19:56056425
|
C | T | 1 | a0001c0085t0001g0236 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3300-1815C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056425 | ||||||
| chr19:56056426
|
G | A | 23 | a0003c0008t0003g0381a0003c0043t0001g0123a0003c0043t0001g0195others(20): Show | 23 | HG00544.hp1 HG00597.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.3300-1814G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056426 | ||||||
| chr19:56056547
|
A | G | 1 | a0001c0002t0001g0043 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3300-1693A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056547 | ||||||
| chr19:56056548
|
C | G | 1 | a0009c0013t0001g0061 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3300-1692C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056548 | ||||||
| chr19:56056549
|
T | A | 1 | a0009c0013t0001g0061 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3300-1691T>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056549 | ||||||
| chr19:56056557
|
T | TA | 4 | a0002c0004t0002g0059a0006c0128t0002g0339a0012c0018t0002g0033others(1): Show | 4 | HG00140.hp2 HG01081.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.3300-1677dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56056557 | |||||
| chr19:56056564
|
C | A | 87 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(84): Show | 87 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.3300-1676C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056564 | ||||||
| chr19:56056639
|
A | G | 90 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(87): Show | 90 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.3300-1601A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056639 | ||||||
| chr19:56056721
|
T | C | 1 | a0001c0056t0001g0384 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3300-1519T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056721 | ||||||
| chr19:56056792
|
C | T | 4 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3300-1448C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056792 | ||||||
| chr19:56056793
|
G | A | 1 | a0001c0056t0001g0382 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3300-1447G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056793 | ||||||
| chr19:56056827
|
C | T | 1 | a0004c0007t0001g0325 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3300-1413C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056827 | ||||||
| chr19:56056877
|
C | T | 130 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(127): Show | 130 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.3300-1363C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056877 | ||||||
| chr19:56056934
|
G | A | 21 | a0003c0008t0003g0381a0003c0043t0001g0123a0003c0043t0001g0195others(18): Show | 21 | HG00544.hp1 HG00597.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.3300-1306G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056934 | ||||||
| chr19:56056969
|
G | A | 6 | a0003c0008t0003g0381a0004c0007t0003g0164a0004c0007t0003g0210others(3): Show | 6 | HG02257.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3300-1271G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056969 | ||||||
| chr19:56056973
|
A | G | 90 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(87): Show | 90 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.3300-1267A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056973 | ||||||
| chr19:56056991
|
T | C | 6 | a0003c0045t0001g0090a0003c0126t0001g0012a0007c0010t0001g0385others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3300-1249T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056991 | ||||||
| chr19:56056996
|
C | T | 22 | a0001c0002t0001g0363a0001c0014t0001g0022a0001c0014t0001g0048others(19): Show | 22 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.3300-1244C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56056996 | ||||||
| chr19:56057011
|
T | C | 238 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(235): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.3300-1229T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057011 | ||||||
| chr19:56057056
|
A | G | 1 | a0001c0009t0001g0283 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3300-1184A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057056 | ||||||
| chr19:56057083
|
T | C | 160 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(157): Show | 160 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.3300-1157T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057083 | ||||||
| chr19:56057084
|
C | T | 8 | a0003c0051t0001g0020a0004c0007t0001g0307a0004c0035t0001g0094others(5): Show | 8 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3300-1156C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057084 | ||||||
| chr19:56057091
|
G | A | 1 | a0037c0091t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3300-1149G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057091 | ||||||
| chr19:56057095
|
C | T | 1 | a0004c0053t0003g0317 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3300-1145C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057095 | ||||||
| chr19:56057100
|
C | T | 1 | a0016c0097t0001g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3300-1140C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057100 | ||||||
| chr19:56057130
|
A | G | 3 | a0003c0118t0001g0357a0004c0070t0001g0069a0016c0129t0001g0100 | 3 | HG02559.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3300-1110A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057130 | ||||||
| chr19:56057173
|
T | G | 2 | a0004c0035t0001g0094a0004c0035t0001g0095 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.3300-1067T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057173 | ||||||
| chr19:56057195
|
C | A | 1 | a0007c0021t0001g0302 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3300-1045C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057195 | ||||||
| chr19:56057199
|
C | T | 56 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0110others(53): Show | 56 | HG00099.hp2 HG00438.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.3300-1041C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057199 | ||||||
| chr19:56057314
|
C | T | 2 | a0013c0026t0002g0143a0013c0026t0002g0228 | 2 | HG00609.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.3300-926C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057314 | ||||||
| chr19:56057388
|
ACC | A | 90 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(87): Show | 90 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.3300-850_3300-849d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56057388 | |||||
| chr19:56057484
|
C | A | 42 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.3300-756C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057484 | ||||||
| chr19:56057536
|
A | C | 90 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(87): Show | 90 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.3300-704A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057536 | ||||||
| chr19:56057536
|
A | G | 6 | a0001c0002t0001g0363a0001c0019t0001g0066a0001c0022t0001g0356others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3300-704A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057536 | ||||||
| chr19:56057547
|
C | T | 8 | a0003c0051t0001g0020a0004c0007t0001g0307a0004c0035t0001g0094others(5): Show | 8 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3300-693C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057547 | ||||||
| chr19:56057612
|
T | C | 90 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(87): Show | 90 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.3300-628T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057612 | ||||||
| chr19:56057657
|
A | G | 2 | a0003c0045t0001g0090a0003c0126t0001g0012 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3300-583A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057657 | ||||||
| chr19:56057715
|
C | T | 3 | a0005c0113t0001g0099a0030c0098t0001g0354a0041c0109t0001g0345 | 3 | HG02615.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3300-525C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057715 | ||||||
| chr19:56057725
|
G | A | 1 | a0005c0025t0001g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3300-515G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057725 | ||||||
| chr19:56057796
|
C | T | 4 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3300-444C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057796 | ||||||
| chr19:56057922
|
G | T | 1 | a0003c0008t0001g0310 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3300-318G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057922 | ||||||
| chr19:56057941
|
C | T | 1 | a0003c0024t0001g0025 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3300-299C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057941 | ||||||
| chr19:56057942
|
G | A | 1 | a0004c0080t0001g0019 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3300-298G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56057942 | ||||||
| chr19:56058028
|
C | CA | 58 | a0001c0001t0001g0007a0001c0001t0001g0049a0001c0001t0001g0199others(55): Show | 58 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.3300-196dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56058028 | |||||
| chr19:56058028
|
C | CAA | 37 | a0001c0014t0001g0120a0001c0015t0001g0045a0003c0008t0001g0245others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.3300-197_3300-196d others(4): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56058028 | |||||
| chr19:56058028
|
C | CAAAA | 6 | a0003c0051t0001g0020a0004c0007t0001g0307a0004c0050t0001g0328others(3): Show | 6 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3300-199_3300-196d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56058028 | |||||
| chr19:56058028
|
CAAAA | C | 6 | a0003c0008t0003g0381a0004c0007t0003g0164a0004c0007t0003g0210others(3): Show | 6 | HG02257.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.3300-199_3300-196d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56058028 | |||||
| chr19:56058045
|
G | A | 4 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3300-195G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56058045 | ||||||
| chr19:56058048
|
G | A | 1 | a0001c0086t0001g0018 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3300-192G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56058048 | ||||||
| chr19:56058124
|
TTTTTG | T | 8 | a0003c0051t0001g0020a0004c0007t0001g0307a0004c0035t0001g0094others(5): Show | 8 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3300-101_3300-97de others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56058124 | |||||
| chr19:56058200
|
C | T | 12 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(9): Show | 12 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3300-40C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56058200 | ||||||
| chr19:56058230
|
G | C | 12 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(9): Show | 12 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3300-10G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 13/14 | chr19 | 56058230 | ||||||
| chr19:56058462
|
C | G | 23 | a0003c0008t0003g0381a0003c0043t0001g0123a0003c0043t0001g0195others(20): Show | 23 | HG00544.hp1 HG00597.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.3470+52C>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058462 | ||||||
| chr19:56058476
|
G | A | 1 | a0005c0006t0001g0056 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3470+66G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058476 | ||||||
| chr19:56058503
|
G | A | 1 | a0001c0056t0001g0384 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3470+93G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058503 | ||||||
| chr19:56058551
|
G | A | 53 | a0001c0001t0001g0047a0001c0001t0001g0110a0001c0001t0001g0117others(50): Show | 53 | HG00099.hp2 HG00438.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.3470+141G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058551 | ||||||
| chr19:56058595
|
G | C | 1 | a0016c0097t0001g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3470+185G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058595 | ||||||
| chr19:56058596
|
A | T | 1 | a0016c0097t0001g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3470+186A>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058596 | ||||||
| chr19:56058614
|
A | C | 1 | a0003c0122t0001g0276 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3470+204A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058614 | ||||||
| chr19:56058698
|
T | C | 1 | a0001c0086t0001g0018 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3470+288T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058698 | ||||||
| chr19:56058810
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3470+400G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058810 | ||||||
| chr19:56058831
|
G | A | 40 | a0001c0002t0001g0363a0001c0014t0001g0022a0001c0014t0001g0048others(37): Show | 40 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.3470+421G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058831 | ||||||
| chr19:56058847
|
G | A | 89 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(86): Show | 89 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.3470+437G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058847 | ||||||
| chr19:56058870
|
A | G | 3 | a0001c0002t0001g0032a0001c0002t0001g0079a0001c0015t0001g0045 | 3 | HG03017.hp2 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.3470+460A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058870 | ||||||
| chr19:56058936
|
C | T | 1 | a0012c0065t0002g0005 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3470+526C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058936 | ||||||
| chr19:56058986
|
C | A | 1 | a0037c0091t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3470+576C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058986 | ||||||
| chr19:56058987
|
G | C | 1 | a0037c0091t0001g0167 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3470+577G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56058987 | ||||||
| chr19:56059191
|
T | G | 1 | a0011c0039t0001g0093 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3470+781T>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56059191 | ||||||
| chr19:56059192
|
C | T | 1 | a0011c0039t0001g0093 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3470+782C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56059192 | ||||||
| chr19:56059226
|
C | T | 36 | a0003c0008t0001g0245a0003c0008t0001g0246a0003c0008t0001g0247others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.3470+816C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56059226 | ||||||
| chr19:56059333
|
A | C | 5 | a0009c0013t0001g0350a0009c0013t0001g0351a0009c0013t0001g0352others(2): Show | 5 | HG02630.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.3470+923A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56059333 | ||||||
| chr19:56059384
|
G | A | 1 | a0003c0024t0001g0025 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3470+974G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56059384 | ||||||
| chr19:56059430
|
C | T | 1 | a0003c0008t0001g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3470+1020C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56059430 | ||||||
| chr19:56059482
|
G | A | 89 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(86): Show | 89 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.3470+1072G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56059482 | ||||||
| chr19:56059554
|
A | G | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(2): Show | 5 | HG02258.hp1 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.3470+1144A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56059554 | ||||||
| chr19:56059678
|
G | A | 42 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0091others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.3470+1268G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56059678 | ||||||
| chr19:56059692
|
G | A | 9 | a0003c0008t0003g0381a0004c0007t0003g0164a0004c0007t0003g0210others(6): Show | 9 | HG02257.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.3470+1282G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56059692 | ||||||
| chr19:56059793
|
T | TG | 14 | a0003c0008t0003g0381a0003c0045t0001g0090a0003c0118t0001g0357others(11): Show | 14 | HG02257.hp2 HG02486.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.3470+1385dupG | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56059793 | |||||
| chr19:56059934
|
C | T | 1 | a0001c0019t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3471-1462C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56059934 | ||||||
| chr19:56059949
|
G | C | 3 | a0007c0010t0001g0385a0007c0010t0001g0391a0007c0032t0001g0254 | 3 | HG02970.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3471-1447G>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56059949 | ||||||
| chr19:56060133
|
G | A | 8 | a0003c0051t0001g0020a0004c0007t0001g0307a0004c0035t0001g0094others(5): Show | 8 | HG01243.hp2 HG01515.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3471-1263G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060133 | ||||||
| chr19:56060181
|
A | C | 22 | a0001c0002t0001g0363a0001c0014t0001g0022a0001c0014t0001g0048others(19): Show | 22 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.3471-1215A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060181 | ||||||
| chr19:56060186
|
G | A | 22 | a0001c0002t0001g0363a0001c0014t0001g0022a0001c0014t0001g0048others(19): Show | 22 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.3471-1210G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060186 | ||||||
| chr19:56060293
|
GTTTA | G | 5 | a0001c0002t0001g0148a0001c0002t0001g0151a0001c0046t0001g0261others(2): Show | 5 | HG01255.hp2 HG01261.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.3471-1099_3471-109 others(8): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56060293 | |||||
| chr19:56060301
|
C | A | 1 | a0015c0044t0002g0153 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3471-1095C>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060301 | ||||||
| chr19:56060362
|
A | G | 246 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0038others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.3471-1034A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060362 | ||||||
| chr19:56060478
|
C | T | 48 | a0001c0001t0001g0047a0001c0001t0001g0110a0001c0001t0001g0117others(45): Show | 48 | HG00099.hp2 HG00438.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.3471-918C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060478 | ||||||
| chr19:56060479
|
G | A | 89 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(86): Show | 89 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.3471-917G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060479 | ||||||
| chr19:56060556
|
C | T | 10 | a0001c0001t0001g0353a0001c0019t0001g0118a0001c0019t0001g0122others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.3471-840C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060556 | ||||||
| chr19:56060584
|
A | G | 12 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(9): Show | 12 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3471-812A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060584 | ||||||
| chr19:56060718
|
G | GT | 89 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(86): Show | 89 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.3471-671dupT | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56060718 | |||||
| chr19:56060725
|
T | TA | 3 | a0012c0018t0002g0033a0012c0018t0002g0389a0018c0036t0002g0035 | 3 | HG03669.hp1 HG03688.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3471-670dupA | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56060725 | |||||
| chr19:56060799
|
G | A | 12 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(9): Show | 12 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3471-597G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060799 | ||||||
| chr19:56060835
|
C | T | 43 | a0003c0008t0001g0119a0003c0008t0001g0245a0003c0008t0001g0246others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.3471-561C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060835 | ||||||
| chr19:56060917
|
A | G | 4 | a0001c0023t0001g0248a0001c0023t0001g0249a0001c0023t0001g0314others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3471-479A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060917 | ||||||
| chr19:56060967
|
T | C | 89 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(86): Show | 89 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.3471-429T>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56060967 | ||||||
| chr19:56061014
|
A | G | 12 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0068others(9): Show | 12 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3471-382A>G | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56061014 | ||||||
| chr19:56061018
|
TTATC | T | 48 | a0001c0001t0001g0047a0001c0001t0001g0110a0001c0001t0001g0117others(45): Show | 48 | HG00099.hp2 HG00438.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.3471-374_3471-371d others(6): Show |
NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56061018 | |||||
| chr19:56061153
|
G | A | 89 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(86): Show | 89 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.3471-243G>A | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56061153 | ||||||
| chr19:56061164
|
G | T | 52 | a0003c0008t0001g0119a0003c0008t0001g0245a0003c0008t0001g0246others(49): Show | 52 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.3471-232G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56061164 | ||||||
| chr19:56061180
|
A | C | 1 | a0023c0057t0004g0360 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3471-216A>C | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56061180 | ||||||
| chr19:56061182
|
G | T | 87 | a0002c0004t0002g0059a0002c0004t0002g0124a0002c0004t0002g0125others(84): Show | 87 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.3471-214G>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56061182 | ||||||
| chr19:56061267
|
C | T | 46 | a0002c0004t0002g0166a0002c0004t0002g0176a0002c0004t0002g0183others(43): Show | 46 | HG00597.hp2 HG01175.hp1 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.3471-129C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56061267 | ||||||
| chr19:56061352
|
C | T | 23 | a0003c0008t0003g0381a0003c0043t0001g0123a0003c0043t0001g0195others(20): Show | 23 | HG00544.hp1 HG00597.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.3471-44C>T | NLRP5 | ENSG00000171487.16 | transcript | ENST00000390649.8 | protein_coding | 14/14 | chr19 | 56061352 |