| geneid | 84726 |
|---|---|
| ensemblid | ENSG00000288701.1 |
| hgncid | 28121 |
| symbol | PRRC2B |
| name | proline rich coiled-coil 2B |
| refseq_nuc | NM_013318.4 |
| refseq_prot | NP_037450.2 |
| ensembl_nuc | ENST00000683519.1 |
| ensembl_prot | ENSP00000508048.1 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 131394086 |
| end | 131500193 |
| strand | + |
| ver | v1.2 |
| region | chr9:131394086-131500193 |
| region5000 | chr9:131389086-131505193 |
| regionname0 | PRRC2B_chr9_131394086_131500193 |
| regionname5000 | PRRC2B_chr9_131389086_131505193 |
| 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 | 2229 | 77 | 14 | 20 | 24 | 8 | 10 | 17 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002 | 0/0 | 2229 | 51 | 27 | 7 | 12 | 3 | 2 | 11 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0003 | 0/0 | 2229 | 28 | 12 | 9 | 4 | 1 | 2 | 4 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0004 | 0/0 | 2229 | 19 | 6 | 6 | 0 | 5 | 2 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0005 | 0/0 | 2229 | 14 | 5 | 5 | 3 | 0 | 1 | 3 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0006 | 1/0 | 2229 | 4 | 3 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0007 | 0/0 | 2229 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0008 | 0/0 | 2229 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0009 | 0/0 | 2229 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0010 | 0/0 | 2229 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0011 | 0/0 | 2229 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0012 | 0/0 | 2229 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0013 | 0/0 | 2229 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0014 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0015 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0016 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0017 | 0/0 | 2229 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0018 | 0/0 | 2229 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0019 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0020 | 0/0 | 2229 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0021 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0022 | 0/0 | 2229 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0023 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0024 | 0/0 | 2229 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| 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 | 0/1 | 6690 | 75 | 14 | 19 | 24 | 8 | 9 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0002 | 0/0 | 6690 | 27 | 11 | 9 | 4 | 1 | 2 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0003 | 0/0 | 6690 | 16 | 1 | 2 | 8 | 3 | 2 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0004 | 0/0 | 6690 | 15 | 2 | 6 | 0 | 5 | 2 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0005 | 0/0 | 6690 | 12 | 5 | 4 | 3 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0006 | 0/0 | 6690 | 7 | 6 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0007 | 0/0 | 6690 | 6 | 6 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0008 | 0/0 | 6690 | 5 | 3 | 2 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0009 | 0/0 | 6690 | 4 | 4 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0010 | 0/0 | 6690 | 3 | 2 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0011 | 1/0 | 6690 | 3 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0012 | 0/0 | 6690 | 2 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0013 | 0/0 | 6690 | 2 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0014 | 0/0 | 6690 | 2 | 0 | 0 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0015 | 0/0 | 6690 | 2 | 0 | 2 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0016 | 0/0 | 6690 | 2 | 0 | 0 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0017 | 0/0 | 6690 | 2 | 0 | 0 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0018 | 0/0 | 6690 | 2 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0019 | 0/0 | 6690 | 2 | 0 | 0 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0020 | 0/0 | 6690 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0021 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0022 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0023 | 0/0 | 6690 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0024 | 0/0 | 6690 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0025 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0026 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0027 | 0/0 | 6690 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0028 | 0/0 | 6690 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0029 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0030 | 0/0 | 6690 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0031 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0032 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0033 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0034 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0035 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0036 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0037 | 0/0 | 6690 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0038 | 0/0 | 6690 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0039 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0040 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0041 | 0/0 | 6690 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0042 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0043 | 0/0 | 6690 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0044 | 0/0 | 6690 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0045 | 0/0 | 6690 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| c0046 | 0/0 | 6690 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| 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 | 0/1 | 4549 | 96 | 21 | 21 | 33 | 8 | 12 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0002 | 0/0 | 4549 | 16 | 10 | 4 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0003 | 0/0 | 4550 | 16 | 1 | 2 | 9 | 3 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0004 | 0/0 | 4550 | 9 | 8 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0005 | 0/0 | 4550 | 8 | 0 | 4 | 0 | 2 | 2 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0006 | 0/0 | 4551 | 7 | 0 | 4 | 0 | 3 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0007 | 0/0 | 4551 | 6 | 5 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0008 | 0/0 | 4550 | 4 | 3 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0009 | 0/0 | 4550 | 3 | 2 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0010 | 0/0 | 4549 | 3 | 3 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0011 | 0/0 | 4550 | 3 | 0 | 0 | 3 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0012 | 0/0 | 4551 | 2 | 0 | 1 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0013 | 0/0 | 4550 | 2 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0014 | 0/0 | 4549 | 2 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0015 | 1/0 | 4549 | 2 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0016 | 0/0 | 4549 | 2 | 0 | 2 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0017 | 0/0 | 4549 | 2 | 0 | 2 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0018 | 0/0 | 4550 | 2 | 1 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0019 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0020 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0021 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0022 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0023 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0024 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0025 | 0/0 | 4550 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0026 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0027 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0028 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0029 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0030 | 0/0 | 4551 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0031 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0032 | 0/0 | 4551 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0033 | 0/0 | 4551 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0034 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0035 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0036 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0037 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0038 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0039 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0040 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0041 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0042 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0043 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0044 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0045 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0046 | 0/0 | 4550 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0047 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0048 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| t0049 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| 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 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0182 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| 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 | 0/1 | 6690 | 75 | 14 | 19 | 24 | 8 | 9 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0041 | 0/0 | 6690 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0046 | 0/0 | 6690 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0003 | 0/0 | 6690 | 16 | 1 | 2 | 8 | 3 | 2 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0006 | 0/0 | 6690 | 7 | 6 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0007 | 0/0 | 6690 | 6 | 6 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0008 | 0/0 | 6690 | 5 | 3 | 2 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0010 | 0/0 | 6690 | 3 | 2 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0012 | 0/0 | 6690 | 2 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0018 | 0/0 | 6690 | 2 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0019 | 0/0 | 6690 | 2 | 0 | 0 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0023 | 0/0 | 6690 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0026 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0033 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0035 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0037 | 0/0 | 6690 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0038 | 0/0 | 6690 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0039 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0040 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0003c0002 | 0/0 | 6690 | 27 | 11 | 9 | 4 | 1 | 2 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0003c0031 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0004c0004 | 0/0 | 6690 | 15 | 2 | 6 | 0 | 5 | 2 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0004c0009 | 0/0 | 6690 | 4 | 4 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0005c0005 | 0/0 | 6690 | 12 | 5 | 4 | 3 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0005c0043 | 0/0 | 6690 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0005c0044 | 0/0 | 6690 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0006c0011 | 1/0 | 6690 | 3 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0006c0022 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0007c0017 | 0/0 | 6690 | 2 | 0 | 0 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0008c0016 | 0/0 | 6690 | 2 | 0 | 0 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0009c0015 | 0/0 | 6690 | 2 | 0 | 2 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0010c0014 | 0/0 | 6690 | 2 | 0 | 0 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0011c0013 | 0/0 | 6690 | 2 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0012c0045 | 0/0 | 6690 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0013c0020 | 0/0 | 6690 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0014c0042 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0015c0021 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0016c0032 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0017c0024 | 0/0 | 6690 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0018c0030 | 0/0 | 6690 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0019c0029 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0020c0028 | 0/0 | 6690 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0021c0034 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0022c0027 | 0/0 | 6690 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0023c0036 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0024c0025 | 0/0 | 6690 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 11238 | 55 | 6 | 12 | 21 | 7 | 8 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0001t0002 | 0/0 | 11238 | 9 | 8 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0001t0011 | 0/0 | 11239 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0001t0016 | 0/0 | 11238 | 2 | 0 | 2 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0001t0017 | 0/0 | 11238 | 2 | 0 | 2 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0001t0022 | 0/0 | 11238 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0001t0033 | 0/0 | 11240 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0001t0043 | 0/0 | 11238 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0001t0044 | 0/0 | 11238 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0001t0045 | 0/0 | 11238 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0001t0049 | 0/0 | 11238 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0041t0001 | 0/0 | 11238 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0001c0046t0001 | 0/0 | 11238 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0003t0003 | 0/0 | 11239 | 15 | 1 | 2 | 8 | 3 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0003t0008 | 0/0 | 11239 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0006t0004 | 0/0 | 11239 | 4 | 4 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0006t0018 | 0/0 | 11239 | 2 | 1 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0006t0026 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0007t0010 | 0/0 | 11238 | 3 | 3 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0007t0014 | 0/0 | 11238 | 2 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0007t0024 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0008t0025 | 0/0 | 11239 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0008t0028 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0008t0034 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0008t0035 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0008t0042 | 0/0 | 11238 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0010t0009 | 0/0 | 11239 | 3 | 2 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0012t0004 | 0/0 | 11239 | 2 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0018t0008 | 0/0 | 11239 | 2 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0019t0001 | 0/0 | 11238 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0019t0011 | 0/0 | 11239 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0023t0012 | 0/0 | 11240 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0026t0040 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0033t0023 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0035t0004 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0037t0003 | 0/0 | 11239 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0038t0012 | 0/0 | 11240 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0039t0008 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0002c0040t0029 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0003c0002t0001 | 0/0 | 11238 | 20 | 9 | 5 | 3 | 1 | 2 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0003c0002t0004 | 0/0 | 11239 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0003c0002t0011 | 0/0 | 11239 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0003c0002t0027 | 0/0 | 11238 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0003c0002t0039 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0003c0002t0041 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0003c0002t0046 | 0/0 | 11239 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0003c0002t0047 | 0/0 | 11238 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0003c0031t0001 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0004c0004t0005 | 0/0 | 11239 | 7 | 0 | 3 | 0 | 2 | 2 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0004c0004t0006 | 0/0 | 11240 | 5 | 0 | 3 | 0 | 2 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0004c0004t0013 | 0/0 | 11239 | 2 | 2 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0004c0004t0030 | 0/0 | 11240 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0004c0009t0007 | 0/0 | 11240 | 4 | 4 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0005c0005t0001 | 0/0 | 11238 | 5 | 3 | 1 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0005c0005t0002 | 0/0 | 11238 | 7 | 2 | 3 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0005c0043t0001 | 0/0 | 11238 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0005c0044t0021 | 0/0 | 11238 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0006c0011t0015 | 1/0 | 11238 | 2 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0006c0011t0037 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0006c0022t0038 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0007c0017t0001 | 0/0 | 11238 | 2 | 0 | 0 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0008c0016t0001 | 0/0 | 11238 | 2 | 0 | 0 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0009c0015t0005 | 0/0 | 11239 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0009c0015t0006 | 0/0 | 11240 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0010c0014t0001 | 0/0 | 11238 | 2 | 0 | 0 | 2 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0011c0013t0031 | 0/0 | 11240 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0011c0013t0036 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0012c0045t0001 | 0/0 | 11238 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0013c0020t0032 | 0/0 | 11240 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0014c0042t0001 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0015c0021t0004 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0016c0032t0019 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0017c0024t0001 | 0/0 | 11238 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0018c0030t0001 | 0/0 | 11238 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0019c0029t0020 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0020c0028t0007 | 0/0 | 11240 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0021c0034t0048 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0022c0027t0006 | 0/0 | 11240 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0023c0036t0007 | 0/0 | 11240 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| a0024c0025t0001 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | copy fasta | chr9 | 131389086 | 131505193 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0011g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0016g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0016g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0017g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0017g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0022g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0033g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0043g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0044g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0045g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0001t0049g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0041t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0001c0046t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0003t0008g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0006t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0006t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0006t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0006t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0006t0018g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0006t0018g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0006t0026g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0007t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0007t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0007t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0007t0014g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0007t0014g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0007t0024g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0008t0025g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0008t0028g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0008t0034g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0008t0035g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0008t0042g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0010t0009g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0010t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0010t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0012t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0012t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0018t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0018t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0019t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0019t0011g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0023t0012g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0026t0040g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0033t0023g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0035t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0037t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0038t0012g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0039t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0002c0040t0029g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0011g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0027g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0039g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0041g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0046g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0002t0047g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0003c0031t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0005g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0005g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0005g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0005g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0005g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0006g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0006g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0006g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0013g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0013g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0004t0030g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0009t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0009t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0009t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0004c0009t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0005t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0005t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0005t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0005t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0005t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0005t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0005t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0005t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0005t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0005t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0005t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0043t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0005c0044t0021g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0006c0011t0015g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0006c0011t0015g0182 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0006c0011t0037g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0006c0022t0038g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0007c0017t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0007c0017t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0008c0016t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0008c0016t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0009c0015t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0009c0015t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0010c0014t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0010c0014t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0011c0013t0031g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0011c0013t0036g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0012c0045t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0013c0020t0032g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0014c0042t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0015c0021t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0016c0032t0019g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0017c0024t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0018c0030t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0019c0029t0020g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0020c0028t0007g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0021c0034t0048g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0022c0027t0006g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0023c0036t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| a0024c0025t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0004 | t0030 | g0142 | EUR | GBR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00140 | hp1 | a0003 | c0002 | t0001 | g0110 | EUR | GBR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00280 | hp1 | a0004 | c0004 | t0006 | g0144 | EUR | FIN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00280 | hp2 | a0001 | c0001 | t0045 | g0121 | EUR | FIN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00323 | hp1 | a0004 | c0004 | t0005 | g0143 | EUR | FIN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00558 | hp1 | a0002 | c0003 | t0003 | g0019 | EAS | CHS | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00621 | hp2 | a0007 | c0017 | t0001 | g0106 | EAS | CHS | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00639 | hp1 | a0009 | c0015 | t0005 | g0094 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00639 | hp2 | a0004 | c0004 | t0005 | g0140 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00642 | hp2 | a0013 | c0020 | t0032 | g0006 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00741 | hp1 | a0003 | c0002 | t0001 | g0130 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG00741 | hp2 | a0009 | c0015 | t0006 | g0115 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01069 | hp1 | a0003 | c0002 | t0001 | g0066 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01069 | hp2 | a0001 | c0001 | t0049 | g0120 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01071 | hp1 | a0003 | c0002 | t0001 | g0128 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01071 | hp2 | a0003 | c0002 | t0001 | g0067 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01099 | hp1 | a0018 | c0030 | t0001 | g0009 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01099 | hp2 | a0001 | c0001 | t0017 | g0008 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01106 | hp1 | a0003 | c0002 | t0004 | g0118 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01167 | hp1 | a0002 | c0006 | t0018 | g0164 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01168 | hp2 | a0003 | c0002 | t0047 | g0061 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01169 | hp1 | a0003 | c0002 | t0046 | g0060 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01175 | hp2 | a0003 | c0002 | t0027 | g0174 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01192 | hp1 | a0002 | c0038 | t0012 | g0171 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01192 | hp2 | a0003 | c0002 | t0001 | g0127 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01243 | hp2 | a0004 | c0004 | t0005 | g0117 | AMR | PUR | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01255 | hp1 | a0004 | c0004 | t0006 | g0138 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01255 | hp2 | a0001 | c0001 | t0016 | g0079 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01256 | hp2 | a0005 | c0005 | t0002 | g0212 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01257 | hp1 | a0004 | c0004 | t0006 | g0137 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01257 | hp2 | a0002 | c0003 | t0003 | g0031 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01258 | hp1 | a0005 | c0005 | t0002 | g0213 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01258 | hp2 | a0004 | c0004 | t0006 | g0139 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01261 | hp1 | a0005 | c0005 | t0002 | g0214 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01358 | hp1 | a0001 | c0041 | t0001 | g0041 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01358 | hp2 | a0001 | c0001 | t0017 | g0007 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01361 | hp1 | a0005 | c0044 | t0021 | g0200 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01361 | hp2 | a0002 | c0010 | t0009 | g0187 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01496 | hp2 | a0001 | c0001 | t0022 | g0192 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01515 | hp1 | a0002 | c0003 | t0003 | g0027 | EUR | IBS | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01516 | hp2 | a0004 | c0004 | t0006 | g0145 | EUR | IBS | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01517 | hp1 | a0002 | c0003 | t0003 | g0026 | EUR | IBS | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01517 | hp2 | a0004 | c0004 | t0005 | g0147 | EUR | IBS | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01891 | hp1 | a0002 | c0008 | t0028 | g0126 | AFR | ACB | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01891 | hp2 | a0002 | c0008 | t0035 | g0039 | AFR | ACB | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01934 | hp1 | a0001 | c0001 | t0016 | g0081 | AMR | PEL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01943 | hp1 | a0002 | c0008 | t0025 | g0125 | AMR | PEL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01943 | hp2 | a0017 | c0024 | t0001 | g0068 | AMR | PEL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01975 | hp1 | a0002 | c0003 | t0003 | g0028 | AMR | PEL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01975 | hp2 | a0004 | c0004 | t0005 | g0123 | AMR | PEL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02055 | hp1 | a0002 | c0007 | t0014 | g0012 | AFR | ACB | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02055 | hp2 | a0002 | c0003 | t0003 | g0032 | AFR | ACB | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02145 | hp1 | a0002 | c0006 | t0004 | g0168 | AFR | ACB | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02145 | hp2 | a0021 | c0034 | t0048 | g0013 | AFR | ACB | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02165 | hp1 | a0007 | c0017 | t0001 | g0056 | EAS | CDX | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02257 | hp1 | a0003 | c0002 | t0001 | g0069 | AFR | ACB | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02451 | hp1 | a0002 | c0006 | t0004 | g0160 | AFR | ACB | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02451 | hp2 | a0011 | c0013 | t0036 | g0037 | AFR | ACB | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02572 | hp1 | a0023 | c0036 | t0007 | g0148 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02572 | hp2 | a0003 | c0002 | t0001 | g0183 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02630 | hp2 | a0003 | c0002 | t0039 | g0047 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02647 | hp1 | a0003 | c0002 | t0001 | g0134 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02647 | hp2 | a0014 | c0042 | t0001 | g0173 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02698 | hp2 | a0003 | c0002 | t0001 | g0065 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02723 | hp2 | a0002 | c0007 | t0010 | g0201 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02735 | hp1 | a0003 | c0002 | t0001 | g0129 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02738 | hp1 | a0001 | c0001 | t0033 | g0077 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02738 | hp2 | a0002 | c0003 | t0008 | g0216 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02809 | hp1 | a0003 | c0002 | t0041 | g0044 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02818 | hp1 | a0002 | c0007 | t0024 | g0186 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02818 | hp2 | a0002 | c0006 | t0004 | g0167 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02886 | hp1 | a0002 | c0006 | t0018 | g0166 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02886 | hp2 | a0016 | c0032 | t0019 | g0215 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02895 | hp2 | a0002 | c0010 | t0009 | g0189 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02896 | hp1 | a0002 | c0018 | t0008 | g0208 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02896 | hp2 | a0002 | c0026 | t0040 | g0178 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02897 | hp1 | a0002 | c0018 | t0008 | g0207 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02897 | hp2 | a0002 | c0010 | t0009 | g0188 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02922 | hp1 | a0015 | c0021 | t0004 | g0005 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02965 | hp1 | a0006 | c0011 | t0015 | g0181 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02965 | hp2 | a0004 | c0004 | t0013 | g0169 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02970 | hp1 | a0004 | c0009 | t0007 | g0159 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02970 | hp2 | a0002 | c0033 | t0023 | g0163 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02976 | hp1 | a0006 | c0011 | t0037 | g0179 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG02976 | hp2 | a0002 | c0012 | t0004 | g0161 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03017 | hp2 | a0005 | c0043 | t0001 | g0086 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03041 | hp1 | a0002 | c0006 | t0004 | g0165 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03130 | hp1 | a0005 | c0005 | t0002 | g0205 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03139 | hp1 | a0002 | c0012 | t0004 | g0162 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03139 | hp2 | a0003 | c0002 | t0001 | g0184 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03209 | hp1 | a0003 | c0002 | t0001 | g0154 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03209 | hp2 | a0004 | c0009 | t0007 | g0136 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03225 | hp1 | a0002 | c0007 | t0010 | g0202 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03239 | hp1 | a0004 | c0004 | t0005 | g0150 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03453 | hp1 | a0004 | c0004 | t0013 | g0170 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03453 | hp2 | a0004 | c0009 | t0007 | g0133 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03486 | hp1 | a0003 | c0002 | t0001 | g0153 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03486 | hp2 | a0006 | c0022 | t0038 | g0180 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03516 | hp1 | a0004 | c0009 | t0007 | g0132 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03516 | hp2 | a0019 | c0029 | t0020 | g0209 | AFR | ESN | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03540 | hp1 | a0003 | c0002 | t0001 | g0185 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03540 | hp2 | a0002 | c0007 | t0010 | g0203 | AFR | GWD | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03579 | hp2 | a0002 | c0035 | t0004 | g0131 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03669 | hp1 | a0004 | c0004 | t0005 | g0149 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03710 | hp1 | a0020 | c0028 | t0007 | g0135 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG04228 | hp1 | a0001 | c0046 | t0001 | g0177 | SAS | STU | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG04228 | hp2 | a0002 | c0003 | t0003 | g0016 | SAS | STU | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18906 | hp1 | a0003 | c0031 | t0001 | g0172 | AFR | YRI | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18906 | hp2 | a0002 | c0039 | t0008 | g0206 | AFR | YRI | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18947 | hp1 | a0002 | c0003 | t0003 | g0030 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18949 | hp2 | a0002 | c0003 | t0003 | g0021 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18951 | hp2 | a0002 | c0003 | t0003 | g0020 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18964 | hp2 | a0008 | c0016 | t0001 | g0089 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18970 | hp1 | a0005 | c0005 | t0001 | g0095 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18971 | hp1 | a0005 | c0005 | t0002 | g0211 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18972 | hp1 | a0003 | c0002 | t0011 | g0158 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18972 | hp2 | a0001 | c0001 | t0011 | g0155 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18975 | hp1 | a0001 | c0001 | t0043 | g0105 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18975 | hp2 | a0003 | c0002 | t0001 | g0156 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18985 | hp2 | a0002 | c0037 | t0003 | g0017 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18990 | hp1 | a0010 | c0014 | t0001 | g0052 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA18990 | hp2 | a0002 | c0019 | t0001 | g0023 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19003 | hp2 | a0005 | c0005 | t0002 | g0210 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19012 | hp2 | a0002 | c0003 | t0003 | g0015 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19030 | hp1 | a0002 | c0040 | t0029 | g0151 | AFR | LWK | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19030 | hp2 | a0002 | c0006 | t0026 | g0146 | AFR | LWK | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19043 | hp1 | a0002 | c0008 | t0034 | g0035 | AFR | LWK | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19043 | hp2 | a0005 | c0005 | t0001 | g0010 | AFR | LWK | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19057 | hp2 | a0002 | c0003 | t0003 | g0018 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19064 | hp1 | a0002 | c0019 | t0011 | g0022 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19066 | hp1 | a0012 | c0045 | t0001 | g0043 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19066 | hp2 | a0003 | c0002 | t0001 | g0046 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19067 | hp2 | a0002 | c0023 | t0012 | g0029 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19077 | hp1 | a0010 | c0014 | t0001 | g0055 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19077 | hp2 | a0002 | c0003 | t0003 | g0014 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19087 | hp2 | a0003 | c0002 | t0001 | g0049 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19088 | hp2 | a0008 | c0016 | t0001 | g0088 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19091 | hp1 | a0001 | c0001 | t0044 | g0051 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19091 | hp2 | a0002 | c0003 | t0003 | g0024 | EAS | JPT | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19240 | hp1 | a0005 | c0005 | t0002 | g0204 | AFR | YRI | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | YRI | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA20129 | hp1 | a0024 | c0025 | t0001 | g0034 | AFR | ASW | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA20129 | hp2 | a0002 | c0007 | t0014 | g0002 | AFR | ASW | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA20752 | hp1 | a0022 | c0027 | t0006 | g0141 | EUR | TSI | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA20805 | hp1 | a0002 | c0003 | t0003 | g0025 | EUR | TSI | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01123 | hp1 | a0005 | c0005 | t0001 | g0107 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG01123 | hp2 | a0002 | c0008 | t0042 | g0038 | AMR | CLM | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG03471 | hp2 | a0005 | c0005 | t0001 | g0011 | AFR | MSL | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG06807 | hp1 | a0003 | c0002 | t0001 | g0152 | AFR | USA | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| HG06807 | hp2 | a0011 | c0013 | t0031 | g0036 | AFR | USA | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA20300 | hp1 | a0003 | c0002 | t0001 | g0045 | AFR | USA | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| NA20300 | hp2 | a0005 | c0005 | t0001 | g0108 | AFR | USA | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0102 | REF | REF | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| homoSapiens_grch38 | hp1 | a0006 | c0011 | t0015 | g0182 | REF | REF | PRRC2B_chr9_131389086_131505193 | PRRC2B | chr9 | 131389086 | 131505193 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131436700
|
C | T | 1 | a0012 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.374C>T | p.Pro125Leu | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/32 | 603/11238 | 374/6690 | 125/2229 | chr9 | 131436700 | ||
| chr9:131446568
|
G | A | 1 | a0013 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.781G>A | p.Val261Ile | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 7/32 | 1010/11238 | 781/6690 | 261/2229 | chr9 | 131446568 | ||
| chr9:131459201
|
A | G | 1 | a0005 | 14 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(11): Show |
missense_variant | MODERATE | c.1249A>G | p.Met417Val | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/32 | 1478/11238 | 1249/6690 | 417/2229 | chr9 | 131459201 | ||
| chr9:131459216
|
A | G | 1 | a0014 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1264A>G | p.Ser422Gly | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/32 | 1493/11238 | 1264/6690 | 422/2229 | chr9 | 131459216 | ||
| chr9:131459280
|
G | A | 1 | a0015 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1328G>A | p.Arg443His | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/32 | 1557/11238 | 1328/6690 | 443/2229 | chr9 | 131459280 | ||
| chr9:131470932
|
A | C | 1 | a0016 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.2056A>C | p.Thr686Pro | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/32 | 2285/11238 | 2056/6690 | 686/2229 | chr9 | 131470932 | ||
| chr9:131473718
|
G | A | 1 | a0017 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.2318G>A | p.Arg773His | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 15/32 | 2547/11238 | 2318/6690 | 773/2229 | chr9 | 131473718 | ||
| chr9:131474918
|
C | A | 1 | a0024 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.2789C>A | p.Pro930Gln | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 3018/11238 | 2789/6690 | 930/2229 | chr9 | 131474918 | ||
| chr9:131474936
|
C | G | 12 | a0001a0003a0005others(9): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
missense_variant | MODERATE | c.2807C>G | p.Thr936Ser | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 3036/11238 | 2807/6690 | 936/2229 | chr9 | 131474936 | ||
| chr9:131475071
|
C | T | 12 | a0001a0003a0005others(9): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
missense_variant | MODERATE | c.2942C>T | p.Pro981Leu | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 3171/11238 | 2942/6690 | 981/2229 | chr9 | 131475071 | ||
| chr9:131475260
|
T | C | 23 | a0001a0002a0003others(20): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
missense_variant | MODERATE | c.3131T>C | p.Met1044Thr | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 3360/11238 | 3131/6690 | 1044/2229 | chr9 | 131475260 | ||
| chr9:131475297
|
A | T | 1 | a0019 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.3168A>T | p.Gln1056His | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 3397/11238 | 3168/6690 | 1056/2229 | chr9 | 131475297 | ||
| chr9:131475451
|
C | T | 1 | a0020 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.3322C>T | p.Arg1108Cys | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 3551/11238 | 3322/6690 | 1108/2229 | chr9 | 131475451 | ||
| chr9:131475464
|
T | C | 1 | a0010 | 2 | NA18990.hp1 NA19077.hp1 |
missense_variant | MODERATE | c.3335T>C | p.Leu1112Pro | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 3564/11238 | 3335/6690 | 1112/2229 | chr9 | 131475464 | ||
| chr9:131475589
|
G | A | 1 | a0011 | 2 | HG02451.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.3460G>A | p.Glu1154Lys | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 3689/11238 | 3460/6690 | 1154/2229 | chr9 | 131475589 | ||
| chr9:131475956
|
C | T | 7 | a0003a0004a0005others(4): Show | 65 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(62): Show |
missense_variant | MODERATE | c.3827C>T | p.Ala1276Val | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 4056/11238 | 3827/6690 | 1276/2229 | chr9 | 131475956 | ||
| chr9:131476069
|
C | T | 1 | a0016 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.3940C>T | p.Arg1314Trp | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 4169/11238 | 3940/6690 | 1314/2229 | chr9 | 131476069 | ||
| chr9:131476343
|
T | G | 1 | a0009 | 2 | HG00639.hp1 HG00741.hp2 |
missense_variant | MODERATE | c.4214T>G | p.Leu1405Arg | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 4443/11238 | 4214/6690 | 1405/2229 | chr9 | 131476343 | ||
| chr9:131477826
|
G | T | 1 | a0021 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.4489G>T | p.Ala1497Ser | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 17/32 | 4718/11238 | 4489/6690 | 1497/2229 | chr9 | 131477826 | ||
| chr9:131478506
|
G | C | 1 | a0008 | 2 | NA18964.hp2 NA19088.hp2 |
missense_variant | MODERATE | c.4645G>C | p.Gly1549Arg | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 18/32 | 4874/11238 | 4645/6690 | 1549/2229 | chr9 | 131478506 | ||
| chr9:131482560
|
A | C | 1 | a0018 | 1 | HG01099.hp1 | missense_variant&splice_region_variant | MODERATE | c.5173A>C | p.Lys1725Gln | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 21/32 | 5402/11238 | 5173/6690 | 1725/2229 | chr9 | 131482560 | ||
| chr9:131483398
|
C | G | 1 | a0022 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.5413C>G | p.Pro1805Ala | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 23/32 | 5642/11238 | 5413/6690 | 1805/2229 | chr9 | 131483398 | ||
| chr9:131485014
|
G | A | 1 | a0023 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.5632G>A | p.Ala1878Thr | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 25/32 | 5861/11238 | 5632/6690 | 1878/2229 | chr9 | 131485014 | ||
| chr9:131495776
|
G | C | 1 | a0007 | 2 | HG00621.hp2 HG02165.hp1 |
missense_variant | MODERATE | c.6592G>C | p.Ala2198Pro | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 6821/11238 | 6592/6690 | 2198/2229 | chr9 | 131495776 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131432744
|
C | G | 1 | a0001c0046 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.243C>G | p.Pro81Pro | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/32 | 472/11238 | 243/6690 | 81/2229 | chr9 | 131432744 | ||
| chr9:131464924
|
G | A | 1 | a0006c0022 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1566G>A | p.Leu522Leu | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/32 | 1795/11238 | 1566/6690 | 522/2229 | chr9 | 131464924 | ||
| chr9:131467570
|
A | G | 1 | a0001c0041 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.1728A>G | p.Pro576Pro | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/32 | 1957/11238 | 1728/6690 | 576/2229 | chr9 | 131467570 | ||
| chr9:131467747
|
A | G | 1 | a0002c0040 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1905A>G | p.Gln635Gln | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/32 | 2134/11238 | 1905/6690 | 635/2229 | chr9 | 131467747 | ||
| chr9:131470835
|
G | A | 1 | a0002c0023 | 1 | NA19067.hp2 | synonymous_variant | LOW | c.1959G>A | p.Pro653Pro | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/32 | 2188/11238 | 1959/6690 | 653/2229 | chr9 | 131470835 | ||
| chr9:131470928
|
T | C | 27 | a0001c0001a0001c0041a0001c0046others(24): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
synonymous_variant | LOW | c.2052T>C | p.Arg684Arg | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/32 | 2281/11238 | 2052/6690 | 684/2229 | chr9 | 131470928 | ||
| chr9:131474601
|
A | G | 2 | a0002c0018a0002c0039 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.2472A>G | p.Arg824Arg | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 2701/11238 | 2472/6690 | 824/2229 | chr9 | 131474601 | ||
| chr9:131474730
|
G | A | 3 | a0002c0012a0002c0033a0015c0021 | 4 | HG02922.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.2601G>A | p.Glu867Glu | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 2830/11238 | 2601/6690 | 867/2229 | chr9 | 131474730 | ||
| chr9:131474844
|
C | T | 5 | a0002c0003a0002c0019a0002c0023others(2): Show | 21 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(18): Show |
synonymous_variant | LOW | c.2715C>T | p.Asn905Asn | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 2944/11238 | 2715/6690 | 905/2229 | chr9 | 131474844 | ||
| chr9:131475042
|
C | G | 1 | a0005c0044 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.2913C>G | p.Thr971Thr | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 3142/11238 | 2913/6690 | 971/2229 | chr9 | 131475042 | ||
| chr9:131475300
|
C | T | 1 | a0002c0038 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.3171C>T | p.Ala1057Ala | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 3400/11238 | 3171/6690 | 1057/2229 | chr9 | 131475300 | ||
| chr9:131475570
|
C | G | 1 | a0001c0041 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.3441C>G | p.Arg1147Arg | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 3670/11238 | 3441/6690 | 1147/2229 | chr9 | 131475570 | ||
| chr9:131475678
|
G | T | 31 | a0001c0001a0001c0041a0001c0046others(28): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
synonymous_variant | LOW | c.3549G>T | p.Gly1183Gly | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 3778/11238 | 3549/6690 | 1183/2229 | chr9 | 131475678 | ||
| chr9:131476044
|
A | G | 3 | a0002c0012a0002c0033a0015c0021 | 4 | HG02922.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.3915A>G | p.Pro1305Pro | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 4144/11238 | 3915/6690 | 1305/2229 | chr9 | 131476044 | ||
| chr9:131476113
|
C | T | 6 | a0002c0003a0002c0019a0002c0023others(3): Show | 22 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(19): Show |
synonymous_variant | LOW | c.3984C>T | p.Pro1328Pro | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 4213/11238 | 3984/6690 | 1328/2229 | chr9 | 131476113 | ||
| chr9:131476383
|
G | A | 10 | a0002c0006a0002c0012a0002c0026others(7): Show | 34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
synonymous_variant | LOW | c.4254G>A | p.Lys1418Lys | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/32 | 4483/11238 | 4254/6690 | 1418/2229 | chr9 | 131476383 | ||
| chr9:131478550
|
C | T | 2 | a0002c0018a0002c0039 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.4689C>T | p.Ile1563Ile | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 18/32 | 4918/11238 | 4689/6690 | 1563/2229 | chr9 | 131478550 | ||
| chr9:131482721
|
A | G | 12 | a0002c0003a0002c0008a0002c0018others(9): Show | 34 | HG00558.hp1 HG00642.hp2 HG01123.hp2 others(31): Show |
synonymous_variant | LOW | c.5187A>G | p.Gln1729Gln | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 22/32 | 5416/11238 | 5187/6690 | 1729/2229 | chr9 | 131482721 | ||
| chr9:131487190
|
G | A | 1 | a0003c0031 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.5880G>A | p.Pro1960Pro | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 27/32 | 6109/11238 | 5880/6690 | 1960/2229 | chr9 | 131487190 | ||
| chr9:131487889
|
G | A | 1 | a0002c0010 | 3 | HG01361.hp2 HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.6018G>A | p.Pro2006Pro | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/32 | 6247/11238 | 6018/6690 | 2006/2229 | chr9 | 131487889 | ||
| chr9:131495778
|
C | T | 7 | a0002c0003a0002c0018a0002c0023others(4): Show | 23 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(20): Show |
synonymous_variant | LOW | c.6594C>T | p.Ala2198Ala | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 6823/11238 | 6594/6690 | 2198/2229 | chr9 | 131495778 | ||
| chr9:131495859
|
G | A | 1 | a0005c0043 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.6675G>A | p.Glu2225Glu | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 6904/11238 | 6675/6690 | 2225/2229 | chr9 | 131495859 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131394110
|
C | T | 1 | a0002c0006t0018 | 2 | HG01167.hp1 HG02886.hp1 |
5_prime_UTR_variant | MODIFIER | c.-205C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/32 | 36035 | chr9 | 131394110 | |||||
| chr9:131394179
|
A | G | 1 | a0001c0001t0049 | 1 | HG01069.hp2 | 5_prime_UTR_variant | MODIFIER | c.-136A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/32 | 35966 | chr9 | 131394179 | |||||
| chr9:131394194
|
G | A | 11 | a0001c0001t0002a0001c0001t0022a0002c0003t0008others(8): Show | 30 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-121G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/32 | 35951 | chr9 | 131394194 | |||||
| chr9:131496115
|
T | G | 7 | a0002c0006t0026a0002c0007t0024a0002c0008t0025others(4): Show | 10 | HG01943.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*241T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 241 | chr9 | 131496115 | |||||
| chr9:131496156
|
T | C | 1 | a0003c0002t0027 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*282T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 282 | chr9 | 131496156 | |||||
| chr9:131496310
|
G | T | 1 | a0001c0001t0049 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*436G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 436 | chr9 | 131496310 | |||||
| chr9:131496551
|
C | T | 1 | a0021c0034t0048 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*677C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 677 | chr9 | 131496551 | |||||
| chr9:131496557
|
C | G | 2 | a0003c0002t0046a0003c0002t0047 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*683C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 683 | chr9 | 131496557 | |||||
| chr9:131496558
|
G | A | 9 | a0002c0003t0003a0002c0003t0008a0002c0008t0028others(6): Show | 24 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*684G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 684 | chr9 | 131496558 | |||||
| chr9:131496593
|
G | A | 7 | a0004c0004t0005a0004c0004t0006a0004c0004t0013others(4): Show | 18 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*719G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 719 | chr9 | 131496593 | |||||
| chr9:131496597
|
G | C | 1 | a0021c0034t0048 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*723G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 723 | chr9 | 131496597 | |||||
| chr9:131496627
|
A | AG | 29 | a0001c0001t0011a0002c0003t0003a0002c0003t0008others(26): Show | 58 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*762dupG | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 763 | INFO_REALIGN_3_PRIME | chr9 | 131496627 | ||||
| chr9:131496627
|
A | AGG | 12 | a0001c0001t0033a0002c0023t0012a0002c0038t0012others(9): Show | 19 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*761_*762dupGG | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 763 | INFO_REALIGN_3_PRIME | chr9 | 131496627 | ||||
| chr9:131496627
|
A | G | 1 | a0002c0040t0029 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*753A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 753 | chr9 | 131496627 | |||||
| chr9:131496766
|
G | A | 1 | a0003c0002t0039 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*892G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 892 | chr9 | 131496766 | |||||
| chr9:131496827
|
T | C | 5 | a0002c0008t0034a0002c0008t0035a0011c0013t0031others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*953T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 953 | chr9 | 131496827 | |||||
| chr9:131496845
|
C | T | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(33): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*971C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 971 | chr9 | 131496845 | |||||
| chr9:131496903
|
A | G | 6 | a0004c0004t0005a0004c0004t0006a0004c0004t0030others(3): Show | 16 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1029A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 1029 | chr9 | 131496903 | |||||
| chr9:131497285
|
C | T | 4 | a0002c0008t0034a0002c0008t0035a0011c0013t0031others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1411C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 1411 | chr9 | 131497285 | |||||
| chr9:131497388
|
C | A | 1 | a0001c0001t0016 | 2 | HG01255.hp2 HG01934.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1514C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 1514 | chr9 | 131497388 | |||||
| chr9:131497426
|
A | G | 1 | a0019c0029t0020 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1552A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 1552 | chr9 | 131497426 | |||||
| chr9:131497488
|
C | T | 1 | a0001c0001t0045 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1614C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 1614 | chr9 | 131497488 | |||||
| chr9:131497614
|
G | T | 8 | a0002c0003t0003a0002c0003t0008a0002c0018t0008others(5): Show | 23 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1740G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 1740 | chr9 | 131497614 | |||||
| chr9:131497881
|
G | A | 2 | a0002c0007t0010a0002c0007t0014 | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2007G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 2007 | chr9 | 131497881 | |||||
| chr9:131498111
|
A | G | 1 | a0001c0001t0044 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2237A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 2237 | chr9 | 131498111 | |||||
| chr9:131498116
|
A | G | 1 | a0004c0004t0030 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2242A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 2242 | chr9 | 131498116 | |||||
| chr9:131498200
|
C | T | 1 | a0001c0001t0043 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2326C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 2326 | chr9 | 131498200 | |||||
| chr9:131498383
|
G | C | 77 | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(74): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*2509G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 2509 | chr9 | 131498383 | |||||
| chr9:131498585
|
G | A | 1 | a0003c0002t0041 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2711G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 2711 | chr9 | 131498585 | |||||
| chr9:131498667
|
T | C | 1 | a0002c0008t0034 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2793T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 2793 | chr9 | 131498667 | |||||
| chr9:131498705
|
C | T | 1 | a0001c0001t0022 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2831C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 2831 | chr9 | 131498705 | |||||
| chr9:131498770
|
C | T | 1 | a0021c0034t0048 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2896C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 2896 | chr9 | 131498770 | |||||
| chr9:131498887
|
C | T | 7 | a0002c0003t0003a0002c0003t0008a0002c0018t0008others(4): Show | 22 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3013C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 3013 | chr9 | 131498887 | |||||
| chr9:131499154
|
C | T | 5 | a0002c0007t0024a0002c0008t0025a0004c0009t0007others(2): Show | 8 | HG01943.hp1 HG02572.hp1 HG02818.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3280C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 3280 | chr9 | 131499154 | |||||
| chr9:131499194
|
A | G | 1 | a0002c0008t0025 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3320A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 3320 | chr9 | 131499194 | |||||
| chr9:131499212
|
C | T | 7 | a0002c0003t0003a0002c0003t0008a0002c0018t0008others(4): Show | 22 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3338C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 3338 | chr9 | 131499212 | |||||
| chr9:131499214
|
C | G | 78 | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(75): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*3340C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 3340 | chr9 | 131499214 | |||||
| chr9:131499285
|
C | T | 5 | a0002c0007t0024a0002c0008t0025a0004c0009t0007others(2): Show | 8 | HG01943.hp1 HG02572.hp1 HG02818.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3411C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 3411 | chr9 | 131499285 | |||||
| chr9:131499442
|
C | T | 1 | a0002c0008t0042 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3568C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 3568 | chr9 | 131499442 | |||||
| chr9:131499471
|
G | A | 1 | a0005c0044t0021 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3597G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 3597 | chr9 | 131499471 | |||||
| chr9:131499495
|
T | C | 7 | a0004c0004t0005a0004c0004t0006a0004c0004t0013others(4): Show | 18 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3621T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 3621 | chr9 | 131499495 | |||||
| chr9:131499495
|
T | G | 12 | a0002c0003t0003a0002c0003t0008a0002c0006t0026others(9): Show | 27 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3621T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 3621 | chr9 | 131499495 | |||||
| chr9:131500045
|
G | A | 1 | a0001c0001t0017 | 2 | HG01099.hp2 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4171G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 4171 | chr9 | 131500045 | |||||
| chr9:131500048
|
G | T | 2 | a0011c0013t0031a0011c0013t0036 | 2 | HG02451.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4174G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 32/32 | 4174 | chr9 | 131500048 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:131394402
|
G | T | 30 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0193others(27): Show | 30 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.-52+139G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131394402 | ||||||
| chr9:131394560
|
C | T | 1 | a0002c0007t0024g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-52+297C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131394560 | ||||||
| chr9:131394659
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.-52+396T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131394659 | ||||||
| chr9:131394720
|
A | G | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-52+457A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131394720 | ||||||
| chr9:131394749
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-52+486G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131394749 | ||||||
| chr9:131394956
|
TG | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0040others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.-52+697delG | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131394956 | |||||
| chr9:131394959
|
GGT | G | 11 | a0001c0001t0017g0007a0001c0001t0017g0008a0002c0018t0008g0207others(8): Show | 11 | HG00642.hp2 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.-52+697_-52+698del others(2): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131394959 | ||||||
| chr9:131394960
|
G | T | 8 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0046t0001g0177others(5): Show | 8 | HG00735.hp2 HG01175.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.-52+697G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131394960 | ||||||
| chr9:131394960
|
GT | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0002g0190others(17): Show | 20 | HG00735.hp1 HG01361.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.-52+710delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131394960 | |||||
| chr9:131394961
|
T | G | 1 | a0006c0011t0037g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-52+698T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131394961 | ||||||
| chr9:131394989
|
C | G | 11 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(8): Show | 11 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-52+726C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131394989 | ||||||
| chr9:131394993
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-52+730T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131394993 | ||||||
| chr9:131395131
|
C | G | 1 | a0003c0002t0011g0158 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-52+868C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131395131 | ||||||
| chr9:131395134
|
G | T | 3 | a0002c0018t0008g0207a0002c0018t0008g0208a0002c0039t0008g0206 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-52+871G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131395134 | ||||||
| chr9:131395160
|
C | CTCA | 2 | a0002c0007t0014g0002a0002c0007t0014g0012 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-52+898_-52+899ins others(3): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131395160 | |||||
| chr9:131395225
|
C | G | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-52+962C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131395225 | ||||||
| chr9:131395339
|
G | C | 2 | a0013c0020t0032g0006a0021c0034t0048g0013 | 2 | HG00642.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-52+1076G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131395339 | ||||||
| chr9:131395362
|
G | C | 1 | a0006c0022t0038g0180 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-52+1099G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131395362 | ||||||
| chr9:131395805
|
A | G | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-52+1542A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131395805 | ||||||
| chr9:131395832
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-52+1569A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131395832 | ||||||
| chr9:131395850
|
G | C | 24 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(21): Show | 24 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-52+1587G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131395850 | ||||||
| chr9:131396239
|
C | G | 2 | a0001c0001t0011g0155a0003c0002t0001g0156 | 2 | NA18972.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-52+1976C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131396239 | ||||||
| chr9:131396246
|
C | T | 26 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.-52+1983C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131396246 | ||||||
| chr9:131396325
|
C | CT | 8 | a0002c0003t0003g0014a0002c0006t0004g0168a0002c0010t0009g0187others(5): Show | 8 | HG01361.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52+2082dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131396325 | |||||
| chr9:131396325
|
C | CTT | 25 | a0002c0003t0003g0015a0002c0003t0003g0016a0002c0003t0003g0018others(22): Show | 25 | HG00558.hp1 HG00642.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.-52+2081_-52+2082d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131396325 | |||||
| chr9:131396325
|
CT | C | 8 | a0001c0001t0001g0033a0002c0006t0004g0160a0002c0026t0040g0178others(5): Show | 8 | HG02451.hp1 HG02896.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-52+2082delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131396325 | |||||
| chr9:131396329
|
T | TC | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0124others(2): Show | 5 | HG01975.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+2066_-52+2067i others(3): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131396329 | ||||||
| chr9:131396330
|
T | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0042others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.-52+2067T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131396330 | ||||||
| chr9:131396331
|
T | C | 2 | a0001c0001t0001g0033a0024c0025t0001g0034 | 2 | NA19003.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-52+2068T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131396331 | ||||||
| chr9:131396351
|
A | G | 10 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-52+2088A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131396351 | ||||||
| chr9:131396575
|
C | G | 3 | a0001c0001t0001g0122a0001c0001t0045g0121a0001c0001t0049g0120 | 3 | HG00280.hp2 HG01069.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-52+2312C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131396575 | ||||||
| chr9:131396893
|
T | C | 9 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+2630T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131396893 | ||||||
| chr9:131396950
|
T | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-52+2687T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131396950 | ||||||
| chr9:131397036
|
C | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.-52+2773C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131397036 | ||||||
| chr9:131397187
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-52+2924G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131397187 | ||||||
| chr9:131397381
|
C | T | 2 | a0005c0005t0001g0010a0005c0005t0001g0011 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-52+3118C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131397381 | ||||||
| chr9:131397563
|
G | GTTT | 13 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(10): Show | 13 | HG00642.hp2 HG01123.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-52+3319_-52+3321d others(5): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131397563 | |||||
| chr9:131397563
|
G | GTTTTT | 19 | a0002c0006t0026g0146a0002c0007t0010g0201a0002c0007t0010g0202others(16): Show | 19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.-52+3317_-52+3321d others(7): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131397563 | |||||
| chr9:131397563
|
G | GTTTTTT | 8 | a0002c0007t0014g0012a0002c0026t0040g0178a0002c0040t0029g0151others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.-52+3316_-52+3321d others(8): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131397563 | |||||
| chr9:131397563
|
GTTT | G | 9 | a0002c0003t0003g0032a0002c0003t0008g0216a0002c0010t0009g0188others(6): Show | 9 | HG01106.hp1 HG01192.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+3319_-52+3321d others(5): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131397563 | |||||
| chr9:131397563
|
GTTTT | G | 45 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0112others(42): Show | 45 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.-52+3318_-52+3321d others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131397563 | |||||
| chr9:131397563
|
GTTTTT | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-52+3317_-52+3321d others(7): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131397563 | |||||
| chr9:131397563
|
GTTTTTTT others(3): Show |
G | 3 | a0004c0009t0007g0132a0004c0009t0007g0159a0015c0021t0004g0005 | 3 | HG02922.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-52+3312_-52+3321d others(12): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131397563 | |||||
| chr9:131397721
|
A | G | 27 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(24): Show | 27 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.-52+3458A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131397721 | ||||||
| chr9:131397741
|
A | G | 12 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(9): Show | 12 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.-52+3478A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131397741 | ||||||
| chr9:131397787
|
C | T | 2 | a0020c0028t0007g0135a0023c0036t0007g0148 | 2 | HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-52+3524C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131397787 | ||||||
| chr9:131397968
|
G | A | 1 | a0004c0004t0005g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-52+3705G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131397968 | ||||||
| chr9:131397981
|
G | C | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+3718G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131397981 | ||||||
| chr9:131398110
|
T | A | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-52+3847T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131398110 | ||||||
| chr9:131398176
|
G | C | 2 | a0002c0003t0003g0014a0002c0003t0003g0015 | 2 | NA19012.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-52+3913G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131398176 | ||||||
| chr9:131398185
|
C | T | 1 | a0004c0004t0005g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-52+3922C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131398185 | ||||||
| chr9:131398360
|
G | A | 24 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(21): Show | 24 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-52+4097G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131398360 | ||||||
| chr9:131398511
|
C | T | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-52+4248C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131398511 | ||||||
| chr9:131398519
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0041t0001g0041 | 3 | HG01358.hp1 HG01496.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-52+4256G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131398519 | ||||||
| chr9:131398528
|
G | A | 1 | a0012c0045t0001g0043 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-52+4265G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131398528 | ||||||
| chr9:131398847
|
G | A | 2 | a0003c0002t0001g0045a0003c0002t0041g0044 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-52+4584G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131398847 | ||||||
| chr9:131398927
|
G | A | 26 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.-52+4664G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131398927 | ||||||
| chr9:131398997
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-52+4734C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131398997 | ||||||
| chr9:131399056
|
A | G | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-52+4793A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131399056 | ||||||
| chr9:131399276
|
C | CA | 50 | a0001c0001t0001g0003a0001c0001t0001g0048a0001c0001t0001g0050others(47): Show | 50 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-52+5034dupA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131399276 | |||||
| chr9:131399276
|
C | CAA | 30 | a0002c0003t0003g0016a0002c0003t0003g0018a0002c0003t0003g0032others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.-52+5033_-52+5034d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131399276 | |||||
| chr9:131399276
|
CA | C | 9 | a0001c0001t0002g0191a0001c0001t0002g0193a0001c0001t0002g0194others(6): Show | 9 | HG00735.hp1 HG01496.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+5034delA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131399276 | |||||
| chr9:131399376
|
G | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-52+5113G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131399376 | ||||||
| chr9:131399437
|
G | A | 1 | a0005c0044t0021g0200 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-52+5174G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131399437 | ||||||
| chr9:131399437
|
G | T | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-52+5174G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131399437 | ||||||
| chr9:131399513
|
A | C | 3 | a0005c0005t0001g0095a0005c0005t0002g0210a0005c0005t0002g0211 | 3 | NA18970.hp1 NA18971.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-52+5250A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131399513 | ||||||
| chr9:131399536
|
G | A | 26 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.-52+5273G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131399536 | ||||||
| chr9:131399548
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-52+5285T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131399548 | ||||||
| chr9:131399923
|
C | T | 27 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(24): Show | 27 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.-52+5660C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131399923 | ||||||
| chr9:131399946
|
G | A | 2 | a0002c0008t0034g0035a0002c0008t0042g0038 | 2 | HG01123.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-52+5683G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131399946 | ||||||
| chr9:131399997
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.-52+5734T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131399997 | ||||||
| chr9:131400097
|
T | C | 2 | a0005c0005t0001g0010a0005c0005t0001g0011 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-52+5834T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131400097 | ||||||
| chr9:131400284
|
GCCATTTT others(1567): Show |
G | 1 | a0002c0003t0003g0019 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-52+6026_-52+7599d others(2): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131400284 | |||||
| chr9:131400370
|
G | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-52+6107G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131400370 | ||||||
| chr9:131400449
|
C | T | 2 | a0009c0015t0005g0094a0009c0015t0006g0115 | 2 | HG00639.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.-52+6186C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131400449 | ||||||
| chr9:131400486
|
T | G | 1 | a0005c0005t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-52+6223T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131400486 | ||||||
| chr9:131400506
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-52+6243C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131400506 | ||||||
| chr9:131400560
|
C | T | 1 | a0003c0002t0004g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-52+6297C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131400560 | ||||||
| chr9:131400608
|
G | T | 1 | a0002c0007t0024g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-52+6345G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131400608 | ||||||
| chr9:131400687
|
C | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.-52+6424C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131400687 | ||||||
| chr9:131400714
|
G | A | 1 | a0002c0008t0042g0038 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-52+6451G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131400714 | ||||||
| chr9:131400906
|
G | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-52+6643G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131400906 | ||||||
| chr9:131400917
|
G | A | 2 | a0005c0005t0001g0010a0005c0005t0001g0011 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-52+6654G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131400917 | ||||||
| chr9:131400951
|
GTTTC | G | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0114 | 3 | HG01168.hp1 HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-52+6700_-52+6703d others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131400951 | |||||
| chr9:131400962
|
TC | T | 10 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0193others(7): Show | 10 | HG00735.hp1 HG01496.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-52+6700delC | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131400962 | ||||||
| chr9:131400963
|
C | CT | 6 | a0002c0007t0024g0186a0002c0008t0035g0039a0002c0008t0042g0038others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+6715dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131400963 | |||||
| chr9:131401018
|
A | G | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+6755A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131401018 | ||||||
| chr9:131401054
|
C | T | 1 | a0002c0003t0003g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-52+6791C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131401054 | ||||||
| chr9:131401163
|
T | C | 1 | a0007c0017t0001g0056 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-52+6900T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131401163 | ||||||
| chr9:131401262
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.-52+6999A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131401262 | ||||||
| chr9:131401350
|
A | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0012c0045t0001g0043 | 3 | NA18949.hp1 NA19012.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-52+7087A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131401350 | ||||||
| chr9:131401358
|
C | T | 2 | a0008c0016t0001g0088a0008c0016t0001g0089 | 2 | NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-52+7095C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131401358 | ||||||
| chr9:131401385
|
C | CT | 6 | a0001c0001t0001g0176a0002c0006t0004g0167a0002c0008t0028g0126others(3): Show | 6 | HG00735.hp2 HG01192.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52+7138dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131401385 | |||||
| chr9:131401524
|
A | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0040others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.-52+7261A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131401524 | ||||||
| chr9:131401539
|
C | T | 1 | a0002c0003t0003g0031 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-52+7276C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131401539 | ||||||
| chr9:131401661
|
A | ATATTT | 6 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(3): Show | 6 | HG00642.hp2 HG02055.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+7413_-52+7417d others(7): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131401661 | |||||
| chr9:131401760
|
A | G | 2 | a0005c0005t0001g0010a0005c0005t0001g0011 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-52+7497A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131401760 | ||||||
| chr9:131401828
|
T | C | 29 | a0001c0001t0043g0105a0002c0003t0003g0014a0002c0003t0003g0015others(26): Show | 29 | HG01192.hp1 HG01257.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.-52+7565T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131401828 | ||||||
| chr9:131401958
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-52+7695G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131401958 | ||||||
| chr9:131402060
|
C | T | 9 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+7797C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131402060 | ||||||
| chr9:131402393
|
G | T | 3 | a0002c0010t0009g0187a0002c0010t0009g0188a0002c0010t0009g0189 | 3 | HG01361.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-52+8130G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131402393 | ||||||
| chr9:131402468
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-52+8205A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131402468 | ||||||
| chr9:131402554
|
A | G | 3 | a0001c0001t0001g0122a0001c0001t0045g0121a0001c0001t0049g0120 | 3 | HG00280.hp2 HG01069.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-52+8291A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131402554 | ||||||
| chr9:131402576
|
G | C | 1 | a0001c0041t0001g0041 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-52+8313G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131402576 | ||||||
| chr9:131402801
|
A | G | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-52+8538A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131402801 | ||||||
| chr9:131402872
|
A | G | 1 | a0002c0003t0003g0018 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-52+8609A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131402872 | ||||||
| chr9:131402883
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-52+8620A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131402883 | ||||||
| chr9:131402965
|
G | C | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+8702G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131402965 | ||||||
| chr9:131403344
|
T | TTTTA | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+9097_-52+9100d others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131403344 | |||||
| chr9:131403360
|
A | T | 5 | a0002c0008t0028g0126a0003c0002t0001g0183a0003c0002t0001g0184others(2): Show | 5 | HG01891.hp1 HG02572.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+9097A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131403360 | ||||||
| chr9:131403364
|
T | A | 12 | a0001c0001t0001g0071a0001c0001t0001g0122a0001c0001t0045g0121others(9): Show | 12 | HG00280.hp2 HG00558.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.-52+9101T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131403364 | ||||||
| chr9:131403386
|
C | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-52+9123C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131403386 | ||||||
| chr9:131403422
|
G | A | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-52+9159G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131403422 | ||||||
| chr9:131403493
|
A | G | 1 | a0002c0008t0025g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-52+9230A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131403493 | ||||||
| chr9:131403662
|
TA | T | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+9416delA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131403662 | |||||
| chr9:131403677
|
AAAC | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0119others(13): Show | 16 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.-52+9417_-52+9419d others(5): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131403677 | |||||
| chr9:131403678
|
AAC | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0040others(145): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-52+9417_-52+9418d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131403678 | |||||
| chr9:131403679
|
AC | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0124others(34): Show | 37 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-52+9417delC | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131403679 | ||||||
| chr9:131403727
|
A | G | 9 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+9464A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131403727 | ||||||
| chr9:131403744
|
C | T | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-52+9481C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131403744 | ||||||
| chr9:131403789
|
C | T | 1 | a0002c0033t0023g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-52+9526C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131403789 | ||||||
| chr9:131403798
|
A | G | 2 | a0005c0005t0001g0010a0005c0005t0001g0011 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-52+9535A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131403798 | ||||||
| chr9:131403946
|
T | C | 1 | a0002c0003t0003g0016 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-52+9683T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131403946 | ||||||
| chr9:131404055
|
A | G | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+9792A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131404055 | ||||||
| chr9:131404167
|
A | G | 1 | a0005c0043t0001g0086 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-52+9904A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131404167 | ||||||
| chr9:131404216
|
C | CT | 16 | a0001c0001t0002g0199a0002c0003t0003g0030a0002c0006t0004g0167others(13): Show | 16 | HG00642.hp2 HG01361.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.-52+9972dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131404216 | |||||
| chr9:131404305
|
C | T | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-52+10042C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131404305 | ||||||
| chr9:131404329
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-52+10066T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131404329 | ||||||
| chr9:131404338
|
G | A | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-52+10075G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131404338 | ||||||
| chr9:131404414
|
A | G | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-52+10151A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131404414 | ||||||
| chr9:131404497
|
C | G | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0114 | 3 | HG01168.hp1 HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-52+10234C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131404497 | ||||||
| chr9:131404502
|
G | A | 1 | a0003c0002t0039g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-52+10239G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131404502 | ||||||
| chr9:131404556
|
C | T | 1 | a0003c0002t0001g0184 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-52+10293C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131404556 | ||||||
| chr9:131404592
|
G | GA | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-52+10338dupA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131404592 | |||||
| chr9:131404605
|
G | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-52+10342G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131404605 | ||||||
| chr9:131404662
|
G | A | 2 | a0002c0012t0004g0161a0002c0012t0004g0162 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-52+10399G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131404662 | ||||||
| chr9:131404805
|
C | A | 2 | a0005c0005t0002g0204a0005c0005t0002g0205 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+10542C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131404805 | ||||||
| chr9:131405257
|
G | A | 1 | a0002c0010t0009g0187 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-52+10994G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131405257 | ||||||
| chr9:131405356
|
C | T | 3 | a0002c0003t0003g0028a0002c0023t0012g0029a0002c0038t0012g0171 | 3 | HG01192.hp1 HG01975.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-52+11093C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131405356 | ||||||
| chr9:131405417
|
G | A | 2 | a0005c0005t0002g0204a0005c0005t0002g0205 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-52+11154G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131405417 | ||||||
| chr9:131405545
|
C | T | 36 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(33): Show | 36 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.-52+11282C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131405545 | ||||||
| chr9:131405753
|
G | A | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-52+11490G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131405753 | ||||||
| chr9:131405810
|
C | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-52+11547C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131405810 | ||||||
| chr9:131405843
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-52+11580A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131405843 | ||||||
| chr9:131406037
|
G | C | 2 | a0008c0016t0001g0088a0008c0016t0001g0089 | 2 | NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-52+11774G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131406037 | ||||||
| chr9:131406039
|
C | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-52+11776C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131406039 | ||||||
| chr9:131406058
|
C | T | 2 | a0001c0001t0011g0155a0003c0002t0011g0158 | 2 | NA18972.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-52+11795C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131406058 | ||||||
| chr9:131406101
|
CG | C | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+11843delG | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131406101 | |||||
| chr9:131406285
|
A | T | 1 | a0001c0001t0001g0085 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-52+12022A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131406285 | ||||||
| chr9:131406371
|
C | T | 36 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(33): Show | 36 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.-52+12108C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131406371 | ||||||
| chr9:131406404
|
G | A | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-52+12141G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131406404 | ||||||
| chr9:131406449
|
A | G | 2 | a0002c0003t0003g0026a0002c0003t0003g0027 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-52+12186A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131406449 | ||||||
| chr9:131406544
|
A | T | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-52+12281A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131406544 | ||||||
| chr9:131406621
|
C | T | 1 | a0001c0001t0002g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-52+12358C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131406621 | ||||||
| chr9:131407167
|
G | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-52+12904G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131407167 | ||||||
| chr9:131407179
|
A | G | 1 | a0002c0003t0003g0025 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-52+12916A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131407179 | ||||||
| chr9:131407462
|
G | T | 7 | a0002c0040t0029g0151a0003c0002t0001g0134a0003c0002t0001g0152others(4): Show | 7 | HG02647.hp1 HG02965.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-52+13199G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131407462 | ||||||
| chr9:131407525
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-52+13262A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131407525 | ||||||
| chr9:131407599
|
C | T | 8 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(5): Show | 8 | HG02055.hp1 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52+13336C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131407599 | ||||||
| chr9:131407699
|
A | C | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-52+13436A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131407699 | ||||||
| chr9:131407822
|
T | C | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-52+13559T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131407822 | ||||||
| chr9:131407901
|
G | A | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-52+13638G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131407901 | ||||||
| chr9:131407966
|
C | T | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-52+13703C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131407966 | ||||||
| chr9:131408063
|
G | A | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-52+13800G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131408063 | ||||||
| chr9:131408463
|
A | G | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-52+14200A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131408463 | ||||||
| chr9:131408516
|
C | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-52+14253C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131408516 | ||||||
| chr9:131408526
|
C | G | 3 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203 | 3 | HG02723.hp2 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-52+14263C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131408526 | ||||||
| chr9:131408757
|
T | G | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-52+14494T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131408757 | ||||||
| chr9:131408822
|
T | A | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-52+14559T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131408822 | ||||||
| chr9:131408912
|
T | G | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-52+14649T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131408912 | ||||||
| chr9:131409010
|
C | T | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+14747C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131409010 | ||||||
| chr9:131409020
|
C | CT | 27 | a0002c0006t0026g0146a0002c0026t0040g0178a0002c0040t0029g0151others(24): Show | 27 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.-52+14773dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131409020 | |||||
| chr9:131409020
|
CT | C | 27 | a0001c0001t0001g0050a0001c0001t0022g0192a0002c0003t0003g0014others(24): Show | 27 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.-52+14773delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131409020 | |||||
| chr9:131409035
|
T | A | 1 | a0001c0001t0002g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-52+14772T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131409035 | ||||||
| chr9:131409037
|
C | T | 9 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+14774C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131409037 | ||||||
| chr9:131409039
|
T | C | 9 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-52+14776T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131409039 | ||||||
| chr9:131409169
|
T | C | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-52+14906T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131409169 | ||||||
| chr9:131409242
|
G | A | 1 | a0002c0007t0024g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-52+14979G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131409242 | ||||||
| chr9:131409368
|
C | T | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-52+15105C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131409368 | ||||||
| chr9:131409452
|
G | T | 2 | a0002c0003t0003g0014a0002c0003t0003g0015 | 2 | NA19012.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-52+15189G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131409452 | ||||||
| chr9:131409603
|
G | T | 1 | a0017c0024t0001g0068 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-52+15340G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131409603 | ||||||
| chr9:131409690
|
G | A | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-52+15427G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131409690 | ||||||
| chr9:131409692
|
A | G | 1 | a0001c0001t0017g0007 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-52+15429A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131409692 | ||||||
| chr9:131409885
|
T | C | 1 | a0002c0006t0004g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-52+15622T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131409885 | ||||||
| chr9:131410141
|
G | A | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52+15878G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131410141 | ||||||
| chr9:131410180
|
G | A | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-52+15917G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131410180 | ||||||
| chr9:131410368
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-52+16105C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131410368 | ||||||
| chr9:131410437
|
T | C | 27 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(24): Show | 27 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.-52+16174T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131410437 | ||||||
| chr9:131410705
|
T | A | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-52+16442T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131410705 | ||||||
| chr9:131410769
|
A | G | 1 | a0002c0008t0035g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-52+16506A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131410769 | ||||||
| chr9:131410813
|
A | G | 1 | a0002c0006t0004g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-52+16550A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131410813 | ||||||
| chr9:131410914
|
A | AT | 5 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0019others(2): Show | 5 | HG00558.hp1 HG01123.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52+16659dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131410914 | |||||
| chr9:131411181
|
C | T | 1 | a0002c0003t0003g0030 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-52+16918C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131411181 | ||||||
| chr9:131411302
|
G | A | 2 | a0002c0008t0028g0126a0015c0021t0004g0005 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-52+17039G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131411302 | ||||||
| chr9:131411353
|
GT | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-52+17101delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131411353 | |||||
| chr9:131411705
|
CT | C | 30 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(27): Show | 30 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-52+17448delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131411705 | |||||
| chr9:131411958
|
C | A | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52+17695C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131411958 | ||||||
| chr9:131411970
|
AT | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-52+17722delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131411970 | |||||
| chr9:131412006
|
T | C | 1 | a0002c0008t0025g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-52+17743T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131412006 | ||||||
| chr9:131412107
|
T | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0040others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.-52+17844T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131412107 | ||||||
| chr9:131412152
|
G | T | 1 | a0002c0006t0004g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-52+17889G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131412152 | ||||||
| chr9:131412467
|
T | TGTGC | 10 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0193others(7): Show | 10 | HG00735.hp1 HG01496.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51-17610_-51-1760 others(8): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131412467 | |||||
| chr9:131412537
|
G | A | 1 | a0002c0006t0004g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-51-17557G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131412537 | ||||||
| chr9:131412620
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-51-17474A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131412620 | ||||||
| chr9:131412654
|
C | T | 2 | a0008c0016t0001g0088a0008c0016t0001g0089 | 2 | NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-51-17440C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131412654 | ||||||
| chr9:131412785
|
T | TTC | 2 | a0003c0002t0001g0045a0003c0002t0041g0044 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-51-17297_-51-1729 others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131412785 | |||||
| chr9:131412797
|
C | CT | 31 | a0001c0001t0001g0092a0001c0001t0001g0124a0002c0003t0003g0014others(28): Show | 31 | HG00639.hp1 HG00642.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-51-17281dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131412797 | |||||
| chr9:131412797
|
C | CTT | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-51-17282_-51-1728 others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131412797 | |||||
| chr9:131412797
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-51-17297C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131412797 | ||||||
| chr9:131412903
|
C | T | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51-17191C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131412903 | ||||||
| chr9:131412929
|
GATTATAG others(13): Show |
G | 1 | a0001c0001t0044g0051 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-51-17163_-51-1714 others(24): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131412929 | |||||
| chr9:131413258
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-51-16836C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131413258 | ||||||
| chr9:131413417
|
C | T | 26 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51-16677C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131413417 | ||||||
| chr9:131413492
|
G | A | 1 | a0002c0003t0003g0018 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-51-16602G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131413492 | ||||||
| chr9:131413556
|
C | T | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-16538C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131413556 | ||||||
| chr9:131413852
|
A | G | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-16242A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131413852 | ||||||
| chr9:131413916
|
C | G | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-51-16178C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131413916 | ||||||
| chr9:131413916
|
C | T | 5 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(2): Show | 5 | HG01167.hp1 HG02451.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-16178C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131413916 | ||||||
| chr9:131413921
|
C | T | 4 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0019others(1): Show | 4 | HG00558.hp1 NA18949.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-16173C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131413921 | ||||||
| chr9:131413962
|
G | A | 2 | a0005c0005t0001g0010a0005c0005t0001g0011 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-51-16132G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131413962 | ||||||
| chr9:131413989
|
A | C | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-51-16105A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131413989 | ||||||
| chr9:131414098
|
G | C | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51-15996G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414098 | ||||||
| chr9:131414231
|
T | G | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-51-15863T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414231 | ||||||
| chr9:131414237
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-51-15857C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414237 | ||||||
| chr9:131414353
|
A | C | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-15741A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414353 | ||||||
| chr9:131414407
|
T | TTATATCT others(3218): Show |
1 | a0001c0001t0049g0120 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-51-15686_-51-1568 others(3229): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414407 | |||||
| chr9:131414407
|
T | TTATATCT others(3399): Show |
1 | a0001c0001t0045g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-51-15686_-51-1568 others(3410): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414407 | |||||
| chr9:131414407
|
T | TTATATCT others(3399): Show |
1 | a0001c0001t0001g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-51-15686_-51-1568 others(3410): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414407 | |||||
| chr9:131414409
|
G | C | 3 | a0001c0001t0001g0122a0001c0001t0045g0121a0001c0001t0049g0120 | 3 | HG00280.hp2 HG01069.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-51-15685G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414409 | ||||||
| chr9:131414409
|
G | GTATCTTT others(2979): Show |
1 | a0001c0001t0002g0193 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(2990): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3335): Show |
1 | a0001c0001t0001g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3346): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3336): Show |
1 | a0001c0001t0001g0058 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3347): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3336): Show |
1 | a0001c0001t0001g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3347): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3337): Show |
1 | a0014c0042t0001g0173 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3348): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3338): Show |
1 | a0005c0044t0021g0200 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3349): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3468): Show |
1 | a0004c0004t0005g0123 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3479): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3389): Show |
1 | a0005c0005t0002g0204 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3400): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3390): Show |
1 | a0005c0005t0002g0205 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3401): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3342): Show |
1 | a0001c0001t0001g0003 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3353): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3395): Show |
1 | a0005c0005t0002g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3406): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3221): Show |
1 | a0003c0002t0011g0158 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3232): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3348): Show |
1 | a0003c0002t0001g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3359): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3227): Show |
1 | a0003c0002t0001g0156 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3238): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2998): Show |
1 | a0003c0002t0027g0174 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3009): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3348): Show |
1 | a0005c0005t0002g0212 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3359): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3360): Show |
1 | a0005c0005t0002g0214 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3371): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3397): Show |
1 | a0001c0001t0001g0097 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3408): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3398): Show |
1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3409): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3398): Show |
1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3409): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3398): Show |
1 | a0003c0002t0001g0185 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3409): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3399): Show |
1 | a0003c0031t0001g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3410): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2994): Show |
1 | a0001c0001t0002g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3005): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2979): Show |
1 | a0001c0001t0002g0199 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(2990): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3396): Show |
1 | a0005c0005t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3407): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3397): Show |
1 | a0005c0005t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3408): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3349): Show |
1 | a0005c0005t0002g0213 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3360): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2948): Show |
1 | a0005c0005t0001g0108 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(2959): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3397): Show |
1 | a0005c0005t0001g0095 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3408): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3349): Show |
1 | a0001c0001t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3360): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3398): Show |
4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3409): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3398): Show |
1 | a0001c0001t0001g0050 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3409): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3399): Show |
2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG01515.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3410): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3399): Show |
1 | a0001c0001t0001g0112 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3410): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3400): Show |
1 | a0001c0001t0001g0001 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3411): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2742): Show |
1 | a0001c0001t0001g0033 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(2753): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3403): Show |
1 | a0001c0001t0001g0175 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3414): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2995): Show |
1 | a0003c0002t0046g0060 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3006): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2996): Show |
1 | a0003c0002t0047g0061 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3007): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2996): Show |
1 | a0003c0002t0001g0069 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3007): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2993): Show |
1 | a0001c0001t0002g0194 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3004): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2992): Show |
3 | a0001c0001t0002g0191a0001c0001t0002g0195a0001c0001t0002g0197 | 3 | HG02723.hp1 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3003): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3349): Show |
1 | a0005c0005t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3360): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3399): Show |
1 | a0005c0005t0002g0211 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3410): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3399): Show |
1 | a0005c0043t0001g0086 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3410): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3350): Show |
1 | a0001c0001t0001g0004 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3361): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3400): Show |
1 | a0018c0030t0001g0009 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3411): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3400): Show |
1 | a0001c0001t0001g0116 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3411): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3399): Show |
3 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0085 | 3 | NA18747.hp2 NA19087.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3410): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3399): Show |
1 | a0001c0041t0001g0041 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3410): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3400): Show |
1 | a0001c0001t0001g0075 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3411): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3401): Show |
1 | a0001c0001t0001g0157 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3412): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3400): Show |
1 | a0001c0001t0001g0119 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3411): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3401): Show |
1 | a0001c0001t0001g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3412): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3400): Show |
1 | a0009c0015t0005g0094 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3411): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3402): Show |
1 | a0001c0001t0001g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3413): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3349): Show |
1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3360): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3349): Show |
1 | a0001c0001t0043g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3360): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2994): Show |
1 | a0001c0001t0002g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3005): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2994): Show |
1 | a0001c0001t0002g0198 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3005): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3400): Show |
1 | a0003c0002t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3411): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3354): Show |
1 | a0003c0002t0001g0184 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3365): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3400): Show |
1 | a0001c0001t0001g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3411): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3419): Show |
1 | a0001c0001t0033g0077 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3430): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3401): Show |
1 | a0010c0014t0001g0052 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3412): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3400): Show |
1 | a0001c0001t0001g0078 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3411): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3803): Show |
1 | a0001c0001t0001g0053 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3814): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3400): Show |
2 | a0001c0001t0001g0071a0007c0017t0001g0056 | 2 | HG00558.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3411): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3400): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0042 | 2 | HG01496.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3411): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3402): Show |
1 | a0001c0001t0016g0079 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3413): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3351): Show |
1 | a0024c0025t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3362): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2512): Show |
1 | a0001c0001t0001g0080 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(2523): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3401): Show |
1 | a0001c0001t0016g0081 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3412): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3402): Show |
1 | a0010c0014t0001g0055 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3413): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3403): Show |
1 | a0001c0046t0001g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3414): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2462): Show |
1 | a0001c0001t0044g0051 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(2473): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3403): Show |
1 | a0001c0001t0001g0096 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3414): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3403): Show |
1 | a0003c0002t0039g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3414): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3401): Show |
1 | a0001c0001t0001g0054 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3412): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3300): Show |
1 | a0001c0001t0001g0124 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3311): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3350): Show |
1 | a0001c0001t0001g0063 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3361): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3352): Show |
1 | a0001c0001t0001g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3363): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3399): Show |
1 | a0008c0016t0001g0088 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3410): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3364): Show |
1 | a0003c0002t0001g0046 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3375): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3401): Show |
1 | a0008c0016t0001g0089 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3412): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3402): Show |
1 | a0001c0001t0001g0082 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3413): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3403): Show |
1 | a0001c0001t0001g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3414): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3402): Show |
1 | a0009c0015t0006g0115 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3413): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3422): Show |
1 | a0001c0001t0001g0093 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3433): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3414): Show |
1 | a0001c0001t0001g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3425): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3351): Show |
1 | a0001c0001t0011g0155 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3362): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3353): Show |
1 | a0001c0001t0001g0109 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3364): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3400): Show |
1 | a0001c0001t0001g0090 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3411): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3401): Show |
1 | a0001c0001t0001g0091 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3412): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3402): Show |
1 | a0003c0002t0041g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3413): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(2996): Show |
1 | a0001c0001t0022g0192 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3007): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3403): Show |
1 | a0007c0017t0001g0106 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3414): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3404): Show |
1 | a0001c0001t0001g0092 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3415): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3403): Show |
1 | a0003c0002t0001g0065 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3414): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3402): Show |
2 | a0003c0002t0001g0066a0017c0024t0001g0068 | 2 | HG01069.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3413): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3404): Show |
1 | a0003c0002t0001g0110 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3415): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3355): Show |
1 | a0003c0002t0001g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3366): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3374): Show |
1 | a0001c0001t0001g0087 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3385): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3359): Show |
1 | a0001c0001t0001g0083 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3370): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3353): Show |
1 | a0001c0001t0001g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3364): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3403): Show |
1 | a0012c0045t0001g0043 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3414): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3355): Show |
1 | a0001c0001t0001g0070 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3366): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3354): Show |
1 | a0001c0001t0017g0007 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3365): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3404): Show |
2 | a0003c0002t0001g0067a0003c0002t0001g0128 | 2 | HG01071.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3415): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3407): Show |
1 | a0003c0002t0004g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3418): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3418): Show |
1 | a0003c0002t0001g0127 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3429): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3361): Show |
1 | a0001c0001t0017g0008 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3372): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3404): Show |
1 | a0003c0002t0001g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3415): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414409
|
G | GTATCTTT others(3406): Show |
1 | a0003c0002t0001g0129 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-51-15670_-51-1566 others(3417): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414409 | |||||
| chr9:131414456
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-51-15638A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414456 | ||||||
| chr9:131414509
|
G | A | 1 | a0006c0011t0037g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-51-15585G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414509 | ||||||
| chr9:131414521
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-51-15573T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414521 | ||||||
| chr9:131414573
|
C | CT | 7 | a0001c0001t0001g0085a0001c0001t0033g0077a0003c0002t0001g0129others(4): Show | 7 | HG00642.hp2 HG02572.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51-15508dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131414573 | |||||
| chr9:131414742
|
G | C | 2 | a0003c0002t0001g0183a0003c0002t0001g0184 | 2 | HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-51-15352G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414742 | ||||||
| chr9:131414744
|
A | G | 15 | a0002c0008t0025g0125a0004c0004t0005g0117a0004c0004t0005g0140others(12): Show | 15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.-51-15350A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414744 | ||||||
| chr9:131414823
|
G | C | 2 | a0002c0012t0004g0161a0002c0012t0004g0162 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-51-15271G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414823 | ||||||
| chr9:131414893
|
G | A | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-51-15201G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414893 | ||||||
| chr9:131414992
|
C | A | 1 | a0002c0033t0023g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-51-15102C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131414992 | ||||||
| chr9:131415306
|
G | A | 14 | a0003c0002t0001g0046a0003c0002t0001g0065a0003c0002t0001g0066others(11): Show | 14 | HG00140.hp1 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-51-14788G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131415306 | ||||||
| chr9:131415359
|
T | G | 3 | a0001c0001t0002g0195a0001c0001t0002g0197a0001c0001t0022g0192 | 3 | HG01496.hp2 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-51-14735T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131415359 | ||||||
| chr9:131415385
|
T | TTAG | 14 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(11): Show | 14 | HG02572.hp1 HG02647.hp1 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.-51-14708_-51-1470 others(7): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131415385 | |||||
| chr9:131415511
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.-51-14583A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131415511 | ||||||
| chr9:131415826
|
C | G | 14 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(11): Show | 14 | HG02572.hp1 HG02647.hp1 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.-51-14268C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131415826 | ||||||
| chr9:131415828
|
T | A | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-14266T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131415828 | ||||||
| chr9:131415883
|
G | C | 43 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(40): Show | 43 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.-51-14211G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131415883 | ||||||
| chr9:131416025
|
G | A | 14 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(11): Show | 14 | HG02572.hp1 HG02647.hp1 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.-51-14069G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416025 | ||||||
| chr9:131416058
|
A | G | 1 | a0001c0001t0044g0051 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-51-14036A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416058 | ||||||
| chr9:131416114
|
C | CT | 19 | a0002c0006t0026g0146a0002c0007t0010g0201a0002c0007t0010g0202others(16): Show | 19 | HG02055.hp1 HG02572.hp1 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51-13968dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131416114 | |||||
| chr9:131416343
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-51-13751A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416343 | ||||||
| chr9:131416607
|
C | A | 1 | a0003c0002t0001g0156 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-51-13487C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416607 | ||||||
| chr9:131416621
|
C | CT | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-51-13463dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131416621 | |||||
| chr9:131416631
|
T | C | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-13463T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416631 | ||||||
| chr9:131416632
|
C | T | 12 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(9): Show | 12 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.-51-13462C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416632 | ||||||
| chr9:131416670
|
A | G | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-13424A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416670 | ||||||
| chr9:131416750
|
A | G | 25 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(22): Show | 25 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51-13344A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416750 | ||||||
| chr9:131416755
|
C | T | 10 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0193others(7): Show | 10 | HG00735.hp1 HG01496.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51-13339C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416755 | ||||||
| chr9:131416758
|
C | T | 11 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(8): Show | 11 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51-13336C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416758 | ||||||
| chr9:131416875
|
GA | G | 6 | a0002c0006t0004g0165a0002c0006t0004g0167a0002c0006t0018g0164others(3): Show | 6 | HG01167.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51-13212delA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131416875 | |||||
| chr9:131416944
|
T | G | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-13150T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416944 | ||||||
| chr9:131416954
|
C | G | 2 | a0011c0013t0031g0036a0011c0013t0036g0037 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-51-13140C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416954 | ||||||
| chr9:131416996
|
A | G | 14 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(11): Show | 14 | HG02572.hp1 HG02647.hp1 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.-51-13098A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131416996 | ||||||
| chr9:131417051
|
G | A | 1 | a0002c0019t0011g0022 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-51-13043G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131417051 | ||||||
| chr9:131417100
|
A | G | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-12994A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131417100 | ||||||
| chr9:131417149
|
G | GTTTTCTT others(5): Show |
1 | a0001c0001t0001g0075 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-51-12944_-51-1293 others(16): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131417149 | |||||
| chr9:131417478
|
C | T | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-51-12616C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131417478 | ||||||
| chr9:131417498
|
C | T | 3 | a0002c0012t0004g0161a0002c0012t0004g0162a0002c0033t0023g0163 | 3 | HG02970.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-51-12596C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131417498 | ||||||
| chr9:131417942
|
G | A | 2 | a0002c0018t0008g0207a0002c0018t0008g0208 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-12152G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131417942 | ||||||
| chr9:131418050
|
C | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-12044C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131418050 | ||||||
| chr9:131418061
|
A | G | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-51-12033A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131418061 | ||||||
| chr9:131418072
|
A | G | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-51-12022A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131418072 | ||||||
| chr9:131418144
|
T | C | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-51-11950T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131418144 | ||||||
| chr9:131418190
|
T | TCATCATC others(15): Show |
1 | a0001c0001t0001g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-51-11903_-51-1188 others(26): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131418190 | |||||
| chr9:131418215
|
C | G | 1 | a0004c0009t0007g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-51-11879C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131418215 | ||||||
| chr9:131418504
|
A | G | 1 | a0004c0009t0007g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-51-11590A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131418504 | ||||||
| chr9:131418732
|
C | T | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-11362C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131418732 | ||||||
| chr9:131418885
|
G | A | 1 | a0002c0003t0003g0019 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-51-11209G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131418885 | ||||||
| chr9:131418893
|
T | C | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-51-11201T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131418893 | ||||||
| chr9:131418939
|
GCTGGTGA others(8): Show |
G | 1 | a0001c0001t0001g0093 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-51-11153_-51-1113 others(19): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131418939 | |||||
| chr9:131419074
|
A | G | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51-11020A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131419074 | ||||||
| chr9:131419145
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-51-10949A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131419145 | ||||||
| chr9:131419253
|
ATCTCCCT others(8): Show |
A | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-51-10840_-51-1082 others(19): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131419253 | ||||||
| chr9:131419345
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-51-10749T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131419345 | ||||||
| chr9:131419488
|
G | A | 2 | a0002c0007t0024g0186a0015c0021t0004g0005 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-51-10606G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131419488 | ||||||
| chr9:131419655
|
CTCT | C | 30 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(27): Show | 30 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-51-10437_-51-1043 others(7): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131419655 | |||||
| chr9:131419877
|
C | T | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51-10217C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131419877 | ||||||
| chr9:131419906
|
G | A | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-10188G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131419906 | ||||||
| chr9:131419918
|
C | T | 6 | a0003c0002t0001g0134a0003c0002t0001g0152a0003c0002t0001g0153others(3): Show | 6 | HG02647.hp1 HG02965.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51-10176C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131419918 | ||||||
| chr9:131420007
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-51-10087T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420007 | ||||||
| chr9:131420317
|
C | T | 1 | a0003c0002t0027g0174 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-51-9777C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420317 | ||||||
| chr9:131420433
|
T | G | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51-9661T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420433 | ||||||
| chr9:131420451
|
C | CTCTTTCT others(1): Show |
3 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0031 | 3 | HG01257.hp2 NA19012.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-51-9642_-51-9641i others(10): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420451 | |||||
| chr9:131420451
|
C | CTCTTTCT others(5): Show |
3 | a0002c0003t0003g0024a0002c0003t0003g0025a0002c0003t0003g0028 | 3 | HG01975.hp1 NA19091.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-51-9642_-51-9641i others(14): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420451 | |||||
| chr9:131420451
|
C | CTCTTTCT others(9): Show |
3 | a0002c0003t0003g0016a0002c0019t0011g0022a0002c0037t0003g0017 | 3 | HG04228.hp2 NA18985.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-51-9642_-51-9641i others(18): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420451 | |||||
| chr9:131420451
|
C | CTCTTTCT others(13): Show |
2 | a0002c0003t0003g0018a0002c0010t0009g0189 | 2 | HG02895.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-51-9642_-51-9641i others(22): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420451 | |||||
| chr9:131420451
|
C | CTCTTTCT others(17): Show |
1 | a0002c0003t0003g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-51-9642_-51-9641i others(26): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420451 | |||||
| chr9:131420451
|
C | CTCTTTCT others(41): Show |
1 | a0002c0003t0008g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-51-9642_-51-9641i others(50): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420451 | |||||
| chr9:131420451
|
C | CTCTTTCT others(45): Show |
1 | a0002c0003t0003g0026 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-51-9642_-51-9641i others(54): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420451 | |||||
| chr9:131420451
|
C | CTCTTTCT others(325): Show |
1 | a0001c0001t0001g0075 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-51-9642_-51-9641i others(334): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420451 | |||||
| chr9:131420452
|
T | TCTTCTCT others(82): Show |
1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-51-9642_-51-9641i others(91): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420452 | ||||||
| chr9:131420453
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0070others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-51-9641T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420453 | ||||||
| chr9:131420453
|
T | TTCTTTCT others(15): Show |
1 | a0005c0043t0001g0086 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-51-9640_-51-9639i others(24): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420453 | |||||
| chr9:131420453
|
T | TTCTTTCT others(442): Show |
1 | a0001c0001t0001g0093 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-51-9640_-51-9639i others(451): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420453 | |||||
| chr9:131420453
|
T | TTTTCTCT others(75): Show |
1 | a0003c0002t0001g0185 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-51-9636_-51-9635i others(84): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420453 | |||||
| chr9:131420453
|
T | TTTTCTTT others(17): Show |
2 | a0001c0001t0001g0098a0001c0001t0001g0100 | 2 | HG01516.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-51-9621_-51-9598d others(26): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420453 | |||||
| chr9:131420453
|
T | TTTTCTTT others(41): Show |
1 | a0001c0001t0033g0077 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(50): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420453 | |||||
| chr9:131420454
|
T | C | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-51-9640T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420454 | ||||||
| chr9:131420454
|
T | TTTCTTTC others(89): Show |
1 | a0005c0005t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(98): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420454 | |||||
| chr9:131420455
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-51-9639T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420455 | ||||||
| chr9:131420461
|
C | CTCTCTTT others(263): Show |
1 | a0004c0004t0006g0137 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-51-9632_-51-9631i others(272): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420461 | |||||
| chr9:131420461
|
C | CTCTCTTT others(237): Show |
1 | a0004c0004t0005g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-51-9632_-51-9631i others(246): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420461 | |||||
| chr9:131420462
|
T | TTTCTTTC others(392): Show |
1 | a0001c0001t0001g0001 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-51-9615_-51-9614i others(401): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420462 | |||||
| chr9:131420465
|
C | CTCTCTTT others(261): Show |
1 | a0004c0009t0007g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-51-9628_-51-9627i others(270): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTCTCTTT others(285): Show |
1 | a0004c0009t0007g0159 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-51-9628_-51-9627i others(294): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTCT others(260): Show |
1 | a0004c0004t0006g0138 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-51-9624_-51-9623i others(269): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTCT others(287): Show |
1 | a0004c0004t0013g0169 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-51-9624_-51-9623i others(296): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTCT others(263): Show |
1 | a0004c0004t0006g0139 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-51-9624_-51-9623i others(272): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTCT others(273): Show |
1 | a0020c0028t0007g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-51-9624_-51-9623i others(282): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTCT others(233): Show |
1 | a0004c0004t0005g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-51-9624_-51-9623i others(242): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTCT others(241): Show |
2 | a0004c0004t0005g0140a0004c0004t0005g0150 | 2 | HG00639.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-51-9624_-51-9623i others(250): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTCT others(249): Show |
1 | a0022c0027t0006g0141 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-51-9624_-51-9623i others(258): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTCT others(257): Show |
1 | a0004c0004t0030g0142 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-51-9624_-51-9623i others(266): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTCT others(249): Show |
1 | a0004c0004t0005g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-51-9624_-51-9623i others(258): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTCT others(257): Show |
1 | a0004c0004t0006g0144 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-51-9624_-51-9623i others(266): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTCT others(241): Show |
2 | a0004c0004t0005g0147a0004c0004t0006g0145 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-51-9624_-51-9623i others(250): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTTT others(56): Show |
1 | a0002c0008t0025g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(65): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420465
|
C | CTTTCTTT others(51): Show |
1 | a0019c0029t0020g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(60): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420465 | |||||
| chr9:131420468
|
TCTTTCTT others(14): Show |
T | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-51-9625_-51-9605d others(23): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420468 | ||||||
| chr9:131420470
|
TTTCTTTC others(16): Show |
T | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51-9621_-51-9599d others(25): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420470 | |||||
| chr9:131420474
|
T | C | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-9620T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420474 | ||||||
| chr9:131420477
|
C | CTCTCTTT others(266): Show |
1 | a0003c0002t0001g0152 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-51-9616_-51-9615i others(275): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420477 | |||||
| chr9:131420477
|
C | CTCTCTTT others(269): Show |
1 | a0023c0036t0007g0148 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-51-9616_-51-9615i others(278): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420477 | |||||
| chr9:131420477
|
C | CTCTCTTT others(237): Show |
2 | a0004c0009t0007g0133a0004c0009t0007g0136 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-51-9616_-51-9615i others(246): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420477 | |||||
| chr9:131420477
|
C | CTCTCTTT others(293): Show |
1 | a0002c0006t0026g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-51-9616_-51-9615i others(302): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420477 | |||||
| chr9:131420477
|
C | CTCTCTTT others(283): Show |
1 | a0004c0004t0013g0170 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-51-9616_-51-9615i others(292): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420477 | |||||
| chr9:131420477
|
C | CTCTCTTT others(265): Show |
1 | a0003c0002t0001g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-51-9616_-51-9615i others(274): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420477 | |||||
| chr9:131420477
|
C | CTCTCTTT others(265): Show |
1 | a0003c0002t0001g0153 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-51-9616_-51-9615i others(274): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420477 | |||||
| chr9:131420477
|
C | G | 2 | a0004c0004t0005g0149a0004c0004t0006g0137 | 2 | HG01257.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-51-9617C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420477 | ||||||
| chr9:131420478
|
T | C | 2 | a0002c0018t0008g0207a0002c0018t0008g0208 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-9616T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420478 | ||||||
| chr9:131420478
|
T | TTTCG | 3 | a0002c0008t0035g0039a0011c0013t0031g0036a0011c0013t0036g0037 | 3 | HG01891.hp2 HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-51-9613_-51-9612i others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420478 | |||||
| chr9:131420478
|
TTTCTTTC others(8): Show |
T | 5 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0194others(2): Show | 5 | HG00735.hp1 HG02895.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-9613_-51-9599d others(17): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420478 | |||||
| chr9:131420480
|
T | TTCCCTTT others(308): Show |
2 | a0002c0018t0008g0207a0002c0018t0008g0208 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-9614_-51-9613i others(317): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420480 | ||||||
| chr9:131420481
|
C | CTTTCTTT others(11): Show |
1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-9606_-51-9605i others(20): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420481 | |||||
| chr9:131420481
|
C | G | 15 | a0004c0004t0005g0117a0004c0004t0005g0140a0004c0004t0005g0143others(12): Show | 15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.-51-9613C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420481 | ||||||
| chr9:131420482
|
T | G | 3 | a0002c0008t0035g0039a0011c0013t0031g0036a0011c0013t0036g0037 | 3 | HG01891.hp2 HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-51-9612T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420482 | ||||||
| chr9:131420483
|
T | C | 1 | a0003c0002t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-51-9611T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420483 | ||||||
| chr9:131420486
|
T | G | 3 | a0002c0008t0035g0039a0011c0013t0031g0036a0011c0013t0036g0037 | 3 | HG01891.hp2 HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-51-9608T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420486 | ||||||
| chr9:131420486
|
T | TTTCGTTC others(5): Show |
2 | a0002c0008t0034g0035a0002c0008t0042g0038 | 2 | HG01123.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-51-9605_-51-9604i others(14): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420486 | |||||
| chr9:131420486
|
TTTCTTTC | T | 6 | a0001c0001t0002g0193a0001c0001t0002g0195a0001c0001t0002g0196others(3): Show | 6 | HG01496.hp2 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-9605_-51-9599d others(9): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420486 | |||||
| chr9:131420487
|
T | C | 1 | a0002c0040t0029g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-51-9607T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420487 | ||||||
| chr9:131420488
|
T | C | 2 | a0002c0018t0008g0207a0002c0018t0008g0208 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-9606T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420488 | ||||||
| chr9:131420489
|
C | CCTTCTTT others(28): Show |
1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51-9605_-51-9604i others(37): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420489 | ||||||
| chr9:131420489
|
C | CTCTTTCT others(166): Show |
1 | a0001c0001t0001g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-51-9604_-51-9603i others(175): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420489 | |||||
| chr9:131420490
|
T | G | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-9604T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420490 | ||||||
| chr9:131420491
|
T | C | 1 | a0003c0002t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-51-9603T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420491 | ||||||
| chr9:131420493
|
C | CTCTCTCT others(132): Show |
1 | a0001c0001t0001g0054 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-51-9600_-51-9599i others(141): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTCTCTTT others(260): Show |
1 | a0002c0040t0029g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-51-9600_-51-9599i others(269): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCT | 6 | a0001c0001t0001g0064a0003c0002t0001g0069a0003c0002t0001g0128others(3): Show | 6 | HG00741.hp1 HG01071.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(7): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(2): Show |
11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0062others(8): Show | 11 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(11): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(6): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0063a0001c0001t0001g0124others(5): Show | 8 | HG02698.hp2 HG02735.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(15): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(7): Show |
1 | a0001c0001t0001g0040 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(16): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(10): Show |
5 | a0001c0001t0001g0048a0001c0001t0001g0109a0002c0003t0003g0030others(2): Show | 5 | HG02027.hp2 HG02630.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(19): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(11): Show |
2 | a0001c0001t0001g0004a0014c0042t0001g0173 | 2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(20): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(14): Show |
3 | a0001c0001t0001g0059a0003c0002t0001g0045a0005c0005t0002g0211 | 3 | HG02809.hp2 NA18971.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(23): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(15): Show |
1 | a0001c0001t0001g0119 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(24): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(16): Show |
1 | a0001c0001t0001g0102 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(25): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(18): Show |
4 | a0001c0001t0001g0070a0001c0001t0001g0101a0001c0001t0017g0008others(1): Show | 4 | HG01099.hp1 HG01099.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(27): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(19): Show |
1 | a0003c0002t0041g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(28): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(22): Show |
5 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0176others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(31): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(24): Show |
1 | a0010c0014t0001g0052 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(33): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(26): Show |
5 | a0001c0001t0001g0114a0001c0001t0011g0155a0001c0001t0045g0121others(2): Show | 5 | HG00280.hp2 HG01069.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(35): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(30): Show |
3 | a0001c0001t0001g0080a0005c0005t0002g0212a0005c0005t0002g0213 | 3 | HG01256.hp2 HG01258.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(39): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(31): Show |
3 | a0001c0001t0001g0085a0003c0002t0001g0049a0007c0017t0001g0106 | 3 | HG00621.hp2 NA19087.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(40): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(32): Show |
1 | a0001c0001t0001g0071 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(41): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(36): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0116 | 2 | NA19067.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(45): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(42): Show |
1 | a0005c0005t0001g0108 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(51): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(44): Show |
1 | a0008c0016t0001g0089 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(53): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(46): Show |
2 | a0001c0001t0001g0111a0002c0003t0003g0027 | 2 | HG01515.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(55): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(56): Show |
1 | a0007c0017t0001g0056 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(65): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(62): Show |
1 | a0001c0001t0001g0092 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(71): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(198): Show |
1 | a0001c0001t0001g0175 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(207): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(190): Show |
1 | a0003c0002t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(199): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(303): Show |
1 | a0001c0001t0001g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(312): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(256): Show |
1 | a0001c0001t0001g0078 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(265): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(191): Show |
1 | a0001c0001t0001g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(200): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(37): Show |
1 | a0008c0016t0001g0088 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(46): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(38): Show |
2 | a0001c0001t0001g0082a0010c0014t0001g0055 | 2 | NA19064.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(47): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(39): Show |
1 | a0012c0045t0001g0043 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(48): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(33): Show |
1 | a0001c0001t0001g0112 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(42): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(34): Show |
1 | a0001c0001t0001g0053 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(43): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(35): Show |
1 | a0001c0001t0001g0091 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(44): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(30): Show |
2 | a0001c0001t0001g0090a0024c0025t0001g0034 | 2 | NA18949.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(39): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(26): Show |
2 | a0001c0001t0001g0050a0001c0001t0016g0079 | 2 | HG01255.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(35): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(27): Show |
1 | a0001c0001t0016g0081 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(36): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(22): Show |
2 | a0001c0001t0001g0157a0001c0046t0001g0177 | 2 | HG04228.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(31): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(23): Show |
1 | a0001c0001t0044g0051 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(32): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(39): Show |
1 | a0009c0015t0005g0094 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(48): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(40): Show |
1 | a0009c0015t0006g0115 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(49): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(19): Show |
1 | a0001c0001t0001g0042 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(28): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(32): Show |
1 | a0002c0033t0023g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(41): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(29): Show |
1 | a0002c0006t0004g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(38): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(24): Show |
1 | a0002c0006t0004g0167 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(33): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(6): Show |
1 | a0001c0001t0001g0073 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(15): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTCTTT others(20): Show |
3 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0018g0164 | 3 | HG01167.hp1 HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(29): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | CTTTTCTT others(16): Show |
1 | a0002c0006t0018g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-51-9597_-51-9596i others(25): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420493 | |||||
| chr9:131420493
|
C | G | 10 | a0002c0006t0026g0146a0003c0002t0001g0134a0003c0002t0001g0152others(7): Show | 10 | HG01257.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51-9601C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420493 | ||||||
| chr9:131420493
|
C | T | 5 | a0001c0001t0001g0113a0002c0012t0004g0161a0002c0012t0004g0162others(2): Show | 5 | HG02145.hp2 HG02922.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-9601C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420493 | ||||||
| chr9:131420494
|
T | C | 2 | a0002c0018t0008g0207a0002c0018t0008g0208 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-9600T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420494 | ||||||
| chr9:131420494
|
T | G | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-9600T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420494 | ||||||
| chr9:131420494
|
T | TTTCTTTC others(12): Show |
3 | a0001c0001t0001g0096a0001c0001t0001g0097a0003c0002t0011g0158 | 3 | HG01175.hp1 HG02698.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(21): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420494 | |||||
| chr9:131420494
|
T | TTTCTTTC others(16): Show |
1 | a0001c0001t0001g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(25): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420494 | |||||
| chr9:131420494
|
T | TTTCTTTC others(72): Show |
1 | a0001c0001t0001g0033 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(81): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420494 | |||||
| chr9:131420494
|
T | TTTCTTTC others(46): Show |
1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(55): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420494 | |||||
| chr9:131420494
|
T | TTTCTTTC others(24): Show |
2 | a0002c0039t0008g0206a0005c0005t0002g0214 | 2 | HG01261.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(33): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420494 | |||||
| chr9:131420494
|
T | TTTCTTTC others(52): Show |
1 | a0003c0002t0001g0184 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(61): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420494 | |||||
| chr9:131420495
|
T | C | 2 | a0002c0035t0004g0131a0002c0040t0029g0151 | 2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-51-9599T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420495 | ||||||
| chr9:131420495
|
T | TTC | 11 | a0001c0001t0001g0093a0002c0006t0026g0146a0003c0002t0001g0134others(8): Show | 11 | HG01257.hp1 HG01261.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420495
|
T | TTCTCTCT others(263): Show |
1 | a0003c0002t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(272): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420495
|
T | TTCTTTCT others(7): Show |
2 | a0002c0003t0003g0020a0005c0005t0001g0011 | 2 | HG03471.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(16): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420495
|
T | TTCTTTCT others(15): Show |
1 | a0002c0010t0009g0188 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(24): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420495
|
T | TTCTTTCT others(75): Show |
4 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0014g0002others(1): Show | 4 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(84): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420495
|
T | TTCTTTCT others(19): Show |
3 | a0002c0010t0009g0187a0002c0019t0001g0023a0005c0005t0002g0205 | 3 | HG01361.hp2 HG03130.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(28): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420495
|
T | TTCTTTCT others(403): Show |
1 | a0001c0001t0001g0083 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(412): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420495
|
T | TTCTTTCT others(403): Show |
1 | a0001c0001t0001g0087 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(412): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420495
|
T | TTCTTTCT others(79): Show |
1 | a0002c0007t0010g0203 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(88): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420495
|
T | TTCTTTCT others(23): Show |
1 | a0002c0038t0012g0171 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(32): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420495
|
T | TTCTTTCT others(99): Show |
1 | a0001c0001t0001g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(108): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420495
|
T | TTCTTTCT others(128): Show |
1 | a0002c0007t0024g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(137): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420495
|
T | TTGTTTC | 15 | a0004c0004t0005g0117a0004c0004t0005g0140a0004c0004t0005g0143others(12): Show | 15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.-51-9598_-51-9597i others(8): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131420495 | |||||
| chr9:131420496
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-51-9598T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420496 | ||||||
| chr9:131420496
|
T | TCTTTCTT others(22): Show |
1 | a0005c0005t0002g0204 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(31): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420496 | ||||||
| chr9:131420496
|
T | TCTTTCTT others(506): Show |
1 | a0001c0001t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-51-9598_-51-9597i others(515): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420496 | ||||||
| chr9:131420497
|
T | C | 9 | a0001c0001t0001g0075a0001c0001t0001g0098a0002c0008t0025g0125others(6): Show | 9 | HG01123.hp2 HG01256.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-9597T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420497 | ||||||
| chr9:131420498
|
T | C | 5 | a0001c0001t0001g0033a0002c0018t0008g0207a0002c0018t0008g0208others(2): Show | 5 | HG00642.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-9596T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420498 | ||||||
| chr9:131420499
|
T | C | 32 | a0001c0001t0001g0083a0001c0001t0001g0087a0002c0006t0026g0146others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.-51-9595T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420499 | ||||||
| chr9:131420500
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-51-9594T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420500 | ||||||
| chr9:131420502
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-51-9592T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420502 | ||||||
| chr9:131420503
|
T | C | 33 | a0001c0001t0001g0083a0001c0001t0001g0087a0002c0006t0026g0146others(30): Show | 33 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.-51-9591T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420503 | ||||||
| chr9:131420504
|
T | C | 2 | a0002c0018t0008g0207a0002c0018t0008g0208 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-9590T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420504 | ||||||
| chr9:131420507
|
T | C | 1 | a0002c0007t0024g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-51-9587T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420507 | ||||||
| chr9:131420508
|
T | C | 2 | a0002c0018t0008g0207a0002c0018t0008g0208 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-9586T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420508 | ||||||
| chr9:131420511
|
G | T | 1 | a0002c0007t0024g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-51-9583G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420511 | ||||||
| chr9:131420532
|
G | A | 4 | a0002c0035t0004g0131a0003c0002t0001g0183a0003c0002t0001g0184others(1): Show | 4 | HG02572.hp2 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51-9562G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420532 | ||||||
| chr9:131420634
|
C | T | 9 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51-9460C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420634 | ||||||
| chr9:131420636
|
T | C | 9 | a0002c0007t0024g0186a0002c0008t0028g0126a0002c0008t0034g0035others(6): Show | 9 | HG01123.hp2 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-9458T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420636 | ||||||
| chr9:131420696
|
G | C | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-51-9398G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420696 | ||||||
| chr9:131420770
|
G | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51-9324G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420770 | ||||||
| chr9:131420944
|
A | G | 1 | a0005c0005t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-51-9150A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131420944 | ||||||
| chr9:131421000
|
G | A | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-9094G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421000 | ||||||
| chr9:131421103
|
A | G | 1 | a0002c0007t0024g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-51-8991A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421103 | ||||||
| chr9:131421159
|
C | G | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-51-8935C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421159 | ||||||
| chr9:131421216
|
T | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-51-8878T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421216 | ||||||
| chr9:131421546
|
G | A | 27 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(24): Show | 27 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.-51-8548G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421546 | ||||||
| chr9:131421588
|
C | G | 27 | a0002c0006t0026g0146a0002c0040t0029g0151a0003c0002t0001g0134others(24): Show | 27 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.-51-8506C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421588 | ||||||
| chr9:131421610
|
G | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51-8484G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421610 | ||||||
| chr9:131421610
|
G | C | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-51-8484G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421610 | ||||||
| chr9:131421652
|
G | A | 1 | a0004c0004t0005g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-51-8442G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421652 | ||||||
| chr9:131421695
|
A | G | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-8399A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421695 | ||||||
| chr9:131421777
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0109 | 3 | HG02027.hp2 NA18747.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-51-8317G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421777 | ||||||
| chr9:131421822
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-51-8272T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421822 | ||||||
| chr9:131421882
|
C | T | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51-8212C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421882 | ||||||
| chr9:131421973
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-51-8121C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131421973 | ||||||
| chr9:131422038
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-51-8056C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131422038 | ||||||
| chr9:131422055
|
A | T | 1 | a0001c0001t0001g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-51-8039A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131422055 | ||||||
| chr9:131422056
|
T | A | 1 | a0001c0001t0001g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-51-8038T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131422056 | ||||||
| chr9:131422063
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-51-8031A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131422063 | ||||||
| chr9:131422096
|
C | T | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-51-7998C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131422096 | ||||||
| chr9:131422135
|
A | T | 1 | a0001c0001t0001g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-51-7959A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131422135 | ||||||
| chr9:131422349
|
C | T | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-7745C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131422349 | ||||||
| chr9:131422570
|
G | C | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-7524G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131422570 | ||||||
| chr9:131422827
|
C | T | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-51-7267C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131422827 | ||||||
| chr9:131422888
|
A | G | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51-7206A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131422888 | ||||||
| chr9:131422947
|
G | A | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-7147G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131422947 | ||||||
| chr9:131423021
|
G | A | 2 | a0011c0013t0031g0036a0011c0013t0036g0037 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-51-7073G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423021 | ||||||
| chr9:131423068
|
C | G | 1 | a0001c0001t0002g0194 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-51-7026C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423068 | ||||||
| chr9:131423083
|
T | C | 1 | a0001c0001t0043g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-51-7011T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423083 | ||||||
| chr9:131423141
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-51-6953G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423141 | ||||||
| chr9:131423279
|
C | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-51-6815C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423279 | ||||||
| chr9:131423369
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-51-6725T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423369 | ||||||
| chr9:131423676
|
T | C | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-6418T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423676 | ||||||
| chr9:131423710
|
C | G | 38 | a0003c0002t0001g0045a0003c0002t0001g0046a0003c0002t0001g0049others(35): Show | 38 | HG00140.hp1 HG00741.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.-51-6384C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423710 | ||||||
| chr9:131423721
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-51-6373C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423721 | ||||||
| chr9:131423729
|
G | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-51-6365G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423729 | ||||||
| chr9:131423806
|
G | A | 6 | a0003c0002t0001g0134a0003c0002t0001g0152a0003c0002t0001g0153others(3): Show | 6 | HG02647.hp1 HG02965.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51-6288G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423806 | ||||||
| chr9:131423904
|
G | A | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-6190G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423904 | ||||||
| chr9:131423941
|
G | GT | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.-51-6141dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131423941 | |||||
| chr9:131423954
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-51-6140A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423954 | ||||||
| chr9:131423993
|
T | G | 37 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(34): Show | 37 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.-51-6101T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131423993 | ||||||
| chr9:131424081
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-51-6013G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131424081 | ||||||
| chr9:131424093
|
G | A | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-6001G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131424093 | ||||||
| chr9:131424109
|
T | A | 4 | a0002c0035t0004g0131a0003c0002t0001g0049a0003c0002t0001g0156others(1): Show | 4 | HG03579.hp2 NA18972.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51-5985T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131424109 | ||||||
| chr9:131424214
|
T | G | 1 | a0004c0004t0005g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-51-5880T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131424214 | ||||||
| chr9:131424220
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.-51-5874G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131424220 | ||||||
| chr9:131424554
|
C | T | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-51-5540C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131424554 | ||||||
| chr9:131424585
|
C | T | 1 | a0004c0009t0007g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-51-5509C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131424585 | ||||||
| chr9:131424647
|
C | G | 3 | a0003c0002t0001g0127a0003c0002t0001g0128a0003c0002t0001g0130 | 3 | HG00741.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-51-5447C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131424647 | ||||||
| chr9:131424716
|
G | A | 2 | a0003c0002t0046g0060a0003c0002t0047g0061 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-51-5378G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131424716 | ||||||
| chr9:131424905
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-51-5189T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131424905 | ||||||
| chr9:131424968
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-51-5126G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131424968 | ||||||
| chr9:131425042
|
C | T | 9 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51-5052C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131425042 | ||||||
| chr9:131425111
|
G | A | 2 | a0003c0002t0046g0060a0003c0002t0047g0061 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-51-4983G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131425111 | ||||||
| chr9:131425169
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-51-4925A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131425169 | ||||||
| chr9:131425174
|
C | T | 1 | a0002c0033t0023g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-51-4920C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131425174 | ||||||
| chr9:131425237
|
C | T | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-4857C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131425237 | ||||||
| chr9:131425519
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-51-4575C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131425519 | ||||||
| chr9:131425540
|
G | A | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-51-4554G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131425540 | ||||||
| chr9:131425661
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0157 | 2 | HG02165.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-51-4433T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131425661 | ||||||
| chr9:131425693
|
G | A | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-51-4401G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131425693 | ||||||
| chr9:131425708
|
C | G | 1 | a0002c0007t0024g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-51-4386C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131425708 | ||||||
| chr9:131426244
|
A | G | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-51-3850A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131426244 | ||||||
| chr9:131426306
|
C | G | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-51-3788C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131426306 | ||||||
| chr9:131426337
|
CAA | C | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51-3735_-51-3734d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131426337 | |||||
| chr9:131426337
|
CAAAA | C | 27 | a0001c0001t0001g0175a0001c0001t0002g0190a0001c0001t0002g0191others(24): Show | 27 | HG00735.hp1 HG01123.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.-51-3737_-51-3734d others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131426337 | |||||
| chr9:131426337
|
CAAAAA | C | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0033others(171): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-51-3738_-51-3734d others(7): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131426337 | |||||
| chr9:131426355
|
A | G | 9 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0019others(6): Show | 9 | HG00558.hp1 HG02738.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51-3739A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131426355 | ||||||
| chr9:131426367
|
GAAA | G | 3 | a0001c0001t0002g0195a0001c0001t0002g0197a0001c0001t0022g0192 | 3 | HG01496.hp2 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-51-3722_-51-3720d others(5): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131426367 | |||||
| chr9:131426497
|
A | C | 1 | a0003c0031t0001g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-51-3597A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131426497 | ||||||
| chr9:131426609
|
G | A | 10 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0193others(7): Show | 10 | HG00735.hp1 HG01496.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51-3485G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131426609 | ||||||
| chr9:131426742
|
T | C | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-51-3352T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131426742 | ||||||
| chr9:131426843
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-51-3251A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131426843 | ||||||
| chr9:131426859
|
T | C | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51-3235T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131426859 | ||||||
| chr9:131426948
|
G | A | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-51-3146G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131426948 | ||||||
| chr9:131426995
|
G | A | 25 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(22): Show | 25 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51-3099G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131426995 | ||||||
| chr9:131427029
|
C | T | 2 | a0005c0005t0002g0204a0005c0005t0002g0205 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-51-3065C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427029 | ||||||
| chr9:131427213
|
G | A | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-51-2881G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427213 | ||||||
| chr9:131427259
|
C | G | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-51-2835C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427259 | ||||||
| chr9:131427272
|
G | A | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-51-2822G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427272 | ||||||
| chr9:131427295
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-51-2799A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427295 | ||||||
| chr9:131427327
|
T | TTG | 25 | a0001c0001t0001g0057a0002c0003t0003g0014a0002c0003t0003g0015others(22): Show | 25 | HG00558.hp1 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-51-2751_-51-2750d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131427327 | |||||
| chr9:131427327
|
T | TTGTG | 5 | a0002c0003t0003g0028a0002c0010t0009g0187a0002c0010t0009g0188others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-2753_-51-2750d others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131427327 | |||||
| chr9:131427343
|
G | T | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-51-2751G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427343 | ||||||
| chr9:131427345
|
T | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-51-2749T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427345 | ||||||
| chr9:131427381
|
A | T | 5 | a0005c0005t0001g0010a0005c0005t0001g0011a0005c0005t0001g0095others(2): Show | 5 | HG03471.hp2 NA18970.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-2713A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427381 | ||||||
| chr9:131427423
|
C | T | 9 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51-2671C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427423 | ||||||
| chr9:131427431
|
C | T | 1 | a0019c0029t0020g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-51-2663C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427431 | ||||||
| chr9:131427506
|
A | G | 1 | a0001c0001t0002g0193 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-51-2588A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427506 | ||||||
| chr9:131427531
|
C | T | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-51-2563C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427531 | ||||||
| chr9:131427585
|
C | T | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-51-2509C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427585 | ||||||
| chr9:131427607
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-51-2487G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427607 | ||||||
| chr9:131427859
|
G | A | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-51-2235G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427859 | ||||||
| chr9:131427963
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-51-2131T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131427963 | ||||||
| chr9:131428246
|
G | A | 1 | a0002c0007t0010g0201 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-51-1848G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131428246 | ||||||
| chr9:131428376
|
A | G | 1 | a0019c0029t0020g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-51-1718A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131428376 | ||||||
| chr9:131428429
|
C | T | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-1665C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131428429 | ||||||
| chr9:131428958
|
T | C | 39 | a0001c0001t0001g0071a0003c0002t0001g0045a0003c0002t0001g0046others(36): Show | 39 | HG00140.hp1 HG00558.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-51-1136T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131428958 | ||||||
| chr9:131428986
|
C | T | 1 | a0002c0003t0008g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-51-1108C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131428986 | ||||||
| chr9:131429109
|
G | T | 1 | a0002c0006t0026g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-51-985G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131429109 | ||||||
| chr9:131429146
|
C | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51-948C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131429146 | ||||||
| chr9:131429238
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-51-856C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131429238 | ||||||
| chr9:131429261
|
T | TTGAG | 20 | a0001c0001t0002g0197a0002c0006t0004g0165a0002c0006t0004g0167others(17): Show | 20 | HG00099.hp1 HG01167.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-51-801_-51-798dup others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131429261 | |||||
| chr9:131429261
|
T | TTGAGTGA others(1): Show |
3 | a0002c0006t0004g0160a0013c0020t0032g0006a0021c0034t0048g0013 | 3 | HG00642.hp2 HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-51-805_-51-798dup others(8): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr9 | 131429261 | |||||
| chr9:131429468
|
G | A | 2 | a0003c0002t0039g0047a0015c0021t0004g0005 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-51-626G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131429468 | ||||||
| chr9:131429679
|
C | G | 2 | a0002c0018t0008g0207a0002c0018t0008g0208 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-51-415C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131429679 | ||||||
| chr9:131429784
|
T | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0012c0045t0001g0043 | 3 | NA18949.hp1 NA19012.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-51-310T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131429784 | ||||||
| chr9:131429788
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-51-306A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131429788 | ||||||
| chr9:131429856
|
G | A | 2 | a0003c0002t0001g0066a0003c0002t0001g0067 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-51-238G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131429856 | ||||||
| chr9:131429880
|
G | A | 1 | a0002c0006t0018g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-51-214G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131429880 | ||||||
| chr9:131429944
|
C | G | 1 | a0003c0002t0004g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-51-150C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131429944 | ||||||
| chr9:131430041
|
C | T | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-51-53C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131430041 | ||||||
| chr9:131430052
|
T | C | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-51-42T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131430052 | ||||||
| chr9:131430062
|
T | C | 1 | a0006c0011t0037g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-51-32T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131430062 | ||||||
| chr9:131430072
|
T | C | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-51-22T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 1/31 | chr9 | 131430072 | ||||||
| chr9:131430488
|
G | C | 6 | a0003c0002t0001g0134a0003c0002t0001g0152a0003c0002t0001g0153others(3): Show | 6 | HG01106.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.115+229G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430488 | ||||||
| chr9:131430494
|
TATATCTA others(3): Show |
T | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.115+249_115+258del others(10): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430494 | |||||
| chr9:131430495
|
A | ATATCTAT others(29): Show |
9 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(6): Show | 9 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.115+256_115+291dup others(36): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430495 | |||||
| chr9:131430510
|
TATAGATA others(1): Show |
T | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.115+263_115+270del others(8): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430510 | |||||
| chr9:131430515
|
A | G | 3 | a0004c0004t0005g0123a0005c0005t0001g0107a0005c0005t0001g0108 | 3 | HG01123.hp1 HG01975.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.115+256A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430515 | ||||||
| chr9:131430516
|
TAGATAGA others(17): Show |
T | 3 | a0004c0004t0005g0123a0005c0005t0001g0107a0005c0005t0001g0108 | 3 | HG01123.hp1 HG01975.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.115+259_115+282del others(24): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430516 | |||||
| chr9:131430518
|
G | GATATCTA others(13): Show |
1 | a0001c0001t0001g0033 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.115+262_115+263ins others(20): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430518 | |||||
| chr9:131430518
|
G | GATATCTA others(55): Show |
1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.115+262_115+263ins others(62): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430518 | |||||
| chr9:131430541
|
A | G | 3 | a0004c0004t0005g0123a0005c0005t0001g0107a0005c0005t0001g0108 | 3 | HG01123.hp1 HG01975.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.115+282A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430541 | ||||||
| chr9:131430543
|
A | G | 3 | a0004c0004t0005g0123a0005c0005t0001g0107a0005c0005t0001g0108 | 3 | HG01123.hp1 HG01975.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.115+284A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430543 | ||||||
| chr9:131430545
|
C | G | 3 | a0004c0004t0005g0123a0005c0005t0001g0107a0005c0005t0001g0108 | 3 | HG01123.hp1 HG01975.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.115+286C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430545 | ||||||
| chr9:131430547
|
A | G | 3 | a0004c0004t0005g0123a0005c0005t0001g0107a0005c0005t0001g0108 | 3 | HG01123.hp1 HG01975.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.115+288A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430547 | ||||||
| chr9:131430550
|
G | GATAGATA others(33): Show |
1 | a0002c0033t0023g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.115+291_115+292ins others(40): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430550 | ||||||
| chr9:131430550
|
G | T | 2 | a0004c0004t0005g0123a0005c0005t0001g0108 | 2 | HG01975.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.115+291G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430550 | ||||||
| chr9:131430550
|
GGTGTGTG others(13): Show |
G | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+302_115+321del others(20): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430550 | |||||
| chr9:131430557
|
G | A | 1 | a0002c0033t0023g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.115+298G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430557 | ||||||
| chr9:131430559
|
GTA | G | 2 | a0002c0007t0010g0203a0004c0009t0007g0159 | 2 | HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.115+302_115+303del others(2): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430559 | |||||
| chr9:131430561
|
A | ATG | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0053others(11): Show | 14 | HG00558.hp2 HG01099.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.115+336_115+337dup others(2): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430561 | |||||
| chr9:131430561
|
A | ATGTG | 43 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0050others(40): Show | 43 | HG00323.hp2 HG00735.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.115+334_115+337dup others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430561 | |||||
| chr9:131430561
|
A | ATGTGTG | 42 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0062others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.115+332_115+337dup others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430561 | |||||
| chr9:131430561
|
A | ATGTGTGT others(1): Show |
11 | a0001c0001t0001g0064a0001c0001t0001g0103a0003c0002t0001g0049others(8): Show | 11 | HG00140.hp1 HG00621.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.115+330_115+337dup others(8): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430561 | |||||
| chr9:131430561
|
A | ATGTGTGT others(3): Show |
11 | a0001c0001t0001g0033a0001c0001t0001g0057a0001c0001t0001g0063others(8): Show | 11 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.115+328_115+337dup others(10): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430561 | |||||
| chr9:131430561
|
A | ATGTGTGT others(5): Show |
7 | a0003c0002t0001g0152a0003c0002t0001g0153a0003c0002t0001g0154others(4): Show | 7 | HG01361.hp1 HG02145.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.115+326_115+337dup others(12): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430561 | |||||
| chr9:131430561
|
A | ATGTGTGT others(7): Show |
3 | a0005c0005t0002g0204a0005c0005t0002g0212a0005c0005t0002g0213 | 3 | HG01256.hp2 HG01258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.115+324_115+337dup others(14): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430561 | |||||
| chr9:131430561
|
A | ATGTGTGT others(9): Show |
1 | a0005c0005t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.115+322_115+337dup others(16): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430561 | |||||
| chr9:131430561
|
A | ATGTGTGT others(11): Show |
1 | a0005c0005t0002g0205 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.115+320_115+337dup others(18): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430561 | |||||
| chr9:131430561
|
A | G | 9 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0014g0002others(6): Show | 9 | HG01123.hp1 HG01891.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+302A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430561 | ||||||
| chr9:131430561
|
ATG | A | 2 | a0002c0037t0003g0017a0006c0011t0037g0179 | 2 | HG02976.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.115+336_115+337del others(2): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430561 | |||||
| chr9:131430561
|
ATGTG | A | 26 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(23): Show | 26 | HG01192.hp1 HG01257.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.115+334_115+337del others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430561 | |||||
| chr9:131430589
|
GTGTGTGT others(3): Show |
G | 1 | a0004c0009t0007g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.115+332_115+341del others(10): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430589 | |||||
| chr9:131430591
|
GTGTGTAT others(1): Show |
G | 6 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(3): Show | 6 | HG01167.hp1 HG02451.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+334_115+341del others(8): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430591 | |||||
| chr9:131430595
|
G | A | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.115+336G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430595 | ||||||
| chr9:131430595
|
GTA | G | 13 | a0002c0006t0026g0146a0002c0012t0004g0161a0002c0012t0004g0162others(10): Show | 13 | HG00099.hp1 HG01255.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.115+344_115+345del others(2): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430595 | |||||
| chr9:131430595
|
GTATA | G | 11 | a0002c0006t0004g0168a0002c0040t0029g0151a0004c0004t0005g0117others(8): Show | 11 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.115+342_115+345del others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430595 | |||||
| chr9:131430597
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.115+338A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430597 | ||||||
| chr9:131430599
|
A | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0048others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.115+340A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430599 | ||||||
| chr9:131430601
|
A | G | 2 | a0001c0001t0049g0120a0004c0004t0013g0170 | 2 | HG01069.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.115+342A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430601 | ||||||
| chr9:131430698
|
G | C | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.115+439G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131430698 | ||||||
| chr9:131430952
|
C | CT | 10 | a0001c0001t0001g0116a0002c0007t0010g0201a0002c0007t0010g0202others(7): Show | 10 | HG00642.hp2 HG01361.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.115+708dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr9 | 131430952 | |||||
| chr9:131431070
|
C | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0087 | 3 | HG01167.hp2 HG01169.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.115+811C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431070 | ||||||
| chr9:131431111
|
C | T | 1 | a0011c0013t0036g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.115+852C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431111 | ||||||
| chr9:131431145
|
T | C | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+886T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431145 | ||||||
| chr9:131431223
|
C | T | 30 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(27): Show | 30 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.115+964C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431223 | ||||||
| chr9:131431273
|
G | A | 10 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.115+1014G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431273 | ||||||
| chr9:131431306
|
A | T | 1 | a0008c0016t0001g0088 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.115+1047A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431306 | ||||||
| chr9:131431321
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(130): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.115+1062G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431321 | ||||||
| chr9:131431345
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.115+1086C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431345 | ||||||
| chr9:131431381
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.115+1122C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431381 | ||||||
| chr9:131431405
|
C | T | 30 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(27): Show | 30 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.115+1146C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431405 | ||||||
| chr9:131431523
|
C | G | 1 | a0002c0003t0003g0031 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.116-1094C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431523 | ||||||
| chr9:131431640
|
G | A | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.116-977G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431640 | ||||||
| chr9:131431741
|
C | G | 1 | a0003c0002t0041g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.116-876C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431741 | ||||||
| chr9:131431744
|
T | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.116-873T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431744 | ||||||
| chr9:131431832
|
C | T | 25 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(22): Show | 25 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.116-785C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431832 | ||||||
| chr9:131431838
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.116-779G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431838 | ||||||
| chr9:131431875
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.116-742C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431875 | ||||||
| chr9:131431889
|
C | T | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.116-728C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131431889 | ||||||
| chr9:131432224
|
A | C | 10 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0193others(7): Show | 10 | HG00735.hp1 HG01496.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.116-393A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131432224 | ||||||
| chr9:131432320
|
C | T | 1 | a0002c0037t0003g0017 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.116-297C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131432320 | ||||||
| chr9:131432360
|
C | G | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.116-257C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131432360 | ||||||
| chr9:131432366
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.116-251A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 2/31 | chr9 | 131432366 | ||||||
| chr9:131433054
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.293+260G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131433054 | ||||||
| chr9:131433061
|
C | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.293+267C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131433061 | ||||||
| chr9:131433104
|
G | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0048others(16): Show | 19 | HG01099.hp2 HG01358.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.293+310G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131433104 | ||||||
| chr9:131433153
|
C | T | 4 | a0002c0010t0009g0187a0002c0010t0009g0188a0002c0010t0009g0189others(1): Show | 4 | HG01361.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.293+359C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131433153 | ||||||
| chr9:131433488
|
A | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.293+694A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131433488 | ||||||
| chr9:131433717
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.293+923C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131433717 | ||||||
| chr9:131433746
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.293+952T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131433746 | ||||||
| chr9:131434080
|
G | A | 2 | a0007c0017t0001g0056a0007c0017t0001g0106 | 2 | HG00621.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.293+1286G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131434080 | ||||||
| chr9:131434395
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.293+1601G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131434395 | ||||||
| chr9:131434399
|
G | A | 3 | a0002c0012t0004g0161a0002c0012t0004g0162a0015c0021t0004g0005 | 3 | HG02922.hp1 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.293+1605G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131434399 | ||||||
| chr9:131434432
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.293+1638G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131434432 | ||||||
| chr9:131434471
|
A | G | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.293+1677A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131434471 | ||||||
| chr9:131434673
|
G | A | 10 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+1879G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131434673 | ||||||
| chr9:131434736
|
G | T | 1 | a0002c0008t0025g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.294-1884G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131434736 | ||||||
| chr9:131434748
|
C | T | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.294-1872C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131434748 | ||||||
| chr9:131434904
|
A | G | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.294-1716A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131434904 | ||||||
| chr9:131434949
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.294-1671T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131434949 | ||||||
| chr9:131435223
|
G | A | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.294-1397G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131435223 | ||||||
| chr9:131435264
|
C | G | 1 | a0024c0025t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.294-1356C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131435264 | ||||||
| chr9:131435267
|
T | C | 1 | a0002c0003t0003g0030 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.294-1353T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131435267 | ||||||
| chr9:131435307
|
G | GA | 28 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(25): Show | 28 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.294-1309dupA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr9 | 131435307 | |||||
| chr9:131435312
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.294-1308G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131435312 | ||||||
| chr9:131435424
|
G | T | 2 | a0002c0008t0025g0125a0019c0029t0020g0209 | 2 | HG01943.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.294-1196G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131435424 | ||||||
| chr9:131435436
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.294-1184G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131435436 | ||||||
| chr9:131435467
|
T | C | 10 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.294-1153T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131435467 | ||||||
| chr9:131435475
|
C | T | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.294-1145C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131435475 | ||||||
| chr9:131435520
|
CAGG | C | 2 | a0001c0001t0001g0093a0005c0005t0002g0214 | 2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.294-1097_294-1095d others(5): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr9 | 131435520 | |||||
| chr9:131435613
|
TA | T | 9 | a0002c0003t0003g0019a0002c0003t0003g0032a0002c0003t0008g0216others(6): Show | 9 | HG00558.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.294-982delA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr9 | 131435613 | |||||
| chr9:131435613
|
TAA | T | 22 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(19): Show | 22 | HG01192.hp1 HG01257.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.294-983_294-982del others(2): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr9 | 131435613 | |||||
| chr9:131435613
|
TAAA | T | 10 | a0002c0003t0003g0018a0002c0003t0003g0028a0002c0007t0024g0186others(7): Show | 10 | HG00642.hp2 HG01123.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.294-984_294-982del others(3): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr9 | 131435613 | |||||
| chr9:131435613
|
TAAAAAAA others(7): Show |
T | 5 | a0002c0012t0004g0161a0002c0012t0004g0162a0002c0033t0023g0163others(2): Show | 5 | HG02572.hp1 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.294-995_294-982del others(14): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr9 | 131435613 | |||||
| chr9:131435613
|
TAAAAAAA others(8): Show |
T | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.294-996_294-982del others(15): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr9 | 131435613 | |||||
| chr9:131435673
|
G | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.294-947G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131435673 | ||||||
| chr9:131435720
|
A | G | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.294-900A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131435720 | ||||||
| chr9:131435731
|
G | A | 2 | a0005c0005t0001g0010a0005c0005t0001g0011 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.294-889G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131435731 | ||||||
| chr9:131436250
|
A | C | 1 | a0004c0004t0005g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.294-370A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 3/31 | chr9 | 131436250 | ||||||
| chr9:131437146
|
G | A | 6 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0082others(3): Show | 6 | HG01255.hp2 HG01934.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.396+424G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/31 | chr9 | 131437146 | ||||||
| chr9:131437180
|
C | T | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.396+458C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/31 | chr9 | 131437180 | ||||||
| chr9:131437414
|
C | G | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.396+692C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/31 | chr9 | 131437414 | ||||||
| chr9:131437527
|
C | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.396+805C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/31 | chr9 | 131437527 | ||||||
| chr9:131437563
|
G | A | 16 | a0002c0040t0029g0151a0004c0004t0005g0117a0004c0004t0005g0140others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.396+841G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/31 | chr9 | 131437563 | ||||||
| chr9:131437650
|
G | T | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.396+928G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/31 | chr9 | 131437650 | ||||||
| chr9:131437961
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18949.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.397-1028T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/31 | chr9 | 131437961 | ||||||
| chr9:131438238
|
G | A | 34 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.397-751G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/31 | chr9 | 131438238 | ||||||
| chr9:131438346
|
T | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.397-643T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/31 | chr9 | 131438346 | ||||||
| chr9:131438373
|
G | T | 3 | a0003c0002t0001g0183a0003c0002t0001g0184a0003c0002t0001g0185 | 3 | HG02572.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.397-616G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/31 | chr9 | 131438373 | ||||||
| chr9:131438409
|
G | A | 4 | a0002c0012t0004g0161a0002c0012t0004g0162a0002c0033t0023g0163others(1): Show | 4 | HG02922.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.397-580G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/31 | chr9 | 131438409 | ||||||
| chr9:131438600
|
C | T | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.397-389C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 4/31 | chr9 | 131438600 | ||||||
| chr9:131439094
|
C | T | 1 | a0005c0005t0002g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.469+33C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131439094 | ||||||
| chr9:131439187
|
C | T | 2 | a0003c0002t0001g0183a0003c0002t0001g0184 | 2 | HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.469+126C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131439187 | ||||||
| chr9:131439495
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.469+434C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131439495 | ||||||
| chr9:131439807
|
C | T | 1 | a0019c0029t0020g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.469+746C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131439807 | ||||||
| chr9:131439827
|
G | A | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.469+766G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131439827 | ||||||
| chr9:131439883
|
A | T | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.469+822A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131439883 | ||||||
| chr9:131439899
|
GA | G | 6 | a0005c0005t0001g0107a0005c0005t0001g0108a0005c0005t0002g0212others(3): Show | 6 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+839delA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131439899 | ||||||
| chr9:131439900
|
AT | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.469+853delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr9 | 131439900 | |||||
| chr9:131439901
|
T | C | 6 | a0005c0005t0001g0107a0005c0005t0001g0108a0005c0005t0002g0212others(3): Show | 6 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+840T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131439901 | ||||||
| chr9:131439962
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.469+901A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131439962 | ||||||
| chr9:131440383
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.469+1322C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131440383 | ||||||
| chr9:131440598
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.469+1537C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131440598 | ||||||
| chr9:131440617
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.469+1556G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131440617 | ||||||
| chr9:131440806
|
A | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18949.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.469+1745A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131440806 | ||||||
| chr9:131440835
|
G | GACATGGT others(5): Show |
214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.469+1777_469+1778i others(14): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr9 | 131440835 | |||||
| chr9:131440892
|
T | C | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.469+1831T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131440892 | ||||||
| chr9:131440897
|
C | T | 12 | a0003c0002t0001g0045a0003c0002t0001g0134a0003c0002t0001g0152others(9): Show | 12 | HG01106.hp1 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.469+1836C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131440897 | ||||||
| chr9:131441041
|
G | A | 1 | a0003c0002t0001g0046 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.469+1980G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131441041 | ||||||
| chr9:131441099
|
C | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.469+2038C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131441099 | ||||||
| chr9:131441159
|
T | C | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.469+2098T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131441159 | ||||||
| chr9:131441229
|
G | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0112 | 2 | HG02027.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.469+2168G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131441229 | ||||||
| chr9:131441381
|
A | G | 1 | a0007c0017t0001g0056 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.469+2320A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131441381 | ||||||
| chr9:131441648
|
T | G | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-2537T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131441648 | ||||||
| chr9:131441709
|
G | A | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.470-2476G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131441709 | ||||||
| chr9:131441805
|
G | A | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.470-2380G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131441805 | ||||||
| chr9:131441980
|
AT | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.470-2194delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr9 | 131441980 | |||||
| chr9:131442130
|
G | T | 2 | a0016c0032t0019g0215a0018c0030t0001g0009 | 2 | HG01099.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.470-2055G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442130 | ||||||
| chr9:131442146
|
T | G | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.470-2039T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442146 | ||||||
| chr9:131442210
|
A | G | 1 | a0023c0036t0007g0148 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.470-1975A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442210 | ||||||
| chr9:131442213
|
G | A | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-1972G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442213 | ||||||
| chr9:131442259
|
A | C | 3 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203 | 3 | HG02723.hp2 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.470-1926A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442259 | ||||||
| chr9:131442352
|
T | C | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.470-1833T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442352 | ||||||
| chr9:131442386
|
C | T | 34 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.470-1799C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442386 | ||||||
| chr9:131442477
|
TC | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.470-1707delC | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442477 | ||||||
| chr9:131442490
|
A | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0112 | 2 | HG02027.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.470-1695A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442490 | ||||||
| chr9:131442516
|
G | A | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.470-1669G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442516 | ||||||
| chr9:131442607
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.470-1578C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442607 | ||||||
| chr9:131442616
|
C | T | 30 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(27): Show | 30 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.470-1569C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442616 | ||||||
| chr9:131442742
|
G | A | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.470-1443G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131442742 | ||||||
| chr9:131443037
|
CAT | C | 26 | a0002c0006t0026g0146a0002c0010t0009g0187a0002c0010t0009g0188others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.470-1147_470-1146d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131443037 | ||||||
| chr9:131443138
|
TA | T | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-1046delA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131443138 | ||||||
| chr9:131443139
|
AT | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.470-1034delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr9 | 131443139 | |||||
| chr9:131443141
|
T | A | 1 | a0002c0008t0035g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.470-1044T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131443141 | ||||||
| chr9:131443142
|
T | A | 16 | a0002c0040t0029g0151a0004c0004t0005g0117a0004c0004t0005g0140others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.470-1043T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131443142 | ||||||
| chr9:131443143
|
T | A | 1 | a0003c0002t0001g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.470-1042T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131443143 | ||||||
| chr9:131443241
|
C | T | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.470-944C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131443241 | ||||||
| chr9:131443299
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.470-886A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131443299 | ||||||
| chr9:131443383
|
G | A | 10 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.470-802G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131443383 | ||||||
| chr9:131443569
|
G | T | 1 | a0001c0001t0033g0077 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.470-616G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131443569 | ||||||
| chr9:131443582
|
C | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.470-603C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131443582 | ||||||
| chr9:131444131
|
G | A | 1 | a0001c0001t0022g0192 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.470-54G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 5/31 | chr9 | 131444131 | ||||||
| chr9:131444447
|
GC | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.613+120delC | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131444447 | ||||||
| chr9:131444458
|
C | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.613+130C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131444458 | ||||||
| chr9:131444463
|
C | T | 1 | a0005c0005t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.613+135C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131444463 | ||||||
| chr9:131444480
|
T | C | 2 | a0005c0005t0002g0204a0005c0005t0002g0205 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.613+152T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131444480 | ||||||
| chr9:131444508
|
G | T | 4 | a0002c0007t0024g0186a0002c0008t0035g0039a0011c0013t0031g0036others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.613+180G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131444508 | ||||||
| chr9:131444823
|
C | T | 14 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0063others(11): Show | 14 | HG01099.hp2 HG01358.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.613+495C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131444823 | ||||||
| chr9:131444883
|
C | T | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.613+555C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131444883 | ||||||
| chr9:131444941
|
G | A | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+613G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131444941 | ||||||
| chr9:131444967
|
G | T | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.613+639G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131444967 | ||||||
| chr9:131445392
|
C | G | 1 | a0001c0001t0001g0073 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.614-1009C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131445392 | ||||||
| chr9:131445405
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.614-996T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131445405 | ||||||
| chr9:131445436
|
G | C | 1 | a0001c0001t0001g0053 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.614-965G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131445436 | ||||||
| chr9:131445437
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.614-964G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131445437 | ||||||
| chr9:131445438
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.614-963C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131445438 | ||||||
| chr9:131445812
|
C | A | 2 | a0002c0007t0010g0201a0002c0007t0010g0202 | 2 | HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.614-589C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131445812 | ||||||
| chr9:131445859
|
G | C | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.614-542G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131445859 | ||||||
| chr9:131445873
|
G | C | 2 | a0004c0004t0013g0169a0004c0004t0013g0170 | 2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.614-528G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131445873 | ||||||
| chr9:131446120
|
T | TGG | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.614-278_614-277dup others(2): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr9 | 131446120 | |||||
| chr9:131446386
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.614-15C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 6/31 | chr9 | 131446386 | ||||||
| chr9:131446682
|
T | C | 1 | a0002c0003t0003g0020 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.855+40T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 7/31 | chr9 | 131446682 | ||||||
| chr9:131446780
|
A | G | 9 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0018others(6): Show | 9 | HG00558.hp1 HG02738.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.855+138A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 7/31 | chr9 | 131446780 | ||||||
| chr9:131446937
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.856-148G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 7/31 | chr9 | 131446937 | ||||||
| chr9:131446946
|
G | A | 2 | a0002c0008t0025g0125a0019c0029t0020g0209 | 2 | HG01943.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.856-139G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 7/31 | chr9 | 131446946 | ||||||
| chr9:131446989
|
T | C | 3 | a0002c0018t0008g0207a0002c0018t0008g0208a0002c0039t0008g0206 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.856-96T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 7/31 | chr9 | 131446989 | ||||||
| chr9:131447231
|
G | C | 3 | a0002c0018t0008g0207a0002c0018t0008g0208a0002c0039t0008g0206 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.977+25G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 8/31 | chr9 | 131447231 | ||||||
| chr9:131447294
|
G | T | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.977+88G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 8/31 | chr9 | 131447294 | ||||||
| chr9:131447378
|
C | G | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.977+172C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 8/31 | chr9 | 131447378 | ||||||
| chr9:131447396
|
C | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.977+190C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 8/31 | chr9 | 131447396 | ||||||
| chr9:131447571
|
C | G | 3 | a0003c0002t0001g0183a0003c0002t0001g0184a0003c0002t0001g0185 | 3 | HG02572.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.978-91C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 8/31 | chr9 | 131447571 | ||||||
| chr9:131447600
|
G | T | 2 | a0002c0019t0001g0023a0002c0019t0011g0022 | 2 | NA18990.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.978-62G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 8/31 | chr9 | 131447600 | ||||||
| chr9:131447601
|
G | A | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.978-61G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 8/31 | chr9 | 131447601 | ||||||
| chr9:131447607
|
G | C | 2 | a0011c0013t0031g0036a0011c0013t0036g0037 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.978-55G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 8/31 | chr9 | 131447607 | ||||||
| chr9:131447853
|
A | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1120+49A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131447853 | ||||||
| chr9:131447977
|
A | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1120+173A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131447977 | ||||||
| chr9:131448145
|
C | T | 1 | a0002c0006t0004g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1120+341C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448145 | ||||||
| chr9:131448342
|
G | A | 1 | a0002c0008t0042g0038 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1120+538G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448342 | ||||||
| chr9:131448449
|
C | A | 2 | a0002c0006t0018g0164a0002c0006t0018g0166 | 2 | HG01167.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1120+645C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448449 | ||||||
| chr9:131448496
|
A | G | 30 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(27): Show | 30 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.1120+692A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448496 | ||||||
| chr9:131448509
|
A | C | 1 | a0003c0002t0001g0152 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1120+705A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448509 | ||||||
| chr9:131448541
|
C | CCCAAAAA others(12): Show |
1 | a0005c0005t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1120+737_1120+738i others(21): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448541 | ||||||
| chr9:131448541
|
CT | C | 8 | a0001c0001t0001g0085a0001c0001t0001g0119a0002c0026t0040g0178others(5): Show | 8 | HG00140.hp2 HG02896.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1120+738delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448541 | ||||||
| chr9:131448542
|
T | A | 1 | a0005c0005t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1120+738T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448542 | ||||||
| chr9:131448542
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1120+738T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448542 | ||||||
| chr9:131448543
|
C | CA | 15 | a0001c0001t0001g0033a0001c0001t0001g0053a0001c0001t0001g0157others(12): Show | 15 | HG01167.hp1 HG01255.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1120+766dupA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAA | 7 | a0001c0001t0001g0098a0001c0001t0001g0116a0002c0006t0004g0168others(4): Show | 7 | HG02145.hp1 HG02165.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1120+765_1120+766d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0087 | 2 | HG01167.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1120+757_1120+766d others(12): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0083 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1120+756_1120+766d others(13): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0002g0194others(1): Show | 4 | HG00735.hp1 HG01256.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120+755_1120+766d others(14): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0071a0001c0001t0002g0199a0009c0015t0005g0094others(1): Show | 4 | HG00558.hp2 HG00639.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+754_1120+766d others(15): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0004a0001c0001t0002g0190a0001c0001t0002g0198others(1): Show | 4 | HG00741.hp2 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+753_1120+766d others(16): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0091a0001c0001t0001g0175a0001c0001t0002g0191others(1): Show | 4 | NA18990.hp1 NA19012.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120+752_1120+766d others(17): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(9): Show |
6 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0109others(3): Show | 6 | HG01496.hp2 HG02027.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120+751_1120+766d others(18): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(10): Show |
4 | a0001c0001t0001g0054a0001c0001t0001g0112a0001c0001t0002g0195others(1): Show | 4 | HG00621.hp1 HG00621.hp2 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+750_1120+766d others(19): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0001a0001c0001t0001g0078a0001c0001t0011g0155 | 3 | HG00099.hp2 NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1120+749_1120+766d others(20): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0090a0001c0001t0002g0196a0012c0045t0001g0043 | 3 | HG03471.hp1 NA18949.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1120+748_1120+766d others(21): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(13): Show |
2 | a0001c0001t0001g0104a0001c0001t0045g0121 | 2 | HG00280.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1120+747_1120+766d others(22): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(14): Show |
5 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0074others(2): Show | 5 | HG00642.hp1 HG01069.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120+746_1120+766d others(23): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0093a0001c0001t0001g0102a0001c0001t0017g0008others(1): Show | 4 | HG01099.hp2 HG01261.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120+745_1120+766d others(24): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(17): Show |
6 | a0001c0001t0001g0059a0001c0001t0001g0097a0001c0001t0001g0100others(3): Show | 6 | HG01099.hp1 HG01358.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120+743_1120+766d others(26): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0070 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1120+742_1120+766d others(27): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0001g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1120+741_1120+766d others(28): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(21): Show |
2 | a0001c0001t0001g0122a0001c0046t0001g0177 | 2 | HG01243.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1120+766_1120+767i others(30): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1120+766_1120+767i others(31): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(23): Show |
1 | a0004c0004t0005g0123 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1120+766_1120+767i others(32): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0096 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1120+766_1120+767i others(33): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(25): Show |
2 | a0001c0001t0033g0077a0001c0041t0001g0041 | 2 | HG01358.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1120+766_1120+767i others(34): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0001g0124 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1120+766_1120+767i others(35): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(28): Show |
1 | a0001c0001t0001g0101 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1120+766_1120+767i others(37): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(29): Show |
1 | a0001c0001t0016g0079 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1120+766_1120+767i others(38): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(37): Show |
1 | a0001c0001t0001g0092 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1120+766_1120+767i others(46): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(13): Show |
1 | a0005c0005t0002g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1120+757_1120+758i others(22): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(15): Show |
1 | a0005c0005t0002g0211 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1120+757_1120+758i others(24): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
C | CAAAAAAA others(16): Show |
1 | a0005c0005t0001g0095 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1120+757_1120+758i others(25): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
CAA | C | 5 | a0001c0001t0001g0076a0001c0001t0043g0105a0002c0008t0035g0039others(2): Show | 5 | HG00323.hp2 HG01891.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120+765_1120+766d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448543
|
CAAAAAAA others(5): Show |
C | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1120+755_1120+766d others(14): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448543 | |||||
| chr9:131448544
|
A | AAAAAAAA others(11): Show |
1 | a0005c0005t0001g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1120+757_1120+758i others(20): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448544 | |||||
| chr9:131448544
|
A | C | 8 | a0001c0001t0001g0085a0001c0001t0001g0119a0002c0026t0040g0178others(5): Show | 8 | HG00140.hp2 HG02896.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1120+740A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448544 | ||||||
| chr9:131448546
|
A | AAAAAAAA others(9): Show |
1 | a0003c0002t0001g0065 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1120+757_1120+758i others(18): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448546 | |||||
| chr9:131448547
|
A | AAAAAAAA others(10): Show |
1 | a0005c0005t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1120+759_1120+760i others(19): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448547 | |||||
| chr9:131448547
|
A | AAAAAAAA others(8): Show |
3 | a0003c0002t0001g0110a0003c0002t0004g0118a0005c0044t0021g0200 | 3 | HG00140.hp1 HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1120+757_1120+758i others(17): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448547 | |||||
| chr9:131448548
|
A | AAAAAAAA others(9): Show |
2 | a0003c0002t0001g0156a0003c0002t0011g0158 | 2 | NA18972.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1120+759_1120+760i others(18): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448548 | |||||
| chr9:131448548
|
A | AAAAAAAA others(8): Show |
3 | a0003c0002t0001g0134a0003c0002t0001g0184a0003c0002t0027g0174 | 3 | HG01175.hp2 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1120+758_1120+759i others(17): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448548 | |||||
| chr9:131448548
|
A | AAAAAAAA others(7): Show |
25 | a0001c0001t0001g0103a0003c0002t0001g0046a0003c0002t0001g0066others(22): Show | 25 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1120+757_1120+758i others(16): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448548 | |||||
| chr9:131448549
|
A | AAAAAAAA others(7): Show |
2 | a0003c0002t0001g0045a0005c0005t0001g0108 | 2 | NA20300.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1120+758_1120+759i others(16): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448549 | |||||
| chr9:131448549
|
A | AAAAAAAA others(6): Show |
1 | a0003c0002t0041g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1120+757_1120+758i others(15): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131448549 | |||||
| chr9:131448568
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1120+764A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448568 | ||||||
| chr9:131448571
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1120+767G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448571 | ||||||
| chr9:131448572
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1120+768G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448572 | ||||||
| chr9:131448576
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1120+772G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448576 | ||||||
| chr9:131448578
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1120+774G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448578 | ||||||
| chr9:131448582
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1120+778G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448582 | ||||||
| chr9:131448583
|
A | AAAAAAAA others(54): Show |
1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1120+779_1120+780i others(63): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448583 | ||||||
| chr9:131448620
|
G | T | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120+816G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448620 | ||||||
| chr9:131448644
|
C | T | 1 | a0005c0044t0021g0200 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1120+840C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448644 | ||||||
| chr9:131448680
|
G | A | 10 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0193others(7): Show | 10 | HG00735.hp1 HG01496.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1120+876G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448680 | ||||||
| chr9:131448711
|
A | G | 3 | a0002c0018t0008g0207a0002c0018t0008g0208a0002c0039t0008g0206 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1120+907A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448711 | ||||||
| chr9:131448718
|
C | G | 2 | a0002c0007t0014g0002a0002c0007t0014g0012 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1120+914C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448718 | ||||||
| chr9:131448733
|
T | G | 1 | a0024c0025t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1120+929T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448733 | ||||||
| chr9:131448749
|
C | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1120+945C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448749 | ||||||
| chr9:131448787
|
T | C | 21 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(18): Show | 21 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1120+983T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448787 | ||||||
| chr9:131448936
|
C | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120+1132C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131448936 | ||||||
| chr9:131449018
|
T | A | 16 | a0002c0040t0029g0151a0004c0004t0005g0117a0004c0004t0005g0140others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.1120+1214T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131449018 | ||||||
| chr9:131449089
|
A | G | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120+1285A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131449089 | ||||||
| chr9:131449198
|
A | G | 1 | a0002c0040t0029g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1120+1394A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131449198 | ||||||
| chr9:131449363
|
C | CT | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1120+1570dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131449363 | |||||
| chr9:131449433
|
C | T | 2 | a0005c0005t0002g0204a0005c0005t0002g0205 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1120+1629C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131449433 | ||||||
| chr9:131449480
|
T | G | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1120+1676T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131449480 | ||||||
| chr9:131450012
|
A | T | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1120+2208A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131450012 | ||||||
| chr9:131450040
|
A | G | 2 | a0003c0002t0046g0060a0003c0002t0047g0061 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1120+2236A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131450040 | ||||||
| chr9:131450218
|
G | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1120+2414G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131450218 | ||||||
| chr9:131450249
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1120+2445C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131450249 | ||||||
| chr9:131450267
|
A | AT | 24 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0048others(21): Show | 24 | HG01099.hp1 HG01099.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.1120+2478dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131450267 | |||||
| chr9:131450337
|
G | A | 2 | a0002c0040t0029g0151a0016c0032t0019g0215 | 2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1120+2533G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131450337 | ||||||
| chr9:131450356
|
C | T | 1 | a0003c0031t0001g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1120+2552C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131450356 | ||||||
| chr9:131450593
|
G | GT | 30 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(27): Show | 30 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.1120+2800dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131450593 | |||||
| chr9:131450836
|
C | T | 1 | a0005c0005t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1120+3032C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131450836 | ||||||
| chr9:131450841
|
G | T | 1 | a0005c0005t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1120+3037G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131450841 | ||||||
| chr9:131450851
|
G | T | 8 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(5): Show | 8 | HG00140.hp2 HG00642.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1120+3047G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131450851 | ||||||
| chr9:131450857
|
G | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1120+3053G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131450857 | ||||||
| chr9:131450965
|
C | A | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1120+3161C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131450965 | ||||||
| chr9:131451028
|
G | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120+3224G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131451028 | ||||||
| chr9:131451137
|
C | T | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120+3333C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131451137 | ||||||
| chr9:131451271
|
C | T | 2 | a0002c0026t0040g0178a0006c0011t0037g0179 | 2 | HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1120+3467C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131451271 | ||||||
| chr9:131451380
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1120+3576C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131451380 | ||||||
| chr9:131451398
|
C | CA | 34 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.1120+3604dupA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131451398 | |||||
| chr9:131451438
|
T | C | 1 | a0020c0028t0007g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1120+3634T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131451438 | ||||||
| chr9:131451563
|
G | A | 45 | a0002c0008t0025g0125a0003c0002t0001g0045a0003c0002t0001g0046others(42): Show | 45 | HG00140.hp1 HG00741.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1121-3513G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131451563 | ||||||
| chr9:131451601
|
A | G | 9 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0193others(6): Show | 9 | HG00735.hp1 HG01496.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1121-3475A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131451601 | ||||||
| chr9:131451609
|
A | G | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1121-3467A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131451609 | ||||||
| chr9:131451634
|
A | T | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1121-3442A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131451634 | ||||||
| chr9:131451639
|
C | A | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1121-3437C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131451639 | ||||||
| chr9:131451644
|
T | A | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1121-3432T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131451644 | ||||||
| chr9:131451655
|
A | G | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1121-3421A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131451655 | ||||||
| chr9:131452030
|
C | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1121-3046C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452030 | ||||||
| chr9:131452047
|
G | A | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-3029G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452047 | ||||||
| chr9:131452072
|
C | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121-3004C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452072 | ||||||
| chr9:131452079
|
AATAAGAT others(21): Show |
A | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1121-2966_1121-293 others(32): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131452079 | |||||
| chr9:131452264
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1121-2812C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452264 | ||||||
| chr9:131452316
|
G | C | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1121-2760G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452316 | ||||||
| chr9:131452349
|
T | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1121-2727T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452349 | ||||||
| chr9:131452350
|
C | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1121-2726C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452350 | ||||||
| chr9:131452360
|
T | G | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1121-2716T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452360 | ||||||
| chr9:131452378
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1121-2698A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452378 | ||||||
| chr9:131452436
|
A | T | 3 | a0002c0018t0008g0207a0002c0018t0008g0208a0002c0039t0008g0206 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1121-2640A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452436 | ||||||
| chr9:131452563
|
T | A | 1 | a0006c0022t0038g0180 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1121-2513T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452563 | ||||||
| chr9:131452579
|
A | G | 2 | a0004c0004t0005g0143a0004c0004t0006g0144 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1121-2497A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452579 | ||||||
| chr9:131452623
|
T | TGTTA | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1121-2450_1121-244 others(8): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131452623 | |||||
| chr9:131452750
|
T | A | 23 | a0002c0006t0026g0146a0002c0040t0029g0151a0004c0004t0005g0117others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1121-2326T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131452750 | ||||||
| chr9:131453041
|
T | C | 10 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1121-2035T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453041 | ||||||
| chr9:131453042
|
G | A | 3 | a0005c0005t0001g0095a0005c0005t0002g0210a0005c0005t0002g0211 | 3 | NA18970.hp1 NA18971.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1121-2034G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453042 | ||||||
| chr9:131453124
|
A | G | 10 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1121-1952A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453124 | ||||||
| chr9:131453144
|
G | A | 3 | a0002c0010t0009g0187a0002c0010t0009g0188a0002c0010t0009g0189 | 3 | HG01361.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1121-1932G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453144 | ||||||
| chr9:131453263
|
C | T | 2 | a0004c0004t0005g0143a0004c0004t0006g0144 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1121-1813C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453263 | ||||||
| chr9:131453314
|
C | T | 1 | a0002c0033t0023g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1121-1762C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453314 | ||||||
| chr9:131453345
|
C | G | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1121-1731C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453345 | ||||||
| chr9:131453463
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0114 | 3 | HG01168.hp1 HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1121-1613C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453463 | ||||||
| chr9:131453477
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1121-1599G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453477 | ||||||
| chr9:131453514
|
A | G | 1 | a0002c0003t0003g0030 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1121-1562A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453514 | ||||||
| chr9:131453524
|
C | T | 5 | a0005c0005t0001g0010a0005c0005t0001g0011a0005c0005t0001g0095others(2): Show | 5 | HG03471.hp2 NA18970.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121-1552C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453524 | ||||||
| chr9:131453570
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1121-1506T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453570 | ||||||
| chr9:131453620
|
T | C | 2 | a0020c0028t0007g0135a0023c0036t0007g0148 | 2 | HG02572.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1121-1456T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453620 | ||||||
| chr9:131453969
|
A | G | 1 | a0001c0001t0022g0192 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1121-1107A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131453969 | ||||||
| chr9:131454116
|
A | C | 6 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0082others(3): Show | 6 | HG01255.hp2 HG01934.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-960A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131454116 | ||||||
| chr9:131454189
|
A | G | 1 | a0015c0021t0004g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1121-887A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131454189 | ||||||
| chr9:131454202
|
C | T | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121-874C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131454202 | ||||||
| chr9:131454440
|
A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1121-636A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131454440 | ||||||
| chr9:131454538
|
G | A | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121-538G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131454538 | ||||||
| chr9:131454633
|
C | CT | 3 | a0003c0002t0001g0049a0003c0002t0001g0156a0003c0002t0011g0158 | 3 | NA18972.hp1 NA18975.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1121-438dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131454633 | |||||
| chr9:131454718
|
C | T | 3 | a0003c0002t0001g0049a0003c0002t0001g0156a0003c0002t0011g0158 | 3 | NA18972.hp1 NA18975.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1121-358C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131454718 | ||||||
| chr9:131454796
|
C | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0091a0008c0016t0001g0088others(2): Show | 5 | NA18949.hp1 NA18964.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121-280C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131454796 | ||||||
| chr9:131454824
|
C | T | 25 | a0002c0006t0026g0146a0002c0040t0029g0151a0004c0004t0005g0117others(22): Show | 25 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.1121-252C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131454824 | ||||||
| chr9:131454847
|
GCTGGTCT others(81): Show |
G | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121-211_1121-124d others(90): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131454847 | |||||
| chr9:131454865
|
ACCTCATG others(81): Show |
A | 13 | a0002c0003t0003g0016a0002c0003t0003g0018a0002c0003t0003g0025others(10): Show | 13 | HG01192.hp1 HG01257.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.1121-151_1121-64de others(89): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr9 | 131454865 | |||||
| chr9:131454962
|
T | G | 23 | a0002c0006t0026g0146a0002c0040t0029g0151a0004c0004t0005g0117others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1121-114T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131454962 | ||||||
| chr9:131455000
|
G | C | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121-76G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 9/31 | chr9 | 131455000 | ||||||
| chr9:131455188
|
A | G | 2 | a0002c0012t0004g0161a0002c0012t0004g0162 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1211+22A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131455188 | ||||||
| chr9:131455216
|
T | G | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1211+50T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131455216 | ||||||
| chr9:131455510
|
CT | C | 12 | a0002c0003t0008g0216a0002c0007t0010g0201a0002c0007t0010g0202others(9): Show | 12 | HG01123.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1211+368delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr9 | 131455510 | |||||
| chr9:131455510
|
CTT | C | 8 | a0001c0001t0001g0054a0001c0001t0001g0111a0002c0008t0025g0125others(5): Show | 8 | HG00621.hp1 HG00642.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1211+367_1211+368d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr9 | 131455510 | |||||
| chr9:131455510
|
CTTT | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0040others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.1211+366_1211+368d others(5): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr9 | 131455510 | |||||
| chr9:131455510
|
CTTTT | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0048others(81): Show | 84 | HG00140.hp1 HG00735.hp1 HG00741.hp1 others(81): Show |
intron_variant | MODIFIER | c.1211+365_1211+368d others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr9 | 131455510 | |||||
| chr9:131455912
|
A | C | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1211+746A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131455912 | ||||||
| chr9:131455924
|
C | T | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1211+758C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131455924 | ||||||
| chr9:131456134
|
T | C | 1 | a0002c0023t0012g0029 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1211+968T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456134 | ||||||
| chr9:131456204
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1211+1038T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456204 | ||||||
| chr9:131456211
|
CT | C | 29 | a0001c0001t0022g0192a0002c0006t0026g0146a0002c0007t0010g0201others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1211+1064delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr9 | 131456211 | |||||
| chr9:131456211
|
CTT | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1211+1063_1211+106 others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr9 | 131456211 | |||||
| chr9:131456211
|
CTTT | C | 6 | a0002c0008t0028g0126a0002c0008t0035g0039a0002c0008t0042g0038others(3): Show | 6 | HG01123.hp2 HG01891.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1211+1062_1211+106 others(7): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr9 | 131456211 | |||||
| chr9:131456214
|
T | C | 24 | a0001c0001t0022g0192a0002c0006t0026g0146a0002c0040t0029g0151others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.1211+1048T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456214 | ||||||
| chr9:131456215
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1211+1049T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456215 | ||||||
| chr9:131456216
|
T | C | 2 | a0002c0008t0028g0126a0002c0010t0009g0189 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1211+1050T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456216 | ||||||
| chr9:131456381
|
T | C | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1211+1215T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456381 | ||||||
| chr9:131456402
|
C | T | 1 | a0002c0003t0003g0016 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1211+1236C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456402 | ||||||
| chr9:131456447
|
C | T | 1 | a0002c0040t0029g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1211+1281C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456447 | ||||||
| chr9:131456448
|
A | G | 1 | a0002c0040t0029g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1211+1282A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456448 | ||||||
| chr9:131456534
|
G | C | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1211+1368G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456534 | ||||||
| chr9:131456562
|
C | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1211+1396C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456562 | ||||||
| chr9:131456774
|
C | T | 2 | a0002c0012t0004g0161a0002c0012t0004g0162 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1211+1608C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456774 | ||||||
| chr9:131456817
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1211+1651A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131456817 | ||||||
| chr9:131457107
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1211+1941A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131457107 | ||||||
| chr9:131457429
|
G | A | 3 | a0003c0002t0001g0067a0003c0002t0001g0127a0003c0002t0001g0130 | 3 | HG00741.hp1 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1212-1735G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131457429 | ||||||
| chr9:131457703
|
C | T | 30 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(27): Show | 30 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.1212-1461C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131457703 | ||||||
| chr9:131457788
|
T | C | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1212-1376T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131457788 | ||||||
| chr9:131457804
|
G | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1212-1360G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131457804 | ||||||
| chr9:131457851
|
C | T | 3 | a0002c0018t0008g0207a0002c0018t0008g0208a0002c0039t0008g0206 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1212-1313C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131457851 | ||||||
| chr9:131457863
|
T | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1212-1301T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131457863 | ||||||
| chr9:131458007
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1212-1157C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131458007 | ||||||
| chr9:131458070
|
C | T | 1 | a0006c0022t0038g0180 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1212-1094C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131458070 | ||||||
| chr9:131458158
|
CT | C | 4 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212-1001delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr9 | 131458158 | |||||
| chr9:131458191
|
T | C | 1 | a0012c0045t0001g0043 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1212-973T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131458191 | ||||||
| chr9:131458371
|
G | A | 3 | a0002c0018t0008g0207a0002c0018t0008g0208a0002c0039t0008g0206 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1212-793G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131458371 | ||||||
| chr9:131458503
|
AT | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.1212-648delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr9 | 131458503 | |||||
| chr9:131458510
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1212-654T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131458510 | ||||||
| chr9:131458537
|
G | C | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1212-627G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131458537 | ||||||
| chr9:131458567
|
C | T | 5 | a0002c0008t0025g0125a0002c0018t0008g0207a0002c0018t0008g0208others(2): Show | 5 | HG01943.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1212-597C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131458567 | ||||||
| chr9:131458733
|
C | A | 4 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0019others(1): Show | 4 | HG00558.hp1 NA18949.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212-431C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131458733 | ||||||
| chr9:131458844
|
G | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1212-320G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131458844 | ||||||
| chr9:131458930
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1212-234C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131458930 | ||||||
| chr9:131459073
|
T | C | 3 | a0004c0004t0005g0117a0004c0004t0005g0140a0004c0004t0005g0150 | 3 | HG00639.hp2 HG01243.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1212-91T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 10/31 | chr9 | 131459073 | ||||||
| chr9:131459592
|
A | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1404+236A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131459592 | ||||||
| chr9:131459634
|
C | T | 30 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(27): Show | 30 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.1404+278C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131459634 | ||||||
| chr9:131459697
|
C | T | 1 | a0004c0004t0005g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1404+341C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131459697 | ||||||
| chr9:131459727
|
C | T | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1404+371C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131459727 | ||||||
| chr9:131459831
|
A | G | 3 | a0002c0018t0008g0207a0002c0018t0008g0208a0002c0039t0008g0206 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1404+475A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131459831 | ||||||
| chr9:131459847
|
T | C | 30 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(27): Show | 30 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.1404+491T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131459847 | ||||||
| chr9:131459890
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1404+534G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131459890 | ||||||
| chr9:131459970
|
CA | C | 28 | a0002c0003t0003g0025a0002c0003t0003g0027a0002c0008t0028g0126others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1404+636delA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131459970 | |||||
| chr9:131459970
|
CAA | C | 14 | a0001c0001t0001g0063a0001c0001t0001g0073a0001c0001t0001g0113others(11): Show | 14 | HG01167.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1404+635_1404+636d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131459970 | |||||
| chr9:131459970
|
CAAA | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.1404+634_1404+636d others(5): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131459970 | |||||
| chr9:131459970
|
CAAAA | C | 5 | a0005c0005t0002g0212a0005c0005t0002g0213a0005c0005t0002g0214others(2): Show | 5 | HG01256.hp2 HG01258.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1404+633_1404+636d others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131459970 | |||||
| chr9:131460020
|
A | G | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1404+664A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131460020 | ||||||
| chr9:131460097
|
G | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1404+741G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131460097 | ||||||
| chr9:131460199
|
G | A | 23 | a0002c0006t0026g0146a0002c0040t0029g0151a0004c0004t0005g0117others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1404+843G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131460199 | ||||||
| chr9:131460206
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1404+850C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131460206 | ||||||
| chr9:131460811
|
G | T | 1 | a0004c0009t0007g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1404+1455G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131460811 | ||||||
| chr9:131460827
|
A | C | 2 | a0003c0002t0001g0156a0003c0002t0011g0158 | 2 | NA18972.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1404+1471A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131460827 | ||||||
| chr9:131460966
|
G | A | 3 | a0002c0010t0009g0187a0002c0010t0009g0188a0002c0010t0009g0189 | 3 | HG01361.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1404+1610G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131460966 | ||||||
| chr9:131461093
|
T | A | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1404+1737T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131461093 | ||||||
| chr9:131461108
|
G | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1404+1752G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131461108 | ||||||
| chr9:131461215
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1404+1859T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131461215 | ||||||
| chr9:131461231
|
G | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0041t0001g0041 | 3 | HG01358.hp1 HG01496.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1404+1875G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131461231 | ||||||
| chr9:131461352
|
C | T | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1404+1996C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131461352 | ||||||
| chr9:131461375
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1404+2019G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131461375 | ||||||
| chr9:131461477
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1404+2121G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131461477 | ||||||
| chr9:131461557
|
T | A | 1 | a0002c0006t0004g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1404+2201T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131461557 | ||||||
| chr9:131461602
|
C | T | 2 | a0001c0001t0001g0040a0001c0041t0001g0041 | 2 | HG01358.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1404+2246C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131461602 | ||||||
| chr9:131461885
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1404+2529C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131461885 | ||||||
| chr9:131461979
|
A | G | 1 | a0002c0007t0024g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1404+2623A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131461979 | ||||||
| chr9:131462063
|
C | T | 28 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(25): Show | 28 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.1405-2700C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131462063 | ||||||
| chr9:131462449
|
G | A | 1 | a0003c0002t0004g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1405-2314G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131462449 | ||||||
| chr9:131462557
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1405-2206T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131462557 | ||||||
| chr9:131462610
|
C | T | 4 | a0002c0012t0004g0161a0002c0012t0004g0162a0002c0033t0023g0163others(1): Show | 4 | HG02922.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1405-2153C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131462610 | ||||||
| chr9:131462621
|
C | T | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1405-2142C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131462621 | ||||||
| chr9:131462673
|
A | G | 2 | a0011c0013t0031g0036a0011c0013t0036g0037 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1405-2090A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131462673 | ||||||
| chr9:131462799
|
C | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1405-1964C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131462799 | ||||||
| chr9:131462836
|
T | TA | 5 | a0002c0008t0028g0126a0002c0018t0008g0207a0002c0018t0008g0208others(2): Show | 5 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1405-1907dupA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131462836 | |||||
| chr9:131462836
|
T | TAAA | 10 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1405-1909_1405-190 others(7): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131462836 | |||||
| chr9:131462836
|
T | TAAAA | 9 | a0002c0026t0040g0178a0003c0002t0001g0183a0003c0002t0001g0184others(6): Show | 9 | HG01261.hp1 HG01361.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1405-1910_1405-190 others(8): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131462836 | |||||
| chr9:131462836
|
T | TAAAAA | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0048others(63): Show | 66 | HG00140.hp1 HG00735.hp1 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.1405-1911_1405-190 others(9): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131462836 | |||||
| chr9:131462836
|
T | TAAAAAA | 55 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0040others(52): Show | 55 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.1405-1912_1405-190 others(10): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131462836 | |||||
| chr9:131462836
|
T | TAAAAAAA | 5 | a0001c0001t0001g0072a0001c0001t0001g0090a0001c0001t0001g0096others(2): Show | 5 | HG01175.hp1 HG01243.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1405-1913_1405-190 others(11): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131462836 | |||||
| chr9:131462836
|
TA | T | 21 | a0002c0003t0003g0020a0002c0006t0026g0146a0002c0040t0029g0151others(18): Show | 21 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.1405-1907delA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131462836 | |||||
| chr9:131462948
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1405-1815C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131462948 | ||||||
| chr9:131462963
|
CTCTGAG | C | 23 | a0002c0006t0026g0146a0002c0040t0029g0151a0004c0004t0005g0117others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1405-1796_1405-179 others(10): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131462963 | |||||
| chr9:131463095
|
G | T | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1405-1668G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131463095 | ||||||
| chr9:131463215
|
C | T | 1 | a0002c0033t0023g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1405-1548C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131463215 | ||||||
| chr9:131463375
|
T | G | 1 | a0003c0002t0004g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1405-1388T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131463375 | ||||||
| chr9:131463463
|
T | A | 1 | a0002c0008t0042g0038 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1405-1300T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131463463 | ||||||
| chr9:131463506
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1405-1257T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131463506 | ||||||
| chr9:131463628
|
C | CT | 10 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0082others(7): Show | 10 | HG01123.hp2 HG01255.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1405-1117dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131463628 | |||||
| chr9:131463628
|
C | CTT | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1405-1118_1405-111 others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131463628 | |||||
| chr9:131463628
|
C | CTTT | 13 | a0001c0001t0001g0084a0001c0001t0001g0122a0002c0003t0008g0216others(10): Show | 13 | HG01167.hp1 HG01243.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1405-1119_1405-111 others(7): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131463628 | |||||
| chr9:131463628
|
CTT | C | 23 | a0002c0006t0026g0146a0002c0040t0029g0151a0004c0004t0005g0117others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1405-1118_1405-111 others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131463628 | |||||
| chr9:131463669
|
C | T | 2 | a0002c0003t0003g0020a0002c0003t0003g0024 | 2 | NA18951.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1405-1094C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131463669 | ||||||
| chr9:131463800
|
T | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1405-963T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131463800 | ||||||
| chr9:131463852
|
C | T | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1405-911C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131463852 | ||||||
| chr9:131463941
|
C | CT | 32 | a0001c0001t0002g0194a0002c0003t0003g0032a0002c0006t0026g0146others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1405-808dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131463941 | |||||
| chr9:131463941
|
C | CTT | 6 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(3): Show | 6 | HG02055.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1405-809_1405-808d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr9 | 131463941 | |||||
| chr9:131463953
|
T | C | 1 | a0002c0037t0003g0017 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1405-810T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131463953 | ||||||
| chr9:131464130
|
C | T | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1405-633C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131464130 | ||||||
| chr9:131464333
|
T | A | 1 | a0001c0001t0001g0071 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1405-430T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131464333 | ||||||
| chr9:131464385
|
C | G | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1405-378C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131464385 | ||||||
| chr9:131464428
|
G | A | 28 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(25): Show | 28 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.1405-335G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131464428 | ||||||
| chr9:131464718
|
G | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1405-45G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 11/31 | chr9 | 131464718 | ||||||
| chr9:131465113
|
C | T | 4 | a0003c0002t0001g0067a0003c0002t0001g0127a0003c0002t0001g0129others(1): Show | 4 | HG00741.hp1 HG01071.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+35C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465113 | ||||||
| chr9:131465127
|
C | T | 2 | a0003c0002t0001g0067a0003c0002t0001g0127 | 2 | HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1720+49C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465127 | ||||||
| chr9:131465193
|
G | A | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1720+115G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465193 | ||||||
| chr9:131465230
|
G | A | 1 | a0004c0004t0013g0169 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1720+152G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465230 | ||||||
| chr9:131465270
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1720+192T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465270 | ||||||
| chr9:131465355
|
A | C | 2 | a0002c0007t0014g0002a0002c0007t0014g0012 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+277A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465355 | ||||||
| chr9:131465373
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1720+295C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465373 | ||||||
| chr9:131465547
|
A | G | 1 | a0005c0005t0001g0108 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1720+469A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465547 | ||||||
| chr9:131465571
|
A | G | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1720+493A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465571 | ||||||
| chr9:131465578
|
C | A | 1 | a0006c0022t0038g0180 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1720+500C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465578 | ||||||
| chr9:131465584
|
T | C | 8 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0014g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1720+506T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465584 | ||||||
| chr9:131465770
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1720+692C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465770 | ||||||
| chr9:131465837
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1720+759A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465837 | ||||||
| chr9:131465965
|
T | C | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1720+887T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465965 | ||||||
| chr9:131465985
|
A | G | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1720+907A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131465985 | ||||||
| chr9:131466077
|
T | C | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1720+999T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131466077 | ||||||
| chr9:131466098
|
T | A | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1720+1020T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131466098 | ||||||
| chr9:131466293
|
T | C | 1 | a0002c0003t0003g0028 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1720+1215T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131466293 | ||||||
| chr9:131466420
|
A | T | 3 | a0001c0001t0001g0053a0007c0017t0001g0056a0007c0017t0001g0106 | 3 | HG00621.hp2 HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1721-1143A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131466420 | ||||||
| chr9:131466458
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1721-1105T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131466458 | ||||||
| chr9:131466624
|
C | CT | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1721-929dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr9 | 131466624 | |||||
| chr9:131466681
|
A | G | 10 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0193others(7): Show | 10 | HG00735.hp1 HG01496.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1721-882A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131466681 | ||||||
| chr9:131466722
|
C | T | 7 | a0001c0001t0001g0074a0001c0001t0001g0112a0002c0007t0010g0201others(4): Show | 7 | HG02027.hp1 HG02055.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1721-841C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131466722 | ||||||
| chr9:131466840
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1721-723C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131466840 | ||||||
| chr9:131466912
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1721-651C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131466912 | ||||||
| chr9:131466958
|
C | T | 1 | a0002c0003t0003g0025 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1721-605C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131466958 | ||||||
| chr9:131466991
|
C | T | 34 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.1721-572C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131466991 | ||||||
| chr9:131467080
|
T | C | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1721-483T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131467080 | ||||||
| chr9:131467100
|
A | AT | 80 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1721-457dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr9 | 131467100 | |||||
| chr9:131467551
|
T | C | 17 | a0003c0002t0001g0046a0003c0002t0001g0049a0003c0002t0001g0065others(14): Show | 17 | HG00140.hp1 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1721-12T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131467551 | ||||||
| chr9:131467552
|
A | G | 13 | a0004c0004t0005g0117a0004c0004t0005g0140a0004c0004t0005g0143others(10): Show | 13 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.1721-11A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 12/31 | chr9 | 131467552 | ||||||
| chr9:131468039
|
T | C | 2 | a0011c0013t0031g0036a0011c0013t0036g0037 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1911+286T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131468039 | ||||||
| chr9:131468050
|
T | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1911+297T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131468050 | ||||||
| chr9:131468055
|
G | A | 3 | a0002c0010t0009g0187a0002c0010t0009g0188a0002c0010t0009g0189 | 3 | HG01361.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1911+302G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131468055 | ||||||
| chr9:131468226
|
G | A | 10 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1911+473G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131468226 | ||||||
| chr9:131468384
|
G | A | 1 | a0024c0025t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1911+631G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131468384 | ||||||
| chr9:131468405
|
A | G | 1 | a0001c0046t0001g0177 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1911+652A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131468405 | ||||||
| chr9:131468410
|
C | G | 1 | a0005c0044t0021g0200 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1911+657C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131468410 | ||||||
| chr9:131468825
|
T | A | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1911+1072T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131468825 | ||||||
| chr9:131468826
|
T | A | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1911+1073T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131468826 | ||||||
| chr9:131468861
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1911+1108C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131468861 | ||||||
| chr9:131469062
|
G | A | 2 | a0003c0002t0001g0065a0003c0002t0001g0110 | 2 | HG00140.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1911+1309G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131469062 | ||||||
| chr9:131469102
|
G | A | 1 | a0002c0008t0028g0126 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1911+1349G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131469102 | ||||||
| chr9:131469108
|
C | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1911+1355C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131469108 | ||||||
| chr9:131469241
|
G | C | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1911+1488G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131469241 | ||||||
| chr9:131469270
|
G | A | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1911+1517G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131469270 | ||||||
| chr9:131469296
|
T | G | 14 | a0003c0002t0001g0046a0003c0002t0001g0065a0003c0002t0001g0066others(11): Show | 14 | HG00140.hp1 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1912-1492T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131469296 | ||||||
| chr9:131469335
|
AAAAAT | A | 3 | a0002c0008t0028g0126a0003c0002t0001g0065a0003c0002t0001g0110 | 3 | HG00140.hp1 HG01891.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1912-1434_1912-143 others(9): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr9 | 131469335 | |||||
| chr9:131469401
|
C | G | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1912-1387C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131469401 | ||||||
| chr9:131469636
|
G | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1912-1152G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131469636 | ||||||
| chr9:131469802
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0083others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1912-986A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131469802 | ||||||
| chr9:131469995
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1912-793C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131469995 | ||||||
| chr9:131470014
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1912-774G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131470014 | ||||||
| chr9:131470232
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1912-556G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131470232 | ||||||
| chr9:131470257
|
C | T | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1912-531C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131470257 | ||||||
| chr9:131470300
|
AG | A | 8 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0019others(5): Show | 8 | HG00558.hp1 HG02738.hp2 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.1912-484delG | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr9 | 131470300 | |||||
| chr9:131470423
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1912-365A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131470423 | ||||||
| chr9:131470487
|
G | A | 6 | a0002c0007t0024g0186a0002c0008t0034g0035a0002c0008t0035g0039others(3): Show | 6 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1912-301G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131470487 | ||||||
| chr9:131470497
|
G | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1912-291G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131470497 | ||||||
| chr9:131470542
|
C | T | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1912-246C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131470542 | ||||||
| chr9:131470567
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1912-221T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131470567 | ||||||
| chr9:131470587
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1912-201C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131470587 | ||||||
| chr9:131470700
|
A | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1912-88A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131470700 | ||||||
| chr9:131470719
|
C | T | 1 | a0002c0007t0024g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1912-69C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131470719 | ||||||
| chr9:131470725
|
T | C | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0114 | 3 | HG01168.hp1 HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1912-63T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | chr9 | 131470725 | ||||||
| chr9:131470766
|
G | GTC | 3 | a0001c0001t0002g0195a0001c0001t0002g0197a0001c0001t0022g0192 | 3 | HG01496.hp2 HG02723.hp1 HG03041.hp2 |
splice_region_variant&intron_variant | LOW | c.1912-10_1912-9dupC others(1): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr9 | 131470766 | |||||
| chr9:131471037
|
G | C | 44 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(41): Show | 44 | HG00558.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.2107+54G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131471037 | ||||||
| chr9:131471061
|
A | G | 1 | a0004c0004t0005g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2107+78A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131471061 | ||||||
| chr9:131471149
|
A | G | 5 | a0002c0008t0034g0035a0002c0008t0035g0039a0002c0008t0042g0038others(2): Show | 5 | HG01123.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107+166A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131471149 | ||||||
| chr9:131471296
|
A | C | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2107+313A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131471296 | ||||||
| chr9:131471357
|
C | T | 2 | a0003c0002t0004g0118a0003c0002t0039g0047 | 2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2107+374C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131471357 | ||||||
| chr9:131471425
|
A | G | 9 | a0002c0008t0025g0125a0002c0008t0034g0035a0002c0008t0035g0039others(6): Show | 9 | HG01123.hp2 HG01891.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.2107+442A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131471425 | ||||||
| chr9:131471666
|
C | T | 25 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(22): Show | 25 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.2107+683C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131471666 | ||||||
| chr9:131471937
|
A | G | 1 | a0003c0002t0001g0185 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2107+954A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131471937 | ||||||
| chr9:131472073
|
T | A | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2107+1090T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472073 | ||||||
| chr9:131472112
|
A | C | 1 | a0002c0006t0004g0165 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2107+1129A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472112 | ||||||
| chr9:131472306
|
T | G | 4 | a0001c0001t0022g0192a0001c0046t0001g0177a0013c0020t0032g0006others(1): Show | 4 | HG00642.hp2 HG01496.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.2108-1202T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472306 | ||||||
| chr9:131472396
|
C | G | 1 | a0002c0040t0029g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2108-1112C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472396 | ||||||
| chr9:131472467
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.2108-1041G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472467 | ||||||
| chr9:131472471
|
A | AT | 55 | a0001c0001t0001g0001a0001c0001t0001g0042a0001c0001t0001g0063others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.2108-1014dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr9 | 131472471 | |||||
| chr9:131472471
|
A | ATT | 17 | a0002c0003t0003g0015a0002c0003t0003g0018a0002c0003t0003g0019others(14): Show | 17 | HG00558.hp1 HG01192.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.2108-1015_2108-101 others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr9 | 131472471 | |||||
| chr9:131472471
|
A | ATTT | 11 | a0002c0003t0003g0014a0002c0003t0003g0016a0002c0003t0003g0021others(8): Show | 11 | HG01123.hp2 HG02451.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2108-1016_2108-101 others(7): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr9 | 131472471 | |||||
| chr9:131472471
|
AT | A | 6 | a0001c0001t0001g0058a0001c0001t0001g0084a0001c0001t0022g0192others(3): Show | 6 | HG01496.hp2 HG02683.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-1014delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr9 | 131472471 | |||||
| chr9:131472614
|
T | C | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2108-894T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472614 | ||||||
| chr9:131472631
|
C | G | 1 | a0004c0004t0005g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2108-877C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472631 | ||||||
| chr9:131472668
|
G | A | 3 | a0002c0018t0008g0207a0002c0018t0008g0208a0002c0039t0008g0206 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2108-840G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472668 | ||||||
| chr9:131472679
|
A | G | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2108-829A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472679 | ||||||
| chr9:131472888
|
A | G | 30 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(27): Show | 30 | HG00558.hp1 HG01123.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2108-620A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472888 | ||||||
| chr9:131472908
|
A | G | 1 | a0006c0022t0038g0180 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2108-600A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472908 | ||||||
| chr9:131472927
|
T | G | 4 | a0003c0002t0001g0134a0003c0002t0001g0152a0003c0002t0001g0153others(1): Show | 4 | HG02647.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2108-581T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472927 | ||||||
| chr9:131472937
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2108-571G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131472937 | ||||||
| chr9:131473001
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.2108-507T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131473001 | ||||||
| chr9:131473044
|
T | C | 34 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.2108-464T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131473044 | ||||||
| chr9:131473229
|
T | C | 6 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2108-279T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131473229 | ||||||
| chr9:131473336
|
G | A | 34 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.2108-172G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131473336 | ||||||
| chr9:131473420
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.2108-88G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131473420 | ||||||
| chr9:131473428
|
C | A | 2 | a0004c0009t0007g0132a0004c0009t0007g0159 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2108-80C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | chr9 | 131473428 | ||||||
| chr9:131473431
|
TG | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.2108-74delG | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr9 | 131473431 | |||||
| chr9:131473765
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.2324+41G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 15/31 | chr9 | 131473765 | ||||||
| chr9:131473781
|
T | C | 3 | a0003c0002t0001g0183a0003c0002t0001g0184a0003c0002t0001g0185 | 3 | HG02572.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2324+57T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 15/31 | chr9 | 131473781 | ||||||
| chr9:131474035
|
A | G | 3 | a0002c0018t0008g0207a0002c0018t0008g0208a0002c0039t0008g0206 | 3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2324+311A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 15/31 | chr9 | 131474035 | ||||||
| chr9:131474055
|
A | C | 1 | a0003c0002t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2324+331A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 15/31 | chr9 | 131474055 | ||||||
| chr9:131474162
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2325-292G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 15/31 | chr9 | 131474162 | ||||||
| chr9:131474206
|
A | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.2325-248A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 15/31 | chr9 | 131474206 | ||||||
| chr9:131474210
|
C | T | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2325-244C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 15/31 | chr9 | 131474210 | ||||||
| chr9:131474224
|
G | A | 4 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2325-230G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 15/31 | chr9 | 131474224 | ||||||
| chr9:131474348
|
A | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2325-106A>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 15/31 | chr9 | 131474348 | ||||||
| chr9:131476842
|
G | T | 1 | a0019c0029t0020g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4406+307G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131476842 | ||||||
| chr9:131476845
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4406+310G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131476845 | ||||||
| chr9:131476966
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.4406+431A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131476966 | ||||||
| chr9:131476994
|
C | T | 1 | a0014c0042t0001g0173 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4406+459C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131476994 | ||||||
| chr9:131477035
|
C | A | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4406+500C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131477035 | ||||||
| chr9:131477099
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.4406+564G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131477099 | ||||||
| chr9:131477134
|
G | A | 31 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(28): Show | 31 | HG00558.hp1 HG01123.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.4406+599G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131477134 | ||||||
| chr9:131477201
|
G | A | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4407-543G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131477201 | ||||||
| chr9:131477352
|
G | A | 2 | a0002c0008t0028g0126a0002c0040t0029g0151 | 2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4407-392G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131477352 | ||||||
| chr9:131477354
|
C | T | 3 | a0002c0010t0009g0187a0002c0010t0009g0188a0002c0010t0009g0189 | 3 | HG01361.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4407-390C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131477354 | ||||||
| chr9:131477429
|
G | C | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.4407-315G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131477429 | ||||||
| chr9:131477440
|
G | A | 1 | a0003c0031t0001g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4407-304G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131477440 | ||||||
| chr9:131477478
|
C | G | 4 | a0001c0001t0016g0079a0001c0001t0016g0081a0005c0005t0002g0212others(1): Show | 4 | HG01255.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.4407-266C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131477478 | ||||||
| chr9:131477592
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.4407-152T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131477592 | ||||||
| chr9:131477706
|
C | G | 34 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(31): Show | 34 | HG00558.hp1 HG00642.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.4407-38C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 16/31 | chr9 | 131477706 | ||||||
| chr9:131478126
|
C | T | 12 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(9): Show | 12 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.4612+177C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 17/31 | chr9 | 131478126 | ||||||
| chr9:131478144
|
C | T | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4612+195C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 17/31 | chr9 | 131478144 | ||||||
| chr9:131478209
|
C | T | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4612+260C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 17/31 | chr9 | 131478209 | ||||||
| chr9:131478230
|
TCA | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.4613-237_4613-236d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr9 | 131478230 | |||||
| chr9:131478308
|
T | C | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4613-166T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 17/31 | chr9 | 131478308 | ||||||
| chr9:131478337
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.4613-137C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 17/31 | chr9 | 131478337 | ||||||
| chr9:131478353
|
C | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.4613-121C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 17/31 | chr9 | 131478353 | ||||||
| chr9:131478355
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4613-119G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 17/31 | chr9 | 131478355 | ||||||
| chr9:131479407
|
G | A | 34 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(31): Show | 34 | HG00558.hp1 HG00642.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.4900+14G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | chr9 | 131479407 | ||||||
| chr9:131479550
|
T | A | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4900+157T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | chr9 | 131479550 | ||||||
| chr9:131479611
|
A | AT | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.4900+220dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr9 | 131479611 | |||||
| chr9:131480034
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.4900+641C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | chr9 | 131480034 | ||||||
| chr9:131480420
|
G | A | 7 | a0002c0008t0025g0125a0002c0008t0034g0035a0002c0008t0035g0039others(4): Show | 7 | HG01123.hp2 HG01891.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.4900+1027G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | chr9 | 131480420 | ||||||
| chr9:131480553
|
G | C | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4900+1160G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | chr9 | 131480553 | ||||||
| chr9:131480619
|
A | AT | 35 | a0001c0001t0001g0063a0001c0001t0001g0072a0002c0003t0003g0014others(32): Show | 35 | HG00558.hp1 HG00642.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.4901-1093dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr9 | 131480619 | |||||
| chr9:131480840
|
G | T | 1 | a0005c0005t0002g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.4901-886G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | chr9 | 131480840 | ||||||
| chr9:131481135
|
C | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.4901-591C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | chr9 | 131481135 | ||||||
| chr9:131481209
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4901-517C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | chr9 | 131481209 | ||||||
| chr9:131481265
|
C | T | 31 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(28): Show | 31 | HG00558.hp1 HG01123.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.4901-461C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | chr9 | 131481265 | ||||||
| chr9:131481311
|
C | CA | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.4901-394dupA | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr9 | 131481311 | |||||
| chr9:131481311
|
C | CAA | 40 | a0001c0001t0001g0085a0001c0001t0001g0090a0001c0001t0001g0096others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.4901-395_4901-394d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr9 | 131481311 | |||||
| chr9:131481311
|
C | CAAAAA | 6 | a0002c0008t0028g0126a0004c0009t0007g0132a0004c0009t0007g0133others(3): Show | 6 | HG00642.hp2 HG01891.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.4901-398_4901-394d others(7): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr9 | 131481311 | |||||
| chr9:131481311
|
CAAA | C | 14 | a0005c0005t0001g0010a0005c0005t0001g0011a0005c0005t0001g0095others(11): Show | 14 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.4901-396_4901-394d others(5): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr9 | 131481311 | |||||
| chr9:131481335
|
A | G | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4901-391A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | chr9 | 131481335 | ||||||
| chr9:131481652
|
G | A | 23 | a0002c0006t0026g0146a0004c0004t0005g0117a0004c0004t0005g0123others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.4901-74G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | chr9 | 131481652 | ||||||
| chr9:131481655
|
C | G | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4901-71C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 19/31 | chr9 | 131481655 | ||||||
| chr9:131481902
|
G | A | 4 | a0003c0002t0001g0045a0003c0002t0004g0118a0003c0002t0039g0047others(1): Show | 4 | HG01106.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4983+94G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 20/31 | chr9 | 131481902 | ||||||
| chr9:131481960
|
A | G | 1 | a0002c0003t0003g0018 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4983+152A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 20/31 | chr9 | 131481960 | ||||||
| chr9:131482314
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4984-57T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 20/31 | chr9 | 131482314 | ||||||
| chr9:131483159
|
C | G | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.5374-200C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 22/31 | chr9 | 131483159 | ||||||
| chr9:131483192
|
C | T | 33 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(30): Show | 33 | HG00558.hp1 HG01123.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.5374-167C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 22/31 | chr9 | 131483192 | ||||||
| chr9:131483241
|
G | A | 2 | a0004c0009t0007g0133a0004c0009t0007g0136 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.5374-118G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 22/31 | chr9 | 131483241 | ||||||
| chr9:131483270
|
G | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.5374-89G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 22/31 | chr9 | 131483270 | ||||||
| chr9:131483270
|
G | T | 1 | a0002c0019t0011g0022 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.5374-89G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 22/31 | chr9 | 131483270 | ||||||
| chr9:131483332
|
G | A | 14 | a0004c0004t0005g0117a0004c0004t0005g0123a0004c0004t0005g0140others(11): Show | 14 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.5374-27G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 22/31 | chr9 | 131483332 | ||||||
| chr9:131483454
|
A | G | 1 | a0001c0001t0017g0008 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.5460+9A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 23/31 | chr9 | 131483454 | ||||||
| chr9:131483461
|
C | A | 2 | a0002c0008t0028g0126a0002c0040t0029g0151 | 2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5460+16C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 23/31 | chr9 | 131483461 | ||||||
| chr9:131483562
|
A | G | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5460+117A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 23/31 | chr9 | 131483562 | ||||||
| chr9:131483613
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.5460+168G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 23/31 | chr9 | 131483613 | ||||||
| chr9:131484004
|
G | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0114 | 3 | HG01168.hp1 HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.5460+559G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 23/31 | chr9 | 131484004 | ||||||
| chr9:131484106
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5461-580C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 23/31 | chr9 | 131484106 | ||||||
| chr9:131484190
|
T | A | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.5461-496T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 23/31 | chr9 | 131484190 | ||||||
| chr9:131484301
|
C | T | 2 | a0005c0005t0001g0010a0005c0005t0001g0011 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5461-385C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 23/31 | chr9 | 131484301 | ||||||
| chr9:131484531
|
G | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.5461-155G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 23/31 | chr9 | 131484531 | ||||||
| chr9:131484553
|
A | G | 1 | a0020c0028t0007g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5461-133A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 23/31 | chr9 | 131484553 | ||||||
| chr9:131484628
|
G | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.5461-58G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 23/31 | chr9 | 131484628 | ||||||
| chr9:131484877
|
G | C | 4 | a0003c0002t0001g0134a0003c0002t0001g0152a0003c0002t0001g0153others(1): Show | 4 | HG02647.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.5566-71G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 24/31 | chr9 | 131484877 | ||||||
| chr9:131485364
|
T | C | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.5758+224T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 25/31 | chr9 | 131485364 | ||||||
| chr9:131485437
|
T | C | 44 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(41): Show | 44 | HG00558.hp1 HG00642.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.5758+297T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 25/31 | chr9 | 131485437 | ||||||
| chr9:131485439
|
G | A | 33 | a0001c0001t0001g0071a0002c0008t0042g0038a0003c0002t0001g0046others(30): Show | 33 | HG00140.hp1 HG00558.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.5758+299G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 25/31 | chr9 | 131485439 | ||||||
| chr9:131485518
|
C | T | 1 | a0002c0008t0042g0038 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.5758+378C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 25/31 | chr9 | 131485518 | ||||||
| chr9:131485636
|
C | T | 1 | a0006c0022t0038g0180 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5759-449C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 25/31 | chr9 | 131485636 | ||||||
| chr9:131485667
|
T | C | 2 | a0005c0005t0001g0107a0005c0005t0001g0108 | 2 | HG01123.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.5759-418T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 25/31 | chr9 | 131485667 | ||||||
| chr9:131485920
|
G | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG02630.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.5759-165G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 25/31 | chr9 | 131485920 | ||||||
| chr9:131485931
|
C | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.5759-154C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 25/31 | chr9 | 131485931 | ||||||
| chr9:131486055
|
T | A | 6 | a0003c0002t0001g0066a0003c0002t0001g0067a0003c0002t0001g0127others(3): Show | 6 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.5759-30T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 25/31 | chr9 | 131486055 | ||||||
| chr9:131486071
|
C | T | 1 | a0011c0013t0031g0036 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5759-14C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 25/31 | chr9 | 131486071 | ||||||
| chr9:131486194
|
T | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.5856+12T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 26/31 | chr9 | 131486194 | ||||||
| chr9:131486240
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.5856+58G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 26/31 | chr9 | 131486240 | ||||||
| chr9:131486359
|
G | C | 4 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.5856+177G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 26/31 | chr9 | 131486359 | ||||||
| chr9:131486394
|
A | C | 1 | a0002c0003t0003g0018 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.5856+212A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 26/31 | chr9 | 131486394 | ||||||
| chr9:131486591
|
C | CTT | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.5856+411_5856+412d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 26/31 | INFO_REALIGN_3_PRIME | chr9 | 131486591 | |||||
| chr9:131486816
|
G | C | 2 | a0002c0012t0004g0161a0002c0012t0004g0162 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5857-351G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 26/31 | chr9 | 131486816 | ||||||
| chr9:131486914
|
G | A | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.5857-253G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 26/31 | chr9 | 131486914 | ||||||
| chr9:131486917
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.5857-250T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 26/31 | chr9 | 131486917 | ||||||
| chr9:131487150
|
C | T | 4 | a0003c0002t0001g0134a0003c0002t0001g0152a0003c0002t0001g0153others(1): Show | 4 | HG02647.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.5857-17C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 26/31 | chr9 | 131487150 | ||||||
| chr9:131487491
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.5984+197T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 27/31 | chr9 | 131487491 | ||||||
| chr9:131487640
|
C | T | 2 | a0005c0005t0002g0212a0005c0005t0002g0213 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.5985-216C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 27/31 | chr9 | 131487640 | ||||||
| chr9:131487748
|
G | A | 1 | a0005c0044t0021g0200 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5985-108G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 27/31 | chr9 | 131487748 | ||||||
| chr9:131488171
|
C | T | 2 | a0003c0002t0001g0066a0003c0002t0001g0128 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.6225+75C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131488171 | ||||||
| chr9:131488194
|
G | A | 1 | a0023c0036t0007g0148 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.6225+98G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131488194 | ||||||
| chr9:131488269
|
C | CT | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.6225+186dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr9 | 131488269 | |||||
| chr9:131488269
|
CT | C | 29 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(26): Show | 29 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.6225+186delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr9 | 131488269 | |||||
| chr9:131488320
|
G | A | 4 | a0003c0002t0001g0134a0003c0002t0001g0152a0003c0002t0001g0153others(1): Show | 4 | HG02647.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.6225+224G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131488320 | ||||||
| chr9:131488454
|
T | A | 1 | a0004c0004t0005g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6225+358T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131488454 | ||||||
| chr9:131488498
|
G | A | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.6225+402G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131488498 | ||||||
| chr9:131488500
|
G | A | 5 | a0005c0005t0001g0010a0005c0005t0001g0011a0005c0005t0001g0095others(2): Show | 5 | HG03471.hp2 NA18970.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.6225+404G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131488500 | ||||||
| chr9:131488746
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.6225+650C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131488746 | ||||||
| chr9:131488926
|
C | A | 1 | a0016c0032t0019g0215 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6225+830C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131488926 | ||||||
| chr9:131488927
|
C | T | 10 | a0002c0006t0004g0160a0002c0006t0004g0165a0002c0006t0004g0167others(7): Show | 10 | HG01167.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.6225+831C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131488927 | ||||||
| chr9:131489184
|
C | CT | 10 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0059others(7): Show | 10 | HG00558.hp1 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.6225+1106dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr9 | 131489184 | |||||
| chr9:131489184
|
C | CTT | 11 | a0002c0003t0003g0021a0002c0007t0010g0201a0002c0007t0010g0202others(8): Show | 11 | HG02055.hp1 HG02647.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.6225+1105_6225+110 others(6): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr9 | 131489184 | |||||
| chr9:131489184
|
CT | C | 5 | a0001c0001t0049g0120a0002c0003t0003g0024a0002c0007t0024g0186others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.6225+1106delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr9 | 131489184 | |||||
| chr9:131489548
|
C | T | 4 | a0003c0002t0001g0134a0003c0002t0001g0152a0003c0002t0001g0153others(1): Show | 4 | HG02647.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.6225+1452C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131489548 | ||||||
| chr9:131489640
|
G | A | 1 | a0003c0002t0001g0069 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6225+1544G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131489640 | ||||||
| chr9:131489696
|
C | T | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.6225+1600C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131489696 | ||||||
| chr9:131489805
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.6226-1620G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131489805 | ||||||
| chr9:131489858
|
C | T | 1 | a0002c0035t0004g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6226-1567C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131489858 | ||||||
| chr9:131489983
|
G | A | 1 | a0002c0007t0024g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6226-1442G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131489983 | ||||||
| chr9:131490025
|
A | G | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6226-1400A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131490025 | ||||||
| chr9:131490036
|
T | A | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.6226-1389T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131490036 | ||||||
| chr9:131490222
|
T | C | 28 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(25): Show | 28 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.6226-1203T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131490222 | ||||||
| chr9:131490408
|
C | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.6226-1017C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131490408 | ||||||
| chr9:131490605
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6226-820T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131490605 | ||||||
| chr9:131490722
|
T | C | 7 | a0001c0001t0001g0083a0001c0001t0001g0087a0001c0001t0001g0122others(4): Show | 7 | HG00280.hp2 HG01167.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.6226-703T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131490722 | ||||||
| chr9:131490853
|
C | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.6226-572C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131490853 | ||||||
| chr9:131490887
|
C | T | 14 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(11): Show | 14 | HG00642.hp2 HG01167.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.6226-538C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131490887 | ||||||
| chr9:131490947
|
C | T | 7 | a0002c0006t0004g0160a0002c0006t0018g0164a0002c0006t0018g0166others(4): Show | 7 | HG01167.hp1 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.6226-478C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131490947 | ||||||
| chr9:131491082
|
A | G | 1 | a0003c0002t0039g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6226-343A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131491082 | ||||||
| chr9:131491165
|
C | T | 5 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(2): Show | 5 | HG01257.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.6226-260C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131491165 | ||||||
| chr9:131491235
|
G | A | 2 | a0005c0005t0002g0204a0005c0005t0002g0205 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6226-190G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131491235 | ||||||
| chr9:131491347
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.6226-78T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 28/31 | chr9 | 131491347 | ||||||
| chr9:131491628
|
C | A | 6 | a0002c0003t0003g0025a0002c0003t0003g0026a0002c0003t0003g0027others(3): Show | 6 | HG00642.hp2 HG01257.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.6381+48C>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 29/31 | chr9 | 131491628 | ||||||
| chr9:131491931
|
C | CT | 16 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(13): Show | 16 | HG00558.hp1 HG01192.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.6382-236dupT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr9 | 131491931 | |||||
| chr9:131492356
|
G | T | 41 | a0002c0003t0003g0014a0002c0003t0003g0015a0002c0003t0003g0016others(38): Show | 41 | HG00558.hp1 HG00642.hp2 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.6473+96G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131492356 | ||||||
| chr9:131492367
|
G | A | 6 | a0004c0009t0007g0132a0004c0009t0007g0133a0004c0009t0007g0136others(3): Show | 6 | HG02572.hp1 HG02970.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.6473+107G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131492367 | ||||||
| chr9:131492575
|
A | G | 4 | a0003c0002t0001g0134a0003c0002t0001g0152a0003c0002t0001g0153others(1): Show | 4 | HG02647.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.6473+315A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131492575 | ||||||
| chr9:131492823
|
G | A | 4 | a0002c0008t0034g0035a0002c0008t0035g0039a0011c0013t0031g0036others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.6473+563G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131492823 | ||||||
| chr9:131492836
|
A | C | 1 | a0001c0001t0001g0085 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.6473+576A>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131492836 | ||||||
| chr9:131492952
|
C | T | 4 | a0002c0010t0009g0187a0002c0010t0009g0188a0002c0010t0009g0189others(1): Show | 4 | HG01361.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.6473+692C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131492952 | ||||||
| chr9:131492981
|
G | A | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.6473+721G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131492981 | ||||||
| chr9:131493125
|
A | G | 1 | a0006c0011t0037g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6473+865A>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493125 | ||||||
| chr9:131493126
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.6473+866C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493126 | ||||||
| chr9:131493138
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.6473+878T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493138 | ||||||
| chr9:131493152
|
TGCCCCAC others(1): Show |
T | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.6473+897_6473+904d others(10): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr9 | 131493152 | |||||
| chr9:131493177
|
C | T | 1 | a0003c0002t0001g0069 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6473+917C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493177 | ||||||
| chr9:131493219
|
G | A | 1 | a0002c0003t0003g0028 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.6473+959G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493219 | ||||||
| chr9:131493466
|
C | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.6474-939C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493466 | ||||||
| chr9:131493517
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG01168.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.6474-888C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493517 | ||||||
| chr9:131493565
|
CAG | C | 2 | a0002c0008t0028g0126a0002c0040t0029g0151 | 2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.6474-838_6474-837d others(4): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr9 | 131493565 | |||||
| chr9:131493629
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.6474-776T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493629 | ||||||
| chr9:131493869
|
C | CG | 3 | a0001c0001t0001g0091a0002c0037t0003g0017a0004c0004t0006g0144 | 3 | HG00280.hp1 NA18985.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.6474-536_6474-535i others(3): Show |
PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493869 | ||||||
| chr9:131493869
|
CT | C | 15 | a0002c0007t0024g0186a0002c0008t0028g0126a0002c0008t0035g0039others(12): Show | 15 | HG01361.hp2 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.6474-525delT | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr9 | 131493869 | |||||
| chr9:131493870
|
T | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.6474-535T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493870 | ||||||
| chr9:131493871
|
T | G | 9 | a0002c0007t0024g0186a0002c0008t0035g0039a0004c0009t0007g0132others(6): Show | 9 | HG01891.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.6474-534T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493871 | ||||||
| chr9:131493875
|
T | A | 3 | a0001c0001t0001g0090a0008c0016t0001g0088a0008c0016t0001g0089 | 3 | NA18949.hp1 NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.6474-530T>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493875 | ||||||
| chr9:131493986
|
T | C | 1 | a0002c0026t0040g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.6474-419T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131493986 | ||||||
| chr9:131494025
|
G | A | 2 | a0002c0012t0004g0161a0002c0012t0004g0162 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6474-380G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131494025 | ||||||
| chr9:131494027
|
C | T | 1 | a0003c0002t0001g0049 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.6474-378C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131494027 | ||||||
| chr9:131494252
|
T | G | 1 | a0010c0014t0001g0052 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.6474-153T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131494252 | ||||||
| chr9:131494293
|
G | A | 1 | a0021c0034t0048g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6474-112G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 30/31 | chr9 | 131494293 | ||||||
| chr9:131494740
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.6555+254T>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 31/31 | chr9 | 131494740 | ||||||
| chr9:131494978
|
C | T | 2 | a0002c0006t0018g0164a0002c0006t0018g0166 | 2 | HG01167.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.6555+492C>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 31/31 | chr9 | 131494978 | ||||||
| chr9:131495072
|
G | C | 1 | a0002c0007t0024g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6555+586G>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 31/31 | chr9 | 131495072 | ||||||
| chr9:131495164
|
T | C | 1 | a0019c0029t0020g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6556-576T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 31/31 | chr9 | 131495164 | ||||||
| chr9:131495174
|
C | G | 1 | a0013c0020t0032g0006 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.6556-566C>G | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 31/31 | chr9 | 131495174 | ||||||
| chr9:131495337
|
G | T | 5 | a0002c0007t0010g0201a0002c0007t0010g0202a0002c0007t0010g0203others(2): Show | 5 | HG02055.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.6556-403G>T | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 31/31 | chr9 | 131495337 | ||||||
| chr9:131495402
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.6556-338G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 31/31 | chr9 | 131495402 | ||||||
| chr9:131495539
|
T | C | 2 | a0002c0008t0028g0126a0002c0040t0029g0151 | 2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.6556-201T>C | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 31/31 | chr9 | 131495539 | ||||||
| chr9:131495564
|
G | A | 1 | a0002c0040t0029g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6556-176G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 31/31 | chr9 | 131495564 | ||||||
| chr9:131495670
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.6556-70G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 31/31 | chr9 | 131495670 | ||||||
| chr9:131495693
|
G | A | 2 | a0002c0008t0028g0126a0002c0040t0029g0151 | 2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.6556-47G>A | PRRC2B | ENSG00000288701.1 | transcript | ENST00000683519.1 | protein_coding | 31/31 | chr9 | 131495693 |