| geneid | 9692 |
|---|---|
| ensemblid | ENSG00000100890.16 |
| hgncid | 19958 |
| symbol | PRORP |
| name | protein only RNase P catalytic subunit |
| refseq_nuc | NM_014672.4 |
| refseq_prot | NP_055487.2 |
| ensembl_nuc | ENST00000534898.9 |
| ensembl_prot | ENSP00000440915.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 35122552 |
| end | 35277622 |
| strand | + |
| ver | v1.2 |
| region | chr14:35122552-35277622 |
| region5000 | chr14:35117552-35282622 |
| regionname0 | PRORP_chr14_35122552_35277622 |
| regionname5000 | PRORP_chr14_35117552_35282622 |
| 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 | 1/1 | 583 | 284 | 79 | 60 | 100 | 11 | 32 | 74 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0002 | 0/0 | 583 | 22 | 2 | 10 | 4 | 1 | 5 | 2 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0003 | 0/0 | 583 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0004 | 0/0 | 583 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0005 | 0/0 | 583 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0006 | 0/0 | 583 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0007 | 0/0 | 583 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| 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 | 1/0 | 1752 | 182 | 52 | 40 | 58 | 7 | 24 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| c0002 | 0/1 | 1752 | 99 | 26 | 18 | 42 | 4 | 8 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| c0003 | 0/0 | 1752 | 22 | 2 | 10 | 4 | 1 | 5 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| c0004 | 0/0 | 1752 | 2 | 0 | 2 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| c0005 | 0/0 | 1752 | 2 | 2 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| c0006 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| c0007 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| c0008 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| c0009 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| c0010 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| c0011 | 0/0 | 1752 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| c0012 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| 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 | 4435 | 115 | 8 | 27 | 61 | 6 | 12 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0002 | 0/0 | 4434 | 61 | 8 | 9 | 28 | 3 | 13 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0003 | 0/0 | 4435 | 51 | 29 | 15 | 4 | 0 | 3 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0004 | 0/0 | 4435 | 17 | 0 | 8 | 3 | 1 | 5 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0005 | 0/0 | 4436 | 9 | 9 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0006 | 1/0 | 4435 | 7 | 5 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0007 | 0/0 | 4438 | 6 | 1 | 3 | 0 | 1 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0008 | 0/0 | 4436 | 4 | 2 | 0 | 1 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0009 | 0/0 | 4433 | 4 | 4 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0010 | 0/0 | 4435 | 3 | 0 | 0 | 3 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0011 | 0/0 | 4433 | 3 | 0 | 2 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0012 | 0/0 | 4432 | 3 | 3 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0013 | 0/0 | 4436 | 2 | 2 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0014 | 0/0 | 4435 | 2 | 2 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0015 | 0/0 | 4436 | 2 | 2 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0016 | 0/0 | 4435 | 2 | 2 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0017 | 0/0 | 4432 | 2 | 2 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0018 | 0/0 | 4434 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0019 | 0/0 | 4435 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0020 | 0/0 | 4435 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0021 | 0/0 | 4435 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0022 | 0/0 | 4435 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0023 | 0/0 | 4435 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0024 | 0/0 | 4436 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0025 | 0/0 | 4435 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0026 | 0/0 | 4435 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0027 | 0/0 | 4434 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0028 | 0/0 | 4435 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0029 | 0/0 | 4435 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0030 | 0/0 | 4436 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0031 | 0/0 | 4436 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0032 | 0/0 | 4434 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0033 | 0/0 | 4435 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0034 | 0/0 | 4435 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0035 | 0/0 | 4435 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0036 | 0/0 | 4436 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0037 | 0/0 | 4435 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| t0038 | 0/0 | 4432 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| 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 | 1/0 | 1752 | 182 | 52 | 40 | 58 | 7 | 24 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002 | 0/1 | 1752 | 99 | 26 | 18 | 42 | 4 | 8 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0004 | 0/0 | 1752 | 2 | 0 | 2 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0006 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0002c0003 | 0/0 | 1752 | 22 | 2 | 10 | 4 | 1 | 5 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0003c0005 | 0/0 | 1752 | 2 | 2 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0003c0007 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0003c0012 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0004c0010 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0005c0009 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0006c0008 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0007c0011 | 0/0 | 1752 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6186 | 49 | 5 | 10 | 23 | 2 | 9 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0002 | 0/0 | 6185 | 51 | 8 | 7 | 24 | 3 | 9 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0003 | 0/0 | 6186 | 39 | 17 | 15 | 4 | 0 | 3 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0005 | 0/0 | 6187 | 4 | 4 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0006 | 1/0 | 6186 | 7 | 5 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0007 | 0/0 | 6189 | 6 | 1 | 3 | 0 | 1 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0008 | 0/0 | 6187 | 3 | 1 | 0 | 1 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0009 | 0/0 | 6184 | 4 | 4 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0010 | 0/0 | 6186 | 2 | 0 | 0 | 2 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0011 | 0/0 | 6184 | 3 | 0 | 2 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0012 | 0/0 | 6183 | 2 | 2 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0015 | 0/0 | 6187 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0017 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0018 | 0/0 | 6185 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0021 | 0/0 | 6186 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0022 | 0/0 | 6186 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0023 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0025 | 0/0 | 6186 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0027 | 0/0 | 6185 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0028 | 0/0 | 6186 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0030 | 0/0 | 6187 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0032 | 0/0 | 6185 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0001t0038 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0001 | 0/1 | 6186 | 65 | 3 | 17 | 37 | 4 | 3 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0002 | 0/0 | 6185 | 7 | 0 | 0 | 3 | 0 | 4 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0003 | 0/0 | 6186 | 12 | 12 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0005 | 0/0 | 6187 | 5 | 5 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0010 | 0/0 | 6186 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0014 | 0/0 | 6186 | 2 | 2 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0015 | 0/0 | 6187 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0017 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0024 | 0/0 | 6187 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0026 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0029 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0031 | 0/0 | 6187 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0002t0033 | 0/0 | 6186 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0004t0002 | 0/0 | 6185 | 2 | 0 | 2 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0001c0006t0008 | 0/0 | 6187 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0002c0003t0004 | 0/0 | 6186 | 17 | 0 | 8 | 3 | 1 | 5 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0002c0003t0016 | 0/0 | 6186 | 2 | 2 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0002c0003t0034 | 0/0 | 6186 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0002c0003t0035 | 0/0 | 6186 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0002c0003t0036 | 0/0 | 6187 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0003c0005t0019 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0003c0005t0020 | 0/0 | 6186 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0003c0007t0013 | 0/0 | 6187 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0003c0012t0013 | 0/0 | 6187 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0004c0010t0002 | 0/0 | 6185 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0005c0009t0001 | 0/0 | 6186 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0006c0008t0012 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| a0007c0011t0037 | 0/0 | 6186 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | copy fasta | chr14 | 35117552 | 35282622 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0006g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0007g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0007g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0008g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0008g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0010g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0010g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0011g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0011g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0011g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0015g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0017g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0018g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0021g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0022g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0023g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0025g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0027g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0028g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0030g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0032g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0001t0038g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0010g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0014g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0014g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0015g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0017g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0024g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0026g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0029g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0031g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0002t0033g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0004t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0004t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0001c0006t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0016g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0016g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0034g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0035g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0002c0003t0036g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0003c0005t0019g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0003c0005t0020g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0003c0007t0013g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0003c0012t0013g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0004c0010t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0005c0009t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0006c0008t0012g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| a0007c0011t0037g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0191 | EUR | GBR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00099 | hp2 | a0001 | c0001 | t0007 | g0176 | EUR | GBR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0300 | EUR | GBR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | CHS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00597 | hp2 | a0002 | c0003 | t0004 | g0295 | EAS | CHS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | CHS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00639 | hp1 | a0001 | c0001 | t0018 | g0174 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00642 | hp1 | a0002 | c0003 | t0004 | g0287 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00733 | hp2 | a0002 | c0003 | t0035 | g0272 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00735 | hp1 | a0002 | c0003 | t0004 | g0297 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00735 | hp2 | a0001 | c0001 | t0011 | g0310 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0172 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01071 | hp1 | a0002 | c0003 | t0004 | g0298 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01081 | hp2 | a0002 | c0003 | t0004 | g0039 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0242 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01175 | hp1 | a0002 | c0003 | t0004 | g0286 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01192 | hp2 | a0002 | c0003 | t0004 | g0299 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01255 | hp1 | a0001 | c0001 | t0027 | g0278 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01255 | hp2 | a0001 | c0001 | t0011 | g0155 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01256 | hp1 | a0001 | c0002 | t0024 | g0226 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01256 | hp2 | a0001 | c0004 | t0002 | g0275 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01257 | hp2 | a0001 | c0001 | t0007 | g0173 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01258 | hp1 | a0001 | c0004 | t0002 | g0276 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0131 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01358 | hp1 | a0002 | c0003 | t0034 | g0271 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0241 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0206 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0313 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01433 | hp2 | a0001 | c0001 | t0021 | g0175 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0101 | EUR | IBS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01516 | hp1 | a0001 | c0001 | t0022 | g0094 | EUR | IBS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0312 | EUR | IBS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0311 | EUR | IBS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | IBS | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0159 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0214 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01891 | hp2 | a0001 | c0002 | t0029 | g0210 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01934 | hp1 | a0002 | c0003 | t0004 | g0296 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0134 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01975 | hp1 | a0001 | c0001 | t0007 | g0050 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0264 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0239 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02004 | hp1 | a0002 | c0003 | t0004 | g0285 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02055 | hp1 | a0006 | c0008 | t0012 | g0143 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02056 | hp1 | a0001 | c0001 | t0025 | g0032 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02074 | hp2 | a0002 | c0003 | t0036 | g0292 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0132 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02257 | hp2 | a0001 | c0002 | t0005 | g0186 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0233 | AMR | PEL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02451 | hp2 | a0001 | c0001 | t0030 | g0073 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02572 | hp1 | a0001 | c0002 | t0005 | g0185 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0171 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02630 | hp1 | a0001 | c0002 | t0014 | g0187 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02717 | hp2 | a0001 | c0002 | t0005 | g0182 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0307 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02818 | hp1 | a0003 | c0012 | t0013 | g0211 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02818 | hp2 | a0003 | c0007 | t0013 | g0139 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0158 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0309 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02896 | hp1 | a0001 | c0002 | t0015 | g0305 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02896 | hp2 | a0001 | c0001 | t0015 | g0144 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0306 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0117 | AFR | ESN | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0096 | AFR | ESN | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0164 | AFR | ESN | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | ESN | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0156 | AFR | ESN | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ESN | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02976 | hp1 | a0001 | c0002 | t0003 | g0213 | AFR | ESN | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0093 | AFR | ESN | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03041 | hp2 | a0001 | c0002 | t0005 | g0183 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0212 | AFR | MSL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03098 | hp2 | a0001 | c0002 | t0017 | g0217 | AFR | MSL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03139 | hp2 | a0001 | c0001 | t0023 | g0161 | AFR | ESN | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03225 | hp1 | a0001 | c0006 | t0008 | g0169 | AFR | MSL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03225 | hp2 | a0001 | c0001 | t0012 | g0168 | AFR | MSL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0157 | AFR | MSL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03453 | hp2 | a0003 | c0005 | t0019 | g0166 | AFR | MSL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0189 | AFR | MSL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | MSL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0202 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03491 | hp2 | a0002 | c0003 | t0004 | g0280 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03492 | hp2 | a0002 | c0003 | t0004 | g0279 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | ESN | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03516 | hp2 | a0001 | c0001 | t0038 | g0165 | AFR | ESN | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0194 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0097 | AFR | GWD | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0184 | AFR | MSL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | MSL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03669 | hp2 | a0001 | c0001 | t0011 | g0154 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | STU | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0223 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0170 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03831 | hp2 | a0002 | c0003 | t0004 | g0302 | SAS | BEB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0224 | SAS | BEB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | BEB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0259 | SAS | BEB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03942 | hp1 | a0002 | c0003 | t0004 | g0294 | SAS | BEB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03942 | hp2 | a0007 | c0011 | t0037 | g0128 | SAS | BEB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0147 | SAS | STU | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | STU | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0225 | SAS | BEB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | STU | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | STU | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0222 | SAS | STU | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG04204 | hp2 | a0002 | c0003 | t0004 | g0284 | SAS | STU | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0146 | SAS | STU | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG04228 | hp2 | a0001 | c0002 | t0031 | g0190 | SAS | STU | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | YRI | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0308 | AFR | YRI | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | CHB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | YRI | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0216 | AFR | YRI | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18943 | hp2 | a0001 | c0001 | t0008 | g0149 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18945 | hp1 | a0004 | c0010 | t0002 | g0110 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18959 | hp2 | a0001 | c0001 | t0028 | g0035 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18966 | hp1 | a0001 | c0002 | t0033 | g0230 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18966 | hp2 | a0001 | c0001 | t0010 | g0047 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18975 | hp2 | a0005 | c0009 | t0001 | g0034 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18990 | hp1 | a0002 | c0003 | t0004 | g0293 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18994 | hp1 | a0001 | c0001 | t0010 | g0025 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19012 | hp1 | a0001 | c0002 | t0010 | g0229 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19030 | hp1 | a0003 | c0005 | t0020 | g0023 | AFR | LWK | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | LWK | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19065 | hp2 | a0002 | c0003 | t0004 | g0019 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19084 | hp1 | a0001 | c0001 | t0032 | g0123 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA19089 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | ASW | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ASW | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA20752 | hp1 | a0002 | c0003 | t0004 | g0282 | EUR | TSI | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0198 | EUR | TSI | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0145 | SAS | GIH | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02486 | hp2 | a0001 | c0002 | t0014 | g0188 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0163 | AFR | ACB | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | MSL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | USA | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| HG06807 | hp2 | a0002 | c0003 | t0016 | g0301 | AFR | USA | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA20300 | hp1 | a0001 | c0002 | t0026 | g0205 | AFR | USA | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0167 | AFR | USA | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0138 | AFR | LWK | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| NA21309 | hp2 | a0002 | c0003 | t0016 | g0288 | AFR | LWK | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0197 | REF | REF | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0121 | REF | REF | PRORP_chr14_35117552_35282622 | PRORP | chr14 | 35117552 | 35282622 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:35123931
|
C | T | 1 | a0007 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.686C>T | p.Ala229Val | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/8 | 1064/6186 | 686/1752 | 229/583 | chr14 | 35123931 | ||
| chr14:35127490
|
C | T | 1 | a0004 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.1046C>T | p.Ser349Leu | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/8 | 1424/6186 | 1046/1752 | 349/583 | chr14 | 35127490 | ||
| chr14:35266752
|
C | A | 1 | a0006 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.1301C>A | p.Ala434Asp | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/8 | 1679/6186 | 1301/1752 | 434/583 | chr14 | 35266752 | ||
| chr14:35266761
|
A | G | 1 | a0002 | 22 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(19): Show |
missense_variant | MODERATE | c.1310A>G | p.Asn437Ser | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/8 | 1688/6186 | 1310/1752 | 437/583 | chr14 | 35266761 | ||
| chr14:35270451
|
A | G | 1 | a0003 | 4 | HG02818.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.1475A>G | p.His492Arg | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/8 | 1853/6186 | 1475/1752 | 492/583 | chr14 | 35270451 | ||
| chr14:35270520
|
G | A | 1 | a0005 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.1544G>A | p.Arg515His | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/8 | 1922/6186 | 1544/1752 | 515/583 | chr14 | 35270520 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:35123332
|
C | G | 2 | a0001c0002a0003c0012 | 100 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(97): Show |
synonymous_variant | LOW | c.87C>G | p.Val29Val | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/8 | 465/6186 | 87/1752 | 29/583 | chr14 | 35123332 | ||
| chr14:35123389
|
T | C | 1 | a0001c0006 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.144T>C | p.Leu48Leu | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/8 | 522/6186 | 144/1752 | 48/583 | chr14 | 35123389 | ||
| chr14:35123473
|
G | A | 1 | a0001c0004 | 2 | HG01256.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.228G>A | p.Lys76Lys | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/8 | 606/6186 | 228/1752 | 76/583 | chr14 | 35123473 | ||
| chr14:35123716
|
G | A | 1 | a0003c0007 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.471G>A | p.Val157Val | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/8 | 849/6186 | 471/1752 | 157/583 | chr14 | 35123716 | ||
| chr14:35270401
|
C | T | 3 | a0003c0005a0003c0007a0003c0012 | 4 | HG02818.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.1425C>T | p.Ile475Ile | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/8 | 1803/6186 | 1425/1752 | 475/583 | chr14 | 35270401 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:35122991
|
G | A | 1 | a0001c0001t0018 | 1 | HG00639.hp1 | 5_prime_UTR_variant | MODIFIER | c.-255G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/8 | 255 | chr14 | 35122991 | |||||
| chr14:35123134
|
A | T | 1 | a0001c0001t0038 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-112A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/8 | 112 | chr14 | 35123134 | |||||
| chr14:35123239
|
C | G | 1 | a0007c0011t0037 | 1 | HG03942.hp2 | 5_prime_UTR_variant | MODIFIER | c.-7C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/8 | 7 | chr14 | 35123239 | |||||
| chr14:35273701
|
A | G | 7 | a0001c0001t0009a0001c0001t0011a0001c0001t0012others(4): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*135A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 135 | chr14 | 35273701 | |||||
| chr14:35273857
|
T | A | 23 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(20): Show | 86 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*291T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 291 | chr14 | 35273857 | |||||
| chr14:35274179
|
A | T | 2 | a0001c0001t0012a0006c0008t0012 | 3 | HG02055.hp1 HG02559.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*613A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 613 | chr14 | 35274179 | |||||
| chr14:35274208
|
C | T | 5 | a0002c0003t0004a0002c0003t0016a0002c0003t0034others(2): Show | 22 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*642C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 642 | chr14 | 35274208 | |||||
| chr14:35274252
|
A | G | 1 | a0001c0002t0033 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*686A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 686 | chr14 | 35274252 | |||||
| chr14:35274293
|
C | T | 1 | a0001c0001t0032 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*727C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 727 | chr14 | 35274293 | |||||
| chr14:35274315
|
A | AT | 5 | a0001c0001t0008a0001c0001t0030a0001c0002t0031others(2): Show | 7 | HG02074.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*766dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 767 | INFO_REALIGN_3_PRIME | chr14 | 35274315 | ||||
| chr14:35274315
|
A | ATT | 6 | a0001c0001t0009a0001c0001t0012a0001c0001t0017others(3): Show | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*765_*766dupTT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 767 | INFO_REALIGN_3_PRIME | chr14 | 35274315 | ||||
| chr14:35274315
|
A | ATTT | 2 | a0001c0001t0007a0001c0001t0011 | 9 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*764_*766dupTTT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 767 | INFO_REALIGN_3_PRIME | chr14 | 35274315 | ||||
| chr14:35274367
|
A | G | 19 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(16): Show | 82 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*801A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 801 | chr14 | 35274367 | |||||
| chr14:35274390
|
C | T | 9 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(6): Show | 61 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*824C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 824 | chr14 | 35274390 | |||||
| chr14:35274517
|
T | C | 1 | a0001c0002t0014 | 2 | HG02486.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*951T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 951 | chr14 | 35274517 | |||||
| chr14:35274712
|
T | C | 1 | a0001c0001t0030 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1146T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 1146 | chr14 | 35274712 | |||||
| chr14:35274851
|
A | G | 1 | a0001c0002t0029 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1285A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 1285 | chr14 | 35274851 | |||||
| chr14:35274986
|
G | A | 2 | a0001c0001t0007a0001c0001t0021 | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1420G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 1420 | chr14 | 35274986 | |||||
| chr14:35275024
|
ACTACT | A | 7 | a0001c0001t0009a0001c0001t0011a0001c0001t0012others(4): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1462_*1466delCTCT others(1): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 1462 | INFO_REALIGN_3_PRIME | chr14 | 35275024 | ||||
| chr14:35275082
|
A | C | 10 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(7): Show | 62 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1516A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 1516 | chr14 | 35275082 | |||||
| chr14:35275219
|
A | G | 1 | a0001c0001t0028 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1653A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 1653 | chr14 | 35275219 | |||||
| chr14:35275362
|
G | T | 10 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(7): Show | 62 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1796G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 1796 | chr14 | 35275362 | |||||
| chr14:35275633
|
G | A | 10 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(7): Show | 62 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2067G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 2067 | chr14 | 35275633 | |||||
| chr14:35275797
|
TA | T | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*2247delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 2247 | INFO_REALIGN_3_PRIME | chr14 | 35275797 | ||||
| chr14:35275816
|
C | T | 5 | a0002c0003t0004a0002c0003t0016a0002c0003t0034others(2): Show | 22 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2250C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 2250 | chr14 | 35275816 | |||||
| chr14:35275859
|
T | TA | 43 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(40): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*2295dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 2296 | INFO_REALIGN_3_PRIME | chr14 | 35275859 | ||||
| chr14:35275875
|
A | G | 1 | a0001c0001t0007 | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2309A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 2309 | chr14 | 35275875 | |||||
| chr14:35275916
|
C | T | 1 | a0002c0003t0016 | 2 | HG06807.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2350C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 2350 | chr14 | 35275916 | |||||
| chr14:35275993
|
C | CT | 1 | a0001c0001t0009 | 4 | HG01884.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2430dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 2431 | INFO_REALIGN_3_PRIME | chr14 | 35275993 | ||||
| chr14:35276436
|
T | C | 43 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(40): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*2870T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 2870 | chr14 | 35276436 | |||||
| chr14:35276529
|
C | T | 1 | a0001c0002t0026 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2963C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 2963 | chr14 | 35276529 | |||||
| chr14:35276621
|
C | G | 1 | a0001c0001t0023 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3055C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 3055 | chr14 | 35276621 | |||||
| chr14:35276915
|
C | T | 1 | a0001c0001t0027 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3349C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 3349 | chr14 | 35276915 | |||||
| chr14:35277106
|
A | G | 10 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(7): Show | 62 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*3540A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 3540 | chr14 | 35277106 | |||||
| chr14:35277213
|
A | G | 2 | a0001c0001t0010a0001c0002t0010 | 3 | NA18966.hp2 NA18994.hp1 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3647A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 3647 | chr14 | 35277213 | |||||
| chr14:35277379
|
G | T | 1 | a0001c0001t0025 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3813G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 3813 | chr14 | 35277379 | |||||
| chr14:35277411
|
C | T | 3 | a0003c0005t0020a0003c0007t0013a0003c0012t0013 | 3 | HG02818.hp1 HG02818.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3845C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 3845 | chr14 | 35277411 | |||||
| chr14:35277451
|
C | T | 2 | a0001c0001t0005a0001c0002t0005 | 9 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3885C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 3885 | chr14 | 35277451 | |||||
| chr14:35277544
|
A | G | 5 | a0002c0003t0004a0002c0003t0016a0002c0003t0034others(2): Show | 22 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3978A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 3978 | chr14 | 35277544 | |||||
| chr14:35277553
|
A | G | 1 | a0002c0003t0035 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3987A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 3987 | chr14 | 35277553 | |||||
| chr14:35277574
|
A | G | 1 | a0002c0003t0034 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4008A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 8/8 | 4008 | chr14 | 35277574 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:35122688
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01346.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-295+53T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 1/7 | chr14 | 35122688 | ||||||
| chr14:35122721
|
C | T | 1 | a0001c0001t0003g0313 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-295+86C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 1/7 | chr14 | 35122721 | ||||||
| chr14:35122784
|
T | C | 1 | a0001c0002t0003g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-295+149T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 1/7 | chr14 | 35122784 | ||||||
| chr14:35124271
|
A | AT | 42 | a0001c0001t0001g0289a0001c0001t0002g0273a0001c0001t0002g0274others(39): Show | 42 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.986+54dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 35124271 | |||||
| chr14:35124326
|
G | A | 1 | a0001c0002t0001g0005 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.986+95G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35124326 | ||||||
| chr14:35124393
|
C | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.986+162C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35124393 | ||||||
| chr14:35124872
|
T | C | 5 | a0001c0002t0003g0306a0001c0002t0003g0307a0001c0002t0003g0308others(2): Show | 5 | HG02723.hp1 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.986+641T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35124872 | ||||||
| chr14:35124900
|
C | G | 99 | a0001c0002t0001g0005a0001c0002t0001g0181a0001c0002t0001g0191others(96): Show | 99 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.986+669C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35124900 | ||||||
| chr14:35124985
|
C | T | 101 | a0001c0001t0001g0137a0001c0001t0003g0136a0001c0002t0001g0005others(98): Show | 101 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.986+754C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35124985 | ||||||
| chr14:35125067
|
G | C | 1 | a0001c0002t0001g0181 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.986+836G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35125067 | ||||||
| chr14:35125103
|
C | T | 4 | a0001c0001t0003g0177a0001c0001t0003g0178a0001c0001t0003g0179others(1): Show | 4 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.986+872C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35125103 | ||||||
| chr14:35125236
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.986+1005G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35125236 | ||||||
| chr14:35125597
|
A | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.987-1138A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35125597 | ||||||
| chr14:35125764
|
G | A | 1 | a0001c0001t0003g0136 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.987-971G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35125764 | ||||||
| chr14:35125809
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.987-926G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35125809 | ||||||
| chr14:35125834
|
C | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.987-901C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35125834 | ||||||
| chr14:35125978
|
G | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.987-757G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35125978 | ||||||
| chr14:35126207
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.987-528T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35126207 | ||||||
| chr14:35126212
|
A | T | 56 | a0001c0001t0001g0137a0001c0002t0001g0005a0001c0002t0001g0181others(53): Show | 56 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.987-523A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35126212 | ||||||
| chr14:35126502
|
G | T | 1 | a0001c0002t0017g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.987-233G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35126502 | ||||||
| chr14:35126636
|
C | T | 7 | a0001c0001t0007g0170a0001c0001t0007g0171a0001c0001t0007g0172others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.987-99C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35126636 | ||||||
| chr14:35126732
|
T | C | 14 | a0001c0002t0003g0189a0001c0002t0003g0306a0001c0002t0003g0307others(11): Show | 14 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.987-3T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 2/7 | chr14 | 35126732 | ||||||
| chr14:35126886
|
C | A | 100 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 100 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1034+104C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 3/7 | chr14 | 35126886 | ||||||
| chr14:35127078
|
G | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0137others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1034+296G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 3/7 | chr14 | 35127078 | ||||||
| chr14:35127117
|
C | T | 44 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(41): Show | 44 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.1034+335C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 3/7 | chr14 | 35127117 | ||||||
| chr14:35127189
|
G | A | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1035-290G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 3/7 | chr14 | 35127189 | ||||||
| chr14:35127235
|
A | T | 10 | a0001c0001t0003g0127a0001c0001t0003g0129a0001c0001t0003g0130others(7): Show | 10 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.1035-244A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 3/7 | chr14 | 35127235 | ||||||
| chr14:35127398
|
CATT | C | 44 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(41): Show | 44 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.1035-80_1035-78del others(3): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 3/7 | chr14 | 35127398 | ||||||
| chr14:35127730
|
A | G | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167+119A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35127730 | ||||||
| chr14:35127818
|
T | C | 1 | a0002c0003t0034g0271 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1167+207T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35127818 | ||||||
| chr14:35127860
|
TG | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(33): Show | 36 | HG01099.hp1 HG01255.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1167+250delG | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35127860 | ||||||
| chr14:35127862
|
C | T | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(33): Show | 36 | HG01099.hp1 HG01255.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.1167+251C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35127862 | ||||||
| chr14:35127894
|
G | T | 1 | a0001c0001t0003g0136 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1167+283G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35127894 | ||||||
| chr14:35127943
|
C | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1167+332C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35127943 | ||||||
| chr14:35128116
|
T | G | 1 | a0001c0001t0005g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1167+505T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35128116 | ||||||
| chr14:35128133
|
A | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0137others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1167+522A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35128133 | ||||||
| chr14:35128166
|
C | G | 1 | a0001c0002t0003g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1167+555C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35128166 | ||||||
| chr14:35128261
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1167+650T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35128261 | ||||||
| chr14:35128278
|
G | GT | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(36): Show | 39 | HG00735.hp2 HG01099.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.1167+677dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35128278 | |||||
| chr14:35128301
|
G | GT | 41 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0072others(38): Show | 41 | HG00735.hp2 HG01099.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.1167+700dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35128301 | |||||
| chr14:35128302
|
T | G | 1 | a0001c0001t0005g0012 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1167+691T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35128302 | ||||||
| chr14:35128431
|
G | C | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167+820G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35128431 | ||||||
| chr14:35128496
|
T | C | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+885T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35128496 | ||||||
| chr14:35128683
|
T | C | 33 | a0001c0001t0001g0289a0001c0001t0002g0273a0001c0001t0002g0274others(30): Show | 33 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1167+1072T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35128683 | ||||||
| chr14:35128870
|
G | A | 1 | a0001c0002t0001g0218 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1167+1259G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35128870 | ||||||
| chr14:35128968
|
T | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1167+1357T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35128968 | ||||||
| chr14:35128969
|
G | A | 1 | a0001c0001t0003g0177 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1167+1358G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35128969 | ||||||
| chr14:35129042
|
C | CA | 49 | a0001c0001t0001g0075a0001c0001t0001g0137a0001c0001t0002g0074others(46): Show | 49 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.1167+1447dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35129042 | |||||
| chr14:35129042
|
C | CAA | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(5): Show | 8 | HG01346.hp1 HG02055.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167+1446_1167+144 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35129042 | |||||
| chr14:35129066
|
G | A | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1167+1455G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35129066 | ||||||
| chr14:35129098
|
C | T | 1 | a0001c0002t0001g0215 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1167+1487C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35129098 | ||||||
| chr14:35129101
|
G | A | 1 | a0001c0001t0003g0178 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1167+1490G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35129101 | ||||||
| chr14:35129164
|
C | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1167+1553C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35129164 | ||||||
| chr14:35129513
|
C | T | 1 | a0001c0002t0003g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1167+1902C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35129513 | ||||||
| chr14:35129537
|
C | T | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1167+1926C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35129537 | ||||||
| chr14:35129625
|
C | T | 7 | a0001c0002t0003g0189a0001c0002t0003g0306a0001c0002t0003g0307others(4): Show | 7 | HG02723.hp1 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+2014C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35129625 | ||||||
| chr14:35129627
|
A | T | 6 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(3): Show | 6 | HG00738.hp1 HG01496.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1167+2016A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35129627 | ||||||
| chr14:35129720
|
C | G | 1 | a0001c0001t0003g0134 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1167+2109C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35129720 | ||||||
| chr14:35129800
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(10): Show | 13 | HG01099.hp1 HG01346.hp1 HG03491.hp1 others(10): Show |
intron_variant | MODIFIER | c.1167+2189G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35129800 | ||||||
| chr14:35129964
|
T | C | 1 | a0001c0002t0002g0222 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1167+2353T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35129964 | ||||||
| chr14:35130030
|
C | CT | 9 | a0001c0001t0001g0068a0001c0001t0001g0137a0001c0001t0003g0133others(6): Show | 9 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1167+2437dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35130030 | |||||
| chr14:35130030
|
CT | C | 11 | a0001c0001t0002g0015a0001c0001t0003g0017a0001c0001t0003g0018others(8): Show | 11 | HG01081.hp1 HG01256.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1167+2437delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35130030 | |||||
| chr14:35130031
|
T | G | 2 | a0001c0001t0002g0013a0001c0001t0002g0014 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1167+2420T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35130031 | ||||||
| chr14:35130039
|
T | TTG | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(31): Show | 34 | HG00735.hp2 HG01099.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1167+2429_1167+243 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35130039 | |||||
| chr14:35130387
|
T | TA | 101 | a0001c0001t0001g0137a0001c0002t0001g0005a0001c0002t0001g0181others(98): Show | 101 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1167+2777dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35130387 | |||||
| chr14:35130484
|
CT | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1167+2884delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35130484 | |||||
| chr14:35130493
|
T | C | 1 | a0001c0001t0003g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1167+2882T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35130493 | ||||||
| chr14:35130520
|
C | T | 2 | a0001c0001t0002g0126a0001c0002t0003g0138 | 2 | HG00597.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1167+2909C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35130520 | ||||||
| chr14:35130703
|
C | T | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1167+3092C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35130703 | ||||||
| chr14:35130717
|
T | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0137others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1167+3106T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35130717 | ||||||
| chr14:35130794
|
T | C | 1 | a0001c0002t0001g0227 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1167+3183T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35130794 | ||||||
| chr14:35130816
|
T | A | 93 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(90): Show | 93 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.1167+3205T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35130816 | ||||||
| chr14:35130983
|
G | A | 14 | a0001c0002t0003g0189a0001c0002t0003g0306a0001c0002t0003g0307others(11): Show | 14 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1167+3372G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35130983 | ||||||
| chr14:35131087
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1167+3476C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35131087 | ||||||
| chr14:35131315
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1167+3704A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35131315 | ||||||
| chr14:35131364
|
A | T | 1 | a0001c0001t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1167+3753A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35131364 | ||||||
| chr14:35131532
|
GT | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1167+3935delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35131532 | |||||
| chr14:35131598
|
G | A | 7 | a0001c0001t0007g0170a0001c0001t0007g0171a0001c0001t0007g0172others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+3987G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35131598 | ||||||
| chr14:35131780
|
C | G | 12 | a0001c0001t0002g0290a0001c0001t0002g0291a0002c0003t0004g0019others(9): Show | 12 | HG00597.hp2 HG00735.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1167+4169C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35131780 | ||||||
| chr14:35132048
|
A | G | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167+4437A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35132048 | ||||||
| chr14:35132086
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0002g0078a0001c0001t0002g0079others(1): Show | 4 | HG02071.hp2 NA18951.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+4475G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35132086 | ||||||
| chr14:35132255
|
C | T | 1 | a0001c0001t0032g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1167+4644C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35132255 | ||||||
| chr14:35132398
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1167+4787C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35132398 | ||||||
| chr14:35132589
|
A | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(32): Show | 35 | HG00735.hp2 HG01099.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1167+4978A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35132589 | ||||||
| chr14:35132654
|
G | A | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1167+5043G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35132654 | ||||||
| chr14:35132784
|
CA | C | 98 | a0001c0001t0001g0008a0001c0001t0001g0071a0001c0001t0002g0122others(95): Show | 98 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1167+5189delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35132784 | |||||
| chr14:35132800
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1167+5189A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35132800 | ||||||
| chr14:35132881
|
T | G | 44 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(41): Show | 44 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1167+5270T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35132881 | ||||||
| chr14:35132902
|
TTTTTG | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(60): Show | 63 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1167+5321_1167+532 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35132902 | |||||
| chr14:35133067
|
T | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1167+5456T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35133067 | ||||||
| chr14:35133141
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0003g0136 | 3 | HG01496.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1167+5530C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35133141 | ||||||
| chr14:35133361
|
A | AT | 31 | a0001c0001t0003g0160a0001c0001t0003g0162a0001c0001t0003g0177others(28): Show | 31 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1167+5758dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35133361 | |||||
| chr14:35133462
|
A | G | 3 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0008g0016 | 3 | HG01081.hp1 HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1167+5851A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35133462 | ||||||
| chr14:35133609
|
A | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1167+5998A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35133609 | ||||||
| chr14:35133750
|
G | A | 55 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(52): Show | 55 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1167+6139G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35133750 | ||||||
| chr14:35133819
|
T | C | 2 | a0001c0002t0002g0223a0001c0002t0002g0224 | 2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1167+6208T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35133819 | ||||||
| chr14:35133873
|
G | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(250): Show | 254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1167+6262G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35133873 | ||||||
| chr14:35133960
|
A | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1167+6349A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35133960 | ||||||
| chr14:35134028
|
T | C | 1 | a0001c0002t0031g0190 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1167+6417T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35134028 | ||||||
| chr14:35134367
|
C | G | 1 | a0001c0002t0001g0264 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1167+6756C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35134367 | ||||||
| chr14:35134738
|
T | C | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167+7127T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35134738 | ||||||
| chr14:35134789
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1167+7178G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35134789 | ||||||
| chr14:35135059
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1167+7448A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135059 | ||||||
| chr14:35135144
|
A | G | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(40): Show | 43 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1167+7533A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135144 | ||||||
| chr14:35135211
|
A | C | 1 | a0001c0001t0001g0060 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1167+7600A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135211 | ||||||
| chr14:35135337
|
C | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 47 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.1167+7726C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135337 | ||||||
| chr14:35135635
|
A | C | 3 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0008g0016 | 3 | HG01081.hp1 HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1167+8024A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135635 | ||||||
| chr14:35135686
|
A | C | 94 | a0001c0001t0001g0124a0001c0002t0001g0005a0001c0002t0001g0181others(91): Show | 94 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1167+8075A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135686 | ||||||
| chr14:35135714
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1167+8103C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135714 | ||||||
| chr14:35135730
|
C | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(30): Show | 33 | HG00735.hp2 HG01099.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1167+8119C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135730 | ||||||
| chr14:35135779
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1167+8168A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135779 | ||||||
| chr14:35135787
|
G | A | 2 | a0001c0001t0002g0290a0001c0001t0002g0291 | 2 | NA18941.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1167+8176G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135787 | ||||||
| chr14:35135867
|
A | C | 1 | a0001c0001t0001g0010 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1167+8256A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135867 | ||||||
| chr14:35135957
|
C | CA | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(35): Show | 38 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1167+8363dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35135957 | |||||
| chr14:35135990
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(32): Show | 35 | HG00735.hp2 HG01099.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1167+8379G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135990 | ||||||
| chr14:35135995
|
A | G | 2 | a0001c0001t0003g0177a0001c0001t0003g0180 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1167+8384A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35135995 | ||||||
| chr14:35136163
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1167+8552G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136163 | ||||||
| chr14:35136168
|
C | A | 1 | a0001c0002t0001g0233 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1167+8557C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136168 | ||||||
| chr14:35136232
|
G | A | 1 | a0003c0005t0019g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1167+8621G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136232 | ||||||
| chr14:35136259
|
G | A | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1167+8648G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136259 | ||||||
| chr14:35136361
|
C | T | 30 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0283others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1167+8750C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136361 | ||||||
| chr14:35136364
|
GT | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1167+8760delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35136364 | |||||
| chr14:35136371
|
T | G | 1 | a0001c0002t0001g0233 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1167+8760T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136371 | ||||||
| chr14:35136372
|
G | T | 1 | a0001c0002t0001g0233 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1167+8761G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136372 | ||||||
| chr14:35136408
|
GTTGTTGC others(9447): Show |
G | 71 | a0001c0002t0001g0005a0001c0002t0001g0181a0001c0002t0001g0191others(68): Show | 71 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1167+8812_1167+182 others(5): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35136408 | |||||
| chr14:35136452
|
G | A | 1 | a0001c0001t0006g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1167+8841G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136452 | ||||||
| chr14:35136469
|
G | C | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1167+8858G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136469 | ||||||
| chr14:35136505
|
G | A | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1167+8894G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136505 | ||||||
| chr14:35136537
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1167+8926G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136537 | ||||||
| chr14:35136597
|
A | G | 29 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0003g0020others(26): Show | 29 | HG00738.hp1 HG01496.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1167+8986A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136597 | ||||||
| chr14:35136653
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1167+9042G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136653 | ||||||
| chr14:35136670
|
T | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(69): Show | 72 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.1167+9059T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136670 | ||||||
| chr14:35136769
|
A | G | 1 | a0002c0003t0016g0288 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1167+9158A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136769 | ||||||
| chr14:35136800
|
C | T | 4 | a0001c0001t0002g0001a0001c0001t0002g0114a0001c0001t0002g0115others(1): Show | 5 | HG02015.hp1 NA18977.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1167+9189C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136800 | ||||||
| chr14:35136810
|
A | G | 29 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0003g0020others(26): Show | 29 | HG00738.hp1 HG01496.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1167+9199A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35136810 | ||||||
| chr14:35137075
|
T | C | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1167+9464T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35137075 | ||||||
| chr14:35137230
|
G | A | 1 | a0001c0001t0007g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1167+9619G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35137230 | ||||||
| chr14:35137272
|
A | AT | 5 | a0001c0001t0007g0170a0001c0001t0007g0171a0001c0001t0007g0172others(2): Show | 5 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+9662dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35137272 | |||||
| chr14:35137604
|
G | T | 14 | a0001c0002t0003g0189a0001c0002t0003g0306a0001c0002t0003g0307others(11): Show | 14 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1167+9993G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35137604 | ||||||
| chr14:35137616
|
G | A | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1167+10005G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35137616 | ||||||
| chr14:35137958
|
T | C | 5 | a0001c0002t0003g0306a0001c0002t0003g0307a0001c0002t0003g0308others(2): Show | 5 | HG02723.hp1 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1167+10347T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35137958 | ||||||
| chr14:35138194
|
C | A | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+10583C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35138194 | ||||||
| chr14:35138355
|
G | A | 6 | a0001c0001t0003g0076a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1167+10744G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35138355 | ||||||
| chr14:35138507
|
A | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(69): Show | 72 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.1167+10896A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35138507 | ||||||
| chr14:35138716
|
G | A | 59 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0002g0277others(56): Show | 59 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1167+11105G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35138716 | ||||||
| chr14:35138794
|
T | C | 3 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022 | 3 | HG00738.hp1 HG01496.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1167+11183T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35138794 | ||||||
| chr14:35138797
|
A | AT | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0059others(40): Show | 43 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1167+11198dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35138797 | |||||
| chr14:35138891
|
C | A | 29 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0003g0020others(26): Show | 29 | HG00738.hp1 HG01496.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1167+11280C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35138891 | ||||||
| chr14:35138947
|
T | C | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1167+11336T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35138947 | ||||||
| chr14:35139112
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1167+11501A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35139112 | ||||||
| chr14:35139141
|
G | C | 29 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0003g0020others(26): Show | 29 | HG00738.hp1 HG01496.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1167+11530G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35139141 | ||||||
| chr14:35139176
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1167+11565T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35139176 | ||||||
| chr14:35139248
|
T | C | 5 | a0001c0002t0005g0182a0001c0002t0005g0183a0001c0002t0005g0184others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+11637T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35139248 | ||||||
| chr14:35139410
|
CAA | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(31): Show | 34 | HG00735.hp2 HG01099.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.1167+11802_1167+11 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35139410 | |||||
| chr14:35139791
|
C | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0003g0136 | 3 | HG01496.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1167+12180C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35139791 | ||||||
| chr14:35140231
|
ATG | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.1167+12634_1167+12 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35140231 | |||||
| chr14:35140379
|
C | G | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(30): Show | 33 | HG00735.hp2 HG01099.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1167+12768C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35140379 | ||||||
| chr14:35140404
|
T | C | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1167+12793T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35140404 | ||||||
| chr14:35140563
|
A | G | 29 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0003g0020others(26): Show | 29 | HG00738.hp1 HG01496.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1167+12952A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35140563 | ||||||
| chr14:35140774
|
G | C | 30 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0283others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1167+13163G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35140774 | ||||||
| chr14:35140831
|
T | C | 5 | a0001c0001t0007g0170a0001c0001t0007g0171a0001c0001t0007g0172others(2): Show | 5 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+13220T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35140831 | ||||||
| chr14:35141231
|
C | G | 30 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0283others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1167+13620C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35141231 | ||||||
| chr14:35141273
|
G | GT | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+13668dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35141273 | |||||
| chr14:35141293
|
A | C | 1 | a0003c0005t0019g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1167+13682A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35141293 | ||||||
| chr14:35141624
|
GATA | G | 29 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0003g0020others(26): Show | 29 | HG00738.hp1 HG01496.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1167+14019_1167+14 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35141624 | |||||
| chr14:35141654
|
A | T | 1 | a0001c0001t0002g0113 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1167+14043A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35141654 | ||||||
| chr14:35141725
|
C | A | 1 | a0001c0001t0002g0303 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1167+14114C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35141725 | ||||||
| chr14:35141738
|
A | T | 1 | a0001c0001t0002g0303 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1167+14127A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35141738 | ||||||
| chr14:35141842
|
G | T | 1 | a0002c0003t0004g0287 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1167+14231G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35141842 | ||||||
| chr14:35142034
|
A | T | 29 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0003g0020others(26): Show | 29 | HG00738.hp1 HG01496.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1167+14423A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35142034 | ||||||
| chr14:35142156
|
G | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(39): Show | 42 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1167+14545G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35142156 | ||||||
| chr14:35142271
|
T | A | 1 | a0001c0001t0001g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1167+14660T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35142271 | ||||||
| chr14:35142343
|
C | CT | 6 | a0001c0001t0002g0291a0001c0001t0002g0300a0001c0002t0002g0232others(3): Show | 6 | HG00140.hp2 HG01891.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+14750dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35142343 | |||||
| chr14:35142343
|
CT | C | 8 | a0001c0001t0001g0028a0001c0001t0001g0071a0001c0001t0002g0087others(5): Show | 8 | HG00738.hp1 HG01169.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167+14750delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35142343 | |||||
| chr14:35142347
|
T | G | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167+14736T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35142347 | ||||||
| chr14:35142360
|
T | C | 1 | a0001c0001t0032g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1167+14749T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35142360 | ||||||
| chr14:35142367
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1167+14756A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35142367 | ||||||
| chr14:35142525
|
TA | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1167+14927delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35142525 | |||||
| chr14:35142538
|
A | T | 14 | a0001c0002t0003g0189a0001c0002t0003g0306a0001c0002t0003g0307others(11): Show | 14 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1167+14927A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35142538 | ||||||
| chr14:35142607
|
C | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1167+14996C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35142607 | ||||||
| chr14:35142653
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1167+15042A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35142653 | ||||||
| chr14:35142846
|
C | CA | 8 | a0001c0001t0007g0170a0001c0001t0007g0171a0001c0001t0007g0172others(5): Show | 8 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1167+15248dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35142846 | |||||
| chr14:35142929
|
C | A | 1 | a0001c0001t0001g0029 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1167+15318C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35142929 | ||||||
| chr14:35143287
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1167+15676G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143287 | ||||||
| chr14:35143300
|
T | G | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(40): Show | 43 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1167+15689T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143300 | ||||||
| chr14:35143323
|
G | T | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+15712G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143323 | ||||||
| chr14:35143350
|
C | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1167+15739C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143350 | ||||||
| chr14:35143457
|
C | T | 1 | a0001c0001t0038g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1167+15846C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143457 | ||||||
| chr14:35143475
|
T | C | 3 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0310 | 3 | HG00735.hp2 HG01255.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1167+15864T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143475 | ||||||
| chr14:35143478
|
A | G | 1 | a0001c0002t0001g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1167+15867A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143478 | ||||||
| chr14:35143485
|
A | G | 14 | a0001c0002t0003g0189a0001c0002t0003g0306a0001c0002t0003g0307others(11): Show | 14 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1167+15874A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143485 | ||||||
| chr14:35143524
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0003g0136 | 3 | HG01496.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1167+15913A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143524 | ||||||
| chr14:35143623
|
C | T | 1 | a0001c0001t0021g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1167+16012C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143623 | ||||||
| chr14:35143631
|
T | TTTTG | 4 | a0001c0001t0001g0071a0001c0001t0003g0069a0001c0001t0003g0070others(1): Show | 4 | HG02258.hp1 HG02559.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+16048_1167+16 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35143631 | |||||
| chr14:35143631
|
TTTTG | T | 4 | a0001c0001t0002g0112a0001c0001t0021g0175a0001c0002t0003g0214others(1): Show | 4 | HG01433.hp2 HG01884.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167+16048_1167+16 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35143631 | |||||
| chr14:35143733
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1167+16122C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143733 | ||||||
| chr14:35143789
|
C | G | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1167+16178C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143789 | ||||||
| chr14:35143795
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG02027.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1167+16184T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143795 | ||||||
| chr14:35143801
|
A | G | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1167+16190A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143801 | ||||||
| chr14:35143940
|
G | A | 64 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 64 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1167+16329G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143940 | ||||||
| chr14:35143985
|
A | C | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167+16374A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35143985 | ||||||
| chr14:35144008
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1167+16397A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144008 | ||||||
| chr14:35144011
|
C | T | 8 | a0001c0001t0001g0124a0001c0002t0001g0209a0001c0002t0003g0004others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167+16400C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144011 | ||||||
| chr14:35144024
|
G | T | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1167+16413G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144024 | ||||||
| chr14:35144045
|
A | G | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1167+16434A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144045 | ||||||
| chr14:35144257
|
G | A | 2 | a0001c0001t0002g0088a0001c0001t0032g0123 | 2 | HG01175.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1167+16646G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144257 | ||||||
| chr14:35144294
|
A | G | 1 | a0001c0001t0003g0136 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1167+16683A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144294 | ||||||
| chr14:35144331
|
G | T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167+16720G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144331 | ||||||
| chr14:35144527
|
A | G | 1 | a0001c0001t0003g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1167+16916A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144527 | ||||||
| chr14:35144538
|
G | C | 1 | a0001c0001t0006g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1167+16927G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144538 | ||||||
| chr14:35144652
|
G | A | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1167+17041G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144652 | ||||||
| chr14:35144672
|
A | G | 4 | a0001c0001t0002g0001a0001c0001t0002g0114a0001c0001t0002g0115others(1): Show | 5 | HG02015.hp1 NA18977.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1167+17061A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144672 | ||||||
| chr14:35144720
|
C | T | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+17109C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144720 | ||||||
| chr14:35144855
|
A | G | 1 | a0001c0001t0017g0164 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1167+17244A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144855 | ||||||
| chr14:35144856
|
A | T | 1 | a0001c0001t0017g0164 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1167+17245A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144856 | ||||||
| chr14:35144918
|
A | C | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1167+17307A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35144918 | ||||||
| chr14:35145032
|
G | A | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1167+17421G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35145032 | ||||||
| chr14:35145119
|
C | T | 14 | a0001c0002t0003g0189a0001c0002t0003g0306a0001c0002t0003g0307others(11): Show | 14 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1167+17508C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35145119 | ||||||
| chr14:35145128
|
G | C | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1167+17517G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35145128 | ||||||
| chr14:35145162
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1167+17551G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35145162 | ||||||
| chr14:35145555
|
A | G | 2 | a0002c0003t0004g0285a0002c0003t0004g0286 | 2 | HG01175.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1167+17944A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35145555 | ||||||
| chr14:35145609
|
A | G | 4 | a0001c0001t0002g0001a0001c0001t0002g0114a0001c0001t0002g0115others(1): Show | 5 | HG02015.hp1 NA18977.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1167+17998A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35145609 | ||||||
| chr14:35145732
|
A | AGAAG | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(21): Show | 24 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1167+18145_1167+18 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35145732 | |||||
| chr14:35145732
|
AGAAGGAA others(1): Show |
A | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1167+18141_1167+18 others(14): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35145732 | |||||
| chr14:35145743
|
AG | A | 50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 50 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1167+18134delG | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35145743 | |||||
| chr14:35145804
|
A | ATTAT | 38 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0065others(35): Show | 38 | HG00408.hp2 HG00639.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1167+18220_1167+18 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35145804 | |||||
| chr14:35145804
|
A | ATTATTTA others(1): Show |
87 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1167+18216_1167+18 others(14): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35145804 | |||||
| chr14:35145804
|
A | ATTATTTA others(5): Show |
46 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(43): Show | 46 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1167+18212_1167+18 others(18): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35145804 | |||||
| chr14:35145804
|
A | ATTATTTA others(9): Show |
8 | a0001c0001t0003g0142a0001c0001t0005g0156a0001c0001t0012g0168others(5): Show | 8 | HG01358.hp1 HG02055.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167+18208_1167+18 others(22): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35145804 | |||||
| chr14:35145835
|
T | A | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(238): Show | 242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1167+18224T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35145835 | ||||||
| chr14:35145843
|
T | A | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+18232T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35145843 | ||||||
| chr14:35145921
|
C | T | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1167+18310C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35145921 | ||||||
| chr14:35146083
|
G | A | 6 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(3): Show | 6 | HG00738.hp1 HG01496.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1167+18472G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35146083 | ||||||
| chr14:35146094
|
G | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | NA18971.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1167+18483G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35146094 | ||||||
| chr14:35146241
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0003g0136 | 3 | HG01496.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1167+18630A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35146241 | ||||||
| chr14:35146254
|
G | A | 30 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0283others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1167+18643G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35146254 | ||||||
| chr14:35146422
|
T | C | 1 | a0001c0001t0003g0136 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1167+18811T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35146422 | ||||||
| chr14:35146442
|
A | AT | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(30): Show | 33 | HG00735.hp2 HG01099.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1167+18840dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35146442 | |||||
| chr14:35146587
|
A | G | 79 | a0001c0001t0001g0124a0001c0002t0001g0005a0001c0002t0001g0181others(76): Show | 79 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1167+18976A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35146587 | ||||||
| chr14:35146662
|
C | A | 3 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0008g0016 | 3 | HG01081.hp1 HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1167+19051C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35146662 | ||||||
| chr14:35146740
|
C | T | 1 | a0001c0002t0003g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1167+19129C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35146740 | ||||||
| chr14:35146748
|
T | C | 49 | a0001c0002t0001g0005a0001c0002t0001g0181a0001c0002t0001g0218others(46): Show | 49 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1167+19137T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35146748 | ||||||
| chr14:35146861
|
G | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(40): Show | 43 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1167+19250G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35146861 | ||||||
| chr14:35146890
|
G | A | 1 | a0001c0001t0025g0032 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1167+19279G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35146890 | ||||||
| chr14:35146928
|
C | A | 1 | a0001c0002t0001g0191 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1167+19317C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35146928 | ||||||
| chr14:35147016
|
C | G | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1167+19405C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35147016 | ||||||
| chr14:35147159
|
A | G | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1167+19548A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35147159 | ||||||
| chr14:35147270
|
A | C | 1 | a0001c0001t0002g0111 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1167+19659A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35147270 | ||||||
| chr14:35147388
|
G | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(40): Show | 43 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1167+19777G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35147388 | ||||||
| chr14:35147500
|
G | A | 1 | a0001c0002t0001g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1167+19889G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35147500 | ||||||
| chr14:35147509
|
A | T | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+19898A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35147509 | ||||||
| chr14:35147694
|
T | G | 3 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024 | 3 | HG02723.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1167+20083T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35147694 | ||||||
| chr14:35147720
|
G | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1167+20109G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35147720 | ||||||
| chr14:35148158
|
C | T | 1 | a0001c0001t0002g0112 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1167+20547C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35148158 | ||||||
| chr14:35148175
|
A | G | 3 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015 | 3 | HG02280.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1167+20564A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35148175 | ||||||
| chr14:35148580
|
G | A | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1167+20969G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35148580 | ||||||
| chr14:35148688
|
TTCTAGAT others(4): Show |
T | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1167+21081_1167+21 others(17): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35148688 | |||||
| chr14:35148782
|
C | G | 7 | a0001c0001t0007g0170a0001c0001t0007g0171a0001c0001t0007g0172others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+21171C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35148782 | ||||||
| chr14:35148911
|
A | AT | 27 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(24): Show | 28 | HG00099.hp2 HG00597.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1167+21325dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35148911 | |||||
| chr14:35148911
|
A | ATT | 78 | a0001c0001t0018g0174a0001c0001t0021g0175a0001c0002t0001g0005others(75): Show | 78 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1167+21324_1167+21 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35148911 | |||||
| chr14:35148911
|
A | ATTT | 10 | a0001c0001t0001g0124a0001c0002t0001g0207a0001c0002t0001g0208others(7): Show | 10 | HG01952.hp1 HG02004.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1167+21323_1167+21 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35148911 | |||||
| chr14:35148911
|
AT | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0140others(41): Show | 44 | HG00735.hp2 HG01070.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.1167+21325delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35148911 | |||||
| chr14:35148911
|
ATTTTTTT others(3): Show |
A | 5 | a0001c0002t0003g0216a0001c0002t0005g0182a0001c0002t0005g0183others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+21316_1167+21 others(16): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35148911 | |||||
| chr14:35148949
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1167+21338C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35148949 | ||||||
| chr14:35148953
|
C | T | 1 | a0001c0001t0038g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1167+21342C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35148953 | ||||||
| chr14:35149005
|
G | A | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1167+21394G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35149005 | ||||||
| chr14:35149057
|
A | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1167+21446A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35149057 | ||||||
| chr14:35149109
|
T | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1167+21498T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35149109 | ||||||
| chr14:35149121
|
G | A | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+21510G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35149121 | ||||||
| chr14:35149154
|
C | T | 3 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0310 | 3 | HG00735.hp2 HG01255.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1167+21543C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35149154 | ||||||
| chr14:35149195
|
A | G | 3 | a0002c0003t0004g0282a0002c0003t0016g0288a0002c0003t0016g0301 | 3 | HG06807.hp2 NA20752.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1167+21584A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35149195 | ||||||
| chr14:35149209
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1167+21598G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35149209 | ||||||
| chr14:35149215
|
G | A | 30 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0283others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1167+21604G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35149215 | ||||||
| chr14:35149238
|
A | G | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1167+21627A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35149238 | ||||||
| chr14:35149254
|
A | G | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+21643A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35149254 | ||||||
| chr14:35149385
|
A | G | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(40): Show | 43 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1167+21774A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35149385 | ||||||
| chr14:35149790
|
G | A | 7 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(4): Show | 7 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+22179G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35149790 | ||||||
| chr14:35150226
|
T | C | 1 | a0001c0002t0017g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1167+22615T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35150226 | ||||||
| chr14:35150341
|
G | T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167+22730G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35150341 | ||||||
| chr14:35150400
|
C | G | 1 | a0001c0001t0002g0074 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1167+22789C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35150400 | ||||||
| chr14:35150408
|
C | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1167+22797C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35150408 | ||||||
| chr14:35150419
|
G | T | 1 | a0001c0001t0005g0012 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1167+22808G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35150419 | ||||||
| chr14:35150610
|
A | G | 93 | a0001c0001t0001g0124a0001c0002t0001g0005a0001c0002t0001g0181others(90): Show | 93 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1167+22999A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35150610 | ||||||
| chr14:35150910
|
A | G | 1 | a0001c0001t0038g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1167+23299A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35150910 | ||||||
| chr14:35150952
|
C | G | 1 | a0001c0002t0001g0005 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1167+23341C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35150952 | ||||||
| chr14:35151019
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1167+23408A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151019 | ||||||
| chr14:35151068
|
T | G | 1 | a0001c0002t0001g0236 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1167+23457T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151068 | ||||||
| chr14:35151153
|
G | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1167+23542G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151153 | ||||||
| chr14:35151194
|
A | T | 3 | a0001c0002t0001g0005a0001c0002t0001g0259a0001c0002t0033g0230 | 3 | HG00438.hp2 HG03927.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1167+23583A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151194 | ||||||
| chr14:35151343
|
A | G | 1 | a0001c0002t0001g0258 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1167+23732A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151343 | ||||||
| chr14:35151364
|
A | G | 1 | a0001c0001t0003g0132 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1167+23753A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151364 | ||||||
| chr14:35151393
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1167+23782G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151393 | ||||||
| chr14:35151438
|
C | T | 4 | a0001c0001t0003g0177a0001c0001t0003g0178a0001c0001t0003g0179others(1): Show | 4 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+23827C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151438 | ||||||
| chr14:35151529
|
T | A | 1 | a0001c0002t0001g0237 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1167+23918T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151529 | ||||||
| chr14:35151573
|
C | T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167+23962C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151573 | ||||||
| chr14:35151639
|
T | C | 1 | a0001c0002t0003g0212 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1167+24028T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151639 | ||||||
| chr14:35151639
|
T | TAC | 41 | a0001c0001t0001g0058a0001c0001t0002g0062a0001c0001t0002g0080others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1167+24066_1167+24 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35151639 | |||||
| chr14:35151639
|
T | TACAC | 11 | a0001c0001t0001g0055a0001c0001t0002g0013a0001c0001t0002g0014others(8): Show | 11 | HG01433.hp2 HG01884.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1167+24064_1167+24 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35151639 | |||||
| chr14:35151639
|
T | TACACAC | 6 | a0001c0001t0001g0054a0001c0002t0005g0182a0001c0002t0005g0183others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+24062_1167+24 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35151639 | |||||
| chr14:35151639
|
T | TACACACA others(3): Show |
2 | a0001c0001t0003g0022a0001c0001t0003g0070 | 2 | HG00738.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1167+24058_1167+24 others(16): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35151639 | |||||
| chr14:35151639
|
T | TACACACA others(5): Show |
2 | a0001c0001t0001g0071a0001c0001t0003g0021 | 2 | HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1167+24056_1167+24 others(18): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35151639 | |||||
| chr14:35151639
|
T | TACACACA others(7): Show |
2 | a0001c0001t0003g0020a0001c0001t0003g0069 | 2 | HG01496.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1167+24054_1167+24 others(20): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35151639 | |||||
| chr14:35151639
|
TAC | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0053others(50): Show | 53 | HG00408.hp2 HG00438.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1167+24066_1167+24 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35151639 | |||||
| chr14:35151639
|
TACAC | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0091a0001c0001t0001g0106others(46): Show | 49 | HG01070.hp2 HG01167.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.1167+24064_1167+24 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35151639 | |||||
| chr14:35151639
|
TACACAC | T | 28 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0283others(25): Show | 28 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1167+24062_1167+24 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35151639 | |||||
| chr14:35151639
|
TACACACA others(1): Show |
T | 5 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(2): Show | 5 | HG02630.hp2 HG03139.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1167+24060_1167+24 others(14): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35151639 | |||||
| chr14:35151639
|
TACACACA others(5): Show |
T | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1167+24056_1167+24 others(18): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35151639 | |||||
| chr14:35151676
|
A | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(11): Show | 14 | HG01099.hp1 HG01167.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.1167+24065A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151676 | ||||||
| chr14:35151747
|
C | T | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1167+24136C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151747 | ||||||
| chr14:35151907
|
T | C | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1167+24296T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151907 | ||||||
| chr14:35151934
|
CT | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(158): Show | 161 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1167+24340delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35151934 | |||||
| chr14:35151985
|
G | C | 2 | a0001c0001t0002g0118a0001c0001t0002g0120 | 2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1167+24374G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35151985 | ||||||
| chr14:35152078
|
G | A | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1167+24467G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152078 | ||||||
| chr14:35152085
|
C | T | 7 | a0001c0001t0007g0170a0001c0001t0007g0171a0001c0001t0007g0172others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+24474C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152085 | ||||||
| chr14:35152109
|
T | G | 1 | a0002c0003t0004g0287 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1167+24498T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152109 | ||||||
| chr14:35152172
|
A | G | 2 | a0002c0003t0004g0285a0002c0003t0004g0286 | 2 | HG01175.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1167+24561A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152172 | ||||||
| chr14:35152175
|
A | G | 4 | a0001c0002t0003g0004a0001c0002t0003g0212a0001c0002t0003g0213others(1): Show | 4 | HG01884.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+24564A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152175 | ||||||
| chr14:35152187
|
G | A | 79 | a0001c0001t0001g0124a0001c0002t0001g0005a0001c0002t0001g0181others(76): Show | 79 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1167+24576G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152187 | ||||||
| chr14:35152218
|
A | G | 1 | a0001c0002t0005g0186 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1167+24607A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152218 | ||||||
| chr14:35152221
|
A | T | 1 | a0001c0002t0002g0232 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1167+24610A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152221 | ||||||
| chr14:35152241
|
G | A | 1 | a0001c0001t0003g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1167+24630G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152241 | ||||||
| chr14:35152242
|
G | A | 1 | a0001c0002t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1167+24631G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152242 | ||||||
| chr14:35152302
|
A | G | 2 | a0001c0001t0009g0157a0001c0001t0009g0158 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1167+24691A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152302 | ||||||
| chr14:35152320
|
A | T | 14 | a0001c0002t0003g0189a0001c0002t0003g0306a0001c0002t0003g0307others(11): Show | 14 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1167+24709A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152320 | ||||||
| chr14:35152326
|
G | A | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1167+24715G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152326 | ||||||
| chr14:35152548
|
C | T | 1 | a0001c0002t0003g0214 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1167+24937C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152548 | ||||||
| chr14:35152559
|
G | GC | 30 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0283others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1167+24954dupC | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35152559 | |||||
| chr14:35152576
|
C | T | 1 | a0001c0002t0002g0231 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1167+24965C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152576 | ||||||
| chr14:35152593
|
C | T | 6 | a0001c0001t0007g0176a0001c0002t0005g0182a0001c0002t0005g0183others(3): Show | 6 | HG00099.hp2 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1167+24982C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152593 | ||||||
| chr14:35152690
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1167+25079C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152690 | ||||||
| chr14:35152721
|
G | A | 7 | a0001c0002t0003g0189a0001c0002t0003g0306a0001c0002t0003g0307others(4): Show | 7 | HG02723.hp1 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+25110G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152721 | ||||||
| chr14:35152751
|
C | CG | 10 | a0001c0001t0001g0033a0001c0001t0002g0063a0001c0001t0002g0277others(7): Show | 10 | HG00642.hp2 HG01243.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1167+25144dupG | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35152751 | |||||
| chr14:35152751
|
C | T | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1167+25140C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152751 | ||||||
| chr14:35152764
|
G | A | 3 | a0001c0001t0002g0001a0001c0001t0002g0115a0001c0001t0002g0116 | 4 | HG02015.hp1 NA18980.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+25153G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152764 | ||||||
| chr14:35152807
|
A | C | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167+25196A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152807 | ||||||
| chr14:35152810
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1167+25199C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152810 | ||||||
| chr14:35152811
|
G | A | 30 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0283others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1167+25200G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152811 | ||||||
| chr14:35152876
|
G | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1167+25265G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152876 | ||||||
| chr14:35152991
|
C | T | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1167+25380C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35152991 | ||||||
| chr14:35153084
|
A | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 52 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1167+25473A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153084 | ||||||
| chr14:35153096
|
G | A | 1 | a0003c0005t0019g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1167+25485G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153096 | ||||||
| chr14:35153099
|
A | G | 4 | a0001c0001t0003g0177a0001c0001t0003g0178a0001c0001t0003g0179others(1): Show | 4 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167+25488A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153099 | ||||||
| chr14:35153127
|
G | A | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1167+25516G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153127 | ||||||
| chr14:35153142
|
C | T | 30 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0283others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1167+25531C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153142 | ||||||
| chr14:35153163
|
G | A | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167+25552G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153163 | ||||||
| chr14:35153208
|
C | T | 1 | a0001c0001t0003g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1167+25597C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153208 | ||||||
| chr14:35153262
|
C | T | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1167+25651C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153262 | ||||||
| chr14:35153274
|
T | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1167+25663T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153274 | ||||||
| chr14:35153340
|
G | A | 1 | a0001c0002t0001g0181 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1167+25729G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153340 | ||||||
| chr14:35153363
|
A | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1167+25752A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153363 | ||||||
| chr14:35153379
|
GGAAAGAG others(7): Show |
G | 1 | a0001c0001t0017g0164 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1167+25770_1167+25 others(20): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35153379 | |||||
| chr14:35153392
|
G | A | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 52 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1167+25781G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153392 | ||||||
| chr14:35153406
|
G | GGAGA | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1167+25799_1167+25 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35153406 | |||||
| chr14:35153655
|
C | G | 1 | a0001c0001t0002g0104 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1167+26044C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153655 | ||||||
| chr14:35153728
|
T | C | 7 | a0001c0001t0007g0170a0001c0001t0007g0171a0001c0001t0007g0172others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167+26117T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153728 | ||||||
| chr14:35153732
|
T | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1167+26121T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153732 | ||||||
| chr14:35153941
|
C | T | 1 | a0001c0002t0001g0257 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1167+26330C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35153941 | ||||||
| chr14:35154046
|
C | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0289 | 2 | HG01167.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1167+26435C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35154046 | ||||||
| chr14:35154280
|
G | T | 49 | a0001c0002t0001g0005a0001c0002t0001g0181a0001c0002t0001g0218others(46): Show | 49 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1168-26390G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35154280 | ||||||
| chr14:35154700
|
CA | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1168-25956delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35154700 | |||||
| chr14:35154712
|
A | G | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1168-25958A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35154712 | ||||||
| chr14:35154839
|
G | A | 1 | a0001c0001t0003g0020 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1168-25831G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35154839 | ||||||
| chr14:35154846
|
T | C | 1 | a0001c0001t0003g0133 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1168-25824T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35154846 | ||||||
| chr14:35154902
|
C | CT | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(33): Show | 36 | HG00735.hp2 HG01099.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1168-25758dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35154902 | |||||
| chr14:35154902
|
C | G | 3 | a0001c0001t0001g0124a0001c0002t0003g0216a0001c0002t0029g0210 | 3 | HG01891.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1168-25768C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35154902 | ||||||
| chr14:35154923
|
C | T | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1168-25747C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35154923 | ||||||
| chr14:35154956
|
A | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG02602.hp2 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1168-25714A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35154956 | ||||||
| chr14:35154958
|
A | G | 30 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0283others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1168-25712A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35154958 | ||||||
| chr14:35154971
|
C | T | 30 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0283others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1168-25699C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35154971 | ||||||
| chr14:35155092
|
C | T | 1 | a0001c0001t0003g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1168-25578C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35155092 | ||||||
| chr14:35155150
|
C | T | 1 | a0001c0002t0001g0221 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1168-25520C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35155150 | ||||||
| chr14:35155508
|
G | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-25162G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35155508 | ||||||
| chr14:35155560
|
TA | T | 171 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(168): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1168-25088delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35155560 | |||||
| chr14:35155560
|
TAA | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(47): Show | 50 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1168-25089_1168-25 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35155560 | |||||
| chr14:35155561
|
A | T | 1 | a0001c0001t0002g0109 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1168-25109A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35155561 | ||||||
| chr14:35155610
|
A | G | 1 | a0001c0002t0001g0005 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1168-25060A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35155610 | ||||||
| chr14:35155625
|
A | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(40): Show | 43 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1168-25045A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35155625 | ||||||
| chr14:35155862
|
C | CAT | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1168-24808_1168-24 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35155862 | ||||||
| chr14:35155951
|
G | C | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1168-24719G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35155951 | ||||||
| chr14:35156011
|
G | T | 99 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0003g0020others(96): Show | 99 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1168-24659G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35156011 | ||||||
| chr14:35156155
|
G | T | 9 | a0001c0002t0003g0189a0001c0002t0003g0306a0001c0002t0003g0307others(6): Show | 9 | HG02486.hp2 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168-24515G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35156155 | ||||||
| chr14:35156402
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1168-24268A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35156402 | ||||||
| chr14:35156429
|
A | T | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1168-24241A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35156429 | ||||||
| chr14:35156465
|
TG | T | 23 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0002g0001others(20): Show | 24 | HG00438.hp1 HG00597.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.1168-24204delG | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35156465 | ||||||
| chr14:35156830
|
G | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(39): Show | 42 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1168-23840G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35156830 | ||||||
| chr14:35156869
|
G | C | 1 | a0001c0002t0001g0203 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1168-23801G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35156869 | ||||||
| chr14:35156924
|
T | C | 1 | a0001c0002t0001g0005 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1168-23746T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35156924 | ||||||
| chr14:35156959
|
C | CT | 298 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(295): Show | 299 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.1168-23697dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35156959 | |||||
| chr14:35157113
|
G | A | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1168-23557G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35157113 | ||||||
| chr14:35157202
|
G | A | 6 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(3): Show | 6 | HG00738.hp1 HG01496.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-23468G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35157202 | ||||||
| chr14:35157250
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1168-23420C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35157250 | ||||||
| chr14:35157252
|
G | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1168-23418G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35157252 | ||||||
| chr14:35157281
|
G | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(30): Show | 33 | HG00735.hp2 HG01099.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1168-23389G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35157281 | ||||||
| chr14:35157313
|
A | T | 2 | a0001c0002t0001g0311a0001c0002t0001g0312 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1168-23357A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35157313 | ||||||
| chr14:35157578
|
G | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1168-23092G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35157578 | ||||||
| chr14:35157676
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1168-22994A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35157676 | ||||||
| chr14:35157682
|
C | A | 1 | a0001c0001t0003g0178 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1168-22988C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35157682 | ||||||
| chr14:35157791
|
T | C | 93 | a0001c0001t0001g0124a0001c0002t0001g0005a0001c0002t0001g0181others(90): Show | 93 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1168-22879T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35157791 | ||||||
| chr14:35157816
|
A | G | 1 | a0001c0002t0001g0256 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1168-22854A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35157816 | ||||||
| chr14:35158005
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0289others(28): Show | 31 | HG00735.hp2 HG01099.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.1168-22665G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35158005 | ||||||
| chr14:35158168
|
A | G | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-22502A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35158168 | ||||||
| chr14:35158607
|
G | A | 1 | a0001c0002t0001g0249 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1168-22063G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35158607 | ||||||
| chr14:35158720
|
A | G | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1168-21950A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35158720 | ||||||
| chr14:35158741
|
T | G | 1 | a0001c0002t0001g0228 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1168-21929T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35158741 | ||||||
| chr14:35158789
|
A | G | 7 | a0001c0001t0007g0170a0001c0001t0007g0171a0001c0001t0007g0172others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1168-21881A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35158789 | ||||||
| chr14:35159066
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1168-21604C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35159066 | ||||||
| chr14:35159071
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1168-21599C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35159071 | ||||||
| chr14:35159205
|
C | T | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1168-21465C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35159205 | ||||||
| chr14:35159239
|
T | A | 2 | a0001c0001t0003g0142a0001c0001t0003g0160 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1168-21431T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35159239 | ||||||
| chr14:35159374
|
A | G | 6 | a0001c0001t0003g0070a0001c0001t0003g0136a0001c0002t0003g0004others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-21296A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35159374 | ||||||
| chr14:35159523
|
T | C | 14 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(11): Show | 14 | HG00099.hp2 HG00741.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.1168-21147T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35159523 | ||||||
| chr14:35159798
|
G | A | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1168-20872G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35159798 | ||||||
| chr14:35159914
|
G | A | 10 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 10 | HG01099.hp1 HG03654.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.1168-20756G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35159914 | ||||||
| chr14:35160097
|
C | T | 1 | a0001c0002t0001g0218 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1168-20573C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35160097 | ||||||
| chr14:35160693
|
G | A | 9 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(6): Show | 9 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168-19977G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35160693 | ||||||
| chr14:35160715
|
AT | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(149): Show | 152 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1168-19948delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35160715 | |||||
| chr14:35160845
|
A | G | 2 | a0001c0001t0011g0155a0001c0001t0011g0310 | 2 | HG00735.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1168-19825A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35160845 | ||||||
| chr14:35160886
|
G | A | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1168-19784G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35160886 | ||||||
| chr14:35160969
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(157): Show | 160 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1168-19701A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35160969 | ||||||
| chr14:35161077
|
CCG | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1168-19592_1168-19 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161077 | ||||||
| chr14:35161078
|
C | T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-19592C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161078 | ||||||
| chr14:35161113
|
C | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1168-19557C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161113 | ||||||
| chr14:35161171
|
C | G | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.1168-19499C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161171 | ||||||
| chr14:35161182
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1168-19488A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161182 | ||||||
| chr14:35161263
|
C | A | 27 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(24): Show | 27 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1168-19407C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161263 | ||||||
| chr14:35161287
|
G | A | 20 | a0001c0001t0005g0156a0001c0001t0012g0168a0001c0002t0003g0004others(17): Show | 20 | HG01884.hp2 HG02257.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1168-19383G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161287 | ||||||
| chr14:35161338
|
G | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1168-19332G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161338 | ||||||
| chr14:35161356
|
C | T | 29 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0290others(26): Show | 29 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.1168-19314C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161356 | ||||||
| chr14:35161514
|
T | A | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1168-19156T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161514 | ||||||
| chr14:35161519
|
C | CT | 26 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(23): Show | 26 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168-19144dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35161519 | |||||
| chr14:35161795
|
C | G | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-18875C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161795 | ||||||
| chr14:35161805
|
G | A | 3 | a0001c0001t0003g0098a0001c0001t0006g0096a0001c0001t0006g0097 | 3 | HG02922.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1168-18865G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161805 | ||||||
| chr14:35161918
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1168-18752C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161918 | ||||||
| chr14:35161978
|
C | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(149): Show | 152 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1168-18692C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35161978 | ||||||
| chr14:35162016
|
G | T | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1168-18654G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35162016 | ||||||
| chr14:35162088
|
A | G | 7 | a0001c0002t0003g0189a0001c0002t0003g0306a0001c0002t0003g0307others(4): Show | 7 | HG02723.hp1 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1168-18582A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35162088 | ||||||
| chr14:35162088
|
A | T | 19 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(16): Show | 19 | HG01081.hp1 HG01099.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1168-18582A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35162088 | ||||||
| chr14:35162131
|
C | T | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-18539C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35162131 | ||||||
| chr14:35162225
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1168-18445A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35162225 | ||||||
| chr14:35162347
|
C | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.1168-18323C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35162347 | ||||||
| chr14:35162536
|
T | C | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-18134T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35162536 | ||||||
| chr14:35162614
|
A | AT | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1168-18048dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35162614 | |||||
| chr14:35162647
|
G | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-18023G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35162647 | ||||||
| chr14:35162743
|
C | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-17927C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35162743 | ||||||
| chr14:35162830
|
C | T | 1 | a0001c0001t0032g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1168-17840C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35162830 | ||||||
| chr14:35162970
|
C | T | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1168-17700C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35162970 | ||||||
| chr14:35163122
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1168-17548T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35163122 | ||||||
| chr14:35163127
|
C | T | 1 | a0001c0002t0001g0255 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1168-17543C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35163127 | ||||||
| chr14:35163233
|
A | G | 1 | a0001c0001t0009g0167 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1168-17437A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35163233 | ||||||
| chr14:35163258
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1168-17412T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35163258 | ||||||
| chr14:35163271
|
G | GA | 5 | a0001c0002t0003g0309a0002c0003t0004g0296a0002c0003t0004g0297others(2): Show | 5 | HG00735.hp1 HG01071.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168-17391dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35163271 | |||||
| chr14:35163281
|
G | T | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1168-17389G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35163281 | ||||||
| chr14:35163346
|
C | T | 44 | a0001c0002t0001g0005a0001c0002t0001g0181a0001c0002t0001g0218others(41): Show | 44 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1168-17324C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35163346 | ||||||
| chr14:35163633
|
A | G | 1 | a0001c0002t0001g0192 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1168-17037A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35163633 | ||||||
| chr14:35163663
|
A | G | 3 | a0001c0002t0001g0248a0001c0002t0001g0254a0001c0002t0001g0268 | 3 | NA18950.hp1 NA18975.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1168-17007A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35163663 | ||||||
| chr14:35163751
|
C | T | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1168-16919C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35163751 | ||||||
| chr14:35163906
|
A | G | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-16764A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35163906 | ||||||
| chr14:35163957
|
G | T | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-16713G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35163957 | ||||||
| chr14:35164140
|
T | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(8): Show | 11 | HG00738.hp1 HG01496.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1168-16530T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35164140 | ||||||
| chr14:35164153
|
G | A | 3 | a0001c0001t0001g0124a0001c0002t0003g0216a0001c0002t0029g0210 | 3 | HG01891.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1168-16517G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35164153 | ||||||
| chr14:35164166
|
A | C | 2 | a0001c0002t0002g0231a0001c0002t0002g0232 | 2 | NA18994.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1168-16504A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35164166 | ||||||
| chr14:35164374
|
C | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(157): Show | 160 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1168-16296C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35164374 | ||||||
| chr14:35164374
|
C | T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-16296C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35164374 | ||||||
| chr14:35164447
|
A | T | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168-16223A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35164447 | ||||||
| chr14:35164589
|
C | T | 10 | a0001c0001t0003g0127a0001c0001t0003g0129a0001c0001t0003g0130others(7): Show | 10 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.1168-16081C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35164589 | ||||||
| chr14:35164839
|
C | G | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-15831C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35164839 | ||||||
| chr14:35164893
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(8): Show | 11 | HG00738.hp1 HG01496.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1168-15777G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35164893 | ||||||
| chr14:35164963
|
C | T | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1168-15707C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35164963 | ||||||
| chr14:35165002
|
G | T | 1 | a0001c0001t0002g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1168-15668G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35165002 | ||||||
| chr14:35165016
|
G | A | 6 | a0001c0001t0003g0076a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-15654G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35165016 | ||||||
| chr14:35165030
|
T | C | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168-15640T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35165030 | ||||||
| chr14:35165082
|
T | C | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1168-15588T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35165082 | ||||||
| chr14:35165130
|
A | G | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1168-15540A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35165130 | ||||||
| chr14:35165432
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1168-15238A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35165432 | ||||||
| chr14:35165645
|
T | TG | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1168-15025_1168-15 others(7): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35165645 | ||||||
| chr14:35165655
|
G | A | 27 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(24): Show | 27 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1168-15015G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35165655 | ||||||
| chr14:35165686
|
GT | G | 10 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(7): Show | 10 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1168-14974delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35165686 | |||||
| chr14:35165764
|
T | C | 27 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(24): Show | 27 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1168-14906T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35165764 | ||||||
| chr14:35165796
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1168-14874C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35165796 | ||||||
| chr14:35166003
|
C | T | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1168-14667C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166003 | ||||||
| chr14:35166023
|
T | A | 1 | a0001c0001t0002g0105 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1168-14647T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166023 | ||||||
| chr14:35166024
|
A | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1168-14646A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166024 | ||||||
| chr14:35166056
|
T | G | 26 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(23): Show | 26 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168-14614T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166056 | ||||||
| chr14:35166074
|
C | G | 26 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(23): Show | 26 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168-14596C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166074 | ||||||
| chr14:35166104
|
C | T | 1 | a0001c0001t0011g0154 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1168-14566C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166104 | ||||||
| chr14:35166114
|
T | C | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1168-14556T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166114 | ||||||
| chr14:35166133
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1168-14537T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166133 | ||||||
| chr14:35166214
|
T | TTCTAGTA others(12): Show |
1 | a0001c0002t0001g0250 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1168-14452_1168-14 others(25): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35166214 | |||||
| chr14:35166275
|
T | C | 4 | a0001c0001t0002g0273a0001c0001t0002g0274a0001c0002t0002g0223others(1): Show | 4 | HG03490.hp1 HG03492.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168-14395T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166275 | ||||||
| chr14:35166277
|
T | G | 1 | a0001c0002t0001g0250 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1168-14393T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166277 | ||||||
| chr14:35166284
|
A | G | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-14386A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166284 | ||||||
| chr14:35166287
|
T | C | 1 | a0001c0001t0003g0313 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1168-14383T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166287 | ||||||
| chr14:35166290
|
A | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-14380A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166290 | ||||||
| chr14:35166354
|
C | T | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-14316C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166354 | ||||||
| chr14:35166448
|
CT | C | 123 | a0001c0001t0001g0048a0001c0001t0001g0065a0001c0001t0001g0077others(120): Show | 124 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1168-14202delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35166448 | |||||
| chr14:35166448
|
CTT | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1168-14203_1168-14 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35166448 | |||||
| chr14:35166448
|
CTTT | C | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-14204_1168-14 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35166448 | |||||
| chr14:35166490
|
G | A | 5 | a0001c0002t0003g0004a0001c0002t0003g0138a0001c0002t0003g0212others(2): Show | 5 | HG01884.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168-14180G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166490 | ||||||
| chr14:35166518
|
A | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1168-14152A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166518 | ||||||
| chr14:35166595
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1168-14075G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166595 | ||||||
| chr14:35166645
|
G | A | 1 | a0001c0002t0002g0238 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1168-14025G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166645 | ||||||
| chr14:35166742
|
T | C | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1168-13928T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166742 | ||||||
| chr14:35166821
|
G | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-13849G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35166821 | ||||||
| chr14:35167069
|
T | C | 2 | a0003c0005t0019g0166a0003c0007t0013g0139 | 2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1168-13601T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167069 | ||||||
| chr14:35167163
|
T | C | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-13507T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167163 | ||||||
| chr14:35167203
|
G | T | 1 | a0001c0002t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1168-13467G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167203 | ||||||
| chr14:35167204
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1168-13466A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167204 | ||||||
| chr14:35167317
|
T | C | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-13353T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167317 | ||||||
| chr14:35167405
|
A | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1168-13265A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167405 | ||||||
| chr14:35167437
|
A | T | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1168-13233A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167437 | ||||||
| chr14:35167476
|
A | T | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1168-13194A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167476 | ||||||
| chr14:35167493
|
T | C | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-13177T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167493 | ||||||
| chr14:35167642
|
T | C | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-13028T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167642 | ||||||
| chr14:35167686
|
T | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1168-12984T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167686 | ||||||
| chr14:35167694
|
T | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-12976T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167694 | ||||||
| chr14:35167708
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1168-12962A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167708 | ||||||
| chr14:35167838
|
G | A | 1 | a0001c0002t0003g0309 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1168-12832G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167838 | ||||||
| chr14:35167839
|
A | G | 1 | a0001c0002t0003g0309 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1168-12831A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35167839 | ||||||
| chr14:35168019
|
T | A | 2 | a0001c0002t0001g0311a0001c0002t0001g0312 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1168-12651T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35168019 | ||||||
| chr14:35168222
|
A | G | 1 | a0001c0001t0011g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1168-12448A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35168222 | ||||||
| chr14:35168305
|
G | A | 26 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(23): Show | 26 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168-12365G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35168305 | ||||||
| chr14:35168326
|
A | G | 1 | a0001c0002t0001g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1168-12344A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35168326 | ||||||
| chr14:35168511
|
C | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-12159C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35168511 | ||||||
| chr14:35168694
|
T | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(8): Show | 11 | HG00738.hp1 HG01496.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1168-11976T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35168694 | ||||||
| chr14:35168696
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1168-11974G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35168696 | ||||||
| chr14:35168698
|
A | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(156): Show | 159 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1168-11972A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35168698 | ||||||
| chr14:35168750
|
G | A | 19 | a0001c0001t0002g0015a0001c0001t0003g0142a0001c0001t0003g0160others(16): Show | 19 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1168-11920G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35168750 | ||||||
| chr14:35168760
|
C | A | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-11910C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35168760 | ||||||
| chr14:35168764
|
C | T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-11906C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35168764 | ||||||
| chr14:35168940
|
A | AT | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-11721dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35168940 | |||||
| chr14:35169080
|
CCTTT | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1168-11581_1168-11 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35169080 | |||||
| chr14:35169085
|
CTTTCT | C | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-11581_1168-11 others(11): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35169085 | |||||
| chr14:35169099
|
T | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-11571T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169099 | ||||||
| chr14:35169324
|
A | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-11346A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169324 | ||||||
| chr14:35169458
|
G | GAGGTTTA others(9): Show |
44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-11206_1168-11 others(22): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35169458 | |||||
| chr14:35169491
|
G | A | 1 | a0001c0001t0003g0136 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1168-11179G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169491 | ||||||
| chr14:35169547
|
C | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1168-11123C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169547 | ||||||
| chr14:35169548
|
G | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-11122G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169548 | ||||||
| chr14:35169629
|
T | C | 3 | a0001c0001t0001g0124a0001c0002t0003g0216a0001c0002t0029g0210 | 3 | HG01891.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1168-11041T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169629 | ||||||
| chr14:35169653
|
A | G | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1168-11017A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169653 | ||||||
| chr14:35169689
|
TCCCTTC | T | 26 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(23): Show | 26 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168-10980_1168-10 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169689 | ||||||
| chr14:35169696
|
A | G | 26 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(23): Show | 26 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168-10974A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169696 | ||||||
| chr14:35169731
|
G | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(52): Show | 55 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1168-10939G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169731 | ||||||
| chr14:35169733
|
G | C | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1168-10937G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169733 | ||||||
| chr14:35169752
|
A | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-10918A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169752 | ||||||
| chr14:35169758
|
A | G | 2 | a0001c0001t0002g0062a0001c0001t0002g0063 | 2 | HG02602.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1168-10912A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169758 | ||||||
| chr14:35169914
|
G | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-10756G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169914 | ||||||
| chr14:35169988
|
C | T | 6 | a0001c0001t0005g0156a0001c0001t0012g0168a0001c0002t0005g0182others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-10682C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35169988 | ||||||
| chr14:35170059
|
C | T | 44 | a0001c0001t0001g0011a0001c0001t0002g0092a0001c0001t0003g0076others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-10611C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170059 | ||||||
| chr14:35170186
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1168-10484G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170186 | ||||||
| chr14:35170318
|
T | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(8): Show | 11 | HG00738.hp1 HG01496.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1168-10352T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170318 | ||||||
| chr14:35170322
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1168-10348G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170322 | ||||||
| chr14:35170350
|
A | T | 47 | a0001c0001t0002g0087a0001c0001t0002g0092a0001c0001t0002g0108others(44): Show | 47 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1168-10320A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170350 | ||||||
| chr14:35170394
|
T | A | 1 | a0001c0001t0003g0148 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1168-10276T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170394 | ||||||
| chr14:35170399
|
TTTTAAAA others(10): Show |
T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-10270_1168-10 others(23): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170399 | ||||||
| chr14:35170400
|
T | G | 2 | a0001c0001t0003g0082a0001c0001t0003g0086 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1168-10270T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170400 | ||||||
| chr14:35170416
|
A | T | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-10254A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170416 | ||||||
| chr14:35170469
|
A | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-10201A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170469 | ||||||
| chr14:35170489
|
T | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-10181T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170489 | ||||||
| chr14:35170495
|
T | C | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-10175T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170495 | ||||||
| chr14:35170660
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1168-10010T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170660 | ||||||
| chr14:35170871
|
C | T | 9 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(6): Show | 9 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168-9799C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170871 | ||||||
| chr14:35170881
|
C | T | 26 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(23): Show | 26 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168-9789C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170881 | ||||||
| chr14:35170911
|
G | A | 1 | a0001c0001t0021g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1168-9759G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170911 | ||||||
| chr14:35170944
|
G | A | 2 | a0001c0002t0001g0270a0002c0003t0004g0296 | 2 | HG01934.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.1168-9726G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35170944 | ||||||
| chr14:35171095
|
C | T | 1 | a0001c0002t0001g0270 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1168-9575C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35171095 | ||||||
| chr14:35171112
|
G | T | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-9558G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35171112 | ||||||
| chr14:35171161
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1168-9509T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35171161 | ||||||
| chr14:35171261
|
A | G | 1 | a0001c0001t0032g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1168-9409A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35171261 | ||||||
| chr14:35171508
|
A | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-9162A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35171508 | ||||||
| chr14:35171696
|
T | C | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-8974T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35171696 | ||||||
| chr14:35171711
|
T | A | 17 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(14): Show | 17 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1168-8959T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35171711 | ||||||
| chr14:35171895
|
C | G | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-8775C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35171895 | ||||||
| chr14:35172025
|
C | T | 1 | a0001c0002t0001g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1168-8645C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172025 | ||||||
| chr14:35172052
|
A | AT | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0003g0142others(26): Show | 29 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1168-8604dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172052 | |||||
| chr14:35172052
|
A | ATT | 42 | a0001c0001t0001g0057a0001c0001t0002g0092a0001c0001t0003g0076others(39): Show | 42 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.1168-8605_1168-860 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172052 | |||||
| chr14:35172052
|
A | ATTT | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1168-8606_1168-860 others(7): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172052 | |||||
| chr14:35172092
|
A | C | 16 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(13): Show | 16 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1168-8578A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172092 | ||||||
| chr14:35172268
|
C | T | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-8402C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172268 | ||||||
| chr14:35172333
|
T | A | 1 | a0001c0001t0002g0088 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1168-8337T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172333 | ||||||
| chr14:35172366
|
C | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1168-8304C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172366 | ||||||
| chr14:35172409
|
T | TTTCCTTC others(1): Show |
4 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0003g0017others(1): Show | 4 | HG02615.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168-8258_1168-825 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172409 | |||||
| chr14:35172409
|
T | TTTCCTTC others(5): Show |
1 | a0001c0001t0002g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1168-8258_1168-825 others(16): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172409 | |||||
| chr14:35172413
|
T | C | 14 | a0001c0001t0001g0011a0001c0001t0002g0013a0001c0001t0002g0014others(11): Show | 14 | HG01081.hp1 HG02257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1168-8257T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172413 | ||||||
| chr14:35172413
|
T | TTTCC | 28 | a0001c0001t0001g0091a0001c0001t0001g0106a0001c0001t0002g0074others(25): Show | 28 | HG00408.hp2 HG01192.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1168-8217_1168-821 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172413 | |||||
| chr14:35172413
|
T | TTTCCTTC others(1): Show |
6 | a0001c0001t0001g0071a0001c0001t0002g0113a0001c0001t0003g0020others(3): Show | 6 | HG01099.hp1 HG01496.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-8221_1168-821 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172413 | |||||
| chr14:35172413
|
T | TTTCCTTC others(5): Show |
10 | a0001c0001t0002g0105a0001c0001t0002g0109a0001c0001t0002g0111others(7): Show | 10 | HG00738.hp1 HG02129.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1168-8225_1168-821 others(16): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172413 | |||||
| chr14:35172413
|
T | TTTCCTTC others(9): Show |
2 | a0001c0001t0002g0088a0001c0001t0003g0069 | 2 | HG01175.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1168-8229_1168-821 others(20): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172413 | |||||
| chr14:35172413
|
TTTCC | T | 24 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0078others(21): Show | 25 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1168-8217_1168-821 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172413 | |||||
| chr14:35172413
|
TTTCCTTC others(1): Show |
T | 21 | a0001c0001t0002g0281a0001c0001t0002g0300a0001c0001t0027g0278others(18): Show | 21 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1168-8221_1168-821 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172413 | |||||
| chr14:35172413
|
TTTCCTTC others(9): Show |
T | 6 | a0001c0001t0002g0290a0001c0001t0002g0291a0002c0003t0004g0296others(3): Show | 6 | HG00735.hp1 HG01071.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1168-8229_1168-821 others(20): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172413 | |||||
| chr14:35172414
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1168-8256T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172414 | ||||||
| chr14:35172453
|
C | CTTCCTTC others(77): Show |
1 | a0001c0002t0015g0305 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(88): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(78): Show |
1 | a0001c0001t0001g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(89): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(94): Show |
1 | a0001c0001t0005g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(105): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(53): Show |
1 | a0001c0002t0005g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(64): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(69): Show |
1 | a0001c0001t0005g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(80): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(70): Show |
1 | a0001c0002t0001g0255 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(81): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(73): Show |
1 | a0001c0002t0003g0306 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(84): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(74): Show |
1 | a0001c0002t0001g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(85): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(82): Show |
1 | a0001c0002t0001g0215 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(93): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(81): Show |
1 | a0001c0002t0001g0201 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(92): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(61): Show |
1 | a0001c0002t0005g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(72): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(69): Show |
1 | a0001c0001t0012g0168 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(80): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(70): Show |
1 | a0001c0002t0001g0219 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(81): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(73): Show |
1 | a0001c0002t0005g0184 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(84): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(41): Show |
1 | a0001c0002t0014g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(52): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(50): Show |
4 | a0001c0002t0001g0233a0001c0002t0001g0236a0001c0002t0001g0250others(1): Show | 4 | HG02135.hp2 HG02273.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(61): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(53): Show |
1 | a0001c0002t0014g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(64): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(54): Show |
3 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0200 | 3 | HG00733.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(65): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(62): Show |
1 | a0001c0001t0001g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(73): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(65): Show |
3 | a0001c0001t0001g0010a0001c0002t0003g0307a0001c0002t0005g0185 | 3 | HG01496.hp1 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(76): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(66): Show |
2 | a0001c0002t0001g0207a0001c0002t0001g0311 | 2 | HG01517.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(77): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(69): Show |
2 | a0001c0002t0003g0212a0001c0002t0017g0217 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(80): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(70): Show |
5 | a0001c0001t0001g0036a0001c0002t0001g0209a0001c0002t0001g0312others(2): Show | 5 | HG01516.hp2 HG02965.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(81): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(73): Show |
1 | a0001c0002t0003g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(84): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(74): Show |
1 | a0001c0001t0001g0030 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(85): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(81): Show |
1 | a0001c0002t0003g0309 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(92): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(82): Show |
1 | a0001c0001t0005g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(93): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(94): Show |
1 | a0001c0001t0005g0012 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(105): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(64): Show |
1 | a0001c0002t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(75): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(21): Show |
8 | a0001c0001t0003g0129a0001c0001t0003g0132a0001c0001t0007g0050others(5): Show | 8 | HG00741.hp1 HG01884.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(32): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(46): Show |
5 | a0001c0002t0001g0005a0001c0002t0001g0220a0001c0002t0001g0239others(2): Show | 5 | HG00438.hp2 HG01952.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(57): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(50): Show |
1 | a0001c0002t0001g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(61): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(53): Show |
1 | a0001c0002t0005g0186 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(64): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(54): Show |
1 | a0001c0002t0001g0192 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(65): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(58): Show |
1 | a0001c0002t0001g0191 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(69): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(62): Show |
1 | a0001c0001t0001g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(73): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(66): Show |
3 | a0001c0001t0001g0037a0001c0001t0001g0054a0001c0001t0025g0032 | 3 | HG02056.hp1 NA18971.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(77): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(70): Show |
1 | a0001c0002t0001g0261 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(81): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(78): Show |
1 | a0001c0001t0001g0048 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(89): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(17): Show |
9 | a0001c0001t0003g0127a0001c0001t0003g0130a0001c0001t0003g0133others(6): Show | 9 | HG00099.hp2 HG00639.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(28): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(59): Show |
1 | a0001c0001t0001g0006 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(70): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(41): Show |
1 | a0001c0001t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(52): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(42): Show |
26 | a0001c0001t0001g0124a0001c0001t0010g0047a0001c0002t0001g0218others(23): Show | 26 | HG00609.hp1 HG01099.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(53): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(46): Show |
2 | a0001c0002t0001g0198a0001c0002t0029g0210 | 2 | HG01891.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(57): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(50): Show |
3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0002t0001g0265 | 3 | HG01346.hp1 HG03491.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(61): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(54): Show |
4 | a0001c0001t0001g0055a0001c0001t0001g0140a0001c0002t0001g0199others(1): Show | 4 | HG01070.hp2 HG02486.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(65): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(58): Show |
9 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0068others(6): Show | 9 | HG03704.hp1 NA18943.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(69): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(62): Show |
5 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG02027.hp2 NA18939.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(73): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(66): Show |
3 | a0001c0001t0001g0067a0001c0001t0002g0062a0001c0001t0010g0025 | 3 | HG02602.hp1 HG02602.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(77): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(70): Show |
2 | a0001c0001t0006g0040a0002c0003t0004g0039 | 2 | HG01081.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(81): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(53): Show |
1 | a0001c0001t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(64): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(13): Show |
10 | a0001c0001t0003g0135a0001c0001t0003g0142a0001c0001t0003g0160others(7): Show | 10 | HG00735.hp2 HG01255.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(24): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(38): Show |
8 | a0001c0001t0001g0059a0001c0002t0001g0234a0001c0002t0001g0244others(5): Show | 8 | HG00408.hp1 HG00741.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(49): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(45): Show |
2 | a0001c0002t0003g0004a0001c0002t0003g0214 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(56): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(49): Show |
1 | a0001c0002t0003g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(60): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(50): Show |
1 | a0001c0001t0001g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(61): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(54): Show |
2 | a0001c0001t0001g0026a0001c0002t0026g0205 | 2 | HG02083.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(65): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(58): Show |
5 | a0001c0001t0001g0066a0001c0001t0002g0063a0001c0002t0001g0202others(2): Show | 5 | HG01361.hp1 HG03490.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(69): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(62): Show |
2 | a0001c0001t0001g0045a0001c0001t0001g0072 | 2 | HG01257.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(73): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(66): Show |
3 | a0001c0001t0001g0033a0001c0001t0001g0044a0001c0001t0001g0053 | 3 | HG00642.hp2 HG00738.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(77): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(70): Show |
2 | a0001c0001t0001g0052a0001c0001t0001g0060 | 2 | HG02015.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(81): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(9): Show |
8 | a0001c0001t0003g0131a0001c0001t0003g0134a0001c0001t0012g0163others(5): Show | 8 | HG01346.hp2 HG01952.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(20): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(34): Show |
3 | a0001c0002t0001g0181a0001c0002t0001g0254a0001c0002t0001g0268 | 3 | NA18950.hp1 NA18978.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(45): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(46): Show |
1 | a0001c0001t0001g0065 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(57): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(54): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(65): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(58): Show |
3 | a0001c0001t0001g0029a0001c0001t0001g0046a0001c0001t0001g0051 | 3 | HG00140.hp1 HG01168.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(69): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(62): Show |
2 | a0001c0001t0001g0027a0005c0009t0001g0034 | 2 | HG02109.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(73): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCCTTC others(5): Show |
2 | a0001c0001t0002g0092a0001c0001t0021g0175 | 2 | HG01433.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1168-8214_1168-821 others(16): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCTTTC others(1): Show |
6 | a0001c0001t0003g0076a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-8209_1168-820 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | CTTCTTTC others(26): Show |
1 | a0001c0002t0001g0263 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1168-8202_1168-820 others(37): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172453 | |||||
| chr14:35172453
|
C | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1168-8217C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172453 | ||||||
| chr14:35172456
|
C | CCTTCCTT others(53): Show |
1 | a0001c0001t0001g0038 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1168-8214_1168-821 others(64): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172456 | ||||||
| chr14:35172458
|
T | C | 1 | a0001c0001t0003g0177 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1168-8212T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172458 | ||||||
| chr14:35172490
|
T | TCCTCTCT others(41): Show |
24 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(21): Show | 24 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1168-8171_1168-817 others(52): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172490 | |||||
| chr14:35172490
|
T | TCCTCTCT others(49): Show |
4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0310others(1): Show | 4 | HG00735.hp2 HG01255.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-8171_1168-817 others(60): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172490 | |||||
| chr14:35172490
|
T | TCCTCTCT others(57): Show |
13 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1168-8171_1168-817 others(68): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172490 | |||||
| chr14:35172490
|
T | TCCTCTCT others(65): Show |
2 | a0003c0005t0020g0023a0003c0007t0013g0139 | 2 | HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1168-8171_1168-817 others(76): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172490 | |||||
| chr14:35172490
|
T | TCCTCTCT others(73): Show |
1 | a0003c0005t0019g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1168-8171_1168-817 others(84): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172490 | |||||
| chr14:35172490
|
TCCTCTCT others(1): Show |
T | 80 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0002g0013others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1168-8147_1168-814 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172490 | |||||
| chr14:35172490
|
TCCTCTCT others(9): Show |
T | 2 | a0001c0001t0003g0017a0001c0001t0003g0018 | 2 | HG01081.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1168-8155_1168-814 others(20): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172490 | |||||
| chr14:35172506
|
C | T | 9 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(6): Show | 9 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168-8164C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172506 | ||||||
| chr14:35172545
|
C | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1168-8125C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172545 | ||||||
| chr14:35172548
|
CTCTT | C | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168-8104_1168-810 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172548 | |||||
| chr14:35172660
|
C | T | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-8010C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172660 | ||||||
| chr14:35172872
|
A | AT | 12 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0289others(9): Show | 12 | HG00738.hp1 HG01167.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1168-7786dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172872 | |||||
| chr14:35172872
|
AT | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-7786delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35172872 | |||||
| chr14:35172928
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1168-7742C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35172928 | ||||||
| chr14:35173068
|
A | G | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-7602A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35173068 | ||||||
| chr14:35173077
|
G | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-7593G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35173077 | ||||||
| chr14:35173162
|
C | A | 6 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(3): Show | 6 | HG00733.hp1 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-7508C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35173162 | ||||||
| chr14:35173396
|
C | T | 1 | a0001c0002t0014g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1168-7274C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35173396 | ||||||
| chr14:35173611
|
A | T | 4 | a0001c0002t0001g0204a0001c0002t0001g0206a0001c0002t0001g0208others(1): Show | 4 | HG01361.hp1 NA19001.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-7059A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35173611 | ||||||
| chr14:35173822
|
A | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-6848A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35173822 | ||||||
| chr14:35173900
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1168-6770C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35173900 | ||||||
| chr14:35174136
|
A | G | 5 | a0001c0001t0003g0150a0001c0001t0003g0151a0001c0001t0003g0152others(2): Show | 5 | NA18943.hp2 NA18977.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168-6534A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174136 | ||||||
| chr14:35174141
|
CA | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1168-6526delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35174141 | |||||
| chr14:35174148
|
TA | T | 43 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(40): Show | 43 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1168-6521delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174148 | ||||||
| chr14:35174213
|
A | G | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1168-6457A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174213 | ||||||
| chr14:35174220
|
C | CT | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1168-6448dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35174220 | |||||
| chr14:35174382
|
C | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(146): Show | 149 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.1168-6288C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174382 | ||||||
| chr14:35174621
|
C | T | 1 | a0007c0011t0037g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1168-6049C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174621 | ||||||
| chr14:35174622
|
C | G | 7 | a0001c0001t0005g0156a0001c0001t0012g0168a0001c0002t0005g0182others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168-6048C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174622 | ||||||
| chr14:35174677
|
C | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1168-5993C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174677 | ||||||
| chr14:35174702
|
A | G | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-5968A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174702 | ||||||
| chr14:35174733
|
ATTCT | A | 26 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168-5935_1168-593 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35174733 | |||||
| chr14:35174733
|
ATTCTTCT others(10): Show |
A | 3 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0310 | 3 | HG00735.hp2 HG01255.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1168-5934_1168-591 others(21): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35174733 | |||||
| chr14:35174734
|
TTCTTCTT others(9): Show |
T | 15 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(12): Show | 15 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1168-5934_1168-591 others(20): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35174734 | |||||
| chr14:35174739
|
CT | C | 10 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 10 | HG01099.hp1 HG03654.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.1168-5921delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35174739 | |||||
| chr14:35174750
|
C | CT | 16 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(13): Show | 16 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1168-5906dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35174750 | |||||
| chr14:35174750
|
CTT | C | 9 | a0001c0001t0006g0040a0001c0001t0007g0050a0001c0001t0007g0170others(6): Show | 9 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1168-5907_1168-590 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35174750 | |||||
| chr14:35174750
|
CTTT | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(145): Show | 148 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1168-5908_1168-590 others(7): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35174750 | |||||
| chr14:35174751
|
T | C | 15 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(12): Show | 15 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1168-5919T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174751 | ||||||
| chr14:35174752
|
T | C | 3 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0310 | 3 | HG00735.hp2 HG01255.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1168-5918T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174752 | ||||||
| chr14:35174753
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1168-5917T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174753 | ||||||
| chr14:35174812
|
A | G | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1168-5858A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174812 | ||||||
| chr14:35174863
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0038others(2): Show | 5 | HG01167.hp2 HG01346.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168-5807C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174863 | ||||||
| chr14:35174893
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1168-5777T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174893 | ||||||
| chr14:35174963
|
A | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-5707A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174963 | ||||||
| chr14:35174967
|
G | C | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-5703G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174967 | ||||||
| chr14:35174986
|
C | G | 1 | a0001c0001t0001g0010 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1168-5684C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35174986 | ||||||
| chr14:35175011
|
C | A | 2 | a0001c0001t0003g0131a0001c0001t0003g0135 | 2 | HG01346.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1168-5659C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175011 | ||||||
| chr14:35175012
|
A | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1168-5658A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175012 | ||||||
| chr14:35175013
|
A | G | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168-5657A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175013 | ||||||
| chr14:35175255
|
A | C | 1 | a0001c0002t0001g0005 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1168-5415A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175255 | ||||||
| chr14:35175291
|
A | G | 1 | a0001c0001t0015g0144 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1168-5379A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175291 | ||||||
| chr14:35175303
|
C | T | 4 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0261others(1): Show | 4 | NA18943.hp1 NA18999.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-5367C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175303 | ||||||
| chr14:35175312
|
C | T | 8 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(5): Show | 8 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1168-5358C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175312 | ||||||
| chr14:35175322
|
T | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1168-5348T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175322 | ||||||
| chr14:35175338
|
A | C | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168-5332A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175338 | ||||||
| chr14:35175342
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1168-5328A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175342 | ||||||
| chr14:35175376
|
T | C | 27 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1168-5294T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175376 | ||||||
| chr14:35175379
|
C | T | 27 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1168-5291C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175379 | ||||||
| chr14:35175393
|
C | G | 1 | a0001c0001t0001g0006 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1168-5277C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175393 | ||||||
| chr14:35175468
|
T | C | 20 | a0001c0001t0005g0156a0001c0001t0012g0168a0001c0002t0003g0004others(17): Show | 20 | HG01884.hp2 HG02257.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1168-5202T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175468 | ||||||
| chr14:35175587
|
G | GTTGT | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1168-5080_1168-507 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35175587 | |||||
| chr14:35175594
|
T | G | 1 | a0001c0002t0001g0005 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1168-5076T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175594 | ||||||
| chr14:35175662
|
A | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1168-5008A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175662 | ||||||
| chr14:35175712
|
G | T | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-4958G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175712 | ||||||
| chr14:35175737
|
G | A | 27 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1168-4933G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175737 | ||||||
| chr14:35175743
|
A | C | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168-4927A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175743 | ||||||
| chr14:35175797
|
A | C | 26 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(23): Show | 26 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168-4873A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175797 | ||||||
| chr14:35175951
|
C | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1168-4719C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35175951 | ||||||
| chr14:35176013
|
C | T | 3 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300 | 3 | HG00140.hp2 HG01243.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1168-4657C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176013 | ||||||
| chr14:35176058
|
C | T | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1168-4612C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176058 | ||||||
| chr14:35176062
|
A | G | 24 | a0001c0001t0027g0278a0001c0004t0002g0275a0001c0004t0002g0276others(21): Show | 24 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1168-4608A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176062 | ||||||
| chr14:35176140
|
A | G | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1168-4530A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176140 | ||||||
| chr14:35176270
|
C | A | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-4400C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176270 | ||||||
| chr14:35176322
|
T | C | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-4348T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176322 | ||||||
| chr14:35176390
|
A | G | 1 | a0001c0001t0011g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1168-4280A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176390 | ||||||
| chr14:35176441
|
G | T | 1 | a0002c0003t0016g0288 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1168-4229G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176441 | ||||||
| chr14:35176457
|
A | G | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1168-4213A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176457 | ||||||
| chr14:35176506
|
T | G | 2 | a0001c0001t0003g0145a0001c0001t0003g0146 | 2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1168-4164T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176506 | ||||||
| chr14:35176558
|
G | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-4112G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176558 | ||||||
| chr14:35176592
|
G | T | 6 | a0001c0001t0003g0076a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-4078G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176592 | ||||||
| chr14:35176718
|
T | C | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-3952T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176718 | ||||||
| chr14:35176735
|
C | G | 8 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(5): Show | 8 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1168-3935C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176735 | ||||||
| chr14:35176760
|
C | T | 17 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(14): Show | 17 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1168-3910C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176760 | ||||||
| chr14:35176820
|
G | T | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-3850G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176820 | ||||||
| chr14:35176892
|
TC | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1168-3777delC | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35176892 | ||||||
| chr14:35177000
|
A | G | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1168-3670A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177000 | ||||||
| chr14:35177056
|
G | A | 24 | a0001c0001t0001g0075a0001c0002t0001g0191a0001c0002t0001g0192others(21): Show | 24 | HG00099.hp1 HG00733.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1168-3614G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177056 | ||||||
| chr14:35177198
|
AT | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1168-3469delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35177198 | |||||
| chr14:35177269
|
G | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG00642.hp2 HG01081.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168-3401G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177269 | ||||||
| chr14:35177348
|
A | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-3322A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177348 | ||||||
| chr14:35177363
|
C | T | 27 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1168-3307C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177363 | ||||||
| chr14:35177364
|
G | A | 9 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(6): Show | 9 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168-3306G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177364 | ||||||
| chr14:35177415
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1168-3255T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177415 | ||||||
| chr14:35177465
|
G | C | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1168-3205G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177465 | ||||||
| chr14:35177486
|
C | T | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-3184C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177486 | ||||||
| chr14:35177528
|
C | T | 7 | a0001c0001t0005g0156a0001c0001t0012g0168a0001c0002t0005g0182others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168-3142C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177528 | ||||||
| chr14:35177579
|
C | T | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-3091C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177579 | ||||||
| chr14:35177632
|
C | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-3038C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177632 | ||||||
| chr14:35177804
|
T | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1168-2866T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177804 | ||||||
| chr14:35177955
|
C | T | 4 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(1): Show | 4 | HG02630.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-2715C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177955 | ||||||
| chr14:35177995
|
A | C | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-2675A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35177995 | ||||||
| chr14:35178010
|
T | G | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1168-2660T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178010 | ||||||
| chr14:35178062
|
T | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1168-2608T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178062 | ||||||
| chr14:35178108
|
C | T | 4 | a0001c0002t0001g0227a0001c0002t0001g0228a0001c0002t0001g0266others(1): Show | 4 | NA18957.hp2 NA18968.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168-2562C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178108 | ||||||
| chr14:35178186
|
A | G | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1168-2484A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178186 | ||||||
| chr14:35178271
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1168-2399G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178271 | ||||||
| chr14:35178278
|
G | A | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1168-2392G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178278 | ||||||
| chr14:35178314
|
G | A | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168-2356G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178314 | ||||||
| chr14:35178402
|
C | G | 2 | a0003c0005t0019g0166a0003c0007t0013g0139 | 2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1168-2268C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178402 | ||||||
| chr14:35178756
|
A | ATTG | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1168-1912_1168-191 others(7): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35178756 | |||||
| chr14:35178759
|
A | T | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1168-1911A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178759 | ||||||
| chr14:35178775
|
A | C | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1168-1895A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178775 | ||||||
| chr14:35178887
|
T | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1168-1783T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178887 | ||||||
| chr14:35178895
|
C | T | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1168-1775C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178895 | ||||||
| chr14:35178898
|
T | A | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168-1772T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178898 | ||||||
| chr14:35178911
|
C | T | 4 | a0001c0001t0003g0177a0001c0001t0003g0178a0001c0001t0003g0179others(1): Show | 4 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-1759C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178911 | ||||||
| chr14:35178975
|
C | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1168-1695C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35178975 | ||||||
| chr14:35179067
|
C | T | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-1603C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179067 | ||||||
| chr14:35179096
|
C | A | 1 | a0001c0001t0001g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1168-1574C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179096 | ||||||
| chr14:35179110
|
G | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-1560G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179110 | ||||||
| chr14:35179174
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1168-1496T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179174 | ||||||
| chr14:35179384
|
A | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1168-1286A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179384 | ||||||
| chr14:35179501
|
C | G | 1 | a0001c0001t0003g0136 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1168-1169C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179501 | ||||||
| chr14:35179511
|
T | C | 1 | a0001c0002t0001g0255 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1168-1159T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179511 | ||||||
| chr14:35179525
|
C | G | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-1145C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179525 | ||||||
| chr14:35179525
|
C | T | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168-1145C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179525 | ||||||
| chr14:35179544
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0027others(3): Show | 6 | HG00140.hp1 HG00738.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-1126T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179544 | ||||||
| chr14:35179578
|
G | T | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1168-1092G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179578 | ||||||
| chr14:35179644
|
C | CT | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-1020dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35179644 | |||||
| chr14:35179713
|
C | T | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1168-957C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179713 | ||||||
| chr14:35179735
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1168-935A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179735 | ||||||
| chr14:35179739
|
A | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-931A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179739 | ||||||
| chr14:35179751
|
G | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-919G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179751 | ||||||
| chr14:35179761
|
G | A | 6 | a0001c0001t0003g0076a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168-909G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179761 | ||||||
| chr14:35179768
|
T | G | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1168-902T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179768 | ||||||
| chr14:35179854
|
T | A | 20 | a0001c0001t0005g0156a0001c0001t0012g0168a0001c0002t0003g0004others(17): Show | 20 | HG01884.hp2 HG02257.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1168-816T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179854 | ||||||
| chr14:35179859
|
A | G | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1168-811A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179859 | ||||||
| chr14:35179920
|
A | C | 1 | a0001c0001t0001g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1168-750A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35179920 | ||||||
| chr14:35180008
|
C | T | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1168-662C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180008 | ||||||
| chr14:35180022
|
A | G | 1 | a0001c0001t0003g0082 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1168-648A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180022 | ||||||
| chr14:35180031
|
G | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-639G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180031 | ||||||
| chr14:35180040
|
A | C | 1 | a0001c0002t0001g0227 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1168-630A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180040 | ||||||
| chr14:35180069
|
A | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1168-601A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180069 | ||||||
| chr14:35180091
|
A | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-579A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180091 | ||||||
| chr14:35180225
|
A | T | 26 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(23): Show | 26 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168-445A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180225 | ||||||
| chr14:35180278
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | NA18971.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1168-392C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180278 | ||||||
| chr14:35180284
|
C | T | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1168-386C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180284 | ||||||
| chr14:35180294
|
C | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1168-376C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180294 | ||||||
| chr14:35180321
|
C | T | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1168-349C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180321 | ||||||
| chr14:35180322
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1168-348A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180322 | ||||||
| chr14:35180347
|
A | T | 1 | a0001c0001t0007g0050 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1168-323A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180347 | ||||||
| chr14:35180413
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1168-257A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180413 | ||||||
| chr14:35180478
|
C | T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-192C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180478 | ||||||
| chr14:35180524
|
A | G | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-146A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180524 | ||||||
| chr14:35180526
|
C | CTG | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(59): Show | 62 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1168-120_1168-119d others(4): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35180526 | |||||
| chr14:35180526
|
C | CTGTG | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0042others(7): Show | 10 | HG02015.hp2 HG02027.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1168-122_1168-119d others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35180526 | |||||
| chr14:35180526
|
C | CTGTGTG | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1168-124_1168-119d others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35180526 | |||||
| chr14:35180526
|
C | CTGTGTGT others(5): Show |
17 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(14): Show | 17 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1168-130_1168-119d others(14): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35180526 | |||||
| chr14:35180526
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0021g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1168-136_1168-119d others(20): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35180526 | |||||
| chr14:35180526
|
C | CTGTGTGT others(13): Show |
2 | a0001c0001t0007g0050a0001c0001t0007g0176 | 2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1168-138_1168-119d others(22): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35180526 | |||||
| chr14:35180526
|
C | CTGTGTGT others(17): Show |
4 | a0001c0001t0007g0170a0001c0001t0007g0171a0001c0001t0007g0172others(1): Show | 4 | HG00741.hp1 HG01257.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-142_1168-119d others(26): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 35180526 | |||||
| chr14:35180526
|
C | G | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1168-144C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 4/7 | chr14 | 35180526 | ||||||
| chr14:35180831
|
C | G | 1 | a0001c0002t0001g0265 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1275+54C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35180831 | ||||||
| chr14:35180915
|
T | C | 1 | a0001c0002t0001g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1275+138T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35180915 | ||||||
| chr14:35180938
|
A | G | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+161A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35180938 | ||||||
| chr14:35181033
|
C | T | 2 | a0001c0002t0001g0209a0001c0002t0001g0265 | 2 | HG02965.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1275+256C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181033 | ||||||
| chr14:35181089
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1275+312C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181089 | ||||||
| chr14:35181152
|
G | C | 2 | a0001c0002t0014g0187a0001c0002t0014g0188 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1275+375G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181152 | ||||||
| chr14:35181165
|
C | G | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275+388C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181165 | ||||||
| chr14:35181171
|
A | G | 3 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015 | 3 | HG02280.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1275+394A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181171 | ||||||
| chr14:35181221
|
A | G | 1 | a0001c0001t0021g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1275+444A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181221 | ||||||
| chr14:35181222
|
G | A | 1 | a0001c0002t0001g0250 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1275+445G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181222 | ||||||
| chr14:35181263
|
G | C | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+486G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181263 | ||||||
| chr14:35181269
|
C | T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+492C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181269 | ||||||
| chr14:35181296
|
C | T | 4 | a0001c0002t0001g0204a0001c0002t0001g0206a0001c0002t0001g0208others(1): Show | 4 | HG01361.hp1 NA19001.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275+519C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181296 | ||||||
| chr14:35181346
|
T | G | 8 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(5): Show | 8 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1275+569T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181346 | ||||||
| chr14:35181352
|
C | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1275+575C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181352 | ||||||
| chr14:35181373
|
A | G | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+596A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181373 | ||||||
| chr14:35181612
|
C | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1275+835C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181612 | ||||||
| chr14:35181678
|
G | A | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275+901G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181678 | ||||||
| chr14:35181740
|
G | A | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1275+963G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181740 | ||||||
| chr14:35181774
|
A | G | 29 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0290others(26): Show | 29 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.1275+997A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181774 | ||||||
| chr14:35181783
|
C | CA | 33 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0277others(30): Show | 33 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1275+1024dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35181783 | |||||
| chr14:35181783
|
C | CCA | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1275+1006_1275+100 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181783 | ||||||
| chr14:35181783
|
C | CCAA | 4 | a0001c0002t0001g0199a0001c0002t0001g0267a0001c0002t0017g0217others(1): Show | 4 | HG02486.hp1 HG03098.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1275+1006_1275+100 others(7): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181783 | ||||||
| chr14:35181783
|
CA | C | 7 | a0001c0001t0001g0091a0001c0001t0001g0106a0001c0001t0002g0074others(4): Show | 7 | HG00408.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1275+1024delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35181783 | |||||
| chr14:35181811
|
A | G | 4 | a0001c0002t0003g0004a0001c0002t0003g0212a0001c0002t0003g0213others(1): Show | 4 | HG01884.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275+1034A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181811 | ||||||
| chr14:35181884
|
A | G | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1275+1107A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181884 | ||||||
| chr14:35181917
|
A | G | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1275+1140A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35181917 | ||||||
| chr14:35182002
|
A | G | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1275+1225A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182002 | ||||||
| chr14:35182061
|
C | G | 1 | a0001c0001t0002g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1275+1284C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182061 | ||||||
| chr14:35182062
|
G | A | 1 | a0001c0001t0002g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1275+1285G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182062 | ||||||
| chr14:35182077
|
A | G | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1275+1300A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182077 | ||||||
| chr14:35182101
|
T | TA | 11 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(8): Show | 11 | HG01099.hp1 HG03225.hp1 HG03654.hp1 others(8): Show |
intron_variant | MODIFIER | c.1275+1329dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35182101 | |||||
| chr14:35182122
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1275+1345C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182122 | ||||||
| chr14:35182125
|
G | A | 1 | a0002c0003t0004g0019 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1275+1348G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182125 | ||||||
| chr14:35182133
|
G | C | 1 | a0001c0002t0001g0240 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1275+1356G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182133 | ||||||
| chr14:35182135
|
G | A | 20 | a0001c0001t0005g0156a0001c0001t0012g0168a0001c0002t0003g0004others(17): Show | 20 | HG01884.hp2 HG02257.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1275+1358G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182135 | ||||||
| chr14:35182191
|
G | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1275+1414G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182191 | ||||||
| chr14:35182259
|
A | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1275+1482A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182259 | ||||||
| chr14:35182261
|
A | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1275+1484A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182261 | ||||||
| chr14:35182502
|
G | T | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1275+1725G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182502 | ||||||
| chr14:35182509
|
G | A | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1275+1732G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182509 | ||||||
| chr14:35182535
|
G | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1275+1758G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182535 | ||||||
| chr14:35182535
|
G | T | 1 | a0001c0002t0001g0202 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1275+1758G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182535 | ||||||
| chr14:35182586
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1275+1809A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182586 | ||||||
| chr14:35182641
|
C | T | 1 | a0001c0002t0001g0247 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1275+1864C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182641 | ||||||
| chr14:35182699
|
T | C | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1275+1922T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182699 | ||||||
| chr14:35182704
|
A | G | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+1927A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182704 | ||||||
| chr14:35182715
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0003g0070a0001c0001t0003g0136 | 3 | HG02258.hp1 HG02280.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1275+1938G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182715 | ||||||
| chr14:35182738
|
T | C | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+1961T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182738 | ||||||
| chr14:35182739
|
T | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1275+1962T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182739 | ||||||
| chr14:35182803
|
A | G | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1275+2026A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182803 | ||||||
| chr14:35182885
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1275+2108C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35182885 | ||||||
| chr14:35183140
|
T | C | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1275+2363T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35183140 | ||||||
| chr14:35183172
|
TTG | T | 4 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0198others(1): Show | 4 | HG00733.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275+2403_1275+240 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35183172 | |||||
| chr14:35183176
|
G | A | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1275+2399G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35183176 | ||||||
| chr14:35183221
|
T | TAC | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0026others(84): Show | 87 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1275+2461_1275+246 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35183221 | |||||
| chr14:35183221
|
T | TACAC | 43 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(40): Show | 43 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1275+2459_1275+246 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35183221 | |||||
| chr14:35183221
|
TAC | T | 19 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(16): Show | 19 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1275+2461_1275+246 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35183221 | |||||
| chr14:35183361
|
T | C | 44 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(41): Show | 44 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1275+2584T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35183361 | ||||||
| chr14:35183558
|
G | A | 1 | a0001c0002t0001g0202 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1275+2781G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35183558 | ||||||
| chr14:35183846
|
T | A | 1 | a0001c0001t0002g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1275+3069T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35183846 | ||||||
| chr14:35183850
|
T | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(149): Show | 152 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1275+3073T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35183850 | ||||||
| chr14:35183904
|
T | C | 2 | a0001c0001t0002g0290a0001c0001t0002g0291 | 2 | NA18941.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1275+3127T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35183904 | ||||||
| chr14:35183933
|
A | G | 4 | a0001c0002t0001g0193a0001c0002t0001g0207a0001c0002t0001g0311others(1): Show | 4 | HG01261.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275+3156A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35183933 | ||||||
| chr14:35183943
|
A | G | 1 | a0001c0002t0031g0190 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1275+3166A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35183943 | ||||||
| chr14:35184094
|
C | T | 4 | a0001c0001t0001g0077a0001c0001t0002g0078a0001c0001t0002g0079others(1): Show | 4 | HG02071.hp2 NA18951.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275+3317C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35184094 | ||||||
| chr14:35184103
|
C | T | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+3326C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35184103 | ||||||
| chr14:35184170
|
AC | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1275+3394delC | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35184170 | ||||||
| chr14:35184289
|
G | A | 1 | a0001c0001t0038g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1275+3512G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35184289 | ||||||
| chr14:35184349
|
A | G | 1 | a0001c0001t0002g0114 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1275+3572A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35184349 | ||||||
| chr14:35184522
|
A | T | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1275+3745A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35184522 | ||||||
| chr14:35184588
|
G | A | 6 | a0001c0001t0003g0127a0001c0001t0003g0129a0001c0001t0003g0130others(3): Show | 6 | HG00639.hp2 HG01074.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+3811G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35184588 | ||||||
| chr14:35184647
|
A | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1275+3870A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35184647 | ||||||
| chr14:35184808
|
G | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+4031G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35184808 | ||||||
| chr14:35184847
|
C | T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+4070C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35184847 | ||||||
| chr14:35184912
|
C | T | 1 | a0001c0002t0001g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1275+4135C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35184912 | ||||||
| chr14:35185261
|
T | G | 68 | a0001c0001t0001g0075a0001c0002t0001g0005a0001c0002t0001g0181others(65): Show | 68 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1275+4484T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35185261 | ||||||
| chr14:35185286
|
T | G | 27 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1275+4509T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35185286 | ||||||
| chr14:35185311
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1275+4534A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35185311 | ||||||
| chr14:35185901
|
T | C | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+5124T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35185901 | ||||||
| chr14:35186149
|
A | AT | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1275+5390dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35186149 | |||||
| chr14:35186149
|
A | ATT | 17 | a0001c0001t0001g0033a0001c0001t0003g0020a0001c0001t0003g0021others(14): Show | 17 | HG00642.hp2 HG00738.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.1275+5389_1275+539 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35186149 | |||||
| chr14:35186274
|
T | C | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+5497T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35186274 | ||||||
| chr14:35186278
|
G | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+5501G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35186278 | ||||||
| chr14:35186345
|
AT | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1275+5577delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35186345 | |||||
| chr14:35186398
|
C | G | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1275+5621C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35186398 | ||||||
| chr14:35186404
|
T | C | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1275+5627T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35186404 | ||||||
| chr14:35186483
|
C | G | 20 | a0001c0001t0005g0156a0001c0001t0012g0168a0001c0002t0003g0004others(17): Show | 20 | HG01884.hp2 HG02257.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1275+5706C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35186483 | ||||||
| chr14:35187005
|
G | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1275+6228G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35187005 | ||||||
| chr14:35187106
|
T | C | 1 | a0001c0002t0003g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1275+6329T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35187106 | ||||||
| chr14:35187147
|
A | G | 1 | a0001c0001t0003g0136 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1275+6370A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35187147 | ||||||
| chr14:35187428
|
G | GT | 141 | a0001c0001t0001g0042a0001c0001t0001g0075a0001c0001t0001g0124others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.1275+6667dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35187428 | |||||
| chr14:35187428
|
G | GTT | 55 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(52): Show | 55 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1275+6666_1275+666 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35187428 | |||||
| chr14:35187460
|
G | A | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1275+6683G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35187460 | ||||||
| chr14:35187631
|
T | C | 1 | a0001c0002t0003g0214 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1275+6854T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35187631 | ||||||
| chr14:35187724
|
C | G | 11 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(8): Show | 11 | HG01099.hp1 HG03225.hp1 HG03654.hp1 others(8): Show |
intron_variant | MODIFIER | c.1275+6947C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35187724 | ||||||
| chr14:35187847
|
C | CT | 26 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(23): Show | 26 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1275+7081dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35187847 | |||||
| chr14:35187970
|
C | G | 1 | a0001c0002t0001g0203 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1275+7193C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35187970 | ||||||
| chr14:35188062
|
C | G | 11 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(8): Show | 11 | HG01099.hp1 HG03225.hp1 HG03654.hp1 others(8): Show |
intron_variant | MODIFIER | c.1275+7285C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35188062 | ||||||
| chr14:35188122
|
G | A | 1 | a0001c0002t0001g0265 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1275+7345G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35188122 | ||||||
| chr14:35188191
|
A | AT | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1275+7431dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35188191 | |||||
| chr14:35188191
|
A | ATT | 16 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(13): Show | 16 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1275+7430_1275+743 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35188191 | |||||
| chr14:35188223
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1275+7446C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35188223 | ||||||
| chr14:35188335
|
C | T | 20 | a0001c0001t0005g0156a0001c0001t0012g0168a0001c0002t0003g0004others(17): Show | 20 | HG01884.hp2 HG02257.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1275+7558C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35188335 | ||||||
| chr14:35188412
|
A | C | 1 | a0001c0002t0001g0262 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1275+7635A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35188412 | ||||||
| chr14:35188510
|
T | G | 26 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(23): Show | 26 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1275+7733T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35188510 | ||||||
| chr14:35188581
|
G | A | 18 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1275+7804G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35188581 | ||||||
| chr14:35188757
|
C | G | 9 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(6): Show | 9 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1275+7980C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35188757 | ||||||
| chr14:35188876
|
G | A | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1275+8099G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35188876 | ||||||
| chr14:35188941
|
T | TA | 14 | a0001c0001t0001g0071a0001c0001t0002g0089a0001c0001t0002g0095others(11): Show | 14 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1275+8187dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35188941 | |||||
| chr14:35188961
|
A | AAAAAAGA others(3): Show |
4 | a0001c0001t0003g0082a0001c0001t0007g0172a0001c0001t0021g0175others(1): Show | 4 | HG00741.hp1 HG01243.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1275+8187_1275+818 others(14): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35188961 | |||||
| chr14:35188961
|
A | AAAAAGAA others(2): Show |
17 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0083others(14): Show | 17 | HG00099.hp2 HG01257.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1275+8187_1275+818 others(13): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35188961 | |||||
| chr14:35188961
|
A | AAAAGAAA others(1): Show |
45 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0003g0127others(42): Show | 45 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1275+8188_1275+818 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35188961 | |||||
| chr14:35188961
|
A | AAGAAAGA others(3): Show |
8 | a0001c0001t0001g0031a0001c0001t0001g0055a0001c0001t0001g0065others(5): Show | 8 | HG02027.hp1 HG02027.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1275+8185_1275+818 others(14): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35188961 | |||||
| chr14:35188961
|
A | AGAAAGAA others(2): Show |
122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1275+8184_1275+818 others(13): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35188961 | ||||||
| chr14:35188961
|
A | G | 1 | a0001c0002t0001g0262 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1275+8184A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35188961 | ||||||
| chr14:35189230
|
A | G | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1275+8453A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35189230 | ||||||
| chr14:35189423
|
T | C | 1 | a0001c0001t0018g0174 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1275+8646T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35189423 | ||||||
| chr14:35189430
|
C | CT | 31 | a0001c0001t0001g0038a0001c0001t0002g0277a0001c0001t0002g0281others(28): Show | 31 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1275+8670dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35189430 | |||||
| chr14:35189430
|
CT | C | 21 | a0001c0001t0001g0140a0001c0001t0002g0014a0001c0001t0002g0092others(18): Show | 21 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1275+8670delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35189430 | |||||
| chr14:35189518
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1275+8741C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35189518 | ||||||
| chr14:35189811
|
T | A | 1 | a0001c0001t0003g0145 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1275+9034T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35189811 | ||||||
| chr14:35189965
|
T | A | 30 | a0001c0001t0001g0030a0001c0001t0002g0277a0001c0001t0002g0281others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1275+9188T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35189965 | ||||||
| chr14:35190050
|
A | G | 305 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(302): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1275+9273A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190050 | ||||||
| chr14:35190087
|
G | A | 1 | a0001c0001t0015g0144 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1275+9310G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190087 | ||||||
| chr14:35190095
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1275+9318G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190095 | ||||||
| chr14:35190130
|
A | G | 9 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(6): Show | 9 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1275+9353A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190130 | ||||||
| chr14:35190175
|
G | C | 1 | a0001c0001t0009g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1275+9398G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190175 | ||||||
| chr14:35190302
|
G | A | 9 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(6): Show | 9 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1275+9525G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190302 | ||||||
| chr14:35190313
|
G | A | 9 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0007g0050others(6): Show | 9 | HG00099.hp2 HG00741.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1275+9536G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190313 | ||||||
| chr14:35190334
|
G | T | 2 | a0001c0001t0002g0109a0004c0010t0002g0110 | 2 | HG02129.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1275+9557G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190334 | ||||||
| chr14:35190392
|
C | G | 1 | a0001c0001t0002g0104 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1275+9615C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190392 | ||||||
| chr14:35190405
|
GA | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(145): Show | 148 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1275+9640delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35190405 | |||||
| chr14:35190591
|
C | T | 7 | a0001c0001t0006g0081a0001c0002t0001g0195a0001c0002t0001g0196others(4): Show | 7 | HG00733.hp1 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1275+9814C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190591 | ||||||
| chr14:35190637
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1275+9860C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190637 | ||||||
| chr14:35190652
|
C | T | 2 | a0001c0002t0001g0191a0001c0002t0001g0204 | 2 | HG00099.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1275+9875C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190652 | ||||||
| chr14:35190781
|
G | A | 1 | a0001c0001t0003g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1275+10004G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190781 | ||||||
| chr14:35190854
|
C | A | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+10077C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35190854 | ||||||
| chr14:35191063
|
A | G | 30 | a0001c0001t0001g0030a0001c0001t0002g0277a0001c0001t0002g0281others(27): Show | 30 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1275+10286A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35191063 | ||||||
| chr14:35191383
|
A | G | 1 | a0001c0001t0006g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1275+10606A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35191383 | ||||||
| chr14:35191476
|
A | T | 1 | a0001c0001t0021g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1275+10699A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35191476 | ||||||
| chr14:35191783
|
G | C | 1 | a0001c0002t0003g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1275+11006G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35191783 | ||||||
| chr14:35191842
|
T | C | 18 | a0001c0001t0002g0092a0001c0001t0003g0076a0001c0001t0003g0082others(15): Show | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1275+11065T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35191842 | ||||||
| chr14:35191844
|
TCCAGTAG others(26): Show |
T | 4 | a0001c0002t0003g0004a0001c0002t0003g0212a0001c0002t0003g0213others(1): Show | 4 | HG01884.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275+11136_1275+11 others(39): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35191844 | |||||
| chr14:35192087
|
A | G | 281 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1275+11310A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35192087 | ||||||
| chr14:35192089
|
C | T | 1 | a0001c0001t0003g0145 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1275+11312C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35192089 | ||||||
| chr14:35192090
|
G | A | 2 | a0001c0002t0014g0187a0001c0002t0014g0188 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1275+11313G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35192090 | ||||||
| chr14:35192130
|
T | A | 2 | a0001c0004t0002g0275a0001c0004t0002g0276 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1275+11353T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35192130 | ||||||
| chr14:35192865
|
G | A | 4 | a0001c0002t0001g0005a0001c0002t0001g0220a0001c0002t0001g0259others(1): Show | 4 | HG00438.hp2 HG02074.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1275+12088G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35192865 | ||||||
| chr14:35192940
|
C | T | 1 | a0001c0002t0001g0203 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1275+12163C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35192940 | ||||||
| chr14:35192966
|
C | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+12189C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35192966 | ||||||
| chr14:35192980
|
A | G | 25 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(22): Show | 25 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1275+12203A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35192980 | ||||||
| chr14:35192981
|
G | A | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+12204G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35192981 | ||||||
| chr14:35192981
|
G | GA | 25 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(22): Show | 25 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1275+12218dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35192981 | |||||
| chr14:35192981
|
GA | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1275+12218delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35192981 | |||||
| chr14:35193113
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0027others(4): Show | 7 | HG00140.hp1 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1275+12336C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35193113 | ||||||
| chr14:35193159
|
T | A | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01081.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+12382T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35193159 | ||||||
| chr14:35193634
|
A | AT | 50 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0037others(47): Show | 50 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1275+12873dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35193634 | |||||
| chr14:35193634
|
A | ATTT | 11 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(8): Show | 11 | HG01255.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1275+12871_1275+12 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35193634 | |||||
| chr14:35193634
|
AT | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0091a0001c0001t0001g0106others(19): Show | 22 | HG00408.hp2 HG00733.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.1275+12873delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35193634 | |||||
| chr14:35193710
|
C | T | 2 | a0001c0002t0001g0218a0001c0002t0001g0253 | 2 | NA18981.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1275+12933C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35193710 | ||||||
| chr14:35193917
|
T | C | 2 | a0001c0001t0003g0070a0001c0001t0003g0136 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1275+13140T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35193917 | ||||||
| chr14:35194007
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1275+13230A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35194007 | ||||||
| chr14:35194084
|
G | A | 1 | a0001c0001t0002g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1275+13307G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35194084 | ||||||
| chr14:35194248
|
C | G | 1 | a0001c0002t0002g0232 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1275+13471C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35194248 | ||||||
| chr14:35194475
|
A | T | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1275+13698A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35194475 | ||||||
| chr14:35194510
|
G | A | 4 | a0001c0001t0002g0273a0001c0001t0002g0274a0001c0002t0002g0223others(1): Show | 4 | HG03490.hp1 HG03492.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1275+13733G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35194510 | ||||||
| chr14:35194927
|
A | G | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+14150A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35194927 | ||||||
| chr14:35194962
|
C | T | 4 | a0001c0001t0003g0150a0001c0001t0003g0151a0001c0001t0003g0152others(1): Show | 4 | NA18943.hp2 NA18977.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275+14185C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35194962 | ||||||
| chr14:35194993
|
T | TAA | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(304): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1275+14216_1275+14 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35194993 | ||||||
| chr14:35195042
|
T | C | 1 | a0001c0002t0001g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1275+14265T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35195042 | ||||||
| chr14:35195126
|
G | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1275+14349G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35195126 | ||||||
| chr14:35195147
|
C | T | 1 | a0001c0002t0001g0263 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1275+14370C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35195147 | ||||||
| chr14:35195294
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1275+14517A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35195294 | ||||||
| chr14:35195335
|
A | C | 1 | a0001c0002t0001g0243 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1275+14558A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35195335 | ||||||
| chr14:35195349
|
G | T | 1 | a0001c0001t0002g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1275+14572G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35195349 | ||||||
| chr14:35195384
|
A | G | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+14607A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35195384 | ||||||
| chr14:35195411
|
A | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1275+14634A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35195411 | ||||||
| chr14:35195940
|
G | A | 1 | a0001c0001t0008g0149 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1275+15163G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35195940 | ||||||
| chr14:35195951
|
G | A | 1 | a0001c0002t0014g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1275+15174G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35195951 | ||||||
| chr14:35196166
|
A | G | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1275+15389A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196166 | ||||||
| chr14:35196168
|
T | G | 194 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.1275+15391T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196168 | ||||||
| chr14:35196204
|
G | A | 1 | a0001c0002t0001g0198 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1275+15427G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196204 | ||||||
| chr14:35196229
|
C | A | 1 | a0001c0002t0001g0251 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1275+15452C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196229 | ||||||
| chr14:35196324
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1275+15547C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196324 | ||||||
| chr14:35196329
|
A | G | 5 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(2): Show | 5 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1275+15552A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196329 | ||||||
| chr14:35196399
|
C | T | 109 | a0001c0001t0001g0048a0001c0001t0001g0091a0001c0001t0001g0106others(106): Show | 110 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1275+15622C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196399 | ||||||
| chr14:35196400
|
G | A | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1275+15623G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196400 | ||||||
| chr14:35196400
|
G | C | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+15623G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196400 | ||||||
| chr14:35196446
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1275+15669G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196446 | ||||||
| chr14:35196453
|
C | T | 1 | a0002c0003t0004g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1275+15676C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196453 | ||||||
| chr14:35196458
|
A | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(229): Show | 233 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.1275+15681A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196458 | ||||||
| chr14:35196459
|
T | G | 1 | a0001c0001t0011g0310 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1275+15682T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196459 | ||||||
| chr14:35196961
|
A | G | 2 | a0001c0002t0014g0187a0001c0002t0014g0188 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1275+16184A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35196961 | ||||||
| chr14:35197059
|
C | G | 2 | a0002c0003t0004g0285a0002c0003t0004g0286 | 2 | HG01175.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1275+16282C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35197059 | ||||||
| chr14:35197255
|
C | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1275+16478C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35197255 | ||||||
| chr14:35197259
|
G | C | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+16482G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35197259 | ||||||
| chr14:35197302
|
A | G | 2 | a0003c0005t0020g0023a0003c0012t0013g0211 | 2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1275+16525A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35197302 | ||||||
| chr14:35197464
|
A | G | 26 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(23): Show | 26 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1275+16687A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35197464 | ||||||
| chr14:35197529
|
A | G | 2 | a0001c0001t0003g0082a0001c0001t0003g0086 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1275+16752A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35197529 | ||||||
| chr14:35197541
|
A | G | 1 | a0001c0001t0002g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1275+16764A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35197541 | ||||||
| chr14:35197599
|
T | G | 4 | a0001c0001t0002g0001a0001c0001t0002g0114a0001c0001t0002g0115others(1): Show | 5 | HG02015.hp1 NA18977.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1275+16822T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35197599 | ||||||
| chr14:35197717
|
T | A | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1275+16940T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35197717 | ||||||
| chr14:35197775
|
T | C | 1 | a0001c0002t0001g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1275+16998T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35197775 | ||||||
| chr14:35197873
|
A | G | 1 | a0001c0002t0001g0248 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1275+17096A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35197873 | ||||||
| chr14:35198331
|
A | G | 2 | a0001c0001t0002g0303a0001c0001t0002g0304 | 2 | HG02135.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1275+17554A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35198331 | ||||||
| chr14:35198348
|
C | T | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275+17571C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35198348 | ||||||
| chr14:35198349
|
G | A | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+17572G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35198349 | ||||||
| chr14:35198848
|
T | C | 1 | a0002c0003t0004g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1275+18071T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35198848 | ||||||
| chr14:35198914
|
C | T | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+18137C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35198914 | ||||||
| chr14:35199013
|
A | G | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1275+18236A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35199013 | ||||||
| chr14:35199061
|
C | T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+18284C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35199061 | ||||||
| chr14:35199122
|
C | T | 4 | a0002c0003t0004g0296a0002c0003t0004g0297a0002c0003t0004g0298others(1): Show | 4 | HG00735.hp1 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1275+18345C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35199122 | ||||||
| chr14:35199123
|
G | A | 15 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(12): Show | 15 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1275+18346G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35199123 | ||||||
| chr14:35199164
|
T | A | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(35): Show | 38 | HG00099.hp2 HG00735.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1275+18387T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35199164 | ||||||
| chr14:35199228
|
G | A | 1 | a0001c0002t0001g0261 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1275+18451G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35199228 | ||||||
| chr14:35199267
|
G | A | 1 | a0001c0001t0003g0136 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1275+18490G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35199267 | ||||||
| chr14:35199311
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1275+18534G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35199311 | ||||||
| chr14:35199332
|
T | TA | 39 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0037others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.1275+18577dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35199332 | |||||
| chr14:35199332
|
TA | T | 30 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0070others(27): Show | 30 | HG01074.hp1 HG01081.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1275+18577delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35199332 | |||||
| chr14:35199615
|
T | C | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(37): Show | 40 | HG00099.hp2 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1275+18838T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35199615 | ||||||
| chr14:35199655
|
A | G | 1 | a0001c0002t0017g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1275+18878A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35199655 | ||||||
| chr14:35199745
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1275+18968G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35199745 | ||||||
| chr14:35200106
|
C | T | 2 | a0001c0001t0009g0157a0001c0001t0009g0158 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1275+19329C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35200106 | ||||||
| chr14:35200150
|
C | T | 1 | a0001c0001t0011g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1275+19373C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35200150 | ||||||
| chr14:35200182
|
TTTTG | T | 22 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(19): Show | 22 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1275+19421_1275+19 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35200182 | |||||
| chr14:35200211
|
G | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1275+19434G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35200211 | ||||||
| chr14:35200254
|
A | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1275+19477A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35200254 | ||||||
| chr14:35200341
|
A | G | 21 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1275+19564A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35200341 | ||||||
| chr14:35200392
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1275+19615A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35200392 | ||||||
| chr14:35200460
|
G | A | 1 | a0001c0001t0008g0147 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1275+19683G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35200460 | ||||||
| chr14:35201029
|
A | C | 1 | a0001c0002t0002g0222 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1275+20252A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201029 | ||||||
| chr14:35201113
|
G | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+20336G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201113 | ||||||
| chr14:35201164
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1275+20387G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201164 | ||||||
| chr14:35201359
|
G | A | 1 | a0001c0001t0015g0144 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1275+20582G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201359 | ||||||
| chr14:35201502
|
C | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1275+20725C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201502 | ||||||
| chr14:35201566
|
TTTA | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1275+20795_1275+20 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35201566 | |||||
| chr14:35201631
|
T | TTTTATTT others(1): Show |
7 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(4): Show | 7 | HG00738.hp1 HG01496.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1275+20875_1275+20 others(14): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35201631 | |||||
| chr14:35201631
|
T | TTTTATTT others(5): Show |
5 | a0001c0001t0003g0098a0001c0001t0003g0177a0001c0001t0003g0178others(2): Show | 5 | HG01891.hp1 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1275+20871_1275+20 others(18): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35201631 | |||||
| chr14:35201705
|
C | T | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1275+20928C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201705 | ||||||
| chr14:35201744
|
C | T | 26 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(23): Show | 26 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1275+20967C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201744 | ||||||
| chr14:35201791
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1275+21014G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201791 | ||||||
| chr14:35201866
|
T | C | 2 | a0001c0001t0009g0157a0001c0001t0009g0158 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1275+21089T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201866 | ||||||
| chr14:35201911
|
G | C | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1275+21134G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201911 | ||||||
| chr14:35201954
|
C | G | 21 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1275+21177C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201954 | ||||||
| chr14:35201972
|
A | AT | 17 | a0001c0001t0002g0113a0001c0001t0002g0291a0001c0001t0003g0020others(14): Show | 17 | HG00738.hp1 HG00741.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1275+21210dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35201972 | |||||
| chr14:35201972
|
A | T | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1275+21195A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201972 | ||||||
| chr14:35201974
|
T | TA | 29 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.1275+21197_1275+21 others(7): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201974 | ||||||
| chr14:35201975
|
T | A | 37 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0066others(34): Show | 37 | HG00438.hp2 HG00639.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1275+21198T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201975 | ||||||
| chr14:35201994
|
G | C | 2 | a0001c0001t0009g0157a0001c0001t0009g0158 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1275+21217G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35201994 | ||||||
| chr14:35202022
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(1): Show | 4 | HG01167.hp2 HG01346.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275+21245T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35202022 | ||||||
| chr14:35202026
|
G | A | 21 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1275+21249G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35202026 | ||||||
| chr14:35202236
|
A | G | 21 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1275+21459A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35202236 | ||||||
| chr14:35202279
|
TA | T | 5 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(2): Show | 5 | HG00140.hp2 HG01243.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1275+21508delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35202279 | |||||
| chr14:35202387
|
G | A | 1 | a0001c0001t0003g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1275+21610G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35202387 | ||||||
| chr14:35202480
|
G | C | 26 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(23): Show | 26 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1275+21703G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35202480 | ||||||
| chr14:35202594
|
C | A | 1 | a0001c0002t0001g0221 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1275+21817C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35202594 | ||||||
| chr14:35202656
|
G | A | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1275+21879G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35202656 | ||||||
| chr14:35202706
|
T | G | 2 | a0001c0001t0009g0157a0001c0001t0009g0158 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1275+21929T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35202706 | ||||||
| chr14:35202744
|
C | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1275+21967C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35202744 | ||||||
| chr14:35202807
|
A | T | 22 | a0001c0001t0001g0071a0001c0001t0003g0020a0001c0001t0003g0021others(19): Show | 22 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1275+22030A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35202807 | ||||||
| chr14:35202912
|
G | T | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1275+22135G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35202912 | ||||||
| chr14:35202957
|
A | G | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+22180A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35202957 | ||||||
| chr14:35203036
|
A | G | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1275+22259A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35203036 | ||||||
| chr14:35203121
|
G | T | 3 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0310 | 3 | HG00735.hp2 HG01255.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1275+22344G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35203121 | ||||||
| chr14:35203213
|
A | C | 2 | a0001c0001t0003g0017a0001c0001t0003g0018 | 2 | HG01081.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1275+22436A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35203213 | ||||||
| chr14:35203385
|
G | A | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1275+22608G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35203385 | ||||||
| chr14:35203392
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1275+22615T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35203392 | ||||||
| chr14:35203574
|
T | C | 1 | a0001c0001t0002g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1275+22797T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35203574 | ||||||
| chr14:35203634
|
G | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+22857G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35203634 | ||||||
| chr14:35203797
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1275+23020G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35203797 | ||||||
| chr14:35203822
|
G | A | 1 | a0001c0001t0011g0310 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1275+23045G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35203822 | ||||||
| chr14:35203862
|
C | T | 19 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(16): Show | 19 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1275+23085C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35203862 | ||||||
| chr14:35203876
|
T | C | 2 | a0001c0001t0003g0017a0001c0001t0003g0018 | 2 | HG01081.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1275+23099T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35203876 | ||||||
| chr14:35203946
|
A | T | 10 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 10 | HG01099.hp1 HG03654.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.1275+23169A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35203946 | ||||||
| chr14:35204024
|
T | G | 10 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 10 | HG01099.hp1 HG03654.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.1275+23247T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35204024 | ||||||
| chr14:35204119
|
A | G | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1275+23342A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35204119 | ||||||
| chr14:35204264
|
A | T | 39 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(36): Show | 39 | HG00099.hp2 HG00735.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1275+23487A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35204264 | ||||||
| chr14:35204339
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1275+23562C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35204339 | ||||||
| chr14:35204729
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1275+23952A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35204729 | ||||||
| chr14:35204924
|
T | C | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+24147T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35204924 | ||||||
| chr14:35204951
|
C | G | 15 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1275+24174C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35204951 | ||||||
| chr14:35205073
|
C | T | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+24296C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35205073 | ||||||
| chr14:35205074
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1275+24297G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35205074 | ||||||
| chr14:35205177
|
G | C | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1275+24400G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35205177 | ||||||
| chr14:35205307
|
G | C | 3 | a0001c0001t0002g0087a0001c0001t0002g0108a0001c0001t0002g0122 | 3 | HG01167.hp1 HG01169.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1275+24530G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35205307 | ||||||
| chr14:35205323
|
A | G | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+24546A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35205323 | ||||||
| chr14:35205410
|
G | A | 1 | a0001c0002t0001g0219 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1275+24633G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35205410 | ||||||
| chr14:35205441
|
C | T | 1 | a0001c0001t0010g0025 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1275+24664C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35205441 | ||||||
| chr14:35205522
|
A | G | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1275+24745A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35205522 | ||||||
| chr14:35205614
|
AC | A | 6 | a0001c0001t0005g0156a0001c0002t0005g0182a0001c0002t0005g0183others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+24840delC | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35205614 | |||||
| chr14:35205731
|
G | T | 2 | a0001c0001t0001g0064a0003c0012t0013g0211 | 2 | HG02818.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1275+24954G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35205731 | ||||||
| chr14:35205765
|
TTTTG | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1275+25000_1275+25 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35205765 | |||||
| chr14:35206020
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1275+25243A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35206020 | ||||||
| chr14:35206032
|
A | G | 20 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(17): Show | 20 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1275+25255A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35206032 | ||||||
| chr14:35206221
|
A | G | 1 | a0002c0003t0035g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1275+25444A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35206221 | ||||||
| chr14:35206275
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1275+25498T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35206275 | ||||||
| chr14:35206340
|
T | C | 1 | a0001c0002t0031g0190 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1275+25563T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35206340 | ||||||
| chr14:35206358
|
A | C | 20 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(17): Show | 20 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1275+25581A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35206358 | ||||||
| chr14:35206623
|
A | T | 1 | a0001c0002t0002g0238 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1275+25846A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35206623 | ||||||
| chr14:35206705
|
G | A | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(198): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1275+25928G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35206705 | ||||||
| chr14:35206782
|
T | A | 1 | a0001c0001t0002g0107 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1275+26005T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35206782 | ||||||
| chr14:35206794
|
T | C | 3 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024 | 3 | HG02723.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1275+26017T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35206794 | ||||||
| chr14:35207097
|
A | AT | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+26329dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35207097 | |||||
| chr14:35207285
|
A | G | 1 | a0001c0002t0003g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1275+26508A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35207285 | ||||||
| chr14:35207293
|
G | T | 1 | a0001c0002t0001g0264 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1275+26516G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35207293 | ||||||
| chr14:35207410
|
T | C | 1 | a0001c0001t0021g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1275+26633T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35207410 | ||||||
| chr14:35207495
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1275+26718C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35207495 | ||||||
| chr14:35207639
|
C | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1275+26862C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35207639 | ||||||
| chr14:35207699
|
A | C | 9 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1275+26922A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35207699 | ||||||
| chr14:35207873
|
C | A | 2 | a0001c0001t0003g0070a0001c0001t0003g0136 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1275+27096C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35207873 | ||||||
| chr14:35207931
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1275+27154C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35207931 | ||||||
| chr14:35207947
|
C | T | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1275+27170C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35207947 | ||||||
| chr14:35208019
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(50): Show | 53 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1275+27242G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35208019 | ||||||
| chr14:35208060
|
G | A | 15 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1275+27283G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35208060 | ||||||
| chr14:35208110
|
A | G | 1 | a0001c0001t0032g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1275+27333A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35208110 | ||||||
| chr14:35208128
|
C | A | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+27351C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35208128 | ||||||
| chr14:35208128
|
C | T | 26 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(23): Show | 26 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1275+27351C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35208128 | ||||||
| chr14:35208149
|
CA | C | 7 | a0001c0001t0001g0033a0001c0001t0001g0044a0001c0001t0001g0045others(4): Show | 7 | HG00642.hp2 HG01074.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275+27385delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35208149 | |||||
| chr14:35208210
|
T | C | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+27433T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35208210 | ||||||
| chr14:35208256
|
A | T | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1275+27479A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35208256 | ||||||
| chr14:35208377
|
G | T | 10 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 10 | HG01099.hp1 HG03654.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.1275+27600G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35208377 | ||||||
| chr14:35208407
|
A | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1275+27630A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35208407 | ||||||
| chr14:35208852
|
A | G | 5 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(2): Show | 5 | HG02630.hp2 HG03139.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1275+28075A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35208852 | ||||||
| chr14:35208945
|
CACTTGAA others(17): Show |
C | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+28169_1275+28 others(30): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35208945 | ||||||
| chr14:35208967
|
G | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1275+28190G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35208967 | ||||||
| chr14:35209123
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1275+28346G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35209123 | ||||||
| chr14:35209173
|
CA | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1275+28408delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35209173 | |||||
| chr14:35209208
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1275+28431G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35209208 | ||||||
| chr14:35209214
|
A | T | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1275+28437A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35209214 | ||||||
| chr14:35209282
|
A | G | 20 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(17): Show | 20 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1275+28505A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35209282 | ||||||
| chr14:35209313
|
G | A | 2 | a0001c0001t0017g0164a0001c0001t0038g0165 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1275+28536G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35209313 | ||||||
| chr14:35209554
|
T | C | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+28777T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35209554 | ||||||
| chr14:35209583
|
G | A | 1 | a0001c0001t0003g0129 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1275+28806G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35209583 | ||||||
| chr14:35209833
|
G | A | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+29056G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35209833 | ||||||
| chr14:35209912
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1275+29135T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35209912 | ||||||
| chr14:35210082
|
A | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1275+29305A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35210082 | ||||||
| chr14:35210273
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1275+29496G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35210273 | ||||||
| chr14:35210604
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1275+29827C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35210604 | ||||||
| chr14:35210668
|
ATAAAT | A | 3 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0008g0016 | 3 | HG01081.hp1 HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1275+29895_1275+29 others(11): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35210668 | |||||
| chr14:35210734
|
T | G | 1 | a0001c0002t0002g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1275+29957T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35210734 | ||||||
| chr14:35210750
|
C | CT | 15 | a0001c0001t0002g0015a0001c0001t0002g0043a0001c0001t0002g0049others(12): Show | 15 | HG00438.hp1 HG00597.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1275+30005dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35210750 | |||||
| chr14:35210750
|
C | CTT | 6 | a0001c0001t0002g0273a0001c0001t0002g0274a0001c0002t0002g0222others(3): Show | 6 | HG03490.hp1 HG03492.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+30004_1275+30 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35210750 | |||||
| chr14:35210750
|
CTTT | C | 19 | a0001c0001t0001g0067a0001c0001t0003g0021a0001c0001t0003g0022others(16): Show | 19 | HG00738.hp1 HG01891.hp2 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1275+30003_1275+30 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35210750 | |||||
| chr14:35210750
|
CTTTT | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 109 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.1275+30002_1275+30 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35210750 | |||||
| chr14:35210750
|
CTTTTT | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0075others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.1275+30001_1275+30 others(11): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35210750 | |||||
| chr14:35210750
|
CTTTTTT | C | 25 | a0001c0001t0001g0077a0001c0001t0003g0070a0001c0001t0003g0136others(22): Show | 25 | HG01099.hp2 HG02257.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1275+30000_1275+30 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35210750 | |||||
| chr14:35210750
|
CTTTTTTT others(9): Show |
C | 3 | a0003c0005t0019g0166a0003c0007t0013g0139a0003c0012t0013g0211 | 3 | HG02818.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1275+29990_1275+30 others(22): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35210750 | |||||
| chr14:35210857
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1275+30080A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35210857 | ||||||
| chr14:35211065
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1275+30288G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35211065 | ||||||
| chr14:35211216
|
TAG | T | 17 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024others(14): Show | 17 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1275+30443_1275+30 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35211216 | |||||
| chr14:35211309
|
C | T | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1275+30532C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35211309 | ||||||
| chr14:35211318
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1275+30541A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35211318 | ||||||
| chr14:35211378
|
A | T | 11 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(8): Show | 11 | HG01099.hp1 HG03225.hp1 HG03654.hp1 others(8): Show |
intron_variant | MODIFIER | c.1275+30601A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35211378 | ||||||
| chr14:35211463
|
C | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1275+30686C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35211463 | ||||||
| chr14:35211500
|
A | G | 306 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1275+30723A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35211500 | ||||||
| chr14:35211586
|
T | C | 1 | a0001c0001t0007g0176 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1275+30809T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35211586 | ||||||
| chr14:35211593
|
G | C | 1 | a0002c0003t0004g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1275+30816G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35211593 | ||||||
| chr14:35211639
|
A | T | 1 | a0001c0001t0003g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1275+30862A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35211639 | ||||||
| chr14:35211658
|
A | G | 28 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0290others(25): Show | 28 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1275+30881A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35211658 | ||||||
| chr14:35211740
|
G | C | 1 | a0001c0002t0001g0249 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1275+30963G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35211740 | ||||||
| chr14:35212019
|
G | A | 1 | a0001c0001t0003g0127 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1275+31242G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35212019 | ||||||
| chr14:35212221
|
A | G | 3 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0310 | 3 | HG00735.hp2 HG01255.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1275+31444A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35212221 | ||||||
| chr14:35212244
|
T | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1275+31467T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35212244 | ||||||
| chr14:35212343
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0140others(1): Show | 4 | HG01167.hp2 HG01346.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275+31566T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35212343 | ||||||
| chr14:35212482
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1275+31705A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35212482 | ||||||
| chr14:35212565
|
A | G | 8 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0142others(5): Show | 8 | HG01081.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1275+31788A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35212565 | ||||||
| chr14:35212761
|
T | C | 5 | a0001c0001t0003g0150a0001c0001t0003g0151a0001c0001t0003g0152others(2): Show | 5 | NA18943.hp2 NA18977.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1275+31984T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35212761 | ||||||
| chr14:35212966
|
T | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(49): Show | 52 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1275+32189T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35212966 | ||||||
| chr14:35212995
|
C | T | 3 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0310 | 3 | HG00735.hp2 HG01255.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1275+32218C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35212995 | ||||||
| chr14:35213061
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1275+32284C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35213061 | ||||||
| chr14:35213295
|
G | C | 17 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024others(14): Show | 17 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1275+32518G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35213295 | ||||||
| chr14:35213355
|
C | T | 15 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1275+32578C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35213355 | ||||||
| chr14:35213609
|
A | G | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+32832A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35213609 | ||||||
| chr14:35213695
|
A | G | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275+32918A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35213695 | ||||||
| chr14:35213779
|
C | A | 3 | a0001c0002t0001g0181a0001c0002t0001g0262a0001c0002t0001g0263 | 3 | NA18939.hp2 NA18951.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1275+33002C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35213779 | ||||||
| chr14:35214002
|
T | C | 14 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(11): Show | 14 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1275+33225T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35214002 | ||||||
| chr14:35214220
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1275+33443A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35214220 | ||||||
| chr14:35214279
|
G | A | 20 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(17): Show | 20 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1275+33502G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35214279 | ||||||
| chr14:35214350
|
A | C | 13 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(10): Show | 13 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1275+33573A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35214350 | ||||||
| chr14:35214400
|
C | T | 1 | a0001c0002t0003g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1275+33623C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35214400 | ||||||
| chr14:35214768
|
G | A | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1275+33991G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35214768 | ||||||
| chr14:35214787
|
A | G | 1 | a0001c0002t0001g0219 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1275+34010A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35214787 | ||||||
| chr14:35214799
|
T | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1275+34022T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35214799 | ||||||
| chr14:35214799
|
T | C | 127 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(124): Show | 127 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.1275+34022T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35214799 | ||||||
| chr14:35214822
|
G | A | 3 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022 | 3 | HG00738.hp1 HG01496.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1275+34045G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35214822 | ||||||
| chr14:35214861
|
C | T | 11 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(8): Show | 11 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1275+34084C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35214861 | ||||||
| chr14:35215105
|
C | T | 1 | a0001c0001t0003g0162 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1275+34328C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35215105 | ||||||
| chr14:35215285
|
T | C | 4 | a0001c0001t0002g0001a0001c0001t0002g0114a0001c0001t0002g0115others(1): Show | 5 | HG02015.hp1 NA18977.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1275+34508T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35215285 | ||||||
| chr14:35215446
|
A | G | 28 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0290others(25): Show | 28 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1275+34669A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35215446 | ||||||
| chr14:35215586
|
A | T | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1275+34809A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35215586 | ||||||
| chr14:35215603
|
A | T | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1275+34826A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35215603 | ||||||
| chr14:35215707
|
A | G | 3 | a0003c0005t0019g0166a0003c0007t0013g0139a0003c0012t0013g0211 | 3 | HG02818.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1275+34930A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35215707 | ||||||
| chr14:35215712
|
G | A | 12 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(9): Show | 12 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1275+34935G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35215712 | ||||||
| chr14:35215734
|
C | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1275+34957C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35215734 | ||||||
| chr14:35215762
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1275+34985T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35215762 | ||||||
| chr14:35215889
|
C | T | 1 | a0001c0002t0001g0235 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1275+35112C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35215889 | ||||||
| chr14:35215973
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1275+35196G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35215973 | ||||||
| chr14:35216037
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1275+35260G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35216037 | ||||||
| chr14:35216057
|
G | A | 5 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(2): Show | 5 | HG02630.hp2 HG03139.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1275+35280G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35216057 | ||||||
| chr14:35216103
|
T | TATATATT others(21): Show |
138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(135): Show | 138 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1275+35339_1275+35 others(34): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35216103 | |||||
| chr14:35216103
|
T | TATATATT others(49): Show |
13 | a0001c0001t0001g0057a0001c0001t0003g0076a0001c0001t0003g0083others(10): Show | 13 | HG00639.hp2 HG01346.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1275+35366_1275+35 others(62): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35216103 | |||||
| chr14:35216103
|
T | TATATATT others(49): Show |
1 | a0001c0001t0003g0133 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1275+35366_1275+35 others(62): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35216103 | |||||
| chr14:35216257
|
G | A | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+35480G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35216257 | ||||||
| chr14:35216313
|
G | T | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1275+35536G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35216313 | ||||||
| chr14:35216414
|
A | T | 1 | a0002c0003t0016g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1275+35637A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35216414 | ||||||
| chr14:35216537
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1275+35760T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35216537 | ||||||
| chr14:35216641
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1275+35864A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35216641 | ||||||
| chr14:35216691
|
T | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1275+35914T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35216691 | ||||||
| chr14:35216702
|
G | A | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1275+35925G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35216702 | ||||||
| chr14:35216876
|
A | G | 9 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1275+36099A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35216876 | ||||||
| chr14:35217062
|
T | C | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1275+36285T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35217062 | ||||||
| chr14:35217162
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1275+36385T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35217162 | ||||||
| chr14:35217329
|
C | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1275+36552C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35217329 | ||||||
| chr14:35217387
|
G | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1275+36610G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35217387 | ||||||
| chr14:35217397
|
A | C | 5 | a0001c0001t0003g0150a0001c0001t0003g0151a0001c0001t0003g0152others(2): Show | 5 | NA18943.hp2 NA18977.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1275+36620A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35217397 | ||||||
| chr14:35217454
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1275+36677T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35217454 | ||||||
| chr14:35217500
|
C | CA | 27 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0003g0082others(24): Show | 27 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1275+36740dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35217500 | |||||
| chr14:35217500
|
C | CAA | 11 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(8): Show | 11 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1275+36739_1275+36 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35217500 | |||||
| chr14:35217596
|
GT | G | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+36827delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35217596 | |||||
| chr14:35217637
|
T | C | 1 | a0001c0002t0001g0246 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1275+36860T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35217637 | ||||||
| chr14:35217850
|
C | G | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1275+37073C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35217850 | ||||||
| chr14:35217996
|
T | C | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1275+37219T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35217996 | ||||||
| chr14:35218410
|
G | C | 1 | a0001c0001t0011g0154 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1275+37633G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35218410 | ||||||
| chr14:35218459
|
T | TA | 40 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0002g0300others(37): Show | 40 | HG00140.hp2 HG01071.hp1 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.1275+37689dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35218459 | |||||
| chr14:35218459
|
T | TAA | 78 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1275+37688_1275+37 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35218459 | |||||
| chr14:35218459
|
T | TAAA | 62 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0031others(59): Show | 62 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1275+37687_1275+37 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35218459 | |||||
| chr14:35218459
|
T | TAAAA | 18 | a0001c0001t0001g0036a0001c0001t0001g0075a0001c0001t0001g0077others(15): Show | 18 | HG01169.hp1 HG01261.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.1275+37686_1275+37 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35218459 | |||||
| chr14:35218459
|
T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1275+37689_1275+37 others(19): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35218459 | |||||
| chr14:35218459
|
T | TTAA | 7 | a0001c0001t0003g0085a0001c0001t0003g0127a0001c0001t0003g0129others(4): Show | 7 | HG00639.hp2 HG01346.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275+37682_1275+37 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35218459 | ||||||
| chr14:35218459
|
T | TTAAA | 6 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(3): Show | 6 | HG01074.hp1 HG02055.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+37682_1275+37 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35218459 | ||||||
| chr14:35218467
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1275+37690G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35218467 | ||||||
| chr14:35218467
|
G | GA | 6 | a0001c0001t0002g0062a0001c0001t0002g0088a0001c0001t0002g0089others(3): Show | 6 | HG01175.hp2 HG02109.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+37708dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35218467 | |||||
| chr14:35218473
|
A | C | 1 | a0001c0001t0021g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1275+37696A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35218473 | ||||||
| chr14:35218485
|
A | AAAAG | 6 | a0001c0001t0011g0155a0001c0001t0011g0310a0001c0001t0038g0165others(3): Show | 6 | HG00735.hp2 HG01255.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+37708_1275+37 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35218485 | ||||||
| chr14:35218485
|
A | AAAG | 6 | a0001c0001t0009g0159a0001c0001t0009g0167a0001c0001t0011g0154others(3): Show | 6 | HG01884.hp1 HG02559.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+37708_1275+37 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35218485 | ||||||
| chr14:35218527
|
TTTTTTTT others(8): Show |
T | 3 | a0002c0003t0004g0297a0002c0003t0004g0298a0002c0003t0004g0299 | 3 | HG00735.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1275+37753_1275+37 others(21): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35218527 | |||||
| chr14:35218536
|
TTTTTTG | T | 14 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(11): Show | 14 | HG00738.hp1 HG01433.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1275+37762_1275+37 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35218536 | |||||
| chr14:35218537
|
TTTTTG | T | 28 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0001t0003g0141others(25): Show | 28 | HG00099.hp2 HG00741.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1275+37763_1275+37 others(11): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35218537 | |||||
| chr14:35218538
|
TTTTG | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(10): Show | 13 | HG01081.hp1 HG01496.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1275+37764_1275+37 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35218538 | |||||
| chr14:35218539
|
TTTG | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1275+37766_1275+37 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35218539 | |||||
| chr14:35218540
|
TTG | T | 42 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0124others(39): Show | 42 | HG00140.hp2 HG00642.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.1275+37765_1275+37 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35218540 | |||||
| chr14:35218541
|
TG | T | 6 | a0001c0002t0005g0186a0002c0003t0004g0282a0002c0003t0004g0286others(3): Show | 6 | HG00597.hp2 HG00733.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+37765delG | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35218541 | ||||||
| chr14:35218585
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1275+37808G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35218585 | ||||||
| chr14:35218682
|
C | T | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+37905C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35218682 | ||||||
| chr14:35218974
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1275+38197A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35218974 | ||||||
| chr14:35219182
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1275+38405C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35219182 | ||||||
| chr14:35219254
|
A | T | 2 | a0001c0001t0001g0091a0001c0001t0002g0074 | 2 | NA18947.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1275+38477A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35219254 | ||||||
| chr14:35219426
|
G | A | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1275+38649G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35219426 | ||||||
| chr14:35219517
|
A | G | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+38740A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35219517 | ||||||
| chr14:35219531
|
G | A | 1 | a0002c0003t0004g0295 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1275+38754G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35219531 | ||||||
| chr14:35219537
|
C | A | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+38760C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35219537 | ||||||
| chr14:35219744
|
G | GT | 22 | a0001c0001t0001g0075a0001c0002t0001g0191a0001c0002t0001g0193others(19): Show | 22 | HG00099.hp1 HG00733.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1275+38968dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35219744 | |||||
| chr14:35219757
|
C | A | 17 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024others(14): Show | 17 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1275+38980C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35219757 | ||||||
| chr14:35219760
|
C | G | 7 | a0001c0001t0001g0066a0001c0001t0003g0082a0001c0001t0003g0086others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1275+38983C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35219760 | ||||||
| chr14:35219783
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1275+39006T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35219783 | ||||||
| chr14:35219959
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1275+39182C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35219959 | ||||||
| chr14:35220271
|
G | A | 1 | a0001c0002t0017g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1275+39494G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35220271 | ||||||
| chr14:35220289
|
A | G | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1275+39512A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35220289 | ||||||
| chr14:35220520
|
G | A | 3 | a0001c0001t0012g0163a0001c0001t0012g0168a0006c0008t0012g0143 | 3 | HG02055.hp1 HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1275+39743G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35220520 | ||||||
| chr14:35220618
|
AGACTGAG | A | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275+39844_1275+39 others(13): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35220618 | |||||
| chr14:35220736
|
C | CT | 23 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(20): Show | 23 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1275+39959_1275+39 others(7): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35220736 | ||||||
| chr14:35220737
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1275+39960A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35220737 | ||||||
| chr14:35220865
|
A | G | 9 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1275+40088A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35220865 | ||||||
| chr14:35221247
|
CTTATAA | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(177): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.1275+40474_1275+40 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35221247 | |||||
| chr14:35221296
|
A | G | 3 | a0001c0001t0001g0091a0001c0001t0002g0074a0001c0001t0002g0090 | 3 | HG00408.hp2 NA18947.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1275+40519A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35221296 | ||||||
| chr14:35221309
|
A | G | 22 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0070others(19): Show | 22 | HG01081.hp1 HG01099.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1275+40532A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35221309 | ||||||
| chr14:35221360
|
T | C | 4 | a0001c0002t0001g0204a0001c0002t0001g0206a0001c0002t0001g0208others(1): Show | 4 | HG01361.hp1 NA19001.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1275+40583T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35221360 | ||||||
| chr14:35221551
|
C | T | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+40774C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35221551 | ||||||
| chr14:35221750
|
C | T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1275+40973C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35221750 | ||||||
| chr14:35221772
|
C | G | 22 | a0001c0001t0001g0075a0001c0002t0001g0191a0001c0002t0001g0193others(19): Show | 22 | HG00099.hp1 HG00733.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1275+40995C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35221772 | ||||||
| chr14:35221868
|
G | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1275+41091G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35221868 | ||||||
| chr14:35221877
|
T | TAA | 3 | a0003c0005t0019g0166a0003c0007t0013g0139a0003c0012t0013g0211 | 3 | HG02818.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1275+41101_1275+41 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35221877 | |||||
| chr14:35221947
|
G | A | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275+41170G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35221947 | ||||||
| chr14:35222118
|
T | TAAG | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1275+41347_1275+41 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35222118 | |||||
| chr14:35222233
|
A | G | 5 | a0001c0001t0003g0150a0001c0001t0003g0151a0001c0001t0003g0152others(2): Show | 5 | NA18943.hp2 NA18977.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1275+41456A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35222233 | ||||||
| chr14:35222283
|
C | A | 2 | a0001c0001t0001g0075a0001c0002t0001g0255 | 2 | HG02027.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1275+41506C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35222283 | ||||||
| chr14:35222317
|
C | A | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+41540C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35222317 | ||||||
| chr14:35222329
|
A | G | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1275+41552A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35222329 | ||||||
| chr14:35222401
|
A | G | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+41624A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35222401 | ||||||
| chr14:35222749
|
A | G | 3 | a0001c0002t0001g0181a0001c0002t0001g0262a0001c0002t0001g0263 | 3 | NA18939.hp2 NA18951.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1275+41972A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35222749 | ||||||
| chr14:35222874
|
T | C | 28 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0290others(25): Show | 28 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1275+42097T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35222874 | ||||||
| chr14:35222942
|
G | C | 1 | a0001c0002t0001g0218 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1275+42165G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35222942 | ||||||
| chr14:35222953
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1275+42176C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35222953 | ||||||
| chr14:35222965
|
T | C | 2 | a0001c0001t0003g0070a0001c0001t0003g0136 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1275+42188T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35222965 | ||||||
| chr14:35223020
|
T | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1275+42243T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35223020 | ||||||
| chr14:35223030
|
G | A | 3 | a0002c0003t0004g0282a0002c0003t0016g0288a0002c0003t0016g0301 | 3 | HG06807.hp2 NA20752.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1275+42253G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35223030 | ||||||
| chr14:35223163
|
T | G | 23 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(20): Show | 23 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1275+42386T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35223163 | ||||||
| chr14:35223225
|
C | CT | 19 | a0001c0001t0003g0070a0001c0001t0003g0136a0001c0001t0003g0141others(16): Show | 19 | HG01099.hp1 HG02258.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.1275+42462dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35223225 | |||||
| chr14:35223225
|
CT | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1275+42462delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35223225 | |||||
| chr14:35223252
|
C | A | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1275+42475C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35223252 | ||||||
| chr14:35223400
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG02602.hp2 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1275+42623C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35223400 | ||||||
| chr14:35223456
|
CT | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(255): Show | 259 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.1275+42700delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35223456 | |||||
| chr14:35223456
|
CTT | C | 45 | a0001c0001t0001g0057a0001c0001t0002g0277a0001c0001t0002g0281others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1275+42699_1275+42 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35223456 | |||||
| chr14:35223609
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1275+42832G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35223609 | ||||||
| chr14:35223616
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1275+42839C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35223616 | ||||||
| chr14:35223827
|
T | G | 2 | a0001c0001t0009g0157a0001c0001t0009g0158 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1276-42900T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35223827 | ||||||
| chr14:35223838
|
C | G | 1 | a0001c0001t0032g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1276-42889C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35223838 | ||||||
| chr14:35224192
|
T | C | 15 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1276-42535T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35224192 | ||||||
| chr14:35224427
|
C | A | 2 | a0001c0001t0002g0290a0001c0001t0002g0291 | 2 | NA18941.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1276-42300C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35224427 | ||||||
| chr14:35224583
|
C | G | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276-42144C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35224583 | ||||||
| chr14:35224584
|
T | G | 24 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0070others(21): Show | 24 | HG01081.hp1 HG01099.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1276-42143T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35224584 | ||||||
| chr14:35224642
|
A | G | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276-42085A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35224642 | ||||||
| chr14:35224651
|
A | G | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-42076A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35224651 | ||||||
| chr14:35224820
|
A | G | 14 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(11): Show | 14 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1276-41907A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35224820 | ||||||
| chr14:35225086
|
G | A | 1 | a0001c0002t0001g0191 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1276-41641G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35225086 | ||||||
| chr14:35225145
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1276-41582G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35225145 | ||||||
| chr14:35225372
|
G | A | 8 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-41355G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35225372 | ||||||
| chr14:35225501
|
C | T | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1276-41226C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35225501 | ||||||
| chr14:35225502
|
A | G | 1 | a0001c0001t0002g0079 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1276-41225A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35225502 | ||||||
| chr14:35225588
|
C | A | 1 | a0001c0001t0002g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1276-41139C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35225588 | ||||||
| chr14:35225639
|
G | A | 1 | a0001c0002t0001g0236 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1276-41088G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35225639 | ||||||
| chr14:35225786
|
C | A | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276-40941C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35225786 | ||||||
| chr14:35225834
|
C | T | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-40893C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35225834 | ||||||
| chr14:35225954
|
T | G | 1 | a0001c0002t0001g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1276-40773T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35225954 | ||||||
| chr14:35225975
|
T | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1276-40752T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35225975 | ||||||
| chr14:35226000
|
G | A | 15 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1276-40727G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35226000 | ||||||
| chr14:35226436
|
A | T | 4 | a0002c0003t0004g0296a0002c0003t0004g0297a0002c0003t0004g0298others(1): Show | 4 | HG00735.hp1 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276-40291A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35226436 | ||||||
| chr14:35226568
|
A | G | 1 | a0001c0002t0003g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1276-40159A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35226568 | ||||||
| chr14:35226619
|
C | A | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1276-40108C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35226619 | ||||||
| chr14:35226725
|
AATTATT | A | 11 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(8): Show | 11 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1276-39992_1276-39 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35226725 | |||||
| chr14:35226742
|
C | T | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1276-39985C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35226742 | ||||||
| chr14:35227003
|
T | C | 1 | a0001c0001t0023g0161 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1276-39724T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35227003 | ||||||
| chr14:35227014
|
C | T | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1276-39713C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35227014 | ||||||
| chr14:35227414
|
A | C | 15 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1276-39313A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35227414 | ||||||
| chr14:35227443
|
C | CA | 8 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0109others(5): Show | 8 | HG02083.hp2 HG02129.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-39272dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35227443 | |||||
| chr14:35227612
|
A | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(50): Show | 53 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1276-39115A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35227612 | ||||||
| chr14:35227620
|
A | G | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276-39107A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35227620 | ||||||
| chr14:35227746
|
T | A | 15 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1276-38981T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35227746 | ||||||
| chr14:35227930
|
GTCAGGAG others(1): Show |
G | 17 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024others(14): Show | 17 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1276-38794_1276-38 others(14): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35227930 | |||||
| chr14:35227940
|
C | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1276-38787C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35227940 | ||||||
| chr14:35227999
|
C | T | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-38728C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35227999 | ||||||
| chr14:35228043
|
T | C | 5 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0310others(2): Show | 5 | HG00735.hp2 HG01255.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276-38684T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228043 | ||||||
| chr14:35228098
|
G | A | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1276-38629G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228098 | ||||||
| chr14:35228099
|
C | T | 28 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0290others(25): Show | 28 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1276-38628C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228099 | ||||||
| chr14:35228101
|
C | T | 3 | a0003c0005t0019g0166a0003c0007t0013g0139a0003c0012t0013g0211 | 3 | HG02818.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1276-38626C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228101 | ||||||
| chr14:35228120
|
G | A | 4 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0198others(1): Show | 4 | HG00733.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276-38607G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228120 | ||||||
| chr14:35228224
|
T | G | 1 | a0001c0001t0001g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1276-38503T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228224 | ||||||
| chr14:35228338
|
G | A | 23 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(20): Show | 23 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1276-38389G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228338 | ||||||
| chr14:35228489
|
G | A | 1 | a0002c0003t0004g0296 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1276-38238G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228489 | ||||||
| chr14:35228759
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1276-37968G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228759 | ||||||
| chr14:35228776
|
A | G | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-37951A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228776 | ||||||
| chr14:35228828
|
A | T | 26 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(23): Show | 26 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1276-37899A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228828 | ||||||
| chr14:35228934
|
T | G | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1276-37793T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228934 | ||||||
| chr14:35228954
|
G | A | 20 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(17): Show | 20 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1276-37773G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35228954 | ||||||
| chr14:35229035
|
C | G | 3 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024 | 3 | HG02723.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1276-37692C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35229035 | ||||||
| chr14:35229212
|
A | G | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-37515A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35229212 | ||||||
| chr14:35229373
|
C | T | 8 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0142others(5): Show | 8 | HG01081.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-37354C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35229373 | ||||||
| chr14:35229558
|
C | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1276-37169C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35229558 | ||||||
| chr14:35229841
|
T | TTCCATTG others(2393): Show |
1 | a0001c0001t0003g0132 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1276-36869_1276-36 others(2406): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35229841 | |||||
| chr14:35229877
|
C | T | 1 | a0001c0001t0002g0277 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1276-36850C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35229877 | ||||||
| chr14:35229905
|
CAT | C | 7 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0001g0197others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276-36821_1276-36 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35229905 | ||||||
| chr14:35230050
|
C | CT | 10 | a0001c0001t0003g0152a0001c0001t0007g0050a0001c0001t0007g0171others(7): Show | 10 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1276-36657dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230050 | |||||
| chr14:35230050
|
C | CTTTTTTT others(1): Show |
11 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(8): Show | 11 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1276-36664_1276-36 others(14): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230050 | |||||
| chr14:35230050
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0003g0132 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1276-36668_1276-36 others(18): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230050 | |||||
| chr14:35230050
|
CT | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1276-36657delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230050 | |||||
| chr14:35230050
|
CTT | C | 9 | a0001c0002t0003g0189a0001c0002t0003g0216a0001c0002t0003g0306others(6): Show | 9 | HG01256.hp1 HG02486.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1276-36658_1276-36 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230050 | |||||
| chr14:35230187
|
G | A | 2 | a0001c0001t0009g0157a0001c0001t0009g0158 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1276-36540G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35230187 | ||||||
| chr14:35230202
|
G | A | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-36525G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35230202 | ||||||
| chr14:35230511
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1276-36216A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35230511 | ||||||
| chr14:35230728
|
G | C | 2 | a0001c0001t0006g0097a0001c0001t0006g0117 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1276-35999G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35230728 | ||||||
| chr14:35230938
|
A | AAC | 41 | a0001c0001t0001g0053a0001c0001t0001g0091a0001c0001t0002g0001others(38): Show | 42 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1276-35748_1276-35 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
A | AACAC | 40 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0106others(37): Show | 40 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1276-35750_1276-35 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
A | AACACAC | 39 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0124others(36): Show | 39 | HG00408.hp1 HG01070.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1276-35752_1276-35 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
A | AACACACA others(1): Show |
19 | a0001c0001t0003g0127a0001c0001t0003g0129a0001c0001t0003g0130others(16): Show | 19 | HG00609.hp1 HG00639.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.1276-35754_1276-35 others(14): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
A | AACACACA others(3): Show |
3 | a0001c0001t0028g0035a0001c0002t0001g0257a0007c0011t0037g0128 | 3 | HG03942.hp2 NA18959.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1276-35756_1276-35 others(16): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
A | AACACACA others(7): Show |
1 | a0001c0001t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1276-35760_1276-35 others(20): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
AAC | A | 23 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0065others(20): Show | 23 | HG00735.hp2 HG01255.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1276-35748_1276-35 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
AACAC | A | 16 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0072others(13): Show | 16 | HG01175.hp2 HG01515.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.1276-35750_1276-35 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
AACACAC | A | 11 | a0001c0001t0002g0102a0001c0001t0002g0125a0001c0001t0003g0017others(8): Show | 11 | HG01081.hp1 HG02109.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1276-35752_1276-35 others(12): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
AACACACA others(1): Show |
A | 31 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(28): Show | 31 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1276-35754_1276-35 others(14): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
AACACACA others(3): Show |
A | 5 | a0001c0001t0003g0150a0001c0001t0003g0151a0001c0001t0003g0152others(2): Show | 5 | NA18943.hp2 NA18977.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276-35756_1276-35 others(16): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
AACACACA others(5): Show |
A | 24 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0003g0069others(21): Show | 24 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1276-35758_1276-35 others(18): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
AACACACA others(7): Show |
A | 2 | a0001c0001t0003g0021a0001c0001t0021g0175 | 2 | HG01433.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1276-35760_1276-35 others(20): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35230938
|
AACACACA others(11): Show |
A | 1 | a0001c0001t0003g0148 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1276-35764_1276-35 others(24): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35230938 | |||||
| chr14:35231044
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1276-35683G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35231044 | ||||||
| chr14:35231183
|
C | A | 8 | a0001c0002t0003g0189a0001c0002t0003g0216a0001c0002t0003g0306others(5): Show | 8 | HG02486.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1276-35544C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35231183 | ||||||
| chr14:35231337
|
T | TA | 12 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(9): Show | 12 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1276-35389dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35231337 | |||||
| chr14:35231356
|
C | T | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1276-35371C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35231356 | ||||||
| chr14:35231541
|
C | G | 1 | a0001c0001t0011g0154 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1276-35186C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35231541 | ||||||
| chr14:35231744
|
A | G | 2 | a0001c0001t0002g0062a0001c0001t0002g0063 | 2 | HG02602.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1276-34983A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35231744 | ||||||
| chr14:35231949
|
A | G | 27 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1276-34778A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35231949 | ||||||
| chr14:35232121
|
T | C | 1 | a0001c0002t0003g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1276-34606T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35232121 | ||||||
| chr14:35232192
|
A | AT | 10 | a0001c0001t0001g0065a0001c0001t0002g0088a0001c0001t0007g0050others(7): Show | 10 | HG00099.hp2 HG00741.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1276-34521dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35232192 | |||||
| chr14:35232284
|
C | T | 1 | a0001c0002t0003g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1276-34443C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35232284 | ||||||
| chr14:35232354
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0002t0001g0234 | 3 | HG01346.hp1 HG03491.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1276-34373C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35232354 | ||||||
| chr14:35232840
|
T | C | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1276-33887T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35232840 | ||||||
| chr14:35232863
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1276-33864C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35232863 | ||||||
| chr14:35232912
|
A | G | 2 | a0001c0001t0002g0303a0001c0001t0002g0304 | 2 | HG02135.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1276-33815A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35232912 | ||||||
| chr14:35233086
|
ACTTCAGT others(579): Show |
A | 15 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1276-33637_1276-33 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35233086 | |||||
| chr14:35233172
|
G | T | 1 | a0001c0002t0001g0221 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1276-33555G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35233172 | ||||||
| chr14:35233323
|
G | A | 2 | a0001c0001t0002g0062a0001c0001t0002g0104 | 2 | HG00438.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1276-33404G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35233323 | ||||||
| chr14:35233412
|
CTTATCTA others(41): Show |
C | 8 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0109others(5): Show | 8 | HG02083.hp2 HG02129.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-33314_1276-33 others(54): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35233412 | ||||||
| chr14:35233490
|
A | G | 9 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-33237A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35233490 | ||||||
| chr14:35233499
|
C | T | 2 | a0001c0002t0001g0311a0001c0002t0001g0312 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1276-33228C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35233499 | ||||||
| chr14:35233508
|
C | T | 1 | a0001c0002t0001g0237 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1276-33219C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35233508 | ||||||
| chr14:35233651
|
A | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1276-33076A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35233651 | ||||||
| chr14:35233705
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1276-33022G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35233705 | ||||||
| chr14:35233717
|
T | G | 2 | a0001c0001t0003g0070a0001c0001t0003g0136 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1276-33010T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35233717 | ||||||
| chr14:35234129
|
A | G | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1276-32598A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35234129 | ||||||
| chr14:35234200
|
G | A | 1 | a0001c0001t0032g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1276-32527G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35234200 | ||||||
| chr14:35234295
|
G | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1276-32432G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35234295 | ||||||
| chr14:35234315
|
G | A | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1276-32412G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35234315 | ||||||
| chr14:35234428
|
G | A | 3 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0310 | 3 | HG00735.hp2 HG01255.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1276-32299G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35234428 | ||||||
| chr14:35234433
|
T | C | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-32294T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35234433 | ||||||
| chr14:35234633
|
T | C | 23 | a0001c0001t0001g0075a0001c0001t0001g0124a0001c0002t0001g0191others(20): Show | 23 | HG00099.hp1 HG00733.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1276-32094T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35234633 | ||||||
| chr14:35234648
|
CCTTT | C | 3 | a0001c0002t0003g0212a0001c0002t0003g0213a0001c0002t0003g0214 | 3 | HG01884.hp2 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1276-32073_1276-32 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35234648 | |||||
| chr14:35234657
|
C | T | 1 | a0001c0001t0021g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1276-32070C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35234657 | ||||||
| chr14:35234676
|
C | CT | 28 | a0001c0001t0001g0075a0001c0001t0003g0020a0001c0001t0003g0021others(25): Show | 28 | HG00735.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1276-32033dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35234676 | |||||
| chr14:35234676
|
C | CTT | 16 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(13): Show | 16 | HG00639.hp2 HG01346.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.1276-32034_1276-32 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35234676 | |||||
| chr14:35234676
|
CT | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(59): Show | 62 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1276-32033delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35234676 | |||||
| chr14:35234676
|
CTT | C | 11 | a0001c0001t0001g0002a0001c0001t0005g0009a0001c0001t0005g0012others(8): Show | 11 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1276-32034_1276-32 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35234676 | |||||
| chr14:35235111
|
T | G | 9 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-31616T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35235111 | ||||||
| chr14:35235274
|
C | T | 1 | a0001c0002t0003g0307 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1276-31453C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35235274 | ||||||
| chr14:35235275
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1276-31452G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35235275 | ||||||
| chr14:35235349
|
G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1276-31378G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35235349 | ||||||
| chr14:35235461
|
C | T | 68 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0106others(65): Show | 68 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1276-31266C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35235461 | ||||||
| chr14:35235599
|
C | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1276-31128C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35235599 | ||||||
| chr14:35235762
|
C | A | 1 | a0001c0001t0008g0016 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1276-30965C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35235762 | ||||||
| chr14:35235824
|
G | C | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276-30903G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35235824 | ||||||
| chr14:35235851
|
G | A | 68 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0106others(65): Show | 68 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1276-30876G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35235851 | ||||||
| chr14:35236038
|
T | C | 1 | a0001c0002t0017g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1276-30689T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35236038 | ||||||
| chr14:35236096
|
C | CA | 95 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0031others(92): Show | 95 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1276-30609dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35236096 | |||||
| chr14:35236096
|
C | CAA | 9 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0002t0001g0193others(6): Show | 9 | HG01261.hp2 HG03927.hp2 NA18978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-30610_1276-30 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35236096 | |||||
| chr14:35236096
|
CA | C | 36 | a0001c0001t0001g0058a0001c0001t0003g0017a0001c0001t0003g0018others(33): Show | 36 | HG00099.hp2 HG01081.hp1 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.1276-30609delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35236096 | |||||
| chr14:35236121
|
A | G | 15 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1276-30606A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35236121 | ||||||
| chr14:35236237
|
A | G | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1276-30490A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35236237 | ||||||
| chr14:35236271
|
A | T | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276-30456A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35236271 | ||||||
| chr14:35236520
|
C | T | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-30207C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35236520 | ||||||
| chr14:35236534
|
T | C | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-30193T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35236534 | ||||||
| chr14:35236554
|
A | G | 1 | a0001c0001t0038g0165 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1276-30173A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35236554 | ||||||
| chr14:35236641
|
C | A | 1 | a0001c0002t0001g0192 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1276-30086C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35236641 | ||||||
| chr14:35236929
|
CTCTT | C | 28 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0070others(25): Show | 28 | HG01081.hp1 HG01099.hp1 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.1276-29794_1276-29 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35236929 | |||||
| chr14:35237019
|
CTCCTTCT others(6): Show |
C | 2 | a0001c0001t0003g0070a0001c0001t0003g0136 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1276-29689_1276-29 others(19): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35237019 | |||||
| chr14:35237039
|
T | TCTTCCTT others(11): Show |
51 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(48): Show | 51 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1276-29669_1276-29 others(24): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35237039 | |||||
| chr14:35237062
|
C | T | 1 | a0001c0002t0001g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1276-29665C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35237062 | ||||||
| chr14:35237067
|
T | TTTCC | 4 | a0001c0001t0002g0087a0001c0001t0002g0108a0001c0001t0002g0122others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276-29644_1276-29 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35237067 | |||||
| chr14:35237084
|
T | TTC | 27 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1276-29627_1276-29 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35237084 | |||||
| chr14:35237096
|
C | G | 11 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(8): Show | 11 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1276-29631C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35237096 | ||||||
| chr14:35237213
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1276-29514A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35237213 | ||||||
| chr14:35237352
|
C | A | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1276-29375C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35237352 | ||||||
| chr14:35237375
|
C | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1276-29352C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35237375 | ||||||
| chr14:35237685
|
G | A | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1276-29042G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35237685 | ||||||
| chr14:35237751
|
C | T | 29 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0141others(26): Show | 29 | HG01081.hp1 HG01099.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1276-28976C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35237751 | ||||||
| chr14:35237819
|
A | AT | 18 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(15): Show | 18 | HG00735.hp2 HG01255.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1276-28900dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35237819 | |||||
| chr14:35237859
|
T | C | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1276-28868T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35237859 | ||||||
| chr14:35238070
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1276-28657A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35238070 | ||||||
| chr14:35238223
|
T | C | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-28504T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35238223 | ||||||
| chr14:35238268
|
C | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1276-28459C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35238268 | ||||||
| chr14:35238330
|
T | C | 1 | a0001c0002t0017g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1276-28397T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35238330 | ||||||
| chr14:35238468
|
A | G | 1 | a0001c0001t0021g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1276-28259A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35238468 | ||||||
| chr14:35238474
|
C | G | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1276-28253C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35238474 | ||||||
| chr14:35238733
|
G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1276-27994G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35238733 | ||||||
| chr14:35238733
|
G | C | 1 | a0001c0001t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1276-27994G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35238733 | ||||||
| chr14:35238873
|
G | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1276-27854G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35238873 | ||||||
| chr14:35238928
|
G | C | 2 | a0001c0001t0012g0168a0006c0008t0012g0143 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1276-27799G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35238928 | ||||||
| chr14:35239046
|
G | C | 1 | a0002c0003t0004g0287 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1276-27681G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35239046 | ||||||
| chr14:35239121
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1276-27606C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35239121 | ||||||
| chr14:35239131
|
G | A | 1 | a0001c0002t0001g0192 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1276-27596G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35239131 | ||||||
| chr14:35239307
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1276-27420C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35239307 | ||||||
| chr14:35239333
|
G | A | 4 | a0001c0001t0001g0106a0001c0002t0001g0240a0001c0002t0001g0257others(1): Show | 4 | HG00609.hp1 HG02129.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276-27394G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35239333 | ||||||
| chr14:35239350
|
G | GA | 7 | a0001c0001t0002g0062a0001c0001t0002g0113a0001c0001t0003g0083others(4): Show | 7 | HG02055.hp2 HG02602.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-27361dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35239350 | |||||
| chr14:35239364
|
A | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(153): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1276-27363A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35239364 | ||||||
| chr14:35239518
|
A | G | 3 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0200 | 3 | HG00733.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1276-27209A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35239518 | ||||||
| chr14:35239803
|
G | A | 27 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1276-26924G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35239803 | ||||||
| chr14:35239977
|
A | C | 1 | a0001c0001t0001g0029 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1276-26750A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35239977 | ||||||
| chr14:35240041
|
C | T | 15 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1276-26686C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240041 | ||||||
| chr14:35240062
|
A | G | 1 | a0001c0002t0001g0192 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1276-26665A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240062 | ||||||
| chr14:35240067
|
T | A | 27 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1276-26660T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240067 | ||||||
| chr14:35240074
|
C | CA | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1276-26637dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35240074 | |||||
| chr14:35240313
|
T | TTG | 57 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(54): Show | 57 | HG00735.hp2 HG01099.hp1 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.1276-26414_1276-26 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240313 | ||||||
| chr14:35240313
|
T | TTTG | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1276-26414_1276-26 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240313 | ||||||
| chr14:35240313
|
T | TTTTG | 34 | a0001c0001t0001g0027a0001c0001t0002g0277a0001c0001t0002g0281others(31): Show | 34 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.1276-26414_1276-26 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240313 | ||||||
| chr14:35240315
|
G | GT | 3 | a0001c0001t0003g0018a0001c0001t0009g0157a0001c0001t0009g0158 | 3 | HG01081.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1276-26409dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35240315 | |||||
| chr14:35240315
|
G | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1276-26412G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240315 | ||||||
| chr14:35240488
|
GGT | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(47): Show | 50 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1276-26236_1276-26 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35240488 | |||||
| chr14:35240517
|
A | G | 15 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(12): Show | 15 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1276-26210A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240517 | ||||||
| chr14:35240624
|
C | T | 16 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(13): Show | 16 | HG00735.hp2 HG01255.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1276-26103C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240624 | ||||||
| chr14:35240729
|
C | A | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1276-25998C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240729 | ||||||
| chr14:35240736
|
A | T | 4 | a0001c0002t0029g0210a0003c0005t0019g0166a0003c0007t0013g0139others(1): Show | 4 | HG01891.hp2 HG02818.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276-25991A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240736 | ||||||
| chr14:35240788
|
G | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1276-25939G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240788 | ||||||
| chr14:35240806
|
A | G | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-25921A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240806 | ||||||
| chr14:35240912
|
G | A | 1 | a0002c0003t0035g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1276-25815G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240912 | ||||||
| chr14:35240923
|
C | T | 1 | a0001c0001t0003g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1276-25804C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35240923 | ||||||
| chr14:35241310
|
A | C | 1 | a0001c0002t0031g0190 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1276-25417A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35241310 | ||||||
| chr14:35241319
|
A | G | 30 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0076others(27): Show | 30 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1276-25408A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35241319 | ||||||
| chr14:35241360
|
A | G | 1 | a0001c0001t0003g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1276-25367A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35241360 | ||||||
| chr14:35241377
|
CA | C | 20 | a0001c0001t0001g0077a0001c0001t0003g0020a0001c0001t0003g0021others(17): Show | 20 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1276-25337delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35241377 | |||||
| chr14:35241412
|
A | G | 4 | a0001c0002t0001g0204a0001c0002t0001g0206a0001c0002t0001g0208others(1): Show | 4 | HG01361.hp1 NA19001.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276-25315A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35241412 | ||||||
| chr14:35241626
|
C | T | 1 | a0001c0001t0002g0303 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1276-25101C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35241626 | ||||||
| chr14:35241696
|
C | T | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276-25031C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35241696 | ||||||
| chr14:35241742
|
C | T | 1 | a0001c0001t0005g0012 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1276-24985C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35241742 | ||||||
| chr14:35241852
|
G | C | 8 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0109others(5): Show | 8 | HG02083.hp2 HG02129.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-24875G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35241852 | ||||||
| chr14:35241991
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1276-24736G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35241991 | ||||||
| chr14:35242088
|
T | C | 4 | a0001c0002t0001g0219a0001c0002t0001g0221a0001c0002t0001g0261others(1): Show | 4 | NA18943.hp1 NA18999.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276-24639T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242088 | ||||||
| chr14:35242109
|
C | T | 1 | a0007c0011t0037g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1276-24618C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242109 | ||||||
| chr14:35242188
|
A | T | 19 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1276-24539A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242188 | ||||||
| chr14:35242201
|
T | G | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-24526T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242201 | ||||||
| chr14:35242293
|
G | A | 1 | a0001c0001t0006g0040 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1276-24434G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242293 | ||||||
| chr14:35242312
|
C | G | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-24415C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242312 | ||||||
| chr14:35242532
|
C | T | 1 | a0001c0001t0021g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1276-24195C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242532 | ||||||
| chr14:35242592
|
A | C | 27 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1276-24135A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242592 | ||||||
| chr14:35242674
|
A | G | 1 | a0002c0003t0016g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1276-24053A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242674 | ||||||
| chr14:35242698
|
A | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(155): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1276-24029A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242698 | ||||||
| chr14:35242722
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1276-24005A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242722 | ||||||
| chr14:35242765
|
G | T | 14 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(11): Show | 14 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1276-23962G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242765 | ||||||
| chr14:35242857
|
G | C | 1 | a0001c0001t0001g0106 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1276-23870G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242857 | ||||||
| chr14:35242911
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1276-23816T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35242911 | ||||||
| chr14:35243067
|
A | G | 1 | a0001c0001t0003g0136 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1276-23660A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243067 | ||||||
| chr14:35243341
|
A | G | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-23386A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243341 | ||||||
| chr14:35243379
|
T | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1276-23348T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243379 | ||||||
| chr14:35243450
|
G | A | 2 | a0001c0001t0002g0109a0004c0010t0002g0110 | 2 | HG02129.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1276-23277G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243450 | ||||||
| chr14:35243514
|
T | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1276-23213T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243514 | ||||||
| chr14:35243534
|
T | TA | 71 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0014others(68): Show | 72 | HG00438.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1276-23179dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35243534 | |||||
| chr14:35243540
|
A | G | 10 | a0001c0001t0003g0127a0001c0001t0003g0129a0001c0001t0003g0130others(7): Show | 10 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.1276-23187A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243540 | ||||||
| chr14:35243607
|
G | C | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-23120G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243607 | ||||||
| chr14:35243694
|
T | C | 6 | a0001c0001t0005g0156a0001c0002t0005g0182a0001c0002t0005g0183others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-23033T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243694 | ||||||
| chr14:35243707
|
G | A | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276-23020G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243707 | ||||||
| chr14:35243743
|
C | T | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1276-22984C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243743 | ||||||
| chr14:35243829
|
G | C | 1 | a0001c0001t0018g0174 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1276-22898G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243829 | ||||||
| chr14:35243997
|
C | A | 2 | a0001c0002t0001g0206a0001c0002t0026g0205 | 2 | HG01361.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1276-22730C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243997 | ||||||
| chr14:35243997
|
C | T | 3 | a0001c0001t0003g0162a0001c0001t0023g0161a0001c0002t0005g0186 | 3 | HG02257.hp2 HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1276-22730C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35243997 | ||||||
| chr14:35244132
|
A | G | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1276-22595A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35244132 | ||||||
| chr14:35244320
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1276-22407A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35244320 | ||||||
| chr14:35244446
|
C | CT | 6 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0046others(3): Show | 6 | HG00140.hp1 HG00738.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-22268dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35244446 | |||||
| chr14:35244516
|
G | A | 2 | a0001c0002t0001g0206a0001c0002t0026g0205 | 2 | HG01361.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1276-22211G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35244516 | ||||||
| chr14:35244626
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0056a0005c0009t0001g0034 | 3 | NA18968.hp2 NA18975.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1276-22101G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35244626 | ||||||
| chr14:35244642
|
G | A | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-22085G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35244642 | ||||||
| chr14:35244699
|
A | G | 1 | a0001c0002t0001g0240 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1276-22028A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35244699 | ||||||
| chr14:35244778
|
C | T | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-21949C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35244778 | ||||||
| chr14:35244922
|
G | GAGGAAGG others(4): Show |
157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(154): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1276-21802_1276-21 others(17): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35244922 | |||||
| chr14:35244931
|
G | A | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-21796G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35244931 | ||||||
| chr14:35244938
|
T | C | 1 | a0001c0001t0028g0035 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1276-21789T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35244938 | ||||||
| chr14:35245293
|
A | G | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1276-21434A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35245293 | ||||||
| chr14:35245408
|
C | T | 1 | a0001c0001t0003g0134 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1276-21319C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35245408 | ||||||
| chr14:35245553
|
G | A | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(154): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1276-21174G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35245553 | ||||||
| chr14:35245614
|
G | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1276-21113G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35245614 | ||||||
| chr14:35245810
|
G | A | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276-20917G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35245810 | ||||||
| chr14:35246031
|
G | C | 8 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0055others(5): Show | 8 | HG02056.hp1 NA18939.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-20696G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35246031 | ||||||
| chr14:35246095
|
A | G | 1 | a0001c0001t0003g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1276-20632A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35246095 | ||||||
| chr14:35246205
|
G | A | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(154): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1276-20522G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35246205 | ||||||
| chr14:35246239
|
T | C | 1 | a0002c0003t0004g0019 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1276-20488T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35246239 | ||||||
| chr14:35246380
|
G | C | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1276-20347G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35246380 | ||||||
| chr14:35246603
|
C | T | 25 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(22): Show | 25 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1276-20124C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35246603 | ||||||
| chr14:35246907
|
G | A | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-19820G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35246907 | ||||||
| chr14:35246926
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1276-19801C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35246926 | ||||||
| chr14:35246927
|
G | A | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1276-19800G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35246927 | ||||||
| chr14:35247207
|
G | A | 45 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0070others(42): Show | 45 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.1276-19520G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35247207 | ||||||
| chr14:35247522
|
C | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0049 | 2 | NA18957.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1276-19205C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35247522 | ||||||
| chr14:35247791
|
C | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0049 | 2 | NA18957.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1276-18936C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35247791 | ||||||
| chr14:35248076
|
C | T | 19 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1276-18651C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35248076 | ||||||
| chr14:35248108
|
GA | G | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-18618delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35248108 | ||||||
| chr14:35248236
|
C | G | 5 | a0001c0002t0001g0227a0001c0002t0001g0228a0001c0002t0001g0266others(2): Show | 5 | NA18957.hp2 NA18968.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276-18491C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35248236 | ||||||
| chr14:35248445
|
C | CTCATTTT others(6): Show |
1 | a0001c0002t0001g0255 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1276-18281_1276-18 others(19): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35248445 | |||||
| chr14:35248496
|
G | A | 2 | a0001c0001t0003g0145a0001c0001t0003g0146 | 2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1276-18231G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35248496 | ||||||
| chr14:35248520
|
C | A | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-18207C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35248520 | ||||||
| chr14:35248609
|
A | G | 19 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1276-18118A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35248609 | ||||||
| chr14:35248705
|
G | A | 19 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1276-18022G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35248705 | ||||||
| chr14:35248792
|
C | T | 2 | a0001c0001t0002g0290a0001c0001t0002g0291 | 2 | NA18941.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1276-17935C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35248792 | ||||||
| chr14:35248857
|
T | C | 15 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(12): Show | 15 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1276-17870T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35248857 | ||||||
| chr14:35248870
|
A | G | 25 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(22): Show | 25 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1276-17857A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35248870 | ||||||
| chr14:35248907
|
C | T | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1276-17820C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35248907 | ||||||
| chr14:35248974
|
T | C | 4 | a0002c0003t0004g0296a0002c0003t0004g0297a0002c0003t0004g0298others(1): Show | 4 | HG00735.hp1 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276-17753T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35248974 | ||||||
| chr14:35249301
|
G | A | 2 | a0001c0001t0003g0017a0001c0001t0003g0018 | 2 | HG01081.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1276-17426G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35249301 | ||||||
| chr14:35249401
|
A | G | 2 | a0001c0001t0003g0142a0001c0001t0003g0160 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1276-17326A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35249401 | ||||||
| chr14:35249552
|
G | T | 1 | a0001c0001t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1276-17175G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35249552 | ||||||
| chr14:35249956
|
C | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0027others(9): Show | 12 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1276-16771C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35249956 | ||||||
| chr14:35249990
|
G | A | 8 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0142others(5): Show | 8 | HG01081.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-16737G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35249990 | ||||||
| chr14:35250145
|
G | A | 4 | a0001c0002t0029g0210a0003c0005t0019g0166a0003c0007t0013g0139others(1): Show | 4 | HG01891.hp2 HG02818.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276-16582G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35250145 | ||||||
| chr14:35250188
|
C | T | 1 | a0001c0002t0001g0208 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1276-16539C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35250188 | ||||||
| chr14:35250492
|
A | C | 2 | a0001c0001t0009g0159a0001c0001t0009g0167 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1276-16235A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35250492 | ||||||
| chr14:35250494
|
C | A | 1 | a0001c0001t0001g0046 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1276-16233C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35250494 | ||||||
| chr14:35250502
|
G | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1276-16225G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35250502 | ||||||
| chr14:35250636
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1276-16091G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35250636 | ||||||
| chr14:35250696
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1276-16031G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35250696 | ||||||
| chr14:35250889
|
C | T | 1 | a0001c0002t0001g0258 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1276-15838C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35250889 | ||||||
| chr14:35250890
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1276-15837G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35250890 | ||||||
| chr14:35250925
|
G | T | 1 | a0001c0002t0001g0233 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1276-15802G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35250925 | ||||||
| chr14:35251121
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1276-15606T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35251121 | ||||||
| chr14:35251476
|
A | T | 1 | a0001c0002t0001g0209 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1276-15251A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35251476 | ||||||
| chr14:35251514
|
A | G | 86 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(83): Show | 86 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.1276-15213A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35251514 | ||||||
| chr14:35251539
|
G | A | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-15188G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35251539 | ||||||
| chr14:35251709
|
C | T | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-15018C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35251709 | ||||||
| chr14:35251776
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1276-14951G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35251776 | ||||||
| chr14:35252005
|
G | A | 25 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(22): Show | 25 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1276-14722G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35252005 | ||||||
| chr14:35252108
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | NA18971.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1276-14619G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35252108 | ||||||
| chr14:35252167
|
G | A | 7 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-14560G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35252167 | ||||||
| chr14:35252279
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1276-14448C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35252279 | ||||||
| chr14:35252374
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1276-14353G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35252374 | ||||||
| chr14:35252381
|
C | T | 2 | a0001c0002t0001g0218a0001c0002t0001g0253 | 2 | NA18981.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1276-14346C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35252381 | ||||||
| chr14:35252403
|
A | G | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276-14324A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35252403 | ||||||
| chr14:35252811
|
T | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1276-13916T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35252811 | ||||||
| chr14:35252872
|
A | G | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-13855A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35252872 | ||||||
| chr14:35253034
|
A | T | 1 | a0001c0001t0002g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1276-13693A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253034 | ||||||
| chr14:35253042
|
A | G | 1 | a0001c0001t0012g0168 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1276-13685A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253042 | ||||||
| chr14:35253275
|
A | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1276-13452A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253275 | ||||||
| chr14:35253331
|
CA | C | 14 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0075others(11): Show | 14 | HG02027.hp1 HG02027.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.1276-13383delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35253331 | |||||
| chr14:35253343
|
A | AAAGAG | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-13383_1276-13 others(11): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35253343 | |||||
| chr14:35253343
|
A | AG | 3 | a0003c0005t0019g0166a0003c0007t0013g0139a0003c0012t0013g0211 | 3 | HG02818.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1276-13384_1276-13 others(7): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253343 | ||||||
| chr14:35253343
|
A | G | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-13384A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253343 | ||||||
| chr14:35253343
|
AAGAG | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(45): Show | 48 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.1276-13372_1276-13 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35253343 | |||||
| chr14:35253355
|
G | A | 7 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0001t0021g0175others(4): Show | 7 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-13372G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253355 | ||||||
| chr14:35253355
|
GAGAA | G | 13 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(10): Show | 13 | HG00735.hp2 HG00738.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1276-13354_1276-13 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35253355 | |||||
| chr14:35253369
|
GAAAGAAA others(11): Show |
G | 1 | a0001c0002t0001g0255 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1276-13354_1276-13 others(24): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35253369 | |||||
| chr14:35253388
|
A | G | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-13339A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253388 | ||||||
| chr14:35253399
|
A | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(6): Show | 9 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-13328A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253399 | ||||||
| chr14:35253403
|
G | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(6): Show | 9 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-13324G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253403 | ||||||
| chr14:35253412
|
G | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(6): Show | 9 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-13315G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253412 | ||||||
| chr14:35253412
|
GA | G | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-13308delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35253412 | |||||
| chr14:35253415
|
A | AAAAG | 74 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(71): Show | 74 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.1276-13309_1276-13 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35253415 | |||||
| chr14:35253415
|
A | G | 9 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(6): Show | 9 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-13312A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253415 | ||||||
| chr14:35253432
|
GAAAC | G | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-13293_1276-13 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35253432 | |||||
| chr14:35253451
|
T | C | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-13276T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253451 | ||||||
| chr14:35253463
|
G | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1276-13264G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35253463 | ||||||
| chr14:35254043
|
G | A | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-12684G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254043 | ||||||
| chr14:35254053
|
TC | T | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-12673delC | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254053 | ||||||
| chr14:35254068
|
G | C | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-12659G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254068 | ||||||
| chr14:35254122
|
G | T | 1 | a0001c0001t0003g0022 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1276-12605G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254122 | ||||||
| chr14:35254209
|
A | G | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-12518A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254209 | ||||||
| chr14:35254253
|
T | A | 2 | a0001c0001t0006g0097a0001c0001t0006g0117 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1276-12474T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254253 | ||||||
| chr14:35254360
|
G | C | 85 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(82): Show | 85 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1276-12367G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254360 | ||||||
| chr14:35254377
|
G | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1276-12350G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254377 | ||||||
| chr14:35254496
|
G | A | 44 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0070others(41): Show | 44 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.1276-12231G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254496 | ||||||
| chr14:35254516
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1276-12211C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254516 | ||||||
| chr14:35254519
|
A | C | 1 | a0007c0011t0037g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1276-12208A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254519 | ||||||
| chr14:35254538
|
A | G | 2 | a0003c0005t0019g0166a0003c0007t0013g0139 | 2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1276-12189A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254538 | ||||||
| chr14:35254552
|
G | C | 4 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0198others(1): Show | 4 | HG00733.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276-12175G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254552 | ||||||
| chr14:35254579
|
A | G | 22 | a0001c0001t0003g0076a0001c0001t0003g0083a0001c0001t0003g0084others(19): Show | 22 | HG00639.hp2 HG01074.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.1276-12148A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254579 | ||||||
| chr14:35254592
|
A | C | 60 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(57): Show | 60 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.1276-12135A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254592 | ||||||
| chr14:35254593
|
T | C | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1276-12134T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254593 | ||||||
| chr14:35254670
|
G | A | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1276-12057G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254670 | ||||||
| chr14:35254762
|
T | C | 44 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0070others(41): Show | 44 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.1276-11965T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254762 | ||||||
| chr14:35254819
|
C | T | 1 | a0001c0001t0007g0176 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1276-11908C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254819 | ||||||
| chr14:35254820
|
C | G | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-11907C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254820 | ||||||
| chr14:35254881
|
A | G | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1276-11846A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254881 | ||||||
| chr14:35254939
|
A | G | 3 | a0001c0002t0003g0212a0001c0002t0003g0213a0001c0002t0003g0214 | 3 | HG01884.hp2 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1276-11788A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254939 | ||||||
| chr14:35254948
|
C | T | 1 | a0001c0001t0005g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1276-11779C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35254948 | ||||||
| chr14:35255284
|
C | T | 27 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0300others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1276-11443C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35255284 | ||||||
| chr14:35255350
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1276-11377G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35255350 | ||||||
| chr14:35255410
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1276-11317A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35255410 | ||||||
| chr14:35255433
|
A | G | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-11294A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35255433 | ||||||
| chr14:35255492
|
GTTC | G | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276-11229_1276-11 others(9): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35255492 | |||||
| chr14:35255573
|
T | C | 25 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(22): Show | 25 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1276-11154T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35255573 | ||||||
| chr14:35255700
|
G | A | 10 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 10 | HG01099.hp1 HG03654.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.1276-11027G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35255700 | ||||||
| chr14:35255722
|
G | A | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-11005G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35255722 | ||||||
| chr14:35255791
|
T | A | 60 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(57): Show | 60 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.1276-10936T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35255791 | ||||||
| chr14:35255888
|
T | C | 3 | a0001c0001t0002g0095a0001c0001t0002g0100a0001c0001t0002g0101 | 3 | HG01515.hp1 HG01517.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1276-10839T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35255888 | ||||||
| chr14:35255933
|
TCATTTAT others(4): Show |
T | 5 | a0001c0001t0001g0077a0001c0002t0001g0234a0001c0002t0001g0235others(2): Show | 5 | HG03453.hp2 NA18941.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276-10779_1276-10 others(17): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35255933 | |||||
| chr14:35256081
|
T | G | 1 | a0001c0002t0001g0270 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1276-10646T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256081 | ||||||
| chr14:35256145
|
G | A | 1 | a0001c0002t0003g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1276-10582G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256145 | ||||||
| chr14:35256155
|
G | A | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276-10572G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256155 | ||||||
| chr14:35256157
|
A | G | 52 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0070others(49): Show | 52 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.1276-10570A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256157 | ||||||
| chr14:35256177
|
G | A | 1 | a0001c0001t0002g0105 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1276-10550G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256177 | ||||||
| chr14:35256192
|
G | T | 1 | a0003c0005t0019g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1276-10535G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256192 | ||||||
| chr14:35256291
|
C | CA | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1276-10423dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35256291 | |||||
| chr14:35256322
|
G | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1276-10405G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256322 | ||||||
| chr14:35256326
|
C | CT | 59 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0002g0063others(56): Show | 59 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.1276-10378dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35256326 | |||||
| chr14:35256326
|
C | CTT | 26 | a0001c0001t0003g0076a0001c0001t0003g0082a0001c0001t0003g0083others(23): Show | 26 | HG00597.hp2 HG00733.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1276-10379_1276-10 others(8): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35256326 | |||||
| chr14:35256326
|
C | CTTTT | 7 | a0001c0001t0003g0020a0001c0001t0003g0069a0001c0001t0003g0177others(4): Show | 7 | HG00735.hp1 HG01496.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276-10381_1276-10 others(10): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35256326 | |||||
| chr14:35256350
|
A | T | 88 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(85): Show | 88 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.1276-10377A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256350 | ||||||
| chr14:35256450
|
G | A | 47 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(44): Show | 47 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1276-10277G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256450 | ||||||
| chr14:35256533
|
T | C | 2 | a0001c0002t0001g0239a0001c0002t0001g0247 | 2 | HG01993.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1276-10194T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256533 | ||||||
| chr14:35256534
|
G | T | 1 | a0001c0001t0001g0029 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1276-10193G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256534 | ||||||
| chr14:35256614
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071 | 3 | HG01496.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1276-10113G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256614 | ||||||
| chr14:35256683
|
T | G | 62 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(59): Show | 62 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.1276-10044T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256683 | ||||||
| chr14:35256701
|
T | C | 6 | a0001c0002t0003g0189a0001c0002t0003g0216a0001c0002t0003g0306others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-10026T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256701 | ||||||
| chr14:35256745
|
G | A | 2 | a0003c0005t0019g0166a0003c0007t0013g0139 | 2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1276-9982G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256745 | ||||||
| chr14:35256845
|
A | T | 12 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(9): Show | 12 | HG01099.hp1 HG01516.hp1 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.1276-9882A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256845 | ||||||
| chr14:35256869
|
CT | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1276-9844delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35256869 | |||||
| chr14:35256887
|
T | G | 22 | a0002c0003t0004g0019a0002c0003t0004g0039a0002c0003t0004g0279others(19): Show | 22 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1276-9840T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256887 | ||||||
| chr14:35256896
|
C | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1276-9831C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35256896 | ||||||
| chr14:35257018
|
G | A | 59 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(56): Show | 59 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.1276-9709G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35257018 | ||||||
| chr14:35257108
|
C | G | 3 | a0001c0001t0002g0087a0001c0001t0002g0108a0001c0001t0002g0122 | 3 | HG01167.hp1 HG01169.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1276-9619C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35257108 | ||||||
| chr14:35257399
|
C | T | 1 | a0001c0001t0003g0136 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1276-9328C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35257399 | ||||||
| chr14:35257405
|
T | C | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1276-9322T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35257405 | ||||||
| chr14:35257582
|
G | A | 8 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0109others(5): Show | 8 | HG02083.hp2 HG02129.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-9145G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35257582 | ||||||
| chr14:35257586
|
T | C | 3 | a0001c0002t0001g0248a0001c0002t0001g0254a0001c0002t0001g0268 | 3 | NA18950.hp1 NA18975.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1276-9141T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35257586 | ||||||
| chr14:35257601
|
A | G | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1276-9126A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35257601 | ||||||
| chr14:35257652
|
T | C | 3 | a0003c0005t0019g0166a0003c0007t0013g0139a0003c0012t0013g0211 | 3 | HG02818.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1276-9075T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35257652 | ||||||
| chr14:35257822
|
A | T | 5 | a0001c0001t0001g0091a0001c0001t0002g0074a0001c0001t0002g0090others(2): Show | 5 | HG00408.hp2 NA18941.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276-8905A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35257822 | ||||||
| chr14:35257839
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1276-8888C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35257839 | ||||||
| chr14:35257965
|
C | G | 2 | a0001c0001t0002g0118a0001c0001t0002g0120 | 2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1276-8762C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35257965 | ||||||
| chr14:35258055
|
T | TA | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-8658dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35258055 | |||||
| chr14:35258055
|
TA | T | 81 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(78): Show | 81 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1276-8658delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35258055 | |||||
| chr14:35258160
|
G | T | 85 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(82): Show | 85 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.1276-8567G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35258160 | ||||||
| chr14:35258380
|
G | A | 4 | a0003c0005t0019g0166a0003c0005t0020g0023a0003c0007t0013g0139others(1): Show | 4 | HG02818.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276-8347G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35258380 | ||||||
| chr14:35258383
|
G | A | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1276-8344G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35258383 | ||||||
| chr14:35258751
|
G | A | 1 | a0001c0002t0001g0255 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1276-7976G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35258751 | ||||||
| chr14:35258767
|
C | T | 20 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(17): Show | 20 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1276-7960C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35258767 | ||||||
| chr14:35258823
|
G | A | 20 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(17): Show | 20 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1276-7904G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35258823 | ||||||
| chr14:35258861
|
G | A | 11 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(8): Show | 11 | HG01099.hp1 HG03225.hp1 HG03654.hp1 others(8): Show |
intron_variant | MODIFIER | c.1276-7866G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35258861 | ||||||
| chr14:35258883
|
T | C | 3 | a0003c0005t0019g0166a0003c0007t0013g0139a0003c0012t0013g0211 | 3 | HG02818.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1276-7844T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35258883 | ||||||
| chr14:35258911
|
A | C | 1 | a0001c0002t0003g0212 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1276-7816A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35258911 | ||||||
| chr14:35259231
|
C | G | 12 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(9): Show | 12 | HG01099.hp1 HG01516.hp1 HG03225.hp1 others(9): Show |
intron_variant | MODIFIER | c.1276-7496C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35259231 | ||||||
| chr14:35259720
|
G | A | 4 | a0001c0002t0003g0306a0001c0002t0003g0307a0001c0002t0003g0308others(1): Show | 4 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276-7007G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35259720 | ||||||
| chr14:35259978
|
T | C | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276-6749T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35259978 | ||||||
| chr14:35259993
|
G | GT | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1276-6712dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35259993 | |||||
| chr14:35259993
|
G | GTT | 94 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0029others(91): Show | 94 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1276-6713_1276-671 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35259993 | |||||
| chr14:35259993
|
G | GTTT | 13 | a0001c0001t0001g0124a0001c0002t0001g0181a0001c0002t0001g0197others(10): Show | 13 | HG00741.hp2 HG01361.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1276-6714_1276-671 others(7): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35259993 | |||||
| chr14:35259993
|
GT | G | 7 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0002t0005g0182others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-6712delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35259993 | |||||
| chr14:35259995
|
T | TTG | 7 | a0001c0001t0003g0070a0001c0002t0003g0189a0001c0002t0003g0216others(4): Show | 7 | HG02258.hp1 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276-6731_1276-673 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35259995 | |||||
| chr14:35259999
|
T | G | 1 | a0001c0002t0003g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1276-6728T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35259999 | ||||||
| chr14:35260038
|
G | T | 1 | a0001c0001t0002g0122 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1276-6689G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35260038 | ||||||
| chr14:35260085
|
C | T | 61 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(58): Show | 61 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.1276-6642C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35260085 | ||||||
| chr14:35260179
|
T | A | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-6548T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35260179 | ||||||
| chr14:35260185
|
T | C | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1276-6542T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35260185 | ||||||
| chr14:35260197
|
G | A | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276-6530G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35260197 | ||||||
| chr14:35260377
|
A | G | 3 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022 | 3 | HG00738.hp1 HG01496.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1276-6350A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35260377 | ||||||
| chr14:35260475
|
T | C | 1 | a0001c0002t0029g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1276-6252T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35260475 | ||||||
| chr14:35260605
|
G | A | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-6122G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35260605 | ||||||
| chr14:35260617
|
A | G | 3 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022 | 3 | HG00738.hp1 HG01496.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1276-6110A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35260617 | ||||||
| chr14:35260663
|
T | C | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276-6064T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35260663 | ||||||
| chr14:35260892
|
G | T | 1 | a0001c0001t0032g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1276-5835G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35260892 | ||||||
| chr14:35261016
|
C | T | 1 | a0003c0012t0013g0211 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1276-5711C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35261016 | ||||||
| chr14:35261088
|
G | A | 1 | a0001c0002t0001g0233 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1276-5639G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35261088 | ||||||
| chr14:35261458
|
C | T | 7 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0008g0016others(4): Show | 7 | HG01081.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276-5269C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35261458 | ||||||
| chr14:35261497
|
A | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1276-5230A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35261497 | ||||||
| chr14:35261501
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1276-5226C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35261501 | ||||||
| chr14:35261593
|
G | T | 22 | a0002c0003t0004g0019a0002c0003t0004g0039a0002c0003t0004g0279others(19): Show | 22 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1276-5134G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35261593 | ||||||
| chr14:35261723
|
T | C | 86 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(83): Show | 86 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.1276-5004T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35261723 | ||||||
| chr14:35261747
|
C | T | 4 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(1): Show | 4 | HG02630.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276-4980C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35261747 | ||||||
| chr14:35261769
|
A | G | 1 | a0003c0005t0019g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1276-4958A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35261769 | ||||||
| chr14:35261826
|
G | C | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276-4901G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35261826 | ||||||
| chr14:35261962
|
A | C | 7 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0008g0016others(4): Show | 7 | HG01081.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276-4765A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35261962 | ||||||
| chr14:35262167
|
T | A | 2 | a0001c0001t0003g0070a0001c0001t0003g0136 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1276-4560T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35262167 | ||||||
| chr14:35262424
|
A | G | 3 | a0003c0005t0019g0166a0003c0007t0013g0139a0003c0012t0013g0211 | 3 | HG02818.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1276-4303A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35262424 | ||||||
| chr14:35262460
|
C | T | 1 | a0001c0006t0008g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276-4267C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35262460 | ||||||
| chr14:35262574
|
A | G | 1 | a0003c0005t0020g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1276-4153A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35262574 | ||||||
| chr14:35262583
|
G | A | 2 | a0001c0001t0003g0142a0001c0001t0003g0160 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1276-4144G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35262583 | ||||||
| chr14:35262762
|
A | C | 1 | a0001c0001t0001g0106 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1276-3965A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35262762 | ||||||
| chr14:35262766
|
C | T | 11 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(8): Show | 11 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1276-3961C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35262766 | ||||||
| chr14:35262864
|
T | C | 22 | a0002c0003t0004g0019a0002c0003t0004g0039a0002c0003t0004g0279others(19): Show | 22 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1276-3863T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35262864 | ||||||
| chr14:35263023
|
C | T | 1 | a0001c0001t0032g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1276-3704C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35263023 | ||||||
| chr14:35263163
|
G | A | 20 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(17): Show | 20 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1276-3564G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35263163 | ||||||
| chr14:35263191
|
C | T | 10 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(7): Show | 10 | HG01099.hp1 HG03654.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.1276-3536C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35263191 | ||||||
| chr14:35263489
|
C | T | 1 | a0001c0001t0003g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1276-3238C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35263489 | ||||||
| chr14:35263547
|
C | T | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1276-3180C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35263547 | ||||||
| chr14:35263549
|
TG | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1276-3175delG | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35263549 | |||||
| chr14:35263626
|
T | C | 1 | a0001c0001t0011g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1276-3101T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35263626 | ||||||
| chr14:35263685
|
C | A | 61 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(58): Show | 61 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.1276-3042C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35263685 | ||||||
| chr14:35263693
|
A | T | 1 | a0001c0001t0015g0144 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1276-3034A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35263693 | ||||||
| chr14:35263696
|
T | A | 2 | a0001c0002t0002g0224a0003c0005t0020g0023 | 2 | HG03834.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1276-3031T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35263696 | ||||||
| chr14:35263752
|
C | T | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-2975C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35263752 | ||||||
| chr14:35264177
|
G | A | 9 | a0001c0002t0001g0239a0001c0002t0001g0241a0001c0002t0001g0242others(6): Show | 9 | HG00741.hp2 HG01099.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1276-2550G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35264177 | ||||||
| chr14:35264274
|
T | C | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-2453T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35264274 | ||||||
| chr14:35264284
|
C | T | 1 | a0001c0001t0012g0168 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1276-2443C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35264284 | ||||||
| chr14:35264634
|
A | G | 1 | a0001c0001t0002g0079 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1276-2093A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35264634 | ||||||
| chr14:35264647
|
A | T | 5 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(2): Show | 5 | HG02630.hp2 HG03139.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276-2080A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35264647 | ||||||
| chr14:35264692
|
T | C | 4 | a0003c0005t0019g0166a0003c0005t0020g0023a0003c0007t0013g0139others(1): Show | 4 | HG02818.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276-2035T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35264692 | ||||||
| chr14:35264745
|
C | T | 4 | a0003c0005t0019g0166a0003c0005t0020g0023a0003c0007t0013g0139others(1): Show | 4 | HG02818.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276-1982C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35264745 | ||||||
| chr14:35264888
|
G | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1276-1839G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35264888 | ||||||
| chr14:35264983
|
C | T | 1 | a0001c0001t0011g0310 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1276-1744C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35264983 | ||||||
| chr14:35265388
|
G | A | 4 | a0003c0005t0019g0166a0003c0005t0020g0023a0003c0007t0013g0139others(1): Show | 4 | HG02818.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276-1339G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35265388 | ||||||
| chr14:35265389
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1276-1338C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35265389 | ||||||
| chr14:35265780
|
G | A | 11 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0003g0146others(8): Show | 11 | HG01099.hp1 HG03225.hp1 HG03654.hp1 others(8): Show |
intron_variant | MODIFIER | c.1276-947G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35265780 | ||||||
| chr14:35265938
|
C | G | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1276-789C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35265938 | ||||||
| chr14:35265956
|
T | G | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276-771T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35265956 | ||||||
| chr14:35265963
|
G | A | 1 | a0001c0002t0001g0250 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1276-764G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35265963 | ||||||
| chr14:35265986
|
G | A | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1276-741G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35265986 | ||||||
| chr14:35266013
|
C | CA | 33 | a0001c0001t0001g0072a0001c0001t0002g0099a0001c0001t0002g0102others(30): Show | 33 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.1276-695dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35266013 | |||||
| chr14:35266013
|
CA | C | 29 | a0001c0001t0001g0002a0001c0001t0003g0020a0001c0001t0003g0021others(26): Show | 29 | HG00738.hp1 HG01255.hp2 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.1276-695delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35266013 | |||||
| chr14:35266013
|
CAA | C | 54 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0070others(51): Show | 54 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1276-696_1276-695d others(4): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35266013 | |||||
| chr14:35266088
|
C | T | 9 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276-639C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35266088 | ||||||
| chr14:35266089
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0002g0281 | 2 | HG01981.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1276-638G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35266089 | ||||||
| chr14:35266176
|
C | G | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1276-551C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35266176 | ||||||
| chr14:35266186
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1276-541G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35266186 | ||||||
| chr14:35266242
|
A | G | 312 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1276-485A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35266242 | ||||||
| chr14:35266301
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0056others(1): Show | 4 | NA18968.hp2 NA18975.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276-426G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35266301 | ||||||
| chr14:35266317
|
CA | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(130): Show | 133 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.1276-392delA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 35266317 | |||||
| chr14:35266346
|
G | T | 20 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(17): Show | 20 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1276-381G>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35266346 | ||||||
| chr14:35266381
|
C | G | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1276-346C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35266381 | ||||||
| chr14:35266421
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0037others(3): Show | 6 | HG00609.hp2 HG02071.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276-306G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35266421 | ||||||
| chr14:35266574
|
A | C | 4 | a0001c0001t0003g0142a0001c0001t0003g0160a0001c0001t0003g0162others(1): Show | 4 | HG02630.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276-153A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 5/7 | chr14 | 35266574 | ||||||
| chr14:35266992
|
T | TA | 67 | a0001c0001t0001g0002a0001c0001t0003g0017a0001c0001t0003g0018others(64): Show | 67 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.1424+130dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr14 | 35266992 | |||||
| chr14:35266992
|
T | TAA | 21 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(18): Show | 21 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1424+129_1424+130d others(4): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr14 | 35266992 | |||||
| chr14:35267009
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1424+134T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35267009 | ||||||
| chr14:35267067
|
C | T | 9 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0109others(6): Show | 9 | HG02083.hp2 HG02109.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1424+192C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35267067 | ||||||
| chr14:35267486
|
G | A | 22 | a0002c0003t0004g0019a0002c0003t0004g0039a0002c0003t0004g0279others(19): Show | 22 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1424+611G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35267486 | ||||||
| chr14:35267697
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1424+822C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35267697 | ||||||
| chr14:35267776
|
A | G | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1424+901A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35267776 | ||||||
| chr14:35267807
|
C | T | 1 | a0001c0002t0001g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1424+932C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35267807 | ||||||
| chr14:35267829
|
A | G | 81 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(78): Show | 81 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.1424+954A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35267829 | ||||||
| chr14:35267978
|
G | A | 306 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1424+1103G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35267978 | ||||||
| chr14:35268155
|
C | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(48): Show | 51 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1424+1280C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35268155 | ||||||
| chr14:35268342
|
C | CA | 29 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0042others(26): Show | 29 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1424+1488dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr14 | 35268342 | |||||
| chr14:35268342
|
C | CAA | 53 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0069others(50): Show | 53 | HG00639.hp2 HG01074.hp1 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.1424+1487_1424+148 others(6): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr14 | 35268342 | |||||
| chr14:35268342
|
C | CAAA | 11 | a0001c0001t0003g0022a0001c0001t0003g0084a0001c0001t0003g0153others(8): Show | 11 | HG00738.hp1 HG01891.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1424+1486_1424+148 others(7): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr14 | 35268342 | |||||
| chr14:35268574
|
T | A | 4 | a0003c0005t0019g0166a0003c0005t0020g0023a0003c0007t0013g0139others(1): Show | 4 | HG02818.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1424+1699T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35268574 | ||||||
| chr14:35268667
|
C | T | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1425-1734C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35268667 | ||||||
| chr14:35268744
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1425-1657C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35268744 | ||||||
| chr14:35268780
|
G | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(52): Show | 55 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1425-1621G>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35268780 | ||||||
| chr14:35269028
|
G | A | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1425-1373G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35269028 | ||||||
| chr14:35269267
|
T | A | 1 | a0003c0007t0013g0139 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1425-1134T>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35269267 | ||||||
| chr14:35269357
|
T | C | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1425-1044T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35269357 | ||||||
| chr14:35269359
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1425-1042G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35269359 | ||||||
| chr14:35270052
|
A | G | 62 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(59): Show | 62 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.1425-349A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 6/7 | chr14 | 35270052 | ||||||
| chr14:35270697
|
C | G | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1620+101C>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35270697 | ||||||
| chr14:35270809
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1620+213C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35270809 | ||||||
| chr14:35270910
|
C | T | 1 | a0001c0001t0005g0009 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1620+314C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35270910 | ||||||
| chr14:35271043
|
C | T | 2 | a0001c0001t0006g0097a0001c0001t0006g0117 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1620+447C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271043 | ||||||
| chr14:35271082
|
G | A | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1620+486G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271082 | ||||||
| chr14:35271156
|
C | CT | 36 | a0001c0001t0001g0058a0001c0001t0002g0013a0001c0001t0002g0014others(33): Show | 36 | HG00735.hp2 HG01192.hp2 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.1620+580dupT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 35271156 | |||||
| chr14:35271156
|
C | CTT | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1620+579_1620+580d others(4): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 35271156 | |||||
| chr14:35271156
|
CT | C | 9 | a0001c0001t0003g0150a0001c0001t0006g0040a0001c0002t0001g0204others(6): Show | 9 | HG01256.hp1 HG02818.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1620+580delT | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 35271156 | |||||
| chr14:35271232
|
C | T | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1620+636C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271232 | ||||||
| chr14:35271287
|
TAGCTGGG others(6): Show |
T | 1 | a0001c0002t0001g0181 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1620+692_1620+704d others(15): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271287 | ||||||
| chr14:35271372
|
T | C | 6 | a0001c0001t0003g0082a0001c0001t0003g0086a0001c0002t0003g0004others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1620+776T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271372 | ||||||
| chr14:35271406
|
C | T | 4 | a0003c0005t0019g0166a0003c0005t0020g0023a0003c0007t0013g0139others(1): Show | 4 | HG02818.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1620+810C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271406 | ||||||
| chr14:35271452
|
C | T | 13 | a0001c0001t0001g0075a0001c0001t0003g0020a0001c0001t0003g0021others(10): Show | 13 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1620+856C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271452 | ||||||
| chr14:35271520
|
A | G | 1 | a0002c0003t0004g0282 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1620+924A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271520 | ||||||
| chr14:35271528
|
T | C | 1 | a0001c0002t0015g0305 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1620+932T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271528 | ||||||
| chr14:35271708
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1620+1112G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271708 | ||||||
| chr14:35271735
|
A | G | 82 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(79): Show | 82 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.1620+1139A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271735 | ||||||
| chr14:35271750
|
C | T | 3 | a0001c0001t0005g0009a0001c0001t0005g0012a0001c0001t0005g0024 | 3 | HG02723.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1620+1154C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271750 | ||||||
| chr14:35271838
|
A | C | 3 | a0003c0005t0019g0166a0003c0007t0013g0139a0003c0012t0013g0211 | 3 | HG02818.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1620+1242A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35271838 | ||||||
| chr14:35272001
|
G | A | 1 | a0001c0001t0009g0157 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1620+1405G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272001 | ||||||
| chr14:35272034
|
C | CA | 62 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(59): Show | 62 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.1621-1392dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 35272034 | |||||
| chr14:35272047
|
C | CA | 10 | a0001c0001t0002g0120a0001c0001t0005g0009a0001c0001t0005g0012others(7): Show | 10 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1621-1378dupA | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 35272047 | |||||
| chr14:35272057
|
A | C | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1621-1378A>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272057 | ||||||
| chr14:35272093
|
A | T | 1 | a0001c0001t0028g0035 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1621-1342A>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272093 | ||||||
| chr14:35272309
|
C | T | 11 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(8): Show | 11 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1621-1126C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272309 | ||||||
| chr14:35272348
|
C | T | 22 | a0002c0003t0004g0019a0002c0003t0004g0039a0002c0003t0004g0279others(19): Show | 22 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.1621-1087C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272348 | ||||||
| chr14:35272378
|
C | T | 7 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1621-1057C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272378 | ||||||
| chr14:35272379
|
G | A | 4 | a0003c0005t0019g0166a0003c0005t0020g0023a0003c0007t0013g0139others(1): Show | 4 | HG02818.hp1 HG02818.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621-1056G>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272379 | ||||||
| chr14:35272496
|
T | G | 2 | a0001c0002t0002g0223a0001c0002t0002g0224 | 2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1621-939T>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272496 | ||||||
| chr14:35272571
|
A | G | 1 | a0001c0001t0003g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1621-864A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272571 | ||||||
| chr14:35272651
|
A | G | 11 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(8): Show | 11 | HG00738.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1621-784A>G | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272651 | ||||||
| chr14:35272700
|
T | C | 1 | a0001c0001t0030g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1621-735T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272700 | ||||||
| chr14:35272842
|
C | T | 5 | a0001c0001t0003g0150a0001c0001t0003g0151a0001c0001t0003g0152others(2): Show | 5 | NA18943.hp2 NA18977.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1621-593C>T | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272842 | ||||||
| chr14:35272970
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1621-465T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35272970 | ||||||
| chr14:35273025
|
T | TTTG | 6 | a0001c0001t0007g0050a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621-395_1621-393d others(5): Show |
PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 35273025 | |||||
| chr14:35273267
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1621-168T>C | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35273267 | ||||||
| chr14:35273280
|
C | A | 13 | a0001c0001t0009g0157a0001c0001t0009g0158a0001c0001t0009g0159others(10): Show | 13 | HG00735.hp2 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1621-155C>A | PRORP | ENSG00000100890.16 | transcript | ENST00000534898.9 | protein_coding | 7/7 | chr14 | 35273280 |