Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6119 |
|---|---|
| ensemblid | ENSG00000106399.11 |
| hgncid | 10291 |
| symbol | RPA3 |
| name | replication protein A3 |
| refseq_nuc | NM_002947.5 |
| refseq_prot | NP_002938.1 |
| ensembl_nuc | ENST00000223129.8 |
| ensembl_prot | ENSP00000223129.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 7636518 |
| end | 7718607 |
| strand | - |
| ver | v1.2 |
| region | chr7:7636518-7718607 |
| region5000 | chr7:7631518-7723607 |
| regionname0 | RPA3_chr7_7636518_7718607 |
| regionname5000 | RPA3_chr7_7631518_7723607 |
| 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 | 121 | 308 | 86 | 60 | 112 | 8 | 40 | 84 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| 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 | 1/1 | 366 | 308 | 86 | 60 | 112 | 8 | 40 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| 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 | 1655 | 170 | 23 | 37 | 77 | 5 | 27 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0002 | 0/0 | 1655 | 28 | 17 | 3 | 5 | 0 | 3 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0003 | 0/0 | 1655 | 23 | 0 | 6 | 14 | 2 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0004 | 1/0 | 1655 | 21 | 3 | 8 | 4 | 0 | 5 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0005 | 0/0 | 1653 | 16 | 16 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0006 | 0/0 | 1655 | 6 | 6 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0007 | 0/0 | 1655 | 6 | 6 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0008 | 0/0 | 1653 | 5 | 5 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0009 | 0/0 | 1655 | 5 | 0 | 0 | 5 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0010 | 0/0 | 1655 | 4 | 0 | 0 | 3 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0011 | 0/0 | 1655 | 3 | 0 | 1 | 1 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0012 | 0/0 | 1655 | 3 | 3 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0013 | 0/0 | 1655 | 3 | 1 | 2 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0014 | 0/0 | 1655 | 2 | 1 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0015 | 0/0 | 1655 | 2 | 1 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0016 | 0/0 | 1655 | 2 | 0 | 0 | 0 | 0 | 2 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0017 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0018 | 0/0 | 1655 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0019 | 0/0 | 1655 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0020 | 0/0 | 1655 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0021 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0022 | 0/0 | 1655 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0023 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0024 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| t0025 | 0/0 | 1655 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| 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 | 3 | 3 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| 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 | 1/1 | 366 | 308 | 86 | 60 | 112 | 8 | 40 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2020 | 170 | 23 | 37 | 77 | 5 | 27 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0002 | 0/0 | 2020 | 28 | 17 | 3 | 5 | 0 | 3 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0003 | 0/0 | 2020 | 23 | 0 | 6 | 14 | 2 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0004 | 1/0 | 2020 | 21 | 3 | 8 | 4 | 0 | 5 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0005 | 0/0 | 2018 | 16 | 16 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0006 | 0/0 | 2020 | 6 | 6 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0007 | 0/0 | 2020 | 6 | 6 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0008 | 0/0 | 2018 | 5 | 5 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0009 | 0/0 | 2020 | 5 | 0 | 0 | 5 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0010 | 0/0 | 2020 | 4 | 0 | 0 | 3 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0011 | 0/0 | 2020 | 3 | 0 | 1 | 1 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0012 | 0/0 | 2020 | 3 | 3 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0013 | 0/0 | 2020 | 3 | 1 | 2 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0014 | 0/0 | 2020 | 2 | 1 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0015 | 0/0 | 2020 | 2 | 1 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0016 | 0/0 | 2020 | 2 | 0 | 0 | 0 | 0 | 2 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0017 | 0/0 | 2020 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0018 | 0/0 | 2020 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0019 | 0/0 | 2020 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0020 | 0/0 | 2020 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0021 | 0/0 | 2018 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0022 | 0/0 | 2020 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0023 | 0/0 | 2020 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0024 | 0/0 | 2020 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| a0001c0001t0025 | 0/0 | 2020 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | copy fasta | chr7 | 7631518 | 7723607 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0009g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0009g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0009g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0009g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0010g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0010g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0010g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0011g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0011g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0011g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0012g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0012g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0013g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0013g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0013g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0014g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0014g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0015g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0015g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0016g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0016g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0017g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0018g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0019g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0020g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0021g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0022g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0023g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0024g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| a0001c0001t0025g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | GBR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | GBR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0173 | EUR | FIN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00438 | hp1 | a0001 | c0001 | t0010 | g0155 | EAS | CHS | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00639 | hp2 | a0001 | c0001 | t0014 | g0211 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01106 | hp1 | a0001 | c0001 | t0011 | g0170 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01109 | hp1 | a0001 | c0001 | t0018 | g0292 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01243 | hp1 | a0001 | c0001 | t0015 | g0297 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0269 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0038 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0040 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01975 | hp1 | a0001 | c0001 | t0013 | g0127 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01993 | hp1 | a0001 | c0001 | t0013 | g0137 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02040 | hp1 | a0001 | c0001 | t0023 | g0167 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0233 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02071 | hp1 | a0001 | c0001 | t0024 | g0164 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02080 | hp1 | a0001 | c0001 | t0010 | g0125 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0169 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0260 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0290 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0209 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0099 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0242 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0148 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0060 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0171 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02647 | hp2 | a0001 | c0001 | t0022 | g0243 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02698 | hp1 | a0001 | c0001 | t0016 | g0152 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0296 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02735 | hp1 | a0001 | c0001 | t0011 | g0272 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0122 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0221 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02886 | hp1 | a0001 | c0001 | t0021 | g0251 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02895 | hp1 | a0001 | c0001 | t0012 | g0288 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02922 | hp2 | a0001 | c0001 | t0020 | g0246 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0182 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0236 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0123 | AFR | MSL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03195 | hp1 | a0001 | c0001 | t0015 | g0298 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03209 | hp2 | a0001 | c0001 | t0019 | g0299 | AFR | MSL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | MSL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0120 | AFR | MSL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03490 | hp2 | a0001 | c0001 | t0025 | g0036 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0258 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0030 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0206 | AFR | GWD | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | MSL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | MSL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0244 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | STU | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG04115 | hp2 | a0001 | c0001 | t0016 | g0104 | SAS | STU | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0225 | SAS | BEB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | STU | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0034 | SAS | STU | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0101 | AFR | YRI | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0291 | AFR | YRI | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | CHB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0187 | AFR | YRI | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18961 | hp2 | a0001 | c0001 | t0009 | g0051 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18963 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19000 | hp2 | a0001 | c0001 | t0009 | g0053 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19011 | hp2 | a0001 | c0001 | t0011 | g0279 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19012 | hp2 | a0001 | c0001 | t0010 | g0180 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0097 | AFR | LWK | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | LWK | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | LWK | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19085 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19086 | hp2 | a0001 | c0001 | t0017 | g0090 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19087 | hp1 | a0001 | c0001 | t0009 | g0052 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | YRI | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0144 | AFR | ASW | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0102 | AFR | ASW | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0065 | EUR | TSI | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0072 | EUR | TSI | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | GIH | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | GIH | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | CLM | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0293 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0200 | AFR | ACB | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0111 | AFR | USA | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | USA | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0082 | REF | REF | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0145 | REF | REF | RPA3_chr7_7631518_7723607 | RPA3 | chr7 | 7631518 | 7723607 |
| 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 |
|---|
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:7636550
|
T | C | 1 | a0001c0001t0008 | 5 | HG02055.hp2 HG02257.hp2 HG02559.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*450A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 8/8 | 450 | chr7 | 7636550 | |||||
| chr7:7636671
|
G | T | 2 | a0001c0001t0006a0001c0001t0022 | 7 | HG02622.hp2 HG02647.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*329C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 8/8 | 329 | chr7 | 7636671 | |||||
| chr7:7636712
|
G | A | 2 | a0001c0001t0003a0001c0001t0010 | 27 | HG00280.hp1 HG00438.hp1 HG01123.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*288C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 8/8 | 288 | chr7 | 7636712 | |||||
| chr7:7636720
|
G | A | 2 | a0001c0001t0008a0001c0001t0013 | 8 | HG01975.hp1 HG01993.hp1 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*280C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 8/8 | 280 | chr7 | 7636720 | |||||
| chr7:7636872
|
G | C | 3 | a0001c0001t0015a0001c0001t0018a0001c0001t0019 | 4 | HG01109.hp1 HG01243.hp1 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*128C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 8/8 | 128 | chr7 | 7636872 | |||||
| chr7:7640468
|
CTG | C | 3 | a0001c0001t0005a0001c0001t0008a0001c0001t0021 | 22 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-52_-51delCA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/8 | 51 | chr7 | 7640468 | |||||
| chr7:7640570
|
A | G | 1 | a0001c0001t0012 | 3 | HG02109.hp1 HG02895.hp1 NA18522.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-152T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/8 | chr7 | 7640570 | ||||||
| chr7:7640577
|
T | C | 1 | a0001c0001t0020 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-159A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/8 | 159 | chr7 | 7640577 | |||||
| chr7:7640624
|
G | A | 1 | a0001c0001t0023 | 1 | HG02040.hp1 | 5_prime_UTR_variant | MODIFIER | c.-206C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/8 | 206 | chr7 | 7640624 | |||||
| chr7:7640804
|
C | T | 2 | a0001c0001t0014a0001c0001t0021 | 3 | HG00639.hp2 HG02886.hp1 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-386G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/8 | 386 | chr7 | 7640804 | |||||
| chr7:7641001
|
G | T | 6 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(3): Show | 42 | HG00741.hp2 HG01081.hp1 HG01346.hp2 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-583C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/8 | 583 | chr7 | 7641001 | |||||
| chr7:7641064
|
G | A | 1 | a0001c0001t0007 | 6 | HG02257.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-646C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/8 | 646 | chr7 | 7641064 | |||||
| chr7:7641066
|
A | C | 3 | a0001c0001t0003a0001c0001t0011a0001c0001t0018 | 27 | HG00280.hp1 HG01106.hp1 HG01109.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-648T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/8 | 648 | chr7 | 7641066 | |||||
| chr7:7641162
|
T | G | 1 | a0001c0001t0016 | 2 | HG02698.hp1 HG04115.hp2 |
5_prime_UTR_variant | MODIFIER | c.-744A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/8 | 744 | chr7 | 7641162 | |||||
| chr7:7685885
|
G | A | 1 | a0001c0001t0024 | 1 | HG02071.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-813C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/8 | chr7 | 7685885 | ||||||
| chr7:7685954
|
C | G | 23 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
5_prime_UTR_variant | MODIFIER | c.-882G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/8 | 45536 | chr7 | 7685954 | |||||
| chr7:7687296
|
A | G | 1 | a0001c0001t0017 | 1 | NA19086.hp2 | 5_prime_UTR_variant | MODIFIER | c.-995T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 3/8 | 46878 | chr7 | 7687296 | |||||
| chr7:7715185
|
T | C | 1 | a0001c0001t0009 | 5 | NA18961.hp2 NA18963.hp1 NA19000.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-1038A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/8 | 74767 | chr7 | 7715185 | |||||
| chr7:7715185
|
T | G | 1 | a0001c0001t0025 | 1 | HG03490.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1038A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/8 | 74767 | chr7 | 7715185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:7637113
|
C | G | 5 | a0001c0001t0008g0200a0001c0001t0008g0233a0001c0001t0008g0236others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-31G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637113 | ||||||
| chr7:7637235
|
C | T | 1 | a0001c0001t0006g0122 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.284-153G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637235 | ||||||
| chr7:7637530
|
G | A | 3 | a0001c0001t0014g0123a0001c0001t0014g0211a0001c0001t0021g0251 | 3 | HG00639.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.283+334C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637530 | ||||||
| chr7:7637565
|
C | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG02717.hp1 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+299G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637565 | ||||||
| chr7:7637575
|
A | C | 1 | a0001c0001t0001g0058 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.283+289T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637575 | ||||||
| chr7:7637575
|
AACTGTTT others(146): Show |
A | 1 | a0001c0001t0003g0273 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.283+136_283+288del | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637575 | ||||||
| chr7:7637613
|
T | C | 2 | a0001c0001t0002g0007a0001c0001t0002g0092 | 2 | NA18985.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.283+251A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637613 | ||||||
| chr7:7637658
|
T | TAGTTATA others(24): Show |
5 | a0001c0001t0008g0200a0001c0001t0008g0233a0001c0001t0008g0236others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+175_283+205dup others(31): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637658 | ||||||
| chr7:7637658
|
T | TAGTTATA others(28): Show |
67 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0024others(64): Show | 68 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.283+171_283+205dup others(35): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637658 | ||||||
| chr7:7637658
|
T | TAGTTATA others(63): Show |
23 | a0001c0001t0001g0013a0001c0001t0001g0068a0001c0001t0001g0071others(20): Show | 23 | HG01243.hp1 HG01346.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.283+136_283+205dup others(70): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637658 | ||||||
| chr7:7637658
|
T | TAGTTATA others(98): Show |
10 | a0001c0001t0001g0095a0001c0001t0002g0007a0001c0001t0002g0087others(7): Show | 12 | HG01109.hp1 HG01346.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+101_283+205dup others(105): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637658 | ||||||
| chr7:7637658
|
T | TAGTTATA others(133): Show |
10 | a0001c0001t0001g0295a0001c0001t0002g0012a0001c0001t0005g0060others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+66_283+205dupG others(139): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637658 | ||||||
| chr7:7637658
|
TAGTTATA others(28): Show |
T | 1 | a0001c0001t0001g0257 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.283+171_283+205del others(35): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637658 | ||||||
| chr7:7637658
|
TAGTTATA others(63): Show |
T | 3 | a0001c0001t0014g0123a0001c0001t0014g0211a0001c0001t0021g0251 | 3 | HG00639.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.283+136_283+205del others(70): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637658 | ||||||
| chr7:7637703
|
A | AAACTGTA others(26): Show |
2 | a0001c0001t0001g0190a0001c0001t0001g0193 | 2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.283+128_283+160dup others(33): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637703 | ||||||
| chr7:7637730
|
G | A | 1 | a0001c0001t0003g0273 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.283+134C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637730 | ||||||
| chr7:7637731
|
T | A | 1 | a0001c0001t0003g0273 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.283+133A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637731 | ||||||
| chr7:7637768
|
A | T | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG02717.hp1 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+96T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 7/7 | chr7 | 7637768 | ||||||
| chr7:7637981
|
C | A | 1 | a0001c0001t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.175-9G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7637981 | ||||||
| chr7:7638017
|
A | C | 1 | a0001c0001t0001g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.175-45T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638017 | ||||||
| chr7:7638025
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.175-53T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638025 | ||||||
| chr7:7638126
|
C | T | 125 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(122): Show | 128 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.175-154G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638126 | ||||||
| chr7:7638165
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.175-193G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638165 | ||||||
| chr7:7638178
|
C | T | 248 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0013others(245): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.175-206G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638178 | ||||||
| chr7:7638225
|
C | T | 1 | a0001c0001t0006g0122 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.175-253G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638225 | ||||||
| chr7:7638236
|
G | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0283 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.175-264C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638236 | ||||||
| chr7:7638264
|
CTA | C | 27 | a0001c0001t0003g0006a0001c0001t0003g0062a0001c0001t0003g0072others(24): Show | 28 | HG00280.hp1 HG00438.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.175-294_175-293del others(2): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638264 | ||||||
| chr7:7638268
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.175-296C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638268 | ||||||
| chr7:7638345
|
C | G | 1 | a0001c0001t0005g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.175-373G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638345 | ||||||
| chr7:7638541
|
AAAAAC | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0067others(32): Show | 36 | HG00733.hp2 HG00741.hp2 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.174+524_174+528del others(5): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638541 | ||||||
| chr7:7638541
|
AAAAACAA others(3): Show |
A | 104 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0023others(101): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.174+519_174+528del others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638541 | ||||||
| chr7:7638541
|
AAAAACAA others(8): Show |
A | 1 | a0001c0001t0006g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.174+514_174+528del others(15): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638541 | ||||||
| chr7:7638655
|
G | C | 1 | a0001c0001t0001g0021 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.174+415C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638655 | ||||||
| chr7:7638912
|
TGA | T | 11 | a0001c0001t0001g0096a0001c0001t0002g0007a0001c0001t0002g0012others(8): Show | 11 | HG01346.hp2 HG02132.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+156_174+157del others(2): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638912 | ||||||
| chr7:7638959
|
C | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0147others(4): Show | 8 | HG00735.hp2 HG00741.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+111G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7638959 | ||||||
| chr7:7639038
|
T | C | 3 | a0001c0001t0014g0123a0001c0001t0014g0211a0001c0001t0021g0251 | 3 | HG00639.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.174+32A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7639038 | ||||||
| chr7:7639042
|
T | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG02717.hp1 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+28A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 6/7 | chr7 | 7639042 | ||||||
| chr7:7639333
|
AT | A | 300 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(297): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.100-190delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/7 | chr7 | 7639333 | ||||||
| chr7:7639476
|
A | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(31): Show | 35 | HG00733.hp2 HG00741.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.100-332T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/7 | chr7 | 7639476 | ||||||
| chr7:7639688
|
C | G | 3 | a0001c0001t0014g0123a0001c0001t0014g0211a0001c0001t0021g0251 | 3 | HG00639.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.100-544G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/7 | chr7 | 7639688 | ||||||
| chr7:7639833
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.99+487G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/7 | chr7 | 7639833 | ||||||
| chr7:7639867
|
C | G | 5 | a0001c0001t0002g0106a0001c0001t0002g0219a0001c0001t0002g0220others(2): Show | 5 | HG02818.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+453G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/7 | chr7 | 7639867 | ||||||
| chr7:7639885
|
A | T | 1 | a0001c0001t0024g0164 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.99+435T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/7 | chr7 | 7639885 | ||||||
| chr7:7640013
|
A | G | 39 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0024others(36): Show | 39 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.99+307T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/7 | chr7 | 7640013 | ||||||
| chr7:7640185
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.99+135T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/7 | chr7 | 7640185 | ||||||
| chr7:7640214
|
G | A | 19 | a0001c0001t0001g0071a0001c0001t0001g0218a0001c0001t0002g0011others(16): Show | 19 | HG01346.hp1 HG02055.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+106C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/7 | chr7 | 7640214 | ||||||
| chr7:7640252
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.99+68G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/7 | chr7 | 7640252 | ||||||
| chr7:7640254
|
G | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0018others(28): Show | 33 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.99+66C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/7 | chr7 | 7640254 | ||||||
| chr7:7640316
|
A | G | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.99+4T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 5/7 | chr7 | 7640316 | ||||||
| chr7:7641232
|
C | G | 1 | a0001c0001t0001g0129 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-757-57G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641232 | ||||||
| chr7:7641311
|
A | G | 1 | a0001c0001t0021g0251 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-757-136T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641311 | ||||||
| chr7:7641317
|
G | A | 151 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0014others(148): Show | 153 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-757-142C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641317 | ||||||
| chr7:7641340
|
G | T | 14 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0068others(11): Show | 14 | HG00140.hp2 HG00639.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.-757-165C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641340 | ||||||
| chr7:7641361
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0005g0099others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-757-186C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641361 | ||||||
| chr7:7641389
|
C | T | 111 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(108): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-757-214G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641389 | ||||||
| chr7:7641480
|
T | C | 1 | a0001c0001t0005g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-757-305A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641480 | ||||||
| chr7:7641500
|
A | G | 40 | a0001c0001t0001g0071a0001c0001t0001g0134a0001c0001t0001g0241others(37): Show | 40 | HG00741.hp2 HG01081.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.-757-325T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641500 | ||||||
| chr7:7641573
|
G | C | 2 | a0001c0001t0002g0009a0001c0001t0002g0011 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-757-398C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641573 | ||||||
| chr7:7641604
|
G | C | 3 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102 | 3 | HG02572.hp1 HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-757-429C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641604 | ||||||
| chr7:7641657
|
C | A | 30 | a0001c0001t0001g0071a0001c0001t0001g0241a0001c0001t0002g0009others(27): Show | 30 | HG01081.hp1 HG01346.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-757-482G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641657 | ||||||
| chr7:7641683
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-757-508C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641683 | ||||||
| chr7:7641945
|
G | A | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(170): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-757-770C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7641945 | ||||||
| chr7:7642019
|
G | C | 20 | a0001c0001t0001g0241a0001c0001t0002g0217a0001c0001t0002g0234others(17): Show | 20 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-757-844C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642019 | ||||||
| chr7:7642064
|
T | C | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(114): Show | 120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-757-889A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642064 | ||||||
| chr7:7642167
|
C | G | 127 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(124): Show | 129 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(126): Show |
intron_variant | MODIFIER | c.-757-992G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642167 | ||||||
| chr7:7642269
|
GGAC | G | 87 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(84): Show | 89 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.-757-1097_-757-109 others(7): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642269 | ||||||
| chr7:7642307
|
A | AT | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(111): Show | 117 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-757-1133dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642307 | ||||||
| chr7:7642307
|
A | T | 1 | a0001c0001t0001g0154 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-757-1132T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642307 | ||||||
| chr7:7642460
|
G | A | 22 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0066others(19): Show | 22 | HG01081.hp2 HG01109.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-757-1285C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642460 | ||||||
| chr7:7642467
|
T | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0157others(5): Show | 9 | HG00673.hp2 HG02135.hp1 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.-757-1292A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642467 | ||||||
| chr7:7642469
|
AT | A | 137 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(134): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-757-1295delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642469 | ||||||
| chr7:7642469
|
ATT | A | 112 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(109): Show | 114 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(111): Show |
intron_variant | MODIFIER | c.-757-1296_-757-129 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642469 | ||||||
| chr7:7642469
|
ATTT | A | 10 | a0001c0001t0001g0061a0001c0001t0001g0114a0001c0001t0001g0115others(7): Show | 10 | HG01243.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-757-1297_-757-129 others(7): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642469 | ||||||
| chr7:7642483
|
TA | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0157others(5): Show | 9 | HG00673.hp2 HG02135.hp1 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.-757-1309delT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642483 | ||||||
| chr7:7642544
|
C | T | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(114): Show | 120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-757-1369G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642544 | ||||||
| chr7:7642808
|
G | T | 24 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0003g0062others(21): Show | 24 | HG00140.hp2 HG00639.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.-757-1633C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642808 | ||||||
| chr7:7642959
|
C | T | 36 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0066others(33): Show | 36 | HG00741.hp2 HG01081.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-757-1784G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7642959 | ||||||
| chr7:7643004
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0018g0292 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-757-1829C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643004 | ||||||
| chr7:7643066
|
C | A | 10 | a0001c0001t0001g0061a0001c0001t0001g0114a0001c0001t0001g0115others(7): Show | 10 | HG01243.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-757-1891G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643066 | ||||||
| chr7:7643233
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-757-2058A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643233 | ||||||
| chr7:7643324
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-757-2149G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643324 | ||||||
| chr7:7643677
|
A | G | 1 | a0001c0001t0017g0090 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-757-2502T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643677 | ||||||
| chr7:7643691
|
C | G | 1 | a0001c0001t0018g0292 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-757-2516G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643691 | ||||||
| chr7:7643715
|
AAAAAAAA others(13): Show |
A | 4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(1): Show | 4 | HG01175.hp2 HG01255.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-757-2560_-757-254 others(24): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643715 | ||||||
| chr7:7643716
|
AAAAAAAA others(12): Show |
A | 112 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(109): Show | 115 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.-757-2560_-757-254 others(23): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643716 | ||||||
| chr7:7643717
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0008g0260 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-757-2559_-757-254 others(21): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643717 | ||||||
| chr7:7643717
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0008 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-757-2560_-757-254 others(22): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643717 | ||||||
| chr7:7643718
|
AAAAAAAA others(10): Show |
A | 95 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0061others(92): Show | 97 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.-757-2560_-757-254 others(21): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643718 | ||||||
| chr7:7643719
|
AAAAAAAC others(9): Show |
A | 17 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0068others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-757-2560_-757-254 others(20): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643719 | ||||||
| chr7:7643720
|
AAAAAACA others(8): Show |
A | 11 | a0001c0001t0001g0085a0001c0001t0002g0007a0001c0001t0002g0012others(8): Show | 11 | HG00741.hp2 HG02132.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-757-2560_-757-254 others(19): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643720 | ||||||
| chr7:7643735
|
G | C | 1 | a0001c0001t0008g0260 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-757-2560C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643735 | ||||||
| chr7:7643745
|
G | A | 3 | a0001c0001t0001g0239a0001c0001t0005g0291a0001c0001t0018g0292 | 3 | HG01109.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-757-2570C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643745 | ||||||
| chr7:7643753
|
G | T | 241 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(238): Show | 246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-757-2578C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643753 | ||||||
| chr7:7643764
|
A | T | 241 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(238): Show | 246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-757-2589T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643764 | ||||||
| chr7:7643798
|
C | T | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(170): Show | 176 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.-757-2623G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643798 | ||||||
| chr7:7643861
|
T | G | 85 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(82): Show | 85 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.-757-2686A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643861 | ||||||
| chr7:7643873
|
C | G | 1 | a0001c0001t0001g0119 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-757-2698G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643873 | ||||||
| chr7:7643927
|
C | T | 30 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.-757-2752G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643927 | ||||||
| chr7:7643979
|
C | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-757-2804G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7643979 | ||||||
| chr7:7644119
|
C | G | 84 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(81): Show | 84 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.-757-2944G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7644119 | ||||||
| chr7:7644287
|
G | A | 1 | a0001c0001t0002g0007 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-757-3112C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7644287 | ||||||
| chr7:7644354
|
C | CT | 8 | a0001c0001t0001g0103a0001c0001t0001g0183a0001c0001t0001g0184others(5): Show | 8 | HG00673.hp1 HG02109.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-757-3180dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7644354 | ||||||
| chr7:7644354
|
C | CTT | 76 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(73): Show | 76 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.-757-3181_-757-318 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7644354 | ||||||
| chr7:7644489
|
T | C | 22 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0068others(19): Show | 22 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-757-3314A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7644489 | ||||||
| chr7:7644639
|
G | A | 202 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(199): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-757-3464C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7644639 | ||||||
| chr7:7644674
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-757-3499C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7644674 | ||||||
| chr7:7644917
|
C | G | 202 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(199): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-757-3742G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7644917 | ||||||
| chr7:7644958
|
T | C | 1 | a0001c0001t0004g0043 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-757-3783A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7644958 | ||||||
| chr7:7645081
|
G | A | 7 | a0001c0001t0001g0058a0001c0001t0005g0055a0001c0001t0005g0056others(4): Show | 7 | HG02486.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-757-3906C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7645081 | ||||||
| chr7:7645155
|
A | G | 4 | a0001c0001t0001g0061a0001c0001t0005g0099a0001c0001t0005g0100others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-757-3980T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7645155 | ||||||
| chr7:7645426
|
G | C | 72 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0064others(69): Show | 74 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.-757-4251C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7645426 | ||||||
| chr7:7645537
|
C | A | 1 | a0001c0001t0012g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-757-4362G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7645537 | ||||||
| chr7:7645537
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-757-4362G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7645537 | ||||||
| chr7:7645545
|
G | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-757-4370C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7645545 | ||||||
| chr7:7645657
|
C | T | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(185): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-757-4482G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7645657 | ||||||
| chr7:7645798
|
G | A | 1 | a0001c0001t0012g0288 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-757-4623C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7645798 | ||||||
| chr7:7645817
|
A | AT | 86 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0071others(83): Show | 86 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.-757-4643dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7645817 | ||||||
| chr7:7645817
|
A | ATT | 22 | a0001c0001t0001g0241a0001c0001t0001g0286a0001c0001t0001g0287others(19): Show | 22 | HG01081.hp1 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-757-4644_-757-464 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7645817 | ||||||
| chr7:7645982
|
G | A | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(114): Show | 120 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-757-4807C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7645982 | ||||||
| chr7:7646177
|
C | T | 25 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0002g0093others(22): Show | 25 | HG00140.hp2 HG00639.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-757-5002G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646177 | ||||||
| chr7:7646237
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-757-5062T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646237 | ||||||
| chr7:7646258
|
T | C | 3 | a0001c0001t0007g0209a0001c0001t0014g0123a0001c0001t0014g0211 | 3 | HG00639.hp2 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-757-5083A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646258 | ||||||
| chr7:7646307
|
G | GT | 202 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(199): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-757-5133_-757-513 others(5): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646307 | ||||||
| chr7:7646390
|
A | T | 14 | a0001c0001t0001g0061a0001c0001t0001g0114a0001c0001t0001g0115others(11): Show | 16 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-757-5215T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646390 | ||||||
| chr7:7646400
|
T | G | 1 | a0001c0001t0002g0253 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-757-5225A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646400 | ||||||
| chr7:7646480
|
A | AT | 44 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(41): Show | 44 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.-757-5306dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646480 | ||||||
| chr7:7646480
|
AT | A | 13 | a0001c0001t0001g0071a0001c0001t0001g0103a0001c0001t0001g0239others(10): Show | 13 | HG00639.hp2 HG01109.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.-757-5306delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646480 | ||||||
| chr7:7646480
|
ATT | A | 7 | a0001c0001t0001g0070a0001c0001t0001g0142a0001c0001t0001g0185others(4): Show | 7 | HG00741.hp2 HG01081.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-757-5307_-757-530 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646480 | ||||||
| chr7:7646480
|
ATTT | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0037others(47): Show | 52 | HG00280.hp1 HG01123.hp1 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.-757-5308_-757-530 others(7): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646480 | ||||||
| chr7:7646480
|
ATTTT | A | 124 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(121): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-757-5309_-757-530 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646480 | ||||||
| chr7:7646480
|
ATTTTT | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0208a0001c0001t0001g0295others(5): Show | 10 | HG01069.hp2 HG02486.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-757-5310_-757-530 others(9): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646480 | ||||||
| chr7:7646515
|
G | T | 2 | a0001c0001t0002g0009a0001c0001t0002g0011 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-757-5340C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646515 | ||||||
| chr7:7646529
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-757-5354T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646529 | ||||||
| chr7:7646534
|
G | A | 14 | a0001c0001t0001g0061a0001c0001t0001g0114a0001c0001t0001g0115others(11): Show | 16 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-757-5359C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646534 | ||||||
| chr7:7646661
|
A | T | 1 | a0001c0001t0001g0203 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-757-5486T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646661 | ||||||
| chr7:7646748
|
C | G | 4 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0002g0252others(1): Show | 4 | HG01081.hp1 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-757-5573G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646748 | ||||||
| chr7:7646883
|
G | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(53): Show | 56 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.-757-5708C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646883 | ||||||
| chr7:7646968
|
G | C | 16 | a0001c0001t0001g0061a0001c0001t0001g0114a0001c0001t0001g0115others(13): Show | 18 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-757-5793C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646968 | ||||||
| chr7:7646998
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-757-5823G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7646998 | ||||||
| chr7:7647066
|
A | G | 16 | a0001c0001t0001g0061a0001c0001t0001g0114a0001c0001t0001g0115others(13): Show | 18 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-757-5891T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7647066 | ||||||
| chr7:7647098
|
G | C | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-757-5923C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7647098 | ||||||
| chr7:7647178
|
T | A | 1 | a0001c0001t0001g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-757-6003A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7647178 | ||||||
| chr7:7647320
|
A | C | 7 | a0001c0001t0001g0058a0001c0001t0005g0055a0001c0001t0005g0056others(4): Show | 7 | HG02486.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-757-6145T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7647320 | ||||||
| chr7:7647386
|
G | C | 216 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(213): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-757-6211C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7647386 | ||||||
| chr7:7647681
|
C | G | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-757-6506G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7647681 | ||||||
| chr7:7647708
|
A | G | 3 | a0001c0001t0001g0239a0001c0001t0005g0291a0001c0001t0018g0292 | 3 | HG01109.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-757-6533T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7647708 | ||||||
| chr7:7647814
|
A | G | 5 | a0001c0001t0002g0217a0001c0001t0002g0234a0001c0001t0002g0235others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-757-6639T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7647814 | ||||||
| chr7:7647957
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-757-6782A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7647957 | ||||||
| chr7:7647982
|
C | T | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(212): Show | 220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-757-6807G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7647982 | ||||||
| chr7:7647988
|
G | T | 250 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(247): Show | 255 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.-757-6813C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7647988 | ||||||
| chr7:7647989
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-757-6814A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7647989 | ||||||
| chr7:7648028
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-757-6853A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648028 | ||||||
| chr7:7648118
|
C | G | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(212): Show | 220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-757-6943G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648118 | ||||||
| chr7:7648139
|
C | A | 1 | a0001c0001t0001g0005 | 2 | NA18957.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-757-6964G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648139 | ||||||
| chr7:7648162
|
T | C | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(212): Show | 220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-757-6987A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648162 | ||||||
| chr7:7648165
|
C | T | 1 | a0001c0001t0005g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-757-6990G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648165 | ||||||
| chr7:7648169
|
C | G | 7 | a0001c0001t0001g0058a0001c0001t0005g0055a0001c0001t0005g0056others(4): Show | 7 | HG02486.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-757-6994G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648169 | ||||||
| chr7:7648195
|
T | G | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(212): Show | 220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-757-7020A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648195 | ||||||
| chr7:7648209
|
G | A | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(116): Show | 122 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-757-7034C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648209 | ||||||
| chr7:7648392
|
C | T | 80 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0071others(77): Show | 80 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.-757-7217G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648392 | ||||||
| chr7:7648640
|
C | G | 8 | a0001c0001t0001g0140a0001c0001t0001g0183a0001c0001t0001g0184others(5): Show | 8 | HG00544.hp1 HG00673.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.-757-7465G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648640 | ||||||
| chr7:7648718
|
G | T | 1 | a0001c0001t0018g0292 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-757-7543C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648718 | ||||||
| chr7:7648727
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-757-7552G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648727 | ||||||
| chr7:7648731
|
T | C | 12 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(9): Show | 12 | HG01109.hp2 HG01175.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.-757-7556A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648731 | ||||||
| chr7:7648885
|
G | A | 8 | a0001c0001t0001g0058a0001c0001t0002g0217a0001c0001t0005g0055others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-757-7710C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648885 | ||||||
| chr7:7648886
|
C | T | 215 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(212): Show | 220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-757-7711G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648886 | ||||||
| chr7:7648912
|
A | G | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(116): Show | 122 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-757-7737T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7648912 | ||||||
| chr7:7649022
|
G | C | 3 | a0001c0001t0001g0239a0001c0001t0005g0291a0001c0001t0018g0292 | 3 | HG01109.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-757-7847C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649022 | ||||||
| chr7:7649136
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-757-7961G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649136 | ||||||
| chr7:7649139
|
C | A | 52 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0096others(49): Show | 52 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.-757-7964G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649139 | ||||||
| chr7:7649142
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-757-7967C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649142 | ||||||
| chr7:7649158
|
C | CA | 12 | a0001c0001t0001g0058a0001c0001t0002g0007a0001c0001t0002g0092others(9): Show | 12 | HG00733.hp2 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-757-7984dupT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649158 | ||||||
| chr7:7649158
|
C | CAA | 24 | a0001c0001t0001g0218a0001c0001t0002g0093a0001c0001t0003g0062others(21): Show | 24 | HG01106.hp1 HG01123.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.-757-7985_-757-798 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649158 | ||||||
| chr7:7649175
|
A | AAAG | 8 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0077others(5): Show | 9 | HG03831.hp1 HG03831.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.-757-8001_-757-800 others(7): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649175 | ||||||
| chr7:7649175
|
A | AAG | 114 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(111): Show | 115 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.-757-8001_-757-800 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649175 | ||||||
| chr7:7649175
|
A | AG | 91 | a0001c0001t0001g0008a0001c0001t0001g0061a0001c0001t0001g0096others(88): Show | 94 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.-757-8001_-757-800 others(5): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649175 | ||||||
| chr7:7649175
|
A | G | 16 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(13): Show | 16 | HG01109.hp2 HG01175.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.-757-8000T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649175 | ||||||
| chr7:7649328
|
G | C | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-757-8153C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649328 | ||||||
| chr7:7649351
|
G | A | 3 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0258 | 3 | HG02735.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-757-8176C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649351 | ||||||
| chr7:7649520
|
C | T | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(211): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-757-8345G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649520 | ||||||
| chr7:7649522
|
G | A | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(116): Show | 122 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-757-8347C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649522 | ||||||
| chr7:7649539
|
G | A | 25 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0002g0093others(22): Show | 25 | HG00140.hp2 HG00639.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-757-8364C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649539 | ||||||
| chr7:7649543
|
G | T | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(211): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-757-8368C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649543 | ||||||
| chr7:7649682
|
G | T | 1 | a0001c0001t0013g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-757-8507C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649682 | ||||||
| chr7:7649686
|
GT | G | 120 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(117): Show | 123 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.-757-8512delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649686 | ||||||
| chr7:7649687
|
T | G | 94 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0061others(91): Show | 96 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.-757-8512A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649687 | ||||||
| chr7:7649694
|
G | C | 209 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(206): Show | 214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.-757-8519C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649694 | ||||||
| chr7:7649736
|
TTG | T | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(211): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-757-8563_-757-856 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649736 | ||||||
| chr7:7649740
|
C | A | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(211): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-757-8565G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649740 | ||||||
| chr7:7649815
|
C | G | 1 | a0001c0001t0001g0183 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-757-8640G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649815 | ||||||
| chr7:7649891
|
G | A | 8 | a0001c0001t0001g0058a0001c0001t0002g0217a0001c0001t0005g0055others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-757-8716C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7649891 | ||||||
| chr7:7650200
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-757-9025T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650200 | ||||||
| chr7:7650271
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0248 | 2 | HG02040.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-757-9096T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650271 | ||||||
| chr7:7650288
|
T | G | 26 | a0001c0001t0001g0054a0001c0001t0001g0064a0001c0001t0001g0066others(23): Show | 26 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.-757-9113A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650288 | ||||||
| chr7:7650350
|
C | T | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(211): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-757-9175G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650350 | ||||||
| chr7:7650418
|
C | T | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-757-9243G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650418 | ||||||
| chr7:7650448
|
C | G | 8 | a0001c0001t0001g0058a0001c0001t0002g0217a0001c0001t0005g0055others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-757-9273G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650448 | ||||||
| chr7:7650522
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0070a0001c0001t0001g0142others(1): Show | 5 | HG01081.hp2 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-757-9347C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650522 | ||||||
| chr7:7650553
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-757-9378T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650553 | ||||||
| chr7:7650576
|
A | C | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(116): Show | 122 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-757-9401T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650576 | ||||||
| chr7:7650700
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-757-9525G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650700 | ||||||
| chr7:7650717
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-757-9542T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650717 | ||||||
| chr7:7650736
|
C | T | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(116): Show | 122 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-757-9561G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650736 | ||||||
| chr7:7650793
|
C | T | 12 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(9): Show | 12 | HG01109.hp2 HG01175.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.-757-9618G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7650793 | ||||||
| chr7:7651015
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-757-9840C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7651015 | ||||||
| chr7:7651202
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-757-10027A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7651202 | ||||||
| chr7:7651225
|
G | T | 5 | a0001c0001t0001g0124a0001c0001t0001g0161a0001c0001t0001g0188others(2): Show | 5 | HG01261.hp2 HG01358.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-757-10050C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7651225 | ||||||
| chr7:7651304
|
T | A | 23 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0241others(20): Show | 23 | HG01081.hp1 HG01346.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-757-10129A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7651304 | ||||||
| chr7:7651461
|
C | T | 25 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0002g0093others(22): Show | 25 | HG00140.hp2 HG00639.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-757-10286G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7651461 | ||||||
| chr7:7651464
|
T | C | 5 | a0001c0001t0007g0010a0001c0001t0007g0169a0001c0001t0007g0171others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-757-10289A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7651464 | ||||||
| chr7:7651488
|
C | T | 1 | a0001c0001t0004g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-757-10313G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7651488 | ||||||
| chr7:7651545
|
C | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(115): Show | 121 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-757-10370G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7651545 | ||||||
| chr7:7651588
|
A | C | 3 | a0001c0001t0001g0239a0001c0001t0005g0291a0001c0001t0018g0292 | 3 | HG01109.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-757-10413T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7651588 | ||||||
| chr7:7651787
|
T | A | 3 | a0001c0001t0002g0238a0001c0001t0002g0240a0001c0001t0002g0253 | 3 | HG02615.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-757-10612A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7651787 | ||||||
| chr7:7651931
|
C | A | 3 | a0001c0001t0002g0093a0001c0001t0003g0072a0001c0001t0003g0073 | 3 | HG01168.hp2 HG01346.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-757-10756G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7651931 | ||||||
| chr7:7651962
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-757-10787G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7651962 | ||||||
| chr7:7652109
|
G | A | 2 | a0001c0001t0002g0252a0001c0001t0021g0251 | 2 | HG01081.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-757-10934C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7652109 | ||||||
| chr7:7652115
|
G | T | 2 | a0001c0001t0002g0252a0001c0001t0021g0251 | 2 | HG01081.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-757-10940C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7652115 | ||||||
| chr7:7652246
|
G | T | 239 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(236): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-757-11071C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7652246 | ||||||
| chr7:7652335
|
C | G | 14 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(11): Show | 14 | HG00280.hp2 HG00323.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-757-11160G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7652335 | ||||||
| chr7:7652467
|
C | G | 2 | a0001c0001t0001g0239a0001c0001t0005g0291 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-757-11292G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7652467 | ||||||
| chr7:7652503
|
T | G | 2 | a0001c0001t0002g0252a0001c0001t0021g0251 | 2 | HG01081.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-757-11328A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7652503 | ||||||
| chr7:7652591
|
G | A | 3 | a0001c0001t0002g0093a0001c0001t0003g0072a0001c0001t0003g0073 | 3 | HG01168.hp2 HG01346.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-757-11416C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7652591 | ||||||
| chr7:7652809
|
C | G | 280 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(277): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-757-11634G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7652809 | ||||||
| chr7:7652821
|
T | G | 1 | a0001c0001t0001g0082 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-757-11646A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7652821 | ||||||
| chr7:7652852
|
G | T | 135 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(132): Show | 138 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-757-11677C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7652852 | ||||||
| chr7:7652915
|
C | T | 8 | a0001c0001t0001g0058a0001c0001t0002g0217a0001c0001t0005g0055others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-757-11740G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7652915 | ||||||
| chr7:7653078
|
T | A | 12 | a0001c0001t0001g0085a0001c0001t0001g0218a0001c0001t0002g0007others(9): Show | 12 | HG00741.hp2 HG02132.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-757-11903A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7653078 | ||||||
| chr7:7653136
|
T | C | 25 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0002g0093others(22): Show | 25 | HG00140.hp2 HG00639.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-757-11961A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7653136 | ||||||
| chr7:7653145
|
G | T | 1 | a0001c0001t0001g0257 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-757-11970C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7653145 | ||||||
| chr7:7653422
|
A | C | 14 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(11): Show | 14 | HG00280.hp2 HG00323.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-757-12247T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7653422 | ||||||
| chr7:7653505
|
C | CA | 16 | a0001c0001t0001g0085a0001c0001t0001g0103a0001c0001t0001g0218others(13): Show | 16 | HG00741.hp2 HG02109.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.-757-12331dupT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7653505 | ||||||
| chr7:7653570
|
C | A | 1 | a0001c0001t0005g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-757-12395G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7653570 | ||||||
| chr7:7653577
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-757-12402T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7653577 | ||||||
| chr7:7653585
|
G | A | 1 | a0001c0001t0005g0289 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-757-12410C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7653585 | ||||||
| chr7:7653614
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01891.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-757-12439G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7653614 | ||||||
| chr7:7653659
|
G | T | 1 | a0001c0001t0001g0105 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-757-12484C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7653659 | ||||||
| chr7:7653777
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-757-12602A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7653777 | ||||||
| chr7:7653858
|
G | T | 25 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0002g0093others(22): Show | 25 | HG00140.hp2 HG00639.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-757-12683C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7653858 | ||||||
| chr7:7654140
|
A | C | 24 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0002g0093others(21): Show | 24 | HG00140.hp2 HG00639.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.-757-12965T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654140 | ||||||
| chr7:7654184
|
A | T | 1 | a0001c0001t0001g0015 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-757-13009T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654184 | ||||||
| chr7:7654288
|
A | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(61): Show | 64 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.-757-13113T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654288 | ||||||
| chr7:7654312
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-757-13137A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654312 | ||||||
| chr7:7654332
|
A | G | 1 | a0001c0001t0004g0046 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-757-13157T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654332 | ||||||
| chr7:7654382
|
G | T | 2 | a0001c0001t0002g0098a0001c0001t0018g0292 | 2 | HG01109.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-757-13207C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654382 | ||||||
| chr7:7654424
|
C | G | 3 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102 | 3 | HG02572.hp1 HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-757-13249G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654424 | ||||||
| chr7:7654706
|
C | A | 12 | a0001c0001t0001g0058a0001c0001t0001g0295a0001c0001t0002g0217others(9): Show | 14 | HG02486.hp1 HG02486.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-757-13531G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654706 | ||||||
| chr7:7654902
|
C | CA | 200 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(197): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.-757-13728dupT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654902 | ||||||
| chr7:7654902
|
C | CAA | 6 | a0001c0001t0001g0239a0001c0001t0001g0285a0001c0001t0002g0098others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.-757-13729_-757-13 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654902 | ||||||
| chr7:7654902
|
CA | C | 47 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(44): Show | 47 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.-757-13728delT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654902 | ||||||
| chr7:7654945
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-757-13770C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654945 | ||||||
| chr7:7654962
|
C | G | 8 | a0001c0001t0001g0058a0001c0001t0002g0217a0001c0001t0005g0055others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-757-13787G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7654962 | ||||||
| chr7:7655010
|
C | G | 2 | a0001c0001t0004g0038a0001c0001t0004g0049 | 2 | HG01261.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-757-13835G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7655010 | ||||||
| chr7:7655097
|
C | G | 24 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0002g0093others(21): Show | 24 | HG00140.hp2 HG00639.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.-757-13922G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7655097 | ||||||
| chr7:7655224
|
G | A | 4 | a0001c0001t0001g0103a0001c0001t0001g0283a0001c0001t0012g0101others(1): Show | 4 | HG02109.hp1 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-757-14049C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7655224 | ||||||
| chr7:7655314
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-757-14139G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7655314 | ||||||
| chr7:7655396
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-757-14221T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7655396 | ||||||
| chr7:7655552
|
T | C | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(137): Show | 143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.-757-14377A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7655552 | ||||||
| chr7:7655618
|
A | G | 4 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0113others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-757-14443T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7655618 | ||||||
| chr7:7655819
|
G | GTC | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(136): Show | 142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-757-14646_-757-14 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7655819 | ||||||
| chr7:7655837
|
C | T | 8 | a0001c0001t0001g0058a0001c0001t0002g0217a0001c0001t0005g0055others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-757-14662G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7655837 | ||||||
| chr7:7655875
|
C | T | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-757-14700G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7655875 | ||||||
| chr7:7656023
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | NA18968.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-757-14848G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656023 | ||||||
| chr7:7656078
|
G | A | 6 | a0001c0001t0001g0214a0001c0001t0006g0120a0001c0001t0006g0144others(3): Show | 6 | HG02622.hp2 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-757-14903C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656078 | ||||||
| chr7:7656127
|
G | A | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-757-14952C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656127 | ||||||
| chr7:7656203
|
G | A | 2 | a0001c0001t0002g0088a0001c0001t0002g0091 | 2 | HG02132.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.-757-15028C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656203 | ||||||
| chr7:7656218
|
G | T | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-757-15043C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656218 | ||||||
| chr7:7656307
|
T | A | 3 | a0001c0001t0008g0200a0001c0001t0008g0233a0001c0001t0008g0236 | 3 | HG02055.hp2 HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-757-15132A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656307 | ||||||
| chr7:7656314
|
A | T | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(218): Show | 224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.-757-15139T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656314 | ||||||
| chr7:7656331
|
T | G | 27 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-757-15156A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656331 | ||||||
| chr7:7656339
|
A | T | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(189): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-757-15164T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656339 | ||||||
| chr7:7656370
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-757-15195C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656370 | ||||||
| chr7:7656384
|
G | A | 4 | a0001c0001t0001g0239a0001c0001t0002g0098a0001c0001t0005g0291others(1): Show | 4 | HG01109.hp1 HG01891.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-757-15209C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656384 | ||||||
| chr7:7656451
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-757-15276A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656451 | ||||||
| chr7:7656479
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-757-15304T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656479 | ||||||
| chr7:7656483
|
C | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(119): Show | 125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-757-15308G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656483 | ||||||
| chr7:7656706
|
C | T | 1 | a0001c0001t0002g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-757-15531G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656706 | ||||||
| chr7:7656749
|
G | A | 161 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(158): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-757-15574C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656749 | ||||||
| chr7:7656760
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-757-15585A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656760 | ||||||
| chr7:7656806
|
T | A | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-757-15631A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656806 | ||||||
| chr7:7656929
|
C | T | 2 | a0001c0001t0002g0252a0001c0001t0021g0251 | 2 | HG01081.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-757-15754G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656929 | ||||||
| chr7:7656937
|
T | G | 25 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.-757-15762A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7656937 | ||||||
| chr7:7657024
|
T | G | 25 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.-757-15849A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7657024 | ||||||
| chr7:7657182
|
G | T | 1 | a0001c0001t0001g0202 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-757-16007C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7657182 | ||||||
| chr7:7657263
|
GC | G | 148 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(145): Show | 151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-757-16089delG | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7657263 | ||||||
| chr7:7657352
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-757-16177C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7657352 | ||||||
| chr7:7657549
|
A | G | 148 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(145): Show | 151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-757-16374T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7657549 | ||||||
| chr7:7657692
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-757-16517G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7657692 | ||||||
| chr7:7657704
|
G | A | 21 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0003g0062others(18): Show | 21 | HG00140.hp2 HG00639.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-757-16529C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7657704 | ||||||
| chr7:7657722
|
G | A | 3 | a0001c0001t0002g0252a0001c0001t0012g0288a0001c0001t0021g0251 | 3 | HG01081.hp1 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-757-16547C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7657722 | ||||||
| chr7:7657742
|
G | T | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-757-16567C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7657742 | ||||||
| chr7:7657824
|
A | G | 4 | a0001c0001t0001g0103a0001c0001t0001g0283a0001c0001t0012g0101others(1): Show | 4 | HG02109.hp1 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-757-16649T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7657824 | ||||||
| chr7:7657887
|
G | A | 49 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.-757-16712C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7657887 | ||||||
| chr7:7658096
|
C | A | 49 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(46): Show | 49 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.-757-16921G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658096 | ||||||
| chr7:7658116
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-757-16941T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658116 | ||||||
| chr7:7658119
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-757-16944T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658119 | ||||||
| chr7:7658172
|
A | C | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-757-16997T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658172 | ||||||
| chr7:7658172
|
A | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA18946.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-757-16997T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658172 | ||||||
| chr7:7658178
|
T | C | 8 | a0001c0001t0001g0058a0001c0001t0002g0217a0001c0001t0005g0055others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-757-17003A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658178 | ||||||
| chr7:7658377
|
T | A | 21 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0003g0062others(18): Show | 21 | HG00140.hp2 HG00639.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-757-17202A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658377 | ||||||
| chr7:7658495
|
A | T | 15 | a0001c0001t0001g0008a0001c0001t0001g0131a0001c0001t0001g0143others(12): Show | 15 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-757-17320T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658495 | ||||||
| chr7:7658538
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-757-17363G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658538 | ||||||
| chr7:7658701
|
G | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-757-17526C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658701 | ||||||
| chr7:7658783
|
G | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0131a0001c0001t0001g0143others(12): Show | 15 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-757-17608C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658783 | ||||||
| chr7:7658785
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-757-17610T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658785 | ||||||
| chr7:7658800
|
C | T | 21 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0003g0062others(18): Show | 21 | HG00140.hp2 HG00639.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-757-17625G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658800 | ||||||
| chr7:7658913
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-757-17738A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658913 | ||||||
| chr7:7658914
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-757-17739C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658914 | ||||||
| chr7:7658926
|
A | G | 2 | a0001c0001t0001g0283a0001c0001t0012g0101 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-757-17751T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7658926 | ||||||
| chr7:7659009
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-757-17834G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7659009 | ||||||
| chr7:7659148
|
A | T | 1 | a0001c0001t0021g0251 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-757-17973T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7659148 | ||||||
| chr7:7659168
|
T | A | 24 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 24 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.-757-17993A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7659168 | ||||||
| chr7:7659245
|
A | T | 1 | a0001c0001t0016g0152 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-757-18070T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7659245 | ||||||
| chr7:7659302
|
C | A | 24 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 24 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.-757-18127G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7659302 | ||||||
| chr7:7659311
|
T | C | 281 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(278): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-757-18136A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7659311 | ||||||
| chr7:7659404
|
C | A | 1 | a0001c0001t0003g0062 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-757-18229G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7659404 | ||||||
| chr7:7659405
|
G | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0020 | 2 | NA18999.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-757-18230C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7659405 | ||||||
| chr7:7659502
|
A | G | 281 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(278): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-757-18327T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7659502 | ||||||
| chr7:7659877
|
A | G | 4 | a0001c0001t0001g0103a0001c0001t0001g0283a0001c0001t0012g0101others(1): Show | 4 | HG02109.hp1 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-757-18702T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7659877 | ||||||
| chr7:7659923
|
T | G | 1 | a0001c0001t0003g0245 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-757-18748A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7659923 | ||||||
| chr7:7659937
|
A | C | 21 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0003g0062others(18): Show | 21 | HG00140.hp2 HG00639.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-757-18762T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7659937 | ||||||
| chr7:7660090
|
A | C | 2 | a0001c0001t0004g0038a0001c0001t0004g0049 | 2 | HG01261.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-757-18915T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7660090 | ||||||
| chr7:7660418
|
A | G | 1 | a0001c0001t0005g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-757-19243T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7660418 | ||||||
| chr7:7660448
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-757-19273G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7660448 | ||||||
| chr7:7660449
|
C | G | 21 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(18): Show | 21 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-757-19274G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7660449 | ||||||
| chr7:7660535
|
G | C | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-757-19360C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7660535 | ||||||
| chr7:7660756
|
GGTGAATC others(10): Show |
G | 21 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0003g0062others(18): Show | 21 | HG00140.hp2 HG00639.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-757-19598_-757-19 others(23): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7660756 | ||||||
| chr7:7660812
|
G | T | 1 | a0001c0001t0001g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-757-19637C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7660812 | ||||||
| chr7:7660910
|
C | G | 2 | a0001c0001t0001g0230a0001c0001t0023g0167 | 2 | HG02040.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-757-19735G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7660910 | ||||||
| chr7:7661009
|
GT | G | 259 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(256): Show | 264 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.-757-19835delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7661009 | ||||||
| chr7:7661226
|
T | C | 15 | a0001c0001t0001g0008a0001c0001t0001g0131a0001c0001t0001g0143others(12): Show | 15 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-757-20051A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7661226 | ||||||
| chr7:7661314
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-757-20139G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7661314 | ||||||
| chr7:7661409
|
C | T | 4 | a0001c0001t0001g0239a0001c0001t0002g0098a0001c0001t0005g0291others(1): Show | 4 | HG01109.hp1 HG01891.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-757-20234G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7661409 | ||||||
| chr7:7661666
|
C | T | 27 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-757-20491G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7661666 | ||||||
| chr7:7661726
|
C | G | 42 | a0001c0001t0001g0008a0001c0001t0001g0064a0001c0001t0001g0066others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.-757-20551G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7661726 | ||||||
| chr7:7661728
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-757-20553T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7661728 | ||||||
| chr7:7661901
|
A | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0131a0001c0001t0001g0143others(12): Show | 15 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-757-20726T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7661901 | ||||||
| chr7:7661937
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-757-20762G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7661937 | ||||||
| chr7:7661957
|
T | C | 15 | a0001c0001t0001g0008a0001c0001t0001g0131a0001c0001t0001g0143others(12): Show | 15 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-757-20782A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7661957 | ||||||
| chr7:7661989
|
T | C | 6 | a0001c0001t0001g0241a0001c0001t0008g0200a0001c0001t0008g0233others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-757-20814A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7661989 | ||||||
| chr7:7662045
|
G | A | 3 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0258 | 3 | HG02735.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-757-20870C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662045 | ||||||
| chr7:7662145
|
C | G | 82 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.-757-20970G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662145 | ||||||
| chr7:7662160
|
C | G | 151 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(148): Show | 154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.-757-20985G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662160 | ||||||
| chr7:7662181
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-757-21006C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662181 | ||||||
| chr7:7662203
|
T | C | 97 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(94): Show | 99 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.-757-21028A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662203 | ||||||
| chr7:7662335
|
C | T | 1 | a0001c0001t0010g0155 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-757-21160G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662335 | ||||||
| chr7:7662389
|
A | G | 281 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(278): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-757-21214T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662389 | ||||||
| chr7:7662436
|
G | C | 281 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(278): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-757-21261C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662436 | ||||||
| chr7:7662448
|
G | T | 1 | a0001c0001t0004g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-757-21273C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662448 | ||||||
| chr7:7662499
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-757-21324C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662499 | ||||||
| chr7:7662515
|
A | G | 16 | a0001c0001t0001g0014a0001c0001t0001g0112a0001c0001t0001g0117others(13): Show | 16 | HG00323.hp1 HG00438.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.-757-21340T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662515 | ||||||
| chr7:7662531
|
C | G | 26 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 26 | HG00544.hp2 HG02004.hp2 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-757-21356G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662531 | ||||||
| chr7:7662593
|
C | G | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-757-21418G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662593 | ||||||
| chr7:7662644
|
C | A | 30 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(27): Show | 30 | HG00140.hp2 HG00639.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.-757-21469G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662644 | ||||||
| chr7:7662676
|
C | T | 3 | a0001c0001t0005g0055a0001c0001t0005g0056a0001c0001t0005g0057 | 3 | HG02486.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-757-21501G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662676 | ||||||
| chr7:7662824
|
T | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0258 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-757-21649A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662824 | ||||||
| chr7:7662825
|
G | A | 227 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(224): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-757-21650C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662825 | ||||||
| chr7:7662848
|
A | C | 227 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(224): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-757-21673T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662848 | ||||||
| chr7:7662932
|
A | G | 32 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(29): Show | 35 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.-757-21757T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7662932 | ||||||
| chr7:7663013
|
GC | G | 194 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(191): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-757-21839delG | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663013 | ||||||
| chr7:7663019
|
T | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0247 | 2 | NA18989.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.-757-21844A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663019 | ||||||
| chr7:7663116
|
T | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(34): Show | 40 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.-757-21941A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663116 | ||||||
| chr7:7663182
|
T | TA | 32 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(29): Show | 33 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-757-22008dupT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663182 | ||||||
| chr7:7663182
|
T | TAA | 183 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(180): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.-757-22009_-757-22 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663182 | ||||||
| chr7:7663258
|
A | T | 182 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(179): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.-757-22083T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663258 | ||||||
| chr7:7663298
|
C | CTTTGTTT others(3): Show |
168 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(165): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-757-22124_-757-22 others(16): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663298 | ||||||
| chr7:7663298
|
C | G | 20 | a0001c0001t0001g0268a0001c0001t0001g0270a0001c0001t0001g0271others(17): Show | 20 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-757-22123G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663298 | ||||||
| chr7:7663356
|
A | ATGCT | 188 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-757-22182_-757-22 others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663356 | ||||||
| chr7:7663382
|
C | G | 96 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0063others(93): Show | 98 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-757-22207G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663382 | ||||||
| chr7:7663386
|
T | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-757-22211A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663386 | ||||||
| chr7:7663450
|
T | C | 188 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-757-22275A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663450 | ||||||
| chr7:7663512
|
A | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(34): Show | 40 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.-758+22318T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663512 | ||||||
| chr7:7663604
|
ATGAATC | A | 9 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(6): Show | 11 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-758+22220_-758+22 others(12): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663604 | ||||||
| chr7:7663606
|
G | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(25): Show | 29 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.-758+22224C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663606 | ||||||
| chr7:7663709
|
A | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(34): Show | 40 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.-758+22121T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663709 | ||||||
| chr7:7663726
|
A | G | 230 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(227): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-758+22104T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663726 | ||||||
| chr7:7663743
|
G | T | 190 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(187): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-758+22087C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663743 | ||||||
| chr7:7663770
|
A | G | 190 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(187): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-758+22060T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663770 | ||||||
| chr7:7663789
|
A | G | 1 | a0001c0001t0022g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-758+22041T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663789 | ||||||
| chr7:7663835
|
A | C | 227 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(224): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-758+21995T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663835 | ||||||
| chr7:7663841
|
C | T | 190 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(187): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-758+21989G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663841 | ||||||
| chr7:7663851
|
A | G | 1 | a0001c0001t0022g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-758+21979T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663851 | ||||||
| chr7:7663948
|
A | C | 228 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(225): Show | 233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-758+21882T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7663948 | ||||||
| chr7:7664174
|
A | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(34): Show | 40 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.-758+21656T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664174 | ||||||
| chr7:7664206
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-758+21624G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664206 | ||||||
| chr7:7664212
|
C | T | 184 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(181): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-758+21618G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664212 | ||||||
| chr7:7664224
|
A | C | 184 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(181): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-758+21606T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664224 | ||||||
| chr7:7664293
|
C | T | 17 | a0001c0001t0001g0061a0001c0001t0001g0239a0001c0001t0001g0241others(14): Show | 17 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-758+21537G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664293 | ||||||
| chr7:7664329
|
G | A | 184 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(181): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-758+21501C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664329 | ||||||
| chr7:7664408
|
T | C | 190 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(187): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-758+21422A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664408 | ||||||
| chr7:7664414
|
G | A | 2 | a0001c0001t0002g0252a0001c0001t0021g0251 | 2 | HG01081.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-758+21416C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664414 | ||||||
| chr7:7664417
|
A | T | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(3): Show | 6 | HG01243.hp1 HG03195.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-758+21413T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664417 | ||||||
| chr7:7664469
|
G | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(23): Show | 27 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-758+21361C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664469 | ||||||
| chr7:7664632
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-758+21198A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664632 | ||||||
| chr7:7664675
|
G | A | 1 | a0001c0001t0002g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-758+21155C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664675 | ||||||
| chr7:7664693
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-758+21137G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664693 | ||||||
| chr7:7664750
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-758+21080A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664750 | ||||||
| chr7:7664757
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-758+21073C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664757 | ||||||
| chr7:7664882
|
T | C | 184 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(181): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-758+20948A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7664882 | ||||||
| chr7:7665002
|
G | GAT | 67 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(64): Show | 70 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-758+20826_-758+20 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665002 | ||||||
| chr7:7665002
|
GAT | G | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+20826_-758+20 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665002 | ||||||
| chr7:7665014
|
T | C | 2 | a0001c0001t0007g0169a0001c0001t0007g0187 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-758+20816A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665014 | ||||||
| chr7:7665016
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-758+20814G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665016 | ||||||
| chr7:7665017
|
A | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(40): Show | 46 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.-758+20813T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665017 | ||||||
| chr7:7665116
|
A | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(3): Show | 6 | HG01243.hp1 HG03195.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-758+20714T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665116 | ||||||
| chr7:7665148
|
A | G | 1 | a0001c0001t0022g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-758+20682T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665148 | ||||||
| chr7:7665258
|
T | C | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+20572A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665258 | ||||||
| chr7:7665440
|
G | A | 158 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(155): Show | 160 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-758+20390C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665440 | ||||||
| chr7:7665508
|
C | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(42): Show | 48 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.-758+20322G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665508 | ||||||
| chr7:7665602
|
A | G | 230 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(227): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-758+20228T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665602 | ||||||
| chr7:7665605
|
G | A | 178 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(175): Show | 182 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.-758+20225C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665605 | ||||||
| chr7:7665611
|
G | A | 9 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(6): Show | 11 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-758+20219C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665611 | ||||||
| chr7:7665644
|
A | G | 208 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(205): Show | 213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.-758+20186T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665644 | ||||||
| chr7:7665728
|
T | C | 4 | a0001c0001t0002g0098a0001c0001t0005g0291a0001c0001t0018g0292others(1): Show | 4 | HG01109.hp1 HG01891.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-758+20102A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665728 | ||||||
| chr7:7665731
|
C | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA18946.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-758+20099G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665731 | ||||||
| chr7:7665745
|
T | G | 1 | a0001c0001t0020g0246 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-758+20085A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665745 | ||||||
| chr7:7665782
|
A | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-758+20048T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665782 | ||||||
| chr7:7665824
|
CT | C | 10 | a0001c0001t0001g0295a0001c0001t0002g0007a0001c0001t0002g0294others(7): Show | 12 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-758+20005delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665824 | ||||||
| chr7:7665861
|
G | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+19969C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665861 | ||||||
| chr7:7665921
|
T | C | 10 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0002g0301others(7): Show | 12 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-758+19909A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665921 | ||||||
| chr7:7665924
|
A | G | 27 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(24): Show | 28 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-758+19906T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665924 | ||||||
| chr7:7665986
|
A | G | 1 | a0001c0001t0005g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-758+19844T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7665986 | ||||||
| chr7:7666051
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-758+19779T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666051 | ||||||
| chr7:7666119
|
C | T | 1 | a0001c0001t0016g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-758+19711G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666119 | ||||||
| chr7:7666140
|
G | C | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-758+19690C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666140 | ||||||
| chr7:7666141
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-758+19689A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666141 | ||||||
| chr7:7666184
|
T | TTTTG | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02723.hp2 HG03209.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+19642_-758+19 others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666184 | ||||||
| chr7:7666184
|
TTTTG | T | 160 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(157): Show | 162 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-758+19642_-758+19 others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666184 | ||||||
| chr7:7666184
|
TTTTGTTT others(1): Show |
T | 9 | a0001c0001t0004g0002a0001c0001t0004g0039a0001c0001t0004g0040others(6): Show | 10 | HG00735.hp2 HG01069.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-758+19638_-758+19 others(14): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666184 | ||||||
| chr7:7666226
|
G | C | 10 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-758+19604C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666226 | ||||||
| chr7:7666328
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-758+19502G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666328 | ||||||
| chr7:7666415
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-758+19415G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666415 | ||||||
| chr7:7666450
|
T | A | 1 | a0001c0001t0008g0260 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-758+19380A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666450 | ||||||
| chr7:7666546
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-758+19284A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666546 | ||||||
| chr7:7666606
|
A | G | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+19224T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666606 | ||||||
| chr7:7666641
|
GC | G | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+19188delG | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666641 | ||||||
| chr7:7666674
|
G | A | 168 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(165): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-758+19156C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666674 | ||||||
| chr7:7666695
|
T | C | 1 | a0001c0001t0004g0244 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-758+19135A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666695 | ||||||
| chr7:7666735
|
T | A | 2 | a0001c0001t0002g0252a0001c0001t0021g0251 | 2 | HG01081.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-758+19095A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666735 | ||||||
| chr7:7666853
|
T | A | 4 | a0001c0001t0002g0219a0001c0001t0007g0209a0001c0001t0014g0123others(1): Show | 4 | HG00639.hp2 HG02451.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-758+18977A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666853 | ||||||
| chr7:7666909
|
A | G | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+18921T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666909 | ||||||
| chr7:7666954
|
T | A | 1 | a0001c0001t0001g0256 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-758+18876A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666954 | ||||||
| chr7:7666956
|
C | T | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(154): Show | 159 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.-758+18874G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7666956 | ||||||
| chr7:7667003
|
T | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+18827A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667003 | ||||||
| chr7:7667055
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-758+18775G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667055 | ||||||
| chr7:7667067
|
G | A | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+18763C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667067 | ||||||
| chr7:7667247
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0010g0065 | 2 | HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-758+18583C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667247 | ||||||
| chr7:7667278
|
G | C | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-758+18552C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667278 | ||||||
| chr7:7667287
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-758+18543T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667287 | ||||||
| chr7:7667291
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-758+18539T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667291 | ||||||
| chr7:7667293
|
T | C | 2 | a0001c0001t0001g0179a0001c0001t0010g0180 | 2 | NA18988.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-758+18537A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667293 | ||||||
| chr7:7667379
|
A | G | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+18451T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667379 | ||||||
| chr7:7667380
|
T | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0283a0001c0001t0012g0293 | 3 | HG02109.hp1 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-758+18450A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667380 | ||||||
| chr7:7667413
|
C | T | 25 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(22): Show | 25 | HG00544.hp2 HG02004.hp2 HG02074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-758+18417G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667413 | ||||||
| chr7:7667500
|
G | C | 166 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(163): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-758+18330C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667500 | ||||||
| chr7:7667525
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-758+18305A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667525 | ||||||
| chr7:7667591
|
AATGTTTA others(1): Show |
A | 4 | a0001c0001t0002g0106a0001c0001t0002g0219a0001c0001t0002g0220others(1): Show | 4 | HG02818.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+18231_-758+18 others(14): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667591 | ||||||
| chr7:7667593
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-758+18237A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667593 | ||||||
| chr7:7667683
|
C | T | 166 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(163): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-758+18147G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667683 | ||||||
| chr7:7667709
|
C | T | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+18121G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667709 | ||||||
| chr7:7667794
|
A | G | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+18036T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667794 | ||||||
| chr7:7667812
|
T | C | 173 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(170): Show | 177 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-758+18018A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667812 | ||||||
| chr7:7667852
|
A | G | 166 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(163): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-758+17978T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667852 | ||||||
| chr7:7667926
|
C | T | 1 | a0001c0001t0010g0125 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-758+17904G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667926 | ||||||
| chr7:7667998
|
C | T | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+17832G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7667998 | ||||||
| chr7:7668003
|
G | A | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+17827C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668003 | ||||||
| chr7:7668075
|
G | C | 173 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(170): Show | 175 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.-758+17755C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668075 | ||||||
| chr7:7668110
|
C | T | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+17720G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668110 | ||||||
| chr7:7668162
|
C | G | 3 | a0001c0001t0007g0209a0001c0001t0014g0123a0001c0001t0014g0211 | 3 | HG00639.hp2 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-758+17668G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668162 | ||||||
| chr7:7668208
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-758+17622A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668208 | ||||||
| chr7:7668269
|
C | T | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+17561G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668269 | ||||||
| chr7:7668304
|
C | A | 24 | a0001c0001t0001g0103a0001c0001t0001g0265a0001c0001t0001g0268others(21): Show | 24 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-758+17526G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668304 | ||||||
| chr7:7668354
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-758+17476C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668354 | ||||||
| chr7:7668371
|
T | A | 166 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(163): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-758+17459A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668371 | ||||||
| chr7:7668488
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-758+17342A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668488 | ||||||
| chr7:7668733
|
T | C | 169 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(166): Show | 171 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-758+17097A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668733 | ||||||
| chr7:7668874
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-758+16956G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668874 | ||||||
| chr7:7668891
|
C | T | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+16939G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668891 | ||||||
| chr7:7668969
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-758+16861T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7668969 | ||||||
| chr7:7669084
|
GT | G | 201 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(198): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.-758+16745delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7669084 | ||||||
| chr7:7669150
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-758+16680T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7669150 | ||||||
| chr7:7669203
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-758+16627A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7669203 | ||||||
| chr7:7669243
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-758+16587G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7669243 | ||||||
| chr7:7669328
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-758+16502C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7669328 | ||||||
| chr7:7669329
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-758+16501G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7669329 | ||||||
| chr7:7669391
|
G | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(22): Show | 26 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.-758+16439C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7669391 | ||||||
| chr7:7669523
|
C | T | 167 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(164): Show | 169 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-758+16307G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7669523 | ||||||
| chr7:7669706
|
A | T | 280 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(277): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-758+16124T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7669706 | ||||||
| chr7:7669948
|
T | C | 159 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(156): Show | 161 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-758+15882A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7669948 | ||||||
| chr7:7670109
|
A | G | 1 | a0001c0001t0001g0005 | 2 | NA18957.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-758+15721T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7670109 | ||||||
| chr7:7670110
|
C | T | 167 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(164): Show | 169 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-758+15720G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7670110 | ||||||
| chr7:7670237
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18985.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-758+15593C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7670237 | ||||||
| chr7:7670271
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0021others(1): Show | 4 | NA18957.hp1 NA18965.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+15559T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7670271 | ||||||
| chr7:7670703
|
A | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0283 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-758+15127T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7670703 | ||||||
| chr7:7670738
|
A | C | 281 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(278): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-758+15092T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7670738 | ||||||
| chr7:7670800
|
G | A | 1 | a0001c0001t0007g0171 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-758+15030C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7670800 | ||||||
| chr7:7670967
|
C | G | 1 | a0001c0001t0002g0087 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-758+14863G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7670967 | ||||||
| chr7:7670991
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-758+14839C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7670991 | ||||||
| chr7:7670992
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-758+14838C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7670992 | ||||||
| chr7:7671091
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-758+14739C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671091 | ||||||
| chr7:7671115
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-758+14715T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671115 | ||||||
| chr7:7671120
|
A | G | 3 | a0001c0001t0001g0213a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG02135.hp1 NA18998.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-758+14710T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671120 | ||||||
| chr7:7671283
|
C | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(29): Show | 33 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-758+14547G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671283 | ||||||
| chr7:7671299
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(22): Show | 26 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.-758+14531G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671299 | ||||||
| chr7:7671440
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-758+14390T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671440 | ||||||
| chr7:7671508
|
A | T | 1 | a0001c0001t0016g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-758+14322T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671508 | ||||||
| chr7:7671577
|
G | A | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(223): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-758+14253C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671577 | ||||||
| chr7:7671670
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-758+14160A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671670 | ||||||
| chr7:7671765
|
TCTCTCCT others(2): Show |
T | 4 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(1): Show | 4 | HG02572.hp1 HG02717.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+14056_-758+14 others(15): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671765 | ||||||
| chr7:7671796
|
C | G | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+14034G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671796 | ||||||
| chr7:7671837
|
T | G | 16 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0198others(13): Show | 17 | HG00280.hp1 HG00558.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-758+13993A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671837 | ||||||
| chr7:7671838
|
A | C | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-758+13992T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671838 | ||||||
| chr7:7671956
|
G | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(29): Show | 33 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-758+13874C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7671956 | ||||||
| chr7:7672101
|
C | G | 225 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(222): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.-758+13729G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672101 | ||||||
| chr7:7672252
|
C | T | 193 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(190): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-758+13578G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672252 | ||||||
| chr7:7672264
|
C | G | 1 | a0001c0001t0001g0004 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-758+13566G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672264 | ||||||
| chr7:7672286
|
T | A | 1 | a0001c0001t0012g0288 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-758+13544A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672286 | ||||||
| chr7:7672374
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-758+13456C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672374 | ||||||
| chr7:7672411
|
C | G | 1 | a0001c0001t0001g0172 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-758+13419G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672411 | ||||||
| chr7:7672466
|
A | G | 1 | a0001c0001t0003g0267 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-758+13364T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672466 | ||||||
| chr7:7672501
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-758+13329G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672501 | ||||||
| chr7:7672515
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-758+13315A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672515 | ||||||
| chr7:7672733
|
G | A | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+13097C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672733 | ||||||
| chr7:7672867
|
T | C | 256 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(253): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-758+12963A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672867 | ||||||
| chr7:7672888
|
G | A | 6 | a0001c0001t0001g0239a0001c0001t0008g0200a0001c0001t0008g0233others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+12942C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672888 | ||||||
| chr7:7672941
|
G | C | 4 | a0001c0001t0001g0203a0001c0001t0001g0261a0001c0001t0001g0285others(1): Show | 4 | HG02148.hp1 HG04184.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-758+12889C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672941 | ||||||
| chr7:7672971
|
C | T | 1 | a0001c0001t0022g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-758+12859G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7672971 | ||||||
| chr7:7673226
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0010g0180 | 3 | NA18988.hp2 NA19011.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-758+12604G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673226 | ||||||
| chr7:7673268
|
G | A | 1 | a0001c0001t0004g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-758+12562C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673268 | ||||||
| chr7:7673310
|
T | TAGC | 40 | a0001c0001t0001g0031a0001c0001t0001g0064a0001c0001t0001g0067others(37): Show | 41 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-758+12517_-758+12 others(9): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
T | TAGCAGC | 16 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0002g0088others(13): Show | 16 | HG00741.hp2 HG01167.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.-758+12514_-758+12 others(12): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
T | TAGCAGCA others(2): Show |
7 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0095others(4): Show | 8 | HG00735.hp2 HG01069.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.-758+12511_-758+12 others(15): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
T | TAGCAGCA others(5): Show |
6 | a0001c0001t0002g0012a0001c0001t0002g0092a0001c0001t0004g0041others(3): Show | 6 | HG01192.hp1 HG01243.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+12508_-758+12 others(18): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
T | TAGCAGCA others(8): Show |
1 | a0001c0001t0015g0298 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-758+12505_-758+12 others(21): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
T | TAGCAGCA others(14): Show |
1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-758+12499_-758+12 others(27): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
TAGC | T | 27 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0058others(24): Show | 28 | HG00280.hp1 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-758+12517_-758+12 others(9): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
TAGCAGC | T | 43 | a0001c0001t0001g0008a0001c0001t0001g0096a0001c0001t0001g0108others(40): Show | 43 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-758+12514_-758+12 others(12): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
TAGCAGCA others(2): Show |
T | 96 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(93): Show | 97 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-758+12511_-758+12 others(15): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
TAGCAGCA others(5): Show |
T | 7 | a0001c0001t0001g0176a0001c0001t0002g0098a0001c0001t0002g0217others(4): Show | 7 | HG00438.hp1 HG01891.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+12508_-758+12 others(18): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
TAGCAGCA others(8): Show |
T | 5 | a0001c0001t0001g0215a0001c0001t0001g0232a0001c0001t0002g0252others(2): Show | 5 | HG00735.hp1 HG01081.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+12505_-758+12 others(21): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
TAGCAGCA others(17): Show |
T | 4 | a0001c0001t0001g0068a0001c0001t0001g0107a0001c0001t0001g0283others(1): Show | 4 | HG02630.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+12496_-758+12 others(30): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
TAGCAGCA others(20): Show |
T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-758+12493_-758+12 others(33): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673310
|
TAGCAGCA others(41): Show |
T | 1 | a0001c0001t0004g0050 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-758+12472_-758+12 others(54): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673310 | ||||||
| chr7:7673334
|
C | T | 1 | a0001c0001t0024g0164 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-758+12496G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673334 | ||||||
| chr7:7673346
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-758+12484G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673346 | ||||||
| chr7:7673368
|
A | G | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+12462T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673368 | ||||||
| chr7:7673441
|
T | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0146a0001c0001t0001g0168 | 3 | HG01952.hp1 HG02004.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-758+12389A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673441 | ||||||
| chr7:7673492
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-758+12338A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673492 | ||||||
| chr7:7673674
|
C | G | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+12156G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673674 | ||||||
| chr7:7673699
|
C | CT | 30 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(27): Show | 30 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.-758+12130dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673699 | ||||||
| chr7:7673704
|
TC | T | 161 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(158): Show | 163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-758+12125delG | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673704 | ||||||
| chr7:7673705
|
C | T | 89 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(86): Show | 92 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.-758+12125G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673705 | ||||||
| chr7:7673706
|
C | T | 161 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(158): Show | 163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-758+12124G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673706 | ||||||
| chr7:7673709
|
C | T | 21 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(18): Show | 21 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-758+12121G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673709 | ||||||
| chr7:7673710
|
C | CTT | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+12119_-758+12 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673710 | ||||||
| chr7:7673710
|
C | T | 31 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(28): Show | 31 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.-758+12120G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673710 | ||||||
| chr7:7673711
|
C | T | 40 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(37): Show | 42 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.-758+12119G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673711 | ||||||
| chr7:7673712
|
T | C | 28 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(25): Show | 28 | HG00544.hp2 HG02074.hp2 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.-758+12118A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673712 | ||||||
| chr7:7673713
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-758+12117A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673713 | ||||||
| chr7:7673773
|
G | C | 2 | a0001c0001t0005g0289a0001c0001t0022g0243 | 2 | HG02647.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-758+12057C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673773 | ||||||
| chr7:7673775
|
C | G | 1 | a0001c0001t0001g0193 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-758+12055G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673775 | ||||||
| chr7:7673859
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-758+11971T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673859 | ||||||
| chr7:7673971
|
C | A | 1 | a0001c0001t0001g0184 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-758+11859G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7673971 | ||||||
| chr7:7674050
|
A | T | 3 | a0001c0001t0005g0055a0001c0001t0005g0056a0001c0001t0005g0057 | 3 | HG02486.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-758+11780T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7674050 | ||||||
| chr7:7674095
|
C | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA18946.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-758+11735G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7674095 | ||||||
| chr7:7674316
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-758+11514G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7674316 | ||||||
| chr7:7674335
|
A | G | 1 | a0001c0001t0003g0266 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-758+11495T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7674335 | ||||||
| chr7:7674389
|
C | G | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-758+11441G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7674389 | ||||||
| chr7:7674679
|
C | A | 166 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(163): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-758+11151G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7674679 | ||||||
| chr7:7675256
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-758+10574G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7675256 | ||||||
| chr7:7675366
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-758+10464T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7675366 | ||||||
| chr7:7675494
|
C | A | 257 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(254): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.-758+10336G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7675494 | ||||||
| chr7:7675570
|
C | G | 1 | a0001c0001t0001g0008 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-758+10260G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7675570 | ||||||
| chr7:7675586
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-758+10244T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7675586 | ||||||
| chr7:7675693
|
G | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0283 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-758+10137C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7675693 | ||||||
| chr7:7675693
|
G | C | 1 | a0001c0001t0002g0217 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-758+10137C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7675693 | ||||||
| chr7:7675724
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-758+10106T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7675724 | ||||||
| chr7:7675754
|
G | A | 193 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(190): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-758+10076C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7675754 | ||||||
| chr7:7675846
|
C | T | 167 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(164): Show | 169 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-758+9984G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7675846 | ||||||
| chr7:7675951
|
C | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+9879G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7675951 | ||||||
| chr7:7676000
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-758+9830G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7676000 | ||||||
| chr7:7676182
|
C | G | 1 | a0001c0001t0005g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-758+9648G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7676182 | ||||||
| chr7:7676196
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-758+9634G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7676196 | ||||||
| chr7:7676217
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-758+9613G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7676217 | ||||||
| chr7:7676443
|
C | G | 1 | a0001c0001t0004g0029 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-758+9387G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7676443 | ||||||
| chr7:7676465
|
T | G | 1 | a0001c0001t0024g0164 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-758+9365A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7676465 | ||||||
| chr7:7676719
|
A | G | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+9111T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7676719 | ||||||
| chr7:7676833
|
A | G | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+8997T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7676833 | ||||||
| chr7:7676856
|
A | G | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+8974T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7676856 | ||||||
| chr7:7677053
|
T | TA | 3 | a0001c0001t0005g0289a0001c0001t0005g0291a0001c0001t0022g0243 | 3 | HG02647.hp2 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-758+8776_-758+877 others(5): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677053 | ||||||
| chr7:7677126
|
G | A | 193 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(190): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-758+8704C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677126 | ||||||
| chr7:7677660
|
T | G | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+8170A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677660 | ||||||
| chr7:7677664
|
G | T | 1 | a0001c0001t0004g0045 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-758+8166C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677664 | ||||||
| chr7:7677664
|
GT | G | 46 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0054others(43): Show | 48 | HG00673.hp2 HG00735.hp2 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.-758+8165delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677664 | ||||||
| chr7:7677664
|
GTT | G | 229 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(226): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-758+8164_-758+816 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677664 | ||||||
| chr7:7677671
|
T | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0026 | 2 | NA18988.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-758+8159A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677671 | ||||||
| chr7:7677672
|
T | G | 23 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(20): Show | 23 | HG00544.hp2 HG02004.hp2 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-758+8158A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677672 | ||||||
| chr7:7677673
|
T | G | 6 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 6 | HG01167.hp2 HG01175.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-758+8157A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677673 | ||||||
| chr7:7677674
|
T | G | 39 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0064others(36): Show | 40 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.-758+8156A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677674 | ||||||
| chr7:7677675
|
T | G | 174 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(171): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-758+8155A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677675 | ||||||
| chr7:7677704
|
C | T | 1 | a0001c0001t0005g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-758+8126G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677704 | ||||||
| chr7:7677712
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-758+8118G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677712 | ||||||
| chr7:7677742
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-758+8088G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677742 | ||||||
| chr7:7677743
|
G | A | 189 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-758+8087C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677743 | ||||||
| chr7:7677759
|
T | C | 273 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(270): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-758+8071A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677759 | ||||||
| chr7:7677774
|
C | T | 24 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 24 | HG00544.hp2 HG02004.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-758+8056G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677774 | ||||||
| chr7:7677822
|
C | T | 1 | a0001c0001t0002g0294 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-758+8008G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677822 | ||||||
| chr7:7677962
|
C | T | 2 | a0001c0001t0002g0009a0001c0001t0002g0011 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-758+7868G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7677962 | ||||||
| chr7:7678042
|
A | G | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+7788T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678042 | ||||||
| chr7:7678140
|
T | C | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+7690A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678140 | ||||||
| chr7:7678143
|
GT | G | 280 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(277): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-758+7686delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678143 | ||||||
| chr7:7678260
|
CT | C | 167 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(164): Show | 169 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-758+7569delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678260 | ||||||
| chr7:7678343
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-758+7487A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678343 | ||||||
| chr7:7678348
|
C | T | 2 | a0001c0001t0002g0238a0001c0001t0002g0240 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-758+7482G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678348 | ||||||
| chr7:7678363
|
C | A | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-758+7467G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678363 | ||||||
| chr7:7678460
|
A | AATAT | 24 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 24 | HG00544.hp2 HG02004.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-758+7366_-758+736 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678460 | ||||||
| chr7:7678471
|
A | C | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+7359T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678471 | ||||||
| chr7:7678490
|
AATATATA others(905): Show |
A | 1 | a0001c0001t0001g0165 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-758+6428_-758+733 others(4): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678490 | ||||||
| chr7:7678519
|
A | AATATATT others(24): Show |
16 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0031others(13): Show | 17 | HG01069.hp2 HG01168.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.-758+7280_-758+731 others(35): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678519 | ||||||
| chr7:7678519
|
A | AATATATT others(55): Show |
2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-758+7310_-758+731 others(66): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678519 | ||||||
| chr7:7678519
|
A | AATATATT others(55): Show |
2 | a0001c0001t0001g0283a0001c0001t0005g0291 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-758+7249_-758+731 others(66): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678519 | ||||||
| chr7:7678519
|
A | AATATATT others(54): Show |
2 | a0001c0001t0005g0289a0001c0001t0022g0243 | 2 | HG02647.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-758+7310_-758+731 others(65): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678519 | ||||||
| chr7:7678567
|
A | AATTTATA others(24): Show |
1 | a0001c0001t0001g0250 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-758+7262_-758+726 others(35): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678567 | ||||||
| chr7:7678626
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-758+7204G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678626 | ||||||
| chr7:7678630
|
A | G | 1 | a0001c0001t0002g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-758+7200T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678630 | ||||||
| chr7:7678637
|
G | GATAAATA others(236): Show |
1 | a0001c0001t0024g0164 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-758+7192_-758+719 others(247): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678637 | ||||||
| chr7:7678637
|
G | GATAAATA others(209): Show |
18 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0001t0001g0105others(15): Show | 18 | HG00140.hp1 HG00438.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-758+7192_-758+719 others(220): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678637 | ||||||
| chr7:7678637
|
G | GATAAATA others(263): Show |
1 | a0001c0001t0001g0191 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-758+7192_-758+719 others(274): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678637 | ||||||
| chr7:7678637
|
G | GATAAATA others(182): Show |
2 | a0001c0001t0001g0063a0001c0001t0001g0168 | 2 | HG01256.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-758+7192_-758+719 others(193): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678637 | ||||||
| chr7:7678643
|
T | TATATATT others(138): Show |
4 | a0001c0001t0005g0099a0001c0001t0005g0102a0001c0001t0005g0290others(1): Show | 4 | HG02280.hp2 HG02572.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+7186_-758+718 others(149): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678643 | ||||||
| chr7:7678643
|
T | TATATATT others(107): Show |
1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-758+7186_-758+718 others(118): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678643 | ||||||
| chr7:7678644
|
A | ATATATTT others(178): Show |
1 | a0001c0001t0001g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-758+7185_-758+718 others(189): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678644 | ||||||
| chr7:7678645
|
T | TATATTTA others(217): Show |
1 | a0001c0001t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-758+7184_-758+718 others(228): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678645 | ||||||
| chr7:7678645
|
T | TATATTTA others(240): Show |
1 | a0001c0001t0018g0292 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-758+7184_-758+718 others(251): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678645 | ||||||
| chr7:7678645
|
T | TATATTTA others(182): Show |
10 | a0001c0001t0001g0008a0001c0001t0001g0054a0001c0001t0001g0107others(7): Show | 10 | HG00733.hp1 HG01496.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-758+7184_-758+718 others(193): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678645 | ||||||
| chr7:7678645
|
T | TATATTTA others(155): Show |
1 | a0001c0001t0001g0184 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-758+7184_-758+718 others(166): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678645 | ||||||
| chr7:7678657
|
T | C | 133 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(130): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-758+7173A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678657 | ||||||
| chr7:7678661
|
G | A | 127 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(124): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-758+7169C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678661 | ||||||
| chr7:7678664
|
T | TATAG | 127 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(124): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-758+7165_-758+716 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678664 | ||||||
| chr7:7678668
|
A | G | 2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-758+7162T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678668 | ||||||
| chr7:7678684
|
T | C | 1 | a0001c0001t0005g0100 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-758+7146A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678684 | ||||||
| chr7:7678688
|
G | A | 1 | a0001c0001t0005g0100 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-758+7142C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678688 | ||||||
| chr7:7678697
|
T | C | 4 | a0001c0001t0005g0099a0001c0001t0005g0102a0001c0001t0005g0290others(1): Show | 4 | HG02280.hp2 HG02572.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+7133A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678697 | ||||||
| chr7:7678697
|
T | TATATATT others(43): Show |
2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-758+7132_-758+713 others(54): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678697 | ||||||
| chr7:7678699
|
T | TATATTTA others(43): Show |
1 | a0001c0001t0001g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-758+7130_-758+713 others(54): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678699 | ||||||
| chr7:7678699
|
T | TATATTTA others(70): Show |
1 | a0001c0001t0001g0232 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-758+7130_-758+713 others(81): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678699 | ||||||
| chr7:7678699
|
T | TATATTTA others(97): Show |
1 | a0001c0001t0001g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-758+7130_-758+713 others(108): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678699 | ||||||
| chr7:7678711
|
T | C | 1 | a0001c0001t0005g0100 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-758+7119A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678711 | ||||||
| chr7:7678715
|
G | A | 1 | a0001c0001t0005g0100 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-758+7115C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678715 | ||||||
| chr7:7678722
|
AAT | A | 13 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0239others(10): Show | 13 | HG01361.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-758+7106_-758+710 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678722 | ||||||
| chr7:7678724
|
T | C | 5 | a0001c0001t0001g0218a0001c0001t0005g0099a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-758+7106A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678724 | ||||||
| chr7:7678724
|
T | TATATTTA others(16): Show |
6 | a0001c0001t0001g0058a0001c0001t0002g0237a0001c0001t0005g0055others(3): Show | 6 | HG02559.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+7105_-758+710 others(27): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678724 | ||||||
| chr7:7678726
|
T | TATATTTA others(70): Show |
1 | a0001c0001t0001g0117 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-758+7103_-758+710 others(81): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678726 | ||||||
| chr7:7678735
|
A | G | 26 | a0001c0001t0001g0146a0001c0001t0001g0188a0001c0001t0001g0197others(23): Show | 26 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-758+7095T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678735 | ||||||
| chr7:7678749
|
AAT | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(35): Show | 39 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.-758+7079_-758+708 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678749 | ||||||
| chr7:7678751
|
T | C | 9 | a0001c0001t0001g0069a0001c0001t0001g0218a0001c0001t0002g0234others(6): Show | 9 | HG01361.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-758+7079A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678751 | ||||||
| chr7:7678762
|
A | G | 58 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0124others(55): Show | 60 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-758+7068T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678762 | ||||||
| chr7:7678776
|
A | AAC | 20 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(17): Show | 20 | HG01109.hp2 HG01175.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.-758+7053_-758+705 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678776 | ||||||
| chr7:7678776
|
A | AAT | 178 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(175): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.-758+7052_-758+705 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678776 | ||||||
| chr7:7678776
|
A | AATATATA others(72): Show |
16 | a0001c0001t0001g0112a0001c0001t0001g0143a0001c0001t0001g0149others(13): Show | 16 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-758+7053_-758+705 others(83): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678776 | ||||||
| chr7:7678776
|
A | AATATATA others(126): Show |
2 | a0001c0001t0001g0147a0001c0001t0013g0111 | 2 | HG00741.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-758+7053_-758+705 others(137): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678776 | ||||||
| chr7:7678776
|
A | AATATATA others(45): Show |
3 | a0001c0001t0005g0289a0001c0001t0016g0152a0001c0001t0022g0243 | 3 | HG02647.hp2 HG02698.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-758+7053_-758+705 others(56): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678776 | ||||||
| chr7:7678776
|
AAT | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0188a0001c0001t0003g0264others(1): Show | 4 | HG01952.hp1 HG02148.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+7052_-758+705 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678776 | ||||||
| chr7:7678778
|
T | TATATATT others(45): Show |
8 | a0001c0001t0001g0108a0001c0001t0001g0153a0001c0001t0001g0166others(5): Show | 8 | HG00642.hp2 HG02523.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-758+7051_-758+705 others(56): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678778 | ||||||
| chr7:7678787
|
A | G | 111 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0103others(108): Show | 113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-758+7043T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678787 | ||||||
| chr7:7678801
|
A | AAC | 46 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 47 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.-758+7028_-758+702 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678801 | ||||||
| chr7:7678801
|
A | AAT | 119 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0074others(116): Show | 121 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.-758+7027_-758+702 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678801 | ||||||
| chr7:7678801
|
AAT | A | 49 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0124others(46): Show | 51 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.-758+7027_-758+702 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678801 | ||||||
| chr7:7678803
|
T | C | 2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-758+7027A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678803 | ||||||
| chr7:7678803
|
T | TATATATT others(41): Show |
2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-758+7026_-758+702 others(52): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678803 | ||||||
| chr7:7678811
|
T | C | 2 | a0001c0001t0003g0264a0001c0001t0003g0278 | 2 | NA18959.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-758+7019A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678811 | ||||||
| chr7:7678812
|
A | G | 64 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(61): Show | 64 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-758+7018T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678812 | ||||||
| chr7:7678826
|
AACAT | A | 59 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0113others(56): Show | 59 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-758+7000_-758+700 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678826 | ||||||
| chr7:7678828
|
C | T | 140 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(137): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-758+7002G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678828 | ||||||
| chr7:7678830
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-758+7000A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678830 | ||||||
| chr7:7678838
|
T | C | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+6992A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678838 | ||||||
| chr7:7678839
|
A | G | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | HG01175.hp2 HG01255.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+6991T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678839 | ||||||
| chr7:7678849
|
T | TATAAATA others(456): Show |
1 | a0001c0001t0001g0157 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-758+6980_-758+698 others(467): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678849 | ||||||
| chr7:7678853
|
A | AATATATA others(350): Show |
1 | a0001c0001t0001g0184 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-758+6976_-758+697 others(361): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678853 | ||||||
| chr7:7678853
|
AACAT | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | HG01175.hp2 HG01255.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+6973_-758+697 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678853 | ||||||
| chr7:7678855
|
C | A | 1 | a0001c0001t0001g0184 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-758+6975G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678855 | ||||||
| chr7:7678855
|
C | T | 193 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(190): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-758+6975G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678855 | ||||||
| chr7:7678857
|
T | TATATTTA others(714): Show |
2 | a0001c0001t0003g0263a0001c0001t0003g0277 | 2 | NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6972_-758+697 others(725): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678857 | ||||||
| chr7:7678865
|
T | C | 20 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(17): Show | 20 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-758+6965A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678865 | ||||||
| chr7:7678873
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-758+6957C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678873 | ||||||
| chr7:7678876
|
T | TATAAATA others(439): Show |
1 | a0001c0001t0001g0255 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-758+6953_-758+695 others(450): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678876 | ||||||
| chr7:7678876
|
T | TATAAATA others(439): Show |
1 | a0001c0001t0001g0136 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-758+6953_-758+695 others(450): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678876 | ||||||
| chr7:7678876
|
T | TATAAATA others(414): Show |
1 | a0001c0001t0020g0246 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-758+6953_-758+695 others(425): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678876 | ||||||
| chr7:7678876
|
T | TATAAATA others(412): Show |
1 | a0001c0001t0001g0190 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-758+6953_-758+695 others(423): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678876 | ||||||
| chr7:7678876
|
T | TATAAATA others(381): Show |
7 | a0001c0001t0001g0054a0001c0001t0001g0107a0001c0001t0001g0134others(4): Show | 7 | HG01496.hp2 HG01928.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+6953_-758+695 others(392): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678876 | ||||||
| chr7:7678876
|
T | TATAAATA others(474): Show |
2 | a0001c0001t0001g0070a0001c0001t0001g0284 | 2 | HG01081.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-758+6953_-758+695 others(485): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678876 | ||||||
| chr7:7678876
|
T | TATAAATA others(505): Show |
6 | a0001c0001t0001g0105a0001c0001t0001g0121a0001c0001t0001g0142others(3): Show | 6 | HG01934.hp2 HG02071.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+6953_-758+695 others(516): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678876 | ||||||
| chr7:7678876
|
T | TATAAATA others(536): Show |
2 | a0001c0001t0001g0063a0001c0001t0010g0155 | 2 | HG00438.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-758+6953_-758+695 others(547): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678876 | ||||||
| chr7:7678876
|
T | TATAAATA others(629): Show |
1 | a0001c0001t0001g0174 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-758+6953_-758+695 others(640): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678876 | ||||||
| chr7:7678876
|
T | TATAAATA others(410): Show |
1 | a0001c0001t0001g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-758+6953_-758+695 others(421): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678876 | ||||||
| chr7:7678876
|
T | TATAAATA others(381): Show |
1 | a0001c0001t0001g0179 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-758+6953_-758+695 others(392): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678876 | ||||||
| chr7:7678876
|
T | TATAAATA others(377): Show |
1 | a0001c0001t0001g0147 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-758+6953_-758+695 others(388): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678876 | ||||||
| chr7:7678880
|
A | AATATATA others(350): Show |
7 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0131others(4): Show | 7 | HG00733.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+6949_-758+695 others(361): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678880 | ||||||
| chr7:7678881
|
A | G | 2 | a0001c0001t0003g0263a0001c0001t0003g0277 | 2 | NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6949T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678881 | ||||||
| chr7:7678882
|
C | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0131others(4): Show | 7 | HG00733.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+6948G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678882 | ||||||
| chr7:7678882
|
C | T | 190 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0054others(187): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-758+6948G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678882 | ||||||
| chr7:7678884
|
T | C | 2 | a0001c0001t0003g0263a0001c0001t0003g0277 | 2 | NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6946A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678884 | ||||||
| chr7:7678884
|
T | TATATTTA others(633): Show |
1 | a0001c0001t0001g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-758+6945_-758+694 others(644): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678884 | ||||||
| chr7:7678892
|
T | C | 21 | a0001c0001t0001g0103a0001c0001t0001g0265a0001c0001t0001g0268others(18): Show | 21 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-758+6938A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678892 | ||||||
| chr7:7678893
|
A | T | 1 | a0001c0001t0013g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-758+6937T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678893 | ||||||
| chr7:7678900
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0131others(4): Show | 7 | HG00733.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+6930C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678900 | ||||||
| chr7:7678903
|
T | TATAAATA others(536): Show |
1 | a0001c0001t0001g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-758+6926_-758+692 others(547): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678903 | ||||||
| chr7:7678903
|
T | TATAAATA others(350): Show |
1 | a0001c0001t0013g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-758+6926_-758+692 others(361): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678903 | ||||||
| chr7:7678903
|
T | TATAG | 34 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(31): Show | 34 | HG00140.hp1 HG00438.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.-758+6926_-758+692 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678903 | ||||||
| chr7:7678907
|
AAC | A | 11 | a0001c0001t0001g0117a0001c0001t0001g0143a0001c0001t0001g0149others(8): Show | 11 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-758+6921_-758+692 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678907 | ||||||
| chr7:7678908
|
A | G | 3 | a0001c0001t0001g0271a0001c0001t0003g0263a0001c0001t0003g0277 | 3 | HG00140.hp2 NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6922T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678908 | ||||||
| chr7:7678909
|
C | T | 188 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(185): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-758+6921G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678909 | ||||||
| chr7:7678911
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0003g0263a0001c0001t0003g0277 | 3 | HG00140.hp2 NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6919A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678911 | ||||||
| chr7:7678919
|
T | C | 21 | a0001c0001t0001g0103a0001c0001t0001g0265a0001c0001t0001g0268others(18): Show | 21 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-758+6911A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678919 | ||||||
| chr7:7678927
|
G | A | 1 | a0001c0001t0003g0263 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-758+6903C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678927 | ||||||
| chr7:7678930
|
T | TATAG | 36 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(33): Show | 36 | HG00140.hp1 HG00438.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-758+6899_-758+690 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678930 | ||||||
| chr7:7678934
|
AAC | A | 5 | a0001c0001t0001g0183a0001c0001t0001g0188a0001c0001t0001g0256others(2): Show | 5 | HG02129.hp1 HG02148.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+6894_-758+689 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678934 | ||||||
| chr7:7678935
|
A | G | 3 | a0001c0001t0001g0271a0001c0001t0003g0263a0001c0001t0003g0277 | 3 | HG00140.hp2 NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6895T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678935 | ||||||
| chr7:7678936
|
C | T | 194 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(191): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-758+6894G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678936 | ||||||
| chr7:7678938
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-758+6892A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678938 | ||||||
| chr7:7678938
|
T | TATATTTA others(18): Show |
2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-758+6867_-758+689 others(29): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678938 | ||||||
| chr7:7678941
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-758+6889T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678941 | ||||||
| chr7:7678946
|
T | C | 21 | a0001c0001t0001g0103a0001c0001t0001g0265a0001c0001t0001g0268others(18): Show | 21 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-758+6884A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678946 | ||||||
| chr7:7678954
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0003g0263a0001c0001t0003g0277 | 3 | HG00140.hp2 NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6876C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678954 | ||||||
| chr7:7678957
|
T | TATAG | 38 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(35): Show | 38 | HG00140.hp1 HG00438.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.-758+6872_-758+687 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678957 | ||||||
| chr7:7678961
|
A | AATATATA others(350): Show |
2 | a0001c0001t0001g0215a0001c0001t0001g0232 | 2 | HG00735.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.-758+6868_-758+686 others(361): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678961 | ||||||
| chr7:7678961
|
AAC | A | 11 | a0001c0001t0001g0112a0001c0001t0001g0124a0001c0001t0001g0146others(8): Show | 11 | HG00544.hp1 HG01261.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.-758+6867_-758+686 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678961 | ||||||
| chr7:7678962
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-758+6868T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678962 | ||||||
| chr7:7678963
|
C | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0232 | 2 | HG00735.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.-758+6867G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678963 | ||||||
| chr7:7678963
|
C | T | 186 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(183): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-758+6867G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678963 | ||||||
| chr7:7678968
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-758+6862T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678968 | ||||||
| chr7:7678970
|
T | TTATATAT others(447): Show |
1 | a0001c0001t0002g0294 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-758+6859_-758+686 others(458): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678970 | ||||||
| chr7:7678970
|
T | TTATATAT others(420): Show |
3 | a0001c0001t0001g0295a0001c0001t0005g0001a0001c0001t0005g0296 | 5 | HG02486.hp1 HG02717.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+6859_-758+686 others(431): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678970 | ||||||
| chr7:7678973
|
T | C | 21 | a0001c0001t0001g0103a0001c0001t0001g0265a0001c0001t0001g0268others(18): Show | 21 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-758+6857A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678973 | ||||||
| chr7:7678973
|
T | TTTAGTTT others(308): Show |
1 | a0001c0001t0015g0298 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-758+6856_-758+685 others(319): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678973 | ||||||
| chr7:7678981
|
G | A | 5 | a0001c0001t0001g0215a0001c0001t0001g0232a0001c0001t0001g0271others(2): Show | 5 | HG00140.hp2 HG00735.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+6849C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678981 | ||||||
| chr7:7678984
|
T | TATAAATA others(381): Show |
8 | a0001c0001t0001g0117a0001c0001t0001g0143a0001c0001t0001g0149others(5): Show | 8 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-758+6845_-758+684 others(392): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678984 | ||||||
| chr7:7678984
|
T | TATAG | 38 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(35): Show | 38 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.-758+6845_-758+684 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678984 | ||||||
| chr7:7678988
|
A | AATATATA others(350): Show |
1 | a0001c0001t0007g0206 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-758+6841_-758+684 others(361): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678988 | ||||||
| chr7:7678988
|
A | AATATATA others(348): Show |
3 | a0001c0001t0007g0010a0001c0001t0007g0169a0001c0001t0007g0187 | 3 | HG02257.hp1 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-758+6841_-758+684 others(359): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678988 | ||||||
| chr7:7678988
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-758+6842T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678988 | ||||||
| chr7:7678988
|
A | T | 2 | a0001c0001t0003g0263a0001c0001t0003g0277 | 2 | NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6842T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678988 | ||||||
| chr7:7678988
|
AAC | A | 25 | a0001c0001t0001g0096a0001c0001t0001g0110a0001c0001t0001g0113others(22): Show | 26 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.-758+6840_-758+684 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678988 | ||||||
| chr7:7678990
|
C | A | 6 | a0001c0001t0003g0263a0001c0001t0003g0277a0001c0001t0007g0010others(3): Show | 6 | HG02257.hp1 HG02965.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+6840G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678990 | ||||||
| chr7:7678990
|
C | T | 168 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(165): Show | 171 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.-758+6840G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678990 | ||||||
| chr7:7678992
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0015g0298 | 2 | HG03195.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-758+6838A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678992 | ||||||
| chr7:7678995
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-758+6835T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7678995 | ||||||
| chr7:7679000
|
T | C | 22 | a0001c0001t0001g0103a0001c0001t0001g0265a0001c0001t0001g0268others(19): Show | 22 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+6830A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679000 | ||||||
| chr7:7679000
|
T | TATATTTA others(420): Show |
1 | a0001c0001t0001g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-758+6829_-758+683 others(431): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679000 | ||||||
| chr7:7679008
|
G | A | 7 | a0001c0001t0001g0271a0001c0001t0003g0263a0001c0001t0003g0277others(4): Show | 7 | HG00140.hp2 HG02257.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-758+6822C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679008 | ||||||
| chr7:7679011
|
T | TATAAATA others(383): Show |
1 | a0001c0001t0002g0219 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-758+6818_-758+681 others(394): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679011 | ||||||
| chr7:7679011
|
T | TATAAATA others(381): Show |
2 | a0001c0001t0001g0188a0001c0001t0001g0227 | 2 | HG00544.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-758+6818_-758+681 others(392): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679011 | ||||||
| chr7:7679011
|
T | TATAG | 50 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(47): Show | 50 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.-758+6818_-758+681 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679011 | ||||||
| chr7:7679013
|
T | TAG | 3 | a0001c0001t0001g0271a0001c0001t0003g0263a0001c0001t0003g0277 | 3 | HG00140.hp2 NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6816_-758+681 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679013 | ||||||
| chr7:7679015
|
A | T | 3 | a0001c0001t0001g0271a0001c0001t0003g0263a0001c0001t0003g0277 | 3 | HG00140.hp2 NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6815T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679015 | ||||||
| chr7:7679015
|
AAC | A | 62 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0108others(59): Show | 63 | HG00438.hp2 HG00558.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-758+6813_-758+681 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679015 | ||||||
| chr7:7679017
|
C | A | 3 | a0001c0001t0001g0271a0001c0001t0003g0263a0001c0001t0003g0277 | 3 | HG00140.hp2 NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6813G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679017 | ||||||
| chr7:7679017
|
C | T | 134 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(131): Show | 137 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.-758+6813G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679017 | ||||||
| chr7:7679019
|
T | C | 1 | a0001c0001t0015g0298 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-758+6811A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679019 | ||||||
| chr7:7679027
|
T | C | 25 | a0001c0001t0001g0103a0001c0001t0001g0265a0001c0001t0001g0268others(22): Show | 25 | HG00639.hp1 HG01081.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.-758+6803A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679027 | ||||||
| chr7:7679027
|
T | TATATTTA others(447): Show |
2 | a0001c0001t0001g0116a0001c0001t0015g0297 | 2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-758+6802_-758+680 others(458): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679027 | ||||||
| chr7:7679035
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0003g0263a0001c0001t0003g0277 | 3 | HG00140.hp2 NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6795C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679035 | ||||||
| chr7:7679038
|
T | TATAAATA others(381): Show |
4 | a0001c0001t0001g0112a0001c0001t0001g0124a0001c0001t0001g0161others(1): Show | 4 | HG01261.hp2 HG01361.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+6791_-758+679 others(392): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679038 | ||||||
| chr7:7679038
|
T | TATAAATA others(443): Show |
1 | a0001c0001t0001g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-758+6791_-758+679 others(454): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679038 | ||||||
| chr7:7679038
|
T | TATAAATA others(629): Show |
1 | a0001c0001t0001g0176 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-758+6791_-758+679 others(640): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679038 | ||||||
| chr7:7679038
|
T | TATAAATA others(753): Show |
2 | a0001c0001t0002g0252a0001c0001t0021g0251 | 2 | HG01081.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-758+6791_-758+679 others(764): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679038 | ||||||
| chr7:7679038
|
T | TATAAATA others(383): Show |
1 | a0001c0001t0002g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-758+6791_-758+679 others(394): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679038 | ||||||
| chr7:7679038
|
T | TATAAATA others(803): Show |
1 | a0001c0001t0012g0288 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-758+6791_-758+679 others(814): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679038 | ||||||
| chr7:7679038
|
T | TATAAATA others(447): Show |
1 | a0001c0001t0001g0103 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-758+6791_-758+679 others(458): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679038 | ||||||
| chr7:7679038
|
T | TATAAATA others(416): Show |
1 | a0001c0001t0012g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-758+6791_-758+679 others(427): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679038 | ||||||
| chr7:7679038
|
T | TATAG | 58 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(55): Show | 60 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.-758+6791_-758+679 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679038 | ||||||
| chr7:7679042
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-758+6788T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679042 | ||||||
| chr7:7679042
|
A | T | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-758+6788T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679042 | ||||||
| chr7:7679042
|
AAC | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0162others(1): Show | 4 | HG01175.hp2 HG01358.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-758+6786_-758+678 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679042 | ||||||
| chr7:7679044
|
C | A | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-758+6786G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679044 | ||||||
| chr7:7679044
|
C | T | 194 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(191): Show | 198 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.-758+6786G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679044 | ||||||
| chr7:7679046
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0015g0298 | 2 | HG01256.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-758+6784A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679046 | ||||||
| chr7:7679049
|
A | ATTTATTT others(749): Show |
1 | a0001c0001t0001g0196 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-758+6780_-758+678 others(760): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679049 | ||||||
| chr7:7679049
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-758+6781T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679049 | ||||||
| chr7:7679054
|
T | C | 22 | a0001c0001t0001g0096a0001c0001t0001g0256a0001c0001t0001g0265others(19): Show | 22 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+6776A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679054 | ||||||
| chr7:7679054
|
T | TATATTTA others(393): Show |
1 | a0001c0001t0002g0300 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-758+6775_-758+677 others(404): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679054 | ||||||
| chr7:7679054
|
T | TTTAGTTT others(143): Show |
1 | a0001c0001t0001g0146 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-758+6775_-758+677 others(154): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679054 | ||||||
| chr7:7679055
|
A | T | 2 | a0001c0001t0013g0127a0001c0001t0013g0137 | 2 | HG01975.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-758+6775T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679055 | ||||||
| chr7:7679062
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-758+6768C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679062 | ||||||
| chr7:7679065
|
T | TATAAATA others(597): Show |
1 | a0001c0001t0005g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-758+6764_-758+676 others(608): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679065 | ||||||
| chr7:7679065
|
T | TATAAATA others(507): Show |
1 | a0001c0001t0001g0205 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-758+6764_-758+676 others(518): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679065 | ||||||
| chr7:7679065
|
T | TATAAATA others(381): Show |
3 | a0001c0001t0006g0120a0001c0001t0006g0144a0001c0001t0006g0148 | 3 | HG02622.hp2 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-758+6764_-758+676 others(392): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679065 | ||||||
| chr7:7679065
|
T | TATAAATA others(443): Show |
5 | a0001c0001t0001g0141a0001c0001t0001g0248a0001c0001t0001g0250others(2): Show | 5 | HG00280.hp1 HG01952.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+6764_-758+676 others(454): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679065 | ||||||
| chr7:7679065
|
T | TATAAATA others(474): Show |
4 | a0001c0001t0001g0110a0001c0001t0002g0009a0001c0001t0007g0209others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-758+6764_-758+676 others(485): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679065 | ||||||
| chr7:7679065
|
T | TATAAATA others(505): Show |
3 | a0001c0001t0001g0204a0001c0001t0001g0249a0001c0001t0011g0170 | 3 | HG00673.hp2 HG01106.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-758+6764_-758+676 others(516): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679065 | ||||||
| chr7:7679065
|
T | TATAAATA others(629): Show |
3 | a0001c0001t0001g0113a0001c0001t0001g0159a0001c0001t0003g0006 | 4 | HG00323.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-758+6764_-758+676 others(640): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679065 | ||||||
| chr7:7679065
|
T | TATAAATA others(381): Show |
1 | a0001c0001t0001g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-758+6764_-758+676 others(392): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679065 | ||||||
| chr7:7679065
|
T | TATAAATA others(443): Show |
2 | a0001c0001t0013g0127a0001c0001t0013g0137 | 2 | HG01975.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-758+6764_-758+676 others(454): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679065 | ||||||
| chr7:7679065
|
T | TATAAATA others(466): Show |
1 | a0001c0001t0001g0202 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-758+6764_-758+676 others(477): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679065 | ||||||
| chr7:7679065
|
T | TATAG | 68 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(65): Show | 70 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.-758+6764_-758+676 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679065 | ||||||
| chr7:7679069
|
A | G | 5 | a0001c0001t0001g0212a0001c0001t0002g0252a0001c0001t0010g0155others(2): Show | 5 | HG00438.hp1 HG01081.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.-758+6761T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679069 | ||||||
| chr7:7679071
|
C | CATATATT others(20): Show |
1 | a0001c0001t0005g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-758+6758_-758+675 others(31): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679071 | ||||||
| chr7:7679071
|
C | T | 200 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(197): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.-758+6759G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679071 | ||||||
| chr7:7679073
|
T | C | 6 | a0001c0001t0001g0146a0001c0001t0001g0212a0001c0001t0002g0252others(3): Show | 6 | HG00438.hp1 HG01081.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-758+6757A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679073 | ||||||
| chr7:7679076
|
A | ATTTATTT others(730): Show |
1 | a0001c0001t0001g0256 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-758+6753_-758+675 others(741): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679076 | ||||||
| chr7:7679076
|
A | ATTTATTT others(780): Show |
1 | a0001c0001t0002g0011 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-758+6753_-758+675 others(791): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679076 | ||||||
| chr7:7679076
|
A | ATTTATTT others(749): Show |
1 | a0001c0001t0002g0253 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-758+6753_-758+675 others(760): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679076 | ||||||
| chr7:7679076
|
A | G | 5 | a0001c0001t0001g0212a0001c0001t0002g0252a0001c0001t0010g0155others(2): Show | 5 | HG00438.hp1 HG01081.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.-758+6754T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679076 | ||||||
| chr7:7679081
|
T | C | 20 | a0001c0001t0001g0181a0001c0001t0001g0265a0001c0001t0001g0268others(17): Show | 20 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.-758+6749A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679081 | ||||||
| chr7:7679083
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-758+6747A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679083 | ||||||
| chr7:7679092
|
T | TATAAATA others(676): Show |
1 | a0001c0001t0003g0278 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(687): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(676): Show |
4 | a0001c0001t0003g0245a0001c0001t0003g0274a0001c0001t0003g0276others(1): Show | 4 | HG02129.hp2 NA18970.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+6737_-758+673 others(687): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(699): Show |
1 | a0001c0001t0003g0266 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(710): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(672): Show |
3 | a0001c0001t0001g0268a0001c0001t0003g0273a0001c0001t0003g0281 | 3 | HG01106.hp2 HG01256.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-758+6737_-758+673 others(683): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(703): Show |
1 | a0001c0001t0003g0262 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(714): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(672): Show |
3 | a0001c0001t0003g0264a0001c0001t0003g0267a0001c0001t0003g0275 | 3 | NA18960.hp2 NA18978.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-758+6737_-758+673 others(683): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(645): Show |
1 | a0001c0001t0011g0272 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(656): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(524): Show |
1 | a0001c0001t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(535): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(679): Show |
1 | a0001c0001t0022g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(690): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(451): Show |
1 | a0001c0001t0001g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(462): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(776): Show |
1 | a0001c0001t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(787): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(520): Show |
1 | a0001c0001t0018g0292 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(531): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(483): Show |
1 | a0001c0001t0005g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(494): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(927): Show |
1 | a0001c0001t0001g0074 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(938): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(687): Show |
1 | a0001c0001t0001g0162 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(698): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(838): Show |
1 | a0001c0001t0001g0075 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(849): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(931): Show |
1 | a0001c0001t0001g0076 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(942): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(491): Show |
1 | a0001c0001t0008g0242 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(502): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(476): Show |
1 | a0001c0001t0002g0220 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(487): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(656): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0224 | 2 | NA18961.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-758+6737_-758+673 others(667): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(842): Show |
1 | a0001c0001t0002g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(853): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(412): Show |
3 | a0001c0001t0001g0230a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02922.hp1 HG03130.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-758+6737_-758+673 others(423): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(474): Show |
17 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0158others(14): Show | 17 | HG01123.hp1 HG01192.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.-758+6737_-758+673 others(485): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(505): Show |
9 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0132others(6): Show | 9 | HG00639.hp2 HG00642.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.-758+6737_-758+673 others(516): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(660): Show |
2 | a0001c0001t0001g0199a0001c0001t0003g0133 | 2 | NA19001.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-758+6737_-758+673 others(671): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(842): Show |
1 | a0001c0001t0001g0129 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(853): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(780): Show |
3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0023g0167 | 3 | HG02040.hp1 NA18953.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-758+6737_-758+673 others(791): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(811): Show |
11 | a0001c0001t0001g0005a0001c0001t0001g0135a0001c0001t0001g0186others(8): Show | 12 | HG00438.hp2 HG00558.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.-758+6737_-758+673 others(822): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(842): Show |
4 | a0001c0001t0001g0128a0001c0001t0001g0175a0001c0001t0003g0072others(1): Show | 4 | HG01168.hp2 NA18959.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.-758+6737_-758+673 others(853): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(780): Show |
1 | a0001c0001t0001g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(791): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(811): Show |
1 | a0001c0001t0001g0166 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(822): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAAATA others(474): Show |
1 | a0001c0001t0001g0126 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-758+6737_-758+673 others(485): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679092
|
T | TATAG | 92 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0054others(89): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-758+6737_-758+673 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679092 | ||||||
| chr7:7679096
|
A | AATATATA others(641): Show |
1 | a0001c0001t0003g0269 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-758+6733_-758+673 others(652): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679096 | ||||||
| chr7:7679096
|
A | AATATATA others(560): Show |
1 | a0001c0001t0001g0270 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-758+6733_-758+673 others(571): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679096 | ||||||
| chr7:7679096
|
A | AATATATA others(404): Show |
1 | a0001c0001t0005g0289 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-758+6733_-758+673 others(415): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679096 | ||||||
| chr7:7679096
|
A | G | 8 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0001g0121others(5): Show | 8 | HG01081.hp2 HG01934.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-758+6734T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679096 | ||||||
| chr7:7679098
|
C | A | 3 | a0001c0001t0001g0270a0001c0001t0003g0269a0001c0001t0005g0289 | 3 | HG00639.hp1 HG01255.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-758+6732G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(807): Show |
1 | a0001c0001t0001g0028 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(818): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(865): Show |
1 | a0001c0001t0001g0257 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(876): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(776): Show |
4 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0021others(1): Show | 4 | NA18957.hp1 NA18965.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+6731_-758+673 others(787): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(795): Show |
1 | a0001c0001t0005g0100 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(806): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(726): Show |
1 | a0001c0001t0025g0036 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(737): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(780): Show |
1 | a0001c0001t0001g0025 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(791): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(753): Show |
2 | a0001c0001t0004g0030a0001c0001t0004g0258 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-758+6731_-758+673 others(764): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(780): Show |
1 | a0001c0001t0001g0019 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(791): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(811): Show |
3 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027 | 3 | HG02135.hp2 NA18986.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-758+6731_-758+673 others(822): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(726): Show |
1 | a0001c0001t0004g0029 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(737): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(757): Show |
1 | a0001c0001t0001g0037 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(768): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(753): Show |
1 | a0001c0001t0001g0015 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(764): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(784): Show |
1 | a0001c0001t0001g0023 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(795): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(695): Show |
1 | a0001c0001t0001g0033 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(706): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(788): Show |
1 | a0001c0001t0004g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(799): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(823): Show |
1 | a0001c0001t0004g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(834): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(672): Show |
1 | a0001c0001t0001g0031 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(683): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(761): Show |
1 | a0001c0001t0001g0032 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(772): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(854): Show |
1 | a0001c0001t0004g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(865): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(552): Show |
1 | a0001c0001t0002g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(563): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(765): Show |
1 | a0001c0001t0004g0046 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(776): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(796): Show |
1 | a0001c0001t0004g0244 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(807): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(796): Show |
1 | a0001c0001t0004g0047 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(807): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(769): Show |
1 | a0001c0001t0004g0041 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(780): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(800): Show |
2 | a0001c0001t0004g0002a0001c0001t0004g0043 | 3 | HG00735.hp2 HG01069.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.-758+6731_-758+673 others(811): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(831): Show |
1 | a0001c0001t0004g0040 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(842): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(556): Show |
1 | a0001c0001t0001g0095 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(567): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(556): Show |
1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(567): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(448): Show |
1 | a0001c0001t0002g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(459): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(769): Show |
1 | a0001c0001t0004g0042 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(780): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(769): Show |
7 | a0001c0001t0004g0044a0001c0001t0004g0049a0001c0001t0004g0050others(4): Show | 8 | HG00733.hp2 HG02056.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-758+6731_-758+673 others(780): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(742): Show |
1 | a0001c0001t0004g0038 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(753): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(746): Show |
1 | a0001c0001t0004g0045 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(757): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(529): Show |
2 | a0001c0001t0001g0064a0001c0001t0010g0065 | 2 | HG01109.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-758+6731_-758+673 others(540): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(560): Show |
2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-758+6731_-758+673 others(571): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(579): Show |
3 | a0001c0001t0005g0099a0001c0001t0005g0102a0001c0001t0012g0101 | 3 | HG02572.hp1 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-758+6731_-758+673 others(590): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(502): Show |
1 | a0001c0001t0001g0069 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(513): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(568): Show |
1 | a0001c0001t0002g0217 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(579): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(622): Show |
1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(633): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(541): Show |
3 | a0001c0001t0005g0055a0001c0001t0005g0056a0001c0001t0005g0057 | 3 | HG02486.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-758+6731_-758+673 others(552): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(626): Show |
2 | a0001c0001t0002g0238a0001c0001t0002g0240 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-758+6731_-758+673 others(637): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(599): Show |
1 | a0001c0001t0006g0122 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(610): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(599): Show |
1 | a0001c0001t0008g0200 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(610): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(630): Show |
1 | a0001c0001t0001g0239 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(641): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(514): Show |
1 | a0001c0001t0001g0058 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(525): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(545): Show |
1 | a0001c0001t0005g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(556): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(568): Show |
1 | a0001c0001t0002g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(579): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(599): Show |
2 | a0001c0001t0008g0233a0001c0001t0008g0236 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-758+6731_-758+673 others(610): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(630): Show |
1 | a0001c0001t0001g0241 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(641): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(572): Show |
1 | a0001c0001t0008g0260 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(583): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(572): Show |
2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-758+6731_-758+673 others(583): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | CATATATT others(545): Show |
1 | a0001c0001t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-758+6731_-758+673 others(556): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679098
|
C | T | 197 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(194): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.-758+6732G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679098 | ||||||
| chr7:7679100
|
T | C | 9 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0001g0121others(6): Show | 9 | HG01081.hp2 HG01934.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-758+6730A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679100 | ||||||
| chr7:7679103
|
A | ATTTATTT others(744): Show |
1 | a0001c0001t0001g0156 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-758+6726_-758+672 others(755): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679103 | ||||||
| chr7:7679103
|
A | ATTTATTT others(749): Show |
2 | a0001c0001t0001g0213a0001c0001t0003g0178 | 2 | NA18998.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-758+6726_-758+672 others(760): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679103 | ||||||
| chr7:7679103
|
A | ATTTATTT others(718): Show |
1 | a0001c0001t0001g0192 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-758+6726_-758+672 others(729): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679103 | ||||||
| chr7:7679103
|
A | G | 8 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0001g0121others(5): Show | 8 | HG01081.hp2 HG01934.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-758+6727T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679103 | ||||||
| chr7:7679108
|
T | C | 3 | a0001c0001t0001g0265a0001c0001t0001g0280a0001c0001t0003g0062 | 3 | HG01123.hp2 NA19081.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-758+6722A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679108 | ||||||
| chr7:7679116
|
G | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0270a0001c0001t0003g0269others(1): Show | 4 | HG00639.hp1 HG01255.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+6714C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(718): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0020 | 2 | NA18999.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-758+6713_-758+671 others(729): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(633): Show |
1 | a0001c0001t0001g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(644): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(552): Show |
1 | a0001c0001t0001g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(563): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(633): Show |
1 | a0001c0001t0001g0081 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(644): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(579): Show |
1 | a0001c0001t0002g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(590): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(552): Show |
1 | a0001c0001t0002g0091 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(563): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(552): Show |
3 | a0001c0001t0001g0066a0001c0001t0002g0087a0001c0001t0017g0090 | 3 | HG01175.hp1 NA18968.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-758+6713_-758+671 others(563): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(525): Show |
1 | a0001c0001t0002g0007 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(536): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(525): Show |
1 | a0001c0001t0002g0092 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(536): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(525): Show |
1 | a0001c0001t0002g0088 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(536): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(525): Show |
2 | a0001c0001t0001g0094a0001c0001t0002g0083 | 2 | HG01975.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-758+6713_-758+671 others(536): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(544): Show |
1 | a0001c0001t0005g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(555): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(498): Show |
3 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0084 | 3 | HG02080.hp2 HG03704.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-758+6713_-758+671 others(509): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(444): Show |
1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(455): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(498): Show |
1 | a0001c0001t0001g0079 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(509): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(471): Show |
1 | a0001c0001t0001g0004 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-758+6713_-758+671 others(482): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(444): Show |
1 | a0001c0001t0001g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(455): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(483): Show |
1 | a0001c0001t0005g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(494): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679116
|
G | GTTTATAA others(610): Show |
1 | a0001c0001t0001g0283 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-758+6713_-758+671 others(621): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679116 | ||||||
| chr7:7679119
|
TATAG | T | 3 | a0001c0001t0001g0114a0001c0001t0002g0300a0001c0001t0019g0299 | 3 | HG02723.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-758+6707_-758+671 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679119 | ||||||
| chr7:7679122
|
A | AAATATAT others(416): Show |
1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-758+6707_-758+670 others(427): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679122 | ||||||
| chr7:7679123
|
G | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0280a0001c0001t0003g0062 | 3 | HG01123.hp2 NA19081.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-758+6707C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679123 | ||||||
| chr7:7679123
|
G | T | 1 | a0001c0001t0001g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-758+6707C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679123 | ||||||
| chr7:7679127
|
A | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0280a0001c0001t0003g0062 | 3 | HG01123.hp2 NA19081.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-758+6703T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679127 | ||||||
| chr7:7679129
|
T | TATTTACA others(614): Show |
2 | a0001c0001t0001g0265a0001c0001t0001g0280 | 2 | NA19081.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-758+6700_-758+670 others(625): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679129 | ||||||
| chr7:7679129
|
T | TATTTACA others(666): Show |
1 | a0001c0001t0003g0062 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-758+6700_-758+670 others(677): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679129 | ||||||
| chr7:7679134
|
A | ATTTATAT others(514): Show |
1 | a0001c0001t0001g0146 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-758+6695_-758+669 others(525): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679134 | ||||||
| chr7:7679134
|
A | ATTTATAT others(50): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0224 | 2 | NA18961.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-758+6695_-758+669 others(61): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679134 | ||||||
| chr7:7679134
|
A | ATTTATAT others(20): Show |
3 | a0001c0001t0001g0054a0001c0001t0001g0190a0001c0001t0006g0182 | 3 | HG00140.hp1 HG01496.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-758+6695_-758+669 others(31): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679134 | ||||||
| chr7:7679134
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-758+6696T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679134 | ||||||
| chr7:7679147
|
G | A | 7 | a0001c0001t0001g0022a0001c0001t0001g0265a0001c0001t0001g0280others(4): Show | 7 | HG00741.hp2 HG01123.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-758+6683C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679147 | ||||||
| chr7:7679153
|
A | AAATATAT others(597): Show |
1 | a0001c0001t0019g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-758+6676_-758+667 others(608): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679153 | ||||||
| chr7:7679154
|
G | T | 1 | a0001c0001t0019g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-758+6676C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679154 | ||||||
| chr7:7679156
|
T | G | 4 | a0001c0001t0001g0271a0001c0001t0003g0263a0001c0001t0003g0277others(1): Show | 4 | HG00140.hp2 NA18959.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-758+6674A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679156 | ||||||
| chr7:7679165
|
A | ATTTATAT others(20): Show |
16 | a0001c0001t0001g0136a0001c0001t0001g0157a0001c0001t0001g0159others(13): Show | 17 | HG00323.hp1 HG00642.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-758+6664_-758+666 others(31): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679165 | ||||||
| chr7:7679178
|
G | A | 1 | a0001c0001t0022g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-758+6652C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679178 | ||||||
| chr7:7679187
|
T | G | 9 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0003g0245others(6): Show | 9 | HG00140.hp2 HG00639.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.-758+6643A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679187 | ||||||
| chr7:7679196
|
A | ATTTATAT others(20): Show |
3 | a0001c0001t0001g0184a0001c0001t0001g0214a0001c0001t0018g0292 | 3 | HG01109.hp1 HG03225.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.-758+6633_-758+663 others(31): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679196 | ||||||
| chr7:7679209
|
G | A | 1 | a0001c0001t0022g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-758+6621C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679209 | ||||||
| chr7:7679218
|
T | G | 14 | a0001c0001t0001g0268a0001c0001t0001g0270a0001c0001t0003g0245others(11): Show | 14 | HG00639.hp1 HG01106.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.-758+6612A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679218 | ||||||
| chr7:7679224
|
T | C | 1 | a0001c0001t0005g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-758+6606A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679224 | ||||||
| chr7:7679227
|
A | ATTTATAT others(20): Show |
10 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0001g0107others(7): Show | 10 | HG00733.hp1 HG00741.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-758+6602_-758+660 others(31): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679227 | ||||||
| chr7:7679227
|
A | G | 1 | a0001c0001t0005g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-758+6603T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679227 | ||||||
| chr7:7679240
|
G | A | 1 | a0001c0001t0022g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-758+6590C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679240 | ||||||
| chr7:7679249
|
T | G | 14 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(11): Show | 14 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.-758+6581A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679249 | ||||||
| chr7:7679258
|
A | ATTTATAT others(20): Show |
2 | a0001c0001t0001g0013a0001c0001t0005g0289 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-758+6571_-758+657 others(31): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679258 | ||||||
| chr7:7679271
|
G | A | 1 | a0001c0001t0022g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-758+6559C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679271 | ||||||
| chr7:7679280
|
T | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0280a0001c0001t0011g0272 | 3 | HG02735.hp1 NA19081.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-758+6550A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679280 | ||||||
| chr7:7679289
|
A | ATTTATAT others(20): Show |
20 | a0001c0001t0001g0215a0001c0001t0001g0232a0001c0001t0004g0002others(17): Show | 22 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+6540_-758+654 others(31): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679289 | ||||||
| chr7:7679302
|
G | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0076a0001c0001t0001g0118others(18): Show | 22 | HG00438.hp2 HG00558.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+6528C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679302 | ||||||
| chr7:7679302
|
G | GTTTATAG others(20): Show |
3 | a0001c0001t0001g0271a0001c0001t0003g0263a0001c0001t0003g0277 | 3 | HG00140.hp2 NA19004.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-758+6527_-758+652 others(31): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679302 | ||||||
| chr7:7679311
|
T | G | 1 | a0001c0001t0011g0272 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-758+6519A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679311 | ||||||
| chr7:7679312
|
A | ACATGTTT others(50): Show |
1 | a0001c0001t0004g0040 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-758+6517_-758+651 others(61): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679312 | ||||||
| chr7:7679320
|
A | ATTTATAT others(20): Show |
1 | a0001c0001t0008g0260 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-758+6509_-758+651 others(31): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679320 | ||||||
| chr7:7679333
|
G | A | 32 | a0001c0001t0001g0005a0001c0001t0001g0074a0001c0001t0001g0076others(29): Show | 33 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.-758+6497C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679333 | ||||||
| chr7:7679340
|
GATA | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02698.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-758+6487_-758+648 others(7): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679340 | ||||||
| chr7:7679342
|
T | TA | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(204): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.-758+6487dupT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(21): Show |
1 | a0001c0001t0003g0278 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-758+6487_-758+648 others(32): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(52): Show |
4 | a0001c0001t0003g0245a0001c0001t0003g0274a0001c0001t0003g0276others(1): Show | 4 | HG02129.hp2 NA18970.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+6487_-758+648 others(63): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(21): Show |
50 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(47): Show | 50 | HG00544.hp2 HG00741.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.-758+6487_-758+648 others(32): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(300): Show |
1 | a0001c0001t0001g0143 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-758+6487_-758+648 others(311): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(331): Show |
2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-758+6487_-758+648 others(342): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(362): Show |
1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-758+6487_-758+648 others(373): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(83): Show |
1 | a0001c0001t0011g0170 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-758+6487_-758+648 others(94): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(145): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-758+6487_-758+648 others(156): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(362): Show |
1 | a0001c0001t0001g0188 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-758+6487_-758+648 others(373): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(424): Show |
1 | a0001c0001t0001g0183 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-758+6487_-758+648 others(435): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(176): Show |
1 | a0001c0001t0001g0208 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-758+6487_-758+648 others(187): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(207): Show |
2 | a0001c0001t0001g0207a0001c0001t0016g0152 | 2 | HG02698.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-758+6487_-758+648 others(218): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(424): Show |
1 | a0001c0001t0006g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-758+6487_-758+648 others(435): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(362): Show |
1 | a0001c0001t0001g0117 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-758+6487_-758+648 others(373): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679342
|
T | TACATGTT others(204): Show |
1 | a0001c0001t0002g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-758+6487_-758+648 others(215): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679342 | ||||||
| chr7:7679347
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02698.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-758+6483A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679347 | ||||||
| chr7:7679350
|
A | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG02698.hp2 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-758+6480T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679350 | ||||||
| chr7:7679363
|
G | A | 56 | a0001c0001t0001g0005a0001c0001t0001g0074a0001c0001t0001g0076others(53): Show | 57 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-758+6467C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679363 | ||||||
| chr7:7679370
|
GATA | G | 11 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(8): Show | 13 | HG01243.hp1 HG02257.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(7): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679370 | ||||||
| chr7:7679372
|
T | TA | 128 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(125): Show | 130 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-758+6457dupT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TAAATATA others(424): Show |
2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(435): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(52): Show |
2 | a0001c0001t0001g0270a0001c0001t0003g0273 | 2 | HG00639.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(63): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(83): Show |
11 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0280others(8): Show | 11 | HG01106.hp2 HG01123.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(94): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(114): Show |
1 | a0001c0001t0003g0266 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(125): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(21): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG02109.hp1 HG03579.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(32): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(331): Show |
5 | a0001c0001t0001g0161a0001c0001t0001g0210a0001c0001t0002g0106others(2): Show | 5 | HG01361.hp2 HG01934.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(342): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(362): Show |
2 | a0001c0001t0002g0219a0001c0001t0002g0220 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(373): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(393): Show |
1 | a0001c0001t0001g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(404): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(424): Show |
1 | a0001c0001t0001g0227 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(435): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(517): Show |
1 | a0001c0001t0001g0202 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(528): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(548): Show |
1 | a0001c0001t0001g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(559): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(455): Show |
1 | a0001c0001t0001g0141 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(466): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(238): Show |
5 | a0001c0001t0001g0154a0001c0001t0001g0172a0001c0001t0001g0254others(2): Show | 5 | HG02080.hp1 HG02135.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(249): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(331): Show |
20 | a0001c0001t0001g0126a0001c0001t0001g0132a0001c0001t0001g0138others(17): Show | 20 | HG00280.hp1 HG01123.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(342): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(362): Show |
5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0007g0209others(2): Show | 5 | HG00639.hp2 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(373): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(331): Show |
1 | a0001c0001t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(342): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(362): Show |
1 | a0001c0001t0002g0093 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(373): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(486): Show |
1 | a0001c0001t0006g0148 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(497): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(517): Show |
1 | a0001c0001t0006g0144 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(528): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(331): Show |
1 | a0001c0001t0001g0249 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(342): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(389): Show |
1 | a0001c0001t0001g0124 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(400): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(331): Show |
1 | a0001c0001t0001g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(342): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(82): Show |
1 | a0001c0001t0001g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-758+6457_-758+645 others(93): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(204): Show |
4 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0094others(1): Show | 4 | HG01975.hp2 HG02523.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(215): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(235): Show |
12 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(9): Show | 12 | HG00280.hp2 HG00323.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(246): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(266): Show |
1 | a0001c0001t0001g0004 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(277): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679372
|
T | TACATGTT others(203): Show |
4 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(1): Show | 4 | HG02572.hp1 HG02717.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-758+6457_-758+645 others(214): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679372 | ||||||
| chr7:7679377
|
T | C | 11 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(8): Show | 13 | HG01243.hp1 HG02257.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-758+6453A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679377 | ||||||
| chr7:7679380
|
A | G | 14 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(11): Show | 16 | HG01243.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-758+6450T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679380 | ||||||
| chr7:7679384
|
A | ATATATTT others(171): Show |
1 | a0001c0001t0005g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-758+6445_-758+644 others(182): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679384 | ||||||
| chr7:7679393
|
A | G | 38 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(35): Show | 40 | HG01069.hp2 HG01081.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.-758+6437T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679393 | ||||||
| chr7:7679400
|
GATA | G | 3 | a0001c0001t0001g0112a0001c0001t0002g0300a0001c0001t0010g0155 | 3 | HG00438.hp1 HG02723.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-758+6427_-758+642 others(7): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679400 | ||||||
| chr7:7679402
|
T | TA | 267 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(264): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-758+6427dupT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679402 | ||||||
| chr7:7679402
|
T | TAATATAT others(24): Show |
4 | a0001c0001t0004g0002a0001c0001t0004g0043a0001c0001t0004g0047others(1): Show | 5 | HG00735.hp2 HG01069.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+6397_-758+642 others(35): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679402 | ||||||
| chr7:7679402
|
T | TACATGTT others(173): Show |
1 | a0001c0001t0001g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-758+6427_-758+642 others(184): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679402 | ||||||
| chr7:7679404
|
ATAT | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+6423_-758+642 others(7): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679404 | ||||||
| chr7:7679407
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0002g0300 | 2 | HG02723.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-758+6423A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679407 | ||||||
| chr7:7679409
|
T | C | 1 | a0001c0001t0003g0277 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-758+6421A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679409 | ||||||
| chr7:7679410
|
A | G | 8 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0115others(5): Show | 8 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.-758+6420T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679410 | ||||||
| chr7:7679412
|
T | TTATATAT others(353): Show |
1 | a0001c0001t0001g0230 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-758+6417_-758+641 others(364): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679412 | ||||||
| chr7:7679414
|
A | ATATATTT others(22): Show |
1 | a0001c0001t0025g0036 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-758+6387_-758+641 others(33): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679414 | ||||||
| chr7:7679423
|
A | G | 16 | a0001c0001t0001g0061a0001c0001t0001g0096a0001c0001t0001g0103others(13): Show | 16 | HG02109.hp1 HG02257.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.-758+6407T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679423 | ||||||
| chr7:7679433
|
A | ACATGTTT others(50): Show |
1 | a0001c0001t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-758+6396_-758+639 others(61): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679433 | ||||||
| chr7:7679441
|
A | G | 5 | a0001c0001t0001g0114a0001c0001t0002g0300a0001c0001t0015g0297others(2): Show | 5 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-758+6389T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679441 | ||||||
| chr7:7679445
|
ATATATTT others(22): Show |
A | 1 | a0001c0001t0001g0165 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-758+6356_-758+638 others(33): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679445 | ||||||
| chr7:7679449
|
A | G | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+6381T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679449 | ||||||
| chr7:7679454
|
A | G | 9 | a0001c0001t0001g0096a0001c0001t0001g0112a0001c0001t0001g0283others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-758+6376T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679454 | ||||||
| chr7:7679468
|
A | G | 2 | a0001c0001t0001g0261a0001c0001t0003g0225 | 2 | HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-758+6362T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679468 | ||||||
| chr7:7679472
|
A | G | 3 | a0001c0001t0002g0300a0001c0001t0015g0298a0001c0001t0019g0299 | 3 | HG02723.hp2 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-758+6358T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679472 | ||||||
| chr7:7679474
|
T | TTA | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(178): Show | 185 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.-758+6354_-758+635 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(57): Show |
12 | a0001c0001t0001g0070a0001c0001t0001g0163a0001c0001t0001g0168others(9): Show | 12 | HG00140.hp1 HG00642.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.-758+6355_-758+635 others(68): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(88): Show |
9 | a0001c0001t0001g0105a0001c0001t0001g0121a0001c0001t0001g0136others(6): Show | 9 | HG01928.hp1 HG01934.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.-758+6355_-758+635 others(99): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(119): Show |
4 | a0001c0001t0001g0075a0001c0001t0001g0157a0001c0001t0001g0159others(1): Show | 5 | HG00323.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+6355_-758+635 others(130): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(150): Show |
8 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0113others(5): Show | 8 | HG00741.hp1 HG01496.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-758+6355_-758+635 others(161): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(181): Show |
3 | a0001c0001t0001g0107a0001c0001t0006g0182a0001c0001t0013g0111 | 3 | HG02630.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-758+6355_-758+635 others(192): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(212): Show |
5 | a0001c0001t0001g0008a0001c0001t0001g0077a0001c0001t0001g0134others(2): Show | 5 | HG02809.hp1 HG02970.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-758+6355_-758+635 others(223): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(243): Show |
1 | a0001c0001t0006g0221 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-758+6355_-758+635 others(254): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(274): Show |
4 | a0001c0001t0001g0131a0001c0001t0001g0140a0001c0001t0001g0215others(1): Show | 4 | HG00733.hp1 HG00735.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.-758+6355_-758+635 others(285): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(336): Show |
1 | a0001c0001t0001g0184 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-758+6355_-758+635 others(347): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(26): Show |
1 | a0001c0001t0007g0187 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-758+6355_-758+635 others(37): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(57): Show |
1 | a0001c0001t0001g0112 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-758+6355_-758+635 others(68): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(301): Show |
1 | a0001c0001t0001g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-758+6355_-758+635 others(312): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATAT others(332): Show |
1 | a0001c0001t0005g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-758+6355_-758+635 others(343): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATTT others(24): Show |
20 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0023others(17): Show | 21 | HG00544.hp2 HG00735.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.-758+6325_-758+635 others(35): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATTT others(55): Show |
8 | a0001c0001t0001g0037a0001c0001t0001g0071a0001c0001t0002g0217others(5): Show | 8 | HG01261.hp1 HG01346.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-758+6294_-758+635 others(66): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679474
|
T | TTATATTT others(55): Show |
2 | a0001c0001t0002g0235a0001c0001t0008g0242 | 2 | HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-758+6355_-758+635 others(66): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679474 | ||||||
| chr7:7679483
|
A | ATTTATAG others(24): Show |
10 | a0001c0001t0001g0239a0001c0001t0002g0234a0001c0001t0002g0237others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-758+6346_-758+634 others(35): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679483 | ||||||
| chr7:7679483
|
A | G | 6 | a0001c0001t0001g0112a0001c0001t0001g0283a0001c0001t0007g0010others(3): Show | 6 | HG02257.hp1 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+6347T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679483 | ||||||
| chr7:7679501
|
A | G | 1 | a0001c0001t0019g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-758+6329T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679501 | ||||||
| chr7:7679503
|
TTA | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02698.hp2 HG03579.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.-758+6325_-758+632 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679503 | ||||||
| chr7:7679514
|
A | G | 9 | a0001c0001t0001g0112a0001c0001t0001g0241a0001c0001t0007g0010others(6): Show | 9 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-758+6316T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679514 | ||||||
| chr7:7679534
|
T | TTATATAT others(113): Show |
1 | a0001c0001t0001g0146 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-758+6176_-758+629 others(124): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679534 | ||||||
| chr7:7679545
|
A | G | 5 | a0001c0001t0001g0112a0001c0001t0007g0010a0001c0001t0007g0169others(2): Show | 5 | HG02257.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+6285T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679545 | ||||||
| chr7:7679567
|
A | ATATTTAA others(20): Show |
1 | a0001c0001t0001g0283 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-758+6262_-758+626 others(31): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679567 | ||||||
| chr7:7679576
|
A | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0112a0001c0001t0007g0010others(3): Show | 6 | HG02257.hp1 HG02965.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-758+6254T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679576 | ||||||
| chr7:7679607
|
A | G | 5 | a0001c0001t0001g0061a0001c0001t0007g0010a0001c0001t0007g0169others(2): Show | 5 | HG02257.hp1 HG02965.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-758+6223T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679607 | ||||||
| chr7:7679638
|
A | ATTTATAG others(144): Show |
1 | a0001c0001t0001g0095 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-758+6191_-758+619 others(155): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679638 | ||||||
| chr7:7679638
|
A | ATTTATAG others(210): Show |
1 | a0001c0001t0002g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-758+6191_-758+619 others(221): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679638 | ||||||
| chr7:7679638
|
A | ATTTATAG others(237): Show |
1 | a0001c0001t0001g0069 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-758+6191_-758+619 others(248): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679638 | ||||||
| chr7:7679638
|
A | ATTTATAG others(175): Show |
5 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | HG01109.hp2 HG01175.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+6191_-758+619 others(186): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679638 | ||||||
| chr7:7679638
|
A | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0079others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.-758+6192T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679638 | ||||||
| chr7:7679649
|
AATAT | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+6177_-758+618 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679649 | ||||||
| chr7:7679669
|
A | G | 7 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0002g0007others(4): Show | 7 | HG02523.hp2 NA18952.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+6161T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679669 | ||||||
| chr7:7679711
|
A | AATATATA others(26): Show |
1 | a0001c0001t0004g0047 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-758+6118_-758+611 others(37): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679711 | ||||||
| chr7:7679711
|
AAT | A | 29 | a0001c0001t0001g0061a0001c0001t0001g0114a0001c0001t0001g0115others(26): Show | 31 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.-758+6117_-758+611 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679711 | ||||||
| chr7:7679724
|
A | T | 1 | a0001c0001t0002g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-758+6106T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679724 | ||||||
| chr7:7679729
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0129a0001c0001t0002g0093 | 3 | HG01346.hp2 HG03704.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-758+6101A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679729 | ||||||
| chr7:7679731
|
T | C | 176 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(173): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-758+6099A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679731 | ||||||
| chr7:7679731
|
T | TAC | 12 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(9): Show | 12 | HG02040.hp1 HG02148.hp1 HG04184.hp1 others(9): Show |
intron_variant | MODIFIER | c.-758+6097_-758+609 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7679731 | ||||||
| chr7:7680109
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-758+5721G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7680109 | ||||||
| chr7:7680308
|
A | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0002g0098 | 3 | HG01891.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-758+5522T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7680308 | ||||||
| chr7:7680356
|
T | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(141): Show | 146 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.-758+5474A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7680356 | ||||||
| chr7:7680386
|
C | T | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+5444G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7680386 | ||||||
| chr7:7680487
|
T | G | 21 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0239others(18): Show | 21 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.-758+5343A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7680487 | ||||||
| chr7:7680540
|
A | G | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+5290T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7680540 | ||||||
| chr7:7680563
|
C | A | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-758+5267G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7680563 | ||||||
| chr7:7680568
|
C | T | 189 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-758+5262G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7680568 | ||||||
| chr7:7680688
|
AT | A | 49 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0061others(46): Show | 50 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.-758+5141delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7680688 | ||||||
| chr7:7680717
|
G | T | 189 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-758+5113C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7680717 | ||||||
| chr7:7681011
|
T | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+4819A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7681011 | ||||||
| chr7:7681044
|
T | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01891.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-758+4786A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7681044 | ||||||
| chr7:7681248
|
A | T | 1 | a0001c0001t0004g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-758+4582T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7681248 | ||||||
| chr7:7681498
|
TG | T | 11 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(8): Show | 13 | HG01243.hp1 HG02486.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.-758+4331delC | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7681498 | ||||||
| chr7:7681683
|
C | T | 1 | a0001c0001t0005g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-758+4147G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7681683 | ||||||
| chr7:7681708
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-758+4122T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7681708 | ||||||
| chr7:7681746
|
C | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0154a0001c0001t0001g0172 | 3 | HG00438.hp2 NA18970.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.-758+4084G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7681746 | ||||||
| chr7:7681909
|
A | T | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+3921T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7681909 | ||||||
| chr7:7682015
|
A | C | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+3815T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7682015 | ||||||
| chr7:7682154
|
C | T | 1 | a0001c0001t0006g0221 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-758+3676G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7682154 | ||||||
| chr7:7682186
|
A | G | 1 | a0001c0001t0011g0170 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-758+3644T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7682186 | ||||||
| chr7:7682330
|
TC | T | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+3499delG | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7682330 | ||||||
| chr7:7682429
|
T | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(13): Show | 17 | HG00280.hp2 HG00323.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-758+3401A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7682429 | ||||||
| chr7:7682443
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-758+3387T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7682443 | ||||||
| chr7:7682497
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-758+3333C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7682497 | ||||||
| chr7:7682707
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-758+3123A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7682707 | ||||||
| chr7:7682761
|
C | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(25): Show | 29 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.-758+3069G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7682761 | ||||||
| chr7:7682762
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-758+3068C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7682762 | ||||||
| chr7:7683020
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-758+2810G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683020 | ||||||
| chr7:7683027
|
G | A | 6 | a0001c0001t0001g0058a0001c0001t0005g0055a0001c0001t0005g0056others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+2803C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683027 | ||||||
| chr7:7683167
|
T | C | 189 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-758+2663A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683167 | ||||||
| chr7:7683631
|
C | T | 188 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-758+2199G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683631 | ||||||
| chr7:7683666
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-758+2164T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683666 | ||||||
| chr7:7683751
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-758+2079A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683751 | ||||||
| chr7:7683774
|
C | T | 1 | a0001c0001t0003g0273 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-758+2056G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683774 | ||||||
| chr7:7683803
|
G | T | 1 | a0001c0001t0004g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-758+2027C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683803 | ||||||
| chr7:7683823
|
A | G | 153 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(150): Show | 155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.-758+2007T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683823 | ||||||
| chr7:7683831
|
C | T | 14 | a0001c0001t0001g0061a0001c0001t0001g0239a0001c0001t0001g0241others(11): Show | 14 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-758+1999G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683831 | ||||||
| chr7:7683835
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-758+1995G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683835 | ||||||
| chr7:7683902
|
C | T | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+1928G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683902 | ||||||
| chr7:7683947
|
T | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0146a0001c0001t0001g0168 | 3 | HG01952.hp1 HG02004.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-758+1883A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683947 | ||||||
| chr7:7683948
|
A | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0146a0001c0001t0001g0168 | 3 | HG01952.hp1 HG02004.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-758+1882T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7683948 | ||||||
| chr7:7684201
|
A | T | 1 | a0001c0001t0001g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-758+1629T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684201 | ||||||
| chr7:7684295
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-758+1535C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684295 | ||||||
| chr7:7684368
|
A | AT | 23 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(20): Show | 23 | HG00544.hp2 HG02004.hp2 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-758+1461dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684368 | ||||||
| chr7:7684460
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-758+1370G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684460 | ||||||
| chr7:7684519
|
A | G | 21 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(18): Show | 21 | HG00544.hp2 HG02004.hp2 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-758+1311T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684519 | ||||||
| chr7:7684563
|
C | T | 189 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-758+1267G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684563 | ||||||
| chr7:7684575
|
T | G | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-758+1255A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684575 | ||||||
| chr7:7684584
|
C | T | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-758+1246G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684584 | ||||||
| chr7:7684615
|
G | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+1215C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684615 | ||||||
| chr7:7684689
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | NA18953.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-758+1141G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684689 | ||||||
| chr7:7684782
|
C | T | 1 | a0001c0001t0001g0082 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-758+1048G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684782 | ||||||
| chr7:7684887
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-758+943C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684887 | ||||||
| chr7:7684906
|
A | T | 1 | a0001c0001t0001g0103 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-758+924T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684906 | ||||||
| chr7:7684985
|
C | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG00140.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.-758+845G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684985 | ||||||
| chr7:7684989
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-758+841A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7684989 | ||||||
| chr7:7685109
|
G | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-758+721C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7685109 | ||||||
| chr7:7685131
|
T | C | 1 | a0001c0001t0008g0200 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-758+699A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7685131 | ||||||
| chr7:7685174
|
T | C | 161 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(158): Show | 163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-758+656A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7685174 | ||||||
| chr7:7685301
|
T | C | 189 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(186): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-758+529A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7685301 | ||||||
| chr7:7685314
|
C | CT | 183 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(180): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.-758+515dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7685314 | ||||||
| chr7:7685434
|
C | T | 2 | a0001c0001t0004g0038a0001c0001t0004g0049 | 2 | HG01261.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-758+396G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7685434 | ||||||
| chr7:7685464
|
C | T | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-758+366G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7685464 | ||||||
| chr7:7685495
|
G | C | 1 | a0001c0001t0005g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-758+335C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 4/7 | chr7 | 7685495 | ||||||
| chr7:7686287
|
A | C | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-926-289T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 3/7 | chr7 | 7686287 | ||||||
| chr7:7686396
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-926-398T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 3/7 | chr7 | 7686396 | ||||||
| chr7:7686496
|
A | C | 1 | a0001c0001t0014g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-926-498T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 3/7 | chr7 | 7686496 | ||||||
| chr7:7686576
|
T | C | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-926-578A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 3/7 | chr7 | 7686576 | ||||||
| chr7:7686612
|
T | G | 166 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(163): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-926-614A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 3/7 | chr7 | 7686612 | ||||||
| chr7:7686764
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-927+464C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 3/7 | chr7 | 7686764 | ||||||
| chr7:7686945
|
C | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0283 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-927+283G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 3/7 | chr7 | 7686945 | ||||||
| chr7:7687000
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-927+228C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 3/7 | chr7 | 7687000 | ||||||
| chr7:7687024
|
G | T | 3 | a0001c0001t0005g0289a0001c0001t0005g0291a0001c0001t0022g0243 | 3 | HG02647.hp2 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-927+204C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 3/7 | chr7 | 7687024 | ||||||
| chr7:7687054
|
A | C | 1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-927+174T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 3/7 | chr7 | 7687054 | ||||||
| chr7:7687376
|
C | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-1027-48G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7687376 | ||||||
| chr7:7687383
|
C | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0131a0001c0001t0001g0143others(10): Show | 13 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1027-55G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7687383 | ||||||
| chr7:7687384
|
A | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0131a0001c0001t0001g0143others(10): Show | 13 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1027-56T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7687384 | ||||||
| chr7:7687435
|
T | C | 24 | a0001c0001t0001g0218a0001c0001t0001g0265a0001c0001t0001g0268others(21): Show | 24 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-1027-107A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7687435 | ||||||
| chr7:7687470
|
G | T | 166 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(163): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-1027-142C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7687470 | ||||||
| chr7:7687575
|
C | G | 5 | a0001c0001t0002g0253a0001c0001t0007g0010a0001c0001t0007g0169others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-247G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7687575 | ||||||
| chr7:7687628
|
A | T | 1 | a0001c0001t0016g0152 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-1027-300T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7687628 | ||||||
| chr7:7687653
|
A | G | 2 | a0001c0001t0016g0104a0001c0001t0016g0152 | 2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-1027-325T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7687653 | ||||||
| chr7:7687974
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-1027-646A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7687974 | ||||||
| chr7:7688130
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-1027-802C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7688130 | ||||||
| chr7:7688145
|
G | T | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1027-817C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7688145 | ||||||
| chr7:7688148
|
A | C | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-1027-820T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7688148 | ||||||
| chr7:7688249
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1027-921G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7688249 | ||||||
| chr7:7688343
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1027-1015G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7688343 | ||||||
| chr7:7688344
|
G | A | 161 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(158): Show | 163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-1027-1016C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7688344 | ||||||
| chr7:7688389
|
AG | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1027-1062delC | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7688389 | ||||||
| chr7:7688440
|
T | C | 4 | a0001c0001t0002g0106a0001c0001t0002g0219a0001c0001t0002g0220others(1): Show | 4 | HG02818.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1027-1112A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7688440 | ||||||
| chr7:7688631
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-1027-1303T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7688631 | ||||||
| chr7:7688704
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-1027-1376C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7688704 | ||||||
| chr7:7688777
|
A | C | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1027-1449T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7688777 | ||||||
| chr7:7688822
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1027-1494T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7688822 | ||||||
| chr7:7689189
|
T | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(23): Show | 27 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-1027-1861A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7689189 | ||||||
| chr7:7689199
|
C | A | 1 | a0001c0001t0001g0283 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-1027-1871G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7689199 | ||||||
| chr7:7689204
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-1027-1876A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7689204 | ||||||
| chr7:7689258
|
A | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0146a0001c0001t0001g0168 | 3 | HG01952.hp1 HG02004.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-1027-1930T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7689258 | ||||||
| chr7:7689300
|
A | G | 1 | a0001c0001t0003g0273 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-1027-1972T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7689300 | ||||||
| chr7:7689315
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1027-1987A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7689315 | ||||||
| chr7:7689479
|
G | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0186others(1): Show | 4 | HG02040.hp2 NA18985.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1027-2151C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7689479 | ||||||
| chr7:7689486
|
A | G | 1 | a0001c0001t0003g0269 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-1027-2158T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7689486 | ||||||
| chr7:7689570
|
A | G | 1 | a0001c0001t0023g0167 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-1027-2242T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7689570 | ||||||
| chr7:7689616
|
C | G | 166 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(163): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-1027-2288G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7689616 | ||||||
| chr7:7689696
|
T | C | 1 | a0001c0001t0004g0045 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-1027-2368A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7689696 | ||||||
| chr7:7689745
|
T | C | 2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-1027-2417A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7689745 | ||||||
| chr7:7690080
|
C | G | 166 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(163): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-1027-2752G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7690080 | ||||||
| chr7:7690256
|
G | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1027-2928C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7690256 | ||||||
| chr7:7690609
|
A | C | 1 | a0001c0001t0004g0244 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-1027-3281T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7690609 | ||||||
| chr7:7690718
|
T | G | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-3390A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7690718 | ||||||
| chr7:7690743
|
G | A | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-3415C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7690743 | ||||||
| chr7:7690791
|
C | CAT | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-3465_-1027-3 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7690791 | ||||||
| chr7:7691013
|
G | A | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-3685C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7691013 | ||||||
| chr7:7691051
|
T | C | 204 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(201): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.-1027-3723A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7691051 | ||||||
| chr7:7691084
|
C | T | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-3756G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7691084 | ||||||
| chr7:7691165
|
T | C | 36 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(33): Show | 36 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.-1027-3837A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7691165 | ||||||
| chr7:7691213
|
T | C | 1 | a0001c0001t0007g0010 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-1027-3885A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7691213 | ||||||
| chr7:7691334
|
G | A | 1 | a0001c0001t0004g0244 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-1027-4006C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7691334 | ||||||
| chr7:7691359
|
C | T | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1027-4031G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7691359 | ||||||
| chr7:7691461
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1027-4133C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7691461 | ||||||
| chr7:7691678
|
G | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(93): Show | 101 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.-1027-4350C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7691678 | ||||||
| chr7:7691775
|
A | G | 1 | a0001c0001t0012g0288 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-1027-4447T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7691775 | ||||||
| chr7:7692139
|
A | C | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-4811T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7692139 | ||||||
| chr7:7692140
|
C | T | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-4812G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7692140 | ||||||
| chr7:7692145
|
G | A | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-4817C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7692145 | ||||||
| chr7:7692335
|
T | G | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-5007A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7692335 | ||||||
| chr7:7692514
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-1027-5186T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7692514 | ||||||
| chr7:7692766
|
T | C | 6 | a0001c0001t0001g0218a0001c0001t0005g0099a0001c0001t0005g0100others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1027-5438A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7692766 | ||||||
| chr7:7692809
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-1027-5481T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7692809 | ||||||
| chr7:7692814
|
G | A | 1 | a0001c0001t0003g0281 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-1027-5486C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7692814 | ||||||
| chr7:7692839
|
C | T | 1 | a0001c0001t0012g0288 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-1027-5511G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7692839 | ||||||
| chr7:7692900
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-1027-5572G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7692900 | ||||||
| chr7:7693032
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-1027-5704G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693032 | ||||||
| chr7:7693054
|
TTA | T | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-5728_-1027-5 others(8): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693054 | ||||||
| chr7:7693160
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0010g0065 | 2 | HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-1027-5832T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693160 | ||||||
| chr7:7693229
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1027-5901A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693229 | ||||||
| chr7:7693293
|
C | CTATCTAT others(3): Show |
3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0249 | 3 | HG00673.hp1 HG00673.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-1027-5966_-1027-5 others(16): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693293 | ||||||
| chr7:7693293
|
C | CTATCTAT others(7): Show |
2 | a0001c0001t0001g0031a0001c0001t0004g0258 | 2 | HG03491.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-1027-5966_-1027-5 others(20): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693293 | ||||||
| chr7:7693295
|
T | C | 5 | a0001c0001t0001g0031a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG00673.hp1 HG00673.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1027-5967A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693295 | ||||||
| chr7:7693295
|
T | TTATC | 50 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0071others(47): Show | 51 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.-1027-5971_-1027-5 others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693295 | ||||||
| chr7:7693295
|
T | TTATCTAT others(1): Show |
101 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(98): Show | 104 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-1027-5975_-1027-5 others(14): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693295 | ||||||
| chr7:7693295
|
T | TTATCTAT others(5): Show |
91 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0023others(88): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-1027-5979_-1027-5 others(18): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693295 | ||||||
| chr7:7693295
|
T | TTATCTAT others(9): Show |
21 | a0001c0001t0001g0069a0001c0001t0001g0196a0001c0001t0001g0197others(18): Show | 21 | HG00558.hp1 HG01358.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.-1027-5983_-1027-5 others(22): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693295 | ||||||
| chr7:7693295
|
T | TTATCTAT others(13): Show |
2 | a0001c0001t0005g0060a0001c0001t0008g0200 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-1027-5987_-1027-5 others(26): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693295 | ||||||
| chr7:7693295
|
TTATC | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0116a0001c0001t0012g0293 | 3 | HG02109.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-1027-5971_-1027-5 others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693295 | ||||||
| chr7:7693295
|
TTATCTAT others(1): Show |
T | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0002g0300others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1027-5975_-1027-5 others(14): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693295 | ||||||
| chr7:7693347
|
G | A | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1027-6019C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693347 | ||||||
| chr7:7693387
|
C | A | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-6059G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693387 | ||||||
| chr7:7693551
|
A | G | 1 | a0001c0001t0002g0217 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-1027-6223T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693551 | ||||||
| chr7:7693594
|
C | G | 1 | a0001c0001t0002g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-1027-6266G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693594 | ||||||
| chr7:7693646
|
A | G | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-6318T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693646 | ||||||
| chr7:7693730
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1027-6402T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7693730 | ||||||
| chr7:7694015
|
G | A | 1 | a0001c0001t0002g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-1027-6687C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694015 | ||||||
| chr7:7694019
|
A | G | 2 | a0001c0001t0002g0009a0001c0001t0002g0011 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-1027-6691T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694019 | ||||||
| chr7:7694066
|
G | A | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-6738C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694066 | ||||||
| chr7:7694072
|
G | C | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1027-6744C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694072 | ||||||
| chr7:7694097
|
G | A | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-6769C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694097 | ||||||
| chr7:7694172
|
C | A | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-6844G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694172 | ||||||
| chr7:7694216
|
A | G | 36 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(33): Show | 36 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.-1027-6888T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694216 | ||||||
| chr7:7694217
|
C | T | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-6889G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694217 | ||||||
| chr7:7694378
|
G | A | 36 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(33): Show | 36 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.-1027-7050C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694378 | ||||||
| chr7:7694498
|
G | A | 1 | a0001c0001t0001g0005 | 2 | NA18957.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-1027-7170C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694498 | ||||||
| chr7:7694563
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-1027-7235G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694563 | ||||||
| chr7:7694572
|
A | G | 3 | a0001c0001t0002g0093a0001c0001t0003g0072a0001c0001t0003g0073 | 3 | HG01168.hp2 HG01346.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-1027-7244T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694572 | ||||||
| chr7:7694609
|
A | T | 1 | a0001c0001t0001g0143 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-1027-7281T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694609 | ||||||
| chr7:7694643
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-1027-7315T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694643 | ||||||
| chr7:7694674
|
A | G | 15 | a0001c0001t0001g0265a0001c0001t0001g0280a0001c0001t0003g0245others(12): Show | 15 | HG02129.hp2 NA18948.hp1 NA18959.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1027-7346T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694674 | ||||||
| chr7:7694740
|
G | C | 1 | a0001c0001t0001g0203 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-1027-7412C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694740 | ||||||
| chr7:7694758
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1027-7430C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694758 | ||||||
| chr7:7694926
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1027-7598G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7694926 | ||||||
| chr7:7695100
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-1027-7772A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7695100 | ||||||
| chr7:7695180
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-1027-7852C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7695180 | ||||||
| chr7:7695198
|
C | T | 144 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(141): Show | 149 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.-1027-7870G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7695198 | ||||||
| chr7:7695439
|
A | AT | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1027-8112dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7695439 | ||||||
| chr7:7695462
|
C | A | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1027-8134G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7695462 | ||||||
| chr7:7695868
|
A | C | 1 | a0001c0001t0018g0292 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-1027-8540T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7695868 | ||||||
| chr7:7695908
|
G | A | 14 | a0001c0001t0001g0265a0001c0001t0001g0280a0001c0001t0003g0245others(11): Show | 14 | HG02129.hp2 NA18948.hp1 NA18959.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1027-8580C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7695908 | ||||||
| chr7:7695943
|
T | C | 31 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(28): Show | 31 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.-1027-8615A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7695943 | ||||||
| chr7:7695981
|
G | GT | 106 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(103): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-1027-8654dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7695981 | ||||||
| chr7:7695981
|
GT | G | 9 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(6): Show | 11 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1027-8654delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7695981 | ||||||
| chr7:7696003
|
A | G | 9 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(6): Show | 11 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1027-8675T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7696003 | ||||||
| chr7:7696040
|
C | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA18946.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-1027-8712G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7696040 | ||||||
| chr7:7696313
|
C | A | 9 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(6): Show | 11 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1027-8985G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7696313 | ||||||
| chr7:7696424
|
T | C | 1 | a0001c0001t0001g0082 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-1027-9096A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7696424 | ||||||
| chr7:7696605
|
C | T | 9 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(6): Show | 11 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1027-9277G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7696605 | ||||||
| chr7:7696655
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-1027-9327T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7696655 | ||||||
| chr7:7696713
|
C | A | 1 | a0001c0001t0001g0218 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-1027-9385G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7696713 | ||||||
| chr7:7696726
|
G | C | 9 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(6): Show | 11 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1027-9398C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7696726 | ||||||
| chr7:7696788
|
G | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(90): Show | 96 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.-1027-9460C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7696788 | ||||||
| chr7:7696840
|
C | CT | 9 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(6): Show | 11 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1027-9513dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7696840 | ||||||
| chr7:7696883
|
A | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18985.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-1027-9555T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7696883 | ||||||
| chr7:7697016
|
G | A | 9 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(6): Show | 11 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1027-9688C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7697016 | ||||||
| chr7:7697044
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-1027-9716T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7697044 | ||||||
| chr7:7697076
|
G | C | 13 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(10): Show | 15 | HG01243.hp1 HG02109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1027-9748C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7697076 | ||||||
| chr7:7697173
|
A | G | 4 | a0001c0001t0001g0070a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG01081.hp2 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1027-9845T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7697173 | ||||||
| chr7:7697200
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-1027-9872G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7697200 | ||||||
| chr7:7697417
|
C | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(89): Show | 95 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-1027-10089G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7697417 | ||||||
| chr7:7697449
|
T | C | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1027-10121A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7697449 | ||||||
| chr7:7697505
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1027-10177C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7697505 | ||||||
| chr7:7697506
|
A | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0140a0001c0001t0001g0141 | 3 | HG03831.hp2 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-1027-10178T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7697506 | ||||||
| chr7:7697590
|
GC | G | 3 | a0001c0001t0005g0289a0001c0001t0005g0291a0001c0001t0022g0243 | 3 | HG02647.hp2 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-1027-10263delG | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7697590 | ||||||
| chr7:7697666
|
G | A | 1 | a0001c0001t0007g0206 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-1027-10338C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7697666 | ||||||
| chr7:7697675
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-1027-10347C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7697675 | ||||||
| chr7:7698114
|
A | G | 1 | a0001c0001t0005g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-1027-10786T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7698114 | ||||||
| chr7:7698233
|
T | C | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1027-10905A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7698233 | ||||||
| chr7:7698262
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-1027-10934T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7698262 | ||||||
| chr7:7698350
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18985.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-1027-11022G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7698350 | ||||||
| chr7:7698411
|
G | A | 1 | a0001c0001t0003g0266 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-1027-11083C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7698411 | ||||||
| chr7:7698831
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-1027-11503G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7698831 | ||||||
| chr7:7698846
|
G | A | 8 | a0001c0001t0001g0085a0001c0001t0002g0007a0001c0001t0002g0086others(5): Show | 8 | HG00741.hp2 HG02132.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1027-11518C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7698846 | ||||||
| chr7:7698870
|
C | CT | 11 | a0001c0001t0001g0022a0001c0001t0001g0079a0001c0001t0001g0114others(8): Show | 11 | HG01243.hp1 HG01993.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1027-11543dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7698870 | ||||||
| chr7:7698870
|
CT | C | 9 | a0001c0001t0001g0208a0001c0001t0001g0295a0001c0001t0002g0098others(6): Show | 11 | HG01069.hp2 HG01109.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1027-11543delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7698870 | ||||||
| chr7:7698930
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-1027-11602G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7698930 | ||||||
| chr7:7698974
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-1027-11646G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7698974 | ||||||
| chr7:7698981
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-1027-11653T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7698981 | ||||||
| chr7:7699034
|
TTG | T | 3 | a0001c0001t0001g0064a0001c0001t0004g0048a0001c0001t0005g0102 | 3 | HG01109.hp2 HG01192.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-1027-11708_-1027- others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699034 | ||||||
| chr7:7699036
|
G | C | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1027-11708C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699036 | ||||||
| chr7:7699049
|
T | G | 11 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00639.hp2 HG01243.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1027-11721A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699049 | ||||||
| chr7:7699049
|
TGG | T | 98 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(95): Show | 103 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.-1027-11723_-1027- others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699049 | ||||||
| chr7:7699051
|
G | T | 36 | a0001c0001t0001g0014a0001c0001t0001g0135a0001c0001t0001g0213others(33): Show | 36 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.-1027-11723C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699051 | ||||||
| chr7:7699053
|
G | T | 4 | a0001c0001t0002g0106a0001c0001t0002g0219a0001c0001t0002g0220others(1): Show | 4 | HG02818.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1027-11725C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699053 | ||||||
| chr7:7699059
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-1027-11731C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699059 | ||||||
| chr7:7699226
|
A | G | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-11898T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699226 | ||||||
| chr7:7699230
|
G | A | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1027-11902C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699230 | ||||||
| chr7:7699334
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-1027-12006G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699334 | ||||||
| chr7:7699365
|
T | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG01175.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-1027-12037A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699365 | ||||||
| chr7:7699494
|
C | CTG | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG01243.hp2 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1027-12168_-1027- others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699494 | ||||||
| chr7:7699575
|
T | C | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1027-12247A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699575 | ||||||
| chr7:7699778
|
A | T | 5 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1027-12450T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699778 | ||||||
| chr7:7699894
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-1027-12566C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699894 | ||||||
| chr7:7699942
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-1027-12614T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699942 | ||||||
| chr7:7699984
|
G | T | 1 | a0001c0001t0003g0133 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-1027-12656C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7699984 | ||||||
| chr7:7700002
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-1027-12674G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700002 | ||||||
| chr7:7700105
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-1027-12777C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700105 | ||||||
| chr7:7700217
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG02135.hp1 NA18998.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-1027-12889C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700217 | ||||||
| chr7:7700429
|
A | G | 13 | a0001c0001t0001g0061a0001c0001t0001g0239a0001c0001t0001g0241others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1027-13101T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700429 | ||||||
| chr7:7700452
|
G | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1027-13124C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700452 | ||||||
| chr7:7700490
|
C | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(89): Show | 95 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-1027-13162G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700490 | ||||||
| chr7:7700504
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-1027-13176G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700504 | ||||||
| chr7:7700567
|
T | G | 31 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(28): Show | 31 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.-1027-13239A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700567 | ||||||
| chr7:7700573
|
CAACA | C | 4 | a0001c0001t0005g0099a0001c0001t0005g0100a0001c0001t0005g0102others(1): Show | 4 | HG02572.hp1 HG02717.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1027-13249_-1027- others(12): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700573 | ||||||
| chr7:7700630
|
G | A | 2 | a0001c0001t0002g0252a0001c0001t0021g0251 | 2 | HG01081.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-1027-13302C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700630 | ||||||
| chr7:7700787
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1027-13459G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700787 | ||||||
| chr7:7700852
|
A | T | 9 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG01243.hp1 HG02109.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1027-13524T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700852 | ||||||
| chr7:7700888
|
TA | T | 9 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG01243.hp1 HG02109.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1027-13561delT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700888 | ||||||
| chr7:7700977
|
G | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1027-13649C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7700977 | ||||||
| chr7:7701028
|
C | T | 20 | a0001c0001t0004g0002a0001c0001t0004g0034a0001c0001t0004g0038others(17): Show | 22 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-1027-13700G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701028 | ||||||
| chr7:7701072
|
C | G | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1027-13744G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701072 | ||||||
| chr7:7701144
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-1027-13816T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701144 | ||||||
| chr7:7701237
|
C | CTG | 20 | a0001c0001t0004g0002a0001c0001t0004g0034a0001c0001t0004g0038others(17): Show | 22 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-1027-13911_-1027- others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701237 | ||||||
| chr7:7701283
|
G | T | 31 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(28): Show | 31 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.-1028+13892C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701283 | ||||||
| chr7:7701392
|
CTA | C | 13 | a0001c0001t0001g0061a0001c0001t0001g0239a0001c0001t0001g0241others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1028+13781_-1028+ others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701392 | ||||||
| chr7:7701495
|
T | G | 1 | a0001c0001t0001g0027 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-1028+13680A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701495 | ||||||
| chr7:7701525
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+13650T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701525 | ||||||
| chr7:7701600
|
G | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1028+13575C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701600 | ||||||
| chr7:7701618
|
T | C | 1 | a0001c0001t0005g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1028+13557A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701618 | ||||||
| chr7:7701815
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-1028+13360C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701815 | ||||||
| chr7:7701853
|
G | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(12): Show | 16 | HG00280.hp2 HG00323.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-1028+13322C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701853 | ||||||
| chr7:7701864
|
T | C | 1 | a0001c0001t0016g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-1028+13311A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701864 | ||||||
| chr7:7701918
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-1028+13257G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701918 | ||||||
| chr7:7701925
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-1028+13250A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7701925 | ||||||
| chr7:7702420
|
A | G | 1 | a0001c0001t0005g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1028+12755T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7702420 | ||||||
| chr7:7702425
|
C | A | 104 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0061others(101): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-1028+12750G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7702425 | ||||||
| chr7:7702435
|
A | T | 1 | a0001c0001t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-1028+12740T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7702435 | ||||||
| chr7:7702447
|
G | T | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1028+12728C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7702447 | ||||||
| chr7:7702533
|
G | C | 11 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(8): Show | 13 | HG01243.hp1 HG02486.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1028+12642C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7702533 | ||||||
| chr7:7702764
|
C | T | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1028+12411G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7702764 | ||||||
| chr7:7702785
|
TTTG | T | 29 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(26): Show | 29 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1028+12387_-1028+ others(11): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7702785 | ||||||
| chr7:7702800
|
G | GTTT | 20 | a0001c0001t0004g0002a0001c0001t0004g0034a0001c0001t0004g0038others(17): Show | 22 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-1028+12374_-1028+ others(11): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7702800 | ||||||
| chr7:7702958
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1028+12217A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7702958 | ||||||
| chr7:7702999
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-1028+12176C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7702999 | ||||||
| chr7:7703125
|
T | A | 7 | a0001c0001t0001g0058a0001c0001t0002g0217a0001c0001t0005g0055others(4): Show | 7 | HG02486.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1028+12050A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7703125 | ||||||
| chr7:7703288
|
G | A | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1028+11887C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7703288 | ||||||
| chr7:7703410
|
G | A | 9 | a0001c0001t0001g0085a0001c0001t0002g0007a0001c0001t0002g0086others(6): Show | 9 | HG00741.hp2 HG02132.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1028+11765C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7703410 | ||||||
| chr7:7703491
|
A | G | 36 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(33): Show | 38 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.-1028+11684T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7703491 | ||||||
| chr7:7703496
|
C | T | 3 | a0001c0001t0005g0055a0001c0001t0005g0056a0001c0001t0005g0057 | 3 | HG02486.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-1028+11679G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7703496 | ||||||
| chr7:7703526
|
A | C | 10 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1028+11649T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7703526 | ||||||
| chr7:7703632
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-1028+11543C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7703632 | ||||||
| chr7:7703706
|
G | A | 1 | a0001c0001t0009g0051 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-1028+11469C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7703706 | ||||||
| chr7:7703755
|
C | T | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1028+11420G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7703755 | ||||||
| chr7:7703912
|
A | C | 1 | a0001c0001t0002g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-1028+11263T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7703912 | ||||||
| chr7:7703947
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1028+11228C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7703947 | ||||||
| chr7:7704135
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-1028+11040T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704135 | ||||||
| chr7:7704139
|
T | C | 10 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1028+11036A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704139 | ||||||
| chr7:7704152
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-1028+11023C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704152 | ||||||
| chr7:7704256
|
A | G | 1 | a0001c0001t0005g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1028+10919T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704256 | ||||||
| chr7:7704298
|
A | C | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+10877T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704298 | ||||||
| chr7:7704330
|
T | C | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1028+10845A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704330 | ||||||
| chr7:7704392
|
G | T | 5 | a0001c0001t0002g0098a0001c0001t0005g0099a0001c0001t0005g0100others(2): Show | 5 | HG01891.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1028+10783C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704392 | ||||||
| chr7:7704580
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+10595G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704580 | ||||||
| chr7:7704598
|
G | GA | 17 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0232others(14): Show | 19 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-1028+10576dupT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704598 | ||||||
| chr7:7704598
|
GA | G | 93 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(90): Show | 96 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.-1028+10576delT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704598 | ||||||
| chr7:7704598
|
GAAAA | G | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1028+10573_-1028+ others(12): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704598 | ||||||
| chr7:7704635
|
A | G | 139 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(136): Show | 144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.-1028+10540T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704635 | ||||||
| chr7:7704645
|
G | A | 1 | a0001c0001t0005g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1028+10530C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704645 | ||||||
| chr7:7704694
|
G | C | 9 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG01243.hp1 HG02109.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1028+10481C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704694 | ||||||
| chr7:7704709
|
G | T | 9 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG01243.hp1 HG02109.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1028+10466C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704709 | ||||||
| chr7:7704766
|
C | CA | 98 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0015others(95): Show | 103 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.-1028+10408dupT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704766 | ||||||
| chr7:7704766
|
C | CAA | 21 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0031others(18): Show | 21 | HG01361.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.-1028+10407_-1028+ others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704766 | ||||||
| chr7:7704766
|
C | CAAAAA | 7 | a0001c0001t0001g0268a0001c0001t0001g0270a0001c0001t0001g0271others(4): Show | 7 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1028+10404_-1028+ others(13): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704766 | ||||||
| chr7:7704766
|
C | CAAAAAAA | 9 | a0001c0001t0001g0280a0001c0001t0003g0245a0001c0001t0003g0274others(6): Show | 9 | HG02129.hp2 NA18948.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1028+10402_-1028+ others(15): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704766 | ||||||
| chr7:7704766
|
CA | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0128others(6): Show | 9 | HG01975.hp1 HG02080.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1028+10408delT | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704766 | ||||||
| chr7:7704766
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0005g0290 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1028+10399_-1028+ others(18): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704766 | ||||||
| chr7:7704769
|
A | AAG | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1028+10405_-1028+ others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7704769 | ||||||
| chr7:7705146
|
A | C | 10 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1028+10029T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7705146 | ||||||
| chr7:7705254
|
T | G | 1 | a0001c0001t0002g0301 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1028+9921A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7705254 | ||||||
| chr7:7705462
|
C | T | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG02074.hp2 NA18957.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1028+9713G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7705462 | ||||||
| chr7:7705578
|
A | G | 13 | a0001c0001t0001g0103a0001c0001t0001g0114a0001c0001t0001g0115others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1028+9597T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7705578 | ||||||
| chr7:7705720
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+9455T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7705720 | ||||||
| chr7:7705937
|
A | C | 1 | a0001c0001t0004g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-1028+9238T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7705937 | ||||||
| chr7:7705953
|
T | C | 1 | a0001c0001t0005g0296 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-1028+9222A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7705953 | ||||||
| chr7:7706408
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+8767G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7706408 | ||||||
| chr7:7706459
|
C | A | 132 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(129): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.-1028+8716G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7706459 | ||||||
| chr7:7706591
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-1028+8584T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7706591 | ||||||
| chr7:7706657
|
C | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | NA18953.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-1028+8518G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7706657 | ||||||
| chr7:7706901
|
G | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-1028+8274C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7706901 | ||||||
| chr7:7706918
|
A | G | 24 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 24 | HG00544.hp2 HG02004.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-1028+8257T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7706918 | ||||||
| chr7:7706951
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-1028+8224G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7706951 | ||||||
| chr7:7707044
|
G | A | 22 | a0001c0001t0001g0265a0001c0001t0001g0268a0001c0001t0001g0270others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1028+8131C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7707044 | ||||||
| chr7:7707177
|
T | A | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1028+7998A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7707177 | ||||||
| chr7:7707247
|
T | G | 2 | a0001c0001t0005g0289a0001c0001t0022g0243 | 2 | HG02647.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-1028+7928A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7707247 | ||||||
| chr7:7707313
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-1028+7862T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7707313 | ||||||
| chr7:7707431
|
C | T | 1 | a0001c0001t0010g0125 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-1028+7744G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7707431 | ||||||
| chr7:7707623
|
C | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(113): Show | 119 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-1028+7552G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7707623 | ||||||
| chr7:7707650
|
G | T | 1 | a0001c0001t0002g0098 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-1028+7525C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7707650 | ||||||
| chr7:7707701
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-1028+7474G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7707701 | ||||||
| chr7:7707763
|
T | G | 1 | a0001c0001t0004g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-1028+7412A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7707763 | ||||||
| chr7:7707967
|
T | G | 1 | a0001c0001t0002g0093 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-1028+7208A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7707967 | ||||||
| chr7:7708148
|
C | T | 22 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0268others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1028+7027G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7708148 | ||||||
| chr7:7708308
|
T | A | 1 | a0001c0001t0020g0246 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-1028+6867A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7708308 | ||||||
| chr7:7708433
|
C | T | 2 | a0001c0001t0005g0289a0001c0001t0005g0291 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-1028+6742G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7708433 | ||||||
| chr7:7708689
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-1028+6486T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7708689 | ||||||
| chr7:7709117
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-1028+6058T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7709117 | ||||||
| chr7:7709332
|
G | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-1028+5843C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7709332 | ||||||
| chr7:7709544
|
G | A | 15 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0002g0098others(12): Show | 15 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-1028+5631C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7709544 | ||||||
| chr7:7709562
|
A | G | 1 | a0001c0001t0014g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1028+5613T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7709562 | ||||||
| chr7:7709747
|
A | G | 1 | a0001c0001t0006g0122 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-1028+5428T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7709747 | ||||||
| chr7:7709781
|
GT | G | 32 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(29): Show | 33 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1028+5393delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7709781 | ||||||
| chr7:7709817
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-1028+5358C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7709817 | ||||||
| chr7:7709958
|
C | T | 1 | a0001c0001t0012g0288 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-1028+5217G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7709958 | ||||||
| chr7:7709970
|
T | A | 1 | a0001c0001t0001g0247 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-1028+5205A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7709970 | ||||||
| chr7:7710049
|
A | G | 3 | a0001c0001t0001g0283a0001c0001t0002g0252a0001c0001t0021g0251 | 3 | HG01081.hp1 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-1028+5126T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710049 | ||||||
| chr7:7710235
|
T | C | 61 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(58): Show | 64 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-1028+4940A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710235 | ||||||
| chr7:7710389
|
A | G | 1 | a0001c0001t0012g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-1028+4786T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710389 | ||||||
| chr7:7710450
|
A | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0283a0001c0001t0002g0252others(2): Show | 5 | HG01081.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1028+4725T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710450 | ||||||
| chr7:7710501
|
A | G | 49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 51 | HG00544.hp2 HG00733.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.-1028+4674T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710501 | ||||||
| chr7:7710512
|
C | G | 1 | a0001c0001t0002g0012 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-1028+4663G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710512 | ||||||
| chr7:7710513
|
T | A | 1 | a0001c0001t0001g0248 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-1028+4662A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710513 | ||||||
| chr7:7710588
|
C | G | 1 | a0001c0001t0005g0099 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-1028+4587G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710588 | ||||||
| chr7:7710626
|
T | G | 28 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(25): Show | 28 | HG00544.hp2 HG02004.hp2 HG02074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-1028+4549A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710626 | ||||||
| chr7:7710673
|
C | T | 1 | a0001c0001t0006g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-1028+4502G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710673 | ||||||
| chr7:7710753
|
A | G | 3 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0007g0010 | 3 | HG02965.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-1028+4422T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710753 | ||||||
| chr7:7710802
|
C | T | 1 | a0001c0001t0002g0007 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-1028+4373G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710802 | ||||||
| chr7:7710816
|
A | T | 8 | a0001c0001t0002g0098a0001c0001t0005g0099a0001c0001t0005g0100others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1028+4359T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710816 | ||||||
| chr7:7710859
|
G | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | NA18953.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-1028+4316C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710859 | ||||||
| chr7:7710993
|
G | A | 129 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(126): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.-1028+4182C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7710993 | ||||||
| chr7:7711062
|
G | T | 6 | a0001c0001t0001g0058a0001c0001t0005g0055a0001c0001t0005g0056others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1028+4113C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7711062 | ||||||
| chr7:7711176
|
G | A | 1 | a0001c0001t0005g0291 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-1028+3999C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7711176 | ||||||
| chr7:7711309
|
T | A | 2 | a0001c0001t0005g0289a0001c0001t0005g0291 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-1028+3866A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7711309 | ||||||
| chr7:7711359
|
G | A | 106 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(103): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-1028+3816C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7711359 | ||||||
| chr7:7711427
|
T | A | 1 | a0001c0001t0001g0249 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-1028+3748A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7711427 | ||||||
| chr7:7711607
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-1028+3568A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7711607 | ||||||
| chr7:7711862
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-1028+3313G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7711862 | ||||||
| chr7:7711946
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+3229A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7711946 | ||||||
| chr7:7712051
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+3124T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712051 | ||||||
| chr7:7712149
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-1028+3026G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712149 | ||||||
| chr7:7712488
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+2687C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712488 | ||||||
| chr7:7712529
|
G | C | 1 | a0001c0001t0004g0050 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-1028+2646C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712529 | ||||||
| chr7:7712532
|
A | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+2643T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712532 | ||||||
| chr7:7712682
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+2493G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712682 | ||||||
| chr7:7712730
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+2445T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712730 | ||||||
| chr7:7712735
|
T | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01891.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-1028+2440A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712735 | ||||||
| chr7:7712780
|
A | G | 24 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0268others(21): Show | 25 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.-1028+2395T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712780 | ||||||
| chr7:7712785
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+2390C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712785 | ||||||
| chr7:7712809
|
G | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0283a0001c0001t0002g0252others(2): Show | 5 | HG01081.hp1 HG02886.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1028+2366C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712809 | ||||||
| chr7:7712874
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+2301C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712874 | ||||||
| chr7:7712885
|
T | C | 1 | a0001c0001t0002g0253 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1028+2290A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712885 | ||||||
| chr7:7712928
|
T | G | 50 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 52 | HG00544.hp2 HG00733.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-1028+2247A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712928 | ||||||
| chr7:7712975
|
T | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01891.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-1028+2200A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7712975 | ||||||
| chr7:7713007
|
A | G | 33 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(30): Show | 34 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1028+2168T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713007 | ||||||
| chr7:7713060
|
C | T | 16 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0002g0098others(13): Show | 16 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-1028+2115G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713060 | ||||||
| chr7:7713061
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+2114C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713061 | ||||||
| chr7:7713194
|
A | T | 48 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(45): Show | 50 | HG00544.hp2 HG00733.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.-1028+1981T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713194 | ||||||
| chr7:7713213
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(30): Show | 34 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1028+1962C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713213 | ||||||
| chr7:7713256
|
A | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(30): Show | 34 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1028+1919T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713256 | ||||||
| chr7:7713276
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0255 | 2 | NA18998.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-1028+1899C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713276 | ||||||
| chr7:7713276
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-1028+1899C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713276 | ||||||
| chr7:7713297
|
T | C | 24 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0268others(21): Show | 25 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.-1028+1878A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713297 | ||||||
| chr7:7713360
|
AAAAC | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0256a0001c0001t0015g0298 | 3 | HG02129.hp1 HG03195.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-1028+1811_-1028+1 others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713360 | ||||||
| chr7:7713385
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+1790C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713385 | ||||||
| chr7:7713390
|
T | A | 1 | a0001c0001t0001g0035 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-1028+1785A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713390 | ||||||
| chr7:7713398
|
G | GT | 14 | a0001c0001t0001g0015a0001c0001t0001g0103a0001c0001t0001g0107others(11): Show | 14 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1028+1776dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713398 | ||||||
| chr7:7713470
|
C | T | 2 | a0001c0001t0015g0297a0001c0001t0015g0298 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-1028+1705G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713470 | ||||||
| chr7:7713474
|
C | A | 1 | a0001c0001t0001g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-1028+1701G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713474 | ||||||
| chr7:7713629
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+1546C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713629 | ||||||
| chr7:7713631
|
GT | G | 24 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 24 | HG00544.hp2 HG02004.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-1028+1543delA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713631 | ||||||
| chr7:7713757
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+1418C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713757 | ||||||
| chr7:7713794
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-1028+1381G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713794 | ||||||
| chr7:7713947
|
GC | G | 7 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0005g0055others(4): Show | 7 | HG02486.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1028+1227delG | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7713947 | ||||||
| chr7:7714093
|
G | A | 25 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0268others(22): Show | 26 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-1028+1082C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714093 | ||||||
| chr7:7714094
|
A | G | 25 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0268others(22): Show | 26 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-1028+1081T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714094 | ||||||
| chr7:7714192
|
A | G | 1 | a0001c0001t0002g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-1028+983T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714192 | ||||||
| chr7:7714228
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+947A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714228 | ||||||
| chr7:7714315
|
C | G | 1 | a0001c0001t0005g0289 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-1028+860G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714315 | ||||||
| chr7:7714432
|
C | G | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+743G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714432 | ||||||
| chr7:7714461
|
T | C | 127 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(124): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.-1028+714A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714461 | ||||||
| chr7:7714558
|
T | A | 1 | a0001c0001t0004g0258 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-1028+617A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714558 | ||||||
| chr7:7714616
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-1028+559A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714616 | ||||||
| chr7:7714733
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0012g0293 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-1028+442C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714733 | ||||||
| chr7:7714734
|
G | A | 21 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0004g0002others(18): Show | 23 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1028+441C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714734 | ||||||
| chr7:7714810
|
T | A | 26 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(23): Show | 26 | HG00544.hp2 HG02004.hp2 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-1028+365A>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714810 | ||||||
| chr7:7714932
|
G | A | 25 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0268others(22): Show | 26 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-1028+243C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7714932 | ||||||
| chr7:7715028
|
G | GT | 3 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0007g0010 | 3 | HG02965.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-1028+146dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 2/7 | chr7 | 7715028 | ||||||
| chr7:7715267
|
G | C | 1 | a0001c0001t0008g0260 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1079-41C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7715267 | ||||||
| chr7:7715291
|
G | A | 42 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 42 | HG00544.hp2 HG01109.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1079-65C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7715291 | ||||||
| chr7:7715294
|
T | G | 1 | a0001c0001t0001g0037 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-1079-68A>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7715294 | ||||||
| chr7:7715327
|
A | ACT | 42 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 42 | HG00544.hp2 HG01109.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1079-102_-1079-10 others(6): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7715327 | ||||||
| chr7:7715337
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-1079-111T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7715337 | ||||||
| chr7:7715384
|
T | C | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1079-158A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7715384 | ||||||
| chr7:7715414
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-1079-188T>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7715414 | ||||||
| chr7:7715440
|
C | G | 21 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0004g0002others(18): Show | 23 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1079-214G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7715440 | ||||||
| chr7:7715853
|
A | G | 42 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 42 | HG00544.hp2 HG01109.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.-1079-627T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7715853 | ||||||
| chr7:7715860
|
C | A | 21 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0004g0002others(18): Show | 23 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1079-634G>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7715860 | ||||||
| chr7:7715960
|
A | G | 24 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0268others(21): Show | 25 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.-1079-734T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7715960 | ||||||
| chr7:7716013
|
A | AT | 25 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0268others(22): Show | 26 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-1079-788dupA | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716013 | ||||||
| chr7:7716166
|
T | C | 128 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(125): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.-1079-940A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716166 | ||||||
| chr7:7716238
|
T | C | 21 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0004g0002others(18): Show | 23 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1079-1012A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716238 | ||||||
| chr7:7716460
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-1079-1234C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716460 | ||||||
| chr7:7716472
|
G | T | 45 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 47 | HG00544.hp2 HG01891.hp1 HG02004.hp2 others(44): Show |
intron_variant | MODIFIER | c.-1079-1246C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716472 | ||||||
| chr7:7716605
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-1079-1379A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716605 | ||||||
| chr7:7716734
|
A | T | 1 | a0001c0001t0016g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-1079-1508T>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716734 | ||||||
| chr7:7716738
|
G | T | 3 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0007g0010 | 3 | HG02965.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-1079-1512C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716738 | ||||||
| chr7:7716789
|
C | T | 1 | a0001c0001t0002g0007 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-1079-1563G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716789 | ||||||
| chr7:7716811
|
T | C | 22 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0103others(19): Show | 24 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-1079-1585A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716811 | ||||||
| chr7:7716838
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-1079-1612G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716838 | ||||||
| chr7:7716856
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-1079-1630C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716856 | ||||||
| chr7:7716881
|
G | C | 30 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0103others(27): Show | 32 | HG01109.hp1 HG01243.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.-1080+1634C>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7716881 | ||||||
| chr7:7717056
|
T | C | 18 | a0001c0001t0004g0002a0001c0001t0004g0038a0001c0001t0004g0039others(15): Show | 20 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1080+1459A>G | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7717056 | ||||||
| chr7:7717056
|
T | TTTTC | 4 | a0001c0001t0001g0295a0001c0001t0002g0294a0001c0001t0005g0001others(1): Show | 6 | HG02486.hp1 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1080+1455_-1080+1 others(10): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7717056 | ||||||
| chr7:7717060
|
C | CTTT | 8 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0103others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1080+1452_-1080+1 others(9): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7717060 | ||||||
| chr7:7717060
|
C | CTTTTTT | 7 | a0001c0001t0001g0096a0001c0001t0002g0098a0001c0001t0005g0097others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1080+1449_-1080+1 others(12): Show |
RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7717060 | ||||||
| chr7:7717137
|
A | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0066others(31): Show | 35 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.-1080+1378T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7717137 | ||||||
| chr7:7717184
|
G | A | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0015g0297others(2): Show | 5 | HG01243.hp1 HG02723.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1080+1331C>T | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7717184 | ||||||
| chr7:7717316
|
C | G | 6 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0067others(3): Show | 6 | HG01109.hp2 HG01175.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1080+1199G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7717316 | ||||||
| chr7:7717356
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-1080+1159G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7717356 | ||||||
| chr7:7717370
|
A | G | 1 | a0001c0001t0003g0062 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-1080+1145T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7717370 | ||||||
| chr7:7717563
|
C | G | 7 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0005g0055others(4): Show | 7 | HG02486.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1080+952G>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7717563 | ||||||
| chr7:7718074
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-1080+441T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7718074 | ||||||
| chr7:7718217
|
G | T | 47 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(44): Show | 49 | HG00544.hp2 HG00733.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.-1080+298C>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7718217 | ||||||
| chr7:7718235
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-1080+280T>C | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7718235 | ||||||
| chr7:7718377
|
C | T | 1 | a0001c0001t0002g0007 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-1080+138G>A | RPA3 | ENSG00000106399.11 | transcript | ENST00000223129.8 | protein_coding | 1/7 | chr7 | 7718377 |