Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 22902 |
|---|---|
| ensemblid | ENSG00000018189.13 |
| hgncid | 30285 |
| symbol | RUFY3 |
| name | RUN and FYVE domain containing 3 |
| refseq_nuc | NM_001037442.4 |
| refseq_prot | NP_001032519.1 |
| ensembl_nuc | ENST00000381006.8 |
| ensembl_prot | ENSP00000370394.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 70721964 |
| end | 70808619 |
| strand | + |
| ver | v1.2 |
| region | chr4:70721964-70808619 |
| region5000 | chr4:70716964-70813619 |
| regionname0 | RUFY3_chr4_70721964_70808619 |
| regionname5000 | RUFY3_chr4_70716964_70813619 |
| 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 | 620 | 250 | 76 | 30 | 101 | 10 | 31 | 73 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0002 | 0/0 | 620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0003 | 0/0 | 620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0004 | 0/0 | 620 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0005 | 0/0 | 620 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| 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 | 1863 | 249 | 76 | 30 | 101 | 10 | 30 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| c0002 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| c0003 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| c0004 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| c0005 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| c0006 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2571 | 65 | 13 | 11 | 28 | 5 | 6 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0002 | 0/0 | 2571 | 46 | 7 | 9 | 19 | 2 | 9 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0003 | 0/0 | 2570 | 32 | 0 | 2 | 28 | 0 | 2 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0004 | 0/0 | 2567 | 13 | 0 | 1 | 8 | 0 | 4 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0005 | 0/0 | 2570 | 13 | 12 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0006 | 0/0 | 2571 | 9 | 3 | 2 | 4 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0007 | 0/0 | 2574 | 7 | 7 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0008 | 0/0 | 2570 | 7 | 4 | 2 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0009 | 0/0 | 2570 | 6 | 6 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0010 | 0/0 | 2572 | 6 | 0 | 0 | 3 | 0 | 3 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0011 | 0/0 | 2575 | 6 | 4 | 0 | 0 | 2 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0012 | 0/0 | 2571 | 5 | 0 | 0 | 5 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0013 | 0/0 | 2574 | 4 | 4 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0014 | 0/0 | 2573 | 4 | 4 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0015 | 0/0 | 2569 | 3 | 0 | 0 | 3 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0016 | 0/0 | 2570 | 2 | 0 | 0 | 0 | 0 | 2 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0017 | 0/0 | 2569 | 2 | 1 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0018 | 0/0 | 2572 | 2 | 0 | 0 | 2 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0019 | 0/0 | 2570 | 2 | 2 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0020 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0021 | 0/0 | 2575 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0022 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0023 | 0/0 | 2569 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0024 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0025 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0026 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0027 | 0/0 | 2570 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0028 | 0/0 | 2572 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0029 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0030 | 0/0 | 2572 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0031 | 0/0 | 2568 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0032 | 0/0 | 2572 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0033 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0034 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0035 | 0/0 | 2570 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0036 | 0/0 | 2572 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0037 | 0/0 | 2571 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0038 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| t0039 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| 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 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| 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 | 1863 | 249 | 76 | 30 | 101 | 10 | 30 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0003 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0002c0005 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0003c0004 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0004c0002 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0005c0006 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4433 | 65 | 13 | 11 | 28 | 5 | 6 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0002 | 0/0 | 4433 | 44 | 7 | 9 | 19 | 2 | 7 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0003 | 0/0 | 4432 | 32 | 0 | 2 | 28 | 0 | 2 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0004 | 0/0 | 4429 | 13 | 0 | 1 | 8 | 0 | 4 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0005 | 0/0 | 4432 | 13 | 12 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0006 | 0/0 | 4433 | 9 | 3 | 2 | 4 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0007 | 0/0 | 4436 | 7 | 7 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0008 | 0/0 | 4432 | 7 | 4 | 2 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0009 | 0/0 | 4432 | 6 | 6 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0010 | 0/0 | 4434 | 6 | 0 | 0 | 3 | 0 | 3 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0011 | 0/0 | 4437 | 6 | 4 | 0 | 0 | 2 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0012 | 0/0 | 4433 | 4 | 0 | 0 | 4 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0013 | 0/0 | 4436 | 4 | 4 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0014 | 0/0 | 4435 | 4 | 4 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0015 | 0/0 | 4431 | 3 | 0 | 0 | 3 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0016 | 0/0 | 4432 | 2 | 0 | 0 | 0 | 0 | 2 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0017 | 0/0 | 4431 | 2 | 1 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0018 | 0/0 | 4434 | 2 | 0 | 0 | 2 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0019 | 0/0 | 4432 | 2 | 2 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0020 | 0/0 | 4432 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0021 | 0/0 | 4437 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0023 | 0/0 | 4431 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0024 | 0/0 | 4432 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0025 | 0/0 | 4435 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0026 | 0/0 | 4436 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0027 | 0/0 | 4432 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0028 | 0/0 | 4434 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0029 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0030 | 0/0 | 4434 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0031 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0032 | 0/0 | 4434 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0033 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0034 | 0/0 | 4432 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0035 | 0/0 | 4432 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0036 | 0/0 | 4434 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0037 | 0/0 | 4433 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0001t0039 | 0/0 | 4432 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0001c0003t0002 | 0/0 | 4433 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0002c0005t0022 | 0/0 | 4433 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0003c0004t0038 | 0/0 | 4432 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0004c0002t0002 | 0/0 | 4433 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| a0005c0006t0012 | 0/0 | 4433 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | copy fasta | chr4 | 70716964 | 70813619 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0008g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0008g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0008g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0009g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0010g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0010g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0010g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0010g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0010g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0010g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0011g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0011g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0011g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0011g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0011g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0011g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0012g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0012g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0012g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0012g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0013g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0013g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0013g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0014g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0014g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0014g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0014g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0015g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0015g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0015g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0016g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0016g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0017g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0017g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0018g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0018g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0019g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0019g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0020g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0021g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0023g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0024g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0025g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0026g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0027g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0028g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0029g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0030g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0031g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0032g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0033g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0034g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0035g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0036g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0037g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0001t0039g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0002c0005t0022g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0003c0004t0038g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0004c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| a0005c0006t0012g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0189 | EUR | GBR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0188 | EUR | FIN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00323 | hp2 | a0001 | c0001 | t0036 | g0228 | EUR | FIN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | CHS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0057 | EAS | CHS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | CHS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00673 | hp2 | a0001 | c0001 | t0006 | g0144 | EAS | CHS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01109 | hp1 | a0001 | c0001 | t0035 | g0251 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01167 | hp2 | a0001 | c0001 | t0017 | g0066 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0249 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0235 | AMR | PUR | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0177 | AMR | CLM | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0178 | AMR | CLM | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | IBS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01515 | hp2 | a0001 | c0001 | t0011 | g0229 | EUR | IBS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01517 | hp1 | a0001 | c0001 | t0011 | g0230 | EUR | IBS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0065 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0250 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0231 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01891 | hp2 | a0001 | c0001 | t0019 | g0221 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01978 | hp1 | a0001 | c0001 | t0028 | g0209 | AMR | PEL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02074 | hp1 | a0001 | c0001 | t0012 | g0036 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02074 | hp2 | a0001 | c0001 | t0010 | g0203 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | KHV | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0246 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | CDX | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02155 | hp2 | a0001 | c0001 | t0015 | g0095 | EAS | CDX | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02258 | hp1 | a0001 | c0001 | t0034 | g0223 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02280 | hp1 | a0001 | c0001 | t0023 | g0015 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02572 | hp2 | a0001 | c0001 | t0026 | g0081 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02602 | hp1 | a0001 | c0001 | t0010 | g0086 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02602 | hp2 | a0001 | c0001 | t0016 | g0248 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02615 | hp2 | a0001 | c0001 | t0033 | g0252 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0242 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0227 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02717 | hp1 | a0001 | c0001 | t0014 | g0226 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02723 | hp1 | a0002 | c0005 | t0022 | g0012 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02723 | hp2 | a0001 | c0001 | t0019 | g0220 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02738 | hp2 | a0001 | c0001 | t0032 | g0155 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0091 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0233 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02818 | hp1 | a0001 | c0001 | t0017 | g0067 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02818 | hp2 | a0001 | c0001 | t0020 | g0237 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02886 | hp2 | a0001 | c0001 | t0021 | g0232 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0243 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0239 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0072 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03017 | hp2 | a0001 | c0001 | t0008 | g0244 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0048 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03130 | hp2 | a0003 | c0004 | t0038 | g0014 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0238 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03195 | hp1 | a0001 | c0001 | t0039 | g0024 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0005 | AFR | MSL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0241 | AFR | MSL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | MSL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0236 | AFR | MSL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03491 | hp1 | a0001 | c0001 | t0010 | g0181 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03491 | hp2 | a0001 | c0001 | t0027 | g0116 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | ESN | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0240 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0004 | AFR | GWD | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | MSL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0006 | AFR | MSL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03654 | hp2 | a0001 | c0001 | t0031 | g0171 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03688 | hp1 | a0001 | c0001 | t0016 | g0247 | SAS | STU | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | STU | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0082 | SAS | PJL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0080 | SAS | BEB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | BEB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0074 | SAS | BEB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | BEB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03927 | hp2 | a0004 | c0002 | t0002 | g0154 | SAS | BEB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0076 | SAS | BEB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG04115 | hp2 | a0001 | c0001 | t0010 | g0196 | SAS | STU | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0212 | SAS | STU | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | STU | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0185 | SAS | STU | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18522 | hp1 | a0001 | c0001 | t0025 | g0016 | AFR | YRI | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0003 | AFR | YRI | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18950 | hp1 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18961 | hp1 | a0001 | c0001 | t0012 | g0039 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18962 | hp1 | a0001 | c0001 | t0015 | g0121 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18975 | hp2 | a0001 | c0001 | t0012 | g0021 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18982 | hp2 | a0001 | c0001 | t0024 | g0045 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18986 | hp2 | a0001 | c0001 | t0010 | g0193 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18990 | hp1 | a0001 | c0001 | t0030 | g0172 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18990 | hp2 | a0005 | c0006 | t0012 | g0029 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19006 | hp2 | a0001 | c0001 | t0018 | g0149 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19009 | hp1 | a0001 | c0001 | t0012 | g0062 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | LWK | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0224 | AFR | LWK | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0068 | AFR | LWK | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0225 | AFR | LWK | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19066 | hp2 | a0001 | c0001 | t0010 | g0118 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19087 | hp2 | a0001 | c0001 | t0018 | g0122 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | YRI | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0245 | AFR | YRI | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ASW | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA20129 | hp2 | a0001 | c0001 | t0014 | g0222 | AFR | ASW | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | GIH | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA20905 | hp2 | a0001 | c0001 | t0037 | g0161 | SAS | GIH | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0085 | AMR | CLM | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02559 | hp1 | a0001 | c0001 | t0029 | g0170 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0069 | AFR | ACB | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0071 | AFR | MSL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | MSL | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0047 | AFR | USA | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0234 | AFR | USA | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18955 | hp1 | a0001 | c0001 | t0015 | g0106 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | LWK | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0165 | REF | REF | RUFY3_chr4_70716964_70813619 | RUFY3 | chr4 | 70716964 | 70813619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70788954
|
A | G | 1 | a0005 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.1220A>G | p.Glu407Gly | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 11/18 | 1830/4433 | 1220/1863 | 407/620 | chr4 | 70788954 | ||
| chr4:70794850
|
A | G | 1 | a0002 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1513A>G | p.Arg505Gly | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/18 | 2123/4433 | 1513/1863 | 505/620 | chr4 | 70794850 | ||
| chr4:70794893
|
T | G | 1 | a0004 | 1 | HG03927.hp2 | missense_variant&splice_region_variant | MODERATE | c.1556T>G | p.Met519Arg | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/18 | 2166/4433 | 1556/1863 | 519/620 | chr4 | 70794893 | ||
| chr4:70806601
|
G | A | 1 | a0003 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1805G>A | p.Arg602Gln | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 2415/4433 | 1805/1863 | 602/620 | chr4 | 70806601 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70806593
|
G | A | 1 | a0001c0003 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.1797G>A | p.Lys599Lys | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 2407/4433 | 1797/1863 | 599/620 | chr4 | 70806593 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70722009
|
C | G | 2 | a0001c0001t0019a0003c0004t0038 | 3 | HG01891.hp2 HG02723.hp2 HG03130.hp2 |
5_prime_UTR_variant | MODIFIER | c.-565C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/18 | 565 | chr4 | 70722009 | |||||
| chr4:70722009
|
C | T | 1 | a0001c0001t0039 | 1 | HG03195.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-565C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/18 | chr4 | 70722009 | ||||||
| chr4:70722084
|
T | C | 1 | a0001c0001t0016 | 2 | HG02602.hp2 HG03688.hp1 |
5_prime_UTR_variant | MODIFIER | c.-490T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/18 | 490 | chr4 | 70722084 | |||||
| chr4:70722231
|
G | A | 3 | a0001c0001t0009a0001c0001t0020a0001c0001t0021 | 8 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-343G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/18 | 343 | chr4 | 70722231 | |||||
| chr4:70722268
|
G | A | 1 | a0001c0001t0020 | 1 | HG02818.hp2 | 5_prime_UTR_variant | MODIFIER | c.-306G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/18 | 306 | chr4 | 70722268 | |||||
| chr4:70722278
|
G | T | 1 | a0001c0001t0037 | 1 | NA20905.hp2 | 5_prime_UTR_variant | MODIFIER | c.-296G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/18 | 296 | chr4 | 70722278 | |||||
| chr4:70722335
|
A | G | 11 | a0001c0001t0008a0001c0001t0009a0001c0001t0011others(8): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-239A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/18 | chr4 | 70722335 | ||||||
| chr4:70722414
|
CT | C | 24 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(21): Show | 108 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(105): Show |
5_prime_UTR_variant | MODIFIER | c.-146delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/18 | 146 | INFO_REALIGN_3_PRIME | chr4 | 70722414 | ||||
| chr4:70722494
|
G | A | 1 | a0002c0005t0022 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-80G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/18 | 80 | chr4 | 70722494 | |||||
| chr4:70806676
|
C | A | 1 | a0001c0001t0023 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 17 | chr4 | 70806676 | |||||
| chr4:70806829
|
C | T | 2 | a0001c0001t0017a0001c0001t0023 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*170C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 170 | chr4 | 70806829 | |||||
| chr4:70806936
|
A | G | 34 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(31): Show | 179 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*277A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 277 | chr4 | 70806936 | |||||
| chr4:70807094
|
T | C | 10 | a0001c0001t0007a0001c0001t0008a0001c0001t0009others(7): Show | 34 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*435T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 435 | chr4 | 70807094 | |||||
| chr4:70807307
|
C | CA | 4 | a0001c0001t0011a0001c0001t0021a0001c0001t0026others(1): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*656dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 657 | INFO_REALIGN_3_PRIME | chr4 | 70807307 | ||||
| chr4:70807420
|
T | C | 14 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(11): Show | 74 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*761T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 761 | chr4 | 70807420 | |||||
| chr4:70807531
|
G | A | 1 | a0001c0001t0032 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*872G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 872 | chr4 | 70807531 | |||||
| chr4:70807565
|
A | G | 1 | a0001c0001t0029 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*906A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 906 | chr4 | 70807565 | |||||
| chr4:70807663
|
C | CT | 11 | a0001c0001t0004a0001c0001t0010a0001c0001t0012others(8): Show | 32 | HG00673.hp1 HG01123.hp1 HG01978.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1021dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 1022 | INFO_REALIGN_3_PRIME | chr4 | 70807663 | ||||
| chr4:70807663
|
C | CTTT | 3 | a0001c0001t0011a0001c0001t0021a0001c0001t0026 | 8 | HG01515.hp2 HG01517.hp1 HG01891.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1019_*1021dupTTT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 1022 | INFO_REALIGN_3_PRIME | chr4 | 70807663 | ||||
| chr4:70807663
|
CT | C | 5 | a0001c0001t0014a0001c0001t0017a0001c0001t0023others(2): Show | 9 | HG01167.hp2 HG02280.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1021delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 1021 | INFO_REALIGN_3_PRIME | chr4 | 70807663 | ||||
| chr4:70807902
|
T | C | 1 | a0001c0001t0028 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1243T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 1243 | chr4 | 70807902 | |||||
| chr4:70808191
|
A | G | 6 | a0001c0001t0008a0001c0001t0009a0001c0001t0016others(3): Show | 18 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1532A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 1532 | chr4 | 70808191 | |||||
| chr4:70808283
|
ATATC | A | 2 | a0001c0001t0004a0001c0001t0031 | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1634_*1637delATCT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 1634 | INFO_REALIGN_3_PRIME | chr4 | 70808283 | ||||
| chr4:70808309
|
C | CTCTT | 4 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(1): Show | 16 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1652_*1655dupCTTT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 1656 | INFO_REALIGN_3_PRIME | chr4 | 70808309 | ||||
| chr4:70808311
|
CTT | C | 1 | a0001c0001t0015 | 3 | HG02155.hp2 NA18955.hp1 NA18962.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1654_*1655delTT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 1654 | INFO_REALIGN_3_PRIME | chr4 | 70808311 | ||||
| chr4:70808384
|
C | T | 1 | a0001c0001t0007 | 7 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1725C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 1725 | chr4 | 70808384 | |||||
| chr4:70808518
|
A | G | 2 | a0001c0001t0004a0001c0001t0031 | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1859A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 1859 | chr4 | 70808518 | |||||
| chr4:70808601
|
A | G | 4 | a0001c0001t0011a0001c0001t0021a0001c0001t0026others(1): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1942A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 18/18 | 1942 | chr4 | 70808601 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70722781
|
C | T | 31 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+30C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70722781 | ||||||
| chr4:70722846
|
C | G | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.178+95C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70722846 | ||||||
| chr4:70722947
|
T | G | 116 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(113): Show | 116 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.178+196T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70722947 | ||||||
| chr4:70723008
|
A | G | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.178+257A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70723008 | ||||||
| chr4:70723109
|
T | C | 31 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+358T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70723109 | ||||||
| chr4:70723390
|
A | G | 31 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+639A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70723390 | ||||||
| chr4:70723424
|
T | C | 9 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+673T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70723424 | ||||||
| chr4:70723431
|
T | C | 31 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+680T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70723431 | ||||||
| chr4:70723513
|
TCTTGA | T | 21 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(18): Show | 21 | HG00673.hp1 HG01123.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.178+767_178+771del others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70723513 | |||||
| chr4:70723515
|
T | C | 14 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(11): Show | 14 | HG01243.hp2 HG02145.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+764T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70723515 | ||||||
| chr4:70723523
|
C | G | 1 | a0001c0001t0004g0085 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.178+772C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70723523 | ||||||
| chr4:70723523
|
C | T | 9 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+772C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70723523 | ||||||
| chr4:70723706
|
C | T | 9 | a0001c0001t0001g0215a0001c0001t0002g0211a0001c0001t0002g0213others(6): Show | 9 | HG02080.hp1 HG03239.hp1 HG03834.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+955C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70723706 | ||||||
| chr4:70723833
|
G | A | 5 | a0001c0001t0014g0222a0001c0001t0014g0224a0001c0001t0014g0225others(2): Show | 5 | HG02258.hp1 HG02717.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+1082G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70723833 | ||||||
| chr4:70723869
|
T | G | 31 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+1118T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70723869 | ||||||
| chr4:70723937
|
T | C | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.178+1186T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70723937 | ||||||
| chr4:70724060
|
G | A | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.178+1309G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70724060 | ||||||
| chr4:70724108
|
T | G | 1 | a0001c0001t0003g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.178+1357T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70724108 | ||||||
| chr4:70724160
|
C | T | 31 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+1409C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70724160 | ||||||
| chr4:70724318
|
G | A | 2 | a0001c0001t0005g0065a0001c0001t0010g0086 | 2 | HG01884.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.178+1567G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70724318 | ||||||
| chr4:70724433
|
C | T | 31 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+1682C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70724433 | ||||||
| chr4:70724484
|
T | C | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | NA19004.hp2 NA19056.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+1733T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70724484 | ||||||
| chr4:70724614
|
A | G | 23 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(20): Show | 23 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.178+1863A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70724614 | ||||||
| chr4:70724671
|
C | T | 30 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(27): Show | 30 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.178+1920C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70724671 | ||||||
| chr4:70724942
|
T | A | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.178+2191T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70724942 | ||||||
| chr4:70725079
|
C | A | 67 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(64): Show | 67 | HG00323.hp2 HG00673.hp1 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.178+2328C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70725079 | ||||||
| chr4:70725158
|
A | G | 2 | a0001c0001t0007g0010a0001c0001t0007g0011 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.178+2407A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70725158 | ||||||
| chr4:70725241
|
C | G | 1 | a0001c0001t0003g0064 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.178+2490C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70725241 | ||||||
| chr4:70725242
|
C | T | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.178+2491C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70725242 | ||||||
| chr4:70725336
|
T | G | 49 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(46): Show | 49 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.178+2585T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70725336 | ||||||
| chr4:70725519
|
C | T | 9 | a0001c0001t0001g0215a0001c0001t0002g0211a0001c0001t0002g0213others(6): Show | 9 | HG02080.hp1 HG03239.hp1 HG03834.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+2768C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70725519 | ||||||
| chr4:70725641
|
T | A | 9 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+2890T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70725641 | ||||||
| chr4:70725751
|
A | C | 1 | a0001c0001t0002g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.178+3000A>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70725751 | ||||||
| chr4:70725822
|
C | T | 31 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+3071C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70725822 | ||||||
| chr4:70726143
|
A | G | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.178+3392A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726143 | ||||||
| chr4:70726159
|
G | A | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.178+3408G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726159 | ||||||
| chr4:70726177
|
C | T | 31 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+3426C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726177 | ||||||
| chr4:70726223
|
A | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0028g0209 | 3 | HG01978.hp1 NA18970.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.178+3472A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726223 | ||||||
| chr4:70726226
|
A | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0028g0209 | 3 | HG01978.hp1 NA18970.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.178+3475A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726226 | ||||||
| chr4:70726227
|
G | GTTCATTC others(1): Show |
3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0028g0209 | 3 | HG01978.hp1 NA18970.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.178+3476_178+3477i others(10): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726227 | ||||||
| chr4:70726229
|
C | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0028g0209 | 3 | HG01978.hp1 NA18970.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.178+3478C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726229 | ||||||
| chr4:70726230
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0028g0209 | 3 | HG01978.hp1 NA18970.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.178+3479A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726230 | ||||||
| chr4:70726231
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0028g0209 | 3 | HG01978.hp1 NA18970.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.178+3480G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726231 | ||||||
| chr4:70726234
|
C | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0028g0209 | 3 | HG01978.hp1 NA18970.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.178+3483C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726234 | ||||||
| chr4:70726284
|
A | G | 3 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009 | 3 | HG02976.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.178+3533A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726284 | ||||||
| chr4:70726337
|
G | A | 31 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+3586G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726337 | ||||||
| chr4:70726423
|
C | T | 21 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(18): Show | 21 | HG00673.hp1 HG01123.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.178+3672C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726423 | ||||||
| chr4:70726444
|
C | A | 1 | a0001c0001t0006g0091 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.178+3693C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726444 | ||||||
| chr4:70726522
|
C | T | 1 | a0001c0001t0004g0084 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.178+3771C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726522 | ||||||
| chr4:70726530
|
C | T | 29 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0002g0180others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.178+3779C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726530 | ||||||
| chr4:70726781
|
G | A | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.178+4030G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726781 | ||||||
| chr4:70726818
|
T | G | 3 | a0001c0001t0019g0220a0001c0001t0019g0221a0003c0004t0038g0014 | 3 | HG01891.hp2 HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.178+4067T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726818 | ||||||
| chr4:70726827
|
T | C | 1 | a0001c0001t0023g0015 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.178+4076T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70726827 | ||||||
| chr4:70726983
|
C | CAG | 31 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+4234_178+4235d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70726983 | |||||
| chr4:70727039
|
C | CT | 22 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0008g0235others(19): Show | 22 | HG01109.hp2 HG01243.hp2 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.178+4308dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70727039 | |||||
| chr4:70727039
|
C | CTTT | 5 | a0001c0001t0014g0222a0001c0001t0014g0224a0001c0001t0014g0225others(2): Show | 5 | HG02258.hp1 HG02717.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+4306_178+4308d others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70727039 | |||||
| chr4:70727039
|
CT | C | 33 | a0001c0001t0001g0087a0001c0001t0001g0092a0001c0001t0001g0093others(30): Show | 33 | HG00609.hp2 HG01070.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.178+4308delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70727039 | |||||
| chr4:70727258
|
AT | A | 31 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+4515delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70727258 | |||||
| chr4:70727286
|
A | G | 1 | a0001c0001t0019g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.178+4535A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727286 | ||||||
| chr4:70727313
|
A | T | 1 | a0001c0001t0003g0063 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.178+4562A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727313 | ||||||
| chr4:70727354
|
C | CT | 24 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(21): Show | 24 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.178+4622dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70727354 | |||||
| chr4:70727354
|
C | CTTTT | 26 | a0001c0001t0008g0241a0001c0001t0008g0242a0001c0001t0008g0244others(23): Show | 26 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+4619_178+4622d others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70727354 | |||||
| chr4:70727354
|
CT | C | 20 | a0001c0001t0002g0210a0001c0001t0004g0070a0001c0001t0004g0073others(17): Show | 20 | HG00673.hp1 HG01123.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.178+4622delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70727354 | |||||
| chr4:70727429
|
C | T | 9 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(6): Show | 9 | HG02615.hp1 HG02630.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.178+4678C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727429 | ||||||
| chr4:70727441
|
T | C | 2 | a0001c0001t0008g0250a0001c0001t0035g0251 | 2 | HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.178+4690T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727441 | ||||||
| chr4:70727486
|
A | G | 1 | a0001c0001t0003g0022 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.178+4735A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727486 | ||||||
| chr4:70727512
|
C | T | 1 | a0001c0001t0002g0219 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.178+4761C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727512 | ||||||
| chr4:70727605
|
C | G | 2 | a0001c0001t0011g0229a0001c0001t0011g0230 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.178+4854C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727605 | ||||||
| chr4:70727634
|
A | T | 2 | a0001c0001t0011g0229a0001c0001t0011g0230 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.178+4883A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727634 | ||||||
| chr4:70727647
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.178+4896C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727647 | ||||||
| chr4:70727721
|
G | A | 9 | a0001c0001t0005g0065a0001c0001t0011g0227a0001c0001t0011g0229others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+4970G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727721 | ||||||
| chr4:70727730
|
T | C | 1 | a0001c0001t0023g0015 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.178+4979T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727730 | ||||||
| chr4:70727758
|
G | A | 4 | a0001c0001t0013g0003a0001c0001t0013g0004a0001c0001t0013g0005others(1): Show | 4 | HG03209.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+5007G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727758 | ||||||
| chr4:70727787
|
C | CA | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0003g0022others(2): Show | 5 | HG00741.hp1 NA18941.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+5051dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70727787 | |||||
| chr4:70727979
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.178+5228A>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727979 | ||||||
| chr4:70727983
|
T | A | 1 | a0001c0001t0001g0174 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.178+5232T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727983 | ||||||
| chr4:70727991
|
A | G | 104 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(101): Show | 104 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.178+5240A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70727991 | ||||||
| chr4:70728034
|
C | T | 14 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(11): Show | 14 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+5283C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70728034 | ||||||
| chr4:70728264
|
C | T | 1 | a0001c0001t0033g0252 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.178+5513C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70728264 | ||||||
| chr4:70728276
|
T | G | 14 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(11): Show | 14 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+5525T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70728276 | ||||||
| chr4:70728458
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(58): Show | 62 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.178+5707G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70728458 | ||||||
| chr4:70728478
|
G | T | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+5727G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70728478 | ||||||
| chr4:70728512
|
G | A | 48 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(45): Show | 48 | HG00323.hp2 HG00673.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.178+5761G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70728512 | ||||||
| chr4:70728547
|
A | G | 52 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(49): Show | 52 | HG00323.hp2 HG00673.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.178+5796A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70728547 | ||||||
| chr4:70728620
|
A | T | 2 | a0001c0001t0016g0247a0001c0001t0016g0248 | 2 | HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.178+5869A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70728620 | ||||||
| chr4:70728740
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.178+5989T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70728740 | ||||||
| chr4:70728881
|
CT | C | 8 | a0001c0001t0001g0173a0001c0001t0003g0056a0001c0001t0005g0071others(5): Show | 8 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+6145delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70728881 | |||||
| chr4:70728897
|
A | T | 1 | a0001c0001t0001g0152 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.178+6146A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70728897 | ||||||
| chr4:70729032
|
G | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+6281G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70729032 | ||||||
| chr4:70729370
|
C | T | 5 | a0001c0001t0014g0222a0001c0001t0014g0224a0001c0001t0014g0225others(2): Show | 5 | HG02258.hp1 HG02717.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+6619C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70729370 | ||||||
| chr4:70729423
|
A | T | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+6672A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70729423 | ||||||
| chr4:70729698
|
C | A | 29 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0002g0180others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.178+6947C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70729698 | ||||||
| chr4:70729713
|
G | T | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+6962G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70729713 | ||||||
| chr4:70729776
|
G | A | 1 | a0001c0001t0023g0015 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.178+7025G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70729776 | ||||||
| chr4:70729881
|
A | ACACAAG | 7 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(4): Show | 7 | HG02615.hp1 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+7130_178+7131i others(8): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70729881 | ||||||
| chr4:70729885
|
A | T | 7 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(4): Show | 7 | HG02615.hp1 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+7134A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70729885 | ||||||
| chr4:70729886
|
A | C | 7 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(4): Show | 7 | HG02615.hp1 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+7135A>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70729886 | ||||||
| chr4:70729887
|
A | AGTT | 7 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(4): Show | 7 | HG02615.hp1 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+7136_178+7137i others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70729887 | ||||||
| chr4:70729935
|
G | GT | 97 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0093others(94): Show | 97 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.178+7200dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70729935 | |||||
| chr4:70729935
|
G | GTT | 11 | a0001c0001t0001g0104a0001c0001t0001g0147a0001c0001t0001g0148others(8): Show | 11 | HG00735.hp2 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+7199_178+7200d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70729935 | |||||
| chr4:70729935
|
GT | G | 19 | a0001c0001t0002g0097a0001c0001t0004g0070a0001c0001t0004g0073others(16): Show | 19 | HG00673.hp1 HG01123.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.178+7200delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70729935 | |||||
| chr4:70729959
|
A | C | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+7208A>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70729959 | ||||||
| chr4:70730003
|
T | C | 46 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(43): Show | 46 | HG00323.hp2 HG00673.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.178+7252T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730003 | ||||||
| chr4:70730145
|
G | T | 29 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0002g0180others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.178+7394G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730145 | ||||||
| chr4:70730169
|
T | C | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+7418T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730169 | ||||||
| chr4:70730188
|
G | C | 1 | a0001c0001t0007g0011 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.178+7437G>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730188 | ||||||
| chr4:70730244
|
A | G | 2 | a0001c0001t0007g0068a0001c0001t0007g0069 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178+7493A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730244 | ||||||
| chr4:70730560
|
G | A | 14 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(11): Show | 14 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+7809G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730560 | ||||||
| chr4:70730572
|
C | CA | 6 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0174others(3): Show | 6 | HG00639.hp2 HG01109.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+7836dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70730572 | |||||
| chr4:70730572
|
C | CAAAAAA | 15 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+7831_178+7836d others(8): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70730572 | |||||
| chr4:70730572
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0011g0233others(3): Show | 6 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+7826_178+7836d others(13): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70730572 | |||||
| chr4:70730572
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0011g0227a0001c0001t0011g0231 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.178+7825_178+7836d others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70730572 | |||||
| chr4:70730610
|
G | A | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.178+7859G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730610 | ||||||
| chr4:70730681
|
G | A | 1 | a0001c0001t0031g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.178+7930G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730681 | ||||||
| chr4:70730750
|
T | TA | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+8006dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70730750 | |||||
| chr4:70730798
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.178+8047G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730798 | ||||||
| chr4:70730811
|
C | G | 1 | a0001c0001t0001g0101 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.178+8060C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730811 | ||||||
| chr4:70730818
|
T | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+8067T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730818 | ||||||
| chr4:70730904
|
G | A | 8 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(5): Show | 8 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+8153G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730904 | ||||||
| chr4:70730967
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.178+8216G>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70730967 | ||||||
| chr4:70731040
|
C | CT | 23 | a0001c0001t0002g0218a0001c0001t0004g0070a0001c0001t0004g0074others(20): Show | 23 | HG00673.hp1 HG01123.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.178+8306dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70731040 | |||||
| chr4:70731040
|
CT | C | 41 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0211others(38): Show | 41 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.178+8306delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70731040 | |||||
| chr4:70731081
|
A | G | 1 | a0001c0001t0006g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.178+8330A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70731081 | ||||||
| chr4:70731123
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.178+8372C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70731123 | ||||||
| chr4:70731124
|
G | A | 1 | a0001c0001t0002g0184 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.178+8373G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70731124 | ||||||
| chr4:70731347
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.178+8596C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70731347 | ||||||
| chr4:70731352
|
T | G | 120 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(117): Show | 120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.178+8601T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70731352 | ||||||
| chr4:70731510
|
C | G | 4 | a0001c0001t0001g0092a0001c0001t0001g0145a0001c0001t0002g0096others(1): Show | 4 | HG00609.hp2 HG00673.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+8759C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70731510 | ||||||
| chr4:70731512
|
A | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.178+8761A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70731512 | ||||||
| chr4:70731519
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.178+8768A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70731519 | ||||||
| chr4:70731632
|
G | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+8881G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70731632 | ||||||
| chr4:70731851
|
G | A | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0147others(1): Show | 4 | HG00280.hp2 HG00639.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+9100G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70731851 | ||||||
| chr4:70731856
|
C | T | 7 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(4): Show | 7 | HG02615.hp1 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+9105C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70731856 | ||||||
| chr4:70732457
|
C | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.178+9706C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70732457 | ||||||
| chr4:70732470
|
C | T | 5 | a0001c0001t0014g0222a0001c0001t0014g0224a0001c0001t0014g0225others(2): Show | 5 | HG02258.hp1 HG02717.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+9719C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70732470 | ||||||
| chr4:70732514
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.178+9763C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70732514 | ||||||
| chr4:70732645
|
G | A | 46 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(43): Show | 46 | HG00323.hp2 HG00673.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.178+9894G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70732645 | ||||||
| chr4:70732771
|
TG | T | 177 | a0001c0001t0001g0107a0001c0001t0001g0199a0001c0001t0001g0206others(174): Show | 178 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.178+10026delG | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70732771 | |||||
| chr4:70732999
|
G | A | 52 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(49): Show | 52 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.178+10248G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70732999 | ||||||
| chr4:70733023
|
C | T | 2 | a0001c0001t0004g0082a0003c0004t0038g0014 | 2 | HG03130.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.178+10272C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733023 | ||||||
| chr4:70733073
|
A | AAG | 3 | a0001c0001t0007g0068a0001c0001t0007g0069a0001c0001t0015g0106 | 3 | HG02559.hp2 NA18955.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.178+10343_178+1034 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733073 | |||||
| chr4:70733073
|
A | AG | 3 | a0001c0001t0002g0201a0001c0001t0007g0011a0001c0001t0010g0086 | 3 | HG02145.hp1 HG02602.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.178+10322_178+1032 others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733073 | ||||||
| chr4:70733073
|
AAGAGAGA others(22): Show |
A | 10 | a0001c0001t0002g0002a0001c0001t0002g0098a0001c0001t0002g0099others(7): Show | 11 | HG00597.hp2 HG01070.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.178+10341_178+1036 others(33): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733073 | |||||
| chr4:70733073
|
AAGAGAGA others(26): Show |
A | 3 | a0001c0001t0002g0097a0001c0001t0002g0162a0001c0001t0002g0163 | 3 | HG01167.hp1 HG01169.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.178+10337_178+1036 others(37): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733073 | |||||
| chr4:70733077
|
G | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+10326G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733077 | ||||||
| chr4:70733078
|
A | AGAGAGAG others(10): Show |
1 | a0001c0001t0005g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.178+10345_178+1036 others(21): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733078 | |||||
| chr4:70733080
|
AGAGAGAG others(8): Show |
A | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.178+10345_178+1035 others(19): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733080 | |||||
| chr4:70733088
|
A | G | 1 | a0001c0001t0039g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.178+10337A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733088 | ||||||
| chr4:70733088
|
AGAGAGAG others(26): Show |
A | 1 | a0001c0001t0032g0155 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.178+10341_178+1037 others(37): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733088 | |||||
| chr4:70733092
|
AGAG | A | 6 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(3): Show | 6 | HG01243.hp2 HG02074.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+10345_178+1034 others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733092 | |||||
| chr4:70733094
|
AG | A | 23 | a0001c0001t0003g0026a0001c0001t0008g0244a0001c0001t0008g0249others(20): Show | 23 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.178+10345delG | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733094 | |||||
| chr4:70733095
|
G | GGA | 36 | a0001c0001t0001g0093a0001c0001t0001g0108a0001c0001t0001g0117others(33): Show | 36 | HG00408.hp1 HG00438.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.178+10368_178+1036 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733095 | |||||
| chr4:70733095
|
GGAGAGAG others(1): Show |
G | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+10362_178+1036 others(12): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733095 | |||||
| chr4:70733096
|
G | A | 1 | a0001c0001t0003g0027 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.178+10345G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733096 | ||||||
| chr4:70733097
|
A | AGAGAGAG others(8): Show |
1 | a0001c0001t0005g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.178+10347_178+1036 others(19): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733097 | |||||
| chr4:70733097
|
A | G | 1 | a0001c0001t0003g0027 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.178+10346A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733097 | ||||||
| chr4:70733100
|
GA | G | 13 | a0001c0001t0008g0244a0001c0001t0008g0249a0001c0001t0008g0250others(10): Show | 13 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+10350delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733100 | ||||||
| chr4:70733102
|
GA | G | 5 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+10352delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733102 | ||||||
| chr4:70733103
|
A | G | 8 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(5): Show | 8 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+10352A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733103 | ||||||
| chr4:70733108
|
GA | G | 13 | a0001c0001t0008g0244a0001c0001t0008g0249a0001c0001t0008g0250others(10): Show | 13 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+10358delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733108 | ||||||
| chr4:70733109
|
A | AGAGGGAG others(5): Show |
2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.178+10361_178+1036 others(16): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733109 | |||||
| chr4:70733110
|
GA | G | 13 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(10): Show | 13 | HG00323.hp2 HG01243.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+10360delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733110 | ||||||
| chr4:70733113
|
A | G | 8 | a0001c0001t0005g0065a0001c0001t0005g0071a0001c0001t0005g0072others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.178+10362A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733113 | ||||||
| chr4:70733117
|
A | AGAGAGAG others(5): Show |
1 | a0001c0001t0025g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.178+10369_178+1037 others(16): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733117 | |||||
| chr4:70733117
|
A | G | 10 | a0001c0001t0001g0113a0001c0001t0005g0065a0001c0001t0005g0071others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.178+10366A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733117 | ||||||
| chr4:70733119
|
AGG | A | 6 | a0001c0001t0001g0147a0001c0001t0002g0102a0001c0001t0003g0064others(3): Show | 6 | HG01952.hp2 HG02895.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+10370_178+1037 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733119 | |||||
| chr4:70733119
|
AGGGAGGG others(7): Show |
A | 7 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(4): Show | 7 | HG00323.hp2 HG01243.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+10370_178+1038 others(18): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733119 | |||||
| chr4:70733119
|
AGGGAGGG others(11): Show |
A | 19 | a0001c0001t0008g0244a0001c0001t0008g0249a0001c0001t0008g0250others(16): Show | 19 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.178+10370_178+1038 others(22): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733119 | |||||
| chr4:70733121
|
G | A | 47 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(44): Show | 47 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.178+10370G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733121 | ||||||
| chr4:70733125
|
G | A | 20 | a0001c0001t0003g0017a0001c0001t0003g0020a0001c0001t0003g0023others(17): Show | 20 | HG00597.hp1 HG01993.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.178+10374G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733125 | ||||||
| chr4:70733129
|
G | A | 1 | a0001c0001t0030g0172 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.178+10378G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733129 | ||||||
| chr4:70733133
|
GGAGGGAG others(3): Show |
G | 2 | a0001c0001t0003g0044a0001c0001t0024g0045 | 2 | NA18982.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.178+10386_178+1039 others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733133 | |||||
| chr4:70733137
|
G | A | 8 | a0001c0001t0002g0186a0001c0001t0008g0235a0001c0001t0008g0241others(5): Show | 8 | HG00323.hp2 HG01243.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.178+10386G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733137 | ||||||
| chr4:70733137
|
G | GA | 3 | a0001c0001t0001g0120a0001c0001t0001g0175a0004c0002t0002g0154 | 3 | HG03927.hp2 NA18975.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.178+10386_178+1038 others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733137 | ||||||
| chr4:70733137
|
G | GGA | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0166others(4): Show | 7 | HG00438.hp2 HG02056.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+10415_178+1041 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733137 | |||||
| chr4:70733137
|
GGA | G | 34 | a0001c0001t0003g0013a0001c0001t0003g0018a0001c0001t0003g0019others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.178+10415_178+1041 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733137 | |||||
| chr4:70733137
|
GGAGA | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0148others(5): Show | 8 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+10413_178+1041 others(8): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733137 | |||||
| chr4:70733139
|
A | AGG | 19 | a0001c0001t0003g0017a0001c0001t0003g0020a0001c0001t0003g0023others(16): Show | 19 | HG00597.hp1 HG01167.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.178+10389_178+1039 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733139 | |||||
| chr4:70733139
|
A | AGGGAGG | 3 | a0001c0001t0005g0065a0001c0001t0023g0015a0001c0001t0030g0172 | 3 | HG01884.hp1 HG02280.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.178+10389_178+1039 others(10): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733139 | |||||
| chr4:70733139
|
A | G | 8 | a0001c0001t0001g0215a0001c0001t0002g0211a0001c0001t0002g0213others(5): Show | 8 | HG02080.hp1 HG03239.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.178+10388A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733139 | ||||||
| chr4:70733141
|
A | G | 21 | a0001c0001t0001g0140a0001c0001t0001g0147a0001c0001t0002g0102others(18): Show | 21 | HG01952.hp2 HG02145.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.178+10390A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733141 | ||||||
| chr4:70733143
|
A | G | 5 | a0001c0001t0005g0065a0001c0001t0019g0220a0001c0001t0019g0221others(2): Show | 5 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+10392A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733143 | ||||||
| chr4:70733145
|
A | G | 10 | a0001c0001t0007g0068a0001c0001t0007g0069a0001c0001t0013g0003others(7): Show | 10 | HG02258.hp1 HG02559.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.178+10394A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733145 | ||||||
| chr4:70733147
|
A | G | 2 | a0001c0001t0005g0065a0001c0001t0019g0221 | 2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.178+10396A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733147 | ||||||
| chr4:70733153
|
A | G | 1 | a0001c0001t0014g0222 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.178+10402A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733153 | ||||||
| chr4:70733154
|
G | A | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.178+10403G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733154 | ||||||
| chr4:70733156
|
GAGAGAGA others(5): Show |
G | 1 | a0001c0001t0014g0222 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.178+10409_178+1042 others(16): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733156 | |||||
| chr4:70733158
|
G | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+10407G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733158 | ||||||
| chr4:70733160
|
GAGAGAGA others(1): Show |
G | 5 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+10413_178+1042 others(12): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733160 | |||||
| chr4:70733161
|
A | G | 3 | a0001c0001t0014g0224a0001c0001t0014g0225a0001c0001t0014g0226 | 3 | HG02717.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.178+10410A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733161 | ||||||
| chr4:70733162
|
G | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+10411G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733162 | ||||||
| chr4:70733162
|
GAGAGAA | G | 5 | a0001c0001t0003g0026a0001c0001t0013g0003a0001c0001t0013g0004others(2): Show | 5 | HG03209.hp1 HG03540.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+10415_178+1042 others(10): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733162 | |||||
| chr4:70733164
|
G | A | 21 | a0001c0001t0002g0156a0001c0001t0004g0070a0001c0001t0004g0073others(18): Show | 21 | HG00673.hp1 HG01123.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.178+10413G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733164 | ||||||
| chr4:70733164
|
GAGAA | G | 4 | a0001c0001t0014g0224a0001c0001t0014g0225a0001c0001t0014g0226others(1): Show | 4 | HG02258.hp1 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+10427_178+1043 others(8): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733164 | |||||
| chr4:70733166
|
G | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+10415G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733166 | ||||||
| chr4:70733168
|
A | G | 3 | a0001c0001t0002g0205a0001c0001t0003g0044a0001c0001t0024g0045 | 3 | HG02129.hp1 NA18982.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.178+10417A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733168 | ||||||
| chr4:70733174
|
G | GAA | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.178+10425_178+1042 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733174 | |||||
| chr4:70733176
|
AAG | A | 17 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(14): Show | 17 | HG00673.hp1 HG01123.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.178+10427_178+1042 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733176 | |||||
| chr4:70733247
|
T | A | 4 | a0001c0001t0013g0003a0001c0001t0013g0004a0001c0001t0013g0005others(1): Show | 4 | HG03209.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+10496T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733247 | ||||||
| chr4:70733337
|
TTAA | T | 2 | a0001c0001t0002g0211a0001c0001t0002g0217 | 2 | NA18992.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.178+10592_178+1059 others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70733337 | |||||
| chr4:70733403
|
T | C | 1 | a0001c0001t0019g0220 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+10652T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733403 | ||||||
| chr4:70733419
|
G | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+10668G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733419 | ||||||
| chr4:70733539
|
T | C | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.178+10788T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733539 | ||||||
| chr4:70733770
|
A | G | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.178+11019A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733770 | ||||||
| chr4:70733897
|
T | C | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.178+11146T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733897 | ||||||
| chr4:70733933
|
T | C | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.178+11182T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70733933 | ||||||
| chr4:70734276
|
G | A | 2 | a0001c0001t0002g0002a0001c0001t0002g0157 | 3 | HG02622.hp2 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.178+11525G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70734276 | ||||||
| chr4:70734464
|
ACTT | A | 5 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+11716_178+1171 others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70734464 | |||||
| chr4:70734522
|
A | G | 1 | a0001c0001t0037g0161 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.178+11771A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70734522 | ||||||
| chr4:70734535
|
C | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+11784C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70734535 | ||||||
| chr4:70734626
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.178+11875G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70734626 | ||||||
| chr4:70734855
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.178+12104A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70734855 | ||||||
| chr4:70734910
|
A | G | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.178+12159A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70734910 | ||||||
| chr4:70735364
|
G | A | 1 | a0001c0001t0006g0057 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.178+12613G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70735364 | ||||||
| chr4:70735376
|
A | G | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+12625A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70735376 | ||||||
| chr4:70735424
|
A | G | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.178+12673A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70735424 | ||||||
| chr4:70735565
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0002g0219 | 2 | NA18950.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.178+12814G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70735565 | ||||||
| chr4:70735621
|
G | T | 28 | a0001c0001t0001g0107a0001c0001t0001g0199a0001c0001t0001g0206others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.178+12870G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70735621 | ||||||
| chr4:70735622
|
C | T | 28 | a0001c0001t0001g0107a0001c0001t0001g0199a0001c0001t0001g0206others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.178+12871C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70735622 | ||||||
| chr4:70735670
|
A | G | 1 | a0001c0001t0002g0205 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.178+12919A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70735670 | ||||||
| chr4:70735895
|
G | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+13144G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70735895 | ||||||
| chr4:70736110
|
C | A | 1 | a0001c0001t0002g0213 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.178+13359C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736110 | ||||||
| chr4:70736132
|
G | A | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.178+13381G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736132 | ||||||
| chr4:70736152
|
C | CA | 6 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0010g0193others(3): Show | 6 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+13418dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70736152 | |||||
| chr4:70736165
|
A | G | 1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.178+13414A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736165 | ||||||
| chr4:70736239
|
T | C | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.178+13488T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736239 | ||||||
| chr4:70736410
|
G | A | 1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.178+13659G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736410 | ||||||
| chr4:70736420
|
A | G | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.178+13669A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736420 | ||||||
| chr4:70736439
|
T | C | 10 | a0001c0001t0003g0025a0001c0001t0003g0034a0001c0001t0003g0035others(7): Show | 10 | HG00408.hp1 HG00438.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.178+13688T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736439 | ||||||
| chr4:70736464
|
G | A | 1 | a0001c0001t0007g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+13713G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736464 | ||||||
| chr4:70736490
|
A | G | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+13739A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736490 | ||||||
| chr4:70736562
|
ATTTCT | A | 14 | a0001c0001t0002g0191a0001c0001t0007g0008a0001c0001t0007g0009others(11): Show | 14 | HG01257.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.178+13825_178+1382 others(9): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70736562 | |||||
| chr4:70736594
|
G | A | 7 | a0001c0001t0009g0236a0001c0001t0009g0238a0001c0001t0009g0239others(4): Show | 7 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+13843G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736594 | ||||||
| chr4:70736629
|
T | A | 2 | a0001c0001t0007g0068a0001c0001t0007g0069 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178+13878T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736629 | ||||||
| chr4:70736662
|
C | T | 1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.178+13911C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736662 | ||||||
| chr4:70736791
|
C | G | 2 | a0001c0001t0002g0189a0001c0001t0002g0190 | 2 | HG00140.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.178+14040C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70736791 | ||||||
| chr4:70737074
|
C | G | 1 | a0001c0001t0002g0217 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.178+14323C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70737074 | ||||||
| chr4:70737103
|
G | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+14352G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70737103 | ||||||
| chr4:70737236
|
T | A | 1 | a0001c0001t0002g0162 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.178+14485T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70737236 | ||||||
| chr4:70737238
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.178+14487C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70737238 | ||||||
| chr4:70737324
|
A | C | 3 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0036g0228 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.178+14573A>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70737324 | ||||||
| chr4:70737676
|
C | CT | 6 | a0001c0001t0001g0101a0001c0001t0005g0072a0001c0001t0010g0181others(3): Show | 6 | HG01167.hp2 HG01517.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+14943dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70737676 | |||||
| chr4:70737676
|
C | CTT | 8 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0231others(5): Show | 8 | HG00323.hp2 HG01515.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+14942_178+1494 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70737676 | |||||
| chr4:70737676
|
C | CTTT | 16 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(13): Show | 16 | HG01243.hp1 HG01243.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.178+14941_178+1494 others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70737676 | |||||
| chr4:70737676
|
CT | C | 19 | a0001c0001t0001g0109a0001c0001t0003g0034a0001c0001t0004g0070others(16): Show | 19 | HG00673.hp1 HG01123.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.178+14943delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70737676 | |||||
| chr4:70737843
|
T | G | 1 | a0001c0001t0008g0250 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.178+15092T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70737843 | ||||||
| chr4:70737964
|
T | A | 2 | a0001c0001t0005g0065a0003c0004t0038g0014 | 2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.178+15213T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70737964 | ||||||
| chr4:70737982
|
C | CT | 51 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0115others(48): Show | 51 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.178+15249dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70737982 | |||||
| chr4:70737982
|
CT | C | 47 | a0001c0001t0001g0088a0001c0001t0001g0120a0001c0001t0001g0123others(44): Show | 47 | HG00323.hp2 HG01109.hp1 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.178+15249delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70737982 | |||||
| chr4:70737982
|
CTT | C | 59 | a0001c0001t0003g0013a0001c0001t0003g0018a0001c0001t0003g0019others(56): Show | 59 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.178+15248_178+1524 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70737982 | |||||
| chr4:70738129
|
ATGC | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+15382_178+1538 others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70738129 | |||||
| chr4:70738356
|
CT | C | 158 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0120others(155): Show | 159 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.178+15629delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70738356 | |||||
| chr4:70738356
|
CTT | C | 13 | a0001c0001t0004g0070a0001c0001t0007g0068a0001c0001t0007g0069others(10): Show | 13 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+15628_178+1562 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70738356 | |||||
| chr4:70738385
|
C | T | 1 | a0001c0001t0014g0226 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.178+15634C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70738385 | ||||||
| chr4:70738426
|
G | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+15675G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70738426 | ||||||
| chr4:70738449
|
G | A | 1 | a0001c0001t0004g0083 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.178+15698G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70738449 | ||||||
| chr4:70738523
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.178+15772C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70738523 | ||||||
| chr4:70738537
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.178+15786T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70738537 | ||||||
| chr4:70738912
|
C | T | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.178+16161C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70738912 | ||||||
| chr4:70738952
|
C | T | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+16201C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70738952 | ||||||
| chr4:70738957
|
C | T | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+16206C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70738957 | ||||||
| chr4:70738958
|
A | G | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+16207A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70738958 | ||||||
| chr4:70738993
|
G | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+16242G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70738993 | ||||||
| chr4:70739080
|
C | CT | 12 | a0001c0001t0001g0145a0001c0001t0003g0023a0001c0001t0011g0229others(9): Show | 12 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.178+16344dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70739080 | |||||
| chr4:70739080
|
CT | C | 8 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(5): Show | 8 | HG02615.hp1 HG02965.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+16344delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70739080 | |||||
| chr4:70739177
|
T | C | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.178+16426T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70739177 | ||||||
| chr4:70739328
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.178+16577T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70739328 | ||||||
| chr4:70739384
|
G | T | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+16633G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70739384 | ||||||
| chr4:70739533
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.178+16782T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70739533 | ||||||
| chr4:70739674
|
A | G | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+16923A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70739674 | ||||||
| chr4:70739688
|
G | A | 4 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015others(1): Show | 4 | HG01167.hp2 HG02280.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+16937G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70739688 | ||||||
| chr4:70739757
|
C | T | 1 | a0001c0001t0003g0059 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.178+17006C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70739757 | ||||||
| chr4:70739781
|
G | A | 3 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0012g0039 | 3 | HG02155.hp1 NA18961.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.178+17030G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70739781 | ||||||
| chr4:70739828
|
T | TAA | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+17092_178+1709 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70739828 | |||||
| chr4:70739839
|
A | G | 1 | a0001c0001t0027g0116 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.178+17088A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70739839 | ||||||
| chr4:70739844
|
A | AT | 20 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0002g0194others(17): Show | 20 | HG02015.hp1 HG02155.hp1 HG03927.hp1 others(17): Show |
intron_variant | MODIFIER | c.178+17093_178+1709 others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70739844 | ||||||
| chr4:70739990
|
C | CA | 28 | a0001c0001t0002g0194a0001c0001t0003g0022a0001c0001t0003g0064others(25): Show | 28 | HG00673.hp1 HG01123.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.178+17258dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70739990 | |||||
| chr4:70739990
|
CA | C | 7 | a0001c0001t0002g0102a0001c0001t0007g0007a0001c0001t0007g0008others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+17258delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70739990 | |||||
| chr4:70740055
|
A | G | 2 | a0001c0001t0013g0005a0001c0001t0013g0006 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.178+17304A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70740055 | ||||||
| chr4:70740174
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG01258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.178+17423A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70740174 | ||||||
| chr4:70740178
|
TAGTAAAG others(5): Show |
T | 3 | a0001c0001t0014g0222a0001c0001t0014g0224a0001c0001t0014g0226 | 3 | HG02717.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.178+17430_178+1744 others(16): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70740178 | |||||
| chr4:70740245
|
G | C | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+17494G>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70740245 | ||||||
| chr4:70740335
|
T | C | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.178+17584T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70740335 | ||||||
| chr4:70740341
|
T | G | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+17590T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70740341 | ||||||
| chr4:70740462
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.178+17711G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70740462 | ||||||
| chr4:70740638
|
A | G | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.178+17887A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70740638 | ||||||
| chr4:70740764
|
ATAG | A | 6 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(3): Show | 6 | HG02615.hp1 HG03130.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+18017_178+1801 others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70740764 | |||||
| chr4:70740848
|
A | T | 1 | a0001c0001t0003g0030 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.178+18097A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70740848 | ||||||
| chr4:70741162
|
A | AT | 18 | a0001c0001t0004g0073a0001c0001t0008g0235a0001c0001t0008g0241others(15): Show | 18 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.178+18425dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70741162 | |||||
| chr4:70741162
|
AT | A | 6 | a0001c0001t0011g0227a0001c0001t0011g0231a0001c0001t0011g0233others(3): Show | 6 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+18425delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70741162 | |||||
| chr4:70741248
|
A | G | 1 | a0001c0001t0008g0249 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.178+18497A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70741248 | ||||||
| chr4:70741435
|
G | A | 51 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(48): Show | 51 | HG00323.hp2 HG00673.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.178+18684G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70741435 | ||||||
| chr4:70741885
|
C | T | 2 | a0001c0001t0011g0227a0001c0001t0011g0233 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.178+19134C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70741885 | ||||||
| chr4:70741900
|
C | T | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.178+19149C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70741900 | ||||||
| chr4:70741977
|
C | A | 1 | a0001c0001t0033g0252 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.178+19226C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70741977 | ||||||
| chr4:70742096
|
T | A | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.178+19345T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70742096 | ||||||
| chr4:70742102
|
C | CT | 122 | a0001c0001t0002g0182a0001c0001t0003g0013a0001c0001t0003g0017others(119): Show | 122 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.178+19353dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70742102 | |||||
| chr4:70742293
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.178+19542G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70742293 | ||||||
| chr4:70742301
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0111 | 2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.178+19550C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70742301 | ||||||
| chr4:70742302
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.178+19551G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70742302 | ||||||
| chr4:70742443
|
C | G | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.178+19692C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70742443 | ||||||
| chr4:70742497
|
C | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.178+19746C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70742497 | ||||||
| chr4:70742756
|
G | C | 1 | a0001c0001t0002g0098 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.179-19763G>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70742756 | ||||||
| chr4:70743108
|
G | A | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.179-19411G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70743108 | ||||||
| chr4:70743144
|
C | T | 19 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(16): Show | 19 | HG00673.hp1 HG01123.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.179-19375C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70743144 | ||||||
| chr4:70743182
|
G | T | 1 | a0001c0001t0005g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.179-19337G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70743182 | ||||||
| chr4:70743185
|
T | C | 1 | a0001c0001t0005g0050 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-19334T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70743185 | ||||||
| chr4:70743347
|
C | T | 2 | a0001c0001t0023g0015a0002c0005t0022g0012 | 2 | HG02280.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.179-19172C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70743347 | ||||||
| chr4:70743420
|
T | G | 8 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(5): Show | 8 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-19099T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70743420 | ||||||
| chr4:70743488
|
T | C | 2 | a0001c0001t0007g0010a0001c0001t0007g0011 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.179-19031T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70743488 | ||||||
| chr4:70743518
|
A | G | 5 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-19001A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70743518 | ||||||
| chr4:70743890
|
G | A | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.179-18629G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70743890 | ||||||
| chr4:70743948
|
G | A | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.179-18571G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70743948 | ||||||
| chr4:70744090
|
G | A | 6 | a0001c0001t0003g0056a0001c0001t0003g0058a0001c0001t0003g0061others(3): Show | 6 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-18429G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70744090 | ||||||
| chr4:70744164
|
G | C | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.179-18355G>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70744164 | ||||||
| chr4:70744250
|
G | A | 1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.179-18269G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70744250 | ||||||
| chr4:70744356
|
T | TTGTATGT others(1): Show |
15 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(12): Show | 15 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.179-18162_179-1816 others(12): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70744356 | |||||
| chr4:70744358
|
T | G | 15 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(12): Show | 15 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.179-18161T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70744358 | ||||||
| chr4:70744358
|
T | TTATG | 7 | a0001c0001t0005g0065a0001c0001t0007g0068a0001c0001t0007g0069others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-18138_179-1813 others(8): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70744358 | |||||
| chr4:70744358
|
T | TTATGTAT others(1): Show |
73 | a0001c0001t0002g0182a0001c0001t0003g0013a0001c0001t0003g0017others(70): Show | 73 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.179-18142_179-1813 others(12): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70744358 | |||||
| chr4:70744358
|
T | TTATGTAT others(9): Show |
1 | a0001c0001t0025g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.179-18150_179-1813 others(20): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70744358 | |||||
| chr4:70744439
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.179-18080G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70744439 | ||||||
| chr4:70744654
|
A | AT | 13 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0001t0004g0080others(10): Show | 13 | HG01167.hp2 HG02615.hp1 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-17848dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70744654 | |||||
| chr4:70744654
|
ATT | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.179-17849_179-1784 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70744654 | |||||
| chr4:70744658
|
T | A | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.179-17861T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70744658 | ||||||
| chr4:70744714
|
C | G | 68 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(65): Show | 68 | HG00323.hp2 HG00673.hp1 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.179-17805C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70744714 | ||||||
| chr4:70744901
|
C | T | 8 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(5): Show | 8 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-17618C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70744901 | ||||||
| chr4:70744947
|
G | A | 2 | a0001c0001t0003g0040a0001c0001t0003g0060 | 2 | NA18998.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.179-17572G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70744947 | ||||||
| chr4:70745023
|
C | T | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.179-17496C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70745023 | ||||||
| chr4:70745152
|
G | T | 1 | a0001c0001t0009g0240 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.179-17367G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70745152 | ||||||
| chr4:70745179
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.179-17340C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70745179 | ||||||
| chr4:70745275
|
A | G | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.179-17244A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70745275 | ||||||
| chr4:70745295
|
T | C | 1 | a0001c0001t0023g0015 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.179-17224T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70745295 | ||||||
| chr4:70745609
|
G | A | 2 | a0001c0001t0002g0162a0004c0002t0002g0154 | 2 | HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.179-16910G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70745609 | ||||||
| chr4:70745789
|
C | T | 47 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(44): Show | 47 | HG00323.hp2 HG00673.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.179-16730C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70745789 | ||||||
| chr4:70745872
|
C | G | 47 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(44): Show | 47 | HG00323.hp2 HG00673.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.179-16647C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70745872 | ||||||
| chr4:70745914
|
G | A | 26 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(23): Show | 26 | HG00323.hp2 HG01109.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.179-16605G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70745914 | ||||||
| chr4:70746019
|
A | G | 53 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(50): Show | 53 | HG00323.hp2 HG00673.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.179-16500A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70746019 | ||||||
| chr4:70746082
|
G | A | 21 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(18): Show | 21 | HG00673.hp1 HG01123.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.179-16437G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70746082 | ||||||
| chr4:70746119
|
G | A | 4 | a0001c0001t0013g0003a0001c0001t0013g0004a0001c0001t0013g0005others(1): Show | 4 | HG03209.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-16400G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70746119 | ||||||
| chr4:70746252
|
G | A | 14 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(11): Show | 14 | HG01243.hp2 HG02145.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.179-16267G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70746252 | ||||||
| chr4:70746275
|
C | T | 2 | a0001c0001t0014g0224a0001c0001t0014g0226 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.179-16244C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70746275 | ||||||
| chr4:70746290
|
G | A | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.179-16229G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70746290 | ||||||
| chr4:70746340
|
T | TA | 48 | a0001c0001t0001g0175a0001c0001t0004g0070a0001c0001t0004g0073others(45): Show | 48 | HG00323.hp2 HG00673.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.179-16162dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70746340 | |||||
| chr4:70746340
|
T | TAAA | 7 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(4): Show | 7 | HG01978.hp1 NA18942.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-16164_179-1616 others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70746340 | |||||
| chr4:70746473
|
T | C | 47 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(44): Show | 47 | HG00323.hp2 HG00673.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.179-16046T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70746473 | ||||||
| chr4:70746504
|
C | CA | 17 | a0001c0001t0003g0063a0001c0001t0004g0082a0001c0001t0005g0047others(14): Show | 17 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-15995dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70746504 | |||||
| chr4:70746504
|
CA | C | 22 | a0001c0001t0001g0135a0001c0001t0001g0176a0001c0001t0001g0207others(19): Show | 22 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.179-15995delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70746504 | |||||
| chr4:70746742
|
A | T | 1 | a0001c0001t0002g0216 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.179-15777A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70746742 | ||||||
| chr4:70746743
|
A | G | 2 | a0001c0001t0005g0065a0001c0001t0034g0223 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.179-15776A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70746743 | ||||||
| chr4:70746800
|
G | T | 1 | a0001c0001t0001g0087 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.179-15719G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70746800 | ||||||
| chr4:70746927
|
A | G | 1 | a0001c0001t0003g0026 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.179-15592A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70746927 | ||||||
| chr4:70746958
|
G | T | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.179-15561G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70746958 | ||||||
| chr4:70747404
|
G | A | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.179-15115G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70747404 | ||||||
| chr4:70747499
|
C | CA | 62 | a0001c0001t0001g0088a0001c0001t0001g0093a0001c0001t0001g0117others(59): Show | 62 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.179-15007dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70747499 | |||||
| chr4:70747499
|
C | CAA | 17 | a0001c0001t0003g0022a0001c0001t0003g0044a0001c0001t0004g0070others(14): Show | 17 | HG00673.hp1 HG01123.hp1 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.179-15008_179-1500 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70747499 | |||||
| chr4:70747558
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(246): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.179-14961C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70747558 | ||||||
| chr4:70748038
|
A | G | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.179-14481A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748038 | ||||||
| chr4:70748072
|
G | A | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.179-14447G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748072 | ||||||
| chr4:70748082
|
A | G | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.179-14437A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748082 | ||||||
| chr4:70748126
|
G | A | 2 | a0001c0001t0014g0224a0001c0001t0014g0226 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.179-14393G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748126 | ||||||
| chr4:70748252
|
A | G | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.179-14267A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748252 | ||||||
| chr4:70748405
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.179-14114A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748405 | ||||||
| chr4:70748605
|
G | C | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-13914G>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748605 | ||||||
| chr4:70748639
|
T | C | 1 | a0001c0001t0030g0172 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.179-13880T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748639 | ||||||
| chr4:70748667
|
G | C | 1 | a0004c0002t0002g0154 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.179-13852G>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748667 | ||||||
| chr4:70748686
|
C | T | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.179-13833C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748686 | ||||||
| chr4:70748784
|
G | T | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.179-13735G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748784 | ||||||
| chr4:70748863
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.179-13656G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748863 | ||||||
| chr4:70748951
|
A | G | 1 | a0001c0001t0029g0170 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.179-13568A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748951 | ||||||
| chr4:70748973
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.179-13546A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70748973 | ||||||
| chr4:70749050
|
C | T | 1 | a0001c0001t0026g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.179-13469C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70749050 | ||||||
| chr4:70749076
|
T | C | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.179-13443T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70749076 | ||||||
| chr4:70749208
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.179-13311G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70749208 | ||||||
| chr4:70749324
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.179-13195T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70749324 | ||||||
| chr4:70749338
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.179-13181G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70749338 | ||||||
| chr4:70749523
|
GT | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(161): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.179-12981delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70749523 | |||||
| chr4:70749525
|
T | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG00280.hp2 HG01952.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.179-12994T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70749525 | ||||||
| chr4:70749585
|
T | A | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.179-12934T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70749585 | ||||||
| chr4:70749653
|
T | C | 4 | a0001c0001t0010g0118a0001c0001t0015g0095a0001c0001t0015g0106others(1): Show | 4 | HG02155.hp2 NA18955.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-12866T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70749653 | ||||||
| chr4:70749657
|
C | CT | 17 | a0001c0001t0001g0103a0001c0001t0001g0113a0001c0001t0004g0083others(14): Show | 17 | HG00323.hp2 HG00673.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.179-12846dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70749657 | |||||
| chr4:70749657
|
C | CTT | 7 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(4): Show | 7 | HG02615.hp1 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-12847_179-1284 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70749657 | |||||
| chr4:70749788
|
T | C | 71 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.179-12731T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70749788 | ||||||
| chr4:70749826
|
T | C | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-12693T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70749826 | ||||||
| chr4:70749905
|
C | T | 1 | a0001c0001t0002g0090 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.179-12614C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70749905 | ||||||
| chr4:70750042
|
C | T | 3 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0036g0228 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.179-12477C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70750042 | ||||||
| chr4:70750263
|
T | C | 1 | a0001c0001t0006g0057 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.179-12256T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70750263 | ||||||
| chr4:70750493
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.179-12026C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70750493 | ||||||
| chr4:70750546
|
C | T | 3 | a0001c0001t0005g0047a0001c0001t0005g0051a0001c0001t0005g0052 | 3 | HG03195.hp2 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.179-11973C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70750546 | ||||||
| chr4:70750749
|
G | GT | 63 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(60): Show | 63 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.179-11761dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70750749 | |||||
| chr4:70750750
|
T | G | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.179-11769T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70750750 | ||||||
| chr4:70750765
|
C | T | 1 | a0001c0001t0032g0155 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.179-11754C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70750765 | ||||||
| chr4:70750914
|
G | A | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.179-11605G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70750914 | ||||||
| chr4:70751479
|
T | C | 4 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0173others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-11040T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70751479 | ||||||
| chr4:70751571
|
G | A | 1 | a0001c0001t0026g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.179-10948G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70751571 | ||||||
| chr4:70751658
|
A | T | 1 | a0001c0001t0034g0223 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.179-10861A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70751658 | ||||||
| chr4:70751972
|
G | C | 1 | a0001c0001t0004g0075 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.179-10547G>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70751972 | ||||||
| chr4:70751992
|
G | C | 1 | a0001c0001t0001g0151 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.179-10527G>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70751992 | ||||||
| chr4:70752073
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.179-10446G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70752073 | ||||||
| chr4:70752097
|
C | G | 1 | a0001c0001t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.179-10422C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70752097 | ||||||
| chr4:70752111
|
T | C | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.179-10408T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70752111 | ||||||
| chr4:70752299
|
G | T | 76 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(73): Show | 76 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.179-10220G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70752299 | ||||||
| chr4:70752308
|
T | TTG | 71 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.179-10196_179-1019 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70752308 | |||||
| chr4:70752328
|
T | G | 1 | a0001c0001t0005g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.179-10191T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70752328 | ||||||
| chr4:70752336
|
A | AT | 62 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(59): Show | 62 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.179-10177dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70752336 | |||||
| chr4:70752434
|
G | A | 71 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.179-10085G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70752434 | ||||||
| chr4:70752438
|
A | G | 34 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(31): Show | 34 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.179-10081A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70752438 | ||||||
| chr4:70752598
|
T | C | 71 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.179-9921T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70752598 | ||||||
| chr4:70752621
|
A | G | 47 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(44): Show | 47 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.179-9898A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70752621 | ||||||
| chr4:70752640
|
A | G | 112 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(109): Show | 112 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.179-9879A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70752640 | ||||||
| chr4:70752661
|
T | C | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-9858T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70752661 | ||||||
| chr4:70752817
|
T | C | 1 | a0001c0001t0002g0211 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.179-9702T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70752817 | ||||||
| chr4:70753098
|
T | A | 1 | a0001c0001t0023g0015 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.179-9421T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753098 | ||||||
| chr4:70753199
|
C | G | 1 | a0001c0001t0008g0249 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.179-9320C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753199 | ||||||
| chr4:70753244
|
T | C | 1 | a0001c0001t0008g0249 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.179-9275T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753244 | ||||||
| chr4:70753260
|
A | G | 1 | a0001c0001t0026g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.179-9259A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753260 | ||||||
| chr4:70753360
|
CAGT | C | 3 | a0001c0001t0008g0244a0001c0001t0016g0247a0001c0001t0016g0248 | 3 | HG02602.hp2 HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.179-9155_179-9153d others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70753360 | |||||
| chr4:70753450
|
G | A | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.179-9069G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753450 | ||||||
| chr4:70753517
|
G | A | 19 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(16): Show | 19 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.179-9002G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753517 | ||||||
| chr4:70753579
|
A | G | 1 | a0001c0001t0004g0083 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.179-8940A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753579 | ||||||
| chr4:70753658
|
T | C | 70 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.179-8861T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753658 | ||||||
| chr4:70753692
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0173 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.179-8827G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753692 | ||||||
| chr4:70753718
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.179-8801A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753718 | ||||||
| chr4:70753726
|
C | G | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.179-8793C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753726 | ||||||
| chr4:70753788
|
A | G | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.179-8731A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753788 | ||||||
| chr4:70753828
|
G | C | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.179-8691G>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753828 | ||||||
| chr4:70753867
|
A | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.179-8652A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753867 | ||||||
| chr4:70753890
|
G | A | 121 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(118): Show | 121 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.179-8629G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753890 | ||||||
| chr4:70753976
|
C | G | 71 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.179-8543C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70753976 | ||||||
| chr4:70754049
|
A | AT | 13 | a0001c0001t0007g0007a0001c0001t0007g0009a0001c0001t0007g0010others(10): Show | 13 | HG02145.hp1 HG02486.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-8455dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70754049 | |||||
| chr4:70754049
|
AT | A | 13 | a0001c0001t0001g0087a0001c0001t0001g0100a0001c0001t0003g0064others(10): Show | 13 | HG00323.hp2 HG01167.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-8455delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70754049 | |||||
| chr4:70754082
|
G | GT | 3 | a0001c0001t0008g0249a0001c0001t0008g0250a0001c0001t0033g0252 | 3 | HG01243.hp1 HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.179-8435dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70754082 | |||||
| chr4:70754138
|
T | C | 71 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.179-8381T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70754138 | ||||||
| chr4:70754288
|
G | A | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.179-8231G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70754288 | ||||||
| chr4:70754304
|
C | T | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.179-8215C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70754304 | ||||||
| chr4:70754528
|
AT | A | 67 | a0001c0001t0001g0112a0001c0001t0003g0013a0001c0001t0003g0017others(64): Show | 67 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.179-7976delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70754528 | |||||
| chr4:70754543
|
T | G | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.179-7976T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70754543 | ||||||
| chr4:70754565
|
G | T | 2 | a0001c0001t0005g0054a0001c0001t0005g0055 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.179-7954G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70754565 | ||||||
| chr4:70754692
|
C | T | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.179-7827C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70754692 | ||||||
| chr4:70754708
|
G | A | 7 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-7811G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70754708 | ||||||
| chr4:70754897
|
CT | C | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.179-7610delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70754897 | |||||
| chr4:70754925
|
C | T | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-7594C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70754925 | ||||||
| chr4:70755049
|
G | A | 1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.179-7470G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70755049 | ||||||
| chr4:70755092
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.179-7427C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70755092 | ||||||
| chr4:70755121
|
C | T | 1 | a0001c0001t0032g0155 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.179-7398C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70755121 | ||||||
| chr4:70755352
|
A | G | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.179-7167A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70755352 | ||||||
| chr4:70755469
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.179-7050G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70755469 | ||||||
| chr4:70755661
|
G | A | 29 | a0001c0001t0001g0105a0001c0001t0001g0206a0001c0001t0002g0096others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.179-6858G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70755661 | ||||||
| chr4:70755951
|
GA | G | 71 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.179-6555delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70755951 | |||||
| chr4:70756079
|
A | G | 1 | a0001c0001t0028g0209 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.179-6440A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70756079 | ||||||
| chr4:70756309
|
T | C | 1 | a0001c0001t0031g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.179-6210T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70756309 | ||||||
| chr4:70756358
|
C | G | 70 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.179-6161C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70756358 | ||||||
| chr4:70756476
|
C | G | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.179-6043C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70756476 | ||||||
| chr4:70756501
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-6018A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70756501 | ||||||
| chr4:70756510
|
G | A | 1 | a0001c0001t0004g0082 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.179-6009G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70756510 | ||||||
| chr4:70756526
|
G | A | 1 | a0001c0001t0021g0232 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.179-5993G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70756526 | ||||||
| chr4:70756704
|
A | G | 112 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(109): Show | 112 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.179-5815A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70756704 | ||||||
| chr4:70757113
|
T | TA | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.179-5396dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70757113 | |||||
| chr4:70757332
|
C | T | 1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.179-5187C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70757332 | ||||||
| chr4:70757368
|
G | A | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.179-5151G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70757368 | ||||||
| chr4:70757465
|
G | A | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.179-5054G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70757465 | ||||||
| chr4:70757560
|
C | T | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.179-4959C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70757560 | ||||||
| chr4:70757640
|
T | C | 1 | a0001c0001t0007g0011 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.179-4879T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70757640 | ||||||
| chr4:70758128
|
A | G | 1 | a0001c0001t0002g0190 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.179-4391A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70758128 | ||||||
| chr4:70758190
|
G | C | 1 | a0001c0001t0004g0070 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.179-4329G>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70758190 | ||||||
| chr4:70758246
|
C | T | 70 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.179-4273C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70758246 | ||||||
| chr4:70758267
|
A | G | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.179-4252A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70758267 | ||||||
| chr4:70758433
|
C | A | 2 | a0001c0001t0005g0065a0001c0001t0034g0223 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.179-4086C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70758433 | ||||||
| chr4:70758449
|
A | G | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.179-4070A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70758449 | ||||||
| chr4:70758735
|
A | T | 1 | a0001c0001t0017g0066 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.179-3784A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70758735 | ||||||
| chr4:70758739
|
TA | T | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.179-3767delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70758739 | |||||
| chr4:70758761
|
A | G | 122 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(119): Show | 122 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.179-3758A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70758761 | ||||||
| chr4:70758763
|
G | A | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.179-3756G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70758763 | ||||||
| chr4:70758898
|
G | A | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.179-3621G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70758898 | ||||||
| chr4:70758939
|
G | A | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.179-3580G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70758939 | ||||||
| chr4:70759035
|
C | CA | 72 | a0001c0001t0002g0201a0001c0001t0003g0013a0001c0001t0003g0017others(69): Show | 72 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.179-3472dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70759035 | |||||
| chr4:70759046
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.179-3473A>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70759046 | ||||||
| chr4:70759119
|
C | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.179-3400C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70759119 | ||||||
| chr4:70759203
|
C | G | 2 | a0001c0001t0013g0003a0001c0001t0013g0004 | 2 | HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.179-3316C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70759203 | ||||||
| chr4:70759331
|
G | T | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-3188G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70759331 | ||||||
| chr4:70759355
|
TTTGTGTG | T | 10 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0075others(7): Show | 10 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.179-3162_179-3156d others(9): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70759355 | |||||
| chr4:70759355
|
TTTGTGTG others(4): Show |
T | 1 | a0001c0001t0026g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.179-3162_179-3152d others(13): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70759355 | |||||
| chr4:70759356
|
T | TGTGTGTG others(6): Show |
1 | a0001c0001t0011g0229 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.179-3163_179-3162i others(15): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70759356 | ||||||
| chr4:70759366
|
GTGTGTA | G | 39 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.179-3147_179-3142d others(8): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70759366 | |||||
| chr4:70759368
|
GTGTA | G | 5 | a0001c0001t0003g0063a0001c0001t0006g0057a0001c0001t0006g0177others(2): Show | 5 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-3147_179-3144d others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70759368 | |||||
| chr4:70759370
|
GTA | G | 3 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0029g0170 | 3 | HG02559.hp1 NA18978.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.179-3147_179-3146d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70759370 | |||||
| chr4:70759372
|
A | G | 26 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(23): Show | 26 | HG00323.hp2 HG00673.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.179-3147A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70759372 | ||||||
| chr4:70759372
|
ATG | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(149): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.179-3119_179-3118d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70759372 | |||||
| chr4:70759372
|
ATGTG | A | 3 | a0001c0001t0001g0175a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG02280.hp1 HG02818.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.179-3121_179-3118d others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70759372 | |||||
| chr4:70759376
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.179-3143G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70759376 | ||||||
| chr4:70759534
|
T | C | 71 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.179-2985T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70759534 | ||||||
| chr4:70759620
|
A | G | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.179-2899A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70759620 | ||||||
| chr4:70759637
|
C | A | 5 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(2): Show | 5 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-2882C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70759637 | ||||||
| chr4:70759794
|
T | C | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-2725T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70759794 | ||||||
| chr4:70759982
|
A | ATTTC | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-2535_179-2534i others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70759982 | |||||
| chr4:70760200
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.179-2319G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760200 | ||||||
| chr4:70760336
|
A | G | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.179-2183A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760336 | ||||||
| chr4:70760363
|
C | G | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.179-2156C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760363 | ||||||
| chr4:70760420
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.179-2099G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760420 | ||||||
| chr4:70760440
|
G | A | 3 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0036g0228 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.179-2079G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760440 | ||||||
| chr4:70760452
|
C | CA | 62 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(59): Show | 62 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.179-2066dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70760452 | |||||
| chr4:70760553
|
T | TG | 7 | a0001c0001t0003g0056a0001c0001t0003g0058a0001c0001t0003g0061others(4): Show | 7 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-1966_179-1965i others(3): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760553 | ||||||
| chr4:70760553
|
TA | T | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-1965delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760553 | ||||||
| chr4:70760554
|
A | AT | 10 | a0001c0001t0001g0139a0001c0001t0001g0145a0001c0001t0002g0102others(7): Show | 10 | HG02056.hp1 HG02559.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.179-1953dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70760554 | |||||
| chr4:70760554
|
A | G | 55 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(52): Show | 55 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.179-1965A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760554 | ||||||
| chr4:70760554
|
A | T | 7 | a0001c0001t0003g0056a0001c0001t0003g0058a0001c0001t0003g0061others(4): Show | 7 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-1965A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760554 | ||||||
| chr4:70760554
|
AT | A | 5 | a0001c0001t0002g0096a0001c0001t0002g0186a0001c0001t0002g0195others(2): Show | 5 | HG00609.hp2 HG02056.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-1953delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 70760554 | |||||
| chr4:70760555
|
T | G | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-1964T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760555 | ||||||
| chr4:70760678
|
T | C | 2 | a0001c0001t0002g0128a0001c0001t0037g0161 | 2 | NA20905.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.179-1841T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760678 | ||||||
| chr4:70760695
|
T | C | 1 | a0001c0001t0014g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-1824T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760695 | ||||||
| chr4:70760855
|
A | G | 70 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.179-1664A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760855 | ||||||
| chr4:70760972
|
G | A | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.179-1547G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70760972 | ||||||
| chr4:70761616
|
A | G | 70 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.179-903A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70761616 | ||||||
| chr4:70761795
|
G | A | 1 | a0001c0001t0016g0247 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.179-724G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70761795 | ||||||
| chr4:70761797
|
G | A | 61 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(58): Show | 61 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.179-722G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70761797 | ||||||
| chr4:70761799
|
A | G | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.179-720A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70761799 | ||||||
| chr4:70762055
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.179-464C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70762055 | ||||||
| chr4:70762056
|
G | A | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.179-463G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70762056 | ||||||
| chr4:70762192
|
A | G | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.179-327A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70762192 | ||||||
| chr4:70762405
|
A | T | 1 | a0001c0001t0001g0120 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.179-114A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70762405 | ||||||
| chr4:70762456
|
A | T | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.179-63A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70762456 | ||||||
| chr4:70762515
|
G | T | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
splice_region_variant&intron_variant | LOW | c.179-4G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 1/17 | chr4 | 70762515 | ||||||
| chr4:70762745
|
C | A | 7 | a0001c0001t0001g0092a0001c0001t0001g0125a0001c0001t0001g0129others(4): Show | 7 | HG00609.hp1 HG01993.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.352+53C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 2/17 | chr4 | 70762745 | ||||||
| chr4:70762754
|
G | A | 5 | a0001c0001t0014g0222a0001c0001t0014g0224a0001c0001t0014g0225others(2): Show | 5 | HG02717.hp1 NA18522.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.352+62G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 2/17 | chr4 | 70762754 | ||||||
| chr4:70762880
|
T | C | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.352+188T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 2/17 | chr4 | 70762880 | ||||||
| chr4:70762965
|
G | A | 1 | a0001c0001t0003g0035 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.352+273G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 2/17 | chr4 | 70762965 | ||||||
| chr4:70763060
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.352+368G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 2/17 | chr4 | 70763060 | ||||||
| chr4:70763222
|
G | A | 1 | a0001c0001t0035g0251 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.353-330G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 2/17 | chr4 | 70763222 | ||||||
| chr4:70763276
|
C | T | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.353-276C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 2/17 | chr4 | 70763276 | ||||||
| chr4:70763453
|
T | C | 2 | a0001c0001t0001g0176a0002c0005t0022g0012 | 2 | HG02723.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.353-99T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 2/17 | chr4 | 70763453 | ||||||
| chr4:70763684
|
G | A | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.470+15G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 3/17 | chr4 | 70763684 | ||||||
| chr4:70763752
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.470+83G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 3/17 | chr4 | 70763752 | ||||||
| chr4:70763820
|
T | C | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.470+151T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 3/17 | chr4 | 70763820 | ||||||
| chr4:70764140
|
A | G | 8 | a0001c0001t0004g0070a0001c0001t0004g0074a0001c0001t0004g0075others(5): Show | 8 | HG00673.hp1 HG01123.hp1 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.471-335A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 3/17 | chr4 | 70764140 | ||||||
| chr4:70764341
|
G | T | 7 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.471-134G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 3/17 | chr4 | 70764341 | ||||||
| chr4:70764360
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.471-115C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 3/17 | chr4 | 70764360 | ||||||
| chr4:70764444
|
T | C | 62 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(59): Show | 62 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.471-31T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 3/17 | chr4 | 70764444 | ||||||
| chr4:70764666
|
C | G | 10 | a0001c0001t0003g0025a0001c0001t0003g0034a0001c0001t0003g0035others(7): Show | 10 | HG00408.hp1 HG00438.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.572+90C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70764666 | ||||||
| chr4:70764704
|
C | A | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.572+128C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70764704 | ||||||
| chr4:70764834
|
T | G | 1 | a0001c0001t0002g0205 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.572+258T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70764834 | ||||||
| chr4:70764908
|
G | T | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.572+332G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70764908 | ||||||
| chr4:70764924
|
G | A | 5 | a0001c0001t0014g0222a0001c0001t0014g0224a0001c0001t0014g0225others(2): Show | 5 | HG02717.hp1 NA18522.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+348G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70764924 | ||||||
| chr4:70765103
|
G | A | 1 | a0001c0001t0017g0066 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.572+527G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70765103 | ||||||
| chr4:70765187
|
C | CA | 10 | a0001c0001t0001g0139a0001c0001t0003g0013a0001c0001t0003g0046others(7): Show | 10 | HG02056.hp1 HG02074.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.572+629dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765187 | |||||
| chr4:70765204
|
A | ATGTGTGT others(22): Show |
1 | a0001c0001t0006g0177 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.572+628_572+629ins others(29): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70765204 | ||||||
| chr4:70765205
|
A | G | 1 | a0001c0001t0034g0223 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.572+629A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70765205 | ||||||
| chr4:70765205
|
AT | A | 3 | a0001c0001t0002g0190a0001c0001t0010g0196a0001c0001t0010g0203 | 3 | HG00741.hp2 HG02074.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.572+630delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70765205 | ||||||
| chr4:70765206
|
T | A | 1 | a0001c0001t0008g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.572+630T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70765206 | ||||||
| chr4:70765207
|
G | A | 4 | a0001c0001t0002g0190a0001c0001t0006g0177a0001c0001t0010g0196others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.572+631G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70765207 | ||||||
| chr4:70765209
|
G | A | 2 | a0001c0001t0002g0218a0001c0001t0006g0177 | 2 | HG01257.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.572+633G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70765209 | ||||||
| chr4:70765209
|
G | GTA | 25 | a0001c0001t0001g0105a0001c0001t0001g0117a0001c0001t0001g0123others(22): Show | 25 | HG00408.hp2 HG01167.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.572+649_572+650dup others(2): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765209 | |||||
| chr4:70765209
|
G | GTATATAT others(1): Show |
3 | a0001c0001t0004g0070a0001c0001t0004g0075a0001c0001t0004g0085 | 3 | HG00673.hp1 HG01123.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.572+643_572+650dup others(8): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765209 | |||||
| chr4:70765209
|
G | GTGTATAT others(57): Show |
1 | a0001c0001t0036g0228 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.572+634_572+635ins others(64): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765209 | |||||
| chr4:70765209
|
G | GTGTATAT others(73): Show |
2 | a0001c0001t0011g0229a0001c0001t0011g0230 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.572+634_572+635ins others(80): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765209 | |||||
| chr4:70765209
|
G | GTGTGTAT others(3): Show |
6 | a0001c0001t0011g0227a0001c0001t0011g0231a0001c0001t0011g0233others(3): Show | 6 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+634_572+635ins others(10): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765209 | |||||
| chr4:70765209
|
G | GTGTGTAT others(5): Show |
10 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0001t0004g0076others(7): Show | 10 | HG03654.hp2 HG03710.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.572+634_572+635ins others(12): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765209 | |||||
| chr4:70765209
|
G | GTGTGTAT others(23): Show |
34 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.572+634_572+635ins others(30): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765209 | |||||
| chr4:70765209
|
G | GTGTGTAT others(25): Show |
8 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0041others(5): Show | 8 | HG00673.hp2 HG02083.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.572+634_572+635ins others(32): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765209 | |||||
| chr4:70765209
|
G | GTGTGTAT others(27): Show |
1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.572+634_572+635ins others(34): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765209 | |||||
| chr4:70765209
|
G | GTGTGTAT others(55): Show |
1 | a0005c0006t0012g0029 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.572+634_572+635ins others(62): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765209 | |||||
| chr4:70765209
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0004g0084 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.572+634_572+635ins others(12): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765209 | |||||
| chr4:70765209
|
GTA | G | 22 | a0001c0001t0002g0096a0001c0001t0002g0180a0001c0001t0002g0182others(19): Show | 22 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.572+649_572+650del others(2): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765209 | |||||
| chr4:70765211
|
A | G | 3 | a0001c0001t0002g0190a0001c0001t0010g0196a0001c0001t0010g0203 | 3 | HG00741.hp2 HG02074.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.572+635A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70765211 | ||||||
| chr4:70765213
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0034g0223 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.572+647_572+648ins others(32): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765213 | |||||
| chr4:70765385
|
A | G | 71 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.572+809A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70765385 | ||||||
| chr4:70765481
|
G | A | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.572+905G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70765481 | ||||||
| chr4:70765654
|
G | T | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.572+1078G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70765654 | ||||||
| chr4:70765758
|
C | CT | 36 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(33): Show | 37 | HG00280.hp1 HG00323.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.572+1198dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765758 | |||||
| chr4:70765758
|
C | CTT | 43 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(40): Show | 43 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.572+1197_572+1198d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70765758 | |||||
| chr4:70766027
|
C | T | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.572+1451C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70766027 | ||||||
| chr4:70766303
|
G | A | 2 | a0001c0001t0007g0068a0001c0001t0007g0069 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.572+1727G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70766303 | ||||||
| chr4:70766369
|
C | T | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.572+1793C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70766369 | ||||||
| chr4:70766381
|
A | G | 16 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(13): Show | 16 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.572+1805A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70766381 | ||||||
| chr4:70766550
|
C | G | 122 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(119): Show | 122 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.572+1974C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70766550 | ||||||
| chr4:70766576
|
A | G | 1 | a0001c0001t0018g0149 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.573-1962A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70766576 | ||||||
| chr4:70766650
|
C | T | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.573-1888C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70766650 | ||||||
| chr4:70766706
|
T | C | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.573-1832T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70766706 | ||||||
| chr4:70766812
|
T | C | 1 | a0001c0001t0017g0067 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.573-1726T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70766812 | ||||||
| chr4:70766938
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.573-1600A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70766938 | ||||||
| chr4:70767086
|
C | CT | 47 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(44): Show | 47 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.573-1443dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70767086 | |||||
| chr4:70767162
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.573-1376C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767162 | ||||||
| chr4:70767259
|
A | AT | 29 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0137others(26): Show | 29 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.573-1249dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70767259 | |||||
| chr4:70767259
|
A | ATT | 7 | a0001c0001t0001g0119a0001c0001t0001g0164a0001c0001t0005g0054others(4): Show | 7 | HG02572.hp1 HG02630.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.573-1250_573-1249d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70767259 | |||||
| chr4:70767259
|
A | ATTT | 5 | a0001c0001t0014g0222a0001c0001t0014g0224a0001c0001t0014g0225others(2): Show | 5 | HG02717.hp1 NA18522.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.573-1251_573-1249d others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70767259 | |||||
| chr4:70767259
|
AT | A | 11 | a0001c0001t0001g0093a0001c0001t0001g0109a0001c0001t0001g0138others(8): Show | 11 | HG00438.hp2 HG01070.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.573-1249delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70767259 | |||||
| chr4:70767259
|
ATTTTTT | A | 12 | a0001c0001t0003g0056a0001c0001t0003g0061a0001c0001t0006g0057others(9): Show | 12 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.573-1254_573-1249d others(8): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70767259 | |||||
| chr4:70767259
|
ATTTTTTT | A | 52 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0019others(49): Show | 52 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.573-1255_573-1249d others(9): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70767259 | |||||
| chr4:70767259
|
ATTTTTTT others(6): Show |
A | 2 | a0001c0001t0002g0211a0001c0001t0002g0217 | 2 | NA18992.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.573-1261_573-1249d others(15): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70767259 | |||||
| chr4:70767289
|
T | C | 2 | a0001c0001t0005g0065a0001c0001t0034g0223 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.573-1249T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767289 | ||||||
| chr4:70767341
|
C | G | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.573-1197C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767341 | ||||||
| chr4:70767356
|
C | T | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.573-1182C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767356 | ||||||
| chr4:70767363
|
A | G | 112 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(109): Show | 112 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.573-1175A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767363 | ||||||
| chr4:70767402
|
G | T | 71 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.573-1136G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767402 | ||||||
| chr4:70767406
|
G | A | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.573-1132G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767406 | ||||||
| chr4:70767522
|
T | C | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.573-1016T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767522 | ||||||
| chr4:70767525
|
A | T | 2 | a0001c0001t0005g0065a0001c0001t0034g0223 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.573-1013A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767525 | ||||||
| chr4:70767576
|
A | G | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.573-962A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767576 | ||||||
| chr4:70767685
|
A | AT | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.573-842dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70767685 | |||||
| chr4:70767713
|
C | T | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.573-825C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767713 | ||||||
| chr4:70767835
|
C | T | 10 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0120others(7): Show | 10 | HG00408.hp2 HG00438.hp2 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.573-703C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767835 | ||||||
| chr4:70767910
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0027g0116 | 2 | HG01070.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.573-628C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70767910 | ||||||
| chr4:70768066
|
C | A | 1 | a0001c0001t0003g0030 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.573-472C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70768066 | ||||||
| chr4:70768082
|
G | A | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.573-456G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70768082 | ||||||
| chr4:70768136
|
C | T | 46 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(43): Show | 46 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.573-402C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70768136 | ||||||
| chr4:70768153
|
G | T | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.573-385G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70768153 | ||||||
| chr4:70768224
|
C | G | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.573-314C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70768224 | ||||||
| chr4:70768397
|
G | GT | 15 | a0001c0001t0001g0107a0001c0001t0004g0070a0001c0001t0004g0073others(12): Show | 15 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(12): Show |
intron_variant | MODIFIER | c.573-131dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 70768397 | |||||
| chr4:70768426
|
T | G | 1 | a0001c0001t0002g0192 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.573-112T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 4/17 | chr4 | 70768426 | ||||||
| chr4:70768860
|
T | C | 71 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.696+199T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70768860 | ||||||
| chr4:70768866
|
C | T | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.696+205C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70768866 | ||||||
| chr4:70769164
|
T | G | 1 | a0001c0001t0003g0060 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.696+503T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70769164 | ||||||
| chr4:70769578
|
T | A | 1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.696+917T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70769578 | ||||||
| chr4:70769615
|
T | C | 62 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(59): Show | 62 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.696+954T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70769615 | ||||||
| chr4:70769638
|
C | T | 2 | a0001c0001t0006g0177a0001c0001t0006g0178 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.696+977C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70769638 | ||||||
| chr4:70769653
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG00639.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.696+992C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70769653 | ||||||
| chr4:70769698
|
T | A | 1 | a0001c0001t0008g0249 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.696+1037T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70769698 | ||||||
| chr4:70769753
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.696+1092C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70769753 | ||||||
| chr4:70769792
|
T | C | 112 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(109): Show | 112 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.696+1131T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70769792 | ||||||
| chr4:70769857
|
G | A | 2 | a0001c0001t0008g0235a0001c0001t0008g0246 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.696+1196G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70769857 | ||||||
| chr4:70769969
|
GCAC | G | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.696+1315_696+1317d others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr4 | 70769969 | |||||
| chr4:70769982
|
T | C | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.696+1321T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70769982 | ||||||
| chr4:70769986
|
T | C | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.696+1325T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70769986 | ||||||
| chr4:70769996
|
A | G | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.696+1335A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70769996 | ||||||
| chr4:70770014
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.696+1353G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70770014 | ||||||
| chr4:70770097
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.696+1436C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70770097 | ||||||
| chr4:70770322
|
G | A | 2 | a0001c0001t0005g0065a0001c0001t0034g0223 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.696+1661G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70770322 | ||||||
| chr4:70770405
|
A | T | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.696+1744A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70770405 | ||||||
| chr4:70770433
|
A | C | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.696+1772A>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70770433 | ||||||
| chr4:70770460
|
A | G | 70 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.696+1799A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70770460 | ||||||
| chr4:70770888
|
C | T | 1 | a0001c0001t0013g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.696+2227C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70770888 | ||||||
| chr4:70770902
|
T | A | 1 | a0001c0001t0003g0027 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.696+2241T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70770902 | ||||||
| chr4:70770916
|
T | C | 35 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(32): Show | 35 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.696+2255T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70770916 | ||||||
| chr4:70770935
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.696+2274G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70770935 | ||||||
| chr4:70770987
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.696+2326C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70770987 | ||||||
| chr4:70771021
|
T | C | 1 | a0001c0001t0035g0251 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.696+2360T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771021 | ||||||
| chr4:70771176
|
C | T | 1 | a0001c0001t0031g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.697-2335C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771176 | ||||||
| chr4:70771189
|
G | A | 1 | a0001c0001t0035g0251 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.697-2322G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771189 | ||||||
| chr4:70771313
|
T | C | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.697-2198T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771313 | ||||||
| chr4:70771346
|
T | A | 3 | a0001c0001t0008g0241a0001c0001t0008g0242a0001c0001t0039g0024 | 3 | HG02622.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.697-2165T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771346 | ||||||
| chr4:70771384
|
A | G | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.697-2127A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771384 | ||||||
| chr4:70771521
|
G | A | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.697-1990G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771521 | ||||||
| chr4:70771580
|
G | A | 1 | a0001c0001t0009g0236 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.697-1931G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771580 | ||||||
| chr4:70771641
|
T | C | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.697-1870T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771641 | ||||||
| chr4:70771652
|
C | G | 1 | a0001c0001t0033g0252 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.697-1859C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771652 | ||||||
| chr4:70771656
|
A | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.697-1855A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771656 | ||||||
| chr4:70771821
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.697-1690C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771821 | ||||||
| chr4:70771822
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.697-1689G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771822 | ||||||
| chr4:70771891
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 6 | HG00280.hp1 HG01258.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-1620T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771891 | ||||||
| chr4:70771992
|
A | G | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.697-1519A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70771992 | ||||||
| chr4:70772006
|
G | T | 43 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(40): Show | 43 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.697-1505G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70772006 | ||||||
| chr4:70772066
|
T | G | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.697-1445T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70772066 | ||||||
| chr4:70772159
|
T | C | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.697-1352T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70772159 | ||||||
| chr4:70772367
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.697-1144G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70772367 | ||||||
| chr4:70772934
|
T | C | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.697-577T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70772934 | ||||||
| chr4:70772942
|
A | T | 70 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.697-569A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70772942 | ||||||
| chr4:70772956
|
C | T | 3 | a0001c0001t0008g0241a0001c0001t0008g0242a0001c0001t0039g0024 | 3 | HG02622.hp1 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.697-555C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70772956 | ||||||
| chr4:70773122
|
T | C | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.697-389T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70773122 | ||||||
| chr4:70773238
|
A | G | 2 | a0001c0001t0005g0065a0001c0001t0034g0223 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.697-273A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70773238 | ||||||
| chr4:70773294
|
T | C | 1 | a0001c0001t0005g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.697-217T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70773294 | ||||||
| chr4:70773391
|
G | A | 1 | a0001c0001t0034g0223 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.697-120G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70773391 | ||||||
| chr4:70773491
|
C | G | 61 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(58): Show | 61 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.697-20C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 5/17 | chr4 | 70773491 | ||||||
| chr4:70773581
|
A | G | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.758+9A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70773581 | ||||||
| chr4:70773632
|
G | A | 112 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(109): Show | 112 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.758+60G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70773632 | ||||||
| chr4:70773695
|
G | T | 1 | a0001c0001t0028g0209 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.758+123G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70773695 | ||||||
| chr4:70773930
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.758+358T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70773930 | ||||||
| chr4:70773985
|
T | G | 1 | a0001c0001t0015g0095 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.758+413T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70773985 | ||||||
| chr4:70774002
|
G | A | 1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.758+430G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774002 | ||||||
| chr4:70774021
|
T | A | 72 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(69): Show | 72 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.758+449T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774021 | ||||||
| chr4:70774131
|
G | A | 1 | a0001c0003t0002g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.758+559G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774131 | ||||||
| chr4:70774202
|
G | T | 1 | a0001c0001t0002g0160 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.758+630G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774202 | ||||||
| chr4:70774453
|
C | CA | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.759-702dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774453 | |||||
| chr4:70774564
|
G | A | 1 | a0001c0001t0002g0159 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.759-604G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774564 | ||||||
| chr4:70774614
|
C | CA | 12 | a0001c0001t0001g0179a0001c0001t0002g0163a0001c0001t0002g0216others(9): Show | 12 | HG01109.hp2 HG01167.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.759-523dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774614 | |||||
| chr4:70774614
|
C | CAA | 7 | a0001c0001t0001g0139a0001c0001t0002g0097a0001c0001t0002g0159others(4): Show | 7 | HG00597.hp2 HG01169.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.759-524_759-523dup others(2): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774614 | |||||
| chr4:70774614
|
CA | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0094others(37): Show | 41 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.759-523delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774614 | |||||
| chr4:70774630
|
A | T | 1 | a0001c0001t0004g0076 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.759-538A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774630 | ||||||
| chr4:70774632
|
A | T | 1 | a0001c0001t0004g0076 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.759-536A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774632 | ||||||
| chr4:70774634
|
A | T | 2 | a0001c0001t0004g0076a0001c0001t0004g0083 | 2 | HG03942.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.759-534A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774634 | ||||||
| chr4:70774636
|
A | T | 3 | a0001c0001t0004g0073a0001c0001t0004g0076a0001c0001t0004g0083 | 3 | HG03942.hp1 NA18995.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.759-532A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774636 | ||||||
| chr4:70774638
|
A | T | 15 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0075others(12): Show | 15 | HG00673.hp1 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.759-530A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774638 | ||||||
| chr4:70774638
|
AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0013g0003a0001c0001t0013g0004 | 2 | HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.759-528_759-519del others(10): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774638 | |||||
| chr4:70774638
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0013g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.759-528_759-517del others(12): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774638 | |||||
| chr4:70774639
|
AAAAAAAT others(4): Show |
A | 1 | a0001c0001t0013g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.759-527_759-517del others(11): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774639 | |||||
| chr4:70774640
|
A | T | 17 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0075others(14): Show | 17 | HG00673.hp1 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.759-528A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774640 | ||||||
| chr4:70774641
|
AAAAATAT others(2): Show |
A | 5 | a0001c0001t0011g0227a0001c0001t0011g0231a0001c0001t0011g0233others(2): Show | 5 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.759-525_759-517del others(9): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774641 | |||||
| chr4:70774642
|
A | AATATATA others(5): Show |
1 | a0001c0001t0003g0040 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.759-525_759-524ins others(12): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774642 | |||||
| chr4:70774642
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0060 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.759-526_759-525ins others(13): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774642 | ||||||
| chr4:70774642
|
A | T | 21 | a0001c0001t0001g0215a0001c0001t0002g0099a0001c0001t0004g0070others(18): Show | 21 | HG00673.hp1 HG01123.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.759-526A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774642 | ||||||
| chr4:70774643
|
A | T | 1 | a0001c0001t0002g0201 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.759-525A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774643 | ||||||
| chr4:70774644
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0008g0249 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.759-523_759-522ins others(37): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0033g0252 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.759-523_759-522ins others(35): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0008g0241 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.759-523_759-522ins others(34): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0008g0246 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.759-523_759-522ins others(26): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0008g0235 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.759-523_759-522ins others(25): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0008g0242 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.759-523_759-522ins others(22): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0039g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.759-523_759-522ins others(30): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0003g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.759-523_759-522ins others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAAATA others(3): Show |
3 | a0001c0001t0017g0066a0001c0001t0017g0067a0002c0005t0022g0012 | 3 | HG01167.hp2 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.759-523_759-522ins others(10): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAAATA others(7): Show |
2 | a0001c0001t0003g0025a0001c0001t0012g0062 | 2 | NA19009.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.759-523_759-522ins others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAAATA others(13): Show |
1 | a0001c0001t0025g0016 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.759-523_759-522ins others(20): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAATAT others(4): Show |
1 | a0001c0001t0009g0240 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.759-523_759-522ins others(11): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAATAT others(6): Show |
5 | a0001c0001t0003g0034a0001c0001t0003g0037a0001c0001t0003g0046others(2): Show | 5 | HG00438.hp1 NA18968.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.759-523_759-522ins others(13): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAATAT others(8): Show |
1 | a0001c0001t0012g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.759-523_759-522ins others(15): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAAATAT others(12): Show |
1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.759-523_759-522ins others(19): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0009g0239 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.759-523_759-522ins others(10): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAAATATA others(5): Show |
4 | a0001c0001t0003g0020a0001c0001t0003g0026a0001c0001t0003g0041others(1): Show | 4 | HG02083.hp1 NA18979.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.759-523_759-522ins others(12): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAATATAT others(6): Show |
3 | a0001c0001t0003g0022a0001c0001t0003g0028a0001c0001t0003g0035 | 3 | HG00408.hp1 NA18978.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.759-523_759-522ins others(13): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAATATAT others(8): Show |
2 | a0001c0001t0003g0030a0001c0001t0003g0038 | 2 | HG02132.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.759-523_759-522ins others(15): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AAT | 7 | a0001c0001t0001g0113a0001c0001t0001g0143a0001c0001t0002g0128others(4): Show | 7 | HG01978.hp1 HG02071.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.759-498_759-497dup others(2): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AATATATA others(3): Show |
3 | a0001c0001t0009g0238a0001c0001t0009g0245a0001c0001t0020g0237 | 3 | HG02818.hp2 HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.759-506_759-497dup others(10): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AATATATA others(5): Show |
10 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(7): Show | 10 | HG01258.hp1 HG01993.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.759-508_759-497dup others(12): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774644
|
A | AT | 14 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0093others(11): Show | 14 | HG00735.hp2 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.759-524_759-523ins others(1): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774644 | ||||||
| chr4:70774644
|
A | ATAT | 4 | a0001c0001t0001g0089a0001c0001t0001g0207a0001c0001t0002g0186others(1): Show | 4 | HG02080.hp2 HG02129.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-524_759-523ins others(3): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774644 | ||||||
| chr4:70774644
|
A | ATATATAT others(4): Show |
3 | a0001c0001t0003g0042a0001c0001t0003g0056a0001c0001t0006g0177 | 3 | HG01257.hp2 HG01975.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.759-524_759-523ins others(11): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774644 | ||||||
| chr4:70774644
|
A | T | 51 | a0001c0001t0001g0103a0001c0001t0001g0112a0001c0001t0001g0125others(48): Show | 51 | HG00609.hp1 HG00609.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.759-524A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774644 | ||||||
| chr4:70774644
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0006g0057 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.759-506_759-497del others(10): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774644 | |||||
| chr4:70774645
|
AT | A | 14 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0166others(11): Show | 14 | HG02258.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.759-522delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774645 | ||||||
| chr4:70774646
|
T | A | 7 | a0001c0001t0001g0139a0001c0001t0002g0216a0001c0001t0006g0169others(4): Show | 7 | HG02056.hp1 HG02080.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.759-522T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774646 | ||||||
| chr4:70774648
|
T | A | 5 | a0001c0001t0001g0134a0001c0001t0005g0047a0001c0001t0007g0068others(2): Show | 5 | HG01517.hp2 HG02559.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.759-520T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774648 | ||||||
| chr4:70774650
|
T | A | 1 | a0001c0001t0014g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.759-518T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774650 | ||||||
| chr4:70774652
|
T | A | 1 | a0001c0001t0014g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.759-516T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774652 | ||||||
| chr4:70774654
|
T | A | 1 | a0001c0001t0014g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.759-514T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774654 | ||||||
| chr4:70774656
|
T | A | 2 | a0001c0001t0006g0057a0001c0001t0014g0225 | 2 | HG00597.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.759-512T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774656 | ||||||
| chr4:70774670
|
T | A | 12 | a0001c0001t0001g0140a0001c0001t0003g0013a0001c0001t0003g0020others(9): Show | 12 | HG03017.hp1 HG03654.hp2 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.759-498T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70774670 | ||||||
| chr4:70774670
|
T | TAA | 4 | a0001c0001t0004g0073a0001c0001t0004g0082a0001c0001t0004g0084others(1): Show | 4 | HG01123.hp1 HG03710.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.759-495_759-494dup others(2): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774670 | |||||
| chr4:70774670
|
T | TATAA | 3 | a0001c0001t0004g0075a0001c0001t0004g0078a0001c0001t0004g0080 | 3 | HG00673.hp1 HG03831.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.759-497_759-496ins others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774670 | |||||
| chr4:70774670
|
T | TATATATA others(3): Show |
1 | a0001c0001t0003g0059 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.759-497_759-496ins others(10): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774670 | |||||
| chr4:70774670
|
T | TATATATA others(5): Show |
6 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0043others(3): Show | 6 | HG00673.hp2 HG02015.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.759-497_759-496ins others(12): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774670 | |||||
| chr4:70774670
|
T | TATATATA others(7): Show |
4 | a0001c0001t0003g0027a0001c0001t0003g0031a0001c0001t0003g0064others(1): Show | 4 | HG02155.hp1 HG03927.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.759-497_759-496ins others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 70774670 | |||||
| chr4:70775033
|
T | C | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.759-135T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 6/17 | chr4 | 70775033 | ||||||
| chr4:70775303
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.824+70G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70775303 | ||||||
| chr4:70775435
|
A | G | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.824+202A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70775435 | ||||||
| chr4:70775499
|
TTAAA | T | 3 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0036g0228 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.824+269_824+272del others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 70775499 | |||||
| chr4:70775688
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.824+455G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70775688 | ||||||
| chr4:70775802
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.824+569C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70775802 | ||||||
| chr4:70775864
|
C | T | 7 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(4): Show | 7 | HG02615.hp1 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.824+631C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70775864 | ||||||
| chr4:70775940
|
T | TAAACAAA others(7): Show |
4 | a0001c0001t0003g0044a0001c0001t0004g0078a0001c0001t0006g0150others(1): Show | 4 | HG02723.hp1 NA18950.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.824+712_824+725dup others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 70775940 | |||||
| chr4:70775944
|
C | CA | 118 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.824+724dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 70775944 | |||||
| chr4:70775944
|
C | CAA | 17 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0130others(14): Show | 17 | HG00408.hp2 HG02738.hp1 HG02738.hp2 others(14): Show |
intron_variant | MODIFIER | c.824+723_824+724dup others(2): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 70775944 | |||||
| chr4:70775944
|
C | CAAAAAAA others(6): Show |
8 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(5): Show | 8 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.824+712_824+724dup others(13): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 70775944 | |||||
| chr4:70775944
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0011g0233a0001c0001t0026g0081 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.824+724_824+725ins others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 70775944 | |||||
| chr4:70775945
|
A | AAAAAAAA others(7): Show |
3 | a0001c0001t0009g0236a0001c0001t0019g0220a0001c0001t0019g0221 | 3 | HG01891.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.824+724_824+725ins others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 70775945 | |||||
| chr4:70775945
|
A | AAAAAAAA others(6): Show |
57 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(54): Show | 57 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.824+713_824+725dup others(13): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 70775945 | |||||
| chr4:70775946
|
A | AAAAAAAA others(7): Show |
3 | a0001c0001t0007g0010a0001c0001t0008g0246a0001c0001t0014g0224 | 3 | HG02145.hp2 HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.824+724_824+725ins others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 70775946 | |||||
| chr4:70775946
|
A | AAAAAAAA others(6): Show |
33 | a0001c0001t0005g0071a0001c0001t0005g0072a0001c0001t0007g0007others(30): Show | 33 | HG01167.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.824+724_824+725ins others(13): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 70775946 | |||||
| chr4:70775946
|
A | AAAAAAAA others(6): Show |
2 | a0001c0001t0013g0005a0001c0001t0013g0006 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.824+722_824+723ins others(13): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 70775946 | |||||
| chr4:70775959
|
G | A | 1 | a0001c0001t0003g0020 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.824+726G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70775959 | ||||||
| chr4:70775961
|
A | G | 6 | a0001c0001t0011g0227a0001c0001t0011g0231a0001c0001t0011g0233others(3): Show | 6 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.824+728A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70775961 | ||||||
| chr4:70776010
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.824+777A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776010 | ||||||
| chr4:70776052
|
A | G | 16 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(13): Show | 16 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.824+819A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776052 | ||||||
| chr4:70776131
|
C | G | 1 | a0001c0001t0023g0015 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.824+898C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776131 | ||||||
| chr4:70776224
|
A | G | 2 | a0001c0001t0005g0065a0001c0001t0034g0223 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.824+991A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776224 | ||||||
| chr4:70776314
|
C | T | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.824+1081C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776314 | ||||||
| chr4:70776340
|
T | C | 74 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(71): Show | 74 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.824+1107T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776340 | ||||||
| chr4:70776443
|
A | G | 5 | a0001c0001t0011g0227a0001c0001t0011g0231a0001c0001t0011g0233others(2): Show | 5 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.824+1210A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776443 | ||||||
| chr4:70776488
|
A | G | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.824+1255A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776488 | ||||||
| chr4:70776504
|
G | A | 1 | a0001c0001t0034g0223 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.824+1271G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776504 | ||||||
| chr4:70776517
|
A | G | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.824+1284A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776517 | ||||||
| chr4:70776566
|
A | G | 2 | a0001c0001t0005g0054a0001c0001t0005g0055 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.824+1333A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776566 | ||||||
| chr4:70776627
|
T | C | 1 | a0001c0001t0018g0122 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.824+1394T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776627 | ||||||
| chr4:70776774
|
TCAAAA | T | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.824+1562_824+1566d others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 70776774 | |||||
| chr4:70776895
|
C | T | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.825-1474C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776895 | ||||||
| chr4:70776964
|
G | A | 1 | a0001c0001t0017g0067 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.825-1405G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70776964 | ||||||
| chr4:70777130
|
T | C | 1 | a0001c0001t0026g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.825-1239T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70777130 | ||||||
| chr4:70777304
|
T | C | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.825-1065T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70777304 | ||||||
| chr4:70777653
|
A | G | 1 | a0001c0001t0008g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.825-716A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70777653 | ||||||
| chr4:70777692
|
G | A | 45 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(42): Show | 45 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.825-677G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70777692 | ||||||
| chr4:70777895
|
A | G | 1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.825-474A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70777895 | ||||||
| chr4:70777992
|
G | T | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.825-377G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70777992 | ||||||
| chr4:70778265
|
A | G | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.825-104A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70778265 | ||||||
| chr4:70778361
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | splice_region_variant&intron_variant | LOW | c.825-8T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 7/17 | chr4 | 70778361 | ||||||
| chr4:70778454
|
G | T | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.894+16G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70778454 | ||||||
| chr4:70778525
|
G | A | 5 | a0001c0001t0014g0222a0001c0001t0014g0224a0001c0001t0014g0225others(2): Show | 5 | HG02717.hp1 NA18522.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+87G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70778525 | ||||||
| chr4:70778573
|
C | CT | 37 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(34): Show | 37 | HG00735.hp2 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.894+158dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 70778573 | |||||
| chr4:70778573
|
C | CTTT | 7 | a0001c0001t0011g0227a0001c0001t0011g0230a0001c0001t0011g0231others(4): Show | 7 | HG00323.hp2 HG01517.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.894+156_894+158dup others(3): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 70778573 | |||||
| chr4:70778573
|
CT | C | 5 | a0001c0001t0001g0140a0001c0001t0002g0219a0001c0001t0005g0048others(2): Show | 5 | HG03017.hp1 HG03130.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+158delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 70778573 | |||||
| chr4:70778573
|
CTTTTTTT others(2): Show |
C | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.894+150_894+158del others(9): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 70778573 | |||||
| chr4:70778657
|
G | A | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.894+219G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70778657 | ||||||
| chr4:70778738
|
C | T | 28 | a0001c0001t0002g0096a0001c0001t0002g0180a0001c0001t0002g0182others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.894+300C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70778738 | ||||||
| chr4:70778753
|
T | A | 1 | a0001c0001t0002g0186 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.894+315T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70778753 | ||||||
| chr4:70778900
|
A | G | 15 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(12): Show | 15 | HG01243.hp2 HG02145.hp2 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.894+462A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70778900 | ||||||
| chr4:70778942
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.894+504A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70778942 | ||||||
| chr4:70779102
|
A | T | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.894+664A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70779102 | ||||||
| chr4:70779146
|
A | G | 3 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0036g0228 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.894+708A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70779146 | ||||||
| chr4:70779493
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.894+1055T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70779493 | ||||||
| chr4:70779669
|
G | A | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.894+1231G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70779669 | ||||||
| chr4:70779675
|
C | T | 1 | a0001c0001t0002g0184 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.894+1237C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70779675 | ||||||
| chr4:70779744
|
G | A | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.894+1306G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70779744 | ||||||
| chr4:70779920
|
T | G | 1 | a0001c0001t0018g0122 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.894+1482T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70779920 | ||||||
| chr4:70779994
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.894+1556A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70779994 | ||||||
| chr4:70779998
|
T | C | 3 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0036g0228 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.894+1560T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70779998 | ||||||
| chr4:70780153
|
T | C | 2 | a0001c0001t0002g0162a0004c0002t0002g0154 | 2 | HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.894+1715T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70780153 | ||||||
| chr4:70780248
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.894+1810C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70780248 | ||||||
| chr4:70780293
|
G | GT | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.894+1861dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 70780293 | |||||
| chr4:70780334
|
C | A | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.894+1896C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70780334 | ||||||
| chr4:70780430
|
A | C | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.894+1992A>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70780430 | ||||||
| chr4:70780439
|
A | G | 1 | a0001c0001t0010g0193 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.894+2001A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70780439 | ||||||
| chr4:70780462
|
A | T | 112 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(109): Show | 112 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.894+2024A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70780462 | ||||||
| chr4:70780482
|
A | G | 1 | a0001c0001t0029g0170 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.894+2044A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70780482 | ||||||
| chr4:70780537
|
C | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.894+2099C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70780537 | ||||||
| chr4:70780615
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.894+2177G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70780615 | ||||||
| chr4:70780866
|
G | A | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.895-2225G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70780866 | ||||||
| chr4:70780987
|
T | C | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.895-2104T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70780987 | ||||||
| chr4:70781016
|
A | G | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.895-2075A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70781016 | ||||||
| chr4:70781084
|
C | CA | 66 | a0001c0001t0001g0113a0001c0001t0003g0013a0001c0001t0003g0017others(63): Show | 66 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.895-1993dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 70781084 | |||||
| chr4:70781101
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.895-1990G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70781101 | ||||||
| chr4:70781192
|
T | C | 2 | a0001c0001t0001g0093a0001c0001t0027g0116 | 2 | HG01070.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.895-1899T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70781192 | ||||||
| chr4:70781234
|
C | T | 1 | a0001c0001t0008g0250 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.895-1857C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70781234 | ||||||
| chr4:70781339
|
C | G | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.895-1752C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70781339 | ||||||
| chr4:70781437
|
C | T | 1 | a0001c0001t0004g0077 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.895-1654C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70781437 | ||||||
| chr4:70781518
|
G | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.895-1573G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70781518 | ||||||
| chr4:70781568
|
T | G | 3 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0036g0228 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.895-1523T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70781568 | ||||||
| chr4:70781585
|
A | G | 3 | a0001c0001t0006g0091a0001c0001t0006g0153a0001c0001t0006g0169 | 3 | HG02809.hp1 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.895-1506A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70781585 | ||||||
| chr4:70781860
|
A | G | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.895-1231A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70781860 | ||||||
| chr4:70781961
|
T | C | 74 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(71): Show | 74 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.895-1130T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70781961 | ||||||
| chr4:70782291
|
C | CT | 7 | a0001c0001t0001g0136a0001c0001t0002g0002a0001c0001t0002g0157others(4): Show | 8 | HG00323.hp2 HG02622.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.895-784dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 70782291 | |||||
| chr4:70782291
|
C | CTT | 8 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(5): Show | 8 | HG01515.hp2 HG01517.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.895-785_895-784dup others(2): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 70782291 | |||||
| chr4:70782340
|
G | A | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.895-751G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70782340 | ||||||
| chr4:70782439
|
T | C | 74 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(71): Show | 74 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.895-652T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70782439 | ||||||
| chr4:70782449
|
T | C | 1 | a0001c0001t0002g0219 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.895-642T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70782449 | ||||||
| chr4:70782526
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.895-565G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70782526 | ||||||
| chr4:70782530
|
G | T | 1 | a0001c0001t0020g0237 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.895-561G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70782530 | ||||||
| chr4:70782571
|
C | T | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.895-520C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70782571 | ||||||
| chr4:70782667
|
C | A | 1 | a0001c0001t0004g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.895-424C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70782667 | ||||||
| chr4:70782679
|
G | A | 3 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0036g0228 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.895-412G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70782679 | ||||||
| chr4:70782694
|
C | G | 2 | a0001c0001t0016g0247a0001c0001t0016g0248 | 2 | HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.895-397C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 8/17 | chr4 | 70782694 | ||||||
| chr4:70783294
|
T | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.987+111T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 9/17 | chr4 | 70783294 | ||||||
| chr4:70783295
|
TTTTATTT others(10): Show |
T | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.987+113_987+129del others(17): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 9/17 | chr4 | 70783295 | ||||||
| chr4:70783313
|
C | A | 1 | a0001c0001t0016g0247 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.987+130C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 9/17 | chr4 | 70783313 | ||||||
| chr4:70783722
|
AT | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.987+541delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 70783722 | |||||
| chr4:70783820
|
T | C | 1 | a0001c0001t0014g0222 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.987+637T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 9/17 | chr4 | 70783820 | ||||||
| chr4:70784023
|
A | G | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.988-773A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 9/17 | chr4 | 70784023 | ||||||
| chr4:70784174
|
G | A | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.988-622G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 9/17 | chr4 | 70784174 | ||||||
| chr4:70784208
|
G | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-588G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 9/17 | chr4 | 70784208 | ||||||
| chr4:70784222
|
G | A | 7 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.988-574G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 9/17 | chr4 | 70784222 | ||||||
| chr4:70784273
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.988-523G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 9/17 | chr4 | 70784273 | ||||||
| chr4:70784281
|
G | A | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.988-515G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 9/17 | chr4 | 70784281 | ||||||
| chr4:70784667
|
T | A | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.988-129T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 9/17 | chr4 | 70784667 | ||||||
| chr4:70785052
|
A | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0129 | 2 | HG02132.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1071+173A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70785052 | ||||||
| chr4:70785182
|
C | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1071+303C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70785182 | ||||||
| chr4:70785206
|
A | G | 1 | a0001c0001t0004g0073 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1071+327A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70785206 | ||||||
| chr4:70785388
|
T | C | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1071+509T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70785388 | ||||||
| chr4:70785674
|
C | CAA | 58 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(55): Show | 58 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1071+807_1071+808d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70785674 | |||||
| chr4:70785689
|
C | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+810C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70785689 | ||||||
| chr4:70785695
|
G | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+816G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70785695 | ||||||
| chr4:70785752
|
C | A | 1 | a0001c0001t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1071+873C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70785752 | ||||||
| chr4:70785852
|
A | G | 7 | a0001c0001t0009g0236a0001c0001t0009g0238a0001c0001t0009g0239others(4): Show | 7 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1071+973A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70785852 | ||||||
| chr4:70785889
|
C | T | 1 | a0001c0001t0018g0122 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1071+1010C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70785889 | ||||||
| chr4:70785929
|
T | C | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1071+1050T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70785929 | ||||||
| chr4:70786138
|
G | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+1259G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70786138 | ||||||
| chr4:70786258
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1071+1379A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70786258 | ||||||
| chr4:70786385
|
GT | G | 110 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(107): Show | 110 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1071+1517delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70786385 | |||||
| chr4:70786564
|
C | CACAA | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+1687_1071+169 others(8): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70786564 | |||||
| chr4:70786625
|
A | G | 2 | a0001c0001t0002g0211a0001c0001t0002g0217 | 2 | NA18992.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1071+1746A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70786625 | ||||||
| chr4:70786638
|
C | G | 2 | a0001c0001t0002g0211a0001c0001t0002g0217 | 2 | NA18992.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1071+1759C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70786638 | ||||||
| chr4:70786715
|
C | G | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+1836C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70786715 | ||||||
| chr4:70786720
|
C | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+1841C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70786720 | ||||||
| chr4:70786741
|
G | A | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1071+1862G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70786741 | ||||||
| chr4:70786988
|
T | C | 2 | a0001c0001t0005g0054a0001c0001t0005g0055 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1072-1818T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70786988 | ||||||
| chr4:70787025
|
C | A | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1072-1781C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787025 | ||||||
| chr4:70787158
|
C | A | 1 | a0001c0001t0023g0015 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1072-1648C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787158 | ||||||
| chr4:70787168
|
G | GA | 9 | a0001c0001t0001g0164a0001c0001t0002g0002a0001c0001t0002g0187others(6): Show | 10 | HG00323.hp1 HG01169.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1072-1618dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787168 | |||||
| chr4:70787168
|
G | GAAAAAAA others(3): Show |
2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1072-1627_1072-161 others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787168 | |||||
| chr4:70787168
|
GA | G | 13 | a0001c0001t0001g0119a0001c0001t0002g0099a0001c0001t0002g0128others(10): Show | 13 | HG00597.hp2 HG01167.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1072-1618delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787168 | |||||
| chr4:70787168
|
GAA | G | 11 | a0001c0001t0001g0114a0001c0001t0001g0207a0001c0001t0001g0208others(8): Show | 11 | HG00639.hp1 HG01978.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.1072-1619_1072-161 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787168 | |||||
| chr4:70787168
|
GAAA | G | 6 | a0001c0001t0013g0003a0001c0001t0013g0004a0001c0001t0014g0222others(3): Show | 6 | HG02717.hp1 HG03540.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.1072-1620_1072-161 others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787168 | |||||
| chr4:70787183
|
A | T | 4 | a0001c0001t0003g0013a0001c0001t0003g0033a0001c0001t0006g0144others(1): Show | 4 | HG00673.hp2 HG02015.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1072-1623A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787183 | ||||||
| chr4:70787185
|
A | AT | 5 | a0001c0001t0003g0022a0001c0001t0003g0034a0001c0001t0003g0056others(2): Show | 5 | HG01975.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072-1621_1072-162 others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787185 | ||||||
| chr4:70787185
|
A | T | 33 | a0001c0001t0003g0013a0001c0001t0003g0020a0001c0001t0003g0025others(30): Show | 33 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1072-1621A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787185 | ||||||
| chr4:70787187
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0019g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1072-1618_1072-161 others(30): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787187 | |||||
| chr4:70787187
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0019g0220 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1072-1618_1072-161 others(34): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787187 | |||||
| chr4:70787187
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0023g0015 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1072-1618_1072-161 others(17): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787187 | |||||
| chr4:70787187
|
A | AT | 9 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158others(6): Show | 9 | HG00323.hp2 HG01952.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1072-1619_1072-161 others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787187 | ||||||
| chr4:70787187
|
A | T | 53 | a0001c0001t0001g0110a0001c0001t0002g0098a0001c0001t0002g0160others(50): Show | 53 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1072-1619A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787187 | ||||||
| chr4:70787187
|
AAT | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(73): Show | 77 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1072-1593_1072-159 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787187 | |||||
| chr4:70787187
|
AATAT | A | 15 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0008g0241others(12): Show | 15 | HG02258.hp2 HG02602.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1072-1595_1072-159 others(8): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787187 | |||||
| chr4:70787187
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0001g0117 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1072-1601_1072-159 others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787187 | |||||
| chr4:70787188
|
AT | A | 15 | a0001c0001t0001g0107a0001c0001t0001g0136a0001c0001t0001g0139others(12): Show | 15 | HG01884.hp1 HG02056.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1072-1617delT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787188 | ||||||
| chr4:70787188
|
ATAT | A | 6 | a0001c0001t0001g0166a0001c0001t0005g0050a0001c0001t0005g0054others(3): Show | 6 | HG02630.hp2 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1072-1617_1072-161 others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787188 | ||||||
| chr4:70787189
|
T | A | 19 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0164others(16): Show | 19 | HG00673.hp1 HG00741.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1072-1617T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787189 | ||||||
| chr4:70787191
|
T | A | 48 | a0001c0001t0001g0133a0001c0001t0002g0096a0001c0001t0002g0102others(45): Show | 48 | HG00140.hp1 HG00609.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.1072-1615T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787191 | ||||||
| chr4:70787193
|
T | A | 33 | a0001c0001t0002g0102a0001c0001t0004g0070a0001c0001t0004g0073others(30): Show | 33 | HG00673.hp1 HG01123.hp1 HG02602.hp2 others(30): Show |
intron_variant | MODIFIER | c.1072-1613T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787193 | ||||||
| chr4:70787195
|
T | A | 5 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0080others(2): Show | 5 | HG02630.hp2 HG03710.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072-1611T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787195 | ||||||
| chr4:70787207
|
T | C | 1 | a0001c0001t0008g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1072-1599T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787207 | ||||||
| chr4:70787211
|
TATA | T | 9 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0077others(6): Show | 9 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(6): Show |
intron_variant | MODIFIER | c.1072-1593_1072-159 others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787211 | |||||
| chr4:70787213
|
TA | T | 45 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(42): Show | 45 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1072-1588delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787213 | |||||
| chr4:70787213
|
TAA | T | 4 | a0001c0001t0001g0127a0001c0001t0001g0173a0001c0001t0002g0182others(1): Show | 4 | HG02976.hp2 NA18956.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1072-1589_1072-158 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787213 | |||||
| chr4:70787214
|
A | AT | 11 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0044others(8): Show | 11 | HG00597.hp1 HG01891.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.1072-1592_1072-159 others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787214 | ||||||
| chr4:70787214
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1072-1592_1072-159 others(17): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787214 | ||||||
| chr4:70787214
|
A | ATATATAT others(10): Show |
1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1072-1592_1072-159 others(21): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787214 | ||||||
| chr4:70787215
|
A | T | 4 | a0001c0001t0001g0140a0001c0001t0002g0099a0001c0001t0002g0157others(1): Show | 4 | HG01978.hp1 HG02896.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1072-1591A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787215 | ||||||
| chr4:70787260
|
G | GT | 10 | a0001c0001t0001g0139a0001c0001t0002g0102a0001c0001t0004g0077others(7): Show | 10 | HG01167.hp2 HG01891.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1072-1531dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70787260 | |||||
| chr4:70787338
|
A | C | 1 | a0001c0001t0032g0155 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1072-1468A>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787338 | ||||||
| chr4:70787695
|
T | C | 1 | a0001c0001t0023g0015 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1072-1111T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787695 | ||||||
| chr4:70787764
|
G | T | 2 | a0001c0001t0003g0064a0005c0006t0012g0029 | 2 | NA18956.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1072-1042G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787764 | ||||||
| chr4:70787810
|
A | G | 3 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0036g0228 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1072-996A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70787810 | ||||||
| chr4:70788058
|
G | A | 1 | a0001c0001t0035g0251 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1072-748G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70788058 | ||||||
| chr4:70788082
|
C | CA | 251 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(248): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1072-723dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70788082 | |||||
| chr4:70788099
|
C | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1072-707C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70788099 | ||||||
| chr4:70788152
|
G | A | 2 | a0001c0001t0011g0231a0001c0001t0011g0234 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1072-654G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70788152 | ||||||
| chr4:70788155
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1072-651T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70788155 | ||||||
| chr4:70788217
|
G | A | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.1072-589G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70788217 | ||||||
| chr4:70788242
|
G | A | 1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1072-564G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70788242 | ||||||
| chr4:70788284
|
C | CA | 15 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0123others(12): Show | 15 | HG00323.hp2 HG00408.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1072-506dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70788284 | |||||
| chr4:70788284
|
C | CAA | 59 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(56): Show | 59 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1072-507_1072-506d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70788284 | |||||
| chr4:70788284
|
CA | C | 36 | a0001c0001t0002g0211a0001c0001t0007g0007a0001c0001t0007g0008others(33): Show | 36 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.1072-506delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 70788284 | |||||
| chr4:70788307
|
C | A | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1072-499C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70788307 | ||||||
| chr4:70788321
|
A | G | 1 | a0001c0001t0003g0035 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1072-485A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70788321 | ||||||
| chr4:70788504
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1072-302G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70788504 | ||||||
| chr4:70788557
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(247): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1072-249A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70788557 | ||||||
| chr4:70788608
|
T | A | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1072-198T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70788608 | ||||||
| chr4:70788711
|
C | T | 1 | a0001c0001t0006g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1072-95C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 10/17 | chr4 | 70788711 | ||||||
| chr4:70788979
|
G | A | 1 | a0001c0001t0010g0196 | 1 | HG04115.hp2 | splice_region_variant&intron_variant | LOW | c.1239+6G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 11/17 | chr4 | 70788979 | ||||||
| chr4:70789114
|
A | G | 1 | a0001c0001t0034g0223 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1239+141A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 11/17 | chr4 | 70789114 | ||||||
| chr4:70789161
|
A | T | 3 | a0001c0001t0002g0098a0001c0001t0002g0156a0001c0001t0002g0158 | 3 | HG01070.hp1 HG01952.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1239+188A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 11/17 | chr4 | 70789161 | ||||||
| chr4:70789283
|
A | G | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1240-212A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 11/17 | chr4 | 70789283 | ||||||
| chr4:70789314
|
C | A | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1240-181C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 11/17 | chr4 | 70789314 | ||||||
| chr4:70789677
|
A | T | 45 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(42): Show | 45 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1337+85A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70789677 | ||||||
| chr4:70789682
|
A | G | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1337+90A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70789682 | ||||||
| chr4:70789722
|
A | G | 1 | a0001c0001t0002g0205 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1337+130A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70789722 | ||||||
| chr4:70789739
|
T | TA | 3 | a0001c0001t0011g0231a0001c0001t0011g0234a0001c0001t0021g0232 | 3 | HG01891.hp1 HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1337+148dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr4 | 70789739 | |||||
| chr4:70789934
|
T | A | 2 | a0001c0001t0002g0180a0001c0001t0010g0203 | 2 | HG02074.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1337+342T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70789934 | ||||||
| chr4:70790287
|
T | C | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1337+695T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70790287 | ||||||
| chr4:70790321
|
T | G | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1337+729T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70790321 | ||||||
| chr4:70790370
|
C | T | 5 | a0001c0001t0014g0222a0001c0001t0014g0224a0001c0001t0014g0225others(2): Show | 5 | HG02717.hp1 NA18522.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1337+778C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70790370 | ||||||
| chr4:70790480
|
A | G | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1337+888A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70790480 | ||||||
| chr4:70790501
|
G | A | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1337+909G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70790501 | ||||||
| chr4:70790501
|
G | T | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1337+909G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70790501 | ||||||
| chr4:70790542
|
C | A | 1 | a0001c0001t0015g0121 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1337+950C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70790542 | ||||||
| chr4:70790624
|
T | C | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1337+1032T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70790624 | ||||||
| chr4:70790678
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1337+1086T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70790678 | ||||||
| chr4:70790947
|
G | A | 1 | a0001c0001t0023g0015 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1337+1355G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70790947 | ||||||
| chr4:70791039
|
T | C | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1337+1447T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70791039 | ||||||
| chr4:70791099
|
CAGAAAG | C | 8 | a0001c0001t0002g0211a0001c0001t0002g0213a0001c0001t0002g0214others(5): Show | 8 | HG03239.hp1 HG03834.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1337+1512_1337+151 others(10): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr4 | 70791099 | |||||
| chr4:70791107
|
G | T | 8 | a0001c0001t0002g0211a0001c0001t0002g0213a0001c0001t0002g0214others(5): Show | 8 | HG03239.hp1 HG03834.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1337+1515G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70791107 | ||||||
| chr4:70791112
|
A | C | 8 | a0001c0001t0002g0211a0001c0001t0002g0213a0001c0001t0002g0214others(5): Show | 8 | HG03239.hp1 HG03834.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1337+1520A>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70791112 | ||||||
| chr4:70791114
|
G | A | 8 | a0001c0001t0002g0211a0001c0001t0002g0213a0001c0001t0002g0214others(5): Show | 8 | HG03239.hp1 HG03834.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1337+1522G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70791114 | ||||||
| chr4:70791116
|
C | A | 8 | a0001c0001t0002g0211a0001c0001t0002g0213a0001c0001t0002g0214others(5): Show | 8 | HG03239.hp1 HG03834.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1337+1524C>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70791116 | ||||||
| chr4:70791117
|
TTA | T | 8 | a0001c0001t0002g0211a0001c0001t0002g0213a0001c0001t0002g0214others(5): Show | 8 | HG03239.hp1 HG03834.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1337+1527_1337+152 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr4 | 70791117 | |||||
| chr4:70791120
|
T | A | 8 | a0001c0001t0002g0211a0001c0001t0002g0213a0001c0001t0002g0214others(5): Show | 8 | HG03239.hp1 HG03834.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1337+1528T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70791120 | ||||||
| chr4:70791170
|
G | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1337+1578G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70791170 | ||||||
| chr4:70791473
|
T | G | 6 | a0001c0001t0003g0056a0001c0001t0003g0058a0001c0001t0003g0061others(3): Show | 6 | HG00597.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1337+1881T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70791473 | ||||||
| chr4:70791474
|
T | C | 1 | a0001c0001t0027g0116 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1337+1882T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70791474 | ||||||
| chr4:70791624
|
A | G | 4 | a0001c0001t0002g0096a0001c0001t0002g0186a0001c0001t0002g0195others(1): Show | 4 | HG00609.hp2 HG02056.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1337+2032A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70791624 | ||||||
| chr4:70791934
|
G | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1338-1851G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70791934 | ||||||
| chr4:70792055
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(246): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1338-1730G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70792055 | ||||||
| chr4:70792143
|
C | T | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1338-1642C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70792143 | ||||||
| chr4:70792172
|
T | A | 7 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1338-1613T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70792172 | ||||||
| chr4:70792351
|
A | G | 1 | a0001c0001t0003g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1338-1434A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70792351 | ||||||
| chr4:70792396
|
T | TAC | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1338-1388_1338-138 others(6): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr4 | 70792396 | |||||
| chr4:70792589
|
G | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1338-1196G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70792589 | ||||||
| chr4:70792691
|
ATCTTT | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1338-1092_1338-108 others(9): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr4 | 70792691 | |||||
| chr4:70792967
|
T | C | 34 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(31): Show | 34 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1338-818T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70792967 | ||||||
| chr4:70793086
|
G | T | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1338-699G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70793086 | ||||||
| chr4:70793118
|
G | A | 2 | a0001c0001t0002g0211a0001c0001t0002g0217 | 2 | NA18992.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1338-667G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70793118 | ||||||
| chr4:70793387
|
A | T | 1 | a0001c0001t0004g0070 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1338-398A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 12/17 | chr4 | 70793387 | ||||||
| chr4:70793917
|
T | C | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1457+13T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 13/17 | chr4 | 70793917 | ||||||
| chr4:70794030
|
T | C | 1 | a0001c0001t0003g0038 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1457+126T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 13/17 | chr4 | 70794030 | ||||||
| chr4:70794044
|
G | T | 1 | a0001c0001t0026g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1457+140G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 13/17 | chr4 | 70794044 | ||||||
| chr4:70794051
|
G | A | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1457+147G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 13/17 | chr4 | 70794051 | ||||||
| chr4:70794095
|
A | G | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1457+191A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 13/17 | chr4 | 70794095 | ||||||
| chr4:70794186
|
C | T | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1457+282C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 13/17 | chr4 | 70794186 | ||||||
| chr4:70794245
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1457+341T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 13/17 | chr4 | 70794245 | ||||||
| chr4:70794253
|
A | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1457+349A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 13/17 | chr4 | 70794253 | ||||||
| chr4:70794633
|
C | CT | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1458-160dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr4 | 70794633 | |||||
| chr4:70794692
|
A | G | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1458-103A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 13/17 | chr4 | 70794692 | ||||||
| chr4:70794758
|
C | T | 1 | a0001c0001t0005g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1458-37C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 13/17 | chr4 | 70794758 | ||||||
| chr4:70795277
|
A | G | 1 | a0001c0001t0013g0006 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1557+383A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70795277 | ||||||
| chr4:70795344
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1557+450C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70795344 | ||||||
| chr4:70795358
|
C | T | 3 | a0001c0001t0017g0066a0001c0001t0017g0067a0001c0001t0023g0015 | 3 | HG01167.hp2 HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1557+464C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70795358 | ||||||
| chr4:70795434
|
A | G | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1557+540A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70795434 | ||||||
| chr4:70795435
|
T | C | 7 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(4): Show | 7 | HG02615.hp1 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1557+541T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70795435 | ||||||
| chr4:70795473
|
G | A | 1 | a0001c0001t0007g0007 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1557+579G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70795473 | ||||||
| chr4:70795878
|
A | G | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1557+984A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70795878 | ||||||
| chr4:70796088
|
A | G | 1 | a0001c0001t0033g0252 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1557+1194A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70796088 | ||||||
| chr4:70796362
|
C | G | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1557+1468C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70796362 | ||||||
| chr4:70796422
|
C | T | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1557+1528C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70796422 | ||||||
| chr4:70796497
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1557+1603A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70796497 | ||||||
| chr4:70796762
|
G | T | 3 | a0001c0001t0008g0249a0001c0001t0008g0250a0001c0001t0033g0252 | 3 | HG01243.hp1 HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1557+1868G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70796762 | ||||||
| chr4:70796926
|
TTTTTCTT others(3): Show |
T | 6 | a0001c0001t0011g0227a0001c0001t0011g0231a0001c0001t0011g0233others(3): Show | 6 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1557+2047_1557+205 others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 70796926 | |||||
| chr4:70796941
|
CTTTTCTT others(3): Show |
C | 3 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0036g0228 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1557+2052_1557+206 others(14): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 70796941 | |||||
| chr4:70796951
|
T | C | 8 | a0001c0001t0002g0211a0001c0001t0002g0213a0001c0001t0002g0214others(5): Show | 8 | HG03239.hp1 HG03834.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1557+2057T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70796951 | ||||||
| chr4:70797025
|
C | T | 2 | a0001c0001t0004g0076a0001c0001t0004g0080 | 2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1557+2131C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70797025 | ||||||
| chr4:70797225
|
G | A | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.1557+2331G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70797225 | ||||||
| chr4:70797269
|
A | T | 1 | a0001c0001t0005g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1557+2375A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70797269 | ||||||
| chr4:70797354
|
A | G | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1557+2460A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70797354 | ||||||
| chr4:70797488
|
A | G | 1 | a0001c0001t0006g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1557+2594A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70797488 | ||||||
| chr4:70797625
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0111 | 2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1558-2516A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70797625 | ||||||
| chr4:70797628
|
A | T | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1558-2513A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70797628 | ||||||
| chr4:70797695
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1558-2446A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70797695 | ||||||
| chr4:70797700
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1558-2441G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70797700 | ||||||
| chr4:70797720
|
A | G | 109 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(106): Show | 109 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1558-2421A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70797720 | ||||||
| chr4:70797861
|
T | TA | 7 | a0001c0001t0009g0236a0001c0001t0009g0238a0001c0001t0009g0239others(4): Show | 7 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-2271dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 70797861 | |||||
| chr4:70797864
|
A | T | 1 | a0001c0001t0008g0249 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1558-2277A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70797864 | ||||||
| chr4:70798046
|
A | T | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG02258.hp2 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1558-2095A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70798046 | ||||||
| chr4:70798226
|
C | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0123others(3): Show | 6 | HG00408.hp2 NA18941.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-1915C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70798226 | ||||||
| chr4:70798371
|
A | AAAAC | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1558-1762_1558-175 others(8): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 70798371 | |||||
| chr4:70798430
|
C | T | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1558-1711C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70798430 | ||||||
| chr4:70798511
|
C | T | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558-1630C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70798511 | ||||||
| chr4:70798518
|
C | T | 5 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(2): Show | 5 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-1623C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70798518 | ||||||
| chr4:70798563
|
C | T | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1558-1578C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70798563 | ||||||
| chr4:70798764
|
C | T | 2 | a0001c0001t0002g0189a0001c0001t0002g0190 | 2 | HG00140.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1558-1377C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70798764 | ||||||
| chr4:70798959
|
G | A | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1558-1182G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70798959 | ||||||
| chr4:70799025
|
A | G | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1558-1116A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799025 | ||||||
| chr4:70799094
|
G | A | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1558-1047G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799094 | ||||||
| chr4:70799144
|
CA | C | 8 | a0001c0001t0001g0087a0001c0001t0011g0227a0001c0001t0011g0231others(5): Show | 8 | HG01167.hp2 HG01891.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1558-980delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 70799144 | |||||
| chr4:70799243
|
G | T | 1 | a0001c0001t0035g0251 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1558-898G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799243 | ||||||
| chr4:70799289
|
C | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1558-852C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799289 | ||||||
| chr4:70799297
|
T | C | 1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1558-844T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799297 | ||||||
| chr4:70799319
|
A | C | 113 | a0001c0001t0001g0110a0001c0001t0003g0013a0001c0001t0003g0017others(110): Show | 113 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1558-822A>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799319 | ||||||
| chr4:70799401
|
A | G | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1558-740A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799401 | ||||||
| chr4:70799420
|
A | T | 1 | a0001c0001t0003g0042 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1558-721A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799420 | ||||||
| chr4:70799557
|
G | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-584G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799557 | ||||||
| chr4:70799618
|
C | T | 2 | a0001c0001t0003g0064a0005c0006t0012g0029 | 2 | NA18956.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1558-523C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799618 | ||||||
| chr4:70799629
|
G | T | 59 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(56): Show | 59 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1558-512G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799629 | ||||||
| chr4:70799654
|
A | G | 1 | a0001c0001t0008g0249 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1558-487A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799654 | ||||||
| chr4:70799749
|
A | T | 1 | a0001c0001t0008g0249 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1558-392A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799749 | ||||||
| chr4:70799939
|
A | G | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-202A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799939 | ||||||
| chr4:70799962
|
A | G | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1558-179A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 14/17 | chr4 | 70799962 | ||||||
| chr4:70800427
|
C | G | 28 | a0001c0001t0002g0090a0001c0001t0002g0096a0001c0001t0002g0180others(25): Show | 28 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1622+222C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70800427 | ||||||
| chr4:70800504
|
C | T | 1 | a0003c0004t0038g0014 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1622+299C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70800504 | ||||||
| chr4:70800563
|
A | G | 1 | a0001c0001t0003g0013 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1622+358A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70800563 | ||||||
| chr4:70800609
|
C | T | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1622+404C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70800609 | ||||||
| chr4:70800628
|
A | G | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1622+423A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70800628 | ||||||
| chr4:70800847
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1622+642A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70800847 | ||||||
| chr4:70800908
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1622+703A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70800908 | ||||||
| chr4:70800935
|
T | C | 9 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(6): Show | 9 | HG02615.hp1 HG02630.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622+730T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70800935 | ||||||
| chr4:70801149
|
C | T | 4 | a0001c0001t0013g0003a0001c0001t0013g0004a0001c0001t0013g0005others(1): Show | 4 | HG03209.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622+944C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70801149 | ||||||
| chr4:70801163
|
CA | C | 61 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(58): Show | 61 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1622+976delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 70801163 | |||||
| chr4:70801163
|
CAA | C | 10 | a0001c0001t0004g0073a0001c0001t0011g0227a0001c0001t0011g0229others(7): Show | 10 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.1622+975_1622+976d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 70801163 | |||||
| chr4:70801185
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1622+980G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70801185 | ||||||
| chr4:70801241
|
T | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1622+1036T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70801241 | ||||||
| chr4:70801282
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1622+1077A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70801282 | ||||||
| chr4:70801288
|
C | T | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1622+1083C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70801288 | ||||||
| chr4:70801295
|
C | CATA | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1622+1092_1622+109 others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 70801295 | |||||
| chr4:70801394
|
G | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1622+1189G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70801394 | ||||||
| chr4:70801401
|
A | G | 1 | a0001c0001t0002g0213 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1622+1196A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70801401 | ||||||
| chr4:70801499
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1622+1294C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70801499 | ||||||
| chr4:70801615
|
G | A | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1623-1341G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70801615 | ||||||
| chr4:70801881
|
C | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1623-1075C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70801881 | ||||||
| chr4:70802029
|
T | C | 1 | a0002c0005t0022g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1623-927T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70802029 | ||||||
| chr4:70802215
|
C | G | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1623-741C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70802215 | ||||||
| chr4:70802246
|
A | T | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1623-710A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70802246 | ||||||
| chr4:70802685
|
A | G | 2 | a0001c0001t0017g0066a0001c0001t0017g0067 | 2 | HG01167.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1623-271A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70802685 | ||||||
| chr4:70802710
|
T | G | 1 | a0001c0001t0005g0050 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1623-246T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70802710 | ||||||
| chr4:70802854
|
T | A | 14 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(11): Show | 14 | HG00673.hp1 HG01123.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.1623-102T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | chr4 | 70802854 | ||||||
| chr4:70802866
|
ATGTT | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1623-86_1623-83del others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 70802866 | |||||
| chr4:70803020
|
A | T | 1 | a0001c0001t0002g0128 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1650+37A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | chr4 | 70803020 | ||||||
| chr4:70803032
|
G | C | 3 | a0001c0001t0011g0229a0001c0001t0011g0230a0001c0001t0036g0228 | 3 | HG00323.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1650+49G>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | chr4 | 70803032 | ||||||
| chr4:70803040
|
G | A | 5 | a0001c0001t0011g0227a0001c0001t0011g0231a0001c0001t0011g0233others(2): Show | 5 | HG01891.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650+57G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | chr4 | 70803040 | ||||||
| chr4:70803257
|
T | G | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1650+274T>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | chr4 | 70803257 | ||||||
| chr4:70803453
|
C | CT | 5 | a0001c0001t0008g0249a0001c0001t0008g0250a0001c0001t0017g0066others(2): Show | 5 | HG01167.hp2 HG01243.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650+483dupT | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr4 | 70803453 | |||||
| chr4:70803453
|
C | CTT | 69 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1650+482_1650+483d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr4 | 70803453 | |||||
| chr4:70803645
|
C | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0157 | 3 | HG02622.hp2 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1650+662C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | chr4 | 70803645 | ||||||
| chr4:70803670
|
C | T | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1651-678C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | chr4 | 70803670 | ||||||
| chr4:70803867
|
C | T | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1651-481C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | chr4 | 70803867 | ||||||
| chr4:70803897
|
TTTA | T | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1651-450_1651-448d others(5): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | chr4 | 70803897 | ||||||
| chr4:70803900
|
AAT | A | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1651-439_1651-438d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr4 | 70803900 | |||||
| chr4:70803902
|
T | A | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1651-446T>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | chr4 | 70803902 | ||||||
| chr4:70803909
|
A | T | 4 | a0001c0001t0013g0003a0001c0001t0013g0004a0001c0001t0013g0005others(1): Show | 4 | HG03209.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1651-439A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | chr4 | 70803909 | ||||||
| chr4:70804029
|
C | G | 18 | a0001c0001t0008g0235a0001c0001t0008g0241a0001c0001t0008g0242others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1651-319C>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | chr4 | 70804029 | ||||||
| chr4:70804198
|
A | T | 2 | a0001c0001t0019g0220a0001c0001t0019g0221 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1651-150A>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 16/17 | chr4 | 70804198 | ||||||
| chr4:70804438
|
C | T | 16 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(13): Show | 16 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1719+22C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | chr4 | 70804438 | ||||||
| chr4:70804644
|
G | A | 7 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0009others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1719+228G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | chr4 | 70804644 | ||||||
| chr4:70804761
|
C | CA | 19 | a0001c0001t0001g0139a0001c0001t0001g0176a0001c0001t0002g0183others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.1719+366dupA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 70804761 | |||||
| chr4:70804761
|
C | CAA | 21 | a0001c0001t0004g0070a0001c0001t0004g0073a0001c0001t0004g0074others(18): Show | 21 | HG00673.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1719+365_1719+366d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 70804761 | |||||
| chr4:70804761
|
CA | C | 18 | a0001c0001t0001g0104a0001c0001t0001g0135a0001c0001t0002g0102others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1719+366delA | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 70804761 | |||||
| chr4:70804761
|
CAA | C | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1719+365_1719+366d others(4): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 70804761 | |||||
| chr4:70804761
|
CAAAAA | C | 44 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 44 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1719+362_1719+366d others(7): Show |
RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 70804761 | |||||
| chr4:70804791
|
C | T | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1719+375C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | chr4 | 70804791 | ||||||
| chr4:70805140
|
A | G | 60 | a0001c0001t0003g0013a0001c0001t0003g0017a0001c0001t0003g0018others(57): Show | 60 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1719+724A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | chr4 | 70805140 | ||||||
| chr4:70805244
|
T | C | 5 | a0001c0001t0014g0222a0001c0001t0014g0224a0001c0001t0014g0225others(2): Show | 5 | HG02717.hp1 NA18522.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1719+828T>C | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | chr4 | 70805244 | ||||||
| chr4:70805306
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1719+890C>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | chr4 | 70805306 | ||||||
| chr4:70805601
|
G | T | 9 | a0001c0001t0011g0227a0001c0001t0011g0229a0001c0001t0011g0230others(6): Show | 9 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720-915G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | chr4 | 70805601 | ||||||
| chr4:70805788
|
G | T | 2 | a0001c0001t0005g0071a0001c0001t0005g0072 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1720-728G>T | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | chr4 | 70805788 | ||||||
| chr4:70806184
|
G | A | 1 | a0001c0001t0026g0081 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1720-332G>A | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | chr4 | 70806184 | ||||||
| chr4:70806241
|
A | G | 1 | a0001c0001t0003g0022 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1720-275A>G | RUFY3 | ENSG00000018189.13 | transcript | ENST00000381006.8 | protein_coding | 17/17 | chr4 | 70806241 |